PMID-sentid Pub_year Sent_text comp_official_name comp_offset protein_name organism prot_offset 7285344-3 1981 10% BCl3:2-chloroethanol is used to derivatize 0.1 ml of urine after evaporation to dryness or lyophilization. Ethylene Chlorohydrin 9-24 BCL3 transcription coactivator Homo sapiens 4-8 3132521-1 1988 A method for preparing glycerophosphoesters from ether phospholipids by dealkylation with boron trichloride (BCl3) is described. glycerophosphoesters 23-43 BCL3 transcription coactivator Homo sapiens 109-113 3132521-1 1988 A method for preparing glycerophosphoesters from ether phospholipids by dealkylation with boron trichloride (BCl3) is described. Phospholipid Ethers 49-68 BCL3 transcription coactivator Homo sapiens 109-113 3132521-1 1988 A method for preparing glycerophosphoesters from ether phospholipids by dealkylation with boron trichloride (BCl3) is described. boron trichloride 90-107 BCL3 transcription coactivator Homo sapiens 109-113 3132521-2 1988 Treatment of ether phospholipids in chloroform with BCl3 for 30 min at room temperature yielded almost quantitatively the corresponding glycerophosphoesters retaining the intact polar head group of the ether phospholipids. Phospholipid Ethers 13-32 BCL3 transcription coactivator Homo sapiens 52-56 3132521-2 1988 Treatment of ether phospholipids in chloroform with BCl3 for 30 min at room temperature yielded almost quantitatively the corresponding glycerophosphoesters retaining the intact polar head group of the ether phospholipids. Chloroform 36-46 BCL3 transcription coactivator Homo sapiens 52-56 3132521-2 1988 Treatment of ether phospholipids in chloroform with BCl3 for 30 min at room temperature yielded almost quantitatively the corresponding glycerophosphoesters retaining the intact polar head group of the ether phospholipids. glycerophosphoesters 136-156 BCL3 transcription coactivator Homo sapiens 52-56 3132521-2 1988 Treatment of ether phospholipids in chloroform with BCl3 for 30 min at room temperature yielded almost quantitatively the corresponding glycerophosphoesters retaining the intact polar head group of the ether phospholipids. Phospholipid Ethers 202-221 BCL3 transcription coactivator Homo sapiens 52-56 3132521-4 1988 BCl3 also cleaved diacyl, alkyl-acyl, and alk-1-enyl-acyl forms of phospholipids to yield corresponding glycerophosphoesters. Phospholipids 67-80 BCL3 transcription coactivator Homo sapiens 0-4 3132521-4 1988 BCl3 also cleaved diacyl, alkyl-acyl, and alk-1-enyl-acyl forms of phospholipids to yield corresponding glycerophosphoesters. glycerophosphoesters 104-124 BCL3 transcription coactivator Homo sapiens 0-4 1244102-3 1975 Carboxylic acid groups have been methylated with BCl3-methanol and phenolic and amine groups have been acylated to pentafluoropropionyl derivatives. Carboxylic Acids 0-15 BCL3 transcription coactivator Homo sapiens 49-53 19684679-0 1978 Heterogeneous condensation of BCl(3) in the presence of CO(2) laser irradiation. co(2) 56-61 BCL3 transcription coactivator Homo sapiens 30-36 1244102-3 1975 Carboxylic acid groups have been methylated with BCl3-methanol and phenolic and amine groups have been acylated to pentafluoropropionyl derivatives. Methanol 54-62 BCL3 transcription coactivator Homo sapiens 49-53 1244102-3 1975 Carboxylic acid groups have been methylated with BCl3-methanol and phenolic and amine groups have been acylated to pentafluoropropionyl derivatives. pentafluoropropionyl derivatives 115-147 BCL3 transcription coactivator Homo sapiens 49-53 33725086-6 2021 This is in contrast to thiazole directed indole borylation with BCl3 where the C7 borylated isomer is the kinetic product too. Thiazoles 23-31 BCL3 transcription coactivator Homo sapiens 64-68 20125978-3 1974 The possibility of chemical reactions induced by CO(2)-laser light is exemplified by the case of BCl(3) molecules. co(2) 49-54 BCL3 transcription coactivator Homo sapiens 97-103 33919816-1 2021 Normally-off p-gallium nitride (GaN) high electron mobility transistor (HEMT) devices with multi-finger layout were successfully fabricated by use of a self-terminating etching technique with Cl2/BCl3/SF6-mixed gas plasma. p-gallium nitride 13-30 BCL3 transcription coactivator Homo sapiens 196-200 33919816-1 2021 Normally-off p-gallium nitride (GaN) high electron mobility transistor (HEMT) devices with multi-finger layout were successfully fabricated by use of a self-terminating etching technique with Cl2/BCl3/SF6-mixed gas plasma. gan 32-35 BCL3 transcription coactivator Homo sapiens 196-200 33725086-6 2021 This is in contrast to thiazole directed indole borylation with BCl3 where the C7 borylated isomer is the kinetic product too. indole 41-47 BCL3 transcription coactivator Homo sapiens 64-68 33100450-3 2020 Within the reaction conditions investigated, the reaction is highly effective on Cl-Si(100) for temperatures below 70 C, at which point both surfaces react with BCl3. cl-si 81-86 BCL3 transcription coactivator Homo sapiens 161-165 33707466-9 2021 These results identify CDK1 as an NF-kappaB target gene regulated by p50 and BCL-3 and suggest that targeting CDK1 may be a strategy to improve the efficacy of TMZ against GBM. Temozolomide 160-163 BCL3 transcription coactivator Homo sapiens 77-82 33068678-0 2021 5-HTP Decreases Goat Mammary Epithelial Cells Apoptosis through MAPK/ERK/Bcl-3 pathway. 5-Hydroxytryptophan 0-5 BCL3 transcription coactivator Homo sapiens 73-78 33068678-5 2021 The aim of this study is to explore the interaction among 5-HTP, MAPK and Bcl-3 in GMEC apoptosis. gmec 83-87 BCL3 transcription coactivator Homo sapiens 74-79 33068678-9 2021 And the results of RT-qPCR and western blotting demonstrated that both 5-HTP and ERK1/2 positively regulated Bcl-3 expression. 5-Hydroxytryptophan 71-76 BCL3 transcription coactivator Homo sapiens 109-114 33068678-10 2021 Sum up all the results, we could draw the conclusion that 5-HTP decreased GMEC apoptosis through MAPK/ERK/Bcl-3 pathway. 5-Hydroxytryptophan 58-63 BCL3 transcription coactivator Homo sapiens 106-111 32432882-1 2020 A variety of appropriately substituted internal alkynes were transformed into the corresponding cyano-substituted phenanthrenes, dihydronaphthalenes, and cyclohepta-1,3,5-trienes in moderate to excellent yields by treatment with imidazolium thiocyanate 1, which serves as an easy to handle [CN]+ precursor, in the presence of BCl3. Alkynes 48-55 BCL3 transcription coactivator Homo sapiens 326-330 33544468-11 2021 Mechanistically, PCAT1 was predominantly localized in the cytoplasm and competitively bound miR-216a-3p to increase BCL3 expression. mir-216a-3p 92-103 BCL3 transcription coactivator Homo sapiens 116-120 32667778-2 2020 Here, we report atomic layer deposition of boron nitride (ALD-BN) using BCl3 and NH3 precursors directly on thermal SiO2 substrates at a relatively low temperature of 600 C. The films were characterized by x-ray photoelectron spectroscopy, atomic force microscopy, and transmission electron microscopy wherein the uniform, atomically smooth, and nanocrystalline layered-BN thin film growth is observed. boron nitride 43-56 BCL3 transcription coactivator Homo sapiens 72-76 32667778-2 2020 Here, we report atomic layer deposition of boron nitride (ALD-BN) using BCl3 and NH3 precursors directly on thermal SiO2 substrates at a relatively low temperature of 600 C. The films were characterized by x-ray photoelectron spectroscopy, atomic force microscopy, and transmission electron microscopy wherein the uniform, atomically smooth, and nanocrystalline layered-BN thin film growth is observed. ald-bn 58-64 BCL3 transcription coactivator Homo sapiens 72-76 32551686-1 2020 Direct intramolecular aminoboration of sulfonamidoallenes was realized using BCl3 as a boron source. sulfonamidoallenes 39-57 BCL3 transcription coactivator Homo sapiens 77-81 32551686-1 2020 Direct intramolecular aminoboration of sulfonamidoallenes was realized using BCl3 as a boron source. Boron 87-92 BCL3 transcription coactivator Homo sapiens 77-81 32432882-1 2020 A variety of appropriately substituted internal alkynes were transformed into the corresponding cyano-substituted phenanthrenes, dihydronaphthalenes, and cyclohepta-1,3,5-trienes in moderate to excellent yields by treatment with imidazolium thiocyanate 1, which serves as an easy to handle [CN]+ precursor, in the presence of BCl3. cyclohepta-1,3,5-trienes 154-178 BCL3 transcription coactivator Homo sapiens 326-330 32551686-2 2020 The reactions benefited from the interaction between BCl3 and sulfonamides and provided a variety of borylvinyl heterocycles in good isolated yields. borylvinyl heterocycles 101-124 BCL3 transcription coactivator Homo sapiens 53-57 32432882-1 2020 A variety of appropriately substituted internal alkynes were transformed into the corresponding cyano-substituted phenanthrenes, dihydronaphthalenes, and cyclohepta-1,3,5-trienes in moderate to excellent yields by treatment with imidazolium thiocyanate 1, which serves as an easy to handle [CN]+ precursor, in the presence of BCl3. imidazolium thiocyanate 229-252 BCL3 transcription coactivator Homo sapiens 326-330 32233410-1 2020 The trilithium compound 1,3-[PhMe2Si-C(Li) C(H)]2C6H3Li (2b) reacted with BCl3, AlCl3, or GaCl3 by salt elimination to yield dinuclear heptacyclic compounds (4). Salts 99-103 BCL3 transcription coactivator Homo sapiens 74-78 32319612-4 2020 In the present study, it was shown for the first time that knocking down BCL-3 expression suppressed cyclooxygenase-2 (COX-2)/prostaglandin E2 (PGE2) signalling in colorectal cancer cells, a pathway known to drive several of the hallmarks of cancer. Dinoprostone 144-148 BCL3 transcription coactivator Homo sapiens 73-78 32319612-9 2020 These results suggest that targeting BCL-3 to suppress PGE2 synthesis may represent an alternative or complementary approach to using non-steroidal anti-inflammatory drugs [(NSAIDs), which inhibit cyclooxygenase activity and suppress the conversion of arachidonic acid to prostaglandin], for prevention and/or recurrence in PGE2-driven tumorigenesis. Dinoprostone 55-59 BCL3 transcription coactivator Homo sapiens 37-42 32319612-9 2020 These results suggest that targeting BCL-3 to suppress PGE2 synthesis may represent an alternative or complementary approach to using non-steroidal anti-inflammatory drugs [(NSAIDs), which inhibit cyclooxygenase activity and suppress the conversion of arachidonic acid to prostaglandin], for prevention and/or recurrence in PGE2-driven tumorigenesis. Arachidonic Acid 252-268 BCL3 transcription coactivator Homo sapiens 37-42 32319612-9 2020 These results suggest that targeting BCL-3 to suppress PGE2 synthesis may represent an alternative or complementary approach to using non-steroidal anti-inflammatory drugs [(NSAIDs), which inhibit cyclooxygenase activity and suppress the conversion of arachidonic acid to prostaglandin], for prevention and/or recurrence in PGE2-driven tumorigenesis. Prostaglandins 272-285 BCL3 transcription coactivator Homo sapiens 37-42 32319612-9 2020 These results suggest that targeting BCL-3 to suppress PGE2 synthesis may represent an alternative or complementary approach to using non-steroidal anti-inflammatory drugs [(NSAIDs), which inhibit cyclooxygenase activity and suppress the conversion of arachidonic acid to prostaglandin], for prevention and/or recurrence in PGE2-driven tumorigenesis. Dinoprostone 324-328 BCL3 transcription coactivator Homo sapiens 37-42 32250118-6 2020 Even though the Cl atomic charge of -0.72 e in BCl3 is more negative than the hydrogen values of -0.67 e in BH3 the hydride out-of-plane intensity of 82.0 km mol-1 is an order of magnitude larger than that of the trichloride, 6.3 km mol-1. 1-butylsulfanylbutane; rhodium(3+); trichloride 213-224 BCL3 transcription coactivator Homo sapiens 47-51 32319612-0 2020 BCL-3 promotes cyclooxygenase-2/prostaglandin E2 signalling in colorectal cancer. Dinoprostone 32-48 BCL3 transcription coactivator Homo sapiens 0-5 32319612-4 2020 In the present study, it was shown for the first time that knocking down BCL-3 expression suppressed cyclooxygenase-2 (COX-2)/prostaglandin E2 (PGE2) signalling in colorectal cancer cells, a pathway known to drive several of the hallmarks of cancer. Dinoprostone 126-142 BCL3 transcription coactivator Homo sapiens 73-78 32355204-0 2020 Bcl-3 promotes Wnt signaling by maintaining the acetylation of beta-catenin at lysine 49 in colorectal cancer. Lysine 79-85 BCL3 transcription coactivator Homo sapiens 0-5 32355204-6 2020 Interestingly, Wnt3a increases the level and nuclear translocation of Bcl-3, which binds directly to beta-catenin and enhances the acetylation of beta-catenin at lysine 49 (Ac-K49-beta-catenin) and transcriptional activity. Lysine 162-168 BCL3 transcription coactivator Homo sapiens 70-75 32134102-2 2020 A stepwise halogen exchange, leading to a mixed-halide Cl-B-F intermediate, is implicated in the conversion of F-aza-BODIPYs to Cl-aza-BODIPYs upon treatment with BCl3. Halogens 11-18 BCL3 transcription coactivator Homo sapiens 163-167 32266478-0 2020 Modeling through space magnetic shielding over the tetrafluoroborate (BF4-) and tetrachloroborate (BCl4-) anions. tetrachloroborate 80-97 BCL3 transcription coactivator Homo sapiens 99-103 32266478-1 2020 The GIAO-B3LYP method was employed to calculate the isotropic NMR shielding increments of a diatomic hydrogen probe above the tetrafluoroborate (BF4-) and tetrachloroborate (BCl4-) anions in tetrahedral (Td) symmetrical structure. Hydrogen 101-109 BCL3 transcription coactivator Homo sapiens 174-178 32266478-1 2020 The GIAO-B3LYP method was employed to calculate the isotropic NMR shielding increments of a diatomic hydrogen probe above the tetrafluoroborate (BF4-) and tetrachloroborate (BCl4-) anions in tetrahedral (Td) symmetrical structure. tetrachloroborate 155-172 BCL3 transcription coactivator Homo sapiens 174-178 32134102-2 2020 A stepwise halogen exchange, leading to a mixed-halide Cl-B-F intermediate, is implicated in the conversion of F-aza-BODIPYs to Cl-aza-BODIPYs upon treatment with BCl3. halide 48-54 BCL3 transcription coactivator Homo sapiens 163-167 32134102-2 2020 A stepwise halogen exchange, leading to a mixed-halide Cl-B-F intermediate, is implicated in the conversion of F-aza-BODIPYs to Cl-aza-BODIPYs upon treatment with BCl3. cl-b-f 55-61 BCL3 transcription coactivator Homo sapiens 163-167 32134102-2 2020 A stepwise halogen exchange, leading to a mixed-halide Cl-B-F intermediate, is implicated in the conversion of F-aza-BODIPYs to Cl-aza-BODIPYs upon treatment with BCl3. f-aza-bodipys 111-124 BCL3 transcription coactivator Homo sapiens 163-167 32134102-2 2020 A stepwise halogen exchange, leading to a mixed-halide Cl-B-F intermediate, is implicated in the conversion of F-aza-BODIPYs to Cl-aza-BODIPYs upon treatment with BCl3. cl-aza-bodipys 128-142 BCL3 transcription coactivator Homo sapiens 163-167 31727944-6 2019 Accordingly, genes involved in the host innate response against pathogens (RUBICON, TRIM25, BCL3) are deregulated in human lung epithelial cells treated with pinometostat. EPZ-5676 158-170 BCL3 transcription coactivator Homo sapiens 92-96 31793036-15 2020 More importantly, re-expression of BCL3 partially reversed miR-627-5p induced inhibitory effects on Hep3B cells. mir-627-5p 59-69 BCL3 transcription coactivator Homo sapiens 35-39 32269848-7 2020 AGS and NCI-N87 cells transfected with si-RNA-Bcl-3 (si-Bcl-3) showed significantly reduced migratory ability and increased chemosensitivity to oxaliplatin, 5-fluorouracil, and irinotecan. Oxaliplatin 144-155 BCL3 transcription coactivator Homo sapiens 46-51 32269848-7 2020 AGS and NCI-N87 cells transfected with si-RNA-Bcl-3 (si-Bcl-3) showed significantly reduced migratory ability and increased chemosensitivity to oxaliplatin, 5-fluorouracil, and irinotecan. Fluorouracil 157-171 BCL3 transcription coactivator Homo sapiens 46-51 32269848-7 2020 AGS and NCI-N87 cells transfected with si-RNA-Bcl-3 (si-Bcl-3) showed significantly reduced migratory ability and increased chemosensitivity to oxaliplatin, 5-fluorouracil, and irinotecan. Irinotecan 177-187 BCL3 transcription coactivator Homo sapiens 46-51 32269848-9 2020 Further, the protective role of si-Bcl-3 on the gastric cancer cells could be reversed by the autophagy inducer, rapamycin. Sirolimus 113-122 BCL3 transcription coactivator Homo sapiens 35-40 31714564-2 2019 The reactions with boranes BX3 SMe2 (X = H, Cl, Br), BF3 OEt2 and BCl3 yield Lewis adducts [BICAAC BH3] (1), [BICAAC BHCl2] (2), [BICAAC BH2Cl] (3), [BICAAC BF3] (4), [BICAAC BCl3] (5) and [BICAAC BBr3] (6) respectively, whereas more hydridic boranes, 9-borabicyclo[3.3.1]nonane (9-BBN) and catecholborane (HBcat), enable the insertion of the carbene carbon into the B-H bond to form [BICAAC(H)-(9-BBN)] (7) and [BICAAC(H)-Bcat] (8). Boranes 19-26 BCL3 transcription coactivator Homo sapiens 66-70 31714564-2 2019 The reactions with boranes BX3 SMe2 (X = H, Cl, Br), BF3 OEt2 and BCl3 yield Lewis adducts [BICAAC BH3] (1), [BICAAC BHCl2] (2), [BICAAC BH2Cl] (3), [BICAAC BF3] (4), [BICAAC BCl3] (5) and [BICAAC BBr3] (6) respectively, whereas more hydridic boranes, 9-borabicyclo[3.3.1]nonane (9-BBN) and catecholborane (HBcat), enable the insertion of the carbene carbon into the B-H bond to form [BICAAC(H)-(9-BBN)] (7) and [BICAAC(H)-Bcat] (8). Boranes 19-26 BCL3 transcription coactivator Homo sapiens 175-179 31714564-2 2019 The reactions with boranes BX3 SMe2 (X = H, Cl, Br), BF3 OEt2 and BCl3 yield Lewis adducts [BICAAC BH3] (1), [BICAAC BHCl2] (2), [BICAAC BH2Cl] (3), [BICAAC BF3] (4), [BICAAC BCl3] (5) and [BICAAC BBr3] (6) respectively, whereas more hydridic boranes, 9-borabicyclo[3.3.1]nonane (9-BBN) and catecholborane (HBcat), enable the insertion of the carbene carbon into the B-H bond to form [BICAAC(H)-(9-BBN)] (7) and [BICAAC(H)-Bcat] (8). 