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For: Miller WL. Disorders in the initial steps of steroid hormone synthesis. The Journal of Steroid Biochemistry and Molecular Biology 2017;165:18-37. [DOI: 10.1016/j.jsbmb.2016.03.009] [Cited by in Crossref: 74] [Cited by in F6Publishing: 58] [Article Influence: 14.8] [Reference Citation Analysis]
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8 Weger M, Weger BD, Görling B, Poschet G, Yildiz M, Hell R, Luy B, Akcay T, Güran T, Dickmeis T, Müller F, Krone N. Glucocorticoid deficiency causes transcriptional and post-transcriptional reprogramming of glutamine metabolism. EBioMedicine 2018;36:376-89. [PMID: 30266295 DOI: 10.1016/j.ebiom.2018.09.024] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
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13 Liang JJ, Rasmusson AM. Overview of the Molecular Steps in Steroidogenesis of the GABAergic Neurosteroids Allopregnanolone and Pregnanolone. Chronic Stress (Thousand Oaks) 2018;2:2470547018818555. [PMID: 32440589 DOI: 10.1177/2470547018818555] [Cited by in Crossref: 7] [Cited by in F6Publishing: 9] [Article Influence: 1.8] [Reference Citation Analysis]
14 Iegaki N, Narita Y, Hattori N, Hirata Y, Ichihara K. Royal jelly reduces depression-like behavior through possible effects on adrenal steroidogenesis in a murine model of unpredictable chronic mild stress. Bioscience, Biotechnology, and Biochemistry 2020;84:606-12. [DOI: 10.1080/09168451.2019.1691496] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
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16 Hannah-shmouni F, Chen W, Merke DP. Genetics of Congenital Adrenal Hyperplasia. Endocrinology and Metabolism Clinics of North America 2017;46:435-58. [DOI: 10.1016/j.ecl.2017.01.008] [Cited by in Crossref: 28] [Cited by in F6Publishing: 17] [Article Influence: 5.6] [Reference Citation Analysis]
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19 Bhargava A, Arnold AP, Bangasser DA, Denton KM, Gupta A, Hilliard Krause LM, Mayer EA, McCarthy M, Miller WL, Raznahan A, Verma R. Considering Sex as a Biological Variable in Basic and Clinical Studies: An Endocrine Society Scientific Statement. Endocr Rev 2021;42:219-58. [PMID: 33704446 DOI: 10.1210/endrev/bnaa034] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 6.0] [Reference Citation Analysis]
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21 Przygrodzka E, Plewes MR, Davis JS. Luteinizing Hormone Regulation of Inter-Organelle Communication and Fate of the Corpus Luteum. Int J Mol Sci 2021;22:9972. [PMID: 34576135 DOI: 10.3390/ijms22189972] [Reference Citation Analysis]
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26 Dabravolski SA, Nikiforov NG, Zhuravlev AD, Orekhov NA, Grechko AV, Orekhov AN. Role of the mtDNA Mutations and Mitophagy in Inflammaging. IJMS 2022;23:1323. [DOI: 10.3390/ijms23031323] [Reference Citation Analysis]
27 Katharopoulos E, Di Iorgi N, Fernandez-Alvarez P, Pandey AV, Groessl M, Dubey S, Camats N, Napoli F, Patti G, Lezzi M, Maghnie M, Flück CE. Characterization of Two Novel Variants of the Steroidogenic Acute Regulatory Protein Identified in a Girl with Classic Lipoid Congenital Adrenal Hyperplasia. Int J Mol Sci 2020;21:E6185. [PMID: 32867102 DOI: 10.3390/ijms21176185] [Reference Citation Analysis]
28 Burget L, Parera LA, Fernandez-Cancio M, Gräni R, Henzen C, Flück CE. A rare cause of primary adrenal insufficiency due to a homozygous Arg188Cys mutation in the STAR gene. Endocrinol Diabetes Metab Case Rep 2018;2018:18-0003. [PMID: 29576868 DOI: 10.1530/EDM-18-0003] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
29 Yang Y, Wang C, Shen H, Fan H, Liu J, Wu N. Cis-bifenthrin inhibits cortisol and aldosterone biosynthesis in human adrenocortical H295R cells via cAMP signaling cascade. Environ Toxicol Pharmacol 2021;89:103784. [PMID: 34896276 DOI: 10.1016/j.etap.2021.103784] [Reference Citation Analysis]
30 Huang H, Wu J, Lu R, Liu X, Chin B, Zhu H, Yin C, Cheng B, Wu Z, Chen X, Liang Y, Song H, Zheng H, Guo H, Su Z. Dynamic urinary metabolomics analysis based on UHPLC-Q-TOF/MS to investigate the potential biomarkers of blood stasis syndrome and the effects of Danggui Sini decoction. Journal of Pharmaceutical and Biomedical Analysis 2020;179:112986. [DOI: 10.1016/j.jpba.2019.112986] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
31 Lara-Velazquez M, Perdomo-Pantoja A, Blackburn PR, Gass JM, Caulfield TR, Atwal PS. A novel splice site variant in CYP11A1 in trans with the p.E314K variant in a male patient with congenital adrenal insufficiency. Mol Genet Genomic Med 2017;5:781-7. [PMID: 29178636 DOI: 10.1002/mgg3.322] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.2] [Reference Citation Analysis]
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33 Larsen MC, Lee J, Jorgensen JS, Jefcoate CR. STARD1 Functions in Mitochondrial Cholesterol Metabolism and Nascent HDL Formation. Gene Expression and Molecular mRNA Imaging Show Novel Splicing and a 1:1 Mitochondrial Association. Front Endocrinol (Lausanne) 2020;11:559674. [PMID: 33193082 DOI: 10.3389/fendo.2020.559674] [Reference Citation Analysis]
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36 Khoury K, Barbar E, Ainmelk Y, Ouellet A, Lavigne P, LeHoux JG. Thirty-Eight-Year Follow-Up of Two Sibling Lipoid Congenital Adrenal Hyperplasia Patients Due to Homozygous Steroidogenic Acute Regulatory (STARD1) Protein Mutation. Molecular Structure and Modeling of the STARD1 L275P Mutation. Front Neurosci 2016;10:527. [PMID: 27917104 DOI: 10.3389/fnins.2016.00527] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 1.5] [Reference Citation Analysis]
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38 Miller WL. Steroidogenic electron-transfer factors and their diseases. Ann Pediatr Endocrinol Metab 2021;26:138-48. [PMID: 34610701 DOI: 10.6065/apem.2142154.077] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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46 Bose HS, Whittal RM, Marshall B, Rajapaksha M, Wang NP, Bose M, Perry EW, Zhao ZQ, Miller WL. A Novel Mitochondrial Complex of Aldosterone Synthase, Steroidogenic Acute Regulatory Protein, and Tom22 Synthesizes Aldosterone in the Rat Heart. J Pharmacol Exp Ther 2021;377:108-20. [PMID: 33526603 DOI: 10.1124/jpet.120.000365] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
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