PMID-sentid	Pub_year	Sent_text	comp_official_name	comp_offset	protein_name	organism	prot_offset
3023378-14	1986	Since this antiestrogen is a complete antagonist in the chick oviduct and prevents estradiol-induced stimulation of ovalbumin gene transcription, it is speculated that Rx to Ry conversion is crucial for ovalbumin gene activation and that Rx may act as a transcriptional repressor.	Estradiol	83-92	ovalbumin (SERPINB14)	Gallus gallus	116-125
2780293-1	1989	To understand the molecular basis of the steroid hormone regulated expression of the ovalbumin gene, we sought to identify and isolate nuclear factors from chicken oviduct which interact specifically with the ovalbumin promoter.	Steroids	41-48	ovalbumin (SERPINB14)	Gallus gallus	85-94
2780293-1	1989	To understand the molecular basis of the steroid hormone regulated expression of the ovalbumin gene, we sought to identify and isolate nuclear factors from chicken oviduct which interact specifically with the ovalbumin promoter.	Steroids	41-48	ovalbumin (SERPINB14)	Gallus gallus	209-218
3410855-1	1988	Substitution of glutamine for asparagine 293 in chicken ovalbumin does not allow glycosylation of asparagine 312.	Asparagine	30-40	ovalbumin (SERPINB14)	Gallus gallus	56-65
3410855-2	1988	It has been shown previously that chicken ovalbumin synthesized and secreted in a heterologous cell system is glycosylated at the correct site and that the oligosaccharides at that site, similar to the protein made in hen oviduct, are predominantly of the hybrid type (Sheares, B. T., and Robbins, P. W. (1986) Proc.	Oligosaccharides	156-172	ovalbumin (SERPINB14)	Gallus gallus	42-51
3410855-9	1988	Using a 20-base oligodeoxynucleotide primer containing a 2-base mismatch, the codon for Asn293 in the chicken ovalbumin gene (AAC) was changed to that for Gln (CAA), thereby preventing glycosylation at amino acid 293.	Glutamine	155-158	ovalbumin (SERPINB14)	Gallus gallus	110-119
3410855-11	1988	Ovalbumin secreted by these cells was recovered by immunoaffinity chromatography and analyzed for the presence of an oligosaccharide attached at Asn312.	Oligosaccharides	117-132	ovalbumin (SERPINB14)	Gallus gallus	0-9
3386256-1	1988	The relative rate of ovalbumin transcription was significantly increased (P less than 0.001) when purified chick liver glucocorticosteroid receptor (GR) was incubated with purified nuclei prepared from the oviducts of diethylstilboestrol (DES)-primed chickens 24 h after oestrogen withdrawal.	diethylstilboestrol	218-237	ovalbumin (SERPINB14)	Gallus gallus	21-30
3386256-1	1988	The relative rate of ovalbumin transcription was significantly increased (P less than 0.001) when purified chick liver glucocorticosteroid receptor (GR) was incubated with purified nuclei prepared from the oviducts of diethylstilboestrol (DES)-primed chickens 24 h after oestrogen withdrawal.	desacetyluvaricin	239-242	ovalbumin (SERPINB14)	Gallus gallus	21-30
3047126-7	1988	The purine contacts in the two promoters are limited to one face of the DNA helix; however, studies on phosphate contacts suggest that the COUP transcription factor wraps around the ovalbumin promoter, while it binds to only one face of the DNA helix in the insulin promoter.	purine	4-10	ovalbumin (SERPINB14)	Gallus gallus	182-191
3047126-7	1988	The purine contacts in the two promoters are limited to one face of the DNA helix; however, studies on phosphate contacts suggest that the COUP transcription factor wraps around the ovalbumin promoter, while it binds to only one face of the DNA helix in the insulin promoter.	Phosphates	103-112	ovalbumin (SERPINB14)	Gallus gallus	182-191
3064812-0	1988	Positive and negative regulatory elements control the steroid-responsive ovalbumin promoter.	Steroids	54-61	ovalbumin (SERPINB14)	Gallus gallus	73-82
3064812-1	1988	Steroid hormones regulate the transcriptional activity of the chicken ovalbumin gene both in vivo and in cell culture.	Steroids	0-16	ovalbumin (SERPINB14)	Gallus gallus	70-79
3064812-3	1988	Induction of the OvCAT genes by estrogen, progesterone, or corticosterone mimics that of the endogenous ovalbumin gene, indicating that the transfected DNA is accurately regulated.	Progesterone	42-54	ovalbumin (SERPINB14)	Gallus gallus	104-113
3064812-3	1988	Induction of the OvCAT genes by estrogen, progesterone, or corticosterone mimics that of the endogenous ovalbumin gene, indicating that the transfected DNA is accurately regulated.	Corticosterone	59-73	ovalbumin (SERPINB14)	Gallus gallus	104-113
3064812-5	1988	Thus, an NRE represses expression of the ovalbumin gene unless steroid hormones relieve this negative control through interactions involving a more distal SRE.	Steroids	63-79	ovalbumin (SERPINB14)	Gallus gallus	41-50
3396330-2	1988	Ovalbumin was fractionated to six fractions according to their phosphate content by high performance anion exchange chromatography.	Phosphates	63-72	ovalbumin (SERPINB14)	Gallus gallus	0-9
3396330-4	1988	This method was applied to analyze the phosphate content of ovalbumin subfractions having different carbohydrate chain from each other which were prepared by concanavalin A/Sepharose chromatography from oviduct slices incubated with [2-3H]mannose.	Phosphates	39-48	ovalbumin (SERPINB14)	Gallus gallus	60-69
3396330-4	1988	This method was applied to analyze the phosphate content of ovalbumin subfractions having different carbohydrate chain from each other which were prepared by concanavalin A/Sepharose chromatography from oviduct slices incubated with [2-3H]mannose.	Carbohydrates	100-112	ovalbumin (SERPINB14)	Gallus gallus	60-69
3396330-4	1988	This method was applied to analyze the phosphate content of ovalbumin subfractions having different carbohydrate chain from each other which were prepared by concanavalin A/Sepharose chromatography from oviduct slices incubated with [2-3H]mannose.	[2-3h]mannose	233-246	ovalbumin (SERPINB14)	Gallus gallus	60-69
3311742-8	1987	Tryptic peptides produced from the ovalbumin and serum albumin derivatives were fractionated by HPLC and subsequently analysed by amino acid analysis, FAB-MS and automated stepwise protein sequence analysis.	Peptides	8-16	ovalbumin (SERPINB14)	Gallus gallus	35-44
3665877-0	1987	The chicken ovalbumin promoter is under negative control which is relieved by steroid hormones.	Steroids	78-94	ovalbumin (SERPINB14)	Gallus gallus	12-21
3665877-1	1987	Steroid hormone regulation of activity of the chicken ovalbumin promoter was studied by microinjection of chimeric genes into the nuclei of primary cultured oviduct tubular gland cells.	Steroids	0-15	ovalbumin (SERPINB14)	Gallus gallus	54-63
3665877-4	1987	The activity of the ovalbumin promoter is cell-specifically repressed in these oviduct cells and the repression is relieved upon addition of steroid hormones.	Steroids	141-157	ovalbumin (SERPINB14)	Gallus gallus	20-29
3665877-5	1987	The -132 to -425 region of the ovalbumin promoter which is responsible for this negative regulation behaves as an independent functional unit containing the regulatory elements necessary for both repression (in the presence of steroid hormone antagonists) and induced derepression (in the presence of steroid hormones) of linked heterologous promoters.	Steroids	227-242	ovalbumin (SERPINB14)	Gallus gallus	31-40
3665877-5	1987	The -132 to -425 region of the ovalbumin promoter which is responsible for this negative regulation behaves as an independent functional unit containing the regulatory elements necessary for both repression (in the presence of steroid hormone antagonists) and induced derepression (in the presence of steroid hormones) of linked heterologous promoters.	Steroids	301-317	ovalbumin (SERPINB14)	Gallus gallus	31-40
3023378-14	1986	Since this antiestrogen is a complete antagonist in the chick oviduct and prevents estradiol-induced stimulation of ovalbumin gene transcription, it is speculated that Rx to Ry conversion is crucial for ovalbumin gene activation and that Rx may act as a transcriptional repressor.	Estradiol	83-92	ovalbumin (SERPINB14)	Gallus gallus	203-212
3021132-1	1986	By means of the DNA-cellulose competitive binding assay, the interaction of estrogen receptor complexed to 17 beta-estradiol with fragments of a cloned DNA region of the estrogen responsive chicken ovalbumin gene spanning from 1343 bps upstream to 373 bps within the transcribed region of the gene (p0V 1.7) was investigated.	Cellulose	20-29	ovalbumin (SERPINB14)	Gallus gallus	198-207
3801455-1	1986	The dependence of chromatin conformation upon salt concentration has been studied for chicken ovalbumin and beta-globin genes isolated from oviduct and adult erythrocytes.	Salts	46-50	ovalbumin (SERPINB14)	Gallus gallus	94-103
3021132-1	1986	By means of the DNA-cellulose competitive binding assay, the interaction of estrogen receptor complexed to 17 beta-estradiol with fragments of a cloned DNA region of the estrogen responsive chicken ovalbumin gene spanning from 1343 bps upstream to 373 bps within the transcribed region of the gene (p0V 1.7) was investigated.	Estradiol	110-124	ovalbumin (SERPINB14)	Gallus gallus	198-207
3487084-2	1986	We used the chicken ovalbumin peptide ovalbumin-(323-339)-Tyr, which is immunogenic in the BALB/c mouse and restricted to I-Ad.	Tyrosine	58-61	ovalbumin (SERPINB14)	Gallus gallus	20-29
3487084-2	1986	We used the chicken ovalbumin peptide ovalbumin-(323-339)-Tyr, which is immunogenic in the BALB/c mouse and restricted to I-Ad.	Tyrosine	58-61	ovalbumin (SERPINB14)	Gallus gallus	38-47
3487084-4	1986	This binding was inhibited by unlabeled ovalbumin-(323-339) but not by ovalbumin-(329-339), which is the longest N-terminally truncated peptide that fails to stimulate any of the I-Ad-restricted hybridomas that have been raised to ovalbumin-(323-339)-Tyr.	Tyrosine	251-254	ovalbumin (SERPINB14)	Gallus gallus	40-49
3707933-8	1986	The lower affinity receptor sediments at 3.5 S on sucrose density gradients compared to 4.2 S for the high-affinity form; it has high specificity for estrogen and is tissue specific, and its nuclear occupancy is associated with increases in ovalbumin gene transcription; thus, this macromolecule meets the criteria of an estrogen receptor.	Sucrose	50-57	ovalbumin (SERPINB14)	Gallus gallus	241-250
3457370-4	1986	As in the case of chicken ovalbumin, the protein synthesized in L cells contains large amounts of hybrid oligosaccharides.	Oligosaccharides	105-121	ovalbumin (SERPINB14)	Gallus gallus	26-35
3457370-6	1986	These results suggest that it is the polypeptide chain of ovalbumin that is responsible for proper glycosylation and subsequent processing of a substantial fraction of the oligosaccharide chains to hybrid structures.	Oligosaccharides	172-187	ovalbumin (SERPINB14)	Gallus gallus	58-67
3457370-5	1986	Approximately 50% of the [3H]mannose incorporated into ovalbumin secreted by L cells is found in such hybrid structures.	Tritium	26-28	ovalbumin (SERPINB14)	Gallus gallus	55-64
3457370-8	1986	The hybrid oligosaccharides of ovalbumin secreted by L cells are completely sialylated and do not contain a bisecting GlcNAc residue, distinguishing them from hybrid chains in chicken ovalbumin.	Oligosaccharides	11-27	ovalbumin (SERPINB14)	Gallus gallus	31-40
3457370-9	1986	In addition to high-mannose and hybrid oligosaccharide chains, ovalbumin synthesized in L cells contains oligosaccharides of the complex type.	Oligosaccharides	105-121	ovalbumin (SERPINB14)	Gallus gallus	63-72
3457370-5	1986	Approximately 50% of the [3H]mannose incorporated into ovalbumin secreted by L cells is found in such hybrid structures.	Mannose	29-36	ovalbumin (SERPINB14)	Gallus gallus	55-64
3457370-11	1986	These differences in fine structure, between the oligosaccharides derived from ovalbumin secreted by L cells and those known to be present in the chicken egg glycoprotein, suggest that the cell type also plays a role in oligosaccharide processing.	Oligosaccharides	49-65	ovalbumin (SERPINB14)	Gallus gallus	79-88
2858488-2	1985	At least 50% of the poly A+ mRNA molecules (9S rabbit globin mRNA, chicken ovalbumin, and lysozyme) were stable in oocytes over a 48-h period, irrespective of the amount injected.	Poly A	20-26	ovalbumin (SERPINB14)	Gallus gallus	75-84
3457370-11	1986	These differences in fine structure, between the oligosaccharides derived from ovalbumin secreted by L cells and those known to be present in the chicken egg glycoprotein, suggest that the cell type also plays a role in oligosaccharide processing.	Oligosaccharides	49-64	ovalbumin (SERPINB14)	Gallus gallus	79-88
3702411-10	1986	In the presence of estradiol (50 and 100 nM), progesterone (50 nM), and both estradiol and progesterone together (50 nM of each), ovalbumin and conalbumin synthesis was increased, when compared to control cultures without hormones, or to oviduct fibroblasts.	Estradiol	19-28	ovalbumin (SERPINB14)	Gallus gallus	130-139
3702411-10	1986	In the presence of estradiol (50 and 100 nM), progesterone (50 nM), and both estradiol and progesterone together (50 nM of each), ovalbumin and conalbumin synthesis was increased, when compared to control cultures without hormones, or to oviduct fibroblasts.	Progesterone	46-58	ovalbumin (SERPINB14)	Gallus gallus	130-139
3702411-10	1986	In the presence of estradiol (50 and 100 nM), progesterone (50 nM), and both estradiol and progesterone together (50 nM of each), ovalbumin and conalbumin synthesis was increased, when compared to control cultures without hormones, or to oviduct fibroblasts.	Estradiol	77-86	ovalbumin (SERPINB14)	Gallus gallus	130-139
3702411-10	1986	In the presence of estradiol (50 and 100 nM), progesterone (50 nM), and both estradiol and progesterone together (50 nM of each), ovalbumin and conalbumin synthesis was increased, when compared to control cultures without hormones, or to oviduct fibroblasts.	Progesterone	91-103	ovalbumin (SERPINB14)	Gallus gallus	130-139
4026804-0	1985	Decreased ovalbumin-gene response to oestrogen in the prenatally diethylstilboestrol-exposed chick oviduct.	diethylstilboestrol	65-84	ovalbumin (SERPINB14)	Gallus gallus	10-19
4026804-1	1985	Prenatal exposure of the female chick-embryo Mullerian duct to diethylstilboestrol (DES) decreases its future capacity for epithelial tubular-gland-cell differentiation and oviduct ovalbumin-gene expression.	diethylstilboestrol	63-82	ovalbumin (SERPINB14)	Gallus gallus	181-190