3-bromoacetoxyandrostan-17-one 48-50 BCL3 transcription coactivator Homo sapiens 66-70 31714564-2 2019 The reactions with boranes BX3 SMe2 (X = H, Cl, Br), BF3 OEt2 and BCl3 yield Lewis adducts [BICAAC BH3] (1), [BICAAC BHCl2] (2), [BICAAC BH2Cl] (3), [BICAAC BF3] (4), [BICAAC BCl3] (5) and [BICAAC BBr3] (6) respectively, whereas more hydridic boranes, 9-borabicyclo[3.3.1]nonane (9-BBN) and catecholborane (HBcat), enable the insertion of the carbene carbon into the B-H bond to form [BICAAC(H)-(9-BBN)] (7) and [BICAAC(H)-Bcat] (8). 3-bromoacetoxyandrostan-17-one 48-50 BCL3 transcription coactivator Homo sapiens 175-179 31714564-2 2019 The reactions with boranes BX3 SMe2 (X = H, Cl, Br), BF3 OEt2 and BCl3 yield Lewis adducts [BICAAC BH3] (1), [BICAAC BHCl2] (2), [BICAAC BH2Cl] (3), [BICAAC BF3] (4), [BICAAC BCl3] (5) and [BICAAC BBr3] (6) respectively, whereas more hydridic boranes, 9-borabicyclo[3.3.1]nonane (9-BBN) and catecholborane (HBcat), enable the insertion of the carbene carbon into the B-H bond to form [BICAAC(H)-(9-BBN)] (7) and [BICAAC(H)-Bcat] (8). 1-(2-ethoxyethyl)-3-(2-methoxyethyl)benzimidazolium 57-61 BCL3 transcription coactivator Homo sapiens 175-179 31714564-2 2019 The reactions with boranes BX3 SMe2 (X = H, Cl, Br), BF3 OEt2 and BCl3 yield Lewis adducts [BICAAC BH3] (1), [BICAAC BHCl2] (2), [BICAAC BH2Cl] (3), [BICAAC BF3] (4), [BICAAC BCl3] (5) and [BICAAC BBr3] (6) respectively, whereas more hydridic boranes, 9-borabicyclo[3.3.1]nonane (9-BBN) and catecholborane (HBcat), enable the insertion of the carbene carbon into the B-H bond to form [BICAAC(H)-(9-BBN)] (7) and [BICAAC(H)-Bcat] (8). Boranes 243-250 BCL3 transcription coactivator Homo sapiens 66-70 31714564-2 2019 The reactions with boranes BX3 SMe2 (X = H, Cl, Br), BF3 OEt2 and BCl3 yield Lewis adducts [BICAAC BH3] (1), [BICAAC BHCl2] (2), [BICAAC BH2Cl] (3), [BICAAC BF3] (4), [BICAAC BCl3] (5) and [BICAAC BBr3] (6) respectively, whereas more hydridic boranes, 9-borabicyclo[3.3.1]nonane (9-BBN) and catecholborane (HBcat), enable the insertion of the carbene carbon into the B-H bond to form [BICAAC(H)-(9-BBN)] (7) and [BICAAC(H)-Bcat] (8). 9-borabicyclo(3,3,1)nonane 252-265 BCL3 transcription coactivator Homo sapiens 66-70 31714564-2 2019 The reactions with boranes BX3 SMe2 (X = H, Cl, Br), BF3 OEt2 and BCl3 yield Lewis adducts [BICAAC BH3] (1), [BICAAC BHCl2] (2), [BICAAC BH2Cl] (3), [BICAAC BF3] (4), [BICAAC BCl3] (5) and [BICAAC BBr3] (6) respectively, whereas more hydridic boranes, 9-borabicyclo[3.3.1]nonane (9-BBN) and catecholborane (HBcat), enable the insertion of the carbene carbon into the B-H bond to form [BICAAC(H)-(9-BBN)] (7) and [BICAAC(H)-Bcat] (8). nonane 272-278 BCL3 transcription coactivator Homo sapiens 66-70 31714564-2 2019 The reactions with boranes BX3 SMe2 (X = H, Cl, Br), BF3 OEt2 and BCl3 yield Lewis adducts [BICAAC BH3] (1), [BICAAC BHCl2] (2), [BICAAC BH2Cl] (3), [BICAAC BF3] (4), [BICAAC BCl3] (5) and [BICAAC BBr3] (6) respectively, whereas more hydridic boranes, 9-borabicyclo[3.3.1]nonane (9-BBN) and catecholborane (HBcat), enable the insertion of the carbene carbon into the B-H bond to form [BICAAC(H)-(9-BBN)] (7) and [BICAAC(H)-Bcat] (8). Catecholborane 291-305 BCL3 transcription coactivator Homo sapiens 66-70 31714564-2 2019 The reactions with boranes BX3 SMe2 (X = H, Cl, Br), BF3 OEt2 and BCl3 yield Lewis adducts [BICAAC BH3] (1), [BICAAC BHCl2] (2), [BICAAC BH2Cl] (3), [BICAAC BF3] (4), [BICAAC BCl3] (5) and [BICAAC BBr3] (6) respectively, whereas more hydridic boranes, 9-borabicyclo[3.3.1]nonane (9-BBN) and catecholborane (HBcat), enable the insertion of the carbene carbon into the B-H bond to form [BICAAC(H)-(9-BBN)] (7) and [BICAAC(H)-Bcat] (8). carbene 343-350 BCL3 transcription coactivator Homo sapiens 66-70 31714564-2 2019 The reactions with boranes BX3 SMe2 (X = H, Cl, Br), BF3 OEt2 and BCl3 yield Lewis adducts [BICAAC BH3] (1), [BICAAC BHCl2] (2), [BICAAC BH2Cl] (3), [BICAAC BF3] (4), [BICAAC BCl3] (5) and [BICAAC BBr3] (6) respectively, whereas more hydridic boranes, 9-borabicyclo[3.3.1]nonane (9-BBN) and catecholborane (HBcat), enable the insertion of the carbene carbon into the B-H bond to form [BICAAC(H)-(9-BBN)] (7) and [BICAAC(H)-Bcat] (8). Carbon 351-357 BCL3 transcription coactivator Homo sapiens 66-70 31714564-2 2019 The reactions with boranes BX3 SMe2 (X = H, Cl, Br), BF3 OEt2 and BCl3 yield Lewis adducts [BICAAC BH3] (1), [BICAAC BHCl2] (2), [BICAAC BH2Cl] (3), [BICAAC BF3] (4), [BICAAC BCl3] (5) and [BICAAC BBr3] (6) respectively, whereas more hydridic boranes, 9-borabicyclo[3.3.1]nonane (9-BBN) and catecholborane (HBcat), enable the insertion of the carbene carbon into the B-H bond to form [BICAAC(H)-(9-BBN)] (7) and [BICAAC(H)-Bcat] (8). Hydrogen 367-370 BCL3 transcription coactivator Homo sapiens 66-70 31714564-2 2019 The reactions with boranes BX3 SMe2 (X = H, Cl, Br), BF3 OEt2 and BCl3 yield Lewis adducts [BICAAC BH3] (1), [BICAAC BHCl2] (2), [BICAAC BH2Cl] (3), [BICAAC BF3] (4), [BICAAC BCl3] (5) and [BICAAC BBr3] (6) respectively, whereas more hydridic boranes, 9-borabicyclo[3.3.1]nonane (9-BBN) and catecholborane (HBcat), enable the insertion of the carbene carbon into the B-H bond to form [BICAAC(H)-(9-BBN)] (7) and [BICAAC(H)-Bcat] (8). 9-borabicyclo(3,3,1)nonane 384-403 BCL3 transcription coactivator Homo sapiens 66-70 31714564-2 2019 The reactions with boranes BX3 SMe2 (X = H, Cl, Br), BF3 OEt2 and BCl3 yield Lewis adducts [BICAAC BH3] (1), [BICAAC BHCl2] (2), [BICAAC BH2Cl] (3), [BICAAC BF3] (4), [BICAAC BCl3] (5) and [BICAAC BBr3] (6) respectively, whereas more hydridic boranes, 9-borabicyclo[3.3.1]nonane (9-BBN) and catecholborane (HBcat), enable the insertion of the carbene carbon into the B-H bond to form [BICAAC(H)-(9-BBN)] (7) and [BICAAC(H)-Bcat] (8). carbene 413-427 BCL3 transcription coactivator Homo sapiens 66-70 31522507-1 2019 Reaction of the bulky N-heterocyclic silylene Si[NB(NArCH)2CH2]2 (3; Ar = 2,6-iPr2C6H3) with BCl3 resulted in ring expansion with formation of the six-membered C2N2SiB heterocycle 4. Argon 53-55 BCL3 transcription coactivator Homo sapiens 93-97 31522507-1 2019 Reaction of the bulky N-heterocyclic silylene Si[NB(NArCH)2CH2]2 (3; Ar = 2,6-iPr2C6H3) with BCl3 resulted in ring expansion with formation of the six-membered C2N2SiB heterocycle 4. 2,6-ipr2c6h3 74-86 BCL3 transcription coactivator Homo sapiens 93-97 31115095-4 2019 Subsequent electrophilic borylation with BCl3 in the presence of AlCl3 and 2,6-di-tert-butylpyridine as a hindered base produced the dichloroborane complexes, which were then in situ reacted with diphenyl or diethyl zinc. Aluminum Chloride 65-70 BCL3 transcription coactivator Homo sapiens 41-45 31215080-5 2019 Dihalogenation of the BH2 entity is observed with BCl3 and BBr3 , whereas BI3 either affords IiPr-BHI2 or proceeds with borylation of the aromatic phenyl ring to give a hydride-bridged bisborylated species. bh2 22-25 BCL3 transcription coactivator Homo sapiens 50-54 31115095-4 2019 Subsequent electrophilic borylation with BCl3 in the presence of AlCl3 and 2,6-di-tert-butylpyridine as a hindered base produced the dichloroborane complexes, which were then in situ reacted with diphenyl or diethyl zinc. 2,6-Di-tert-butylpyridine 75-100 BCL3 transcription coactivator Homo sapiens 41-45 31115095-4 2019 Subsequent electrophilic borylation with BCl3 in the presence of AlCl3 and 2,6-di-tert-butylpyridine as a hindered base produced the dichloroborane complexes, which were then in situ reacted with diphenyl or diethyl zinc. Dichloroboron 133-147 BCL3 transcription coactivator Homo sapiens 41-45 31115095-4 2019 Subsequent electrophilic borylation with BCl3 in the presence of AlCl3 and 2,6-di-tert-butylpyridine as a hindered base produced the dichloroborane complexes, which were then in situ reacted with diphenyl or diethyl zinc. diphenyl 196-204 BCL3 transcription coactivator Homo sapiens 41-45 31115095-4 2019 Subsequent electrophilic borylation with BCl3 in the presence of AlCl3 and 2,6-di-tert-butylpyridine as a hindered base produced the dichloroborane complexes, which were then in situ reacted with diphenyl or diethyl zinc. diethylzinc 208-220 BCL3 transcription coactivator Homo sapiens 41-45 31120094-1 2019 The borylative cyclisation of 1,2-dialkynyl benzenes with BCl3 leads to dibenzopentalenes (via intramolecular SEAr) or benzofulvenes (via chloride addition) depending on substituents, with stabilised vinyl cation intermediates (e.g. with a p-MeO-C6H4-group) favouring the latter. 1,2-dialkynyl benzenes 30-52 BCL3 transcription coactivator Homo sapiens 58-62 30974025-3 2019 In addition to the classical B2 X4 L2 diborane(4) bis-adducts, certain more sterically demanding carbene ligands induce a halide displacement which led to the first halide-bridged monocationic diboron species, [B2 X3 L2 ]A (A=BCl4 , Br, I). carbene 97-104 BCL3 transcription coactivator Homo sapiens 226-230 30974025-3 2019 In addition to the classical B2 X4 L2 diborane(4) bis-adducts, certain more sterically demanding carbene ligands induce a halide displacement which led to the first halide-bridged monocationic diboron species, [B2 X3 L2 ]A (A=BCl4 , Br, I). halide 122-128 BCL3 transcription coactivator Homo sapiens 226-230 30974025-3 2019 In addition to the classical B2 X4 L2 diborane(4) bis-adducts, certain more sterically demanding carbene ligands induce a halide displacement which led to the first halide-bridged monocationic diboron species, [B2 X3 L2 ]A (A=BCl4 , Br, I). halide 165-171 BCL3 transcription coactivator Homo sapiens 226-230 30974025-3 2019 In addition to the classical B2 X4 L2 diborane(4) bis-adducts, certain more sterically demanding carbene ligands induce a halide displacement which led to the first halide-bridged monocationic diboron species, [B2 X3 L2 ]A (A=BCl4 , Br, I). Boron dimer 193-200 BCL3 transcription coactivator Homo sapiens 226-230 31120094-1 2019 The borylative cyclisation of 1,2-dialkynyl benzenes with BCl3 leads to dibenzopentalenes (via intramolecular SEAr) or benzofulvenes (via chloride addition) depending on substituents, with stabilised vinyl cation intermediates (e.g. with a p-MeO-C6H4-group) favouring the latter. dibenzopentalenes 72-89 BCL3 transcription coactivator Homo sapiens 58-62 31120094-1 2019 The borylative cyclisation of 1,2-dialkynyl benzenes with BCl3 leads to dibenzopentalenes (via intramolecular SEAr) or benzofulvenes (via chloride addition) depending on substituents, with stabilised vinyl cation intermediates (e.g. with a p-MeO-C6H4-group) favouring the latter. benzofulvenes 119-132 BCL3 transcription coactivator Homo sapiens 58-62 31120094-1 2019 The borylative cyclisation of 1,2-dialkynyl benzenes with BCl3 leads to dibenzopentalenes (via intramolecular SEAr) or benzofulvenes (via chloride addition) depending on substituents, with stabilised vinyl cation intermediates (e.g. with a p-MeO-C6H4-group) favouring the latter. Chlorides 138-146 BCL3 transcription coactivator Homo sapiens 58-62 31120094-1 2019 The borylative cyclisation of 1,2-dialkynyl benzenes with BCl3 leads to dibenzopentalenes (via intramolecular SEAr) or benzofulvenes (via chloride addition) depending on substituents, with stabilised vinyl cation intermediates (e.g. with a p-MeO-C6H4-group) favouring the latter. p-meo-c6h4 240-250 BCL3 transcription coactivator Homo sapiens 58-62 30789171-0 2019 Computational and experimental investigation on the BCl3 promoted intramolecular amination of alkenes and alkynes. Alkenes 94-101 BCL3 transcription coactivator Homo sapiens 52-56 30624005-3 2019 For BCl3 , the formation of the isocyanide adduct [(CN)BCl3 ]- and the corresponding Wheland complex was verified by mass spectrometry. Cyanides 32-42 BCL3 transcription coactivator Homo sapiens 4-8 30624005-3 2019 For BCl3 , the formation of the isocyanide adduct [(CN)BCl3 ]- and the corresponding Wheland complex was verified by mass spectrometry. Cyanides 32-42 BCL3 transcription coactivator Homo sapiens 55-59 30624005-5 2019 The success of this transfer hydrocyanation depends on the Lewis acid employed; catalytic amounts of BCl3 and (C6 F5 )2 BCl are shown to be effective while B(C6 F5 )3 and BF3 OEt2 are not. Lewis Acids 59-69 BCL3 transcription coactivator Homo sapiens 101-105 31460023-2 2019 Capitalizing on the condensation reaction approach, the desired products were formed using a mixture of p-phenylendiamine and aniline with BCl3, followed by the addition of an aryl lithium derivative. 4-phenylenediamine 104-121 BCL3 transcription coactivator Homo sapiens 139-143 31460023-2 2019 Capitalizing on the condensation reaction approach, the desired products were formed using a mixture of p-phenylendiamine and aniline with BCl3, followed by the addition of an aryl lithium derivative. aniline 126-133 BCL3 transcription coactivator Homo sapiens 139-143 30973169-6 2019 Treatment of 1 with the haloboranes Et2O BF3, BCl3, BBr3 and Me2S BBr3 resulted in the formation of the Lewis acid base adducts 1 BX3 (X = F, Cl, Br) and an equilibrium with their auto-ionization products [12BX2]+[BX4]- slowly develops. haloboranes 24-35 BCL3 transcription coactivator Homo sapiens 46-50 30973169-6 2019 Treatment of 1 with the haloboranes Et2O BF3, BCl3, BBr3 and Me2S BBr3 resulted in the formation of the Lewis acid base adducts 1 BX3 (X = F, Cl, Br) and an equilibrium with their auto-ionization products [12BX2]+[BX4]- slowly develops. Ether 36-40 BCL3 transcription coactivator Homo sapiens 46-50 31183061-1 2019 The one-electron reduction of (CAACMe)BCl3 (CAACMe = 1-(2,6-diisopropylphenyl)-3,3,5,5-tetramethylpyrrolidin-2-ylidene) yields the dichloroboryl radical [(CAACMe)BCl2] . caacme 31-37 BCL3 transcription coactivator Homo sapiens 38-42 31183061-1 2019 The one-electron reduction of (CAACMe)BCl3 (CAACMe = 1-(2,6-diisopropylphenyl)-3,3,5,5-tetramethylpyrrolidin-2-ylidene) yields the dichloroboryl radical [(CAACMe)BCl2] . caacme 44-50 BCL3 transcription coactivator Homo sapiens 38-42 31183061-1 2019 The one-electron reduction of (CAACMe)BCl3 (CAACMe = 1-(2,6-diisopropylphenyl)-3,3,5,5-tetramethylpyrrolidin-2-ylidene) yields the dichloroboryl radical [(CAACMe)BCl2] . 