Achermann JC - Search Results

1

Analysis of genetic variability in Turner syndrome linked to long-term clinical features.

Suntharalingham JP, Ishida M, Cameron-Pimblett A, McGlacken-Byrne SM, Buonocore F, Del Valle I, Madhan GK, Brooks T, Conway GS, Achermann JC. Suntharalingham JP, et al. Among authors: achermann jc. Front Endocrinol (Lausanne). 2023 Sep 20;14:1227164. doi: 10.3389/fendo.2023.1227164. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37800145 Free PMC article.

2

Mutational analysis of DAX1 in patients with hypogonadotropic hypogonadism or pubertal delay.

Achermann JC, Gu WX, Kotlar TJ, Meeks JJ, Sabacan LP, Seminara SB, Habiby RL, Hindmarsh PC, Bick DP, Sherins RJ, Crowley WF Jr, Layman LC, Jameson JL. Achermann JC, et al. J Clin Endocrinol Metab. 1999 Dec;84(12):4497-500. doi: 10.1210/jcem.84.12.6269. J Clin Endocrinol Metab. 1999. PMID: 10599708

3

Clinical and functional effects of mutations in the DAX-1 gene in patients with adrenal hypoplasia congenita.

Reutens AT, Achermann JC, Ito M, Ito M, Gu WX, Habiby RL, Donohoue PA, Pang S, Hindmarsh PC, Jameson JL. Reutens AT, et al. Among authors: achermann jc. J Clin Endocrinol Metab. 1999 Feb;84(2):504-11. doi: 10.1210/jcem.84.2.5468. J Clin Endocrinol Metab. 1999. PMID: 10022408 Free article.

4

Advances in the molecular genetics of hypogonadotropic hypogonadism.

Achermann JC, Jameson JL. Achermann JC, et al. J Pediatr Endocrinol Metab. 2001 Jan;14(1):3-15. doi: 10.1515/jpem.2001.14.1.3. J Pediatr Endocrinol Metab. 2001. PMID: 11220702 Review.

5

Birth weight influences the initial response to growth hormone treatment in growth hormone-insufficient children.

Achermann JC, Hamdani K, Hindmarsh PC, Brook CG. Achermann JC, et al. Pediatrics. 1998 Aug;102(2 Pt 1):342-5. doi: 10.1542/peds.102.2.342. Pediatrics. 1998. PMID: 9685436

6

Aromatase (Cyp19) expression is up-regulated by targeted disruption of Dax1.

Wang ZJ, Jeffs B, Ito M, Achermann JC, Yu RN, Hales DB, Jameson JL. Wang ZJ, et al. Among authors: achermann jc. Proc Natl Acad Sci U S A. 2001 Jul 3;98(14):7988-93. doi: 10.1073/pnas.141543298. Epub 2001 Jun 26. Proc Natl Acad Sci U S A. 2001. PMID: 11427738 Free PMC article.

7

X-linked adrenal hypoplasia congenita: a mutation in DAX1 expands the phenotypic spectrum in males and females.

Seminara SB, Achermann JC, Genel M, Jameson JL, Crowley WF Jr. Seminara SB, et al. Among authors: achermann jc. J Clin Endocrinol Metab. 1999 Dec;84(12):4501-9. doi: 10.1210/jcem.84.12.6172. J Clin Endocrinol Metab. 1999. PMID: 10599709

8

A novel mutation in DAX1 causes delayed-onset adrenal insufficiency and incomplete hypogonadotropic hypogonadism.

Tabarin A, Achermann JC, Recan D, Bex V, Bertagna X, Christin-Maitre S, Ito M, Jameson JL, Bouchard P. Tabarin A, et al. Among authors: achermann jc. J Clin Invest. 2000 Feb;105(3):321-8. doi: 10.1172/JCI7212. J Clin Invest. 2000. PMID: 10675358 Free PMC article.

9

A naturally occurring steroidogenic factor-1 mutation exhibits differential binding and activation of target genes.

Ito M, Achermann JC, Jameson JL. Ito M, et al. Among authors: achermann jc. J Biol Chem. 2000 Oct 13;275(41):31708-14. doi: 10.1074/jbc.M002892200. J Biol Chem. 2000. PMID: 10913126 Free article.

10

Fertility and infertility: genetic contributions from the hypothalamic-pituitary-gonadal axis.

Achermann JC, Jameson JL. Achermann JC, et al. Mol Endocrinol. 1999 Jun;13(6):812-8. doi: 10.1210/mend.13.6.0301. Mol Endocrinol. 1999. PMID: 10379880 Review. No abstract available.

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