PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
30148830-6	2018	Ultrastructural analyses in the female carrying combined mutations in MNS1 and DNAH5 indicated a role for MNS1 in the process of ODA docking (ODA-DC) in the distal respiratory axonemes.	oda	129-132	meiosis specific nuclear structural 1	Homo sapiens	106-110
30148830-6	2018	Ultrastructural analyses in the female carrying combined mutations in MNS1 and DNAH5 indicated a role for MNS1 in the process of ODA docking (ODA-DC) in the distal respiratory axonemes.	oda	129-132	dynein axonemal heavy chain 5	Homo sapiens	79-84
30471717-8	2018	Paramecium DNAH9 knockdown confirms an evolutionarily conserved function for DNAH9 in cilia motility and ODA stability.	oda	105-108	dynein axonemal heavy chain 9	Homo sapiens	11-16
30471717-8	2018	Paramecium DNAH9 knockdown confirms an evolutionarily conserved function for DNAH9 in cilia motility and ODA stability.	oda	105-108	dynein axonemal heavy chain 9	Homo sapiens	77-82
30133350-8	2018	Transient docking still occurred in the docking complex mutant oda3 indicating that the docking complex stabilizes rather than initiates ODA-microtubule interactions.	oda	137-140	uncharacterized protein	Chlamydomonas reinhardtii	63-67
30148830-7	2018	Furthermore, co-immunoprecipitation and yeast two hybrid analyses demonstrated that MNS1 dimerizes and interacts with the ODA docking complex component CCDC114.	oda	122-125	meiosis specific nuclear structural 1	Homo sapiens	84-88
30148830-7	2018	Furthermore, co-immunoprecipitation and yeast two hybrid analyses demonstrated that MNS1 dimerizes and interacts with the ODA docking complex component CCDC114.	oda	122-125	outer dynein arm docking complex subunit 1	Homo sapiens	152-159
25192045-7	2014	We demonstrate that CCDC151 encodes an axonemal coiled coil protein, mutations in which abolish assembly of CCDC151 into respiratory cilia and cause a failure in axonemal assembly of the ODA component DNAH5 and the ODA-DC-associated components CCDC114 and ARMC4.	oda	187-190	outer dynein arm docking complex subunit 3	Mus musculus	20-27
26893459-7	2016	Together, these results demonstrate that PTCH1 mutations contribute to as much as 10% of ODA, identify the SHH signaling pathway as a novel effector of SOX2 activity during human ocular development, and indicate that ODA is likely the result of overactive SHH signaling in humans harboring mutations in either PTCH1 or SOX2.	oda	89-92	patched 1	Homo sapiens	41-46
26893459-7	2016	Together, these results demonstrate that PTCH1 mutations contribute to as much as 10% of ODA, identify the SHH signaling pathway as a novel effector of SOX2 activity during human ocular development, and indicate that ODA is likely the result of overactive SHH signaling in humans harboring mutations in either PTCH1 or SOX2.	oda	217-220	patched 1	Homo sapiens	41-46
25192045-7	2014	We demonstrate that CCDC151 encodes an axonemal coiled coil protein, mutations in which abolish assembly of CCDC151 into respiratory cilia and cause a failure in axonemal assembly of the ODA component DNAH5 and the ODA-DC-associated components CCDC114 and ARMC4.	oda	187-190	outer dynein arm docking complex subunit 1	Mus musculus	244-251
25192045-7	2014	We demonstrate that CCDC151 encodes an axonemal coiled coil protein, mutations in which abolish assembly of CCDC151 into respiratory cilia and cause a failure in axonemal assembly of the ODA component DNAH5 and the ODA-DC-associated components CCDC114 and ARMC4.	oda	187-190	outer dynein arm docking complex subunit 2	Mus musculus	256-261
22143341-4	2012	METHODS: We studied the MIB-1 labeling index in cases of IPMN and ordinary ductal adenocarcinoma (ODA).	oda	98-101	MIB E3 ubiquitin protein ligase 1	Homo sapiens	24-29