4026804-1	1985	Prenatal exposure of the female chick-embryo Mullerian duct to diethylstilboestrol (DES) decreases its future capacity for epithelial tubular-gland-cell differentiation and oviduct ovalbumin-gene expression.	desacetyluvaricin	84-87	ovalbumin (SERPINB14)	Gallus gallus	181-190
4026804-4	1985	Comparisons among these three parameters revealed that the expression of the ovalbumin gene was affected most by DES exposure.	desacetyluvaricin	113-116	ovalbumin (SERPINB14)	Gallus gallus	77-86
4026804-5	1985	Exposure to high doses of DES suppressed ovalbumin-gene expression by 75-78%, and inhibited tubular-gland-cell differentiation and thus decreased the DNA content by 29 and 32% respectively.	desacetyluvaricin	26-29	ovalbumin (SERPINB14)	Gallus gallus	41-50
4026804-6	1985	Exposure to low doses of DES caused suppression of ovalbumin-gene expression by 47-53%, but it did not affect the other two parameters.	desacetyluvaricin	25-28	ovalbumin (SERPINB14)	Gallus gallus	51-60
4016253-2	1985	Guinea-pigs which fasted for 96, 48 and 12 (control) hours were fed intragastrically 300 mg chick ovalbumin in saline, and after 3 hours immunoreactive OA was measured in blood serum by competitive radioimmunoassay.	Sodium Chloride	111-117	ovalbumin (SERPINB14)	Gallus gallus	98-107
3987617-3	1985	Ovalbumin accounted for 25% of oviduct protein synthesis in chicks treated with low dose of diethylstilbestrol (DES; 0.5 mg/day) for 14 days.	Diethylstilbestrol	92-110	ovalbumin (SERPINB14)	Gallus gallus	0-9
3987617-3	1985	Ovalbumin accounted for 25% of oviduct protein synthesis in chicks treated with low dose of diethylstilbestrol (DES; 0.5 mg/day) for 14 days.	Diethylstilbestrol	112-115	ovalbumin (SERPINB14)	Gallus gallus	0-9
3987617-9	1985	Ovalbumin synthesis fluctuated, but overall decreased from 25% of oviduct protein synthesis after priming with DES pellets to 16% of oviduct protein synthesis after 7-12 days of injections of estradiol benzoate (1 mg/day).	estradiol 3-benzoate	192-210	ovalbumin (SERPINB14)	Gallus gallus	0-9
3937332-3	1985	Significant differences in BSA and OVA digestion by the gastric juice--FGS system were detected both with respect to amino nitrogen content and to the degree of their antigenic structure decomposition, whereas no such differences were observed when the four-enzymic system was used.	hydrazine	117-131	ovalbumin (SERPINB14)	Gallus gallus	35-38
3996320-2	1985	The simultaneous injection of equal doses of DEX and progesterone resulted in an additive effect on the relative rate of ovalbumin synthesis at all doses tested (range: 0.05-15 mg/chick), even when the induction of ovalbumin synthesis was maximal at 6 h, for either hormone injected alone.	Dexamethasone	45-48	ovalbumin (SERPINB14)	Gallus gallus	121-130
3996320-2	1985	The simultaneous injection of equal doses of DEX and progesterone resulted in an additive effect on the relative rate of ovalbumin synthesis at all doses tested (range: 0.05-15 mg/chick), even when the induction of ovalbumin synthesis was maximal at 6 h, for either hormone injected alone.	Dexamethasone	45-48	ovalbumin (SERPINB14)	Gallus gallus	215-224
3996320-2	1985	The simultaneous injection of equal doses of DEX and progesterone resulted in an additive effect on the relative rate of ovalbumin synthesis at all doses tested (range: 0.05-15 mg/chick), even when the induction of ovalbumin synthesis was maximal at 6 h, for either hormone injected alone.	Progesterone	53-65	ovalbumin (SERPINB14)	Gallus gallus	121-130
3996320-2	1985	The simultaneous injection of equal doses of DEX and progesterone resulted in an additive effect on the relative rate of ovalbumin synthesis at all doses tested (range: 0.05-15 mg/chick), even when the induction of ovalbumin synthesis was maximal at 6 h, for either hormone injected alone.	Progesterone	53-65	ovalbumin (SERPINB14)	Gallus gallus	215-224
3996320-3	1985	Moreover, the simultaneous injection of DEX and progesterone yielded an additive effect on the relative rates of ovalbumin and conalbumin gene transcription.	Dexamethasone	40-43	ovalbumin (SERPINB14)	Gallus gallus	113-122
3996320-3	1985	Moreover, the simultaneous injection of DEX and progesterone yielded an additive effect on the relative rates of ovalbumin and conalbumin gene transcription.	Progesterone	48-60	ovalbumin (SERPINB14)	Gallus gallus	113-122
3996320-5	1985	The simultaneous injection of tamoxifen and DEX potentiated the effect of DEX on the relative rates of ovalbumin and conalbumin synthesis, and amplified the DEX-induced increase in the relative rates of ovalbumin and conalbumin gene transcription.	Tamoxifen	30-39	ovalbumin (SERPINB14)	Gallus gallus	103-112
3996320-5	1985	The simultaneous injection of tamoxifen and DEX potentiated the effect of DEX on the relative rates of ovalbumin and conalbumin synthesis, and amplified the DEX-induced increase in the relative rates of ovalbumin and conalbumin gene transcription.	Tamoxifen	30-39	ovalbumin (SERPINB14)	Gallus gallus	203-212
3996320-5	1985	The simultaneous injection of tamoxifen and DEX potentiated the effect of DEX on the relative rates of ovalbumin and conalbumin synthesis, and amplified the DEX-induced increase in the relative rates of ovalbumin and conalbumin gene transcription.	Dexamethasone	44-47	ovalbumin (SERPINB14)	Gallus gallus	103-112
3996320-5	1985	The simultaneous injection of tamoxifen and DEX potentiated the effect of DEX on the relative rates of ovalbumin and conalbumin synthesis, and amplified the DEX-induced increase in the relative rates of ovalbumin and conalbumin gene transcription.	Dexamethasone	44-47	ovalbumin (SERPINB14)	Gallus gallus	203-212
3996320-5	1985	The simultaneous injection of tamoxifen and DEX potentiated the effect of DEX on the relative rates of ovalbumin and conalbumin synthesis, and amplified the DEX-induced increase in the relative rates of ovalbumin and conalbumin gene transcription.	Dexamethasone	74-77	ovalbumin (SERPINB14)	Gallus gallus	103-112
3996320-5	1985	The simultaneous injection of tamoxifen and DEX potentiated the effect of DEX on the relative rates of ovalbumin and conalbumin synthesis, and amplified the DEX-induced increase in the relative rates of ovalbumin and conalbumin gene transcription.	Dexamethasone	74-77	ovalbumin (SERPINB14)	Gallus gallus	103-112
2580958-2	1985	The immunogenic hexapeptide H-Gly-Arg-Gly-Thr-Lys-Phe-OH was coupled to chicken egg-albumin with dimethylsuberimidate.	H-Gly-Arg-Gly-Thr-Lys-Phe-OH	28-56	ovalbumin (SERPINB14)	Gallus gallus	80-91
2580958-2	1985	The immunogenic hexapeptide H-Gly-Arg-Gly-Thr-Lys-Phe-OH was coupled to chicken egg-albumin with dimethylsuberimidate.	Dimethyl Suberimidate	97-117	ovalbumin (SERPINB14)	Gallus gallus	80-91
3880544-1	1985	A primary cell culture from estrogen-withdrawn chicken oviduct has been developed in which the genes for the major egg white proteins, ovalbumin and conalbumin, are induced by steroid hormones.	Steroids	176-192	ovalbumin (SERPINB14)	Gallus gallus	135-144
4000950-7	1985	Whereas 40-45% of the beta A chromatin is recovered in the supernatant fraction from n-butyrate incubated immature erythrocytes, nucleohistone containing ovalbumin DNA sequences remains insoluble.	nucleohistone	129-142	ovalbumin (SERPINB14)	Gallus gallus	154-163
4005225-5	1985	After its administration together with or 6 h after diethylstilbestrol (a synthetic estrogen), tamoxifen stopped or suppressed the estrogen-dependent increase of ovalbumin and conalbumin gene transcription.	Tamoxifen	95-104	ovalbumin (SERPINB14)	Gallus gallus	162-171
3880544-4	1985	Both insulin and a second steroid (a glucocorticoid, progestin, or androgen) are required for the induction of the ovalbumin gene by estradiol to the extent reached in vivo.	Steroids	26-33	ovalbumin (SERPINB14)	Gallus gallus	115-124
3880544-4	1985	Both insulin and a second steroid (a glucocorticoid, progestin, or androgen) are required for the induction of the ovalbumin gene by estradiol to the extent reached in vivo.	Estradiol	133-142	ovalbumin (SERPINB14)	Gallus gallus	115-124
3880544-7	1985	The data obtained with the cultured cells demonstrate that the induction of the ovalbumin gene requires the permissive effects of insulin and a second steroid (probably a glucocorticoid in vivo) to facilitate the response to estradiol.	Steroids	151-158	ovalbumin (SERPINB14)	Gallus gallus	80-89
3880544-7	1985	The data obtained with the cultured cells demonstrate that the induction of the ovalbumin gene requires the permissive effects of insulin and a second steroid (probably a glucocorticoid in vivo) to facilitate the response to estradiol.	Estradiol	225-234	ovalbumin (SERPINB14)	Gallus gallus	80-89
6329659-0	1984	Regulation of the ovalbumin gene: effects of insulin, adenosine 3",5"-monophosphate, and estrogen.	Cyclic AMP	54-83	ovalbumin (SERPINB14)	Gallus gallus	18-27
6332146-3	1984	A 17-amino acid tryptic peptide of chicken ovalbumin, designated P323-339, that substituted for processed antigen when presented by glutaraldehyde prefixed accessory cells to specific I-restricted T hybridomas was characterized.	17-amino acid	2-15	ovalbumin (SERPINB14)	Gallus gallus	43-52
6332146-3	1984	A 17-amino acid tryptic peptide of chicken ovalbumin, designated P323-339, that substituted for processed antigen when presented by glutaraldehyde prefixed accessory cells to specific I-restricted T hybridomas was characterized.	Peptides	24-31	ovalbumin (SERPINB14)	Gallus gallus	43-52
6332146-3	1984	A 17-amino acid tryptic peptide of chicken ovalbumin, designated P323-339, that substituted for processed antigen when presented by glutaraldehyde prefixed accessory cells to specific I-restricted T hybridomas was characterized.	Glutaral	132-146	ovalbumin (SERPINB14)	Gallus gallus	43-52
6329659-7	1984	We found that cyclic nucleotide derivatives, such as 8-bromo-cAMP, can mimic the effect of insulin on ovalbumin gene expression and that the phosphodiesterase inhibitor isobutylmethylxanthine can potentiate this response to 8-bromo-cAMP.	Nucleotides, Cyclic	14-31	ovalbumin (SERPINB14)	Gallus gallus	102-111
6329659-7	1984	We found that cyclic nucleotide derivatives, such as 8-bromo-cAMP, can mimic the effect of insulin on ovalbumin gene expression and that the phosphodiesterase inhibitor isobutylmethylxanthine can potentiate this response to 8-bromo-cAMP.	8-Bromo Cyclic Adenosine Monophosphate	53-65	ovalbumin (SERPINB14)	Gallus gallus	102-111
6329659-7	1984	We found that cyclic nucleotide derivatives, such as 8-bromo-cAMP, can mimic the effect of insulin on ovalbumin gene expression and that the phosphodiesterase inhibitor isobutylmethylxanthine can potentiate this response to 8-bromo-cAMP.	1-Methyl-3-isobutylxanthine	169-191	ovalbumin (SERPINB14)	Gallus gallus	102-111
6329659-7	1984	We found that cyclic nucleotide derivatives, such as 8-bromo-cAMP, can mimic the effect of insulin on ovalbumin gene expression and that the phosphodiesterase inhibitor isobutylmethylxanthine can potentiate this response to 8-bromo-cAMP.	8-Bromo Cyclic Adenosine Monophosphate	224-236	ovalbumin (SERPINB14)	Gallus gallus	102-111
6329659-10	1984	We conclude that insulin and cAMP are producing their effects on activation of the ovalbumin gene via convergent pathways.	Cyclic AMP	29-33	ovalbumin (SERPINB14)	Gallus gallus	83-92
6329659-11	1984	The involvement of an activator of protein kinase, cAMP, strongly suggests that protein phosphorylation events play a regulatory role in the expression of the ovalbumin gene.	Cyclic AMP	51-55	ovalbumin (SERPINB14)	Gallus gallus	159-168
6646237-1	1983	In the chicken oviduct, it has been well documented that steroid hormones stimulate the transcription of specific genes such as the ovalbumin gene.	Steroids	57-73	ovalbumin (SERPINB14)	Gallus gallus	132-141
6313672-1	1983	To study the regulation of expression of the chicken ovalbumin gene by steroid hormones, the entire ovalbumin gene and its flanking sequences were cloned together with the bacterial gene for xanthine-guanine phosphoribosyltransferase in plasmid pBR322.	Steroids	71-87	ovalbumin (SERPINB14)	Gallus gallus	53-62
6313672-6	1983	An 8- to 10-fold increase in the amount of ovalbumin mRNA was observed to be present in cells cultured in 10(-8)M estradiol.	Estradiol	114-123	ovalbumin (SERPINB14)	Gallus gallus	43-52
6314276-8	1983	When recombinants are introduced into eukaryotic cells by either calcium phosphate coprecipitation or protoplast fusion, expression of chicken ovalbumin or conalbumin may be detected by indirect immunofluorescence.	calcium phosphate	65-82	ovalbumin (SERPINB14)	Gallus gallus	143-152
6621702-1	1983	Ovalbumin gene transcripts are not detectable in unstimulated chick oviducts but comprise about half of oviduct cell transcripts after steroid hormone induction.	Steroids	135-150	ovalbumin (SERPINB14)	Gallus gallus	0-9
7160465-0	1982	The effect of estrogen on the concentration of ovalbumin gene sequence in the 2 M NaCl residual fraction of oviduct chromatin.	Sodium Chloride	82-86	ovalbumin (SERPINB14)	Gallus gallus	47-56
6571991-3	1983	About a 10-fold preference was seen for DNA fragments flanking the 5" end of the steroid-regulated genes ovalbumin and gene Y.	Steroids	81-88	ovalbumin (SERPINB14)	Gallus gallus	105-114
6557011-1	1983	The ovalbumin gene and the ovalbumin-related X and Y genes are expressed in the chicken oviduct in response to steroid hormones.	Steroids	111-127	ovalbumin (SERPINB14)	Gallus gallus	4-13
6557011-1	1983	The ovalbumin gene and the ovalbumin-related X and Y genes are expressed in the chicken oviduct in response to steroid hormones.	Steroids	111-127	ovalbumin (SERPINB14)	Gallus gallus	27-36
7130193-1	1982	We have examined the effects of steroid hormones in the chromatin sensitivity of the ovalbumin gene to micrococcal nuclease and have attempted to define the importance of the nucleosome core, higher order chromatin folding, and transcription in the maintenance of the nuclease-sensitive conformation of the ovalbumin chromatin.	Steroids	32-39	ovalbumin (SERPINB14)	Gallus gallus	85-94
7084121-2	1982	In estrogen differentiated, hormone-withdrawn animals, biochemical and ultrastructural data indicated that the combined treatment with progesterone plus tamoxifen increased conalbumin (+100%) and ovalbumin (+30%) more than progesterone alone and displayed estrogen-like growth-promoting properties (+50% in DNA content per oviduct).	Progesterone	135-147	ovalbumin (SERPINB14)	Gallus gallus	196-205
