Jean G - Search Results

1

High-resolution mapping of the gene for cystinosis, using combined biochemical and linkage analysis.

Jean G, Fuchshuber A, Town MM, Gribouval O, Schneider JA, Broyer M, van't Hoff W, Niaudet P, Antignac C. Jean G, et al. Am J Hum Genet. 1996 Mar;58(3):535-43. Am J Hum Genet. 1996. PMID: 8644713 Free PMC article.

2

Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis.

Fuchshuber A, Jean G, Gribouval O, Gubler MC, Broyer M, Beckmann JS, Niaudet P, Antignac C. Fuchshuber A, et al. Among authors: jean g. Hum Mol Genet. 1995 Nov;4(11):2155-8. doi: 10.1093/hmg/4.11.2155. Hum Mol Genet. 1995. PMID: 8589695

3

Congenital nephrotic syndrome of the Finnish type: linkage to the locus in a non-Finnish population.

Fuchshuber A, Niaudet P, Gribouval O, Jean G, Gubler MC, Broyer M, Antignac C. Fuchshuber A, et al. Among authors: jean g. Pediatr Nephrol. 1996 Apr;10(2):135-8. doi: 10.1007/BF00862052. Pediatr Nephrol. 1996. PMID: 8703694

4

Molecular characterization of CTNS deletions in nephropathic cystinosis: development of a PCR-based detection assay.

Forestier L, Jean G, Attard M, Cherqui S, Lewis C, van't Hoff W, Broyer M, Town M, Antignac C. Forestier L, et al. Among authors: jean g. Am J Hum Genet. 1999 Aug;65(2):353-9. doi: 10.1086/302509. Am J Hum Genet. 1999. PMID: 10417278 Free PMC article.

5

Severity of phenotype in cystinosis varies with mutations in the CTNS gene: predicted effect on the model of cystinosin.

Attard M, Jean G, Forestier L, Cherqui S, van't Hoff W, Broyer M, Antignac C, Town M. Attard M, et al. Among authors: jean g. Hum Mol Genet. 1999 Dec;8(13):2507-14. doi: 10.1093/hmg/8.13.2507. Hum Mol Genet. 1999. PMID: 10556299

6

Characterization of a putative founder mutation that accounts for the high incidence of cystinosis in Brittany.

Kalatzis V, Cherqui S, Jean G, Cordier B, Cochat P, Broyer M, Antignac C. Kalatzis V, et al. Among authors: jean g. J Am Soc Nephrol. 2001 Oct;12(10):2170-2174. doi: 10.1681/ASN.V12102170. J Am Soc Nephrol. 2001. PMID: 11562417

7

A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis.

Town M, Jean G, Cherqui S, Attard M, Forestier L, Whitmore SA, Callen DF, Gribouval O, Broyer M, Bates GP, van't Hoff W, Antignac C. Town M, et al. Among authors: jean g. Nat Genet. 1998 Apr;18(4):319-24. doi: 10.1038/ng0498-319. Nat Genet. 1998. PMID: 9537412

8

[Intra-leukocyte cystine in cystinosis treated with cysteamine].

Ged C, Jean G, Tete MJ, Broyer M, Kamoun P. Ged C, et al. Among authors: jean g. Ann Biol Clin (Paris). 1991;49(9):482-6. Ann Biol Clin (Paris). 1991. PMID: 1789502 French.

9

Anti-OKT3 response following prophylactic treatment in paediatric kidney transplant recipients.

Niaudet P, Jean G, Broyer M, Chatenoud L. Niaudet P, et al. Among authors: jean g. Pediatr Nephrol. 1993 Jun;7(3):263-7. doi: 10.1007/BF00853215. Pediatr Nephrol. 1993. PMID: 8518095

10

Blood transfusions under cyclosporine coverage before renal transplantation in children.

Niaudet P, Bouvattier C, Gouda H, Mattlinger B, Caillat-Zucman S, Gagnadoux MF, Broyer M, Jean G. Niaudet P, et al. Among authors: jean g. Transplant Proc. 1995 Apr;27(2):1723-4. Transplant Proc. 1995. PMID: 7725470 No abstract available.

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