Found: 19
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Effects of Progesterone and Selective Ligands of Membrane Progesterone Receptors in HepG2 Cells of Human Hepatocellular Carcinoma.
- Published in:
- Biochemistry (00062979), 2023, v. 88, n. 11, p. 1920, doi. 10.1134/S0006297923110202
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- Article
Cytotoxic Effects of the Selective Ligands of Membrane Progesterone Receptors in Human Pancreatic Adenocarcinoma Cells BxPC3.
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- Biochemistry (00062979), 2021, v. 86, n. 11, p. 1446, doi. 10.1134/S0006297921110080
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- Article
A Founder Mutation in the POMC 5′-UTR Causes Proopiomelanocortin Deficiency Through SplicingMediated Decrease of mRNA.
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- Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 9, p. e3654, doi. 10.1210/clinem/dgac397
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- Article
Aberrant Splicing of INS Impairs Beta-Cell Differentiation and Proliferation by ER Stress in the Isogenic iPSC Model of Neonatal Diabetes.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 15, p. 8824, doi. 10.3390/ijms23158824
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- Article
Subtype of Neuroblastoma Cells with High KIT Expression Are Dependent on KIT and Its Knockdown Induces Compensatory Activation of Pro-Survival Signaling.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 14, p. 7724, doi. 10.3390/ijms23147724
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- Article
Late Diagnosis of POMC Deficiency and In Vitro Evidence of Residual Translation From Allele With c.-11C>A Mutation.
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- 2016
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- Publication type:
- journal article
Lipid Regulators during Atherogenesis: Expression of LXR, PPAR, and SREBP mRNA in the Human Aorta
- Published in:
- PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0063374
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- Article
A Novel Homozygous Mutation in CYP11A1 Gene Is Associated with Late-Onset Adrenal Insufficiency and Hypospadias in a 46,XY Patient.
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- Journal of Clinical Endocrinology & Metabolism, 2009, v. 94, n. 3, p. 936, doi. 10.1210/jc.2008-1118
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- Publication type:
- Article
A Familial Insulin-Like Growth Factor-I Receptor Mutant Leads to Short Stature: Clinical and Biochemical Characterization.
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- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 4, p. 1542, doi. 10.1210/jc.2006-2354
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- Article
Four novel missense mutations in the CYP21A2 gene detected in Russian patients suffering from the classical form of congenital adrenal hyperplasia: identification, functional characterization, and structural analysis.
- Published in:
- 2006
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- Publication type:
- journal article
A Potential Rearrangement between CYP19 and TRPM7 Genes on Chromosome 15q21.2 as a Cause of Aromatase Excess Syndrome.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 7, p. 4184, doi. 10.1210/jc.2004-2176
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- Publication type:
- Article
A Novel C-Terminal Growth Hormone Receptor (GHR) Mutation Results in Impaired GHR-STAT5 But Normal STAT-3 Signaling.
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- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 1, p. 542, doi. 10.1210/jc.2003-2133
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- Publication type:
- Article
Partial deficiency of 17γ-hydroxylase/17,20-lyase caused by a novel missense mutation in the canonical cytochrome heme-interacting motif.
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- European Journal of Endocrinology, 2015, v. 172, n. 5, p. K19, doi. 10.1530/EJE-14-0834
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- Publication type:
- Article
Changes of lysosomes in the earliest stages of the development of atherosclerosis.
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- Journal of Cellular & Molecular Medicine, 2013, v. 17, n. 5, p. 626, doi. 10.1111/jcmm.12042
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- Article
GATA1, GATA2, and TAL1 Regulate the Expression of Neurotrophic Receptor Tyrosine Kinase in Leukemia Cells.
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- FASEB Journal, 2021, v. 35, p. N.PAG, doi. 10.1096/fasebj.2021.35.S1.03640
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- Article
Hepatitis Delta Virus Antigens Trigger Oxidative Stress, Activate Antioxidant Nrf2/ARE Pathway, and Induce Unfolded Protein Response.
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- Antioxidants, 2023, v. 12, n. 4, p. 974, doi. 10.3390/antiox12040974
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- Publication type:
- Article
A Novel Mutation in the Critical P-Box Residue of Steroidogenic Factor-1 Presenting with XY Sex Reversal and Transient Adrenal Failure.
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- Hormone Research in Paediatrics, 2018, v. 89, n. 6, p. 450, doi. 10.1159/000481776
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- Article
Minigene splicing assessment of 20 novel synonymous and intronic glucokinase gene variants identified in patients with maturity‐onset diabetes of the young.
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- Human Mutation, 2020, v. 41, n. 1, p. 129, doi. 10.1002/humu.23919
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- Article
Growth Hormone Insensitivity (Laron Syndrome) in a Russian Girl of Slavic Origin Caused by a Common Mutation of the GH Receptor Gene.
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- International Journal on Disability & Human Development (De Gruyter), 1999, v. 1, n. 2, p. 95, doi. 10.1515/ijdhd.1999.1.2.95
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- Article