24421334-7	2014	Our results suggest that Pih1d3 contributes to cytoplasmic preassembly of dynein complexes in spermatogenic cells by stabilizing and promoting complex formation by ODA and IDA proteins.	oda	164-167	dynein axonemal assembly factor 6	Mus musculus	25-31
23891471-2	2013	Using whole-exome and candidate-gene Sanger resequencing in PCD-affected families afflicted with combined IDA and ODA defects, we found that 6/38 (16%) carried biallelic mutations in the conserved zinc-finger gene BLU (ZMYND10).	oda	114-117	blu	Drosophila melanogaster	214-217
22699229-2	2012	This new monomer (DGMI) was copolymerized with octadecyl acrylate (ODA) from 3-mercaptopropyltrimethoxysilane-grafted silica to produce Sil-poly(ODA-alt-DGMI).	oda	67-70	STIL centriolar assembly protein	Homo sapiens	136-139
22204937-6	2012	Higher molecular-linearity selectivity toward PAHs was obtained on Sil-poy(ODA-alt-OMI) regardless of temperature changes but at temperature below 40  C, Sil-poly(ODA) showed better planarity selectivity than that of Sil-poy(ODA-alt-OMI).	oda	75-78	STIL centriolar assembly protein	Homo sapiens	67-70
22204937-3	2012	Both of the polymer-grafted silicas (Sil-poly(ODA-alt-OMI) and Sil-poly(ODA), respectively) were prepared by radical polymerization on 3-mercaptopropyltrimethoxysilane-modified silica.	oda	46-49	STIL centriolar assembly protein	Homo sapiens	37-40
8755606-3	1996	cis-9,10-Octadecenamide (ODA) markedly potentiated the action of 5-hydroxytryptamine (5-HT) on 5-HT2A and 5-HT2C receptors, but this action was not shared by related compounds such as oleic acid and trans-9,10-octacenamide.	oda	25-28	5-hydroxytryptamine receptor 2C	Rattus norvegicus	106-112
20402656-8	2010	Besides, VO(oda) induced a dissipation of the mitochondria membrane potential (MMP) and promoted an increase in ERK cascade phosphorylation, which is involved in the regulation of cellular death and survival.	oda	12-15	mitogen-activated protein kinase 1	Homo sapiens	112-115
20402656-11	2010	These results suggest that VO(oda) stimulated ERKs phosphorilation by induction of free radicals involving kinases upstream of ERK pathway.	oda	30-33	mitogen-activated protein kinase 1	Homo sapiens	46-50
20402656-11	2010	These results suggest that VO(oda) stimulated ERKs phosphorilation by induction of free radicals involving kinases upstream of ERK pathway.	oda	30-33	mitogen-activated protein kinase 1	Homo sapiens	46-49
17407161-7	2007	The spatial distribution of the ODA patches for the different members of the family is in relation to the origin and function of the particular MCP, which allowed distinguishing between them.	oda	32-35	capping actin protein, gelsolin like	Homo sapiens	144-147
18950741-11	2008	Thus, DNAI2 and DNAH5 mutations affect assembly of proximal and distal ODA complexes, whereas DNAI1 mutations mainly disrupt assembly of proximal ODA complexes.	oda	71-74	dynein axonemal intermediate chain 2	Homo sapiens	6-11
18950741-11	2008	Thus, DNAI2 and DNAH5 mutations affect assembly of proximal and distal ODA complexes, whereas DNAI1 mutations mainly disrupt assembly of proximal ODA complexes.	oda	71-74	dynein axonemal heavy chain 5	Homo sapiens	16-21
15750039-8	2005	In contrast to respiratory cilia, sperm tails from a patient with DNAH5 mutations had normal ODA heavy chain distribution, suggesting different modes of ODA generation in these cell types.	oda	153-156	dynein axonemal heavy chain 5	Homo sapiens	66-71
15750039-9	2005	Blinded investigation of a large cohort of patients with PCD and control subjects identified DNAH5 mislocalization in all patients diagnosed with ODA defects by electron microscopy (n = 16).	oda	146-149	dynein axonemal heavy chain 5	Homo sapiens	93-98
11713099-3	2001	The aims of the current study were to test for novel DNAI1 mutations in 13 PCD patients with ODA defects (from 7 unrelated families) and to assess genotype/phenotype correlations in patients and family members.	oda	93-96	dynein axonemal intermediate chain 1	Homo sapiens	53-58
