Walter L. Miller
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Most Influential Person Across History
American endocrinologist
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Walter L. Miller 's Degrees
- Doctorate Medicine Harvard University
Why Is Walter L. Miller Influential?
(Suggest an Edit or Addition)According to Wikipedia, Walter L. Miller is an American endocrinologist and professor emeritus of pediatrics at the University of California, San Francisco . Miller is expert in the field of human steroid biosynthesis and disorders of steroid metabolism. Over the past 40 years Miller's group at UCSF has described molecular basis of several metabolic disorders including, congenital adrenal hyperplasia, pseudo vitamin D dependent rickets, severe, recessive form of Ehlers-Danlos syndrome, 17,20 lyase deficiency caused by CYP17A1 defects, P450scc deficiency caused by CYP11A1 defects, P450 oxidoreductase deficiency .
Walter L. Miller 's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders. (2011) (1626)
- Molecular biology of steroid hormone synthesis. (1988) (1333)
- Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline. (2010) (1132)
- Role of steroidogenic acute regulatory protein in adrenal and gonadal steroidogenesis. (1995) (971)
- The pathophysiology and genetics of congenital lipoid adrenal hyperplasia. (1996) (605)
- Cytochrome b 5 Augments the 17,20-Lyase Activity of Human P450c17 without Direct Electron Transfer* (1998) (526)
- Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome (2004) (457)
- Serine phosphorylation of human P450c17 increases 17,20-lyase activity: implications for adrenarche and the polycystic ovary syndrome. (1995) (456)
- Cloning of human 25-hydroxyvitamin D-1 alpha-hydroxylase and mutations causing vitamin D-dependent rickets type 1. (1997) (435)
- Cytochrome P450c17 (steroid 17 alpha-hydroxylase/17,20 lyase): cloning of human adrenal and testis cDNAs indicates the same gene is expressed in both tissues. (1987) (418)
- Early steps in steroidogenesis: intracellular cholesterol trafficking (2011) (415)
- Cloning and sequence of the human gene for P450c17 (steroid 17 alpha-hydroxylase/17,20 lyase): similarity with the gene for P450c21. (1987) (414)
- Consensus Statement on 21-Hydroxylase Deficiency from The European Society for Paediatric Endocrinology and The Lawson Wilkins Pediatric Endocrine Society (2002) (393)
- Human cytochromes P450 in health and disease (2013) (392)
- Human steroidogenic acute regulatory protein: functional activity in COS-1 cells, tissue-specific expression, and mapping of the structural gene to 8p11.2 and a pseudogene to chromosome 13. (1995) (371)
- Structure and evolution of the growth hormone gene family. (1983) (352)
- A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiency. (2001) (350)
- Human cholesterol side-chain cleavage enzyme, P450scc: cDNA cloning, assignment of the gene to chromosome 15, and expression in the placenta. (1986) (334)
- Rapid regulation of steroidogenesis by mitochondrial protein import (2002) (331)
- Tenascin–X deficiency is associated with Ehlers–Danlos syndrome (1997) (328)
- Diversity and function of mutations in p450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesis. (2005) (328)
- Nephrogenic syndrome of inappropriate antidiuresis. (2005) (325)
- Minireview: regulation of steroidogenesis by electron transfer. (2005) (304)
- Steroid hormone synthesis in mitochondria (2013) (302)
- Steroidogenic acute regulatory protein (StAR), a novel mitochondrial cholesterol transporter. (2007) (299)
- The genetic and functional basis of isolated 17,20–lyase deficiency (1997) (294)
- Tenascin-X: a novel extracellular matrix protein encoded by the human XB gene overlapping P450c21B (1993) (286)
- Steroidogenic acute regulatory protein (StAR) retains activity in the absence of its mitochondrial import sequence: implications for the mechanism of StAR action. (1996) (276)
- Hormonal regulation of P450scc (20,22-desmolase) and P450c17 (17 alpha-hydroxylase/17,20-lyase) in cultured human granulosa cells. (1986) (240)
- The regulation of 17,20 lyase activity (1997) (227)
- Peripheral-type benzodiazepine receptor-mediated action of steroidogenic acute regulatory protein on cholesterol entry into leydig cell mitochondria. (2005) (219)
- The active form of the steroidogenic acute regulatory protein, StAR, appears to be a molten globule. (1999) (219)
- Why boys will be boys: two pathways of fetal testicular androgen biosynthesis are needed for male sexual differentiation. (2011) (217)
- Structure of the human steroidogenic acute regulatory protein (StAR) gene: StAR stimulates mitochondrial cholesterol 27-hydroxylase activity. (1995) (209)
- Role of mitochondria in steroidogenesis. (2012) (209)
- StAR search--what we know about how the steroidogenic acute regulatory protein mediates mitochondrial cholesterol import. (2007) (203)
- Molecular modeling of human P450c17 (17alpha-hydroxylase/17,20-lyase): insights into reaction mechanisms and effects of mutations. (1999) (203)
- Consensus statement on 21-hydroxylase deficiency from the Lawson Wilkins Pediatric Endocrine Society and the European Society for Paediatric Endocrinology. (2002) (201)
- Regulation of steroidogenesis in NCI-H295 cells: a cellular model of the human fetal adrenal. (1993) (199)
- Genetics of P450 oxidoreductase: Sequence variation in 842 individuals of four ethnicities and activities of 15 missense mutations (2008) (197)
- Cholesterol side-chain cleavage P450 messenger ribonucleic acid: evidence for hormonal regulation in rat ovarian follicles and constitutive expression in corpora lutea. (1987) (178)
