Curnow KM - Search Results

1

Recombinant CYP11B genes encode enzymes that can catalyze conversion of 11-deoxycortisol to cortisol, 18-hydroxycortisol, and 18-oxocortisol.

Mulatero P, Curnow KM, Aupetit-Faisant B, Foekling M, Gomez-Sanchez C, Veglio F, Jeunemaitre X, Corvol P, Pascoe L. Mulatero P, et al. Among authors: curnow km. J Clin Endocrinol Metab. 1998 Nov;83(11):3996-4001. doi: 10.1210/jcem.83.11.5237. J Clin Endocrinol Metab. 1998. PMID: 9814482

2

Structural analysis and evaluation of the aldosterone synthase gene in hypertension.

Brand E, Chatelain N, Mulatero P, Féry I, Curnow K, Jeunemaitre X, Corvol P, Pascoe L, Soubrier F. Brand E, et al. Hypertension. 1998 Aug;32(2):198-204. doi: 10.1161/01.hyp.32.2.198. Hypertension. 1998. PMID: 9719043

3

Glucocorticoid-suppressible hyperaldosteronism and adrenal tumors occurring in a single French pedigree.

Pascoe L, Jeunemaitre X, Lebrethon MC, Curnow KM, Gomez-Sanchez CE, Gasc JM, Saez JM, Corvol P. Pascoe L, et al. Among authors: curnow km. J Clin Invest. 1995 Nov;96(5):2236-46. doi: 10.1172/JCI118279. J Clin Invest. 1995. PMID: 7593610 Free PMC article.

4

Genetic recombination as a cause of inherited disorders of aldosterone and cortisol biosynthesis and a contributor to genetic variation in blood pressure.

Pascoe L, Curnow KM. Pascoe L, et al. Among authors: curnow km. Steroids. 1995 Jan;60(1):22-7. doi: 10.1016/0039-128x(94)00003-u. Steroids. 1995. PMID: 7792811 Review.

5

Isolated aldosterone synthase deficiency caused by simultaneous E198D and V386A mutations in the CYP11B2 gene.

Portrat-Doyen S, Tourniaire J, Richard O, Mulatero P, Aupetit-Faisant B, Curnow KM, Pascoe L, Morel Y. Portrat-Doyen S, et al. Among authors: curnow km. J Clin Endocrinol Metab. 1998 Nov;83(11):4156-61. doi: 10.1210/jcem.83.11.5258. J Clin Endocrinol Metab. 1998. PMID: 9814506

6

Deletion hybrid genes, due to unequal crossing over between CYP11B1 (11beta-hydroxylase) and CYP11B2(aldosterone synthase) cause steroid 11beta-hydroxylase deficiency and congenital adrenal hyperplasia.

Portrat S, Mulatero P, Curnow KM, Chaussain JL, Morel Y, Pascoe L. Portrat S, et al. Among authors: curnow km. J Clin Endocrinol Metab. 2001 Jul;86(7):3197-201. doi: 10.1210/jcem.86.7.7671. J Clin Endocrinol Metab. 2001. PMID: 11443188

7

Alternatively spliced human type 1 angiotensin II receptor mRNAs are translated at different efficiencies and encode two receptor isoforms.

Curnow KM, Pascoe L, Davies E, White PC, Corvol P, Clauser E. Curnow KM, et al. Mol Endocrinol. 1995 Sep;9(9):1250-62. doi: 10.1210/mend.9.9.7491117. Mol Endocrinol. 1995. PMID: 7491117

8

Disorders of steroid 11 beta-hydroxylase isozymes.

White PC, Curnow KM, Pascoe L. White PC, et al. Among authors: curnow km. Endocr Rev. 1994 Aug;15(4):421-38. doi: 10.1210/edrv-15-4-421. Endocr Rev. 1994. PMID: 7988480 Review.

9

The amino acid substitutions Ser288Gly and Val320Ala convert the cortisol producing enzyme, CYP11B1, into an aldosterone producing enzyme.

Curnow KM, Mulatero P, Emeric-Blanchouin N, Aupetit-Faisant B, Corvol P, Pascoe L. Curnow KM, et al. Nat Struct Biol. 1997 Jan;4(1):32-5. doi: 10.1038/nsb0197-32. Nat Struct Biol. 1997. PMID: 8989319

10

Prenatal diagnosis and treatment of 11beta-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitalia.

Cerame BI, Newfield RS, Pascoe L, Curnow KM, Nimkarn S, Roe TF, New MI, Wilson RC. Cerame BI, et al. Among authors: curnow km. J Clin Endocrinol Metab. 1999 Sep;84(9):3129-34. doi: 10.1210/jcem.84.9.5976. J Clin Endocrinol Metab. 1999. PMID: 10487675

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