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Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian Insufficiency.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2016, p. 4541, doi. 10.1210/jc.2016-2152
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- Article
Corticosteroid receptors adopt distinct cyclical transcriptional signatures.
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- FASEB Journal, 2018, v. 32, n. 10, p. 5626, doi. 10.1096/fj.201800391RR
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- Article
Cistrome of the aldosterone-activated mineralocorticoid receptor in human renal cells.
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- FASEB Journal, 2015, v. 29, n. 9, p. 3977, doi. 10.1096/fj.15-274266
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- Article
Mechanistic aspects of mineralocorticoid receptor activation.
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- Kidney International, 2000, v. 57, n. 4, p. 1250, doi. 10.1046/j.1523-1755.2000.00958.x
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- Article
Antagonism in the human mineralocorticoid receptor.
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- EMBO Journal, 1998, v. 17, n. 12, p. 3317, doi. 10.1093/emboj/17.12.3317
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- Article
Familial Multiplicity of Estrogen Insensitivity Associated With a Loss-of-Function ESR1 Mutation.
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- 2016
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- Publication type:
- journal article
Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian Insufficiency.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Synthesis of [<sup>3</sup>H<sub>2</sub>]-21-diazoprogesterone as a potent photoaffinity labelling reagent for the mineralocorticoid receptor.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 1997, v. 39, n. 10, p. 791, doi. 10.1002/(SICI)1099-1344(199710)39:10<791::AID-JLCR25>3.0.CO;2-X
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- Publication type:
- Article
RNA-binding protein HuR enhances mineralocorticoid signaling in renal KC3AC1 cells under hypotonicity.
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- Cellular & Molecular Life Sciences, 2017, v. 74, n. 24, p. 4587, doi. 10.1007/s00018-017-2594-x
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- Publication type:
- Article
Two Families with Normosmic Congenital Hypogonadotropic Hypogonadism and Biallelic Mutations in KISS1R (KISS1 Receptor): Clinical Evaluation and Molecular Characterization of a Novel Mutation.
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- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0053896
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- Publication type:
- Article
Normosmic Congenital Hypogonadotropic Hypogonadism Due to TAC3/TACR3 Mutations: Characterization of Neuroendocrine Phenotypes and Novel Mutations.
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- PLoS ONE, 2011, v. 6, n. 10, p. 1, doi. 10.1371/journal.pone.0025614
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- Article
Cover Image, Volume 37, Issue 8.
- Published in:
- Human Mutation, 2016, v. 37, n. 8, p. i, doi. 10.1002/humu.23039
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- Publication type:
- Article
Three Novel Heterozygous Point Mutations of NR3C1 Causing Glucocorticoid Resistance.
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- Human Mutation, 2016, v. 37, n. 8, p. 794, doi. 10.1002/humu.23008
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- Publication type:
- Article
Mineralocorticoid receptor mutations are the principal cause of renal type 1 pseudohypoaldosteronism.
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- Human Mutation, 2007, v. 28, n. 1, p. 33, doi. 10.1002/humu.20371
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- Article
A new model for 20-hydroxyecdysone and dibenzoylhydrazine binding: A homology modeling and docking approach.
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- Protein Science: A Publication of the Protein Society, 2000, v. 9, n. 6, p. 1073
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- Publication type:
- Article
Crystal structure of a mutant mineralocorticoid receptor responsible for hypertension.
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- Nature Structural & Molecular Biology, 2005, v. 12, n. 6, p. 554, doi. 10.1038/nsmb939
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- Publication type:
- Article
Antagonistic effects of finerenone and spironolactone on the aldosterone-regulated transcriptome of human kidney cells.
- Published in:
- FASEB Journal, 2021, v. 35, n. 2, p. 1, doi. 10.1096/fj.202002043RR
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- Publication type:
- Article
A novel mutation in the NR3C1 gene associated with reversible glucocorticoid resistance.
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- European Journal of Endocrinology, 2024, v. 190, n. 4, p. 284, doi. 10.1093/ejendo/lvae031
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- Article