Gribouval O - Search Results

1

Absence of cell surface expression of human ACE leads to perinatal death.

Michaud A, Acharya KR, Masuyer G, Quenech'du N, Gribouval O, Morinière V, Gubler MC, Corvol P. Michaud A, et al. Among authors: gribouval o. Hum Mol Genet. 2014 Mar 15;23(6):1479-91. doi: 10.1093/hmg/ddt535. Epub 2013 Oct 24. Hum Mol Genet. 2014. PMID: 24163131 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: gribouval o. 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: gribouval o. Pediatr Nephrol. 1996 Apr;10(2):135-8. doi: 10.1007/BF00862052. Pediatr Nephrol. 1996. PMID: 8703694

4

NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome.

Boute N, Gribouval O, Roselli S, Benessy F, Lee H, Fuchshuber A, Dahan K, Gubler MC, Niaudet P, Antignac C. Boute N, et al. Among authors: gribouval o. Nat Genet. 2000 Apr;24(4):349-54. doi: 10.1038/74166. Nat Genet. 2000. PMID: 10742096

5

Podocin localizes in the kidney to the slit diaphragm area.

Roselli S, Gribouval O, Boute N, Sich M, Benessy F, Attié T, Gubler MC, Antignac C. Roselli S, et al. Among authors: gribouval o. Am J Pathol. 2002 Jan;160(1):131-9. doi: 10.1016/S0002-9440(10)64357-X. Am J Pathol. 2002. PMID: 11786407 Free PMC article.

6

NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.

Weber S, Gribouval O, Esquivel EL, Morinière V, Tête MJ, Legendre C, Niaudet P, Antignac C. Weber S, et al. Among authors: gribouval o. Kidney Int. 2004 Aug;66(2):571-9. doi: 10.1111/j.1523-1755.2004.00776.x. Kidney Int. 2004. PMID: 15253708 Free article.

7

[Mutations in genes in the renin-angiotensin system and renal tubular dysgenesis].

Gribouval O, Antignac C, Gubler MC. Gribouval O, et al. Med Sci (Paris). 2006 Mar;22(3):246-8. doi: 10.1051/medsci/2006223246. Med Sci (Paris). 2006. PMID: 16527202 Free article. French. No abstract available.

8

Inherited renal tubular dysgenesis: the first patients surviving the neonatal period.

Zingg-Schenk A, Bacchetta J, Corvol P, Michaud A, Stallmach T, Cochat P, Gribouval O, Gubler MC, Neuhaus TJ. Zingg-Schenk A, et al. Among authors: gribouval o. Eur J Pediatr. 2008 Mar;167(3):311-6. doi: 10.1007/s00431-007-0492-1. Epub 2007 Apr 19. Eur J Pediatr. 2008. PMID: 17443344 Free article.

9

Can we live without a functional renin-angiotensin system?

Corvol P, Michaud A, Gribouval O, Gasc JM, Gubler MC. Corvol P, et al. Among authors: gribouval o. Clin Exp Pharmacol Physiol. 2008 Apr;35(4):431-3. doi: 10.1111/j.1440-1681.2008.04891.x. Clin Exp Pharmacol Physiol. 2008. PMID: 18307735

10

[Mutations in renin-angiotensin system genes and kidney developmental anomalies].

Gubler MC, Gribouval O, Morinière V, Pawtowski A, Antignac C. Gubler MC, et al. Among authors: gribouval o. J Soc Biol. 2009;203(4):311-8. doi: 10.1051/jbio/2009035. Epub 2010 Feb 1. J Soc Biol. 2009. PMID: 20122389 Review. French.

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