Duriez B - Search Results

1

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: duriez b. Acta Paediatr Suppl. 1992 Sep;383:132-3. Acta Paediatr Suppl. 1992. PMID: 1458008 Review. No abstract available.

2

[Molecular genetics of growth hormone resistance syndrome].

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

3

An exon-skipping mutation in the btk gene of a patient with X-linked agammaglobulinemia and isolated growth hormone deficiency.

Duriez B, Duquesnoy P, Dastot F, Bougnères P, Amselem S, Goossens M. Duriez B, et al. FEBS Lett. 1994 Jun 13;346(2-3):165-70. doi: 10.1016/0014-5793(94)00457-9. FEBS Lett. 1994. PMID: 8013627 Free article.

4

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: duriez b. 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.

5

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. Mol Endocrinol. 1993 Jun;7(6):806-14. doi: 10.1210/mend.7.6.8361502. Mol Endocrinol. 1993. PMID: 8361502

6

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: duriez b. 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.

7

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: duriez b. Hum Mol Genet. 1993 Apr;2(4):355-9. doi: 10.1093/hmg/2.4.355. Hum Mol Genet. 1993. PMID: 8504296

8

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: duriez b. 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.

9

Alternatively spliced forms in the cytoplasmic domain of the human growth hormone (GH) receptor regulate its ability to generate a soluble GH-binding protein.

Dastot F, Sobrier ML, Duquesnoy P, Duriez B, Goossens M, Amselem S. Dastot F, et al. Among authors: duriez b. Proc Natl Acad Sci U S A. 1996 Oct 1;93(20):10723-8. doi: 10.1073/pnas.93.20.10723. Proc Natl Acad Sci U S A. 1996. PMID: 8855247 Free PMC article.

10

Isolation of several human axonemal dynein heavy chain genes: genomic structure of the catalytic site, phylogenetic analysis and chromosomal assignment.

Chapelin C, Duriez B, Magnino F, Goossens M, Escudier E, Amselem S. Chapelin C, et al. Among authors: duriez b. FEBS Lett. 1997 Jul 28;412(2):325-30. doi: 10.1016/s0014-5793(97)00800-4. FEBS Lett. 1997. PMID: 9256245 Free article.

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