7171239-2	1982	In estrogen differentiated, hormone withdrawn animals, biochemical and ultrastructural data indicated that the combined treatment with progesterone plus tamoxifen increased conalbumin (+ 100%) and ovalbumin (+ 30%) more than progesterone alone, and displayed estrogen-like growth promoting properties (+ 50% in DNA content/oviduct).	Progesterone	135-147	ovalbumin (SERPINB14)	Gallus gallus	173-206
7171239-2	1982	In estrogen differentiated, hormone withdrawn animals, biochemical and ultrastructural data indicated that the combined treatment with progesterone plus tamoxifen increased conalbumin (+ 100%) and ovalbumin (+ 30%) more than progesterone alone, and displayed estrogen-like growth promoting properties (+ 50% in DNA content/oviduct).	Tamoxifen	153-162	ovalbumin (SERPINB14)	Gallus gallus	173-206
7084121-2	1982	In estrogen differentiated, hormone-withdrawn animals, biochemical and ultrastructural data indicated that the combined treatment with progesterone plus tamoxifen increased conalbumin (+100%) and ovalbumin (+30%) more than progesterone alone and displayed estrogen-like growth-promoting properties (+50% in DNA content per oviduct).	Tamoxifen	153-162	ovalbumin (SERPINB14)	Gallus gallus	196-205
7263632-0	1981	Steroid hormone regulation of ovalbumin and conalbumin gene transcription.	Steroids	0-15	ovalbumin (SERPINB14)	Gallus gallus	30-39
6272839-8	1981	Similarly, the hexanucleotide sequence AATAAA common to all eucaryotic messenger RNAs at the 3"-untranslated region occurs seven additional times within the ovalbumin gene.	hexanucleotide	15-29	ovalbumin (SERPINB14)	Gallus gallus	157-166
7263632-6	1981	These ideas are combined with our recent observations that protein synthesis inhibitors and butyrate selectively, but reversibly, inhibit ovalbumin and conalbumin gene transcription.	Butyrates	92-100	ovalbumin (SERPINB14)	Gallus gallus	138-147
6257282-7	1980	R0t analysis has demonstrated that, similar to the ovalbumin gene, the level of X and Y gene transcripts is increased by the steroid hormone estrogen, but to varying degrees.	Steroids	125-140	ovalbumin (SERPINB14)	Gallus gallus	51-60
6162638-4	1981	However, ovalbumin, which is transferred across the endoplasmic reticulum in the presence of tunicamycin and which is indistinguishable by immunoprecipitation, by two-dimensional gel electrophoresis and by concanavalin-A--Sepharose binding from the cytosolic form, is still secreted.	Tunicamycin	93-104	ovalbumin (SERPINB14)	Gallus gallus	9-18
6162638-4	1981	However, ovalbumin, which is transferred across the endoplasmic reticulum in the presence of tunicamycin and which is indistinguishable by immunoprecipitation, by two-dimensional gel electrophoresis and by concanavalin-A--Sepharose binding from the cytosolic form, is still secreted.	Sepharose	222-231	ovalbumin (SERPINB14)	Gallus gallus	9-18
7284304-0	1981	Demonstration of heterogeneity of chick ovalbumin glycopeptides using 360-MHz proton magnetic resonance spectroscopy.	Glycopeptides	50-63	ovalbumin (SERPINB14)	Gallus gallus	40-49
7278996-2	1981	In the chicken oviduct the synthesis of the egg-white proteins ovalbumin, conalbumin, ovomucoid and lysozyme is controlled by the female sex steroids.	Steroids	141-149	ovalbumin (SERPINB14)	Gallus gallus	63-72
7448870-1	1980	The short chain aliphatic acid salts, butyrate and propionate, are effective inhibitors of histone deacetylation in chick oviduct at 2--5 mM; they also prevent the hormonal induction of the ovalbumin and transferrin genes.	aliphatic acid salts	16-36	ovalbumin (SERPINB14)	Gallus gallus	190-199
7448870-1	1980	The short chain aliphatic acid salts, butyrate and propionate, are effective inhibitors of histone deacetylation in chick oviduct at 2--5 mM; they also prevent the hormonal induction of the ovalbumin and transferrin genes.	Butyrates	38-46	ovalbumin (SERPINB14)	Gallus gallus	190-199
7448870-1	1980	The short chain aliphatic acid salts, butyrate and propionate, are effective inhibitors of histone deacetylation in chick oviduct at 2--5 mM; they also prevent the hormonal induction of the ovalbumin and transferrin genes.	Propionates	51-61	ovalbumin (SERPINB14)	Gallus gallus	190-199
7448870-4	1980	In addition to preventing the induction, butyrate also causes a rapid deinduction when added to preinduced cultures; ovalbumin and transferrin gene transcription decline with a half-life of 15--30 min.	Butyrates	41-49	ovalbumin (SERPINB14)	Gallus gallus	117-126
7419588-8	1980	When 3-d-withdrawn oviducts were restimulated with either estrogen or progesterone, in situ hybridization revealed that greater than or equal to 98% of the tubular gland cells contained ovalbumin mRNA.	Progesterone	70-82	ovalbumin (SERPINB14)	Gallus gallus	186-195
7418002-1	1980	The X, Y and ovalbumin genes, which are found within a 40 kb region of the chicken genome, are all expressed in oviduct under steroid hormone control, and share some sequence homologies.	Steroids	126-141	ovalbumin (SERPINB14)	Gallus gallus	13-22
6891480-0	1980	[Control mechanisms of ovalbumin and conalbumin synthesis in chicken oviducts by estradiol and progesterone.	Estradiol	81-90	ovalbumin (SERPINB14)	Gallus gallus	23-32
7387999-0	1980	Ovalbumin messenger ribonucleic acid accumulation in the chick oviduct during secondary stimulation: influence of combinations of steroid hormones and circannual rhythms.	Steroids	130-146	ovalbumin (SERPINB14)	Gallus gallus	0-9
7387999-1	1980	We have analyzed by hybridization the accumulation of ovalbumin mRNA after the administration of estrogen, progesterone, these two hormones together, or each hormone with testosterone to "withdrawn" chicks (chicks previously stimulated with estrogen but then withdrawn from the hormone).	Progesterone	107-119	ovalbumin (SERPINB14)	Gallus gallus	54-63
7398635-0	1980	Effect of tamoxifen on oestradiol and progesterone-induced synthesis of ovalbumin and conalbumin in chick oviduct.	Tamoxifen	10-19	ovalbumin (SERPINB14)	Gallus gallus	72-81
7398635-0	1980	Effect of tamoxifen on oestradiol and progesterone-induced synthesis of ovalbumin and conalbumin in chick oviduct.	Progesterone	38-50	ovalbumin (SERPINB14)	Gallus gallus	72-81
6891480-0	1980	[Control mechanisms of ovalbumin and conalbumin synthesis in chicken oviducts by estradiol and progesterone.	Progesterone	95-107	ovalbumin (SERPINB14)	Gallus gallus	23-32
508284-5	1979	The results were correlated with diethylstilboestrol-induced ovalbumin-gene expression as measured by ovalbumin-mRNA (mRNAov) accumulation and the relative rate of ovalbumin synthesis.	diethylstilboestrol	33-52	ovalbumin (SERPINB14)	Gallus gallus	61-70
479179-0	1979	Transcriptional regulation of the ovalbumin and conalbumin genes by steroid hormones in chick oviduct.	Steroids	68-84	ovalbumin (SERPINB14)	Gallus gallus	34-43
519756-8	1979	Thirty nucleotides before the start of the messenger RNA coding sequence is the heptanucleotide TATATAT, which is also present in a similar location relative to the chicken ovalbumin gene and other unique sequence eucaryotic genes.	heptanucleotide	80-95	ovalbumin (SERPINB14)	Gallus gallus	173-182
508284-5	1979	The results were correlated with diethylstilboestrol-induced ovalbumin-gene expression as measured by ovalbumin-mRNA (mRNAov) accumulation and the relative rate of ovalbumin synthesis.	diethylstilboestrol	33-52	ovalbumin (SERPINB14)	Gallus gallus	102-111
508284-5	1979	The results were correlated with diethylstilboestrol-induced ovalbumin-gene expression as measured by ovalbumin-mRNA (mRNAov) accumulation and the relative rate of ovalbumin synthesis.	diethylstilboestrol	33-52	ovalbumin (SERPINB14)	Gallus gallus	102-111
104296-2	1978	When a plasmid containing the hybrid gene was introduced into E. coli, a protein identified as ovalbumin by immunoreactivity and sodium dodecyl sulfate/polyacrylamide gel electrophoresis was synthesized.	Sodium Dodecyl Sulfate	129-151	ovalbumin (SERPINB14)	Gallus gallus	95-104
286292-3	1979	Of the RNA synthesized by oviduct nuclei from chickens chronically stimulated with diethylstilbestrol, 0.23% corresponded to ovalbumin mRNA and 0.17% were transcripts of intervening sequences.	Diethylstilbestrol	83-101	ovalbumin (SERPINB14)	Gallus gallus	125-134
286292-8	1979	Previously we had identified multiple species of putative precursors of ovalbumin mRNA in oviduct nuclei from chickens chronically stimulated with diethylstilbestrol.	Diethylstilbestrol	147-165	ovalbumin (SERPINB14)	Gallus gallus	72-81
286292-9	1979	We demonstrate here that withdrawal of diethylstilbestrol resulted in a depletion of high-molecular-weight ovalbumin RNA and of mature ovalbumin mRNA and that readministration of the estrogen induced the nuclear accumulation of both forms of ovalbumin RNA.	Diethylstilbestrol	39-57	ovalbumin (SERPINB14)	Gallus gallus	107-116
286292-9	1979	We demonstrate here that withdrawal of diethylstilbestrol resulted in a depletion of high-molecular-weight ovalbumin RNA and of mature ovalbumin mRNA and that readministration of the estrogen induced the nuclear accumulation of both forms of ovalbumin RNA.	Diethylstilbestrol	39-57	ovalbumin (SERPINB14)	Gallus gallus	135-144
286292-9	1979	We demonstrate here that withdrawal of diethylstilbestrol resulted in a depletion of high-molecular-weight ovalbumin RNA and of mature ovalbumin mRNA and that readministration of the estrogen induced the nuclear accumulation of both forms of ovalbumin RNA.	Diethylstilbestrol	39-57	ovalbumin (SERPINB14)	Gallus gallus	135-144
104296-2	1978	When a plasmid containing the hybrid gene was introduced into E. coli, a protein identified as ovalbumin by immunoreactivity and sodium dodecyl sulfate/polyacrylamide gel electrophoresis was synthesized.	polyacrylamide	152-166	ovalbumin (SERPINB14)	Gallus gallus	95-104
78523-1	1978	Kepone induces ovalbumin and conalbumin synthesis in explants of chick oviduct in vitro by acting as a weak estrogen.	Chlordecone	0-6	ovalbumin (SERPINB14)	Gallus gallus	15-24
358194-5	1978	Five out of approximately 20,000 recombinant phage plaques were capable of hybridizing with a (32)P-labeled Hha I fragment of a recombinant plasmid pOV230 containing the entire structural ovalbumin gene.	Phosphorus-32	94-99	ovalbumin (SERPINB14)	Gallus gallus	188-197
273231-6	1978	The synthesis of ovalbumin RNA progressed during the incubation of nuclei and was sensitive to actinomycin D and low concentrations of alpha-amanitin.	Dactinomycin	95-108	ovalbumin (SERPINB14)	Gallus gallus	17-26
661981-1	1978	The complete sequence of chicken ovalbumin mRNA is presented; it is 1,859 residues long, excluding its terminal "cap" and poly(A).	Poly A	122-129	ovalbumin (SERPINB14)	Gallus gallus	33-42
273231-6	1978	The synthesis of ovalbumin RNA progressed during the incubation of nuclei and was sensitive to actinomycin D and low concentrations of alpha-amanitin.	Alpha-Amanitin	135-149	ovalbumin (SERPINB14)	Gallus gallus	17-26
845159-6	1977	The concentration of nuclear estrogen receptors achieved by administering different dosages of 17beta-estradiol, 17beta-estradiol-benzoate, or diethylstilbestrol is related to the rate of accumulation  of ovalbumin and conalbumin mRNA.	Estradiol	95-111	ovalbumin (SERPINB14)	Gallus gallus	205-214
563592-2	1977	Hybridisation with terminally 32P-labelled ovalbumin mRNA fragments or with RNA populations transcribed from the DNA of a hybrid plasmid containing ovalbumin sequences was used to locate the DNA fragments coding for ovalbumin.	Phosphorus-32	30-33	ovalbumin (SERPINB14)	Gallus gallus	43-52
318336-9	1978	The carbohydrate compositions were slightly higher in hexose and lower in hexosamine than chicken ovalbumin.	Carbohydrates	4-16	ovalbumin (SERPINB14)	Gallus gallus	98-107
845159-6	1977	The concentration of nuclear estrogen receptors achieved by administering different dosages of 17beta-estradiol, 17beta-estradiol-benzoate, or diethylstilbestrol is related to the rate of accumulation  of ovalbumin and conalbumin mRNA.	estradiol-17 beta-benzoate	113-138	ovalbumin (SERPINB14)	Gallus gallus	205-214
845159-6	1977	The concentration of nuclear estrogen receptors achieved by administering different dosages of 17beta-estradiol, 17beta-estradiol-benzoate, or diethylstilbestrol is related to the rate of accumulation  of ovalbumin and conalbumin mRNA.	Diethylstilbestrol	143-161	ovalbumin (SERPINB14)	Gallus gallus	205-214
55272-6	1976	When such a complete ovalbumin [3H]cDNA was synthesized with a specific activity of 10(8) cpm/mug and hyfridized to an excess of chick DNA, the kinetics of hybridization indicated that the cDNA was comprised of a nonrepetitive sequence.	Tritium	32-34	ovalbumin (SERPINB14)	Gallus gallus	21-30
941868-8	1976	Substitution of beef, lamb, pork, liver, fish, and chicken for the egg ovalbumin in the sannisynthetic meal resulted in a significant, 2-fold to 4-fold increase in iron absorption whereas no increase was observed with milk, cheese, or egg.	Iron	164-168	ovalbumin (SERPINB14)	Gallus gallus	71-80
932010-3	1976	The coding strand of the ovalbumin gene was partially purified from sheared chick DNA by affinity column chromatography using ovalbumin mRNA immobilized on phosphocellulose.	phosphocellulose	156-172	ovalbumin (SERPINB14)	Gallus gallus	25-34
932010-4	1976	The concentrations of the ovalbumin DNA sequence in various DNA fractions were quantitated by measuring their rates of hybridization with 125I-labeled ovalbumin mRNA.	Iodine-125	138-142	ovalbumin (SERPINB14)	Gallus gallus	26-35
932010-4	1976	The concentrations of the ovalbumin DNA sequence in various DNA fractions were quantitated by measuring their rates of hybridization with 125I-labeled ovalbumin mRNA.	Iodine-125	138-142	ovalbumin (SERPINB14)	Gallus gallus	151-160
987847-10	1976	Ethionine induces ovalbumin and conalbumin synthesis in immature chick oviducts that were withdrawn from estrogen for 3 to 4 weeks following primary estrogen stimulation.	Ethionine	0-9	ovalbumin (SERPINB14)	Gallus gallus	18-27
182385-0	1976	A significant lag in the induction of ovalbumin messenger RNA by steroid hormones: a receptor translocation hypothesis.	Steroids	65-81	ovalbumin (SERPINB14)	Gallus gallus	38-47
182385-7	1976	Treatment of chicks with hydroxyurea shortens the lag for ovalbumin induction with either hormone.	Hydroxyurea	25-36	ovalbumin (SERPINB14)	Gallus gallus	58-67
182385-9	1976	With cycloheximide, however, ovalbumin mRNA accumulation can be prevented.	Cycloheximide	5-18	ovalbumin (SERPINB14)	Gallus gallus	29-38
1250407-0	1976	Induction of ovalbumin and conalbumin synthesis in immature chick oviducts by ethionine.	Ethionine	78-87	ovalbumin (SERPINB14)	Gallus gallus	13-22