1-(2,6-diisopropylphenyl)-3,3,5,5-tetramethylpyrrolidin-2-ylidene 53-118 BCL3 transcription coactivator Homo sapiens 38-42 31183061-1 2019 The one-electron reduction of (CAACMe)BCl3 (CAACMe = 1-(2,6-diisopropylphenyl)-3,3,5,5-tetramethylpyrrolidin-2-ylidene) yields the dichloroboryl radical [(CAACMe)BCl2] . dichloroboryl radical 131-152 BCL3 transcription coactivator Homo sapiens 38-42 31183061-1 2019 The one-electron reduction of (CAACMe)BCl3 (CAACMe = 1-(2,6-diisopropylphenyl)-3,3,5,5-tetramethylpyrrolidin-2-ylidene) yields the dichloroboryl radical [(CAACMe)BCl2] . caacme 44-50 BCL3 transcription coactivator Homo sapiens 38-42 31183061-2 2019 Furthermore, the twofold reduction of (CAACMe)BCl3 in the presence of a range of Lewis bases (L = CAACMe, N-heterocyclic carbene, phosphine) yields a series of doubly base-supported (CAACMe)LBCl chloroborylenes, all of which were structurally characterised. caacme 39-45 BCL3 transcription coactivator Homo sapiens 46-50 31183061-2 2019 Furthermore, the twofold reduction of (CAACMe)BCl3 in the presence of a range of Lewis bases (L = CAACMe, N-heterocyclic carbene, phosphine) yields a series of doubly base-supported (CAACMe)LBCl chloroborylenes, all of which were structurally characterised. l 81-82 BCL3 transcription coactivator Homo sapiens 46-50 31183061-2 2019 Furthermore, the twofold reduction of (CAACMe)BCl3 in the presence of a range of Lewis bases (L = CAACMe, N-heterocyclic carbene, phosphine) yields a series of doubly base-supported (CAACMe)LBCl chloroborylenes, all of which were structurally characterised. caacme 98-104 BCL3 transcription coactivator Homo sapiens 46-50 31183061-2 2019 Furthermore, the twofold reduction of (CAACMe)BCl3 in the presence of a range of Lewis bases (L = CAACMe, N-heterocyclic carbene, phosphine) yields a series of doubly base-supported (CAACMe)LBCl chloroborylenes, all of which were structurally characterised. phosphine 130-139 BCL3 transcription coactivator Homo sapiens 46-50 31183061-2 2019 Furthermore, the twofold reduction of (CAACMe)BCl3 in the presence of a range of Lewis bases (L = CAACMe, N-heterocyclic carbene, phosphine) yields a series of doubly base-supported (CAACMe)LBCl chloroborylenes, all of which were structurally characterised. caacme 98-104 BCL3 transcription coactivator Homo sapiens 46-50 31183061-2 2019 Furthermore, the twofold reduction of (CAACMe)BCl3 in the presence of a range of Lewis bases (L = CAACMe, N-heterocyclic carbene, phosphine) yields a series of doubly base-supported (CAACMe)LBCl chloroborylenes, all of which were structurally characterised. lbcl chloroborylenes 190-210 BCL3 transcription coactivator Homo sapiens 46-50 30789171-0 2019 Computational and experimental investigation on the BCl3 promoted intramolecular amination of alkenes and alkynes. Alkynes 106-113 BCL3 transcription coactivator Homo sapiens 52-56 30789171-2 2019 In 2015, the Li group reported a BCl3 mediated aminoboration of unfunctionalized olefins. Alkenes 81-88 BCL3 transcription coactivator Homo sapiens 33-37 30789171-5 2019 Based on this new mechanism, we then calculated the energy profiles for the BCl3 promoted corresponding aminoboration of alkynes. Alkynes 121-128 BCL3 transcription coactivator Homo sapiens 76-80 31459646-0 2019 BCl3-Mediated C-N, C-S, and C-O Bond Formation of Imidazo[1,2-a]pyridine Benzylic Ethers. Nitrogen 16-17 BCL3 transcription coactivator Homo sapiens 0-4 31459646-0 2019 BCl3-Mediated C-N, C-S, and C-O Bond Formation of Imidazo[1,2-a]pyridine Benzylic Ethers. Cesium 19-22 BCL3 transcription coactivator Homo sapiens 0-4 31459646-0 2019 BCl3-Mediated C-N, C-S, and C-O Bond Formation of Imidazo[1,2-a]pyridine Benzylic Ethers. imidazo[1,2-a]pyridine benzylic ethers 50-88 BCL3 transcription coactivator Homo sapiens 0-4 31459646-1 2019 An efficient BCl3-mediated reaction of imidazo[1,2-a]pyridines has been developed for the C-N, C-S, and C-O bond formation. imidazo(1,2-a)pyridine 39-62 BCL3 transcription coactivator Homo sapiens 13-17 31459646-1 2019 An efficient BCl3-mediated reaction of imidazo[1,2-a]pyridines has been developed for the C-N, C-S, and C-O bond formation. c-n 90-93 BCL3 transcription coactivator Homo sapiens 13-17 31459646-1 2019 An efficient BCl3-mediated reaction of imidazo[1,2-a]pyridines has been developed for the C-N, C-S, and C-O bond formation. Cesium 95-98 BCL3 transcription coactivator Homo sapiens 13-17 29781115-1 2018 Benzothiadiazole (BT) directed C-H borylation using BCl3 , followed by B-Cl hydrolysis and Suzuki-Miyaura cross-coupling enables facile access to twisted donor-acceptor compounds. benzo-1,2,3-thiadiazole 0-16 BCL3 transcription coactivator Homo sapiens 52-56 30547574-4 2019 With a selected cluster ion BCl4-, we are able to achieve high-room-temperature Na-ionic conductivity over 10-3 S/cm and low activation energies below 0.2 eV in the antiperovskite crystals Na3S(BCl4) and Na3S(BCl4)0.5I0.5. na3s 189-193 BCL3 transcription coactivator Homo sapiens 28-32 30547574-4 2019 With a selected cluster ion BCl4-, we are able to achieve high-room-temperature Na-ionic conductivity over 10-3 S/cm and low activation energies below 0.2 eV in the antiperovskite crystals Na3S(BCl4) and Na3S(BCl4)0.5I0.5. na3s 189-193 BCL3 transcription coactivator Homo sapiens 194-198 30547574-4 2019 With a selected cluster ion BCl4-, we are able to achieve high-room-temperature Na-ionic conductivity over 10-3 S/cm and low activation energies below 0.2 eV in the antiperovskite crystals Na3S(BCl4) and Na3S(BCl4)0.5I0.5. na3s 189-193 BCL3 transcription coactivator Homo sapiens 194-198 30547574-4 2019 With a selected cluster ion BCl4-, we are able to achieve high-room-temperature Na-ionic conductivity over 10-3 S/cm and low activation energies below 0.2 eV in the antiperovskite crystals Na3S(BCl4) and Na3S(BCl4)0.5I0.5. na3s 204-208 BCL3 transcription coactivator Homo sapiens 28-32 30547574-4 2019 With a selected cluster ion BCl4-, we are able to achieve high-room-temperature Na-ionic conductivity over 10-3 S/cm and low activation energies below 0.2 eV in the antiperovskite crystals Na3S(BCl4) and Na3S(BCl4)0.5I0.5. na3s 204-208 BCL3 transcription coactivator Homo sapiens 194-198 30547574-4 2019 With a selected cluster ion BCl4-, we are able to achieve high-room-temperature Na-ionic conductivity over 10-3 S/cm and low activation energies below 0.2 eV in the antiperovskite crystals Na3S(BCl4) and Na3S(BCl4)0.5I0.5. na3s 204-208 BCL3 transcription coactivator Homo sapiens 194-198 30135206-5 2018 The mechanism consists of an IFN-induced, Bcl3- and p300-dependent PD-L1 promoter occupancy by Lys-314/315 acetylated p65 NF-kappaB. Lysine 95-98 BCL3 transcription coactivator Homo sapiens 42-46 30168329-4 2018 In analogy to the isoelectronic BCl3, the trichloroberyllate anion exhibits Lewis acidic behavior toward electron-pair donors and was probed for the electronic and steric influence of the Lewis base. trichloroberyllate anion 42-66 BCL3 transcription coactivator Homo sapiens 32-36 29781115-1 2018 Benzothiadiazole (BT) directed C-H borylation using BCl3 , followed by B-Cl hydrolysis and Suzuki-Miyaura cross-coupling enables facile access to twisted donor-acceptor compounds. benzo-1,2,3-thiadiazole 18-20 BCL3 transcription coactivator Homo sapiens 52-56 29267498-8 2017 Furthermore, the down-regulations of p-PI3K, p-AKT, and up-regulations of PTEN, p-IkappaBalpha, p-p65, Bcl-3 induced by LPS were recovered to some extent after ginsenoside Rg1 treatment. Ginsenosides 160-171 BCL3 transcription coactivator Homo sapiens 103-108 29973405-3 2018 We identify the nuclear factor kappaB (NF-kappaB) co-regulator B cell CLL/lymphoma 3 (BCL-3) as an independent predictor of response to temozolomide (TMZ) treatment. Temozolomide 136-148 BCL3 transcription coactivator Homo sapiens 63-84 29973405-3 2018 We identify the nuclear factor kappaB (NF-kappaB) co-regulator B cell CLL/lymphoma 3 (BCL-3) as an independent predictor of response to temozolomide (TMZ) treatment. Temozolomide 136-148 BCL3 transcription coactivator Homo sapiens 86-91 29973405-3 2018 We identify the nuclear factor kappaB (NF-kappaB) co-regulator B cell CLL/lymphoma 3 (BCL-3) as an independent predictor of response to temozolomide (TMZ) treatment. Temozolomide 150-153 BCL3 transcription coactivator Homo sapiens 63-84 29973405-3 2018 We identify the nuclear factor kappaB (NF-kappaB) co-regulator B cell CLL/lymphoma 3 (BCL-3) as an independent predictor of response to temozolomide (TMZ) treatment. Temozolomide 150-153 BCL3 transcription coactivator Homo sapiens 86-91 29973405-4 2018 In glioma patients with tumors that have a methylated O6-methylguanine DNA methyltransferase (MGMT) promoter, high BCL-3 expression was associated with a poor response to TMZ. Temozolomide 171-174 BCL3 transcription coactivator Homo sapiens 115-120 28857264-2 2018 It is confirmed that stronger Lewis acid properties of the boron center are observed for the BCl3 moiety than for the BF3 one in complexes with the strong Lewis base (NH3 ); while the opposite order is observed for complexes with the weak Lewis base (N2 ). Lewis Acids 30-40 BCL3 transcription coactivator Homo sapiens 93-97 28857264-2 2018 It is confirmed that stronger Lewis acid properties of the boron center are observed for the BCl3 moiety than for the BF3 one in complexes with the strong Lewis base (NH3 ); while the opposite order is observed for complexes with the weak Lewis base (N2 ). Boron 59-64 BCL3 transcription coactivator Homo sapiens 93-97 28857264-2 2018 It is confirmed that stronger Lewis acid properties of the boron center are observed for the BCl3 moiety than for the BF3 one in complexes with the strong Lewis base (NH3 ); while the opposite order is observed for complexes with the weak Lewis base (N2 ). bf3 one 118-125 BCL3 transcription coactivator Homo sapiens 93-97 28857264-2 2018 It is confirmed that stronger Lewis acid properties of the boron center are observed for the BCl3 moiety than for the BF3 one in complexes with the strong Lewis base (NH3 ); while the opposite order is observed for complexes with the weak Lewis base (N2 ). Nitrogen 251-253 BCL3 transcription coactivator Homo sapiens 93-97 29236061-4 2017 Further research found that a gas flow ratio of TiCl4/BCl3 had an influence on the film properties and microstructures. titanium tetrachloride 48-53 BCL3 transcription coactivator Homo sapiens 54-58 28712132-7 2018 However, LA with DSA significantly upregulated the whole blood expression of early growth response protein (EGR)1 (1.94-fold, P = .02), EGR3 (1.56-fold, P = .0008) and B-cell lymphoma 3-encoded protein (BCL3; 1.25-fold, P = .03). dsa 17-20 BCL3 transcription coactivator Homo sapiens 168-201 28712132-7 2018 However, LA with DSA significantly upregulated the whole blood expression of early growth response protein (EGR)1 (1.94-fold, P = .02), EGR3 (1.56-fold, P = .0008) and B-cell lymphoma 3-encoded protein (BCL3; 1.25-fold, P = .03). dsa 17-20 BCL3 transcription coactivator Homo sapiens 203-207 28634385-4 2017 As for the large-angle bevel structures, BCl3 + N2 gas mixtures show better characteristics, exhibiting a controllable and large etching angle range from 40 to 80 through the adjustment of the mixture ratio. Nitrogen 48-50 BCL3 transcription coactivator Homo sapiens 41-45 29071315-2 2017 In the presence of BCl3 as the sole boron source, the boryl group and thiol group are added to the C-C double bonds simultaneously. Boron 36-41 BCL3 transcription coactivator Homo sapiens 19-23 29071315-2 2017 In the presence of BCl3 as the sole boron source, the boryl group and thiol group are added to the C-C double bonds simultaneously. boryl 54-59 BCL3 transcription coactivator Homo sapiens 19-23 29071315-2 2017 In the presence of BCl3 as the sole boron source, the boryl group and thiol group are added to the C-C double bonds simultaneously. Sulfhydryl Compounds 70-75 BCL3 transcription coactivator Homo sapiens 19-23 28876892-3 2017 WO3 ALE was achieved by a "conversion-fluorination" mechanism using an AB exposure sequence with boron trichloride (BCl3) and hydrogen fluoride (HF). wo3 ale 0-7 BCL3 transcription coactivator Homo sapiens 116-120 28876892-4 2017 BCl3 converts the WO3 surface to a B2O3 layer while forming volatile WOxCly products. boron oxide 35-39 BCL3 transcription coactivator Homo sapiens 0-4 28876892-10 2017 Subsequently, the WO3 layer is etched with BCl3 and HF. wo3 18-21 BCL3 transcription coactivator Homo sapiens 43-47 29136381-0 2017 Structural and Energetic Properties of Haloacetonitrile-BCl3 Complexes: Computations and Matrix-IR Spectroscopy. haloacetonitrile 39-55 BCL3 transcription coactivator Homo sapiens 56-60 29136381-7 2017 In addition, several IR bands of both FCH2CN-BCl3 and ClCH2CN-BCl3 were observed in nitrogen matrices, but the assigned bands are consistent with M06-2X predictions for the short-bond, minimum-energy structures. Nitrogen 84-92 BCL3 transcription coactivator Homo sapiens 38-49 29136381-7 2017 In addition, several IR bands of both FCH2CN-BCl3 and ClCH2CN-BCl3 were observed in nitrogen matrices, but the assigned bands are consistent with M06-2X predictions for the short-bond, minimum-energy structures. Nitrogen 84-92 BCL3 transcription coactivator Homo sapiens 45-49 28817208-1 2017 A variety of terminal and internal alkynes were converted regio- and stereoselectively into (Z)-3-chloroacrylonitriles by treatment with BCl3 in the presence of stoichiometric amounts of imidazolium thiocyanates. Alkynes 35-42 BCL3 transcription coactivator Homo sapiens 137-141 28817208-1 2017 A variety of terminal and internal alkynes were converted regio- and stereoselectively into (Z)-3-chloroacrylonitriles by treatment with BCl3 in the presence of stoichiometric amounts of imidazolium thiocyanates. (z)-3-chloroacrylonitriles 92-118 BCL3 transcription coactivator Homo sapiens 137-141 28817208-1 2017 A variety of terminal and internal alkynes were converted regio- and stereoselectively into (Z)-3-chloroacrylonitriles by treatment with BCl3 in the presence of stoichiometric amounts of imidazolium thiocyanates. imidazolium thiocyanates 187-211 BCL3 transcription coactivator Homo sapiens 137-141 28481553-3 2017 The tandem reaction proceeds in the presence of BCl3 to generate three new carbon-carbon bonds, a quaternary carbon, and two stereogenic centers with excellent diastereocontrol. Carbon 75-81 BCL3 transcription coactivator Homo sapiens 48-52 28772986-0 2017 Effect of the SiCl4 Flow Rate on SiBN Deposition Kinetics in SiCl4-BCl3-NH3-H2-Ar Environment. sibn 33-37 BCL3 transcription coactivator Homo sapiens 67-71 28481553-3 2017 The tandem reaction proceeds in the presence of BCl3 to generate three new carbon-carbon bonds, a quaternary carbon, and two stereogenic centers with excellent diastereocontrol. Carbon 82-88 BCL3 transcription coactivator Homo sapiens 48-52 28481553-3 2017 The tandem reaction proceeds in the presence of BCl3 to generate three new carbon-carbon bonds, a quaternary carbon, and two stereogenic centers with excellent diastereocontrol. Carbon 82-88 BCL3 transcription coactivator Homo sapiens 48-52 27897368-0 2017 BCl3 -Induced Annulative Oxo- and Thioboration for the Formation of C3-Borylated Benzofurans and Benzothiophenes. Benzofurans 81-92 BCL3 transcription coactivator Homo sapiens 0-4 27897368-0 2017 BCl3 -Induced Annulative Oxo- and Thioboration for the Formation of C3-Borylated Benzofurans and Benzothiophenes. benzothiophene 97-112 BCL3 transcription coactivator Homo sapiens 0-4 27897368-1 2017 BCl3 -induced borylative cyclization of aryl-alkynes possessing ortho-EMe (E=S, O) groups represents a simple, metal-free method for the formation of C3-borylated benzothiophenes and benzofurans. aryl-alkynes 40-52 BCL3 transcription coactivator Homo sapiens 0-4 27897368-1 2017 BCl3 -induced borylative cyclization of aryl-alkynes possessing ortho-EMe (E=S, O) groups represents a simple, metal-free method for the formation of C3-borylated benzothiophenes and benzofurans. Metals 111-116 BCL3 transcription coactivator Homo sapiens 0-4 27897368-1 2017 BCl3 -induced borylative cyclization of aryl-alkynes possessing ortho-EMe (E=S, O) groups represents a simple, metal-free method for the formation of C3-borylated benzothiophenes and benzofurans. benzothiophene 163-178 BCL3 transcription coactivator Homo sapiens 0-4 27897368-1 2017 BCl3 -induced borylative cyclization of aryl-alkynes possessing ortho-EMe (E=S, O) groups represents a simple, metal-free method for the formation of C3-borylated benzothiophenes and benzofurans. Benzofurans 183-194 BCL3 transcription coactivator Homo sapiens 0-4 27405060-6 2016 RESULTS: Hepatocyte-specific overexpression of Bcl-3 led to pronounced metabolic derangement, characterized by enhanced hepatic steatosis from increased de novo lipogenesis and uptake, as well as decreased hydrolysis and export of fatty acids. Fatty Acids 231-242 BCL3 transcription coactivator Homo sapiens 47-52 27748795-2 2016 B-cell CLL/lymphoma 3 (BCL3) was previously found to be a putative proto-oncogene in human cancers and the decoy receptor DcR1 is induced in a p50/Bcl3-dependent manner and attenuates the efficacy of temozolomide in glioblastoma cells. Temozolomide 200-212 BCL3 transcription coactivator Homo sapiens 0-21 27748795-2 2016 B-cell CLL/lymphoma 3 (BCL3) was previously found to be a putative proto-oncogene in human cancers and the decoy receptor DcR1 is induced in a p50/Bcl3-dependent manner and attenuates the efficacy of temozolomide in glioblastoma cells. Temozolomide 200-212 BCL3 transcription coactivator Homo sapiens 23-27 27351275-3 2016 Synthesis of a chloroborenium species [LBCl](+) [BCl4 ](-) (9) without involvement of a weakly coordinating anion was also demonstrated from a reaction of LBH2 (4) with three equivalents of BCl3 . chloroborenium 15-29 BCL3 transcription coactivator Homo sapiens 190-194 27489104-3 2016 Here we show that IkappaBzeta productively interacts with p50 via Asp-451 in the N terminus of ANK1, a residue that is evolutionarily conserved among IkappaBzeta and the related nuclear IkappaB proteins Bcl-3 and IkappaBNS Threonine substitution for Asp-451 abrogates direct association with the kappaB-site-binding protein p50, complex formation with the Lcn2 promoter DNA, and activation of Lcn2 transcription. Aspartic Acid 66-69 BCL3 transcription coactivator Homo sapiens 203-208 27489104-5 2016 Both termini of the ANK domain in Bcl-3 and IkappaBNS function in a manner similar to that of IkappaBzeta to interact with promoter DNA, indicating a common mechanism in which the nuclear IkappaBs form a regulatory complex with NF-kappaB and promoter DNA via the invariant aspartate in ANK1 and the conserved basic residues in ANK7. Aspartic Acid 273-282 BCL3 transcription coactivator Homo sapiens 34-39 27503798-2 2016 BCl3-mediated dehydrative cyclization of 1,3-diaryloxyacetones under mild conditions permitted regioselective ring closure to afford 3-((2-iodoaryloxy)methyl)benzofurans which were converted to the corresponding pterocarpenes by Pd-catalyzed intramolecular direct arylation. 