Jeske YW - Search Results

1

Genomic structure of the human gene for protein kinase A regulatory subunit R1-beta (PRKAR1B) on 7p22: no evidence for mutations in familial hyperaldosteronism type II in a large affected kindred.

Elphinstone MS, Gordon RD, So A, Jeske YW, Stratakis CA, Stowasser M. Elphinstone MS, et al. Among authors: jeske yw. Clin Endocrinol (Oxf). 2004 Dec;61(6):716-23. doi: 10.1111/j.1365-2265.2004.02155.x. Clin Endocrinol (Oxf). 2004. PMID: 15579186

2

Further evidence for linkage of familial hyperaldosteronism type II at chromosome 7p22 in Italian as well as Australian and South American families.

Sukor N, Mulatero P, Gordon RD, So A, Duffy D, Bertello C, Kelemen L, Jeske Y, Veglio F, Stowasser M. Sukor N, et al. J Hypertens. 2008 Aug;26(8):1577-82. doi: 10.1097/HJH.0b013e3283028352. J Hypertens. 2008. PMID: 18622235

3

Examination of chromosome 7p22 candidate genes RBaK, PMS2 and GNA12 in familial hyperaldosteronism type II.

Jeske YW, So A, Kelemen L, Sukor N, Willys C, Bulmer B, Gordon RD, Duffy D, Stowasser M. Jeske YW, et al. Clin Exp Pharmacol Physiol. 2008 Apr;35(4):380-5. doi: 10.1111/j.1440-1681.2008.04882.x. Clin Exp Pharmacol Physiol. 2008. PMID: 18307725

4

Familial hyperaldosteronism type II is linked to the chromosome 7p22 region but also shows predicted heterogeneity.

So A, Duffy DL, Gordon RD, Jeske YW, Lin-Su K, New MI, Stowasser M. So A, et al. Among authors: jeske yw. J Hypertens. 2005 Aug;23(8):1477-84. doi: 10.1097/01.hjh.0000174299.66369.26. J Hypertens. 2005. PMID: 16003173

5

No evidence for coding region mutations in the retinoblastoma-associated Kruppel-associated box protein gene (RBaK) causing familial hyperaldosteronism type II.

So A, Jeske YW, Gordon RD, Duffy D, Kelemen L, Stowasser M. So A, et al. Among authors: jeske yw. Clin Endocrinol (Oxf). 2006 Dec;65(6):829-31. doi: 10.1111/j.1365-2265.2006.02674.x. Clin Endocrinol (Oxf). 2006. PMID: 17121540 No abstract available.

6

Combined pituitary hormone deficiency in Australian children: clinical and genetic correlates.

McLennan K, Jeske Y, Cotterill A, Cowley D, Penfold J, Jones T, Howard N, Thomsett M, Choong C. McLennan K, et al. Clin Endocrinol (Oxf). 2003 Jun;58(6):785-94. doi: 10.1046/j.1365-2265.2003.01781.x. Clin Endocrinol (Oxf). 2003. PMID: 12780757

7

Sertoli-Leydig cell tumor of the ovary, a rare cause of precocious puberty in a 12-month-old infant.

Choong CS, Fuller PJ, Chu S, Jeske Y, Bowling F, Brown R, Borzi P, Balazs ND, Suppiah R, Cotterill AM, Payton D, Robertson DM, Burger HG. Choong CS, et al. J Clin Endocrinol Metab. 2002 Jan;87(1):49-56. doi: 10.1210/jcem.87.1.8162. J Clin Endocrinol Metab. 2002. PMID: 11788622

8

Androgen receptor genotyping in a large Australasian cohort with androgen insensitivity syndrome; identification of four novel mutations.

Jeske YW, McGown IN, Cowley DM, Oley C, Thomsett MJ, Choong CS, Cotterill AM. Jeske YW, et al. J Pediatr Endocrinol Metab. 2007 Aug;20(8):893-908. doi: 10.1515/jpem.2007.20.8.893. J Pediatr Endocrinol Metab. 2007. PMID: 17937062

9

Expression of a linear Sry transcript in the mouse genital ridge.

Jeske YW, Bowles J, Greenfield A, Koopman P. Jeske YW, et al. Nat Genet. 1995 Aug;10(4):480-2. doi: 10.1038/ng0895-480. Nat Genet. 1995. PMID: 7670499

10

21-hydroxylase genotyping in Australasian patients with congenital adrenal hyperplasia.

Jeske YW, McGown IN, Harris M, Bowling FG, Choong CS, Cowley DM, Cotterill AM. Jeske YW, et al. J Pediatr Endocrinol Metab. 2009 Feb;22(2):127-41. doi: 10.1515/jpem.2009.22.2.127. J Pediatr Endocrinol Metab. 2009. PMID: 19449670 Free article.

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