- Heterozygous mutation in the cholesterol side chain cleavage enzyme (p450scc) gene in a patient with 46,XY sex reversal and adrenal insufficiency. (2001) (173)
- Clinical and molecular genetics of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. (1991) (166)
- P450c17 mutations R347H and R358Q selectively disrupt 17,20-lyase activity by disrupting interactions with P450 oxidoreductase and cytochrome b5. (1999) (166)
- Genetics of Vitamin D 1α-Hydroxylase Deficiency in 17 Families (1998) (161)
- Steroid 17 alpha-hydroxylase and 17,20-lyase activities of P450c17: contributions of serine106 and P450 reductase. (1993) (159)
- Clinical review 54: Genetics, diagnosis, and management of 21-hydroxylase deficiency. (1994) (156)
- Molecular pathology and mechanism of action of the steroidogenic acute regulatory protein, StARProceedings of Xth International Congress on Hormonal Steroids, Quebec, Canada, 17–21 June 1998. (1999) (155)
- Androgen biosynthesis from cholesterol to DHEA (2002) (155)
- Nonclassic congenital lipoid adrenal hyperplasia: a new disorder of the steroidogenic acute regulatory protein with very late presentation and normal male genitalia. (2006) (154)
- Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline. (2018) (153)
- The 17, 20-lyase activity of cytochrome p450c17 from human fetal testis favors the delta5 steroidogenic pathway. (2003) (152)
- Transcript encoded on the opposite strand of the human steroid 21-hydroxylase/complement component C4 gene locus. (1989) (151)
- Thiazolidinediones but Not Metformin Directly Inhibit the Steroidogenic Enzymes P450c17 and 3β-Hydroxysteroid Dehydrogenase* (2001) (148)
- Long-term outcome in children and adolescents after transsphenoidal surgery for Cushing's disease. (1997) (145)
- Spontaneous feminization in a 46,XX female patient with congenital lipoid adrenal hyperplasia due to a homozygous frameshift mutation in the steroidogenic acute regulatory protein. (1997) (144)
- Regulation of 17,20 Lyase Activity by Cytochrome b5 and by Serine Phosphorylation of P450c17* (2005) (144)
- Regional mapping of genes encoding human steroidogenic enzymes: P450scc to 15q23-q24, adrenodoxin to 11q22; adrenodoxin reductase to 17q24-q25; and P450c17 to 10q24-q25. (1991) (144)
- ASSIGNMENT OF THE GENE FOR ADRENAL P450cl7 (STEROID 17α-HYDR0XYLASE⁄17,20 LYASE) TO HUMAN CHROMOSOME 10. (1986) (141)
- Construction and function of fusion enzymes of the human cytochrome P450scc system. (1993) (139)
- Molecular cloning of DNA complementary to bovine growth hormone mRNA. (1980) (138)
- Molecular and clinical advances in congenital adrenal hyperplasia. (1987) (136)
- CONGENITAL ADRENAL HYPERPLASIA DUE TO DEFICIENT CHOLESTEROL SIDE‐CHAIN CLEAVAGE ACTIVITY (20, 22‐DESMOLASE) IN A PATIENT TREATED FOR 18 YEARS (1985) (134)
- GATA-4 and GATA-6 modulate tissue-specific transcription of the human gene for P450c17 by direct interaction with Sp1. (2004) (133)
- Congenital lipoid adrenal hyperplasia: the human gene knockout for the steroidogenic acute regulatory protein. (1997) (132)
- Protein Phosphatase 2A and Phosphoprotein SET Regulate Androgen Production by P450c17* (2003) (131)
- Tissue-specific, cyclic adenosine 3',5'-monophosphate-induced, and phorbol ester-repressed transcription from the human P450c17 promoter in mouse cells. (1990) (131)
- Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenital adrenal hyperplasia. (1989) (129)
- Missense mutation serine106----proline causes 17 alpha-hydroxylase deficiency. (1991) (126)
- Steroidogenic enzymes. (2008) (123)
- Mutations in the steroidogenic acute regulatory protein (StAR) in six patients with congenital lipoid adrenal hyperplasia. (2000) (122)
- Normal genes for the cholesterol side chain cleavage enzyme, P450scc, in congenital lipoid adrenal hyperplasia. (1991) (121)
- Mitochondrial specificity of the early steps in steroidogenesis (1995) (120)
- Steroidogenic Activity of StAR Requires Contact with Mitochondrial VDAC1 and Phosphate Carrier Protein* (2008) (119)
- T-->A transversion 11 bp from a splice acceptor site in the human gene for steroidogenic acute regulatory protein causes congenital lipoid adrenal hyperplasia. (1995) (118)
- Disorders in the initial steps of steroid hormone synthesis (2017) (118)
- Severe combined adrenal and gonadal deficiency caused by novel mutations in the cholesterol side chain cleavage enzyme, P450scc. (2008) (117)
- Steroidogenesis: Unanswered Questions (2017) (116)
- How safe is long-term prenatal glucocorticoid treatment? (1997) (115)
- Extraadrenal steroid 21-hydroxylation is not mediated by P450c21. (1989) (115)
- Complete Structure of the Human Gene for the Vitamin D 1α-Hydroxylase, P450c1α (1997) (111)
- Substrate-specific modulation of CYP3A4 activity by genetic variants of cytochrome P450 oxidoreductase (2010) (111)
- Human P450scc gene transcription is induced by cyclic AMP and repressed by 12-O-tetradecanoylphorbol-13-acetate and A23187 through independent cis elements (1990) (111)
- Mechanism and consequences of the duplication of the human C4/P450c21/gene X locus (1992) (111)
- Pharmacogenetics of P450 oxidoreductase: effect of sequence variants on activities of CYP1A2 and CYP2C19 (2008) (111)
- The serine phosphorylation hypothesis of polycystic ovary syndrome: a unifying mechanism for hyperandrogenemia and insulin resistance. (2008) (108)
- The mitochondrial environment is required for activity of the cholesterol side-chain cleavage enzyme, cytochrome P450scc. (1994) (108)
- Androgen synthesis in adrenarche (2009) (107)
