Antignac C - Search Results

1

Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumor.

Jeanpierre C, Antignac C, Beroud C, Lavedan C, Henry I, Saunders G, Williams B, Glaser T, Junien C. Jeanpierre C, et al. Among authors: antignac c. Genomics. 1990 Jul;7(3):434-8. doi: 10.1016/0888-7543(90)90179-x. Genomics. 1990. PMID: 1973142

2

[Antioncogenes: models for tumors in children].

Junien C, Henry I, Jeanpierre C, Lavedan C, Antignac C, Puech A, Beroud C. Junien C, et al. Among authors: antignac c. Bull Cancer. 1991 Jan;78(1):57-68. Bull Cancer. 1991. PMID: 2021687 French.

3

Physical and genetic mapping of the dipeptidase gene DPEP1 to 16q24.3.

Austruy E, Jeanpierre C, Antignac C, Whitmore SA, Van Cong N, Bernheim A, Callen DF, Junien C. Austruy E, et al. Among authors: antignac c. Genomics. 1993 Mar;15(3):684-7. doi: 10.1006/geno.1993.1126. Genomics. 1993. PMID: 7682195

4

Refined mapping of a gene (NPH1) causing familial juvenile nephronophthisis and evidence for genetic heterogeneity.

Medhioub M, Cherif D, Benessy F, Silbermann F, Gubler MC, Le Paslier D, Cohen D, Weissenbach J, Beckmann J, Antignac C. Medhioub M, et al. Among authors: antignac c. Genomics. 1994 Jul 15;22(2):296-301. doi: 10.1006/geno.1994.1387. Genomics. 1994. PMID: 7806215

5

Isolation of kidney complementary DNAs down-expressed in Wilms' tumor by a subtractive hybridization approach.

Austruy E, Cohen-Salmon M, Antignac C, Béroud C, Henry I, Nguyen VC, Brugières L, Junien C, Jeanpierre C. Austruy E, et al. Among authors: antignac c. Cancer Res. 1993 Jun 15;53(12):2888-94. Cancer Res. 1993. PMID: 7916648

6

A 11 Mb YAC-based contig spanning the familial juvenile nephronophthisis region (NPH1) located on chromosome 2q.

Konrad M, Saunier S, Silbermann F, Benessy F, Le Paslier D, Weissenbach J, Broyer M, Gubler MC, Antignac C. Konrad M, et al. Among authors: antignac c. Genomics. 1995 Dec 10;30(3):514-20. doi: 10.1006/geno.1995.1272. Genomics. 1995. PMID: 8825638

7

[Genetics and nephrotic syndrome].

Niaudet P, Broyer M, Gubler MC, Jeanpierre C, Barbaux S, Antignac C. Niaudet P, et al. Among authors: antignac c. Arch Pediatr. 1998;5 Suppl 2:152s-155s. Arch Pediatr. 1998. PMID: 9759244 Review. French. No abstract available.

8

WNT/beta-catenin pathway activation in Wilms tumors: a unifying mechanism with multiple entries?

Corbin M, de Reyniès A, Rickman DS, Berrebi D, Boccon-Gibod L, Cohen-Gogo S, Fabre M, Jaubert F, Faussillon M, Yilmaz F, Sarnacki S, Landman-Parker J, Patte C, Schleiermacher G, Antignac C, Jeanpierre C. Corbin M, et al. Among authors: antignac c. Genes Chromosomes Cancer. 2009 Sep;48(9):816-27. doi: 10.1002/gcc.20686. Genes Chromosomes Cancer. 2009. PMID: 19530245

9

RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects.

Jeanpierre C, Macé G, Parisot M, Morinière V, Pawtowsky A, Benabou M, Martinovic J, Amiel J, Attié-Bitach T, Delezoide AL, Loget P, Blanchet P, Gaillard D, Gonzales M, Carpentier W, Nitschke P, Tores F, Heidet L, Antignac C, Salomon R; Société Française de Foetopathologie. Jeanpierre C, et al. Among authors: antignac c. J Med Genet. 2011 Jul;48(7):497-504. doi: 10.1136/jmg.2010.088526. Epub 2011 Apr 13. J Med Genet. 2011. PMID: 21490379 Free article.

10

Large homozygous deletions of the 2q13 region are a major cause of juvenile nephronophthisis.

Konrad M, Saunier S, Heidet L, Silbermann F, Benessy F, Calado J, Le Paslier D, Broyer M, Gubler MC, Antignac C. Konrad M, et al. Among authors: antignac c. Hum Mol Genet. 1996 Mar;5(3):367-71. doi: 10.1093/hmg/5.3.367. Hum Mol Genet. 1996. PMID: 8852662

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