1176463-1	1975	A complementary DNA synthesized from ovalbumin mRNA was used in hybridization experiments to study the early effect of estrogen and progesterone on the accumulation of ovalbumin mRNA sequences in the chick oviduct.	Progesterone	132-144	ovalbumin (SERPINB14)	Gallus gallus	168-177
4329151-5	1971	Ovalbumin is undetectable in the unstimulated chick oviduct and in oviducts of chicks treated with progesterone (P) for up to 5 days.	Progesterone	99-111	ovalbumin (SERPINB14)	Gallus gallus	0-9
1158896-1	1975	Preparative agarose gel electrophoresis under denaturing conditions has been successfully employed to purify large quantities of ovalbumin mRNA from hen oviducts.	Sepharose	12-19	ovalbumin (SERPINB14)	Gallus gallus	129-138
1158896-4	1975	It is also not contaminated by other biologically active messenger RNAs because, when it is added to the cell-free wheat germ translation system, the only protein product synthesized is ovalbumin as analyzed by polyacrylamide gel electrophoresis in the presence of sodium dodecyl sulfate and specific immunoprecipitation.	polyacrylamide	211-225	ovalbumin (SERPINB14)	Gallus gallus	186-195
4531006-4	1974	Furthermore, poly(A)-free globin mRNA competed with the same efficiency as authentic globin mRNA against chick ovalbumin mRNA when translated under total mRNA saturation conditions.	Poly A	13-20	ovalbumin (SERPINB14)	Gallus gallus	111-120
4129926-0	1973	Synthesis of (3H)DNA complementary to ovalbumin messenger RNA: evidence for limited copies of the ovalbumin gene in chick oviduct.	Tritium	14-16	ovalbumin (SERPINB14)	Gallus gallus	38-47
4515943-0	1973	Rates of induction of specific translatable messenger RNAs for ovalbumin and avidin by steroid hormones.	Steroids	87-103	ovalbumin (SERPINB14)	Gallus gallus	63-72
4515943-1	1973	In the chick oviduct, injections of estrogen and progesterone induce synthesis of the specific proteins ovalbumin and avidin, respectively.	Progesterone	49-61	ovalbumin (SERPINB14)	Gallus gallus	104-113
4515943-4	1973	Single injections of estrogen in chicks previously withdrawn from all steroid hormones for 2 weeks led to rapid increases in ovalbumin mRNA with 3 hr, which coincided with increases in the rate of ovalbumin synthesis.	Steroids	70-86	ovalbumin (SERPINB14)	Gallus gallus	125-134
5542686-0	1971	Modulation of ovalbumin synthesis by estradiol-17 beta and actinomycin D as studied in explants of chick oviduct in culture.	Estradiol	37-54	ovalbumin (SERPINB14)	Gallus gallus	14-23
5542686-0	1971	Modulation of ovalbumin synthesis by estradiol-17 beta and actinomycin D as studied in explants of chick oviduct in culture.	Dactinomycin	59-72	ovalbumin (SERPINB14)	Gallus gallus	14-23
5350180-4	1969	Such function, as measured by the increase in specific cell products such as lysozyme and ovalbumin, requires the continuous presence of estrogen or progesterone.	Progesterone	149-161	ovalbumin (SERPINB14)	Gallus gallus	90-99
5814004-4	1969	Progesterone administered concomitantly with estrogen antagonizes the estrogen-induced tissue growth as well as appearance of tubular gland cells and their specific products, lysozyme and ovalbumin.	Progesterone	0-12	ovalbumin (SERPINB14)	Gallus gallus	188-197
5814004-7	1969	The above results of progesterone antagonism can best be explained by the hypothesis that progesterone inhibits the initial proliferation of cells which become tubular gland cells but does not antagonize the subsequent cytodifferentiation leading to the synthesis of lysozyme and ovalbumin once such cell proliferation has occurred.	Progesterone	21-33	ovalbumin (SERPINB14)	Gallus gallus	280-289
4694721-2	1973	Mechanism of ovalbumin "superinduction" by actinomycin D.	Dactinomycin	43-56	ovalbumin (SERPINB14)	Gallus gallus	13-22
4114403-0	1972	Investigation of the antigenicity of the carbohydrate moiety of chicken ovalbumin.	Carbohydrates	41-53	ovalbumin (SERPINB14)	Gallus gallus	72-81
6007449-37	1966	After short periods of incubation of minced tissue with [(14)C]lysine some of the radioactive protein of the isolated I particles behaved as ovalbumin.	[(14)c]lysine	56-69	ovalbumin (SERPINB14)	Gallus gallus	141-150
4329151-8	1971	When E + P are administered together there is initially a synergistic effect on ovalbumin synthesis, however, after 2 days ovalbumin synthesis slows and by 5 days there is only 1/20th as much ovalbumin per magnum as in the E-treated controls.	e + p	5-10	ovalbumin (SERPINB14)	Gallus gallus	80-89
32729901-4	2021	Using a doxycycline-driven gene expression system, we generated murine MC38, CT26 (colorectal cancer) and B16 (melanoma) cell lines with inducible expression of model immunogenic neoantigens such as chicken ovalbumin and human NY-ESO-1.	Doxycycline	8-19	ovalbumin (SERPINB14)	Gallus gallus	207-216
33519467-0	2020	3-Hydroxyphthalic Anhydride-Modified Chicken Ovalbumin as a Potential Candidate Inhibits SARS-CoV-2 Infection by Disrupting the Interaction of Spike Protein With Host ACE2 Receptor.	3-hydroxyphthalic anhydride	0-27	ovalbumin (SERPINB14)	Gallus gallus	45-54
33519467-3	2020	Our previous studies have reported that 3-hydroxyphthalic anhydride-modified chicken ovalbumin (HP-OVA) serves as a viral entry inhibitor to prevent several kinds of virus infection.	3-hydroxyphthalic anhydride	40-67	ovalbumin (SERPINB14)	Gallus gallus	85-94
33096433-0	2021	A broad-spectrum sensing strategy for the tetracycline family of antibiotics based on an ovalbumin-stabilized gold nanocluster and its application in a pump-free microfluidic sensing platform.	Tetracycline	42-54	ovalbumin (SERPINB14)	Gallus gallus	89-98
33096433-3	2021	The OVA-stabilized AuNCs (AuNCs@OVA) manifest intriguing multicolour fluorescence and a gradually declining fluorescence intensity at 650 nm with an increasing concentration of tetracycline family antibiotics (TCs) including tetracycline, chlorotetracycline, oxytetracycline, and doxycycline, which are a widely used class of antibiotics for treating infections in food-producing animals.	tetracycline family antibiotics	177-208	ovalbumin (SERPINB14)	Gallus gallus	4-7
33096433-3	2021	The OVA-stabilized AuNCs (AuNCs@OVA) manifest intriguing multicolour fluorescence and a gradually declining fluorescence intensity at 650 nm with an increasing concentration of tetracycline family antibiotics (TCs) including tetracycline, chlorotetracycline, oxytetracycline, and doxycycline, which are a widely used class of antibiotics for treating infections in food-producing animals.	9-ethyl-N-(3,4,5-trimethoxyphenyl)carbazole-3-sulfonamide	210-213	ovalbumin (SERPINB14)	Gallus gallus	4-7
33096433-3	2021	The OVA-stabilized AuNCs (AuNCs@OVA) manifest intriguing multicolour fluorescence and a gradually declining fluorescence intensity at 650 nm with an increasing concentration of tetracycline family antibiotics (TCs) including tetracycline, chlorotetracycline, oxytetracycline, and doxycycline, which are a widely used class of antibiotics for treating infections in food-producing animals.	Tetracycline	177-189	ovalbumin (SERPINB14)	Gallus gallus	4-7
33096433-3	2021	The OVA-stabilized AuNCs (AuNCs@OVA) manifest intriguing multicolour fluorescence and a gradually declining fluorescence intensity at 650 nm with an increasing concentration of tetracycline family antibiotics (TCs) including tetracycline, chlorotetracycline, oxytetracycline, and doxycycline, which are a widely used class of antibiotics for treating infections in food-producing animals.	Chlortetracycline	239-257	ovalbumin (SERPINB14)	Gallus gallus	4-7
33096433-3	2021	The OVA-stabilized AuNCs (AuNCs@OVA) manifest intriguing multicolour fluorescence and a gradually declining fluorescence intensity at 650 nm with an increasing concentration of tetracycline family antibiotics (TCs) including tetracycline, chlorotetracycline, oxytetracycline, and doxycycline, which are a widely used class of antibiotics for treating infections in food-producing animals.	Oxytetracycline	259-274	ovalbumin (SERPINB14)	Gallus gallus	4-7
33096433-3	2021	The OVA-stabilized AuNCs (AuNCs@OVA) manifest intriguing multicolour fluorescence and a gradually declining fluorescence intensity at 650 nm with an increasing concentration of tetracycline family antibiotics (TCs) including tetracycline, chlorotetracycline, oxytetracycline, and doxycycline, which are a widely used class of antibiotics for treating infections in food-producing animals.	Doxycycline	280-291	ovalbumin (SERPINB14)	Gallus gallus	4-7
33096433-4	2021	This performance makes AuNCs@OVA particularly attractive as a broad-spectrum detector for TCs sensing, and we demonstrate that this simple sensing procedure can be realized in real time by directly mixing the target sample and AuNCs@OVA components.	9-ethyl-N-(3,4,5-trimethoxyphenyl)carbazole-3-sulfonamide	90-93	ovalbumin (SERPINB14)	Gallus gallus	29-32
33718858-9	2021	In co-cultures of naive DO11.10 T cells and OVA peptide-loaded antigen-presenting cells (APCs), pre-exposure of the T cells (but not pre-exposure of APCs) to 4MU inhibited early T cell activation (CD69 expression).	Hymecromone	158-161	ovalbumin (SERPINB14)	Gallus gallus	44-47
31386980-8	2019	Our data suggest that mangiferin exerted anti-asthmatic effect through decreasing Th9 and Th17 responses and increasing Treg response in OVA-induced asthmatic mouse model.	mangiferin	22-32	ovalbumin (SERPINB14)	Gallus gallus	137-140
32459249-2	2020	Herein, in order to prevent intermolecular accumulation and improve photostability, indocyanine green (ICG) is spontaneously adsorbed onto a covalent organic framework (COF) with high affinity through pi-pi conjugation, and then chicken ovalbumin (OVA) is coated on the surface of COF@ICG via an electrostatic interaction force.	Indocyanine Green	84-101	ovalbumin (SERPINB14)	Gallus gallus	237-246
32459249-2	2020	Herein, in order to prevent intermolecular accumulation and improve photostability, indocyanine green (ICG) is spontaneously adsorbed onto a covalent organic framework (COF) with high affinity through pi-pi conjugation, and then chicken ovalbumin (OVA) is coated on the surface of COF@ICG via an electrostatic interaction force.	Indocyanine Green	84-101	ovalbumin (SERPINB14)	Gallus gallus	248-251
32026252-4	2020	Two types of reductive N-glycans were released from chicken egg albumin (ovalbumin) and soy protein using an ammonia catalysis method and labeled with benzenesulfonyl hydrazide (BSH).	n-glycans	23-32	ovalbumin (SERPINB14)	Gallus gallus	60-71
32026252-4	2020	Two types of reductive N-glycans were released from chicken egg albumin (ovalbumin) and soy protein using an ammonia catalysis method and labeled with benzenesulfonyl hydrazide (BSH).	n-glycans	23-32	ovalbumin (SERPINB14)	Gallus gallus	73-82
32026252-4	2020	Two types of reductive N-glycans were released from chicken egg albumin (ovalbumin) and soy protein using an ammonia catalysis method and labeled with benzenesulfonyl hydrazide (BSH).	benzenesulfohydrazide	178-181	ovalbumin (SERPINB14)	Gallus gallus	73-82
32026252-8	2020	A total of 21 and 8 N-glycan-AEAB conjugates were obtained from ovalbumin and soy protein, respectively.	n-glycan-aeab	20-33	ovalbumin (SERPINB14)	Gallus gallus	64-73
31466032-0	2020	How black tea pigment theaflavin dyes chicken eggs: Binding affinity study of theaflavin with ovalbumin.	theaflavin	22-32	ovalbumin (SERPINB14)	Gallus gallus	94-103
31466032-0	2020	How black tea pigment theaflavin dyes chicken eggs: Binding affinity study of theaflavin with ovalbumin.	theaflavin	78-88	ovalbumin (SERPINB14)	Gallus gallus	94-103
32010807-2	2020	The hapten DIG was coupled to bovine serum albumin or chicken ovalbumin by sodium periodate oxidation.	metaperiodate	75-91	ovalbumin (SERPINB14)	Gallus gallus	62-71
32012983-8	2020	In a murine tolerogenic antigen challenge model, chronic systemic exposure to BPA was sufficient to induce airway sensitization to innocuous chicken egg ovalbumin in the complete absence of adjuvants.	bisphenol A	78-81	ovalbumin (SERPINB14)	Gallus gallus	153-162
29149729-4	2018	Nevertheless, naturally available glycoproteins, such as ovalbumin in chicken egg whites, are good sources for fabricating glycan-immobilized nanoprobes.	Polysaccharides	123-129	ovalbumin (SERPINB14)	Gallus gallus	57-66
30184130-0	2019	Large-scale purification of ovalbumin using polyethylene glycol precipitation and isoelectric precipitation.	Polyethylene Glycols	44-63	ovalbumin (SERPINB14)	Gallus gallus	28-37
30101285-0	2019	Hydroxyl radical-induced early stage oxidation improves the foaming and emulsifying properties of ovalbumin.	Hydroxyl Radical	0-16	ovalbumin (SERPINB14)	Gallus gallus	98-107
30101285-2	2019	The present study investigated the effects of hydroxyl radical-induced early stage oxidation on the physicochemical and interfacial properties of chicken egg white ovalbumin.	Hydroxyl Radical	46-62	ovalbumin (SERPINB14)	Gallus gallus	164-173
30101285-4	2019	Sodium dodecyl sulfate polyacrylamide gel electrophoresis analysis showed that the exposure of ovalbumin to hydroxyl radicals caused self-cross-linking and resulted in the formation of dimers and trimers.	Sodium Dodecyl Sulfate	0-22	ovalbumin (SERPINB14)	Gallus gallus	95-104
30101285-4	2019	Sodium dodecyl sulfate polyacrylamide gel electrophoresis analysis showed that the exposure of ovalbumin to hydroxyl radicals caused self-cross-linking and resulted in the formation of dimers and trimers.	polyacrylamide	23-37	ovalbumin (SERPINB14)	Gallus gallus	95-104
30101285-4	2019	Sodium dodecyl sulfate polyacrylamide gel electrophoresis analysis showed that the exposure of ovalbumin to hydroxyl radicals caused self-cross-linking and resulted in the formation of dimers and trimers.	Hydroxyl Radical	108-125	ovalbumin (SERPINB14)	Gallus gallus	95-104
30101285-7	2019	Hydroxyl radical-induced oxidation changed the surface chemical groups and structures of ovalbumin, thereby affecting the surface properties.	Hydroxyl Radical	0-16	ovalbumin (SERPINB14)	Gallus gallus	89-98
29580801-8	2018	Moreover, Con A-Cu(II)-IDA-MCM displays weak nonspecific adsorption for the impurities and is able to successfully enrich glycoprotein ovalbumin (OVA) from diluted chicken egg white.	con a-cu(ii)-ida-mcm	10-30	ovalbumin (SERPINB14)	Gallus gallus	135-144
29580801-8	2018	Moreover, Con A-Cu(II)-IDA-MCM displays weak nonspecific adsorption for the impurities and is able to successfully enrich glycoprotein ovalbumin (OVA) from diluted chicken egg white.	con a-cu(ii)-ida-mcm	10-30	ovalbumin (SERPINB14)	Gallus gallus	146-149