- The molecular genetics of 21-hydroxylase deficiency. (1989) (106)
- Regulation of the gene for estrogenic 17-ketosteroid reductase lying on chromosome 17cen----q25. (1989) (104)
- Structure and function of the hepatic form of 11 beta-hydroxysteroid dehydrogenase in the squirrel monkey, an animal model of glucocorticoid resistance. (1993) (103)
- Molecular evolution of adrenarche: structural and functional analysis of p450c17 from four primate species. (2002) (103)
- Expression and characterization of truncated human heme oxygenase (hHO-1) and a fusion protein of hHO-1 with human cytochrome P450 reductase. (1995) (102)
- Transcription of the human genes for cytochrome P450scc and P450c17 is regulated differently in human adrenal NCI-H295 cells than in mouse adrenal Y1 cells. (1997) (98)
- N-218 MLN64, a protein with StAR-like steroidogenic activity, is folded and cleaved similarly to StAR. (2000) (95)
- Genetic and Clinical Features of P450 Oxidoreductase Deficiency (2008) (93)
- Steroid hormone biosynthesis and actions in the materno-feto-placental unit. (1998) (92)
- The syndrome of 17,20 lyase deficiency. (2012) (91)
- Congenital adrenal hyperplasia - current insights in pathophysiology, diagnostics and management. (2021) (88)
- Partial defect in the cholesterol side-chain cleavage enzyme P450scc (CYP11A1) resembling nonclassic congenital lipoid adrenal hyperplasia. (2011) (87)
- P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasia. (1987) (86)
- The human peripheral benzodiazepine receptor gene: cloning and characterization of alternative splicing in normal tissues and in a patient with congenital lipoid adrenal hyperplasia. (1993) (85)
- Effects of 8-bromo-cAMP on expression of endocrine functions by cultured human trophoblast cells. Regulation of specific mRNAs (1989) (85)
- Human adrenodoxin reductase: two mRNAs encoded by a single gene on chromosome 17cen----q25 are expressed in steroidogenic tissues. (1988) (84)
- Rainbow trout cytochrome P‐450c17 (17α‐hydroxylase/17,20‐lyase) cDNA cloning, enzymatic properties and temporal pattern of ovarian P‐450c17 mRNA expression during oogenesis (1992) (83)
- NF-1C, Sp1, and Sp3 are essential for transcription of the human gene for P450c17 (steroid 17alpha-hydroxylase/17,20 lyase) in human adrenal NCI-H295A cells. (2001) (80)
- Structure of a bovine gene for P-450c21 (steroid 21-hydroxylase) defines a novel cytochrome P-450 gene family. (1986) (79)
- Homozygous mutation G539R in the gene for P450 oxidoreductase in a family previously diagnosed as having 17,20-lyase deficiency. (2008) (79)
- A pH-dependent Molten Globule Transition Is Required for Activity of the Steroidogenic Acute Regulatory Protein, StAR* (2005) (78)
- Consequences of POR mutations and polymorphisms (2011) (78)
- Prenatal diagnosis of congenital lipoid adrenal hyperplasia. (1995) (77)
- Vitamin D 1α-Hydroxylase Gene Mutations in Patients with 1α-Hydroxylase Deficiency (2007) (77)
- Abundant adrenal-specific transcription of the human P450c21A "pseudogene". (1993) (77)
- Cloning of Factors Related to HIV-inducible LBP Proteins That Regulate Steroidogenic Factor-1-independent Human Placental Transcription of the Cholesterol Side-chain Cleavage Enzyme, P450scc* (2000) (77)
- Cholesterol Binding Does Not Predict Activity of the Steroidogenic Acute Regulatory Protein, StAR* (2007) (76)
- Guidelines for the Development of Comprehensive Care Centers for Congenital Adrenal Hyperplasia: Guidance from the CARES Foundation Initiative (2010) (76)
- Extraadrenal 21-hydroxylation by CYP2C19 and CYP3A4: effect on 21-hydroxylase deficiency. (2009) (75)
- The Mechanism of 1,25-Dihydroxyvitamin D3Autoregulation in Keratinocytes* (2002) (75)
- P450 oxidoreductase deficiency: a new disorder of steroidogenesis with multiple clinical manifestations (2004) (75)
- Genetic variation in P450c11AS in Chilean patients with low renin hypertension. (1996) (75)
- Homologous sequences in steroidogenic enzymes, steroid receptors and a steroid binding protein suggest a consensus steroid-binding sequence. (1988) (75)
- Medroxyprogesterone acetate and dexamethasone are competitive inhibitors of different human steroidogenic enzymes. (1999) (74)
- Differential Regulation of Steroid Hormone Biosynthesis in R2C and MA-10 Leydig Tumor Cells: Role of SR-B1-Mediated Selective Cholesteryl Ester Transport1 (2003) (73)
- A ring-20 chromosome. (1972) (73)
- Novel gene mutations in patients with 1alpha-hydroxylase deficiency that confer partial enzyme activity in vitro. (2002) (73)
- Dietary Phosphorus Transcriptionally Regulates 25-Hydroxyvitamin D-1α-Hydroxylase Gene Expression in the Proximal Renal Tubule. (2002) (72)
- Mutation of histidine 373 to leucine in cytochrome P450c17 causes 17 alpha-hydroxylase deficiency. (1993) (72)
- Clinical, genetic, and functional characterization of four patients carrying partial loss-of-function mutations in the steroidogenic acute regulatory protein (StAR). (2010) (71)
- Study of cholesterol side-chain cleavage (20,22 desmolase) deficiency causing congenital lipoid adrenal hyperplasia using bovine-sequence P450scc oligodeoxyribonucleotide probes. (1986) (70)
- StAR-like activity and molten globule behavior of StARD6, a male germ-line protein. (2008) (70)
- Apparent manifesting heterozygosity in P450 oxidoreductase deficiency and its effect on coexisting 21-hydroxylase deficiency. (2007) (70)
- Transcriptional regulation of human genes for steroidogenic enzymes. (1993) (70)
- Effects of genetic variants of human P450 oxidoreductase on catalysis by CYP2D6 in vitro (2010) (69)