1,3-diaryloxyacetones 41-62 BCL3 transcription coactivator Homo sapiens 0-4 27503798-2 2016 BCl3-mediated dehydrative cyclization of 1,3-diaryloxyacetones under mild conditions permitted regioselective ring closure to afford 3-((2-iodoaryloxy)methyl)benzofurans which were converted to the corresponding pterocarpenes by Pd-catalyzed intramolecular direct arylation. 3-((2-iodoaryloxy)methyl)benzofurans 133-169 BCL3 transcription coactivator Homo sapiens 0-4 27503798-2 2016 BCl3-mediated dehydrative cyclization of 1,3-diaryloxyacetones under mild conditions permitted regioselective ring closure to afford 3-((2-iodoaryloxy)methyl)benzofurans which were converted to the corresponding pterocarpenes by Pd-catalyzed intramolecular direct arylation. pterocarpenes 212-225 BCL3 transcription coactivator Homo sapiens 0-4 27503798-2 2016 BCl3-mediated dehydrative cyclization of 1,3-diaryloxyacetones under mild conditions permitted regioselective ring closure to afford 3-((2-iodoaryloxy)methyl)benzofurans which were converted to the corresponding pterocarpenes by Pd-catalyzed intramolecular direct arylation. Palladium 229-231 BCL3 transcription coactivator Homo sapiens 0-4 27351275-3 2016 Synthesis of a chloroborenium species [LBCl](+) [BCl4 ](-) (9) without involvement of a weakly coordinating anion was also demonstrated from a reaction of LBH2 (4) with three equivalents of BCl3 . chloroborenium 15-29 BCL3 transcription coactivator Homo sapiens 49-53 27351275-3 2016 Synthesis of a chloroborenium species [LBCl](+) [BCl4 ](-) (9) without involvement of a weakly coordinating anion was also demonstrated from a reaction of LBH2 (4) with three equivalents of BCl3 . lbcl 39-43 BCL3 transcription coactivator Homo sapiens 49-53 27351275-3 2016 Synthesis of a chloroborenium species [LBCl](+) [BCl4 ](-) (9) without involvement of a weakly coordinating anion was also demonstrated from a reaction of LBH2 (4) with three equivalents of BCl3 . lbcl 39-43 BCL3 transcription coactivator Homo sapiens 190-194 27351275-3 2016 Synthesis of a chloroborenium species [LBCl](+) [BCl4 ](-) (9) without involvement of a weakly coordinating anion was also demonstrated from a reaction of LBH2 (4) with three equivalents of BCl3 . lbh2 155-159 BCL3 transcription coactivator Homo sapiens 49-53 27351275-3 2016 Synthesis of a chloroborenium species [LBCl](+) [BCl4 ](-) (9) without involvement of a weakly coordinating anion was also demonstrated from a reaction of LBH2 (4) with three equivalents of BCl3 . lbh2 155-159 BCL3 transcription coactivator Homo sapiens 190-194 30452171-2 2016 Selective demethylation of 2 using either BBr or BCl3/TBAI (tetrabutylammonium iodide) gave five O-methylquercetins (3-6), with satisfactory yields. o-methylquercetins 97-115 BCL3 transcription coactivator Homo sapiens 49-53 26033966-8 2016 Treatment with 5-ASA suppressed BCL-3 expression in colorectal cancer cells. Mesalamine 15-20 BCL3 transcription coactivator Homo sapiens 32-37 26515727-3 2015 In search for the mechanism, we found that MSCs and CAFs similarly increased the activity of the PI3K/AKT and the JAK/STAT3 pathways and upregulated the expression of integrin beta1, IGF1R, HIF1alpha, CAIX and Bcl-3 in MCF-7 cells. cafs 52-56 BCL3 transcription coactivator Homo sapiens 210-215 26822161-2 2016 In the case of 1 and 2 reaction with two equivalents of BCl3 affording the corresponding cation via chloride abstraction. Chlorides 100-108 BCL3 transcription coactivator Homo sapiens 56-60 26822161-3 2016 These cations coordinate MeCN to give the six coordinate Ru cation salts [(L)Ru(CHPh)- (NCMe)(O(CH2CH2S)2BCl2)][BCl4] L = SIMes 17, PCy3 18). acetonitrile 25-29 BCL3 transcription coactivator Homo sapiens 112-116 26822161-3 2016 These cations coordinate MeCN to give the six coordinate Ru cation salts [(L)Ru(CHPh)- (NCMe)(O(CH2CH2S)2BCl2)][BCl4] L = SIMes 17, PCy3 18). ru cation salts 57-72 BCL3 transcription coactivator Homo sapiens 112-116 26822161-4 2016 The generated five coordinate cations derived from 2-9 via addition of two equivalents of BCl3 were evaluated in standard preliminary tests for olefin metathesis catalysis. Alkenes 144-150 BCL3 transcription coactivator Homo sapiens 90-94 26515727-10 2015 In conclusion, our data suggest that, by targeting IGFBP5 expression in ERalpha-positive breast cancer cells, such as MCF-7 cells, MSCs and CAFs are able to orchestrate a variety of events, particularly activation of the PI3K/AKT pathway, upregulation of Bcl-3 expression and desensitization to anti-estrogen. cafs 140-144 BCL3 transcription coactivator Homo sapiens 255-260 26493883-0 2015 Heterolysis of H2 Across a Classical Lewis Pair, 2,6-Lutidine BCl3 : Synthesis, Characterization, and Mechanism. Hydrogen 15-17 BCL3 transcription coactivator Homo sapiens 62-66 26426745-6 2015 A neutral adduct (dpma)(BCl3)2 was obtained from the reaction between dpma and BCl3 in Et2O using 1 : 2 stoichiometry. DPMA 18-22 BCL3 transcription coactivator Homo sapiens 24-28 26426745-6 2015 A neutral adduct (dpma)(BCl3)2 was obtained from the reaction between dpma and BCl3 in Et2O using 1 : 2 stoichiometry. DPMA 18-22 BCL3 transcription coactivator Homo sapiens 79-83 26426745-6 2015 A neutral adduct (dpma)(BCl3)2 was obtained from the reaction between dpma and BCl3 in Et2O using 1 : 2 stoichiometry. Ether 87-91 BCL3 transcription coactivator Homo sapiens 24-28 26426745-6 2015 A neutral adduct (dpma)(BCl3)2 was obtained from the reaction between dpma and BCl3 in Et2O using 1 : 2 stoichiometry. Ether 87-91 BCL3 transcription coactivator Homo sapiens 79-83 26493883-0 2015 Heterolysis of H2 Across a Classical Lewis Pair, 2,6-Lutidine BCl3 : Synthesis, Characterization, and Mechanism. 2,6-lutidine 49-61 BCL3 transcription coactivator Homo sapiens 62-66 26493883-1 2015 We report that 2,6-lutidine trichloroborane (Lut BCl3 ) reacts with H2 in toluene, bromobenzene, dichloromethane, and Lut solvents producing the neutral hydride, Lut BHCl2 . 2,6-lutidine trichloroborane 15-43 BCL3 transcription coactivator Homo sapiens 49-53 26493883-1 2015 We report that 2,6-lutidine trichloroborane (Lut BCl3 ) reacts with H2 in toluene, bromobenzene, dichloromethane, and Lut solvents producing the neutral hydride, Lut BHCl2 . Hydrogen 68-70 BCL3 transcription coactivator Homo sapiens 49-53 26493883-1 2015 We report that 2,6-lutidine trichloroborane (Lut BCl3 ) reacts with H2 in toluene, bromobenzene, dichloromethane, and Lut solvents producing the neutral hydride, Lut BHCl2 . Toluene 74-81 BCL3 transcription coactivator Homo sapiens 49-53 26493883-1 2015 We report that 2,6-lutidine trichloroborane (Lut BCl3 ) reacts with H2 in toluene, bromobenzene, dichloromethane, and Lut solvents producing the neutral hydride, Lut BHCl2 . bromobenzene 83-95 BCL3 transcription coactivator Homo sapiens 49-53 26493883-1 2015 We report that 2,6-lutidine trichloroborane (Lut BCl3 ) reacts with H2 in toluene, bromobenzene, dichloromethane, and Lut solvents producing the neutral hydride, Lut BHCl2 . Methylene Chloride 97-112 BCL3 transcription coactivator Homo sapiens 49-53 26493883-1 2015 We report that 2,6-lutidine trichloroborane (Lut BCl3 ) reacts with H2 in toluene, bromobenzene, dichloromethane, and Lut solvents producing the neutral hydride, Lut BHCl2 . Creatinine 153-160 BCL3 transcription coactivator Homo sapiens 49-53 26493883-1 2015 We report that 2,6-lutidine trichloroborane (Lut BCl3 ) reacts with H2 in toluene, bromobenzene, dichloromethane, and Lut solvents producing the neutral hydride, Lut BHCl2 . lut bhcl2 162-171 BCL3 transcription coactivator Homo sapiens 49-53 26493883-3 2015 Lut BCl3 was calculated to react with H2 and form the ion pair, [LutH(+) ][HBCl3 (-) ], with a barrier of DeltaH( ) =24.7 kcal mol(-1) (DeltaG( ) =29.8 kcal mol(-1) ). Hydrogen 38-40 BCL3 transcription coactivator Homo sapiens 4-8 26493883-9 2015 Conversion of the intermediate 2-(BHCl2 CH2 )-6-Me(C5 H3 NH) to Lut BHCl2 may occur by intermolecular steps involving proton/hydride transfers to Lut/BCl3 . 2-(bhcl2 ch2 )-6-me 31-50 BCL3 transcription coactivator Homo sapiens 150-154 26493883-9 2015 Conversion of the intermediate 2-(BHCl2 CH2 )-6-Me(C5 H3 NH) to Lut BHCl2 may occur by intermolecular steps involving proton/hydride transfers to Lut/BCl3 . lut bhcl2 64-73 BCL3 transcription coactivator Homo sapiens 150-154 26331979-2 2015 In the presence of BCl3 (1 equiv) as the sole boron source, intramolecular aminoboration of sulfonamide derivatives of 4-penten-1-amines, 5-hexen-1-amines, and 2-allylanilines proceeded readily without the use of any catalyst. Sulfonamides 92-103 BCL3 transcription coactivator Homo sapiens 19-23 26331979-2 2015 In the presence of BCl3 (1 equiv) as the sole boron source, intramolecular aminoboration of sulfonamide derivatives of 4-penten-1-amines, 5-hexen-1-amines, and 2-allylanilines proceeded readily without the use of any catalyst. 4-penten-1-amines 119-136 BCL3 transcription coactivator Homo sapiens 19-23 26331979-2 2015 In the presence of BCl3 (1 equiv) as the sole boron source, intramolecular aminoboration of sulfonamide derivatives of 4-penten-1-amines, 5-hexen-1-amines, and 2-allylanilines proceeded readily without the use of any catalyst. 5-hexen-1-amines 138-154 BCL3 transcription coactivator Homo sapiens 19-23 26331979-2 2015 In the presence of BCl3 (1 equiv) as the sole boron source, intramolecular aminoboration of sulfonamide derivatives of 4-penten-1-amines, 5-hexen-1-amines, and 2-allylanilines proceeded readily without the use of any catalyst. 2-allylanilines 160-175 BCL3 transcription coactivator Homo sapiens 19-23 26304772-1 2015 The reaction of a recently synthesized dihydroboron species complexed with bis(phosphinimino)amide, LBH2 (), (L = [N(Ph2PN(2,4,6-Me3C6H2))2](-)) with 3 equivalents of BH2Cl SMe2 or one equivalent of BCl3 affords the first stable monohydridoborenium ion, [LBH](+)[HBCl3](-) () that is stable without a weakly coordinating bulky anion. dihydroboron 39-51 BCL3 transcription coactivator Homo sapiens 199-203 25944662-8 2015 Thus, our results suggest that PPARgamma can induce growth suppression of ovarian cancer by upregulating miR-125b which inhibition of proto-oncogene BCL3. mir-125b 105-113 BCL3 transcription coactivator Homo sapiens 149-153 26274826-7 2015 The B-F sigma-bond cleavage of BF2Ar(F) (Ar(F)=3,5-bis(trifluoromethyl)phenyl) and the B-Cl sigma-bond cleavage of BCl3 by 1 are accelerated by the participation of the second borane. 3,5-bis(trifluoromethyl)phenyl) 47-78 BCL3 transcription coactivator Homo sapiens 115-119 26237115-0 2015 Formation of C(sp(2))-boronate esters by borylative cyclization of alkynes using BCl3. Alkynes 67-74 BCL3 transcription coactivator Homo sapiens 81-85 26237115-1 2015 BCl3 is an inexpensive electrophile which induces the borylative cyclization of a wide range of substituted alkynes to regioselectively form polycycles containing synthetically versatile C(sp(2) ) boronate esters. Alkynes 108-115 BCL3 transcription coactivator Homo sapiens 0-4 26237115-1 2015 BCl3 is an inexpensive electrophile which induces the borylative cyclization of a wide range of substituted alkynes to regioselectively form polycycles containing synthetically versatile C(sp(2) ) boronate esters. (sp(2) ) boronate esters 188-212 BCL3 transcription coactivator Homo sapiens 0-4 26237115-3 2015 Intermolecular 1,2-carboboration of alkynes is also achieved using BCl3 to generate trisubstituted vinyl boronate esters. Alkynes 36-43 BCL3 transcription coactivator Homo sapiens 67-71 26237115-3 2015 Intermolecular 1,2-carboboration of alkynes is also achieved using BCl3 to generate trisubstituted vinyl boronate esters. trisubstituted vinyl boronate esters 84-120 BCL3 transcription coactivator Homo sapiens 67-71 25808868-7 2015 Loss-of-function and gain-of-function studies reveal that the atypical IkappaB protein, Bcl3, is also required for induction of DcR1 by temozolomide. Temozolomide 136-148 BCL3 transcription coactivator Homo sapiens 88-92 24984763-10 2014 Furthermore, these analyses indicate that the barrier along the B-N potential of CH3CN-BCl3 results from Pauli repulsion between the pi electrons on the nitrile moiety and the chlorine atoms in BCl3, which is significant at relatively long distances where attractive bonding interactions fail to overcome it. Nitriles 153-160 BCL3 transcription coactivator Homo sapiens 81-91 25462569-3 2015 Although these thiolate derivatives are shown to exhibit modest metathesis activities, the reactivity is enhanced in the presence of BCl3. thiolate 15-23 BCL3 transcription coactivator Homo sapiens 133-137 25407641-1 2015 This paper reports a complete ammonia borane (AB) regeneration process in which Bu3SnH was utilized as a reductant for the reductive dechlorination of BCl3, and Et2PhN was selected as a "helper ligand" to generate Et2PhN BH3, which gives rise to a high yield of AB by a base-exchange reaction at ambient temperature. Ammonia borane 30-44 BCL3 transcription coactivator Homo sapiens 151-155 25407641-1 2015 This paper reports a complete ammonia borane (AB) regeneration process in which Bu3SnH was utilized as a reductant for the reductive dechlorination of BCl3, and Et2PhN was selected as a "helper ligand" to generate Et2PhN BH3, which gives rise to a high yield of AB by a base-exchange reaction at ambient temperature. Tributyltin hydride 80-86 BCL3 transcription coactivator Homo sapiens 151-155 25089799-7 2014 Bcl3 expression is regulated by bortezomib (BZ)-mediated proteasome inhibition, and BZ inhibits Bcl3 recruitment to its target promoters, resulting in decreased expression of cIAP1 and cIAP2, but increased expression of IL-8 and IL-17. Bortezomib 32-42 BCL3 transcription coactivator Homo sapiens 0-4 25089799-7 2014 Bcl3 expression is regulated by bortezomib (BZ)-mediated proteasome inhibition, and BZ inhibits Bcl3 recruitment to its target promoters, resulting in decreased expression of cIAP1 and cIAP2, but increased expression of IL-8 and IL-17. Bortezomib 44-46 BCL3 transcription coactivator Homo sapiens 0-4 25089799-7 2014 Bcl3 expression is regulated by bortezomib (BZ)-mediated proteasome inhibition, and BZ inhibits Bcl3 recruitment to its target promoters, resulting in decreased expression of cIAP1 and cIAP2, but increased expression of IL-8 and IL-17. Bortezomib 84-86 BCL3 transcription coactivator Homo sapiens 96-100 25313303-2 2014 FeCl3 that has rarely been utilized before is introduced not only as a catalyst but also as an efficient transforming agent which converts boron powder into boron chloride (BCl3) vapor in situ. ferric chloride 0-5 BCL3 transcription coactivator Homo sapiens 173-177 25313303-2 2014 FeCl3 that has rarely been utilized before is introduced not only as a catalyst but also as an efficient transforming agent which converts boron powder into boron chloride (BCl3) vapor in situ. Boron 139-144 BCL3 transcription coactivator Homo sapiens 173-177 25313303-2 2014 FeCl3 that has rarely been utilized before is introduced not only as a catalyst but also as an efficient transforming agent which converts boron powder into boron chloride (BCl3) vapor in situ. boron trichloride 157-171 BCL3 transcription coactivator Homo sapiens 173-177 25138585-1 2014 The reaction of 8-(trimethylsiloxy)quinoline (QOTMS) with BCl3 and (aryl)BCl2 forms QOBCl2 and QOBCl(aryl). Quinoline, 8-[(trimethylsilyl)oxy]- 16-44 BCL3 transcription coactivator Homo sapiens 58-62 25582820-1 2015 Haloarenes undergo direct borylation using amine : BCl3 : AlCl3 in the ratio of 1 : 1 : 2. haloarenes 0-10 BCL3 transcription coactivator Homo sapiens 51-55 25582820-1 2015 Haloarenes undergo direct borylation using amine : BCl3 : AlCl3 in the ratio of 1 : 1 : 2. Aluminum Chloride 58-63 BCL3 transcription coactivator Homo sapiens 51-55 25573559-7 2015 The radicals have been prepared in a pulsed electric discharge jet using a precursor mixture of BCl3 and H2 or D2 in high pressure argon. Argon 131-136 BCL3 transcription coactivator Homo sapiens 96-100 25089799-9 2014 In untreated cells, the Bcl3 promoter is occupied predominantly by p65/p50 heterodimers, inducing Bcl3 expression; however, in BZ-treated cells, the p65/50 heterodimers are replaced by p52 subunits, resulting in Bcl3 transcriptional repression. Bortezomib 127-129 BCL3 transcription coactivator Homo sapiens 24-28 25089799-9 2014 In untreated cells, the Bcl3 promoter is occupied predominantly by p65/p50 heterodimers, inducing Bcl3 expression; however, in BZ-treated cells, the p65/50 heterodimers are replaced by p52 subunits, resulting in Bcl3 transcriptional repression. Bortezomib 127-129 BCL3 transcription coactivator Homo sapiens 98-102 25089799-9 2014 In untreated cells, the Bcl3 promoter is occupied predominantly by p65/p50 heterodimers, inducing Bcl3 expression; however, in BZ-treated cells, the p65/50 heterodimers are replaced by p52 subunits, resulting in Bcl3 transcriptional repression. Bortezomib 127-129 BCL3 transcription coactivator Homo sapiens 98-102 24984763-10 2014 Furthermore, these analyses indicate that the barrier along the B-N potential of CH3CN-BCl3 results from Pauli repulsion between the pi electrons on the nitrile moiety and the chlorine atoms in BCl3, which is significant at relatively long distances where attractive bonding interactions fail to overcome it. Nitriles 153-160 BCL3 transcription coactivator Homo sapiens 87-91 24984763-10 2014 Furthermore, these analyses indicate that the barrier along the B-N potential of CH3CN-BCl3 results from Pauli repulsion between the pi electrons on the nitrile moiety and the chlorine atoms in BCl3, which is significant at relatively long distances where attractive bonding interactions fail to overcome it. Chlorine 176-184 BCL3 transcription coactivator Homo sapiens 81-91 24984763-10 2014 Furthermore, these analyses indicate that the barrier along the B-N potential of CH3CN-BCl3 results from Pauli repulsion between the pi electrons on the nitrile moiety and the chlorine atoms in BCl3, which is significant at relatively long distances where attractive bonding interactions fail to overcome it. Chlorine 176-184 BCL3 transcription coactivator Homo sapiens 87-91 23562784-5 2013 Arsenic dependent regulation of AATF (Apoptosis Antagonizing Transcription factor) and BCL3 (B-cell Lymphoma 3) were also found to be modulated through its capacity to induce miR-2909 expression. Arsenic 0-7 BCL3 transcription coactivator Homo sapiens 87-91 24898448-1 2014 Chiral binaphthyl-linked subphthalocyanines (SubPcs) (1) have been prepared by the cyclotrimerization reaction of a phthalonitrile linked with (R)- and (S)-2,2"-binaphthyl in the presence of BCl3, and characterized by various spectroscopies including NMR, electronic absorption, CD, and MCD, as well as electrochemistry. binaphthyl-linked subphthalocyanines 7-43 BCL3 transcription coactivator Homo sapiens 191-195 24992107-1 2014 The crystal structures of three products of the reaction of 2-phenylphenol and BCl3 have been determined. 2-phenylphenol 60-74 BCL3 transcription coactivator Homo sapiens 79-83 24484404-4 2014 We have selected AlCl3, BCl3, BF3, and GdCl3 as binding Lewis acids, in that they exhibit sufficiently strong binding affinity toward the aromatic ketone derivatives to afford stable complexes and yet do not possess low-lying electronic transitions vs the ligands. Lewis Acids 56-67 BCL3 transcription coactivator Homo sapiens 24-28 24484404-4 2014 We have selected AlCl3, BCl3, BF3, and GdCl3 as binding Lewis acids, in that they exhibit sufficiently strong binding affinity toward the aromatic ketone derivatives to afford stable complexes and yet do not possess low-lying electronic transitions vs the ligands. Ketones 147-153 BCL3 transcription coactivator Homo sapiens 24-28 24328213-7 2013 This analysis predicts that (BF)4 and (BCl)4, which are isoelectronic with, respectively, (CO)4 and (CS)4, should both prefer a Td to a D4h equilibrium geometry. (2~{R})-2-[(~{S})-(3-methylphenyl)-phenyl-methyl]pyrrolidine 136-139 BCL3 transcription coactivator Homo sapiens 39-44 23933549-0 2013 QTAIM charge-charge flux-dipole flux models for the fundamental infrared intensities of BF3 and BCl3. dipole 25-31 BCL3 transcription coactivator Homo sapiens 96-100 23933549-1 2013 Quantum Theory of Atoms in Molecules Charge-Charge Flux-Dipole Flux (QTAIM/CCFDF) models have been determined for the BF3 and BCl3 molecules. dipole 56-62 BCL3 transcription coactivator Homo sapiens 126-130 23933549-6 2013 The MP2/6-31G(2d,2p) BCl3 stretching intensity can be accurately estimated by equilibrium charge movement since the charge and dipole fluxes almost exactly cancel one another. dipole 127-133 BCL3 transcription coactivator Homo sapiens 21-25 23933549-7 2013 Both in-plane and out-of-plane BF3 and BCl3 bending deformations are described by equilibrium charge movements that are partially canceled by opposing dipole fluxes that measure the effect on the dipole moment change from electron densities polarized in the opposite direction. dipole 151-157 BCL3 transcription coactivator Homo sapiens 39-43 23933549-7 2013 Both in-plane and out-of-plane BF3 and BCl3 bending deformations are described by equilibrium charge movements that are partially canceled by opposing dipole fluxes that measure the effect on the dipole moment change from electron densities polarized in the opposite direction. dipole 196-202 BCL3 transcription coactivator Homo sapiens 39-43 24236758-7 2013 The impact of the orientation of the perchlorate counterions is disclosed by comparison to J(AB) studies using structurally similar ligands but with different electronegativity (namely, BF4(-), BCl4(-), and BBr4(-)). perchlorate 37-48 BCL3 transcription coactivator Homo sapiens 194-198 23562784-5 2013 Arsenic dependent regulation of AATF (Apoptosis Antagonizing Transcription factor) and BCL3 (B-cell Lymphoma 3) were also found to be modulated through its capacity to induce miR-2909 expression. Arsenic 0-7 BCL3 transcription coactivator Homo sapiens 93-110 23149915-6 2013 Bcl3 knockdown resulted in a 61% decrease in tumor cell motility and a concomitant increase in the cell migration inhibitors Nme1, Nme2, and Nme3, the GDP dissociation inhibitor Arhgdib, and the metalloprotease inhibitors Timp1 and Timp2. arhgdib 178-185 BCL3 transcription coactivator Homo sapiens 0-4 23494744-3 2013 We found that, in Bcl-3-silenced cells, caspase-3, caspase-8 and caspase-9 activation is accelerated and tBid mitochondrial content is increased. tBID 105-109 BCL3 transcription coactivator Homo sapiens 18-23 22931421-8 2013 AZT down-regulated the pro-proliferative genes encoding AKT1, MYC, STAT1, MAPK8, MAPK9, CCL-3, Bcl-3, and cyclin D2; pro-angiogenenic genes encoding VEGF and IL8; and genes involved in cell adhesion (ICAM1 and FN1) and the NF-kappaB pathway. Zidovudine 0-3 BCL3 transcription coactivator Homo sapiens 95-100 22674228-2 2012 Subsequent reaction of 1 with BCl(3) led to the chloroborane (p-C(6)F(4)H)(2)BCl (2), which was converted to the borane [(p-C(6)F(4)H)(2)BH](2) (3) by treatment with the hydride source Me(2)SiHCl. Chloroborane 48-60 BCL3 transcription coactivator Homo sapiens 30-36 24088350-4 2013 The utility of this reaction has been fully demonstrated through a total synthesis of yatakemycin, which features the regioselective ring opening of (S)-epichlorohydrin with 2,6-dibromophenyllithium species and the efficient deprotection of benzyl groups of aryl benzyl ether with BCl3 in the presence of pentamethylbenzene. yatakemycin 86-97 BCL3 transcription coactivator Homo sapiens 281-285 24088350-4 2013 The utility of this reaction has been fully demonstrated through a total synthesis of yatakemycin, which features the regioselective ring opening of (S)-epichlorohydrin with 2,6-dibromophenyllithium species and the efficient deprotection of benzyl groups of aryl benzyl ether with BCl3 in the presence of pentamethylbenzene. Epichlorohydrin 149-168 BCL3 transcription coactivator Homo sapiens 281-285 23102377-0 2012 Theoretical study of the binding of silane (SiH4) with borane (BH3), diborane (B2H6), and boron trichloride (BCl3): the role of core-electron correlation. Silanes 36-42 BCL3 transcription coactivator Homo sapiens 109-113 23102377-0 2012 Theoretical study of the binding of silane (SiH4) with borane (BH3), diborane (B2H6), and boron trichloride (BCl3): the role of core-electron correlation. monosilane 44-48 BCL3 transcription coactivator Homo sapiens 109-113 23102377-0 2012 Theoretical study of the binding of silane (SiH4) with borane (BH3), diborane (B2H6), and boron trichloride (BCl3): the role of core-electron correlation. boron trichloride 90-107 BCL3 transcription coactivator Homo sapiens 109-113 23097381-0 2012 A self-contained regeneration scheme for spent ammonia borane based on the catalytic hydrodechlorination of BCl3. Ammonia borane 47-61 BCL3 transcription coactivator Homo sapiens 108-112 22674228-2 2012 Subsequent reaction of 1 with BCl(3) led to the chloroborane (p-C(6)F(4)H)(2)BCl (2), which was converted to the borane [(p-C(6)F(4)H)(2)BH](2) (3) by treatment with the hydride source Me(2)SiHCl. Chlorosilicon 190-195 BCL3 transcription coactivator Homo sapiens 30-36 22022702-1 2011 Electrophilic direct borylation is facilitated, and arene substrate scope enhanced, by using electrophiles derived from inexpensive reagents; specifically an amine, BCl(3) and AlCl(3). arene 52-57 BCL3 transcription coactivator Homo sapiens 165-170 22662961-0 2012 Decomposition reaction rate of BCl3-C3H6(propene)-H2 in the gas phase. Hydrogen 50-52 BCL3 transcription coactivator Homo sapiens 31-35 20845419-2 2010 The key steps involve a transmetallation reaction between BCl(3) and an appropriate stannacyclic precursor, and the dehydrochlorination of the H(2)IMes adduct of the chloroborane product. h(2)imes 143-151 BCL3 transcription coactivator Homo sapiens 58-64 21913687-0 2011 Reaction mechanism for the thermal decomposition of BCl3/CH4/H2 gas mixtures. Methane 57-60 BCL3 transcription coactivator Homo sapiens 52-56 21913687-0 2011 Reaction mechanism for the thermal decomposition of BCl3/CH4/H2 gas mixtures. Hydrogen 61-63 BCL3 transcription coactivator Homo sapiens 52-56 21491857-0 2011 Theoretical study of the decomposition of BCl3 induced by a H radical. h radical 60-69 BCL3 transcription coactivator Homo sapiens 42-46 20658525-0 2011 MiR-125b targets BCL3 and suppresses ovarian cancer proliferation. mir-125b 0-8 BCL3 transcription coactivator Homo sapiens 17-21 20658525-5 2011 This inhibitory effect on OC cell growth was mediated by miR-125b inhibition of the translation of an mRNA encoding a proto-oncogene, BCL3. mir-125b 57-65 BCL3 transcription coactivator Homo sapiens 134-138 20845419-2 2010 The key steps involve a transmetallation reaction between BCl(3) and an appropriate stannacyclic precursor, and the dehydrochlorination of the H(2)IMes adduct of the chloroborane product. Chloroborane 166-178 BCL3 transcription coactivator Homo sapiens 58-64 20420878-11 2010 The up-regulation of cyclin D1 mediated by the p52-Bcl3 complex in response to low concentration arsenite might be important in assessing the health risk of low concentration arsenite and understanding the mechanisms of the harmful effects of arsenite. arsenite 97-105 BCL3 transcription coactivator Homo sapiens 51-55 20558726-6 2010 The N-terminal part of BCL-3 includes lysines 13 and 26 required for the Lys(48)-linked polyubiquitination of BCL-3. Lysine 38-45 BCL3 transcription coactivator Homo sapiens 23-28 20558726-6 2010 The N-terminal part of BCL-3 includes lysines 13 and 26 required for the Lys(48)-linked polyubiquitination of BCL-3. Lysine 38-45 BCL3 transcription coactivator Homo sapiens 110-115 20558726-6 2010 The N-terminal part of BCL-3 includes lysines 13 and 26 required for the Lys(48)-linked polyubiquitination of BCL-3. Lysine 73-76 BCL3 transcription coactivator Homo sapiens 23-28 20558726-6 2010 The N-terminal part of BCL-3 includes lysines 13 and 26 required for the Lys(48)-linked polyubiquitination of BCL-3. Lysine 73-76 BCL3 transcription coactivator Homo sapiens 110-115 20547759-4 2010 CtBP is also required for the oncogenic potential of BCL-3 and for its ability to inhibit UV-mediated cell apoptosis in keratinocytes. ctbp 0-4 BCL3 transcription coactivator Homo sapiens 53-58 20737317-1 2010 OBJECTIVE: To study the effects of NS398, a selective cyclooxygenase-2 (COX-2) inhibitor, on the transcription and translation of BCL-3 and its regulatory gene cyclin D1 in colon cancer cell line SW480. N-(2-cyclohexyloxy-4-nitrophenyl)methanesulfonamide 35-40 BCL3 transcription coactivator Homo sapiens 130-135 20420878-0 2010 p52-Bcl3 complex promotes cyclin D1 expression in BEAS-2B cells in response to low concentration arsenite. arsenite 97-105 BCL3 transcription coactivator Homo sapiens 4-8 20420878-9 2010 Activation and nuclear localization of p52 and Bcl3 in response to low concentration arsenite indicated that the non-canonical NF-kappaB pathway was involved in arsenite-induced cyclin D1 expression. arsenite 85-93 BCL3 transcription coactivator Homo sapiens 47-51 20420878-9 2010 Activation and nuclear localization of p52 and Bcl3 in response to low concentration arsenite indicated that the non-canonical NF-kappaB pathway was involved in arsenite-induced cyclin D1 expression. arsenite 161-169 BCL3 transcription coactivator Homo sapiens 47-51 20420878-11 2010 The up-regulation of cyclin D1 mediated by the p52-Bcl3 complex in response to low concentration arsenite might be important in assessing the health risk of low concentration arsenite and understanding the mechanisms of the harmful effects of arsenite. arsenite 175-183 BCL3 transcription coactivator Homo sapiens 51-55 20420878-11 2010 The up-regulation of cyclin D1 mediated by the p52-Bcl3 complex in response to low concentration arsenite might be important in assessing the health risk of low concentration arsenite and understanding the mechanisms of the harmful effects of arsenite. arsenite 175-183 BCL3 transcription coactivator Homo sapiens 51-55 19908792-0 2009 Low damage atomic layer etching of ZrO2 by using BCl3 gas and ar neutral beam. zirconium oxide 35-39 BCL3 transcription coactivator Homo sapiens 49-53 20471514-5 2010 When bortezomib was added, some proapoptotic genes (CARD9, TRAIL) were upregulated, and some antiapoptotic genes (BCL2, BCL3, FLICE) were downregulated. Bortezomib 5-15 BCL3 transcription coactivator Homo sapiens 120-124 20056886-2 2010 Using a copper-catalyzed, vapor-liquid-solid-growth process, SiCl4 and BCl3 were used to grow ordered arrays of crystalline p-type silicon (p-Si) microwires on p+-Si(111) substrates. Copper 8-14 BCL3 transcription coactivator Homo sapiens 71-75 20056886-2 2010 Using a copper-catalyzed, vapor-liquid-solid-growth process, SiCl4 and BCl3 were used to grow ordered arrays of crystalline p-type silicon (p-Si) microwires on p+-Si(111) substrates. Silicon 131-138 BCL3 transcription coactivator Homo sapiens 71-75 20056886-2 2010 Using a copper-catalyzed, vapor-liquid-solid-growth process, SiCl4 and BCl3 were used to grow ordered arrays of crystalline p-type silicon (p-Si) microwires on p+-Si(111) substrates. Silicon 142-144 BCL3 transcription coactivator Homo sapiens 71-75 20397251-0 2010 BCl3-mediated ene reaction of sulfur dioxide