29149729-6	2018	The generated Au@cew NPs are mainly encapsulated by ovalbumin, in which the surface is decorated by abundant hybrid mannose and Galbeta(1 4)GlcNAc-terminated glycan ligands.	Mannose	116-123	ovalbumin (SERPINB14)	Gallus gallus	52-61
29149729-6	2018	The generated Au@cew NPs are mainly encapsulated by ovalbumin, in which the surface is decorated by abundant hybrid mannose and Galbeta(1 4)GlcNAc-terminated glycan ligands.	galbeta	128-135	ovalbumin (SERPINB14)	Gallus gallus	52-61
29149729-6	2018	The generated Au@cew NPs are mainly encapsulated by ovalbumin, in which the surface is decorated by abundant hybrid mannose and Galbeta(1 4)GlcNAc-terminated glycan ligands.	2-acetamido-2-deoxy-4-O-(beta-2-acetamid-2-deoxyglucopyranosyl)glucopyranose	140-146	ovalbumin (SERPINB14)	Gallus gallus	52-61
29149729-6	2018	The generated Au@cew NPs are mainly encapsulated by ovalbumin, in which the surface is decorated by abundant hybrid mannose and Galbeta(1 4)GlcNAc-terminated glycan ligands.	Polysaccharides	158-164	ovalbumin (SERPINB14)	Gallus gallus	52-61
26842584-5	2016	METHODS: Released N-glycans from the glycoproteins bovine fetuin, ribonuclease B, chicken ovalbumin, and porcine thyroglobulin were reduced with sodium cyanoborohydride and both negative ion CID spectra and ion mobility properties of their phosphate adducts were examined with a Waters Synapt G2Si travelling-wave ion mobility mass spectrometer with electrospray sample introduction.	n-glycans	18-27	ovalbumin (SERPINB14)	Gallus gallus	90-99
27534448-2	2016	In rodent models, acute respiratory, subcutaneous, and direct immune cell exposure to CBNPs has been shown to enhance allergic sensitization to co-administered ovalbumin (OVA) protein from chicken egg.	cbnps	86-91	ovalbumin (SERPINB14)	Gallus gallus	160-169
27534448-2	2016	In rodent models, acute respiratory, subcutaneous, and direct immune cell exposure to CBNPs has been shown to enhance allergic sensitization to co-administered ovalbumin (OVA) protein from chicken egg.	cbnps	86-91	ovalbumin (SERPINB14)	Gallus gallus	171-174
28220659-0	2017	In situ self-assembled reduced graphene oxide aerogel embedded with nickel oxide nanoparticles for the high-efficiency separation of ovalbumin.	graphene oxide	31-45	ovalbumin (SERPINB14)	Gallus gallus	133-142
28220659-0	2017	In situ self-assembled reduced graphene oxide aerogel embedded with nickel oxide nanoparticles for the high-efficiency separation of ovalbumin.	nickel monoxide	68-80	ovalbumin (SERPINB14)	Gallus gallus	133-142
28220659-7	2017	The adsorption behavior of ovalbumin on the reduced graphene oxide composite well fitted to the Langmuir adsorption model, and a corresponding theoretical maximum adsorption capacity was 1695.2 mg/g.	graphene oxide	52-66	ovalbumin (SERPINB14)	Gallus gallus	27-36
28220659-8	2017	A sodium dodecyl sulfate polyacrylamide gel electrophoresis assay demonstrated that the aerogel could selectively isolate ovalbumin from chicken egg white.	Sodium Dodecyl Sulfate	2-24	ovalbumin (SERPINB14)	Gallus gallus	122-131
28220659-8	2017	A sodium dodecyl sulfate polyacrylamide gel electrophoresis assay demonstrated that the aerogel could selectively isolate ovalbumin from chicken egg white.	polyacrylamide	25-39	ovalbumin (SERPINB14)	Gallus gallus	122-131
27477117-3	2016	Some isomers, such as Man3 GlcNAc3 from chicken ovalbumin and Man3 GlcNAc3 Fuc1 from thyroglobulin could be partially resolved and identified by their negative ion fragmentation spectra obtained by collision-induced decomposition (CID).	man3 glcnac3	22-34	ovalbumin (SERPINB14)	Gallus gallus	48-57
26842584-5	2016	METHODS: Released N-glycans from the glycoproteins bovine fetuin, ribonuclease B, chicken ovalbumin, and porcine thyroglobulin were reduced with sodium cyanoborohydride and both negative ion CID spectra and ion mobility properties of their phosphate adducts were examined with a Waters Synapt G2Si travelling-wave ion mobility mass spectrometer with electrospray sample introduction.	sodium cyanoborohydride	145-168	ovalbumin (SERPINB14)	Gallus gallus	90-99
26842584-5	2016	METHODS: Released N-glycans from the glycoproteins bovine fetuin, ribonuclease B, chicken ovalbumin, and porcine thyroglobulin were reduced with sodium cyanoborohydride and both negative ion CID spectra and ion mobility properties of their phosphate adducts were examined with a Waters Synapt G2Si travelling-wave ion mobility mass spectrometer with electrospray sample introduction.	Phosphates	240-249	ovalbumin (SERPINB14)	Gallus gallus	90-99
26886334-3	2016	Poly(lactic-co-glycolic acid) particles (size range: 250-600 nm) were successfully formulated to include PET lipid A and/or the model tumor antigen, chicken ovalbumin (OVA).	Polylactic Acid-Polyglycolic Acid Copolymer	0-29	ovalbumin (SERPINB14)	Gallus gallus	157-166
25982752-0	2015	Transition of serine residues to the D-form during the conversion of ovalbumin into heat stable S-ovalbumin.	Serine	14-20	ovalbumin (SERPINB14)	Gallus gallus	69-78
25982752-0	2015	Transition of serine residues to the D-form during the conversion of ovalbumin into heat stable S-ovalbumin.	Serine	14-20	ovalbumin (SERPINB14)	Gallus gallus	98-107
25982752-5	2015	A time-dependent increase in the D-Ser contents in native ovalbumin was observed over a period of 7 days, reaching approximately 8%.	D-serine	33-38	ovalbumin (SERPINB14)	Gallus gallus	58-67
25982752-2	2015	Our previous X-ray crystallographic study indicated that S-ovalbumin contains three D-Ser residues (S164, S236, and S320), which may account for its thermostability.	D-serine	84-89	ovalbumin (SERPINB14)	Gallus gallus	59-68
25982752-3	2015	Here, we confirmed the presence of these D-Ser residues in ovalbumin using a technique combining deuterium labeling of alpha-protons of amino acids and liquid chromatography-tandem mass spectrometry (LC-MS/MS).	D-serine	41-46	ovalbumin (SERPINB14)	Gallus gallus	59-68
25982752-3	2015	Here, we confirmed the presence of these D-Ser residues in ovalbumin using a technique combining deuterium labeling of alpha-protons of amino acids and liquid chromatography-tandem mass spectrometry (LC-MS/MS).	Deuterium	97-106	ovalbumin (SERPINB14)	Gallus gallus	59-68
25982752-4	2015	Ovalbumin from chicken egg white and recombinant ovalbumin were incubated for approximately 12 days at pH 9.5 and 37 C. They were then hydrolyzed in DCl/D2O vapor, derivatized with 4-fluoro-7-nitro-2,1,3-benzoxadiazole (NBD-F), and analyzed by LC-MS/MS.	dcl	149-152	ovalbumin (SERPINB14)	Gallus gallus	0-9
25982752-4	2015	Ovalbumin from chicken egg white and recombinant ovalbumin were incubated for approximately 12 days at pH 9.5 and 37 C. They were then hydrolyzed in DCl/D2O vapor, derivatized with 4-fluoro-7-nitro-2,1,3-benzoxadiazole (NBD-F), and analyzed by LC-MS/MS.	dcl	149-152	ovalbumin (SERPINB14)	Gallus gallus	49-58
25982752-4	2015	Ovalbumin from chicken egg white and recombinant ovalbumin were incubated for approximately 12 days at pH 9.5 and 37 C. They were then hydrolyzed in DCl/D2O vapor, derivatized with 4-fluoro-7-nitro-2,1,3-benzoxadiazole (NBD-F), and analyzed by LC-MS/MS.	Deuterium Oxide	153-156	ovalbumin (SERPINB14)	Gallus gallus	0-9
25982752-4	2015	Ovalbumin from chicken egg white and recombinant ovalbumin were incubated for approximately 12 days at pH 9.5 and 37 C. They were then hydrolyzed in DCl/D2O vapor, derivatized with 4-fluoro-7-nitro-2,1,3-benzoxadiazole (NBD-F), and analyzed by LC-MS/MS.	Deuterium Oxide	153-156	ovalbumin (SERPINB14)	Gallus gallus	49-58
25982752-4	2015	Ovalbumin from chicken egg white and recombinant ovalbumin were incubated for approximately 12 days at pH 9.5 and 37 C. They were then hydrolyzed in DCl/D2O vapor, derivatized with 4-fluoro-7-nitro-2,1,3-benzoxadiazole (NBD-F), and analyzed by LC-MS/MS.	7-fluoro-4-nitrobenzo-2-oxa-1,3-diazole	181-218	ovalbumin (SERPINB14)	Gallus gallus	0-9
25982752-4	2015	Ovalbumin from chicken egg white and recombinant ovalbumin were incubated for approximately 12 days at pH 9.5 and 37 C. They were then hydrolyzed in DCl/D2O vapor, derivatized with 4-fluoro-7-nitro-2,1,3-benzoxadiazole (NBD-F), and analyzed by LC-MS/MS.	7-fluoro-4-nitrobenzo-2-oxa-1,3-diazole	181-218	ovalbumin (SERPINB14)	Gallus gallus	49-58
26335373-6	2015	Application of the strategy to chicken ovalbumin, normal mouse mammary epithelial cells (NMuMG), and human serum resulted in detection of 5, 6, and 11 additional N-glycan structures, respectively.	n-glycan	162-170	ovalbumin (SERPINB14)	Gallus gallus	39-48
32262779-0	2015	Preparation of a cobalt mono-substituted silicotungstic acid doped with aniline for the selective adsorption of ovalbumin.	cobalt mono-substituted silicotungstic acid	17-60	ovalbumin (SERPINB14)	Gallus gallus	112-121
32262779-0	2015	Preparation of a cobalt mono-substituted silicotungstic acid doped with aniline for the selective adsorption of ovalbumin.	aniline	72-79	ovalbumin (SERPINB14)	Gallus gallus	112-121
32262779-3	2015	5.0 mg of SiW11Co-PANI composite gives rise to an adsorption efficiency of >70% for 100 mg L-1 ovalbumin in 1.0 mL of sample solution within a wide pH range of 3-9, and a maximum adsorption efficiency of 92% is achieved at pH 9.	siw11co-pani	10-22	ovalbumin (SERPINB14)	Gallus gallus	95-104
32262779-5	2015	The retained ovalbumin could be readily recovered by using a 0.1 mol L-1 phosphate buffer at pH 5.6 as a stripping reagent, providing a recovery of 84.4%.	Phosphates	73-82	ovalbumin (SERPINB14)	Gallus gallus	13-22
32262779-7	2015	The SiW11Co-PANI composite has been applied for the selective adsorption of ovalbumin from the chicken egg white, and SDS-PAGE assay demonstrates that high purity of ovalbumin is obtained.	Sodium Dodecyl Sulfate	118-121	ovalbumin (SERPINB14)	Gallus gallus	76-85
32262779-7	2015	The SiW11Co-PANI composite has been applied for the selective adsorption of ovalbumin from the chicken egg white, and SDS-PAGE assay demonstrates that high purity of ovalbumin is obtained.	Sodium Dodecyl Sulfate	118-121	ovalbumin (SERPINB14)	Gallus gallus	166-175
23181906-5	2012	Furthermore, they were covalently linked to Sepharose and used as an affinity matrix for ovalbumin depletion.	Sepharose	44-53	ovalbumin (SERPINB14)	Gallus gallus	89-98
25683505-0	2015	Effect of nitric oxide on conformational changes of ovalbumin accompanying self-assembly into non-disease-associated fibrils.	Nitric Oxide	10-22	ovalbumin (SERPINB14)	Gallus gallus	52-61
24446294-6	2014	Moreover, the relative OVA expression level in pigeon oviduct epithelial cells could be upregulated by a constant concentration of steroid hormones.	Steroids	131-147	ovalbumin (SERPINB14)	Gallus gallus	23-26
24010128-8	2013	The proposed derivatization technique is successfully applied to the profiling of N-linked glycans derived from chicken ovalbumin.	n-linked glycans	82-98	ovalbumin (SERPINB14)	Gallus gallus	120-129
23995439-5	2013	At pH 6.0, use of 5 mg PIL@SiO2 nanocomposite results in a sorption efficiency of up to 95 % for 200 mg L(-1) ovalbumin in 1 mL sample solution.	Silicon Dioxide	27-31	ovalbumin (SERPINB14)	Gallus gallus	110-119
23995439-8	2013	The retained ovalbumin is recovered by elution with 0.2 % SDS solution.	Sodium Dodecyl Sulfate	58-61	ovalbumin (SERPINB14)	Gallus gallus	13-22
23995439-10	2013	In summary, high-purity ovalbumin is isolated from chicken egg-white by use of the PIL@SiO2 nanocomposite as adsorbent.	Silicon Dioxide	87-91	ovalbumin (SERPINB14)	Gallus gallus	24-33
23090025-2	2013	Conformational changes on ovalbumin at various concentrations of glyoxal, ethylene glycol (EG) and polyethylene glycol-400 (PEG-400) were investigated by fluorescence spectroscopy, circular dichroism, attenuated total reflection Fourier transform infra red spectroscopy, 8-anilino-1-naphthalenesulfonic acid and thioflavin T assay.	Glyoxal	65-72	ovalbumin (SERPINB14)	Gallus gallus	26-35
23090025-2	2013	Conformational changes on ovalbumin at various concentrations of glyoxal, ethylene glycol (EG) and polyethylene glycol-400 (PEG-400) were investigated by fluorescence spectroscopy, circular dichroism, attenuated total reflection Fourier transform infra red spectroscopy, 8-anilino-1-naphthalenesulfonic acid and thioflavin T assay.	Ethylene Glycol	74-89	ovalbumin (SERPINB14)	Gallus gallus	26-35
23090025-2	2013	Conformational changes on ovalbumin at various concentrations of glyoxal, ethylene glycol (EG) and polyethylene glycol-400 (PEG-400) were investigated by fluorescence spectroscopy, circular dichroism, attenuated total reflection Fourier transform infra red spectroscopy, 8-anilino-1-naphthalenesulfonic acid and thioflavin T assay.	Ethylene Glycol	91-93	ovalbumin (SERPINB14)	Gallus gallus	26-35
23090025-2	2013	Conformational changes on ovalbumin at various concentrations of glyoxal, ethylene glycol (EG) and polyethylene glycol-400 (PEG-400) were investigated by fluorescence spectroscopy, circular dichroism, attenuated total reflection Fourier transform infra red spectroscopy, 8-anilino-1-naphthalenesulfonic acid and thioflavin T assay.	polyethylene glycol 400	99-122	ovalbumin (SERPINB14)	Gallus gallus	26-35
23090025-2	2013	Conformational changes on ovalbumin at various concentrations of glyoxal, ethylene glycol (EG) and polyethylene glycol-400 (PEG-400) were investigated by fluorescence spectroscopy, circular dichroism, attenuated total reflection Fourier transform infra red spectroscopy, 8-anilino-1-naphthalenesulfonic acid and thioflavin T assay.	polyethylene glycol 400	124-131	ovalbumin (SERPINB14)	Gallus gallus	26-35
23090025-2	2013	Conformational changes on ovalbumin at various concentrations of glyoxal, ethylene glycol (EG) and polyethylene glycol-400 (PEG-400) were investigated by fluorescence spectroscopy, circular dichroism, attenuated total reflection Fourier transform infra red spectroscopy, 8-anilino-1-naphthalenesulfonic acid and thioflavin T assay.	8-anilino-1-naphthalenesulfonic acid	271-307	ovalbumin (SERPINB14)	Gallus gallus	26-35
23090025-2	2013	Conformational changes on ovalbumin at various concentrations of glyoxal, ethylene glycol (EG) and polyethylene glycol-400 (PEG-400) were investigated by fluorescence spectroscopy, circular dichroism, attenuated total reflection Fourier transform infra red spectroscopy, 8-anilino-1-naphthalenesulfonic acid and thioflavin T assay.	thioflavin T	312-324	ovalbumin (SERPINB14)	Gallus gallus	26-35