- Deletion of amino acids Asp487-Ser488-Phe489 in human cytochrome P450c17 causes severe 17 alpha-hydroxylase deficiency. (1993) (69)
- Regulation of ovine follicle-stimulating hormone beta-chain mRNA by 17 beta-estradiol in vivo and in vitro. (1982) (69)
- A genetic isolate of congenital lipoid adrenal hyperplasia with atypical clinical findings. (2005) (69)
- Vitamin D 1α-Hydroxylase (2000) (69)
- Binding of Steroidogenic Acute Regulatory Protein to Synthetic Membranes Suggests an Active Molten Globule* (2001) (69)
- Modeling and mutagenesis of the active site of human P450c17. (1994) (68)
- Early steps in androgen biosynthesis: from cholesterol to DHEA. (1998) (68)
- Dexamethasone treatment of congenital adrenal hyperplasia in utero: an experimental therapy of unproven safety. (1999) (65)
- Clinical, genetic, and enzymatic characterization of P450 oxidoreductase deficiency in four patients. (2009) (63)
- pH-dependent Interactions of the Carboxyl-terminal Helix of Steroidogenic Acute Regulatory Protein with Synthetic Membranes* (2005) (63)
- Point mutation of Arg440 to His in cytochrome P450c17 causes severe 17 alpha-hydroxylase deficiency. (1994) (60)
- Mutation T318M in the CYP11B2 gene encoding P450c11AS (aldosterone synthase) causes corticosterone methyl oxidase II deficiency. (1995) (60)
- Identification of positive and negative placenta-specific basal elements and a cyclic adenosine 3',5'-monophosphate response element in the human gene for P450scc. (1992) (60)
- Transfer of Cholesterol between Phospholipid Vesicles Mediated by the Steroidogenic Acute Regulatory Protein (StAR)* (2002) (59)
- Clinical, genetic, and functional characterization of adrenocorticotropin receptor mutations using a novel receptor assay. (2002) (59)
- FGF-23 Regulates CYP27B1 Transcription in the Kidney and in Extra-Renal Tissues (2013) (59)
- cAMP post-transcriptionally diminishes the abundance of adrenodoxin reductase mRNA. (1992) (58)
- Mutation of proline 409 to arginine in the meander region of cytochrome p450c17 causes severe 17 alpha-hydroxylase deficiency. (2001) (58)
- Lack of defects in androgen production in children with hypospadias. (2004) (57)
- Molten globule structure and steroidogenic activity of N-218 MLN64 in human placental mitochondria. (2004) (57)
- Isolation of nine different biologically and immunologically active molecular variants of bovine follicular inhibin. (1995) (56)
- Gene conversion in the CYP11B2 gene encoding P450c11AS is associated with, but does not cause, the syndrome of corticosterone methyloxidase II deficiency. (1996) (55)
- Mechanism of StAR's regulation of mitochondrial cholesterol import (2007) (55)
- Incorrect folding of steroidogenic acute regulatory protein (StAR) in congenital lipoid adrenal hyperplasia. (1998) (55)
- MECHANISMS IN ENDOCRINOLOGY: Rare defects in adrenal steroidogenesis. (2018) (55)
- Cloning and sequence of the human adrenodoxin reductase gene. (1990) (54)
- Molecular biology of mineralocorticoid metabolism. (1996) (54)
- Genetic disorders of Vitamin D biosynthesis and degradation (2017) (54)
- Human proopiomelanocortin-(79-96), a proposed androgen stimulatory hormone, does not affect steroidogenesis in cultured human fetal adrenal cells. (1991) (54)
- Gene conversions, deletions, and polymorphisms in congenital adrenal hyperplasia. (1988) (53)
- Cloning and structure of the human adrenodoxin gene. (1988) (53)
- Disorders of Androgen Synthesis – from Cholesterol to Dehydroepiandrosterone (2005) (53)
- Of marsupials and men: “Backdoor” dihydrotestosterone synthesis in male sexual differentiation (2013) (52)
- Prenatal treatment of congenital adrenal hyperplasia: risks outweigh benefits. (2013) (52)
- Sequences promoting the transcription of the human XA gene overlapping P450c21A correctly predict the presence of a novel, adrenal-specific, truncated form of tenascin-X. (1995) (52)
- Regulation of proteins in the cholesterol side-chain cleavage system in JEG-3 and Y-1 cells. (1993) (52)
- Genetics of vitamin D 1alpha-hydroxylase deficiency in 17 families. (1998) (51)
- A Summary of the Endocrine Society Clinical Practice Guidelines on Congenital Adrenal Hyperplasia due to Steroid 21-Hydroxylase Deficiency (2010) (51)
- The molecular basis of premature adrenarche: an hypothesis (1999) (50)
- Human cytochromes P 450 in health and disease (2012) (50)
- Coordinate tropic hormone regulation of mRNAs for insulin-like growth factor II and the cholesterol side-chain-cleavage enzyme, P450ssc, in human steroidogenic tissues (49)
- THE STEROIDOGENIC ACUTE REGULATORY PROTEIN, StAR, WORKS ONLY AT THE OUTER MITOCHONDRIAL MEMBRANE (2002) (49)
- Genetic variation in human P450 oxidoreductase (2009) (48)
- The common P450 oxidoreductase variant A503V is not a modifier gene for 21-hydroxylase deficiency. (2008) (48)
- Varied clinical presentations of seven patients with mutations in CYP11A1 encoding the cholesterol side-chain cleavage enzyme, P450scc. (2013) (48)
- Considering Sex as a Biological Variable in Basic and Clinical Studies: An Endocrine Society Scientific Statement. (2021) (47)
- Effect of P450 oxidoreductase variants on the metabolism of model substrates mediated by CYP2C9.1, CYP2C9.2, and CYP2C9.3 (2012) (47)
- Rainbow trout ovarian cholesterol side‐chain cleavage cytochrome P450 (P450scc) (1993) (46)
- A promoter within intron 35 of the human C4A gene initiates abundant adrenal-specific transcription of a 1 kb RNA: location of a cryptic CYP21 promoter element? (1995) (46)
- Defects in Androgen Biosynthesis Causing 46,XY Disorders of Sexual Development (2012) (46)