and unfunctionalized alkenes. Sulfur Dioxide 30-44 BCL3 transcription coactivator Homo sapiens 0-4 20397251-0 2010 BCl3-mediated ene reaction of sulfur dioxide and unfunctionalized alkenes. Alkenes 66-73 BCL3 transcription coactivator Homo sapiens 0-4 20397251-3 2010 Indeed, in the presence of one equivalent of BCl(3), the unstable sulfinic acid form stable sulfinic acid.BCl(3) complexes that can be reacted in situ with NCS to generate corresponding sulfonyl chlorides, or with a base to generate corresponding sulfinates. Sulfinic Acids 66-79 BCL3 transcription coactivator Homo sapiens 45-51 20397251-3 2010 Indeed, in the presence of one equivalent of BCl(3), the unstable sulfinic acid form stable sulfinic acid.BCl(3) complexes that can be reacted in situ with NCS to generate corresponding sulfonyl chlorides, or with a base to generate corresponding sulfinates. Sulfinic Acids 66-79 BCL3 transcription coactivator Homo sapiens 106-112 20397251-3 2010 Indeed, in the presence of one equivalent of BCl(3), the unstable sulfinic acid form stable sulfinic acid.BCl(3) complexes that can be reacted in situ with NCS to generate corresponding sulfonyl chlorides, or with a base to generate corresponding sulfinates. Sulfinic Acids 92-105 BCL3 transcription coactivator Homo sapiens 45-51 20397251-3 2010 Indeed, in the presence of one equivalent of BCl(3), the unstable sulfinic acid form stable sulfinic acid.BCl(3) complexes that can be reacted in situ with NCS to generate corresponding sulfonyl chlorides, or with a base to generate corresponding sulfinates. Sulfinic Acids 92-105 BCL3 transcription coactivator Homo sapiens 106-112 20397251-3 2010 Indeed, in the presence of one equivalent of BCl(3), the unstable sulfinic acid form stable sulfinic acid.BCl(3) complexes that can be reacted in situ with NCS to generate corresponding sulfonyl chlorides, or with a base to generate corresponding sulfinates. sulfonyl chloride 186-204 BCL3 transcription coactivator Homo sapiens 45-51 20397251-3 2010 Indeed, in the presence of one equivalent of BCl(3), the unstable sulfinic acid form stable sulfinic acid.BCl(3) complexes that can be reacted in situ with NCS to generate corresponding sulfonyl chlorides, or with a base to generate corresponding sulfinates. sulfonyl chloride 186-204 BCL3 transcription coactivator Homo sapiens 106-112 20397251-3 2010 Indeed, in the presence of one equivalent of BCl(3), the unstable sulfinic acid form stable sulfinic acid.BCl(3) complexes that can be reacted in situ with NCS to generate corresponding sulfonyl chlorides, or with a base to generate corresponding sulfinates. sulfinates 247-257 BCL3 transcription coactivator Homo sapiens 45-51 20397251-3 2010 Indeed, in the presence of one equivalent of BCl(3), the unstable sulfinic acid form stable sulfinic acid.BCl(3) complexes that can be reacted in situ with NCS to generate corresponding sulfonyl chlorides, or with a base to generate corresponding sulfinates. sulfinates 247-257 BCL3 transcription coactivator Homo sapiens 106-112 20397251-5 2010 The sulfinic acid.BCl(3) complexes can be reacted with ethers that act as oxygen nucleophiles to produce corresponding sulfinic esters. Sulfinic Acids 4-17 BCL3 transcription coactivator Homo sapiens 18-24 20397251-5 2010 The sulfinic acid.BCl(3) complexes can be reacted with ethers that act as oxygen nucleophiles to produce corresponding sulfinic esters. Ethers 55-61 BCL3 transcription coactivator Homo sapiens 18-24 20397251-5 2010 The sulfinic acid.BCl(3) complexes can be reacted with ethers that act as oxygen nucleophiles to produce corresponding sulfinic esters. sulfinic esters 119-134 BCL3 transcription coactivator Homo sapiens 18-24 20226764-5 2010 We found that Bcl-3 interacts with the pleckstrin homology domain and the phosphotyrosine binding domain of IRS-3, and that IRS-3 interacts with the ankyrin repeat domain of Bcl-3. Phosphotyrosine 74-89 BCL3 transcription coactivator Homo sapiens 14-19 19908792-1 2009 This study examined the etch characteristics of ZrO2 etched using an atomic layer etching (ALET) system with BCl3 gas for adsorption and an Ar neutral beam for desorption. zirconium oxide 48-52 BCL3 transcription coactivator Homo sapiens 109-113 19494302-7 2009 Chromatin immunoprecipitation assay demonstrated that p52 and Bcl-3 bind the MIEP in acutely HCMV-infected MDMs. miep 77-81 BCL3 transcription coactivator Homo sapiens 62-67 19282837-5 2009 Bcl-3 silencing enhanced vitamin D3 (1,25D3)-induced gene expression of cathelicidin AMP in keratinocytes, suggesting a negative regulatory function on cathelicidin transcription. Cholecalciferol 25-35 BCL3 transcription coactivator Homo sapiens 0-5 19282837-5 2009 Bcl-3 silencing enhanced vitamin D3 (1,25D3)-induced gene expression of cathelicidin AMP in keratinocytes, suggesting a negative regulatory function on cathelicidin transcription. Adenosine Monophosphate 85-88 BCL3 transcription coactivator Homo sapiens 0-5 18570375-0 2008 Novel polyhydroxylated cyclic nitrones and N-hydroxypyrrolidines through BCl3-mediated deprotection. cyclic nitrones 23-38 BCL3 transcription coactivator Homo sapiens 73-77 18796561-0 2009 Oxidative, multistep activation of the noncanonical NF-kappaB pathway via disulfide Bcl-3/p50 complex. Disulfides 74-83 BCL3 transcription coactivator Homo sapiens 84-89 18796561-4 2009 The early phase, coinciding with substantial thiol depletion, produces a cytosolic preparative complex, consisting of p50 and its interactor Bcl-3 linked by interprotein disulfide bridges. Sulfhydryl Compounds 45-50 BCL3 transcription coactivator Homo sapiens 141-146 18796561-4 2009 The early phase, coinciding with substantial thiol depletion, produces a cytosolic preparative complex, consisting of p50 and its interactor Bcl-3 linked by interprotein disulfide bridges. Disulfides 170-179 BCL3 transcription coactivator Homo sapiens 141-146 19229118-9 2009 CONCLUSIONS: BCL3 appears to influence risk of CL/P through a parent-of-origin effect with excess maternal transmission. Phosphorus 50-51 BCL3 transcription coactivator Homo sapiens 13-17 18766214-1 2008 The reaction of BCl3 with two equivalents of LiN(H)Dipp (Dipp = 2,6-diisopropylphenyl) in THF produces DippN(H)BO(CH2)4NDipp, which contains a puckered seven-membered C4OBN ring. lin(h)dipp 45-55 BCL3 transcription coactivator Homo sapiens 16-20 18766214-1 2008 The reaction of BCl3 with two equivalents of LiN(H)Dipp (Dipp = 2,6-diisopropylphenyl) in THF produces DippN(H)BO(CH2)4NDipp, which contains a puckered seven-membered C4OBN ring. 2,6-diisopropylphenyl) in thf 64-93 BCL3 transcription coactivator Homo sapiens 16-20 18766214-1 2008 The reaction of BCl3 with two equivalents of LiN(H)Dipp (Dipp = 2,6-diisopropylphenyl) in THF produces DippN(H)BO(CH2)4NDipp, which contains a puckered seven-membered C4OBN ring. dippn(h) 103-111 BCL3 transcription coactivator Homo sapiens 16-20 19049460-3 2008 The properties of the carbon complexes as donor ligands were studied by calculating the geometries and bond dissociation energies of the Lewis acid-base adducts with the Lewis acids M(CO)5 (M = Cr, Mo, W), PdCl2SMe2, BH3, BCl3, and Fe2(CO)8. Carbon 22-28 BCL3 transcription coactivator Homo sapiens 222-226 18570375-0 2008 Novel polyhydroxylated cyclic nitrones and N-hydroxypyrrolidines through BCl3-mediated deprotection. n-hydroxypyrrolidines 43-64 BCL3 transcription coactivator Homo sapiens 73-77 18570375-3 2008 The same reagent (BCl3) also allowed the efficient synthesis of a polyhydroxylated N-hydroxypyrrolidine, giving access to a novel class of N-hydroxyiminosugars. n-hydroxypyrrolidine 83-103 BCL3 transcription coactivator Homo sapiens 18-22 18570375-3 2008 The same reagent (BCl3) also allowed the efficient synthesis of a polyhydroxylated N-hydroxypyrrolidine, giving access to a novel class of N-hydroxyiminosugars. n-hydroxyiminosugars 139-159 BCL3 transcription coactivator Homo sapiens 18-22 18247493-5 2008 For 8, the debenzylation of precursor leaving the chlorine untouched was achieved by judicious use of BCl3. Chlorine 50-58 BCL3 transcription coactivator Homo sapiens 102-106 18318543-3 2008 During the investigation, it was also discovered that, at low temperatures, the reaction of BCl3 with alkynes produces monovinylboron dichloride rather than the reported divinylboron chloride. monovinylboron dichloride 119-144 BCL3 transcription coactivator Homo sapiens 92-96 18318543-3 2008 During the investigation, it was also discovered that, at low temperatures, the reaction of BCl3 with alkynes produces monovinylboron dichloride rather than the reported divinylboron chloride. divinylboron chloride 170-191 BCL3 transcription coactivator Homo sapiens 92-96 18454522-2 2008 The chemistry involves a pyrolysis of the designed boron-containing polymeric precursors, which are the polyaddition and polycondensation adducts between BCl3 and phenylene diacetylene and lithiated phenylene diacetylene, respectively. Boron 51-56 BCL3 transcription coactivator Homo sapiens 154-158 18318543-3 2008 During the investigation, it was also discovered that, at low temperatures, the reaction of BCl3 with alkynes produces monovinylboron dichloride rather than the reported divinylboron chloride. Alkynes 102-109 BCL3 transcription coactivator Homo sapiens 92-96 18000998-4 2008 The efficient and chemoselective debenzylation of aryl benzyl ether with BCl3 in the presence of pentamethylbenzene was developed. aryl benzyl ether 50-67 BCL3 transcription coactivator Homo sapiens 73-77 18000998-4 2008 The efficient and chemoselective debenzylation of aryl benzyl ether with BCl3 in the presence of pentamethylbenzene was developed. pentamethylbenzene 97-115 BCL3 transcription coactivator Homo sapiens 73-77 18097489-1 2008 BCl3 cyclizes diazadiene (2,6-Pr(i)2C6H3NCH)2 1 through a dichloroborated intermediate [(2,6-Pr(i)2C6H3NCHCl)2BCl] to give, in polar aprotic solvents, a spontaneously dehyrochlorinated C-chloro diazaborole 4. diazadiene 14-24 BCL3 transcription coactivator Homo sapiens 0-4 18464388-4 2008 Various silica pretreatments are utilized to alter the silica surface prior to reaction with AlEt3, AlEtxCl(3-x), BEt3, BCl3, and TiCl4. Silicon Dioxide 8-14 BCL3 transcription coactivator Homo sapiens 120-124 18464388-4 2008 Various silica pretreatments are utilized to alter the silica surface prior to reaction with AlEt3, AlEtxCl(3-x), BEt3, BCl3, and TiCl4. Silicon Dioxide 55-61 BCL3 transcription coactivator Homo sapiens 120-124 18097489-1 2008 BCl3 cyclizes diazadiene (2,6-Pr(i)2C6H3NCH)2 1 through a dichloroborated intermediate [(2,6-Pr(i)2C6H3NCHCl)2BCl] to give, in polar aprotic solvents, a spontaneously dehyrochlorinated C-chloro diazaborole 4. 2,6-pr(i)2c6h3nch) 26-44 BCL3 transcription coactivator Homo sapiens 0-4 18097489-1 2008 BCl3 cyclizes diazadiene (2,6-Pr(i)2C6H3NCH)2 1 through a dichloroborated intermediate [(2,6-Pr(i)2C6H3NCHCl)2BCl] to give, in polar aprotic solvents, a spontaneously dehyrochlorinated C-chloro diazaborole 4. (2,6-pr(i)2c6h3nchcl)2bcl 88-113 BCL3 transcription coactivator Homo sapiens 0-4 18097489-1 2008 BCl3 cyclizes diazadiene (2,6-Pr(i)2C6H3NCH)2 1 through a dichloroborated intermediate [(2,6-Pr(i)2C6H3NCHCl)2BCl] to give, in polar aprotic solvents, a spontaneously dehyrochlorinated C-chloro diazaborole 4. c-chloro diazaborole 185-205 BCL3 transcription coactivator Homo sapiens 0-4 18097489-7 2008 Reduction of 2/BCl3, in which additional phenyl groups on the diazadiene C-2 and C-3 atoms hinder the radical coupling observed in , gave predominantly diazaborole .BCl, (9a) contaminated with .BCl2, (9b) the first such stable radical diazadiene complex of boron. diazadiene 62-72 BCL3 transcription coactivator Homo sapiens 15-19 18097489-7 2008 Reduction of 2/BCl3, in which additional phenyl groups on the diazadiene C-2 and C-3 atoms hinder the radical coupling observed in , gave predominantly diazaborole .BCl, (9a) contaminated with .BCl2, (9b) the first such stable radical diazadiene complex of boron. diazaborole 152-163 BCL3 transcription coactivator Homo sapiens 15-19 18097489-7 2008 Reduction of 2/BCl3, in which additional phenyl groups on the diazadiene C-2 and C-3 atoms hinder the radical coupling observed in , gave predominantly diazaborole .BCl, (9a) contaminated with .BCl2, (9b) the first such stable radical diazadiene complex of boron. diazadiene 235-245 BCL3 transcription coactivator Homo sapiens 15-19 18097489-7 2008 Reduction of 2/BCl3, in which additional phenyl groups on the diazadiene C-2 and C-3 atoms hinder the radical coupling observed in , gave predominantly diazaborole .BCl, (9a) contaminated with .BCl2, (9b) the first such stable radical diazadiene complex of boron. Boron 257-262 BCL3 transcription coactivator Homo sapiens 15-19 18324655-1 2008 A series of technically and economically important element chlorides-such as SiCl4, BCl3, AlCl3, FeCl2, PCl3 and TiCl4-was synthesized through reactions between hydrogen chloride and the corresponding element oxides in the presence of different carbon sources with microwave assistance. Chlorides 59-68 BCL3 transcription coactivator Homo sapiens 84-88 18324655-1 2008 A series of technically and economically important element chlorides-such as SiCl4, BCl3, AlCl3, FeCl2, PCl3 and TiCl4-was synthesized through reactions between hydrogen chloride and the corresponding element oxides in the presence of different carbon sources with microwave assistance. Hydrochloric Acid 161-178 BCL3 transcription coactivator Homo sapiens 84-88 17547404-2 2007 Selectively controlled chlorination of H3SiGeH3 is provided by reactions with BCl3 to produce ClH2SiGeH3 (1) and Cl2HSiGeH3 (2). h3sigeh3 39-47 BCL3 transcription coactivator Homo sapiens 78-82 17644518-9 2007 Treatment with trichostatin A, a potent inhibitor of the transcriptional co-repressor HDAC, partially reversed the inhibitory effect of BCL3. trichostatin A 15-29 BCL3 transcription coactivator Homo sapiens 136-140 17547404-2 2007 Selectively controlled chlorination of H3SiGeH3 is provided by reactions with BCl3 to produce ClH2SiGeH3 (1) and Cl2HSiGeH3 (2). clh2sigeh3 94-104 BCL3 transcription coactivator Homo sapiens 78-82 17547404-2 2007 Selectively controlled chlorination of H3SiGeH3 is provided by reactions with BCl3 to produce ClH2SiGeH3 (1) and Cl2HSiGeH3 (2). cl2hsigeh3 113-123 BCL3 transcription coactivator Homo sapiens 78-82 17373851-4 2007 The sequence is completed by BCl3-promoted cleavage of 7 and 9 to form the sn-1,2- and sn-2,3-diacylglycerols, respectively. sn-1,2- and sn-2,3-diacylglycerols 75-109 BCL3 transcription coactivator Homo sapiens 29-33 17160181-1 2007 The reaction between [Pt(nbe)3] (nbe=norbornene), two equivalents of the phosphines PPh3, PMePh2 or PMe2Ph and 1 equivalent of BCl3 affords the platinum dichloroboryl species [PtCl(BCl2)(PPh3)2], [PtCl(BCl2)(PMePh2)2] and [PtCl(BCl2)(PMe2Ph)2]. pt(nbe)3] 22-31 BCL3 transcription coactivator Homo sapiens 127-131 17288388-8 2007 BCl3, AlCl3, and GaCl3 are predicted to be efficient catalysts for the silicon-directed aldol reaction as they strongly activate the formaldehyde electrophile. Silicon 71-78 BCL3 transcription coactivator Homo sapiens 0-4 17288388-8 2007 BCl3, AlCl3, and GaCl3 are predicted to be efficient catalysts for the silicon-directed aldol reaction as they strongly activate the formaldehyde electrophile. Formaldehyde 133-145 BCL3 transcription coactivator Homo sapiens 0-4 17378556-9 2007 The reaction of the lithium salt [t-Bu3PNLi]4 (13) with BCl3 proceeds smoothly to give t-Bu3PNBCl2 (14), which is readily alkylated to give t-Bu3PNBMe2 (15). lithium salt [t-bu3pnli]4 20-45 BCL3 transcription coactivator Homo sapiens 56-60 17378556-9 2007 The reaction of the lithium salt [t-Bu3PNLi]4 (13) with BCl3 proceeds smoothly to give t-Bu3PNBCl2 (14), which is readily alkylated to give t-Bu3PNBMe2 (15). t-bu3pnbcl2 87-98 BCL3 transcription coactivator Homo sapiens 56-60 17378556-9 2007 The reaction of the lithium salt [t-Bu3PNLi]4 (13) with BCl3 proceeds smoothly to give t-Bu3PNBCl2 (14), which is readily alkylated to give t-Bu3PNBMe2 (15). t-bu3pnbme2 140-151 BCL3 transcription coactivator Homo sapiens 56-60 17378556-11 2007 The reaction of 13 in a 2:1 ratio with BCl3 gives the salt [(t-Bu3PN)2B]Cl (17). Salts 54-58 BCL3 transcription coactivator Homo sapiens 39-43 17378556-11 2007 The reaction of 13 in a 2:1 ratio with BCl3 gives the salt [(t-Bu3PN)2B]Cl (17). [(t-bu3pn)2b]cl 59-74 BCL3 transcription coactivator Homo sapiens 39-43 17160181-1 2007 The reaction between [Pt(nbe)3] (nbe=norbornene), two equivalents of the phosphines PPh3, PMePh2 or PMe2Ph and 1 equivalent of BCl3 affords the platinum dichloroboryl species [PtCl(BCl2)(PPh3)2], [PtCl(BCl2)(PMePh2)2] and [PtCl(BCl2)(PMe2Ph)2]. platinum dichloroboryl 144-166 BCL3 transcription coactivator Homo sapiens 127-131 17160181-1 2007 The reaction between [Pt(nbe)3] (nbe=norbornene), two equivalents of the phosphines PPh3, PMePh2 or PMe2Ph and 1 equivalent of BCl3 affords the platinum dichloroboryl species [PtCl(BCl2)(PPh3)2], [PtCl(BCl2)(PMePh2)2] and [PtCl(BCl2)(PMe2Ph)2]. 