Pandey AV - Search Results

1

The cytochrome P450 aromatase lacking exon 5 is associated with a phenotype of nonclassic aromatase deficiency and is also present in normal human steroidogenic tissues.

Pepe CM, Saraco NI, Baquedano MS, Guercio G, Vaiani E, Marino R, Pandey AV, Flück CE, Rivarola MA, Belgorosky A. Pepe CM, et al. Among authors: pandey av. Clin Endocrinol (Oxf). 2007 Nov;67(5):698-705. doi: 10.1111/j.1365-2265.2007.02948.x. Epub 2007 Jul 2. Clin Endocrinol (Oxf). 2007. PMID: 17608756

2

Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome.

Flück CE, Tajima T, Pandey AV, Arlt W, Okuhara K, Verge CF, Jabs EW, Mendonça BB, Fujieda K, Miller WL. Flück CE, et al. Among authors: pandey av. Nat Genet. 2004 Mar;36(3):228-30. doi: 10.1038/ng1300. Epub 2004 Feb 1. Nat Genet. 2004. PMID: 14758361

3

P450 oxidoreductase deficiency.

Miller WL, Huang N, Flück CE, Pandey AV. Miller WL, et al. Among authors: pandey av. Lancet. 2004 Nov 6-12;364(9446):1663. doi: 10.1016/S0140-6736(04)17344-3. Lancet. 2004. PMID: 15530620 No abstract available.

4

P450 oxidoreductase deficiency: a new disorder of steroidogenesis affecting all microsomal P450 enzymes.

Pandey AV, Flück CE, Huang N, Tajima T, Fujieda K, Miller WL. Pandey AV, et al. Endocr Res. 2004 Nov;30(4):881-8. doi: 10.1081/erc-200044134. Endocr Res. 2004. PMID: 15666840

5

Diversity and function of mutations in p450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesis.

Huang N, Pandey AV, Agrawal V, Reardon W, Lapunzina PD, Mowat D, Jabs EW, Van Vliet G, Sack J, Flück CE, Miller WL. Huang N, et al. Among authors: pandey av. Am J Hum Genet. 2005 May;76(5):729-49. doi: 10.1086/429417. Epub 2005 Mar 25. Am J Hum Genet. 2005. PMID: 15793702 Free PMC article.

6

P450 oxidoreductase deficiency: a new disorder of steroidogenesis.

Miller WL, Huang N, Pandey AV, Flück CE, Agrawal V. Miller WL, et al. Among authors: pandey av. Ann N Y Acad Sci. 2005 Dec;1061:100-8. doi: 10.1196/annals.1336.012. Ann N Y Acad Sci. 2005. PMID: 16467261 Review.

7

Clinical and biochemical description of a novel CYP21A2 gene mutation 962_963insA using a new 3D model for the P450c21 protein.

Janner M, Pandey AV, Mullis PE, Flück CE. Janner M, et al. Among authors: pandey av. Eur J Endocrinol. 2006 Jul;155(1):143-51. doi: 10.1530/eje.1.02172. Eur J Endocrinol. 2006. PMID: 16793961

8

Modulation of human CYP19A1 activity by mutant NADPH P450 oxidoreductase.

Pandey AV, Kempná P, Hofer G, Mullis PE, Flück CE. Pandey AV, et al. Mol Endocrinol. 2007 Oct;21(10):2579-95. doi: 10.1210/me.2007-0245. Epub 2007 Jun 26. Mol Endocrinol. 2007. PMID: 17595315

9

Clinical, structural and functional implications of mutations and polymorphisms in human NADPH P450 oxidoreductase.

Flück CE, Nicolo C, Pandey AV. Flück CE, et al. Among authors: pandey av. Fundam Clin Pharmacol. 2007 Aug;21(4):399-410. doi: 10.1111/j.1472-8206.2007.00520.x. Fundam Clin Pharmacol. 2007. PMID: 17635179 Review.

10

P450 oxidoreductase deficiency - a new form of congenital adrenal hyperplasia.

Flück CE, Pandey AV, Huang N, Agrawal V, Miller WL. Flück CE, et al. Among authors: pandey av. Endocr Dev. 2008;13:67-81. doi: 10.1159/000134826. Endocr Dev. 2008. PMID: 18493134 Review.

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