- Pathways leading to phosphorylation of p450c17 and to the posttranslational regulation of androgen biosynthesis. (2008) (45)
- The Adrenal Cortex and its Disorders (2019) (45)
- Human 25-hydroxyvitamin D-1α-hydroxylase: cloning, mutations, and gene expression (2000) (45)
- Transcriptional Regulatory Elements of the Human Gene for Cytochrome P450c21 (Steroid 21-Hydroxylase) Lie within Intron 35 of the Linked C4B Gene* (1999) (44)
- Why nobody has P450scc (20,22 desmoslase) deficiency. (1998) (44)
- Characterization of placental transcriptional activation of the human gene for P450scc. (1995) (44)
- Gene conversions and rearrangements cause discordance between inheritance of forms of 21-hydroxylase deficiency and HLA types. (1989) (42)
- Transcriptional regulation of the human P450 oxidoreductase gene: hormonal regulation and influence of promoter polymorphisms. (2011) (42)
- Congenital Adrenal Hyperplasia: Time to Replace 17OHP with 21-Deoxycortisol (2019) (41)
- Regulation of cytochrome b5 gene transcription by Sp3, GATA-6, and steroidogenic factor 1 in human adrenal NCI-H295A cells. (2005) (41)
- The Regulation of Human P450c17 Activity: Relationship to Premature Adrenarche, Insulin Resistance and the Polycystic Ovary Syndrome (1998) (41)
- Prenatal Treatment of Congenital Adrenal Hyperplasia: A Promising Experimental Therapy of Unproven Safety (1998) (41)
- An infant with Cushing's disease due to an adrenocorticotropin-producing pituitary adenoma. (1979) (40)
- Phosphorylation of Human Cytochrome P450c17 by p38α Selectively Increases 17,20 Lyase Activity and Androgen Biosynthesis* (2013) (40)
- Molten-globule structure and membrane binding of the N-terminal protease-resistant domain (63-193) of the steroidogenic acute regulatory protein (StAR). (2001) (40)
- The “backdoor pathway” of androgen synthesis in human male sexual development (2019) (39)
- Vitamin D 1alpha-hydroxylase gene mutations in patients with 1alpha-hydroxylase deficiency. (2007) (39)
- Tenascin-X, Congenital Adrenal Hyperplasia, and the CAH-X Syndrome (2018) (39)
- Near-miss apparent SIDS from adrenal crisis. (2004) (39)
- P450 oxidoreductase deficiency: a new form of congenital adrenal hyperplasia (2006) (39)
- The Hypothalamic-Pituitary-Adrenal Axis: A Brief History (2018) (38)
- Cloning and characterization of the bovine gene for steroid 21-hydroxylase (P-450c21). (1985) (38)
- P450 oxidoreductase deficiency - a new form of congenital adrenal hyperplasia. (2008) (37)
- Hormonal regulation of growth hormone secretion and messenger ribonucleic acid accumulation in cultured bovine pituitary cells. (1988) (37)
- Synteny mapping of the genes for 21 steroid hydroxylase, alpha A crystallin, and class I bovine leukocyte antigen in cattle. (1988) (37)
- Evidence That Star and MLN64 act on the Outer Mitochondrial Membrane as Molten Globules (2000) (37)
- Alternate promoters and alternate splicing of human tenascin-X, a gene with 5' and 3' ends buried in other genes. (1996) (36)
- Regulation of growth hormone (GH) secretion by GH-releasing factor, somatostatin, and insulin-like growth factor I in ovine fetal and neonatal pituitary cells in vitro. (1989) (36)
- Cloning of bovine prolactin cDNA and evolutionary implications of its sequence. (1981) (35)
- Molecular characterization of a Leydig cell tumor presenting as congenital adrenal hyperplasia. (1989) (35)
- The molecular basis of isolated 17,20 lyase deficiency (1998) (35)
- Assignment of the gene for adrenal P450c17 (steroid 17 alpha-hydroxylase/17,20 lyase) to human chromosome 10. (1986) (34)
- Nomenclature for alleles of the cytochrome P450 oxidoreductase gene. (2009) (34)
- Molecular genetics of familial central diabetes insipidus. (1993) (34)
- P450 Oxidoreductase Deficiency: A New Disorder of Steroidogenesis Affecting All Microsomal P450 Enzymes (2004) (34)
- Enzymatic activities of P450c17 stably expressed in fibroblasts from patients with the polycystic ovary syndrome. (2000) (34)
- The post-translational regulation of 17,20 lyase activity (2015) (33)
- Steroidogenic adrenocortical cell lines produced by genetically targeted tumorigenesis in transgenic mice. (1994) (33)
- Basal transcriptional activity and cyclic adenosine 3',5'-monophosphate responsiveness of the human cytochrome P450scc promoter transfected into MA-10 Leydig cells. (1993) (33)
- A brief history of adrenal research Steroidogenesis – The soul of the adrenal (2013) (32)
- Fetal endocrine therapy for congenital adrenal hyperplasia should not be done. (2015) (32)
- P450 oxidoreductase deficiency (2004) (32)
- Steroid 17α-Hydroxylase Deficiency—Not Rare Everywhere (2004) (32)
- The role of transcriptional regulation in steroid hormone biosynthesis (1991) (32)
- Cortisol response to operative stress with anesthesia in healthy children. (2013) (31)
- Molecular and Clinical Advances in Congenital Adrenal Hyperplasia (1987) (31)
- Regulation of Steroidogenesis (2014) (31)
- High-yield expression of a catalytically active membrane-bound protein: human P450 oxidoreductase. (2011) (30)
- Artificial mutations in P450c11AS (aldosterone synthase) can increase enzymatic activity: a model for low-renin hypertension? (1995) (29)
- Clinical, biochemical, and molecular characterization of macronodular adrenocortical hyperplasia of the zona reticularis: a new syndrome. (2010) (29)
- LBP proteins modulate SF1-independent expression of P450scc in human placental JEG-3 cells. (2005) (29)
- Prenatal Treatment of Congenital Adrenal Hyperplasia—Not Standard of Care (2012) (28)
- Identification, characterization and rescue of a novel vasopressin‐2 receptor mutation causing nephrogenic diabetes insipidus (2009) (28)
