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Page 1
Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database.
Jeanpierre C, Denamur E, Henry I, Cabanis MO, Luce S, Cécille A, Elion J, Peuchmaur M, Loirat C, Niaudet P, Gubler MC, Junien C. Jeanpierre C, et al. Am J Hum Genet. 1998 Apr;62(4):824-33. doi: 10.1086/301806. Am J Hum Genet. 1998. PMID: 9529364 Free PMC article.
[Genetics and nephrotic syndrome].
Niaudet P, Broyer M, Gubler MC, Jeanpierre C, Barbaux S, Antignac C. Niaudet P, et al. Among authors: jeanpierre c. Arch Pediatr. 1998;5 Suppl 2:152s-155s. Arch Pediatr. 1998. PMID: 9759244 Review. French. No abstract available.
WT1, renal development, and glomerulopathies.
Gubler MC, Yang Y, Jeanpierre C, Barbaux S, Niaudet P. Gubler MC, et al. Among authors: jeanpierre c. Adv Nephrol Necker Hosp. 1999;29:299-315. Adv Nephrol Necker Hosp. 1999. PMID: 10561752 Review. No abstract available.
WT1 splicing alterations in Wilms' tumors.
Baudry D, Hamelin M, Cabanis MO, Fournet JC, Tournade MF, Sarnacki S, Junien C, Jeanpierre C. Baudry D, et al. Among authors: jeanpierre c. Clin Cancer Res. 2000 Oct;6(10):3957-65. Clin Cancer Res. 2000. PMID: 11051244
Severe prenatal renal anomalies associated with mutations in HNF1B or PAX2 genes.
Madariaga L, Morinière V, Jeanpierre C, Bouvier R, Loget P, Martinovic J, Dechelotte P, Leporrier N, Thauvin-Robinet C, Jensen UB, Gaillard D, Mathieu M, Turlin B, Attie-Bitach T, Salomon R, Gübler MC, Antignac C, Heidet L. Madariaga L, et al. Among authors: jeanpierre c. Clin J Am Soc Nephrol. 2013 Jul;8(7):1179-87. doi: 10.2215/CJN.10221012. Epub 2013 Mar 28. Clin J Am Soc Nephrol. 2013. PMID: 23539225 Free PMC article.
80 results