2-((4-pyridyl)methyl)amino-N-(3-(trifluoromethyl)phenyl)benzamide 234-240 BCL3 transcription coactivator Homo sapiens 127-131 17160181-4 2007 Crystals were obtained of a product shown by X-ray crystallography to be the unusual dinuclear species [Pt2(BCl2)2(PMe3)4(micro-Cl)][BCl4] which reveals an arrangement in which two square planar platinum(II) centres are linked by a single bridging chloride which is trans to a BCl2 group on each platinum centre. platinum(ii) 195-207 BCL3 transcription coactivator Homo sapiens 133-137 17160181-1 2007 The reaction between [Pt(nbe)3] (nbe=norbornene), two equivalents of the phosphines PPh3, PMePh2 or PMe2Ph and 1 equivalent of BCl3 affords the platinum dichloroboryl species [PtCl(BCl2)(PPh3)2], [PtCl(BCl2)(PMePh2)2] and [PtCl(BCl2)(PMe2Ph)2]. phenylhydroxylamine 25-28 BCL3 transcription coactivator Homo sapiens 127-131 17160181-4 2007 Crystals were obtained of a product shown by X-ray crystallography to be the unusual dinuclear species [Pt2(BCl2)2(PMe3)4(micro-Cl)][BCl4] which reveals an arrangement in which two square planar platinum(II) centres are linked by a single bridging chloride which is trans to a BCl2 group on each platinum centre. Chlorides 248-256 BCL3 transcription coactivator Homo sapiens 133-137 17160181-4 2007 Crystals were obtained of a product shown by X-ray crystallography to be the unusual dinuclear species [Pt2(BCl2)2(PMe3)4(micro-Cl)][BCl4] which reveals an arrangement in which two square planar platinum(II) centres are linked by a single bridging chloride which is trans to a BCl2 group on each platinum centre. Platinum 195-203 BCL3 transcription coactivator Homo sapiens 133-137 17160181-1 2007 The reaction between [Pt(nbe)3] (nbe=norbornene), two equivalents of the phosphines PPh3, PMePh2 or PMe2Ph and 1 equivalent of BCl3 affords the platinum dichloroboryl species [PtCl(BCl2)(PPh3)2], [PtCl(BCl2)(PMePh2)2] and [PtCl(BCl2)(PMe2Ph)2]. 2-norbornene 37-47 BCL3 transcription coactivator Homo sapiens 127-131 16878923-1 2006 cis-3,4-Dicyano-3-hexene undergoes cyclotrimerization with BCl3 to form the new subtriazaporphyrin chloro[hexaethylsubtriazaporphyrinato]boron(III). subtriazaporphyrin chloro[hexaethylsubtriazaporphyrinato]boron 80-142 BCL3 transcription coactivator Homo sapiens 59-63 16004507-0 2005 Microwave-assisted synthesis of salicylamide via BCl3 mediated coupling. salicylamide 32-44 BCL3 transcription coactivator Homo sapiens 49-53 16734447-2 2006 The synthesis features the regioselective ring opening of (S)-epichlorohydrin with 2,6-dibromophenyllithium species, the mild copper-mediated aryl amination utilizing the combination of CuI and CsOAc, and the efficient deprotection of benzyl groups of aryl benzyl ether with BCl3 in the presence of pentamethylbenzene. Epichlorohydrin 58-77 BCL3 transcription coactivator Homo sapiens 275-279 16734447-2 2006 The synthesis features the regioselective ring opening of (S)-epichlorohydrin with 2,6-dibromophenyllithium species, the mild copper-mediated aryl amination utilizing the combination of CuI and CsOAc, and the efficient deprotection of benzyl groups of aryl benzyl ether with BCl3 in the presence of pentamethylbenzene. Copper 126-132 BCL3 transcription coactivator Homo sapiens 275-279 16468798-2 2006 TiCl4, TiBr4, BCl3, and BBr3 promoted syn-selective cyclizations to sterically congested chloro- and bromohydrins, while SnCl4, SnBr4, InCl3, ZrCl4, and several other Lewis acids effected highly anti-selective reactions to furnish the corresponding trans halohydrins. chloro- and bromohydrins 89-113 BCL3 transcription coactivator Homo sapiens 14-18 16468798-2 2006 TiCl4, TiBr4, BCl3, and BBr3 promoted syn-selective cyclizations to sterically congested chloro- and bromohydrins, while SnCl4, SnBr4, InCl3, ZrCl4, and several other Lewis acids effected highly anti-selective reactions to furnish the corresponding trans halohydrins. Tin(IV) bromide 128-133 BCL3 transcription coactivator Homo sapiens 14-18 16468798-2 2006 TiCl4, TiBr4, BCl3, and BBr3 promoted syn-selective cyclizations to sterically congested chloro- and bromohydrins, while SnCl4, SnBr4, InCl3, ZrCl4, and several other Lewis acids effected highly anti-selective reactions to furnish the corresponding trans halohydrins. Indium chloride (InCl3) 135-140 BCL3 transcription coactivator Homo sapiens 14-18 16468798-2 2006 TiCl4, TiBr4, BCl3, and BBr3 promoted syn-selective cyclizations to sterically congested chloro- and bromohydrins, while SnCl4, SnBr4, InCl3, ZrCl4, and several other Lewis acids effected highly anti-selective reactions to furnish the corresponding trans halohydrins. zirconium chloride 142-147 BCL3 transcription coactivator Homo sapiens 14-18 16468798-2 2006 TiCl4, TiBr4, BCl3, and BBr3 promoted syn-selective cyclizations to sterically congested chloro- and bromohydrins, while SnCl4, SnBr4, InCl3, ZrCl4, and several other Lewis acids effected highly anti-selective reactions to furnish the corresponding trans halohydrins. halohydrins 255-266 BCL3 transcription coactivator Homo sapiens 14-18 16004507-1 2005 A novel and efficient microwave-assisted, BCl3-mediated coupling reaction to synthesize salicylamide structures from phenols and isocyanates is described. salicylamide 88-100 BCL3 transcription coactivator Homo sapiens 42-46 16004507-1 2005 A novel and efficient microwave-assisted, BCl3-mediated coupling reaction to synthesize salicylamide structures from phenols and isocyanates is described. Phenols 117-124 BCL3 transcription coactivator Homo sapiens 42-46 16004507-1 2005 A novel and efficient microwave-assisted, BCl3-mediated coupling reaction to synthesize salicylamide structures from phenols and isocyanates is described. Isocyanates 129-140 BCL3 transcription coactivator Homo sapiens 42-46 14573596-4 2004 These findings suggest an enzymatic role for Pirin, most likely in biological redox reactions involving oxygen, and provide compelling evidence that Pirin requires the participation of the metal ion for its interaction with Bcl-3 to co-regulate the NF-kappaB transcription pathway and the interaction with NFI in DNA replication. Oxygen 104-110 BCL3 transcription coactivator Homo sapiens 224-229 19787977-1 2005 The pulsed field ionization-photoelectron (PFI-PE) spectrum of boron trichloride (BCl3) in the region of 93 590-95 640 cm(-1) has been measured using vacuum ultraviolet (VUV) laser. boron trichloride 63-80 BCL3 transcription coactivator Homo sapiens 82-86 19787977-5 2005 Furthermore, the CCSD(T)/CBS calculations predict the existence of two BCl3+ transitional structures with D3h and C2v symmetries lying 800 and 1300 cm(-1), respectively, above the BCl3+ (X 2B2) ground state. D3H 106-109 BCL3 transcription coactivator Homo sapiens 71-75 19787977-5 2005 Furthermore, the CCSD(T)/CBS calculations predict the existence of two BCl3+ transitional structures with D3h and C2v symmetries lying 800 and 1300 cm(-1), respectively, above the BCl3+ (X 2B2) ground state. N-[2-(dimethylamino)ethyl]-3-[6-(thiophen-2-yl)imidazo[1,2-b]pyridazin-3-yl]benzamide 114-117 BCL3 transcription coactivator Homo sapiens 71-75 19787977-8 2005 Combining this 0 K AE value and the IE (BCl3), we have determined the 0 K bond dissociation energy (D0) for Cl2B(+) -Cl as 0.854 +/- 0.002 eV. cl2b(+) -cl 108-119 BCL3 transcription coactivator Homo sapiens 40-44 15838378-8 2005 The adjuvant effects of poly(I:C) appear to be at least partially dependent on an increase in the transcription of the anti-apoptotic molecules Bcl-3 and Bcl-xL and a concomitant decrease in apoptosis during the contraction phase of the primary T-cell response. Poly I-C 24-32 BCL3 transcription coactivator Homo sapiens 144-149 15796509-1 2005 The first example of a stable oxoborane monomer (LB=O) stabilized by complexation to AlCl3 has been prepared by the reaction of LAlCl2 with BCl3 followed by treatment with H2O in CH2Cl2 (L = [HC(CMe)2(NC6F5)2]). borage oil 30-39 BCL3 transcription coactivator Homo sapiens 140-144 15796509-1 2005 The first example of a stable oxoborane monomer (LB=O) stabilized by complexation to AlCl3 has been prepared by the reaction of LAlCl2 with BCl3 followed by treatment with H2O in CH2Cl2 (L = [HC(CMe)2(NC6F5)2]). Aluminum Chloride 85-90 BCL3 transcription coactivator Homo sapiens 140-144 15796509-1 2005 The first example of a stable oxoborane monomer (LB=O) stabilized by complexation to AlCl3 has been prepared by the reaction of LAlCl2 with BCl3 followed by treatment with H2O in CH2Cl2 (L = [HC(CMe)2(NC6F5)2]). lalcl2 128-134 BCL3 transcription coactivator Homo sapiens 140-144 15796509-1 2005 The first example of a stable oxoborane monomer (LB=O) stabilized by complexation to AlCl3 has been prepared by the reaction of LAlCl2 with BCl3 followed by treatment with H2O in CH2Cl2 (L = [HC(CMe)2(NC6F5)2]). Methylene Chloride 179-185 BCL3 transcription coactivator Homo sapiens 140-144 14573596-4 2004 These findings suggest an enzymatic role for Pirin, most likely in biological redox reactions involving oxygen, and provide compelling evidence that Pirin requires the participation of the metal ion for its interaction with Bcl-3 to co-regulate the NF-kappaB transcription pathway and the interaction with NFI in DNA replication. Metals 189-194 BCL3 transcription coactivator Homo sapiens 224-229 12932292-0 2003 The triterpenoid CDDO inhibits expression of matrix metalloproteinase-1, matrix metalloproteinase-13 and Bcl-3 in primary human chondrocytes. triterpenoid TP-222 4-16 BCL3 transcription coactivator Homo sapiens 105-110 12456498-6 2003 The BCL3 gene contains 2 cytosine-guanine dinucleotide (CpG) islands, and the intragenic 3" CpG was entirely demethylated in SU-DHL-1 and DEL. cytidylyl-3'-5'-guanosine 25-54 BCL3 transcription coactivator Homo sapiens 4-8 12456498-6 2003 The BCL3 gene contains 2 cytosine-guanine dinucleotide (CpG) islands, and the intragenic 3" CpG was entirely demethylated in SU-DHL-1 and DEL. su-dhl 125-131 BCL3 transcription coactivator Homo sapiens 4-8 12932292-8 2003 In human primary chondrocytes, IL-1-induced Bcl-3 expression was inhibited when cells were pretreated with CDDO. 2-cyano-3,12-dioxoolean-1,9-dien-28-oic acid 107-111 BCL3 transcription coactivator Homo sapiens 44-49 12932292-9 2003 To determine whether the inhibitory effect of CDDO on MMP worked through inhibition of Bcl-3 gene expression, SW-1353 cells stably transfected with a Bcl-3 expression plasmid were treated with IL-1 and/or CDDO, and MMP gene expression was assayed. 2-cyano-3,12-dioxoolean-1,9-dien-28-oic acid 46-50 BCL3 transcription coactivator Homo sapiens 87-92 14632517-0 2003 Why is BCl3 a stronger Lewis acid with respect to strong bases than BF3? Lewis Acids 23-33 BCL3 transcription coactivator Homo sapiens 7-11 14632517-0 2003 Why is BCl3 a stronger Lewis acid with respect to strong bases than BF3? boron trifluoride 68-71 BCL3 transcription coactivator Homo sapiens 7-11 14632517-4 2003 The higher Lewis acid strength of BCl(3) in X(3)B[bond]H(3) compared with BF(3) is an intrinsic property of the molecule. Lewis Acids 11-21 BCL3 transcription coactivator Homo sapiens 34-40 14632517-4 2003 The higher Lewis acid strength of BCl(3) in X(3)B[bond]H(3) compared with BF(3) is an intrinsic property of the molecule. boron trifluoride 74-79 BCL3 transcription coactivator Homo sapiens 34-40 14632517-5 2003 The energy partitioning analysis of Cl(3)B[bond]NH(3) and F(3)B[bond]NH(3) shows that the stronger bond in the former complex comes from enhanced covalent interactions between the Lewis acid and the Lewis base which can be explained with the energetically lower lying LUMO of BCl(3). Lewis Acids 180-190 BCL3 transcription coactivator Homo sapiens 276-282 12932292-11 2003 Furthermore, overexpressed Bcl-3 could sustain the CDDO-dependent inhibition of IL-1-induced MMP-1 expression. 2-cyano-3,12-dioxoolean-1,9-dien-28-oic acid 51-55 BCL3 transcription coactivator Homo sapiens 27-32 12932292-0 2003 The triterpenoid CDDO inhibits expression of matrix metalloproteinase-1, matrix metalloproteinase-13 and Bcl-3 in primary human chondrocytes. 2-cyano-3,12-dioxoolean-1,9-dien-28-oic acid 17-21 BCL3 transcription coactivator Homo sapiens 105-110 12483727-4 2002 SW-1353 cells were transfected with antisense oligonucleotides to Bcl-3, and IL-1-induced MMP-1 mRNA expression was assayed by quantitative RT-PCR. Oligonucleotides 46-62 BCL3 transcription coactivator Homo sapiens 66-71 12932292-13 2003 CDDO also inhibits the expression of Bcl-3, an IL-1-responsive gene that preferentially contributes to MMP-1 gene expression. 2-cyano-3,12-dioxoolean-1,9-dien-28-oic acid 0-4 BCL3 transcription coactivator Homo sapiens 37-42 11908218-2 2002 BCl3-Ar chemistry was found to give satisfactory results; N2 and Cl2 were added to change the selectivity between GaAs and e-beam resist. Nitrogen 58-60 BCL3 transcription coactivator Homo sapiens 0-4 11908218-2 2002 BCl3-Ar chemistry was found to give satisfactory results; N2 and Cl2 were added to change the selectivity between GaAs and e-beam resist. Chlorine 65-68 BCL3 transcription coactivator Homo sapiens 0-4 11908218-2 2002 BCl3-Ar chemistry was found to give satisfactory results; N2 and Cl2 were added to change the selectivity between GaAs and e-beam resist. gallium arsenide 114-118 BCL3 transcription coactivator Homo sapiens 0-4 11300564-2 2001 The method is illustrated by describing the vibrational modes of BCl3-NH3 and BCl3-pyridine electron donor-acceptor complexes in terms of motions of BCl3 and either NH3 or pyridine. Ammonia 70-73 BCL3 transcription coactivator Homo sapiens 65-69 11300564-2 2001 The method is illustrated by describing the vibrational modes of BCl3-NH3 and BCl3-pyridine electron donor-acceptor complexes in terms of motions of BCl3 and either NH3 or pyridine. pyridine 83-91 BCL3 transcription coactivator Homo sapiens 65-69 11300564-2 2001 The method is illustrated by describing the vibrational modes of BCl3-NH3 and BCl3-pyridine electron donor-acceptor complexes in terms of motions of BCl3 and either NH3 or pyridine. pyridine 83-91 BCL3 transcription coactivator Homo sapiens 78-82 11300564-2 2001 The method is illustrated by describing the vibrational modes of BCl3-NH3 and BCl3-pyridine electron donor-acceptor complexes in terms of motions of BCl3 and either NH3 or pyridine. pyridine 83-91 BCL3 transcription coactivator Homo sapiens 78-82 11300564-6 2001 For the BCl3-pyridine complex, a band observed at 1107 cm(-1) is re-assigned as a combination of C-H in-plane bending and a ring-breathing mode of the pyridine fragment. pyridine 13-21 BCL3 transcription coactivator Homo sapiens 8-12 11077296-2 2000 The cation has a near-tetrahedral P atom and the BCl(4)(-) anion is near-tetrahedral at boron. Boron 88-93 BCL3 transcription coactivator Homo sapiens 49-54 11034849-2 2000 The molecule was produced by reacting oxygen atoms, produced in a microwave discharge containing an O(2)/He mixture, with BCl(3). Oxygen 38-44 BCL3 transcription coactivator Homo sapiens 122-128 11034849-2 2000 The molecule was produced by reacting oxygen atoms, produced in a microwave discharge containing an O(2)/He mixture, with BCl(3). Oxygen 100-104 BCL3 transcription coactivator Homo sapiens 122-128 11034849-2 2000 The molecule was produced by reacting oxygen atoms, produced in a microwave discharge containing an O(2)/He mixture, with BCl(3). Helium 105-107 BCL3 transcription coactivator Homo sapiens 122-128 10985724-3 2000 Most likely due to steric constraints, a triferrocenylborane was not obtained even from the reaction of BCl3 with an excess of 1a, whereas facile formation of the diferrocenylphenylborane 2c from PhBCl2 and two equivalents of 1a was observed. triferrocenylborane 41-60 BCL3 transcription coactivator Homo sapiens 104-108 10775131-6 2000 Synthesis of Bcl-3, a protein whose translation is controlled by an mTOR-dependent pathway, was induced by flow and inhibited by