- Vitamin D 1 alpha-hydroxylase. (2000) (27)
- Recombinant DNA — A new source of insulin (1980) (27)
- Genetic disorders of vitamin D biosynthesis. (1999) (27)
- Disorders of androgen biosynthesis. (2002) (27)
- 150 years of congenital adrenal hyperplasia: translation and commentary of De Crecchio's classic paper from 1865. (2015) (27)
- Assignment of the functional gene for human adrenodoxin to chromosome 11q13----qter and of adrenodoxin pseudogenes to chromosome 20cen----q13.1. (1988) (26)
- The transcriptional response of the human chorionic gonadotropin beta-subunit gene to cAMP is cycloheximide sensitive and is mediated by cis-acting sequences different from that found in the alpha-subunit gene. (1989) (26)
- Alternative splicing of DENND1A, a PCOS candidate gene, generates variant 2 (2016) (26)
- Regulation of mRNAs for human steroidogenic enzymes. (1989) (26)
- Human cytochrome p450c17: single step purification and phosphorylation of serine 258 by protein kinase a. (2010) (26)
- Genetics of vitamin D biosynthesis and its disorders. (2001) (24)
- Regulation of human cytochrome P450scc and adrenodoxin messenger ribonucleic acids in JEG-3 cytotrophoblast cells. (1992) (24)
- CHAPTER 13 – Adrenal cortex and its disorders (2014) (24)
- Processing of the precursor to corticotropin and beta-lipotropin in humans. (1980) (24)
- Rat insulin-like growth factor-I and -II mRNAs are unchanged during compensatory adrenal growth but decrease during ACTH-induced adrenal growth. (1990) (24)
- Renal arteriography following systemic reaction to contrast material (1975) (23)
- Dexamethasone does not exert direct intracellular feedback on steroidogenesis in human adrenal NCI-H295A cells. (2003) (23)
- Dietary phosphorus transcriptionally regulates 25-hydroxyvitamin D-1alpha-hydroxylase gene expression in the proximal renal tubule. (2002) (23)
- Structure of genes encoding steroidogenic enzymes. (1987) (23)
- P450 Oxidoreductase Deficiency (2005) (23)
- Role of mitochondria in steroidogenesis. (2011) (22)
- Complete structure of the human gene for the vitamin D 1alpha-hydroxylase, P450c1alpha. (1997) (22)
- P450 Oxidoreductase Deficiency: A Disorder of Steroidogenesis with Multiple Clinical Manifestations (2012) (22)
- Effects of Anticonvulsants on Human P450c17 (17α‐Hydroxylase/17,20 Lyase) and 3β‐Hydroxysteroid Dehydrogenase Type 2 (2005) (21)
- Cloning of DNA complementary to bovine prolactin mRNA. (1980) (21)
- The human genome contains only two CYP11B (P450c11) genes. (1996) (21)
- P450 enzymes in steroid processing (2015) (20)
- Pathophysiology, genetics, and treatment of hyperandrogenism. (1997) (20)
- Vitamin D 25-hydroxylase deficiency. (2004) (20)
- Vitamin D Biosynthesis and Vitamin D 1α-Hydroxylase Deficiency (2003) (20)
- Cinnamic acid based thiazolidinediones inhibit human P450c17 and 3beta-hydroxysteroid dehydrogenase and improve insulin sensitivity independent of PPARgamma agonist activity. (2004) (19)
- Lack of mutations in CYP2D6 and CYP27 in patients with apparent deficiency of vitamin D 25-hydroxylase. (2003) (19)
- Congenital adrenal hyperplasia--more dogma bites the dust. (2012) (18)
- Expression of P450c17 in the human fetal nervous system. (2012) (18)
- Phosphorylation of human cytochrome P450c17 by p38α selectively increases 17,20 lyase activity and androgen biosynthesis. (2014) (18)
- Human 25-hydroxyvitamin D-1alpha-hydroxylase: cloning, mutations, and gene expression. (2000) (18)
- Distinguishing deficiencies in the steroidogenic acute regulatory protein and the cholesterol side chain cleavage enzyme causing neonatal adrenal failure. (2013) (17)
- Novel P450c17 mutation H373D causing combined 17alpha-hydroxylase/17,20-lyase deficiency. (2009) (17)
- Insulins, Growth Hormone, and Recombinant DNA Technology (1982) (17)
- Endocrine, histological, and biochemical studies of adrenocorticotropin-producing islet cell carcinoma of the pancreas in childhood with characterization of proopiomelanocortin. (1983) (17)
- Increased efficiency in liquid scintillation counting: Glass fiber discs and a new scintillator (1967) (16)
- Genetic causes of rickets. (1999) (16)
- mRNA for ovine follicle-stimulating hormone beta-chain. An in vitro translational assay. (1981) (16)
- Infection of cultured human adrenal cells by different strains of HIV (1992) (16)
- Construction of a P450c27 fusion enzyme: a useful tool for analysis of vitamin D3 25-hydroxylase activity. (1996) (16)
- Immunoassays for human müllerian inhibitory factor (MIF): new insights into the physiology of MIF. (1990) (16)
- Vitamin D biosynthesis and vitamin D 1 alpha-hydroxylase deficiency. (2003) (16)
- SEQUENTIAL CHANGES IN CLASSES OF RNA DURING COMPENSATORY GROWTH OF THE KIDNEY (1967) (16)
- Molecular cloning of DNA complementary to bovine adrenal P450scc mRNA. (1984) (16)
- Functional Characterization of Vasopressin Receptor 2 Mutations Causing Partial and Complete Congenital Nephrogenic Diabetes Insipidus in Thai Families (2010) (15)
- Synthesis and glycosylation of proopiomelanocortin by a Cushing tumor. (1982) (14)
- Probing Structural and Functional Domains of Human P450c17 (2000) (14)
- CHAPTER 12 – The Adrenal Cortex and Its Disorders (2008) (13)
- Gene expression in normal and regenerating mouse kidney. (1979) (12)
- Quantitation of CYP24A1 enzymatic activity with a simple two-hybrid system. (2015) (12)
- Formation and functioning of fused cholesterol side-chain cleavage enzymes. (2003) (12)
- Congenital Lipoid Adrenal Hyperplasia (2001) (12)
- Did Akhenaten Have the AntleyBixler Syndrome? (2009) (12)
- Lessons from congenital lipoid adrenal hyperplasia (1998) (11)