23090025-3	2013	A partially folded state of ovalbumin at 50 % v/v glyoxal was detected that preceded the onset of the aggregation process at the maximum concentration (90 % v/v) of this aldehyde.	Glyoxal	50-57	ovalbumin (SERPINB14)	Gallus gallus	28-37
23090025-3	2013	A partially folded state of ovalbumin at 50 % v/v glyoxal was detected that preceded the onset of the aggregation process at the maximum concentration (90 % v/v) of this aldehyde.	Aldehydes	170-178	ovalbumin (SERPINB14)	Gallus gallus	28-37
23090025-4	2013	Aggregates of ovalbumin in the presence EG and PEG-400 were deduced at 70 and 80 % v/v respectively.	Ethylene Glycol	40-42	ovalbumin (SERPINB14)	Gallus gallus	14-23
23090025-4	2013	Aggregates of ovalbumin in the presence EG and PEG-400 were deduced at 70 and 80 % v/v respectively.	polyethylene glycol 400	47-54	ovalbumin (SERPINB14)	Gallus gallus	14-23
23090025-5	2013	Maximum aggregation of ovalbumin was observed at 80 % v/v PEG-400, followed by 70 % v/v EG and 90 % v/v glyoxal.	polyethylene glycol 400	58-65	ovalbumin (SERPINB14)	Gallus gallus	23-32
23090025-5	2013	Maximum aggregation of ovalbumin was observed at 80 % v/v PEG-400, followed by 70 % v/v EG and 90 % v/v glyoxal.	Ethylene Glycol	59-61	ovalbumin (SERPINB14)	Gallus gallus	23-32
23090025-5	2013	Maximum aggregation of ovalbumin was observed at 80 % v/v PEG-400, followed by 70 % v/v EG and 90 % v/v glyoxal.	Glyoxal	104-111	ovalbumin (SERPINB14)	Gallus gallus	23-32
23505104-2	2013	METHODS: The derivative of DES (DES-HS) was synthesized from diethylstilbestrol, ethyl bromoacetate,bovine serum albumin (BSA) and chicken ovalbumin (OVA) with the nucleophilic substitution reaction; the compound was identified by electrospray ionization mass spectrometry(ESI-MS).	Diethylstilbestrol	27-30	ovalbumin (SERPINB14)	Gallus gallus	139-148
23505104-2	2013	METHODS: The derivative of DES (DES-HS) was synthesized from diethylstilbestrol, ethyl bromoacetate,bovine serum albumin (BSA) and chicken ovalbumin (OVA) with the nucleophilic substitution reaction; the compound was identified by electrospray ionization mass spectrometry(ESI-MS).	des-hs	32-38	ovalbumin (SERPINB14)	Gallus gallus	139-148
20194691-0	2010	3-hydroxyphthalic anhydride-modified chicken ovalbumin exhibits potent and broad anti-HIV-1 activity: a potential microbicide for preventing sexual transmission of HIV-1.	3-hydroxyphthalic anhydride	0-27	ovalbumin (SERPINB14)	Gallus gallus	45-54
22991893-11	2012	Five of the major known proteins including three glycoisoforms of ovalbumin in chicken egg white were identified in a single run on the GO@column with phosphate buffer (5 mM, pH 7.0) and an applied voltage of 20 kV.	Phosphates	151-160	ovalbumin (SERPINB14)	Gallus gallus	66-75
23281756-7	2012	In the allantoic fluid, especially on day 7, considerable proportions of cystatin and ovalbumin were phosphorylated and contained phosphorylated serine.	Serine	145-151	ovalbumin (SERPINB14)	Gallus gallus	86-95
21239999-2	2011	Our previous studies demonstrated that 3-hydroxyphthalic anhydride-modified chicken ovalbumin (HP-OVA) exhibited potent antiviral activity against a broad spectrum of HIV, simian immunodeficiency virus, and herpes simplex virus, making it a promising candidate as a component of combination microbicide.	3-hydroxyphthalic anhydride	39-66	ovalbumin (SERPINB14)	Gallus gallus	84-93
21715713-5	2011	Results showed that oviduct-specific levels of avidin, ovalbumin, ovomucin, lysozyme, ESR1, and PGR gene expression were significantly elevated in steroid hormone-treated OECs compared with those of untreated cells (P < 0.05).	Steroids	147-162	ovalbumin (SERPINB14)	Gallus gallus	55-64
21728232-4	2011	Polyacrylamide gels containing immobilized Fe(III) ions were used to study the electrophoretic behavior of two model proteins differing in their phosphate group content: chicken ovalbumin and bovine alpha-casein.	polyacrylamide	0-14	ovalbumin (SERPINB14)	Gallus gallus	178-187
21159849-4	2011	Afterwards, mice were sensitized to chicken egg ovalbumin (OVA) precipitated in aluminium sulphate and then intranasally challenged with OVA to induce allergic lung inflammation.	aluminum sulfate	80-98	ovalbumin (SERPINB14)	Gallus gallus	48-57
21159849-4	2011	Afterwards, mice were sensitized to chicken egg ovalbumin (OVA) precipitated in aluminium sulphate and then intranasally challenged with OVA to induce allergic lung inflammation.	aluminum sulfate	80-98	ovalbumin (SERPINB14)	Gallus gallus	59-62
20147736-3	2010	To drive tissue-specific expression of rhIL1RN, a 1.35-kb fragment of the chicken ovalbumin promoter, which contains both the steroid-dependent regulatory element and the negative regulatory element, was used.	Steroids	126-133	ovalbumin (SERPINB14)	Gallus gallus	82-91
20194691-3	2010	Here we report that 3-hydroxyphthalic anhydride-modified chicken ovalbumin (HP-OVA) exhibits potent antiviral activity against a broad spectrum of human immunodeficiency virus type 1 (HIV-1) isolates with different genotypes and biotypes.	3-hydroxyphthalic anhydride	20-47	ovalbumin (SERPINB14)	Gallus gallus	65-74
15838100-3	2004	The key discovery that set the scientific tone for the lab over the ensuing few decades began with the discovery that steroid hormones induced the nuclear production of specific mRNAs for ovalbumin and avidin in the chick oviduct.	Steroids	118-134	ovalbumin (SERPINB14)	Gallus gallus	188-197
19558425-4	2009	Sensitized rats received chicken egg albumin (EA, 1 mg mL(-1)) in drinking water for 2 weeks (day 1-14).	Drinking Water	66-80	ovalbumin (SERPINB14)	Gallus gallus	33-44
19341784-1	2009	Although the ovalbumin (Ov) gene has served as a model to study tissue-specific, steroid hormone-induced gene expression in vertebrates for decades, the mechanisms responsible for regulating this gene remain elusive.	Steroids	81-96	ovalbumin (SERPINB14)	Gallus gallus	13-22
19341784-1	2009	Although the ovalbumin (Ov) gene has served as a model to study tissue-specific, steroid hormone-induced gene expression in vertebrates for decades, the mechanisms responsible for regulating this gene remain elusive.	Steroids	81-96	ovalbumin (SERPINB14)	Gallus gallus	24-26
18672356-4	2008	The equilibrium constants of the newly selected tetrapeptides increased slightly respect to the dipeptides (Pro-Lys-His-Phe for Npt II, K(eq) 7.88 x 10(4)M(-1); Trp-Gln-Ala-Phe for Cry 1A, K(eq) 5.65 x 10(4)M(-1)), but selectivity towards other proteins (wheat gliadins, bovine gamma-globulins, bovine serum albumin and chicken ovalbumin) became higher.	Dipeptides	96-106	ovalbumin (SERPINB14)	Gallus gallus	328-337
18672356-4	2008	The equilibrium constants of the newly selected tetrapeptides increased slightly respect to the dipeptides (Pro-Lys-His-Phe for Npt II, K(eq) 7.88 x 10(4)M(-1); Trp-Gln-Ala-Phe for Cry 1A, K(eq) 5.65 x 10(4)M(-1)), but selectivity towards other proteins (wheat gliadins, bovine gamma-globulins, bovine serum albumin and chicken ovalbumin) became higher.	Pro-Lys-His	108-119	ovalbumin (SERPINB14)	Gallus gallus	328-337
18672356-4	2008	The equilibrium constants of the newly selected tetrapeptides increased slightly respect to the dipeptides (Pro-Lys-His-Phe for Npt II, K(eq) 7.88 x 10(4)M(-1); Trp-Gln-Ala-Phe for Cry 1A, K(eq) 5.65 x 10(4)M(-1)), but selectivity towards other proteins (wheat gliadins, bovine gamma-globulins, bovine serum albumin and chicken ovalbumin) became higher.	Phenylalanine	120-123	ovalbumin (SERPINB14)	Gallus gallus	328-337
18179854-2	2008	It has been reported previously that certain commonly used phthalate plasticizers, such as di-(2-ethylhexyl) phthalate (DEHP), are able to modify immune responses induced in mice by the common hens" egg allergen ovalbumin (OVA).	phthalic acid	59-68	ovalbumin (SERPINB14)	Gallus gallus	212-221
18179854-2	2008	It has been reported previously that certain commonly used phthalate plasticizers, such as di-(2-ethylhexyl) phthalate (DEHP), are able to modify immune responses induced in mice by the common hens" egg allergen ovalbumin (OVA).	Diethylhexyl Phthalate	91-118	ovalbumin (SERPINB14)	Gallus gallus	212-221
18179854-2	2008	It has been reported previously that certain commonly used phthalate plasticizers, such as di-(2-ethylhexyl) phthalate (DEHP), are able to modify immune responses induced in mice by the common hens" egg allergen ovalbumin (OVA).	Diethylhexyl Phthalate	120-124	ovalbumin (SERPINB14)	Gallus gallus	212-221
16380189-2	2006	TMC nanoparticles were prepared by ionic crosslinking of TMC solution (with or without ovalbumin) with tripolyphosphate, at ambient temperature while stirring.	N-trimethyl chitosan chloride	0-3	ovalbumin (SERPINB14)	Gallus gallus	87-96
15751107-1	2005	N-Linked glycans from bovine ribonuclease B, chicken ovalbumin, bovine fetuin, porcine thyroglobulin and human alpha(1)-acid glycoprotein were derivatized with 2-aminobenzoic acid by reductive amination and their tandem mass spectra were recorded by negative ion electrospray ionization with a quadrupole time-of-flight mass spectrometer.	n-linked glycans	0-16	ovalbumin (SERPINB14)	Gallus gallus	53-62
15659378-0	2005	Reversible self-association of ovalbumin at air-water interfaces and the consequences for the exerted surface pressure.	Water	48-53	ovalbumin (SERPINB14)	Gallus gallus	31-40
14719827-2	2003	A gene encoding for chicken ovalbumin (Gad dI) was isolated from chicken oviduct by PCR amplification and was cloned under the control of T5 promoter fused with a six-histidine tag at the N-terminal end.	Histidine	167-176	ovalbumin (SERPINB14)	Gallus gallus	28-37
14983084-2	2003	Native ovalbumin (N-OVA) is converted on the hours time-scale into more heat-stable forms denoted I- (intermediate) and S-OVA, that have denaturation temperatures 4.8 and 8.4 degrees C, respectively, higher than that of N-OVA.	n-ova	18-23	ovalbumin (SERPINB14)	Gallus gallus	7-16
14983084-2	2003	Native ovalbumin (N-OVA) is converted on the hours time-scale into more heat-stable forms denoted I- (intermediate) and S-OVA, that have denaturation temperatures 4.8 and 8.4 degrees C, respectively, higher than that of N-OVA.	n-ova	220-225	ovalbumin (SERPINB14)	Gallus gallus	7-16
15283599-5	2004	Despite the general recognition that the production of signals of oligosaccharides under MALDI conditions would be highly dependent on the matrix, most of the known N-glycans from chicken ovalbumin could be detected upon Cye derivatization nearly independent of the kind of matrix tested (e.g., nor-harman, 2,5-dihydroxybenzoic acid and alpha-cyano-4-hydroxycinnamic acid) without spoiling the signal strength.	n-glycans	165-174	ovalbumin (SERPINB14)	Gallus gallus	188-197
15283599-5	2004	Despite the general recognition that the production of signals of oligosaccharides under MALDI conditions would be highly dependent on the matrix, most of the known N-glycans from chicken ovalbumin could be detected upon Cye derivatization nearly independent of the kind of matrix tested (e.g., nor-harman, 2,5-dihydroxybenzoic acid and alpha-cyano-4-hydroxycinnamic acid) without spoiling the signal strength.	45-(3-AMINOPROPYL)-5,11,22,28,34-PENTAMETHYL-3,9,15,20,26,32,38,43-OCTAOXO-2,5,8,14,19,22,25,28,31,34,37,42,45,48-TETRADECAAZA-11-AZONIAHEPTACYCLO[42.2.1.1~4,7~.1~10,13~.1~21,24~.1~27,30~.1~33,36~]DOPENTACONTA-1(46),4(52),6,10(51),12,21(50),23,27(49),29,33(48),35,44(47)-DODECAENE	221-224	ovalbumin (SERPINB14)	Gallus gallus	188-197
12609095-5	2002	After multiple ovalbumin exposures, airway responsiveness to intravenous injection of acetylcholine decreased significantly (-LogPC(200): 4.006 +/- 0.554 vs 2.059 +/- 0.262; P < 0.01).	Acetylcholine	86-99	ovalbumin (SERPINB14)	Gallus gallus	15-24
14600204-2	2003	In this study, the immunodominant IgE-binding epitopes of ovalbumin were mapped using arrays of overlapping peptides synthesized on activated cellulose membranes.	Cellulose	142-151	ovalbumin (SERPINB14)	Gallus gallus	58-67
9403346-1	1997	The effect of the histamine H2-receptor antagonist, cimetidine, on the cutaneous Arthus-like hypersensitivity to oxazolone elicited injecting subcutaneously oxazolone conjugated to egg-albumin (EA-OX) has been examined in the chicken.	Cimetidine	52-62	ovalbumin (SERPINB14)	Gallus gallus	181-192
10833030-0	2000	Composition of N-linked carbohydrates from ovalbumin and co-purified glycoproteins.	n-linked carbohydrates	15-37	ovalbumin (SERPINB14)	Gallus gallus	43-52
10833030-4	2000	Ovalbumin was found to be glycosylated mainly with high-mannose and hybrid structures, consistent with profiles obtained on the intact glycoprotein by electrospray.	Mannose	56-63	ovalbumin (SERPINB14)	Gallus gallus	0-9
10833030-5	2000	The other glycoproteins contained mainly larger, complex glycans with up to five antennae, many of which had earlier been associated with ovalbumin.	Polysaccharides	57-64	ovalbumin (SERPINB14)	Gallus gallus	138-147
10457454-6	1999	Their glycoform patterns were highly similar except for the conspicuous decrease in quantity of four glycoforms in the ovalbumin containing less mannose, compared to that of the other with more mannose.	Mannose	145-152	ovalbumin (SERPINB14)	Gallus gallus	119-128
12207461-1	2002	Bisphenol A was coupled, after derivatization into a suitable hapten, to bovine serum albumin and ovalbumin in order to produce immunizing and coating antigens.	bisphenol A	0-11	ovalbumin (SERPINB14)	Gallus gallus	98-107
10073574-10	1999	These results demonstrate that the Ov NRE contains not only sites responsible for the repression of the gene but also a positive element that is required for responsiveness to steroid hormones.	Steroids	176-192	ovalbumin (SERPINB14)	Gallus gallus	35-37
9832435-3	1998	The ovalbumin gene contains one such unit, known as the steroid-dependent regulatory element.	Steroids	56-63	ovalbumin (SERPINB14)	Gallus gallus	4-13
9541491-3	1998	A single exposure of the EC sensitized mice to aerosolized OVA induced eosinophilia in the bronchoalveolar lavage fluid and airway hyperresponsiveness to intravenous methacholine as assessed by measurement of pulmonary dynamic compliance (Cdyn).	Methacholine Chloride	166-178	ovalbumin (SERPINB14)	Gallus gallus	59-62
9541491-3	1998	A single exposure of the EC sensitized mice to aerosolized OVA induced eosinophilia in the bronchoalveolar lavage fluid and airway hyperresponsiveness to intravenous methacholine as assessed by measurement of pulmonary dynamic compliance (Cdyn).	cdyn	239-243	ovalbumin (SERPINB14)	Gallus gallus	59-62
