Goossens M - Search Results

1

Molecular genetics of Laron-type GH insensitivity syndrome.

Goossens M, Amselem S, Duquesnoy P, Sobrier ML. Goossens M, et al. Recent Prog Horm Res. 1993;48:165-78. doi: 10.1016/b978-0-12-571148-7.50010-5. Recent Prog Horm Res. 1993. PMID: 8441847 Review. No abstract available.

2

A single amino acid substitution in the exoplasmic domain of the human growth hormone (GH) receptor confers familial GH resistance (Laron syndrome) with positive GH-binding activity by abolishing receptor homodimerization.

Duquesnoy P, Sobrier ML, Duriez B, Dastot F, Buchanan CR, Savage MO, Preece MA, Craescu CT, Blouquit Y, Goossens M, et al. Duquesnoy P, et al. Among authors: goossens m. EMBO J. 1994 Mar 15;13(6):1386-95. doi: 10.1002/j.1460-2075.1994.tb06392.x. EMBO J. 1994. PMID: 8137822 Free PMC article.

3

A naturally occurring growth hormone receptor mutation: in vivo and in vitro evidence for the functional importance of the WS motif common to all members of the cytokine receptor superfamily.

Duriez B, Sobrier ML, Duquesnoy P, Tixier-Boichard M, Decuypere E, Coquerelle G, Zeman M, Goossens M, Amselem S. Duriez B, et al. Among authors: goossens m. Mol Endocrinol. 1993 Jun;7(6):806-14. doi: 10.1210/mend.7.6.8361502. Mol Endocrinol. 1993. PMID: 8361502

4

Expression and binding properties of two isoforms of the human growth hormone receptor.

Sobrier ML, Duquesnoy P, Duriez B, Amselem S, Goossens M. Sobrier ML, et al. Among authors: goossens m. FEBS Lett. 1993 Mar 15;319(1-2):16-20. doi: 10.1016/0014-5793(93)80028-s. FEBS Lett. 1993. PMID: 8454051 Free article.

5

Spectrum of growth hormone receptor mutations and associated haplotypes in Laron syndrome.

Amselem S, Duquesnoy P, Duriez B, Dastot F, Sobrier ML, Valleix S, Goossens M. Amselem S, et al. Among authors: goossens m. Hum Mol Genet. 1993 Apr;2(4):355-9. doi: 10.1093/hmg/2.4.355. Hum Mol Genet. 1993. PMID: 8504296

6

Molecular basis of inherited growth hormone resistance in childhood.

Amselem S, Sobrier ML, Dastot F, Duquesnoy P, Duriez B, Goossens M. Amselem S, et al. Among authors: goossens m. Baillieres Clin Endocrinol Metab. 1996 Jul;10(3):353-69. doi: 10.1016/s0950-351x(96)80485-x. Baillieres Clin Endocrinol Metab. 1996. PMID: 8853444 Review.

7

Nine novel growth hormone receptor gene mutations in patients with Laron syndrome.

Sobrier ML, Dastot F, Duquesnoy P, Kandemir N, Yordam N, Goossens M, Amselem S. Sobrier ML, et al. Among authors: goossens m. J Clin Endocrinol Metab. 1997 Feb;82(2):435-7. doi: 10.1210/jcem.82.2.3725. J Clin Endocrinol Metab. 1997. PMID: 9024232

8

[Molecular genetics of growth hormone resistance syndrome].

Amselem S, Duriez B, Duquesnoy P, Sobrier ML, Goossens M. Amselem S, et al. Among authors: goossens m. C R Seances Soc Biol Fil. 1992;186(4):354-62. C R Seances Soc Biol Fil. 1992. PMID: 1301223 Review. French.

9

Point mutations in the growth hormone receptor gene of patients with Laron syndrome.

Amselem S, Duriez B, Sobrier ML, Duquesnoy P, Goossens M. Amselem S, et al. Among authors: goossens m. Acta Paediatr Suppl. 1992 Sep;383:132-3. Acta Paediatr Suppl. 1992. PMID: 1458008 Review. No abstract available.

10

Defective membrane expression of human growth hormone (GH) receptor causes Laron-type GH insensitivity syndrome.

Duquesnoy P, Sobrier ML, Amselem S, Goossens M. Duquesnoy P, et al. Among authors: goossens m. Proc Natl Acad Sci U S A. 1991 Nov 15;88(22):10272-6. doi: 10.1073/pnas.88.22.10272. Proc Natl Acad Sci U S A. 1991. PMID: 1719554 Free PMC article.

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