- Ovarian and Adrenal Androgen Biosynthesis and Metabolism (2006) (11)
- Localization and analysis of the principal promoter for human tenascin-X. (2002) (10)
- Bovine prolactin: corrected cDNA sequence and genetic polymorphisms. (1982) (10)
- Congenital lipoid adrenal hyperplasia—Genes for P450scc, side chain cleavage enzyme, are normal (1993) (10)
- Use of recombinant DNA technology for the production of polypeptides. (1979) (10)
- Congenital adrenal hyperplasia. (1987) (10)
- Rickets Due to Hereditary Abnormalities of Vitamin D Synthesis or Action (2012) (10)
- Binding of StAR to Synthetic Membranes Suggests an Active Molten Globule (2001) (10)
- Effects of anticonvulsants on human p450c17 (17alpha-hydroxylase/17,20 lyase) and 3beta-hydroxysteroid dehydrogenase type 2. (2005) (10)
- Genetic and Clinical Features of P 450 Oxidoreductase Deficiency (2008) (9)
- Creation and activity of COS-1 cells stably expressing the F2 fusion of the human cholesterol side-chain cleavage enzyme system. (2001) (9)
- Steroid 17alpha-hydroxylase deficiency--not rare everywhere. (2004) (9)
- Disorders of the Human Adrenal Cortex (2008) (8)
- Role of cytochrome b5 in the 17,20-lyase activity of P450c17. (2000) (8)
- Interaction of Catalytic Domains in Cytochrome P450scc–Adrenodoxin Reductase–Adrenodoxin Fusion Protein Imported into Yeast Mitochondria (2000) (8)
- Potential Relevance of Mullerian-Inhibiting Substance to Ovarian Physiology (1989) (8)
- Tenascin-X—Discovery and Early Research (2021) (7)
- Analysis of the duplicated human C4/P450c21/X gene cluster (1992) (7)
- Potential role of increased oxygenation in altering perinatal adrenal steroidogenesis (2015) (6)
- Electron transfer by human wild-type and A287P mutant P450 oxidoreductase assessed by transient kinetics: functional basis of P450 oxidoreductase deficiency. (2015) (6)
- CHAPTER 24 – Rickets Due to Hereditary Abnormalities of Vitamin D Synthesis or Action (2003) (6)
- Naturally-occurring mutation in the calcium-sensing receptor reveals the significance of extracellular domain loop III region for class C G-protein-coupled receptor function. (2010) (6)
- P45OXXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasia (5)
- Hybridization of the complementary mRNAs for P450c21 (steroid 21-hydroxylase) and tenascin-X is prevented by sequence-specific binding of nuclear proteins. (1995) (5)
- Restoration of hemorrhaged plasma volume by gastrointestinal fluid in the dog. (1978) (5)
- An Approach to the Molecular Biology of Congenital Adrenal Hyperplasia a (1985) (4)
- Regulation of β-chain mRNA of ovine follicle-stimulating hormone by 17β-estradiol (2004) (4)
- HumanP450scc GeneTranscription IsInduced byCyclic AMP and Repressed by12-O-Tetradecanoylphorbol-13-Acetate andA23187 through Independent cisElements (1990) (4)
- Biochemistry and Genetics of Human P450c17 (2000) (4)
- Steroidogenic electron-transfer factors and their diseases (2021) (4)
- Hereditary rickets revealed. (1998) (4)
- 17α-Hydroxylase/17, 20-Lyase Deficiency (2004) (4)
- Response to Letter to the Editor: "Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline". (2019) (4)
- Congenital adrenal hyperplasia in the adult patient. (1999) (4)
- P450c17—The Qualitative Regulator of Steroidogenesis (1999) (3)
- The First Defect in Electron Transfer to Mitochondrial P450 Enzymes. (2016) (3)
- Characterization of the Protein Responsible for the Acute Regulation of Steroidogenesis in Mouse Leydig Tumor Cells (1996) (3)
- THE MOLECULAR BASIS OF ISOLATED 17,20 LYASE DEFICIENCY. • 519 (1996) (3)
- Disorders in the Initial Steps in Steroidogenesis (2014) (3)
- A Novel Mitochondrial Complex of Aldosterone Synthase, Steroidogenic Acute Regulatory Protein, and Tom22 Synthesizes Aldosterone in the Rat Heart (2021) (3)
- Cinnamic acid based thiazolidinediones inhibit human P 450 c 17 and 3-hydroxysteroid dehydrogenase and improve insulin sensitivity independent of PPAR agonist activity (2004) (3)
- Adrenocortical carcinoma in a 17th-century girl (2017) (3)
- Medroxyprogesterone Acetate (MPA) Inhibits Pituitary-Independent Steroidogenesis by Inhibiting 3 β-Hydroxysteroid Dehydrogenase Type II (3 β-HSDII) (1999) (2)
- Genetic Disorders Of Vitamin D Synthesis and Action (2018) (2)
- Mechanism and consequences of the duplication of the human C4/P450c21/gene X locus (1992) (2)
- Activity and Cyclic Adenosine 3',5'-Monophosphate Responsiveness of the Human Cytochrome P45Oscc Promoter Transfected into MA- 10 Leydig Cells* (1993) (2)
- A novel mitochondrial complex of P450c11AS, StAR and Tom22 synthesizes aldosterone in the rat heart. (2021) (2)
- P450 oxidoreductase: genotyping, expression, purification of recombinant protein, and activity assessments of wild-type and mutant protein. (2013) (2)
- History of adrenal research: from ancient anatomy to contemporary molecular biology. (2022) (2)
- A Brief History of Congenital Adrenal Hyperplasia (2022) (2)
- Evolution and Regulation of Genes for Growth Hormone and Prolactin (1983) (2)
- Cloning of human adrenal and testis cDNAs (2)
- Chapter 33 – Genetic Disorders of Vitamin D Synthesis and Action (2013) (2)
- Rickets, Vitamin D, and Ca/P Metabolism (2022) (1)
- Errata (1910) (1)
- Chapter 97 – The Principles, Enzymes, and Pathways of Human Steroidogenesis (2016) (1)
- Evolution of the genes for growth hormone (GH) and Prolactin (Prl) (1981) (1)
- Responses of plasma renin activity and dopamine-beta-hydroxylase to increased intravascular volume (2005) (1)
- Mutation T318M in the CYP II B2 Gene Encoding P450c II AS (Aldosterone Synthase) Causes Corticosterone Methyl Oxidase 11 Deficiency (2007) (1)