9403346-1	1997	The effect of the histamine H2-receptor antagonist, cimetidine, on the cutaneous Arthus-like hypersensitivity to oxazolone elicited injecting subcutaneously oxazolone conjugated to egg-albumin (EA-OX) has been examined in the chicken.	Oxazolone	113-122	ovalbumin (SERPINB14)	Gallus gallus	181-192
8947831-4	1996	The half-life of OVA mRNA as determined using a transcription inhibitor (actinomycin D) was estimated to be about 24 h irrespective of the hormone treatment, though the half-life was about 6 h in the absence of hormones.	Dactinomycin	73-86	ovalbumin (SERPINB14)	Gallus gallus	17-20
9175273-5	1997	By using free-solution CE with polyacrylamide-coated capillaries and boric acid-alcohol amine (BA) buffers, ovalbumin of agarose electrophoresis purity can be split into more than twenty peaks at pH 8.0 +/- 0.3 (0.2-0.4 mol/l BA).	polyacrylamide	31-45	ovalbumin (SERPINB14)	Gallus gallus	108-117
9175273-5	1997	By using free-solution CE with polyacrylamide-coated capillaries and boric acid-alcohol amine (BA) buffers, ovalbumin of agarose electrophoresis purity can be split into more than twenty peaks at pH 8.0 +/- 0.3 (0.2-0.4 mol/l BA).	boric acid-alcohol amine	69-93	ovalbumin (SERPINB14)	Gallus gallus	108-117
9175273-5	1997	By using free-solution CE with polyacrylamide-coated capillaries and boric acid-alcohol amine (BA) buffers, ovalbumin of agarose electrophoresis purity can be split into more than twenty peaks at pH 8.0 +/- 0.3 (0.2-0.4 mol/l BA).	Barium	95-97	ovalbumin (SERPINB14)	Gallus gallus	108-117
9175273-5	1997	By using free-solution CE with polyacrylamide-coated capillaries and boric acid-alcohol amine (BA) buffers, ovalbumin of agarose electrophoresis purity can be split into more than twenty peaks at pH 8.0 +/- 0.3 (0.2-0.4 mol/l BA).	Sepharose	121-128	ovalbumin (SERPINB14)	Gallus gallus	108-117
9175273-5	1997	By using free-solution CE with polyacrylamide-coated capillaries and boric acid-alcohol amine (BA) buffers, ovalbumin of agarose electrophoresis purity can be split into more than twenty peaks at pH 8.0 +/- 0.3 (0.2-0.4 mol/l BA).	Barium	226-228	ovalbumin (SERPINB14)	Gallus gallus	108-117
9149392-1	1997	The role of estrogen receptor on ovalbumin mRNA induction by steroid hormones was investigated in primary cultures of oviduct cells from estrogen-stimulated immature chicks of genetically selected high- and low-albumen egg laying lines (H- and L-lines).	Steroids	61-77	ovalbumin (SERPINB14)	Gallus gallus	33-42
8947831-0	1996	Steroid hormones differentially induce transcription of the chicken ovalbumin gene, but stabilize the mRNA with the same half-life.	Steroids	0-16	ovalbumin (SERPINB14)	Gallus gallus	68-77
8947831-1	1996	The stabilization of chicken ovalbumin (OVA) mRNA by different classes of steroid hormones (estrogen, progesterone, glucocorticoid, and androgen) was studied in the oviducts of chicks treated with combinations of four steroids.	Steroids	74-90	ovalbumin (SERPINB14)	Gallus gallus	40-43
8947831-5	1996	These results suggested that the prolongation of the half-life of OVA mRNA by steroid hormones is constant irrespective of differential transcription rates of the OVA gene.	Steroids	78-94	ovalbumin (SERPINB14)	Gallus gallus	66-69
8916422-5	1996	The method is illustrated by the analysis of isolated glycans and complex mixtures derived from chicken ovalbumin and human immunoglobulin G.	Polysaccharides	54-61	ovalbumin (SERPINB14)	Gallus gallus	104-113
8546694-3	1996	Run-on analysis with oviduct nuclei isolated from E2-treated chicks showed that TAM treatment completely blocked E2-induced transcription of the OVA gene within 24 h without affecting ER gene expression.	Tamoxifen	80-83	ovalbumin (SERPINB14)	Gallus gallus	145-148
8819508-9	1996	However, GaAs-exposed macrophages activated hen egg lysozyme- and chicken ovalbumin-specific T cells as efficiently as vehicle control cells.	gallium arsenide	9-13	ovalbumin (SERPINB14)	Gallus gallus	74-83
8901111-0	1996	Steroid hormone-induced expression of the chicken ovalbumin gene and the levels of nuclear steroid hormone receptors in chick oviduct.	Steroids	0-15	ovalbumin (SERPINB14)	Gallus gallus	50-59
8901111-1	1996	The induction of the chicken ovalbumin (OVA) gene by different classes of steroid hormones and the mRNA levels of estrogen (ER), progesterone (PR), and glucocorticoid (GR) receptors were studied in chick oviducts.	Steroids	74-90	ovalbumin (SERPINB14)	Gallus gallus	29-38
8901111-1	1996	The induction of the chicken ovalbumin (OVA) gene by different classes of steroid hormones and the mRNA levels of estrogen (ER), progesterone (PR), and glucocorticoid (GR) receptors were studied in chick oviducts.	Steroids	74-90	ovalbumin (SERPINB14)	Gallus gallus	40-43
8833539-17	1996	There was significantly more reducible selenium in ovalbumin from control eggs than from all other samples but even so non-reducible selenium accounted for two thirds of the selenium present.	Selenium	39-47	ovalbumin (SERPINB14)	Gallus gallus	51-60
8628267-0	1996	Regulation of the chicken ovalbumin gene by estrogen and corticosterone requires a novel DNA element that binds a labile protein, Chirp-1.	Corticosterone	57-71	ovalbumin (SERPINB14)	Gallus gallus	26-35
8628267-1	1996	Because induction of the chicken ovalbumin (Ov) gene by steroid hormones requires concomitant protein synthesis, efforts have focused on defining the binding site in the Ov gene for a labile transcription factor.	Steroids	56-72	ovalbumin (SERPINB14)	Gallus gallus	33-42
8628267-1	1996	Because induction of the chicken ovalbumin (Ov) gene by steroid hormones requires concomitant protein synthesis, efforts have focused on defining the binding site in the Ov gene for a labile transcription factor.	Steroids	56-72	ovalbumin (SERPINB14)	Gallus gallus	44-46
8628267-3	1996	To ascertain whether estrogen and glucocorticoid affect the binding of this labile protein, genomic footprinting of the Ov gene was done by treating primary oviduct cell cultures with dimethyl sulfate.	dimethyl sulfate	184-200	ovalbumin (SERPINB14)	Gallus gallus	120-122
8628267-11	1996	These data support the contention that the ovalbumin gene is regulated by a steroid hormone-induced transcriptional cascade that culminates in the binding of chicken ovalbumin induced regulatory protein or protein complex (Chirp-I) to a DNA element from -891 to -878 in the SDRE.	Steroids	76-91	ovalbumin (SERPINB14)	Gallus gallus	43-52
8628267-11	1996	These data support the contention that the ovalbumin gene is regulated by a steroid hormone-induced transcriptional cascade that culminates in the binding of chicken ovalbumin induced regulatory protein or protein complex (Chirp-I) to a DNA element from -891 to -878 in the SDRE.	Steroids	76-91	ovalbumin (SERPINB14)	Gallus gallus	166-175
8546694-6	1996	However, in the chicks treated with TAM and E2, OVA mRNA was degraded slowly over 48 h with a half-life of 24 h, suggesting that TAM does not inhibit E2-induced mRNA stabilization.	Tamoxifen	36-39	ovalbumin (SERPINB14)	Gallus gallus	48-51
7584852-0	1995	Induction of ovalbumin mRNA by ascorbic acid in primary cultures of tubular gland cells of the chicken oviduct.	Ascorbic Acid	31-44	ovalbumin (SERPINB14)	Gallus gallus	13-22
18623494-4	1995	Lysozyme and ovalbumin CD spectra in the corresponding GuHCl aqueous solutions revealed no changes in the higher order structures of the proteins.	Cadmium	23-25	ovalbumin (SERPINB14)	Gallus gallus	13-22
18623494-4	1995	Lysozyme and ovalbumin CD spectra in the corresponding GuHCl aqueous solutions revealed no changes in the higher order structures of the proteins.	Guanidine	55-60	ovalbumin (SERPINB14)	Gallus gallus	13-22
7584852-1	1995	The present study was conducted to investigate the effects of aging and medium supplements on steroid-induced ovalbumin mRNA in primary cultures of tubular gland cells from the chicken oviduct.	Steroids	94-101	ovalbumin (SERPINB14)	Gallus gallus	110-119
7584852-5	1995	The results indicated that the oviduct cells from immature chicks had clearer induction of ovalbumin mRNA by the steroid treatment than did those from laying hens.	Steroids	113-120	ovalbumin (SERPINB14)	Gallus gallus	91-100
7584852-7	1995	The drastic induction of ovalbumin mRNA by ascorbic acid supplementation was exerted only when the steroid hormones were present in the medium, implying that the effect of ascorbic acid may be auxiliary in steroid-induced transcription of the ovalbumin gene.	Ascorbic Acid	43-56	ovalbumin (SERPINB14)	Gallus gallus	25-34
7584852-7	1995	The drastic induction of ovalbumin mRNA by ascorbic acid supplementation was exerted only when the steroid hormones were present in the medium, implying that the effect of ascorbic acid may be auxiliary in steroid-induced transcription of the ovalbumin gene.	Ascorbic Acid	43-56	ovalbumin (SERPINB14)	Gallus gallus	243-252
7584852-7	1995	The drastic induction of ovalbumin mRNA by ascorbic acid supplementation was exerted only when the steroid hormones were present in the medium, implying that the effect of ascorbic acid may be auxiliary in steroid-induced transcription of the ovalbumin gene.	Steroids	99-106	ovalbumin (SERPINB14)	Gallus gallus	25-34
7584852-7	1995	The drastic induction of ovalbumin mRNA by ascorbic acid supplementation was exerted only when the steroid hormones were present in the medium, implying that the effect of ascorbic acid may be auxiliary in steroid-induced transcription of the ovalbumin gene.	Ascorbic Acid	172-185	ovalbumin (SERPINB14)	Gallus gallus	25-34
7584852-7	1995	The drastic induction of ovalbumin mRNA by ascorbic acid supplementation was exerted only when the steroid hormones were present in the medium, implying that the effect of ascorbic acid may be auxiliary in steroid-induced transcription of the ovalbumin gene.	Ascorbic Acid	172-185	ovalbumin (SERPINB14)	Gallus gallus	243-252
7584852-7	1995	The drastic induction of ovalbumin mRNA by ascorbic acid supplementation was exerted only when the steroid hormones were present in the medium, implying that the effect of ascorbic acid may be auxiliary in steroid-induced transcription of the ovalbumin gene.	Steroids	206-213	ovalbumin (SERPINB14)	Gallus gallus	25-34
7584852-7	1995	The drastic induction of ovalbumin mRNA by ascorbic acid supplementation was exerted only when the steroid hormones were present in the medium, implying that the effect of ascorbic acid may be auxiliary in steroid-induced transcription of the ovalbumin gene.	Steroids	206-213	ovalbumin (SERPINB14)	Gallus gallus	243-252
7665081-4	1995	SDS-PAGE and Western blotting analysis revealed that re-Ova immunoreacting with the egg ovalbumin antibody is not glycosylated.	Sodium Dodecyl Sulfate	0-3	ovalbumin (SERPINB14)	Gallus gallus	56-59
7490131-2	1995	Here we report that chicken ovalbumin (OVA) denatured by heat or sodium dodecyl sulphate (SDS) effectively induced CD8+ cytolytic T cells in vivo.	Sodium Dodecyl Sulfate	65-88	ovalbumin (SERPINB14)	Gallus gallus	28-37
7490131-2	1995	Here we report that chicken ovalbumin (OVA) denatured by heat or sodium dodecyl sulphate (SDS) effectively induced CD8+ cytolytic T cells in vivo.	Sodium Dodecyl Sulfate	65-88	ovalbumin (SERPINB14)	Gallus gallus	39-42
7490131-2	1995	Here we report that chicken ovalbumin (OVA) denatured by heat or sodium dodecyl sulphate (SDS) effectively induced CD8+ cytolytic T cells in vivo.	Sodium Dodecyl Sulfate	90-93	ovalbumin (SERPINB14)	Gallus gallus	28-37
7490131-2	1995	Here we report that chicken ovalbumin (OVA) denatured by heat or sodium dodecyl sulphate (SDS) effectively induced CD8+ cytolytic T cells in vivo.	Sodium Dodecyl Sulfate	90-93	ovalbumin (SERPINB14)	Gallus gallus	39-42
7490131-7	1995	In contrast, class I-restricted presentation of denatured OVA was sensitive to lysosomotropic agents (NH4Cl, vinblastine and leupeptin), indicating that endosomal-like compartments are involved in the presentation of denatured OVA.	Ammonium Chloride	102-107	ovalbumin (SERPINB14)	Gallus gallus	58-61
7490131-7	1995	In contrast, class I-restricted presentation of denatured OVA was sensitive to lysosomotropic agents (NH4Cl, vinblastine and leupeptin), indicating that endosomal-like compartments are involved in the presentation of denatured OVA.	Ammonium Chloride	102-107	ovalbumin (SERPINB14)	Gallus gallus	227-230
7490131-7	1995	In contrast, class I-restricted presentation of denatured OVA was sensitive to lysosomotropic agents (NH4Cl, vinblastine and leupeptin), indicating that endosomal-like compartments are involved in the presentation of denatured OVA.	Vinblastine	109-120	ovalbumin (SERPINB14)	Gallus gallus	58-61
7490131-7	1995	In contrast, class I-restricted presentation of denatured OVA was sensitive to lysosomotropic agents (NH4Cl, vinblastine and leupeptin), indicating that endosomal-like compartments are involved in the presentation of denatured OVA.	Vinblastine	109-120	ovalbumin (SERPINB14)	Gallus gallus	227-230
7490131-7	1995	In contrast, class I-restricted presentation of denatured OVA was sensitive to lysosomotropic agents (NH4Cl, vinblastine and leupeptin), indicating that endosomal-like compartments are involved in the presentation of denatured OVA.	leupeptin	125-134	ovalbumin (SERPINB14)	Gallus gallus	58-61
7490131-7	1995	In contrast, class I-restricted presentation of denatured OVA was sensitive to lysosomotropic agents (NH4Cl, vinblastine and leupeptin), indicating that endosomal-like compartments are involved in the presentation of denatured OVA.	leupeptin	125-134	ovalbumin (SERPINB14)	Gallus gallus	227-230
7490131-8	1995	Sensitization was inhibited at low temperature, yet took place in the presence of sucrose and in the absence of K+, indicating that denatured OVA enters the cell via fluid-phase endocytosis.	Sucrose	82-89	ovalbumin (SERPINB14)	Gallus gallus	142-145
7491104-2	1995	Two major regulatory elements reside in the chicken ovalbumin gene, a steroid-dependent regulatory element (SDRE, -892 to -780) and a negative regulatory element (NRE, -308 to -88).	Steroids	70-77	ovalbumin (SERPINB14)	Gallus gallus	52-61
7665081-4	1995	SDS-PAGE and Western blotting analysis revealed that re-Ova immunoreacting with the egg ovalbumin antibody is not glycosylated.	Sodium Dodecyl Sulfate	0-3	ovalbumin (SERPINB14)	Gallus gallus	88-97
7665081-5	1995	The re-Ova was purified by anion exchange chromatography into homogeneity, as evaluated by SDS-PAGE.	Sodium Dodecyl Sulfate	91-94	ovalbumin (SERPINB14)	Gallus gallus	7-10
