Taymans S - Search Results

1

Developmental focus on disorders of sex development: special issue overview.

Freund LS, Taymans S, Wehr E, Stratakis CA. Freund LS, et al. Among authors: taymans s. Horm Metab Res. 2015 May;47(5):309-11. doi: 10.1055/s-0035-1549880. Epub 2015 May 13. Horm Metab Res. 2015. PMID: 25970708 No abstract available.

2

Structure of the gene coding for calcineurin B (PPP3R1) and mapping to D2S358-D2S1778 (chromosomal region 2p15).

Stratakis CA, Taymans SE. Stratakis CA, et al. Among authors: taymans se. DNA Seq. 1998;9(4):227-30. doi: 10.3109/10425179809105209. DNA Seq. 1998. PMID: 10520753

3

Chromosome 2 (2p16) abnormalities in Carney complex tumours.

Matyakhina L, Pack S, Kirschner LS, Pak E, Mannan P, Jaikumar J, Taymans SE, Sandrini F, Carney JA, Stratakis CA. Matyakhina L, et al. Among authors: taymans se. J Med Genet. 2003 Apr;40(4):268-77. doi: 10.1136/jmg.40.4.268. J Med Genet. 2003. PMID: 12676898 Free PMC article.

4

Familial hyperaldosteronism type II: description of a large kindred and exclusion of the aldosterone synthase (CYP11B2) gene.

Torpy DJ, Gordon RD, Lin JP, Huggard PR, Taymans SE, Stowasser M, Chrousos GP, Stratakis CA. Torpy DJ, et al. Among authors: taymans se. J Clin Endocrinol Metab. 1998 Sep;83(9):3214-8. doi: 10.1210/jcem.83.9.5086. J Clin Endocrinol Metab. 1998. PMID: 9745430

5

Characterization of the adrenal gland pathology of Carney complex, and molecular genetics of the disease.

Kirschner LS, Taymans SE, Stratakis CA. Kirschner LS, et al. Among authors: taymans se. Endocr Res. 1998 Aug-Nov;24(3-4):863-4. doi: 10.3109/07435809809032698. Endocr Res. 1998. PMID: 9888588 No abstract available.

6

Radiation hybrid mapping of chromosomal region 2p15-p16: integration of expressed and polymorphic sequences maps at the Carney complex (CNC) and Doyne honeycomb retinal dystrophy (DHRD) loci.

Taymans SE, Kirschner LS, Giatzakis C, Stratakis CA. Taymans SE, et al. Genomics. 1999 Mar 15;56(3):344-9. doi: 10.1006/geno.1998.5720. Genomics. 1999. PMID: 10087203

7

The human vitamin D receptor gene (VDR) is localized to region 12cen-q12 by fluorescent in situ hybridization and radiation hybrid mapping: genetic and physical VDR map.

Taymans SE, Pack S, Pak E, Orban Z, Barsony J, Zhuang Z, Stratakis CA. Taymans SE, et al. J Bone Miner Res. 1999 Jul;14(7):1163-6. doi: 10.1359/jbmr.1999.14.7.1163. J Bone Miner Res. 1999. PMID: 10404016 Free article.

8

Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex.

Kirschner LS, Carney JA, Pack SD, Taymans SE, Giatzakis C, Cho YS, Cho-Chung YS, Stratakis CA. Kirschner LS, et al. Among authors: taymans se. Nat Genet. 2000 Sep;26(1):89-92. doi: 10.1038/79238. Nat Genet. 2000. PMID: 10973256

9

Anisomastia associated with interstitial duplication of chromosome 16, mental retardation, obesity, dysmorphic facies, and digital anomalies: molecular mapping of a new syndrome by fluorescent in situ hybridization and microsatellites to 16q13 (D16S419-D16S503).

Stratakis CA, Lafferty A, Taymans SE, Gafni RI, Meck JM, Blancato J. Stratakis CA, et al. Among authors: taymans se. J Clin Endocrinol Metab. 2000 Sep;85(9):3396-401. doi: 10.1210/jcem.85.9.6776. J Clin Endocrinol Metab. 2000. PMID: 10999840

10

A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22).

Lafferty AR, Torpy DJ, Stowasser M, Taymans SE, Lin JP, Huggard P, Gordon RD, Stratakis CA. Lafferty AR, et al. Among authors: taymans se. J Med Genet. 2000 Nov;37(11):831-5. doi: 10.1136/jmg.37.11.831. J Med Genet. 2000. PMID: 11073536 Free PMC article.

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