- Marsupial pathway in humans (2013) (1)
- Proteins Involved in Mitochondrial Cholesterol Transport (2000) (1)
- Synthesis of biologically active proteins by recombinant DNA technology (1981) (1)
- Introduction to the 2016 Keith L. Parker Memorial Lecturer: Douglas M. Stocco, Ph.D. (2017) (1)
- HOMOZYGOUS DELETION OF AMINO ACIDS 487–489 IN P450c17 CAUSES SEVERE 17α-HYDROXYLASE (17-OH) DEFICIENCY (1993) (1)
- Structure of a bovine gene for P-450 c 21 ( steroid 21-hydroxylase ) defines a novel cytochrome P-450 gene family ( adrenal gland / steroid hormone / molecular evolution / DNA sequence ) (1)
- STEROID 21-HYDROXYLASE GENE ANALYSIS IN CONGENITAL ADRENAL HYPERPLASIA (1987) (0)
- Disorders of the adrenal cortex. (2008) (0)
- DNA... and Cell Biology: What's in a Name? (1990) (0)
- Processing of the precursor to corticotropin and j 3-lipotropin in humans ( immunoprecipitations / peptide analysis / peptide hormones / Nelson syndrome / ectopic corticotropin ) (0)
- Serine Phosphorylation, Insulin Resistance, and the Regulation of Androgen Synthesis (2007) (0)
- 437 MOLECULAR CLONING OF THE BOVINE 21 HYDROXYLASE GENE (1985) (0)
- 119 CLONING AND STRUCTURE OF THE BOVINE 21 HYDROXYLASE GENE (1985) (0)
- Endocrinologic, biochemical and histologic characterization of an ectopic ACTH producing carcinoma in childhood (1981) (0)
- In Memoriam: Melvin M. Grumbach, MD, (1925-2016) Pediatric Endocrinologist, Scientist, Educator, Leader. (2017) (0)
- THE TENASCIN-X GENE OVERLAPPING THE P450c21B GENE USES DIFFERENT PROMOTERS FOR ADRENAL, MUSCLE AND ADRENAL CARCINOMA EXPRESSION. • 583 (1996) (0)
- Processing of pro-opiocortin in Cushing tumors (1981) (0)
- Molecular Genetic Analysis of Human Vitamin D-Dependent Rickets Type 1(VDDR-1) by Direct Analysis of the CYP40 Gene • 714 (1998) (0)
- 431 MOLECULAR CLONING OF DNA COMPLEMENTARY TO BOVINE PROLACTIN MESSENGER RNA (1981) (0)
- MESSENGER RNA TRANSCRIPTION IN REGENERATING KIDNEY (1977) (0)
- Production of bovine pre-growthhormone and growth hormone (1996) (0)
- Phenotypic heterogeneity associated with the splicing mutation in congenital adrenal hyperplasia due to 21-hydroxylase deficiency. (1997) (0)
- Ambiguous Genitalia in the Newborn (2021) (0)
- CHANGES IN RNA DURING GROWTH OF KIDNEY (2003) (0)
- 315 ACTH-PRODUCING INTRACRANIAL TUMOR IN AN INFANT (1978) (0)
- Congenital Adrenal Hyperplasia and Adult Sexual Behavior-Reply (1997) (0)
- Congenital adrenal hyperplasia. (1986) (0)
- Chapter 2 / Adrenal and Ovarian Steroidogenesis 19 19 (2006) (0)
- “Antley-Bixler Syndrome”—A Reply to Cragun and Hopkin (2005) (0)
- Transcriptional Regulationof HumanGenesfor Steroidogenic Enzymes (1993) (0)
- Enzymologic Defect in the R347H and R358Q Mutations in P450c17 that Cause Selective 17,20-Lyase Deficiency • 425 (1998) (0)
- Molecular Cloning of DNA Complementary t< Bovine Growth (1980) (0)
- REGULATION OF mRNA FOR INSULIN-LIKE GROWTH FACTOR II (IGF-II) IN THE FETAL TESTIS (1987) (0)
- CLONING OF cDNA ENCODING BOVINE 21-HYDROXYLASE (1984) (0)
- Insulin like growth factor i messenger rna abundance during rat adrenal regeneration (1990) (0)
- Regulation of beta-chain mRNA of ovine follicle-stimulating hormone by 17 beta-estradiol. (1983) (0)
- A Brief History of the Pediatric Endocrine Society (PES) (2022) (0)
- Recombinant DNA technology: a fundamental tool for studying development. (1987) (0)
- A process for preparing a DNA transfer vector containing a sequence coding for growth hormone or oksepraevaekst (1981) (0)
- LEYDIG CELL TUMOR PRESENTING AS CONGENITAL ADRENAL HYPERPLASIA (CAH) (1987) (0)
- In Memoriam, Melvin M. Grumbach (1925–2016) (2017) (0)
- Regulation of growth hormone secretion and mRNA in the ovine fetus and neonate (1988) (0)
- Foerfarande Foer framstaellning of a DNA oeverfoeringsvektor vilken innehaoller of sequence I which encodes oxens vaexthormon eller foerstadiet of oxens vaexthormon (1981) (0)
- ABUNDANT ADRENAL-SPECTI IC TRANSCRIPTION OF THE P450c21A PSEUDOGENE—IMPLICATIONS FOR CONGENITAL ADRENAL HYPERPLASIA (1993) (0)
- COMPUTATIONAL MODEL OF HUMAN P450C17 (1999) (0)
- P450 Oxidoreductase Deficiency and Antley-Bixler Syndrome (2016) (0)
- 839 USE OF OLIGONUCLEOTIDES WITH NON-HUMAN SEQUENCES FOR PROBING HUMAN DNA (1985) (0)
- PRENATAL DIAGNOSIS OF CONGENITAL LIPOID ADRENAL HYPERPLASIA (LIPOID CAH) (1993) (0)
- Translation of messenger RNA from fetal and adult mouse kidney. (1979) (0)
- Celebrating 50 Years of the Pediatric Endocrine Society (PES): Histories of Pediatric Endocrine Topics (2022) (0)
- Human Tenascin-X Deficiency is a Cause of Ehlers-Danlos Syndrome. • 595 (1997) (0)
- In Memoriam: Melvin M. Grumbach (1925-2016). (2016) (0)
- Errata (1819) (0)
- CONGENITAL ADRENAL HYPERPLASIA AND ADULT SEXUAL BEHAVIOR. AUTHORS' REPLY (1997) (0)
- 84 STUDY OF THE HUMAN GENE FOR THE CHOLESTEROL SIDE- CHAIN CLEAVAGE ENZYME, P450SCC (20,22 DESMOLASE) IN CONGENITAL LIPOID ADRENAL HYPERPLASIA (1985) (0)
- Effect of Anticonvulsants on Activities of P450c17 and 3βHSDII (2004) (0)
- Partial Loss-of-Function Mutations in the Steroidogenic Acute Regulatory Clinical, Genetic, and Functional Characterization of Four Patients Carrying (2010) (0)
- Session Summary (2004) (0)
- SAT-562 Angiotensin II Induces Aldosterone Synthesis in the Rat Heart Stressed by Angiotensin II (2020) (0)
- In Memoriam: Melvin M. Grumbach (1925-2016). (2016) (0)
- Phosphate Carrier Protein Contact with Mitochondrial VDAC 1 and Steroidogenic Activity of StAR Requires and Biogenesis : Membrane Transport , Structure , Function (2008) (0)
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