11713099-8	2001	Mutations in DNAI1 are causative for PCD with ODA defects, and are likely the genetic origin of clinical disease in some PCD patients with ultrastructural defects in the ODA.	oda	46-49	dynein axonemal intermediate chain 1	Homo sapiens	13-18
11713099-8	2001	Mutations in DNAI1 are causative for PCD with ODA defects, and are likely the genetic origin of clinical disease in some PCD patients with ultrastructural defects in the ODA.	oda	170-173	dynein axonemal intermediate chain 1	Homo sapiens	13-18
11208923-4	2001	The present study examined the possible role of NF-kappaB in ODA (auto-oxidized dopamine)-induced apoptosis to understand the process of PD.	oda	61-64	nuclear factor kappa B subunit 1	Homo sapiens	48-57
11208923-5	2001	Using the electrophoretic mobility shift assay, it was found that ODA activated the DNA binding activity of NF-kappaB.	oda	66-69	nuclear factor kappa B subunit 1	Homo sapiens	108-117
11208923-6	2001	Suppression of the transcriptional activity of NF-kappaB in PC12 cells by overexpression of a wild-type and a dominant negative mutant form (S32A/S36A) of inhibitor kappa B (IkappaB)-alpha led to increase of apoptotic cell death induced by treatment of ODA.	oda	253-256	nuclear factor kappa B subunit 1	Homo sapiens	47-56
11208923-7	2001	In addition, overexpression of NF-kappaB in PC12 cells blocked ODA-induced cell death.	oda	63-66	nuclear factor kappa B subunit 1	Homo sapiens	31-40
11208923-9	2001	Therefore, these results suggest that activation of NF-kappaB during ODA-induced apoptosis may have a counteracting activity against the signals mediating apoptotic cell death and thereby delay the process of Parkinson"s disease.	oda	69-72	nuclear factor kappa B subunit 1	Homo sapiens	52-61
31178125-9	2019	Overall, this study demonstrates that mutations in DNAH17 are responsible for isolated male infertility and provides information regarding ODA composition in human spermatozoa.	oda	139-142	dynein axonemal heavy chain 17	Homo sapiens	51-57
33812606-2	2021	The N,O-CS/ODA hydrogels have a good suitable gelation time, good cytocompatibility and hemocompatibility, good antibacterial activity, excellent biodegradable and biocompatible, and can effectively inhibit the adhesion of fibroblasts to the wound, thereby suggesting that N,O-CS/ODA hydrogels are suitable for preventing post-operative adhesion.	oda	11-14	citrate synthase	Rattus norvegicus	8-10
33812606-2	2021	The N,O-CS/ODA hydrogels have a good suitable gelation time, good cytocompatibility and hemocompatibility, good antibacterial activity, excellent biodegradable and biocompatible, and can effectively inhibit the adhesion of fibroblasts to the wound, thereby suggesting that N,O-CS/ODA hydrogels are suitable for preventing post-operative adhesion.	oda	11-14	citrate synthase	Rattus norvegicus	277-279
33812606-2	2021	The N,O-CS/ODA hydrogels have a good suitable gelation time, good cytocompatibility and hemocompatibility, good antibacterial activity, excellent biodegradable and biocompatible, and can effectively inhibit the adhesion of fibroblasts to the wound, thereby suggesting that N,O-CS/ODA hydrogels are suitable for preventing post-operative adhesion.	oda	280-283	citrate synthase	Rattus norvegicus	8-10
33812606-4	2021	A significant reduction of peritoneal adhesions (10% rat with lower score adhesion) is observed in the N,O-CS/ODA-hydrogel-treated group compared with the commercial hydrogel and control groups.	oda	110-113	citrate synthase	Rattus norvegicus	107-109
33812606-6	2021	Therefore, the N,O-CS/ODA hydrogels with multi-functional properties exhibit great potential for the prevention and treatment of postoperative adhesion.	oda	22-25	citrate synthase	Rattus norvegicus	19-21