rapamycin and wortmannin. Sirolimus 129-138 BCL3 transcription coactivator Homo sapiens 13-18 10775131-6 2000 Synthesis of Bcl-3, a protein whose translation is controlled by an mTOR-dependent pathway, was induced by flow and inhibited by rapamycin and wortmannin. Wortmannin 143-153 BCL3 transcription coactivator Homo sapiens 13-18 12526571-9 2000 New procedures for the generation of diborane were also developed by the reaction of NaBF4 with NaBH4 in triglyme (or tetraglyme) in the presence of Lewis acids such as AlCl3 and BCl3. diborane 37-45 BCL3 transcription coactivator Homo sapiens 179-183 12526571-9 2000 New procedures for the generation of diborane were also developed by the reaction of NaBF4 with NaBH4 in triglyme (or tetraglyme) in the presence of Lewis acids such as AlCl3 and BCl3. Sodium tetrafluoroborate 85-90 BCL3 transcription coactivator Homo sapiens 179-183 12526571-9 2000 New procedures for the generation of diborane were also developed by the reaction of NaBF4 with NaBH4 in triglyme (or tetraglyme) in the presence of Lewis acids such as AlCl3 and BCl3. sodium borohydride 96-101 BCL3 transcription coactivator Homo sapiens 179-183 11671188-1 1999 The unexpected greater Lewis acidity of BCl(3) than BF(3) with respect to strong bases such as NH(3) has been the subject of much discussion. Ammonia 95-100 BCL3 transcription coactivator Homo sapiens 40-46 10836034-2 1999 The acrylate esters of these alcohols undergo BCl3-catalyzed Diels-Alder reactions with a variety of dienes at -78 to -55 degrees C in CH2Cl2 or C7H8 with high dienophile face selectivity (Table 1). acrylate esters 4-19 BCL3 transcription coactivator Homo sapiens 46-50 10836034-2 1999 The acrylate esters of these alcohols undergo BCl3-catalyzed Diels-Alder reactions with a variety of dienes at -78 to -55 degrees C in CH2Cl2 or C7H8 with high dienophile face selectivity (Table 1). Alcohols 29-37 BCL3 transcription coactivator Homo sapiens 46-50 10836034-2 1999 The acrylate esters of these alcohols undergo BCl3-catalyzed Diels-Alder reactions with a variety of dienes at -78 to -55 degrees C in CH2Cl2 or C7H8 with high dienophile face selectivity (Table 1). diels 61-66 BCL3 transcription coactivator Homo sapiens 46-50 10836034-2 1999 The acrylate esters of these alcohols undergo BCl3-catalyzed Diels-Alder reactions with a variety of dienes at -78 to -55 degrees C in CH2Cl2 or C7H8 with high dienophile face selectivity (Table 1). dienes 101-107 BCL3 transcription coactivator Homo sapiens 46-50 10836034-2 1999 The acrylate esters of these alcohols undergo BCl3-catalyzed Diels-Alder reactions with a variety of dienes at -78 to -55 degrees C in CH2Cl2 or C7H8 with high dienophile face selectivity (Table 1). Methylene Chloride 135-141 BCL3 transcription coactivator Homo sapiens 46-50 10836034-2 1999 The acrylate esters of these alcohols undergo BCl3-catalyzed Diels-Alder reactions with a variety of dienes at -78 to -55 degrees C in CH2Cl2 or C7H8 with high dienophile face selectivity (Table 1). c7h8 145-149 BCL3 transcription coactivator Homo sapiens 46-50 11671188-3 1999 In contrast, toward weak bases such as CO, BF(3) is a stronger Lewis acid than BCl(3). Carbon Monoxide 39-41 BCL3 transcription coactivator Homo sapiens 79-85 11671188-3 1999 In contrast, toward weak bases such as CO, BF(3) is a stronger Lewis acid than BCl(3). boron trifluoride 43-48 BCL3 transcription coactivator Homo sapiens 79-85 11671188-6 1999 It takes more energy to lengthen the short strong BF bonds than the longer weaker BCl bonds and it is for this reason that BCl(3) is a stronger Lewis acid than BF(3) toward a strong base such as NH(3). Lewis Acids 144-154 BCL3 transcription coactivator Homo sapiens 123-129 11671188-6 1999 It takes more energy to lengthen the short strong BF bonds than the longer weaker BCl bonds and it is for this reason that BCl(3) is a stronger Lewis acid than BF(3) toward a strong base such as NH(3). benzo(b)fluoranthene 50-52 BCL3 transcription coactivator Homo sapiens 123-129 11671188-7 1999 In contrast, in the formation of a complex with a weak base such as CO, the BX(3) is barely distorted from planarity and so the acidity of BF(3) is greater than that of BCl(3) because the charge on boron is greater in BF(3) than BCl(3). benzo(b)fluoranthene 139-141 BCL3 transcription coactivator Homo sapiens 229-235 11671188-7 1999 In contrast, in the formation of a complex with a weak base such as CO, the BX(3) is barely distorted from planarity and so the acidity of BF(3) is greater than that of BCl(3) because the charge on boron is greater in BF(3) than BCl(3). Boron 198-203 BCL3 transcription coactivator Homo sapiens 169-175 11671188-7 1999 In contrast, in the formation of a complex with a weak base such as CO, the BX(3) is barely distorted from planarity and so the acidity of BF(3) is greater than that of BCl(3) because the charge on boron is greater in BF(3) than BCl(3). Boron 198-203 BCL3 transcription coactivator Homo sapiens 229-235 9812988-5 1998 The Bcl3 interaction involved two distinct subregions of RXR, i.e. constitutive interactions of the N-terminal ABC domains and 9-cis-RA-dependent interactions of the C-terminal DEF domains. Alitretinoin 133-135 BCL3 transcription coactivator Homo sapiens 4-8 9477565-2 1998 Because of safety concerns with diazomethane, the reagent used to form methyl esters, a less toxic and dangerous reagent, BCl3/2-chloroethanol, was considered. methyl esters 71-84 BCL3 transcription coactivator Homo sapiens 122-126 9484493-4 1998 Butynyl intermediate 7 is prepared from 2-(benzyloxy)-5-deoxyascorbic acid (15) by iodination (I2, PPh3, Imd), iodo substitution with lithium acetylide ethylenediamine complex (LiAEDA, HMPA, -5 degrees C), and benzyl group cleavage (Ac2O, Pyr, BCl3). but-1-yne 0-7 BCL3 transcription coactivator Homo sapiens 244-248 9770398-2 1998 The DBO molecule was generated by an ac discharge in a mixture of BCl3, D2, O2, and He. 6,8-dichloro-2,3-dihydro-3-hydroxymethyl-1,4-benzoxazine 4-7 BCL3 transcription coactivator Homo sapiens 66-70 9477565-2 1998 Because of safety concerns with diazomethane, the reagent used to form methyl esters, a less toxic and dangerous reagent, BCl3/2-chloroethanol, was considered. Ethylene Chlorohydrin 127-142 BCL3 transcription coactivator Homo sapiens 122-126 7881537-3 1995 Triclopyr was extracted from the matrices and derivatized separately to 2-chloroethylene ester with 2-chloroethanol-BCl3 and methyl ester with diazomethane. triclopyr 0-9 BCL3 transcription coactivator Homo sapiens 116-120 8979999-1 1996 BN was formed in a microwave discharge of He with a trace of BCl3 and N2. 6-bromo-2-naphthyl sulfate 0-2 BCL3 transcription coactivator Homo sapiens 61-65 7668251-12 1995 These results suggest that BCL3, or a nearby gene, plays a role in the etiology of CL/P in some families. Phosphorus 86-87 BCL3 transcription coactivator Homo sapiens 27-31 7881537-3 1995 Triclopyr was extracted from the matrices and derivatized separately to 2-chloroethylene ester with 2-chloroethanol-BCl3 and methyl ester with diazomethane. 2-chloroethylene ester 72-94 BCL3 transcription coactivator Homo sapiens 116-120 1459457-6 1992 Two dimensional phosphotryptic peptide maps of the human bcl-3 and the human 37-kD (I kappa B alpha) proteins reveal that the phosphopeptides from the 37-kD (I kappa B alpha) protein are nested within the bcl-3 protein. Peptides 31-38 BCL3 transcription coactivator Homo sapiens 57-62 1459457-9 1992 Comparison of tryptic peptide maps of the bcl-3 protein synthesized in vitro, and p56 and p38 from HeLa cells, shows that they are all structurally related. Peptides 22-29 BCL3 transcription coactivator Homo sapiens 42-47 34198270-0 2021 Reactivity of the Si(100)-2x1-Cl surface with respect to PH3, PCl3, and BCl3: Comparison with PH3 on Si(100)-2x1-H. Silicon 18-20 BCL3 transcription coactivator Homo sapiens 72-76 34405671-0 2021 B-Doped delta-Layers and Nanowires from Area-Selective Deposition of BCl3 on Si(100). Silicon 77-79 BCL3 transcription coactivator Homo sapiens 69-73 34405671-3 2021 Here, B-doped delta-layers were fabricated in Si(100) by using BCl3 as an acceptor dopant precursor in ultrahigh vacuum. Silicon 46-48 BCL3 transcription coactivator Homo sapiens 63-67 34405671-4 2021 Additionally, we demonstrate compatibility of BCl3 with both H and Cl monatomic resists to achieve area-selective deposition on Si. Silicon 128-130 BCL3 transcription coactivator Homo sapiens 46-50 34752072-1 2021 An aromatic tricoordinated organo B(III) complex of benzitriphyrin(2.1.1) was synthesized by treating the nonaromatic phlorin analogue of meso-fused benzitriphyrin(2.1.1) with BCl3 in triethylamine/toluene and refluxing for 2 h. The X-ray structure revealed that B(III) was in a trigonal-planar geometry and was coordinated to two nitrogen atoms and one carbon. organo b(iii) 27-40 BCL3 transcription coactivator Homo sapiens 176-180 34752072-1 2021 An aromatic tricoordinated organo B(III) complex of benzitriphyrin(2.1.1) was synthesized by treating the nonaromatic phlorin analogue of meso-fused benzitriphyrin(2.1.1) with BCl3 in triethylamine/toluene and refluxing for 2 h. The X-ray structure revealed that B(III) was in a trigonal-planar geometry and was coordinated to two nitrogen atoms and one carbon. benzitriphyrin 52-66 BCL3 transcription coactivator Homo sapiens 176-180 34752072-1 2021 An aromatic tricoordinated organo B(III) complex of benzitriphyrin(2.1.1) was synthesized by treating the nonaromatic phlorin analogue of meso-fused benzitriphyrin(2.1.1) with BCl3 in triethylamine/toluene and refluxing for 2 h. The X-ray structure revealed that B(III) was in a trigonal-planar geometry and was coordinated to two nitrogen atoms and one carbon. phlorin porphyrin 118-125 BCL3 transcription coactivator Homo sapiens 176-180 34612655-0 2021 Borylative Cyclization of 1,6-Allenynes Driven by BCl3. 1,6-allenynes 26-39 BCL3 transcription coactivator Homo sapiens 50-54 34612655-1 2021 A metal-free intramolecular borylative cyclization of 1,6-allenynes driven by BCl3 was developed. Metals 2-7 BCL3 transcription coactivator Homo sapiens 78-82 34612655-1 2021 A metal-free intramolecular borylative cyclization of 1,6-allenynes driven by BCl3 was developed. 1,6-allenynes 54-67 BCL3 transcription coactivator Homo sapiens 78-82 34198270-2 2021 We used the density functional theory to evaluate whether a chlorine monolayer on Si(100) is suitable as a resist for PH3, PCl3, and BCl3molecules. Chlorine 60-68 BCL3 transcription coactivator Homo sapiens 133-137 34198270-2 2021 We used the density functional theory to evaluate whether a chlorine monolayer on Si(100) is suitable as a resist for PH3, PCl3, and BCl3molecules. Silicon 82-84 BCL3 transcription coactivator Homo sapiens 133-137 34198270-3 2021 We calculated reaction pathways for PH3, PCl3, and BCl3adsorption on a bare and Cl-terminated Si(100)-2x1 surface, as well as for PH3adsorption on H-terminated Si(100)-2x1, which is widely used in current technologies for atomically precise doping of Si(100) with phosphorus. Silicon 94-96 BCL3 transcription coactivator Homo sapiens 51-55 35425053-2 2022 Demethylation of the key intermediate methyl 3-arylbenzofuran-4-carboxylate was achieved successfully through bromination followed by BBr3-or BCl3/TBAI-mediated ether cleavage reaction. methyl 3-arylbenzofuran-4-carboxylate 38-75 BCL3 transcription coactivator Homo sapiens 142-146 34169715-2 2021 In the present work, the structure of active sites of ZN catalysts in the absence of ethylene, referred to as dormant active sites, is elucidated from magnetic resonance experiments carried out on samples reacted with increasing amounts of BCl3 so as to enhance the concentration of active sites and observe clear spectroscopic signatures. Zinc 54-56 BCL3 transcription coactivator Homo sapiens 240-244 34169715-2 2021 In the present work, the structure of active sites of ZN catalysts in the absence of ethylene, referred to as dormant active sites, is elucidated from magnetic resonance experiments carried out on samples reacted with increasing amounts of BCl3 so as to enhance the concentration of active sites and observe clear spectroscopic signatures. ethylene 85-93 BCL3 transcription coactivator Homo sapiens 240-244 35457894-1 2022 A systematic study of the selective etching of p-GaN over AlGaN was carried out using a BCl3/SF6 inductively coupled plasma (ICP) process. aluminum gallium nitride 58-63 BCL3 transcription coactivator Homo sapiens 88-92 35457894-4 2022 MIS-capacitor devices fabricated on the AlGaN surface with ALD-Al2O3 as the gate dielectric after p-GaN etch showed the significant benefit of BCl3/SF6 selective etch process. aluminum gallium nitride 40-45 BCL3 transcription coactivator Homo sapiens 143-147 35510716-0 2022 Metal-Free Temperature-Controlled Regiodivergent Borylative Cyclizations of Enynes: BCl3-Promoted Skeletal Rearrangement. Metals 0-5 BCL3 transcription coactivator Homo sapiens 84-88 35510716-1 2022 Metal-free borylative cyclization of biphenyl-embedded 1,3,5-trien-7-ynes in the presence of simple and inexpensive BCl3 provided synthetically useful borylated building blocks. Metals 0-5 BCL3 transcription coactivator Homo sapiens 116-120 35510716-1 2022 Metal-free borylative cyclization of biphenyl-embedded 1,3,5-trien-7-ynes in the presence of simple and inexpensive BCl3 provided synthetically useful borylated building blocks. 1,3,5-trien-7-ynes 55-73 BCL3 transcription coactivator Homo sapiens 116-120 35510716-3 2022 Based on DFT calculations, a mechanism for these novel transformations has been proposed, which involves an uncommon skeletal rearrangement, including migration of a methyl group and alkyne fragmentation, unprecedented in BCl3-promoted cyclization reactions. Alkynes 183-189 BCL3 transcription coactivator Homo sapiens 222-226 35425053-2 2022 Demethylation of the key intermediate methyl 3-arylbenzofuran-4-carboxylate was achieved successfully through bromination followed by BBr3-or BCl3/TBAI-mediated ether cleavage reaction. Tetrabutylammonium iodide 147-151 BCL3 transcription coactivator Homo sapiens 142-146 35425053-2 2022 Demethylation of the key intermediate methyl 3-arylbenzofuran-4-carboxylate was achieved successfully through bromination followed by BBr3-or BCl3/TBAI-mediated ether cleavage reaction. Ether 161-166 BCL3 transcription coactivator Homo sapiens 142-146 35020071-0 2022 BCL3 expression is strongly associated with the occurrence of breast cancer relapse under tamoxifen treatment in a retrospective cohort study. Tamoxifen 90-99 BCL3 transcription coactivator Homo sapiens 0-4 35020071-5 2022 Formaldehyde-fixed, paraffin-embedded samples of 180 breast cancer patients were analyzed for BCL3 expression by immunohistochemistry. Formaldehyde 0-12 BCL3 transcription coactivator Homo sapiens 94-98 35020071-8 2022 A tamoxifen-adapted MCF-7 derived cell line was investigated for BCL3 localization by immunofluorescence. Tamoxifen 2-11 BCL3 transcription coactivator Homo sapiens 65-69 35020071-9 2022 The cytosolic BCL3-IRS significantly correlated with the proliferation marker Ki-67, and with the occurrence of a relapse under tamoxifen treatment. Tamoxifen 128-137 BCL3 transcription coactivator Homo sapiens 14-18 35020071-13 2022 Tamoxifen-treated, but not aromatase-treated patients had a poor survival when BCL3 scores were high. Tamoxifen 0-9 BCL3 transcription coactivator Homo sapiens 79-83 35020071-14 2022 A tamoxifen adapted cell line exhibited a reduced expression and mainly nuclear localization of BCL3, compared to the parental estrogen receptor positive cell-line MCF-7. Tamoxifen 2-11 BCL3 transcription coactivator Homo sapiens 96-100 35020071-15 2022 Altogether, these data strongly support a function of BCL3 in tamoxifen resistance and its potential use as a predictive biomarker for tamoxifen resistance. Tamoxifen 62-71 BCL3 transcription coactivator Homo sapiens 54-58 35176335-2 2022 The chloride anions form NH Cl- hydrogen bonds in BCl-4ABA and OH Cl- hydrogen bonds in BCl-4HBA. Chlorides 4-12 BCL3 transcription coactivator Homo sapiens 52-57 35176335-2 2022 The chloride anions form NH Cl- hydrogen bonds in BCl-4ABA and OH Cl- hydrogen bonds in BCl-4HBA. Hydrogen 34-42 BCL3 transcription coactivator Homo sapiens 52-57 35176335-5 2022 Compared to BCl, the dissolution rates of BCl-4ABA and BCl-4HBA in water are higher but that of (B)+(26DHBA)- is lower. Water 67-72 BCL3 transcription coactivator Homo sapiens 55-60