8311248-1	1993	High-performance liquid chromatography (HPLC) interface to inductively coupled plasma mass spectrometry (ICPMS) has been applied for the first time to determine the sulfhydryl groups (SHs) in chicken ovalbumin (OVA) after their conversion into mercaptides with organic mercury compounds.	mercaptides	244-255	ovalbumin (SERPINB14)	Gallus gallus	200-209
8311248-1	1993	High-performance liquid chromatography (HPLC) interface to inductively coupled plasma mass spectrometry (ICPMS) has been applied for the first time to determine the sulfhydryl groups (SHs) in chicken ovalbumin (OVA) after their conversion into mercaptides with organic mercury compounds.	mercaptides	244-255	ovalbumin (SERPINB14)	Gallus gallus	211-214
8311248-1	1993	High-performance liquid chromatography (HPLC) interface to inductively coupled plasma mass spectrometry (ICPMS) has been applied for the first time to determine the sulfhydryl groups (SHs) in chicken ovalbumin (OVA) after their conversion into mercaptides with organic mercury compounds.	Mercury	269-276	ovalbumin (SERPINB14)	Gallus gallus	200-209
8311248-1	1993	High-performance liquid chromatography (HPLC) interface to inductively coupled plasma mass spectrometry (ICPMS) has been applied for the first time to determine the sulfhydryl groups (SHs) in chicken ovalbumin (OVA) after their conversion into mercaptides with organic mercury compounds.	Mercury	269-276	ovalbumin (SERPINB14)	Gallus gallus	211-214
8311248-3	1993	The rates of reaction of five mercaptide-forming reagents with SHs in OVA were in the order ethylmercuric chloride > mersalyl acid > p-chloromercuribenzoate > p-(chloromercuri)benzenesulfonic acid > fluorescein mercuric acetate.	mercaptide	30-40	ovalbumin (SERPINB14)	Gallus gallus	70-73
8311248-3	1993	The rates of reaction of five mercaptide-forming reagents with SHs in OVA were in the order ethylmercuric chloride > mersalyl acid > p-chloromercuribenzoate > p-(chloromercuri)benzenesulfonic acid > fluorescein mercuric acetate.	Ethylmercuric Chloride	92-114	ovalbumin (SERPINB14)	Gallus gallus	70-73
8311248-3	1993	The rates of reaction of five mercaptide-forming reagents with SHs in OVA were in the order ethylmercuric chloride > mersalyl acid > p-chloromercuribenzoate > p-(chloromercuri)benzenesulfonic acid > fluorescein mercuric acetate.	Mersalyl	120-133	ovalbumin (SERPINB14)	Gallus gallus	70-73
8311248-3	1993	The rates of reaction of five mercaptide-forming reagents with SHs in OVA were in the order ethylmercuric chloride > mersalyl acid > p-chloromercuribenzoate > p-(chloromercuri)benzenesulfonic acid > fluorescein mercuric acetate.	p-chloromercuribenzoate	139-162	ovalbumin (SERPINB14)	Gallus gallus	70-73
8311248-3	1993	The rates of reaction of five mercaptide-forming reagents with SHs in OVA were in the order ethylmercuric chloride > mersalyl acid > p-chloromercuribenzoate > p-(chloromercuri)benzenesulfonic acid > fluorescein mercuric acetate.	4-Chloromercuribenzenesulfonate	168-205	ovalbumin (SERPINB14)	Gallus gallus	70-73
8311248-3	1993	The rates of reaction of five mercaptide-forming reagents with SHs in OVA were in the order ethylmercuric chloride > mersalyl acid > p-chloromercuribenzoate > p-(chloromercuri)benzenesulfonic acid > fluorescein mercuric acetate.	fluorescein mercuric acetate	211-239	ovalbumin (SERPINB14)	Gallus gallus	70-73
8514758-0	1993	A complex array of double-stranded and single-stranded DNA-binding proteins mediates induction of the ovalbumin gene by steroid hormones.	Steroids	120-136	ovalbumin (SERPINB14)	Gallus gallus	102-111
8404652-6	1993	As expected, ovalbumin gene transcription is increased only after a lag period of 4 h following Pg treatment.	Progesterone	96-98	ovalbumin (SERPINB14)	Gallus gallus	13-22
8399219-3	1993	In analogy with hen egg ovalbumin, where the same proteases all cleaved the polypeptide chain very specifically around Ala-352, Ala-323 of Mib-CK may be located in an exposed surface loop that is sensitive to protease attack.	Alanine	119-122	ovalbumin (SERPINB14)	Gallus gallus	24-33
8399219-3	1993	In analogy with hen egg ovalbumin, where the same proteases all cleaved the polypeptide chain very specifically around Ala-352, Ala-323 of Mib-CK may be located in an exposed surface loop that is sensitive to protease attack.	Alanine	128-131	ovalbumin (SERPINB14)	Gallus gallus	24-33
8113098-0	1993	Ovalbumin-like immunoreactivity detected in chicken sensory neurons by antibodies to aldehyde-treated ovalbumin.	Aldehydes	85-93	ovalbumin (SERPINB14)	Gallus gallus	0-9
8113098-0	1993	Ovalbumin-like immunoreactivity detected in chicken sensory neurons by antibodies to aldehyde-treated ovalbumin.	Aldehydes	85-93	ovalbumin (SERPINB14)	Gallus gallus	102-111
8113098-2	1993	Ovalbumin-like immunoreactivity has been identified in a subpopulation of chicken dorsal root ganglion neurons by the generation of antibodies to aldehyde-conjugated ovalbumin but not by the antibodies to native ovalbumin, although both antibodies recognize the much higher concentrations of ovalbumin in sections of the oviduct.	Aldehydes	146-154	ovalbumin (SERPINB14)	Gallus gallus	0-9
8113098-2	1993	Ovalbumin-like immunoreactivity has been identified in a subpopulation of chicken dorsal root ganglion neurons by the generation of antibodies to aldehyde-conjugated ovalbumin but not by the antibodies to native ovalbumin, although both antibodies recognize the much higher concentrations of ovalbumin in sections of the oviduct.	Aldehydes	146-154	ovalbumin (SERPINB14)	Gallus gallus	166-175
8514758-1	1993	The transcriptional induction of the chicken ovalbumin gene by steroid hormones is abolished by inhibitors of protein synthesis such as cycloheximide, suggesting that a labile protein mediates this process.	Steroids	63-79	ovalbumin (SERPINB14)	Gallus gallus	45-54
8514758-1	1993	The transcriptional induction of the chicken ovalbumin gene by steroid hormones is abolished by inhibitors of protein synthesis such as cycloheximide, suggesting that a labile protein mediates this process.	Cycloheximide	136-149	ovalbumin (SERPINB14)	Gallus gallus	45-54
1279383-0	1992	Regulation of expression of the chicken ovalbumin gene: interactions between steroid hormones and second messenger systems.	Steroids	77-93	ovalbumin (SERPINB14)	Gallus gallus	40-49
1291045-1	1992	Resolution and structural characterization of ovalbumin glycans.	Polysaccharides	56-63	ovalbumin (SERPINB14)	Gallus gallus	46-55
1291045-2	1992	The microheterogeneous mixture of fluoresceinated glycopeptides (FGPs) obtained from the single site of glycosylation of chicken ovalbumin was resolved by a combination of discontinuous electrophoresis in a high-density poly(acrylamide) gel (PAGE) for sizing, in conjunction with borate-PAGE.	fluoresceinated glycopeptides	34-63	ovalbumin (SERPINB14)	Gallus gallus	129-138
1291045-2	1992	The microheterogeneous mixture of fluoresceinated glycopeptides (FGPs) obtained from the single site of glycosylation of chicken ovalbumin was resolved by a combination of discontinuous electrophoresis in a high-density poly(acrylamide) gel (PAGE) for sizing, in conjunction with borate-PAGE.	polyacrylamide	220-236	ovalbumin (SERPINB14)	Gallus gallus	129-138
1279383-7	1992	The results indicate that phorbol 12-myristilate 13-acetate causes a dramatic destabilization of ovalbumin message, resulting in a reduction in ovalbumin mRNA levels.	phorbol 12-myristilate 13-acetate	26-59	ovalbumin (SERPINB14)	Gallus gallus	97-106
1279383-7	1992	The results indicate that phorbol 12-myristilate 13-acetate causes a dramatic destabilization of ovalbumin message, resulting in a reduction in ovalbumin mRNA levels.	phorbol 12-myristilate 13-acetate	26-59	ovalbumin (SERPINB14)	Gallus gallus	144-153
1279383-8	1992	In contrast, the activators of the PKA system can substitute for insulin and, thereby, increase expression of the ovalbumin gene synergistically with the steroids.	Steroids	154-162	ovalbumin (SERPINB14)	Gallus gallus	114-123
1279383-10	1992	Thus, in chicken oviduct cell cultures, the PKA and PKC signal transduction pathways act in opposing ways to modulate the steroid-induced expression of the ovalbumin gene.	Steroids	122-129	ovalbumin (SERPINB14)	Gallus gallus	156-165
2332444-0	1990	The steroid-dependent regulatory element in the ovalbumin gene does not function as a typical steroid response element.	Steroids	4-11	ovalbumin (SERPINB14)	Gallus gallus	48-57
1546973-1	1992	The equilibrium binding of the apolar fluorescent dye 1-anilinonaphthalene-8-sulphonate (ANS) to bacteriorhodopsin, BSA, chicken egg lysozyme, ovalbumin, porcine somatotrophin (PST) and bovine pancreatic ribonuclease (RNAase) was quantitatively evaluated using Scatchard- and Klotz-plot analyses.	1-anilinonaphthalene-8-sulphonate	54-87	ovalbumin (SERPINB14)	Gallus gallus	143-152
1694878-0	1990	Different roles for thiol and aspartyl proteases in antigen presentation of ovalbumin.	Sulfhydryl Compounds	20-25	ovalbumin (SERPINB14)	Gallus gallus	76-85
2141621-2	1990	Tryptic digest and cyanogen bromide fragments of chicken ovalbumin and synthetic peptides of ovalbumin (323-339) and influenza virus (NP 365-380) were used to generate CTL and T helper lines from unprimed T cells.	Cyanogen Bromide	19-35	ovalbumin (SERPINB14)	Gallus gallus	57-66
1562535-0	1992	In situ hybridization of ovalbumin mRNA in the chick oviduct reveals target cell specificity for estrogen and progesterone.	Progesterone	110-122	ovalbumin (SERPINB14)	Gallus gallus	25-34
1562535-1	1992	An in situ hybridization method using paraffin-embedded sections was used to characterize the chicken oviduct cells synthesizing ovalbumin mRNA due to the action of estrogen and progesterone.	Paraffin	38-46	ovalbumin (SERPINB14)	Gallus gallus	129-138
1562535-1	1992	An in situ hybridization method using paraffin-embedded sections was used to characterize the chicken oviduct cells synthesizing ovalbumin mRNA due to the action of estrogen and progesterone.	Progesterone	178-190	ovalbumin (SERPINB14)	Gallus gallus	129-138
1562535-6	1992	Administration of progesterone induced the expression of ovalbumin mRNA in the surface epithelial cells.	Progesterone	18-30	ovalbumin (SERPINB14)	Gallus gallus	57-66
1562535-9	1992	We conclude that the expression of ovalbumin in the surface epithelial cells and in the tubular gland cells is specific for progesterone and estrogen, respectively.	Progesterone	124-136	ovalbumin (SERPINB14)	Gallus gallus	35-44
1450986-16	1992	Butyrate inhibits the induction of proteins, including enzymes, by steroid hormones as has been shown for the induction of tyrosine aminotransferase by glucocorticoids, of ovalbumin and transferrin by estradiol in chick oviduct.	Butyrates	0-8	ovalbumin (SERPINB14)	Gallus gallus	172-181
1450986-16	1992	Butyrate inhibits the induction of proteins, including enzymes, by steroid hormones as has been shown for the induction of tyrosine aminotransferase by glucocorticoids, of ovalbumin and transferrin by estradiol in chick oviduct.	Steroids	67-83	ovalbumin (SERPINB14)	Gallus gallus	172-181
2037595-0	1991	A protein with a binding specificity similar to NF-kappa B binds to a steroid-dependent regulatory element in the ovalbumin gene.	Steroids	70-77	ovalbumin (SERPINB14)	Gallus gallus	114-123
2037595-1	1991	The chicken ovalbumin gene is regulated at the level of transcription by four classes of steroid hormones.	Steroids	89-105	ovalbumin (SERPINB14)	Gallus gallus	12-21
2037595-4	1991	Fusion genes containing the mutant ovalbumin 5"-flanking sequences linked to the chloramphenicol acetyltransferase structural gene (CAT) were transfected into steroid-responsive primary oviduct cells.	Steroids	159-166	ovalbumin (SERPINB14)	Gallus gallus	35-44
2037595-12	1991	These data suggest that a protein binding to sequences in the SDRE that are similar to an NF-kappa B-binding site participates in the steroid-mediated increase in transcription of the chicken ovalbumin gene.	Steroids	134-141	ovalbumin (SERPINB14)	Gallus gallus	192-201
2332444-1	1990	Transcription of the chicken ovalbumin gene is induced both in vivo and in vitro by four classes of steroid hormones.	Steroids	100-116	ovalbumin (SERPINB14)	Gallus gallus	29-38
2332444-4	1990	When the ovalbumin-chloramphenicol acetyltransferase fusion genes were transfected into steroid-responsive primary oviduct cells, mutants lacking sequences between -900 and -732 were no longer responsive to estrogen, corticosterone, progesterone, or dihydrotestosterone.	Steroids	88-95	ovalbumin (SERPINB14)	Gallus gallus	9-18
2332444-4	1990	When the ovalbumin-chloramphenicol acetyltransferase fusion genes were transfected into steroid-responsive primary oviduct cells, mutants lacking sequences between -900 and -732 were no longer responsive to estrogen, corticosterone, progesterone, or dihydrotestosterone.	Corticosterone	217-231	ovalbumin (SERPINB14)	Gallus gallus	9-18
2332444-4	1990	When the ovalbumin-chloramphenicol acetyltransferase fusion genes were transfected into steroid-responsive primary oviduct cells, mutants lacking sequences between -900 and -732 were no longer responsive to estrogen, corticosterone, progesterone, or dihydrotestosterone.	Progesterone	233-245	ovalbumin (SERPINB14)	Gallus gallus	9-18
2332444-4	1990	When the ovalbumin-chloramphenicol acetyltransferase fusion genes were transfected into steroid-responsive primary oviduct cells, mutants lacking sequences between -900 and -732 were no longer responsive to estrogen, corticosterone, progesterone, or dihydrotestosterone.	Dihydrotestosterone	250-269	ovalbumin (SERPINB14)	Gallus gallus	9-18
2332444-10	1990	These data indicate that induction of the ovalbumin gene by steroid hormones requires complex interactions involving both the SDRE and the negative regulatory element.	Steroids	60-76	ovalbumin (SERPINB14)	Gallus gallus	42-51
2404743-11	1990	After 2-week stimulation with DES, avidin was expressed predominantly by cells of the basal layer of pseudostratified surface epithelium, and ovalbumin mainly by tubular glands and cells of the luminal layer of surface epithelium.	Diethylstilbestrol	30-33	ovalbumin (SERPINB14)	Gallus gallus	142-151
2139364-4	1990	In mice treated with 400 ng of PT and 1 mg of chicken egg albumin (EA), the percentage of these cells increased, 14 days after immunization, to an average value of 31.1 +/- 2.2%.	Platinum	31-33	ovalbumin (SERPINB14)	Gallus gallus	67-69
16667406-5	1990	Both activities comigrated with chicken ovalbumin during gel filtration through Sephacryl S-200, indicating a native molecular mass of 45 kilodaltons.	sephacryl S 200	80-95	ovalbumin (SERPINB14)	Gallus gallus	40-49