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C Jeanpierre

Showing results (11-20 of 27) with videos related to

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Bulletin Du Cancer|January 1, 1991
[Antioncogenes: models for tumors in children]C Junien, I Henry, C Jeanpierre, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Chromosomal assignment of the uromodulin gene (UMOD) to 16p13.11C Jeanpierre, S A Whitmore, E Austruy, et al.
Genomics|July 1, 1990
Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumorC Jeanpierre, C Antignac, C Beroud, et al.
Journal of Pediatric Surgery|February 20, 2003
Surgical management and genotype/phenotype correlations in WT1 gene-related diseases (Drash, Frasier syndromes)F Auber, S Lortat-Jacob, S Sarnacki, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 29, 2000
WT1 splicing alterations in Wilms' tumorsD Baudry, M Hamelin, M O Cabanis, et al.
Genomics|March 1, 1993
Physical and genetic mapping of the dipeptidase gene DPEP1 to 16q24.3E Austruy, C Jeanpierre, C Antignac, et al.
Genes, Chromosomes & Cancer|December 1, 1995
Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesisE Austruy, S Candon, I Henry, et al.
Human Molecular Genetics|November 11, 1999
Spectrum of hSNF5/INI1 somatic mutations in human cancer and genotype-phenotype correlationsN Sévenet, A Lellouch-Tubiana, D Schofield, et al.
Cancer Research|June 15, 1993
Isolation of kidney complementary DNAs down-expressed in Wilms' tumor by a subtractive hybridization approachE Austruy, M Cohen-Salmon, C Antignac, et al.
Genomics|August 1, 1992
11p15.5-specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesisA Puech, L Ahnine, H J Lüdecke, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Bulletin Du Cancer|January 1, 1991
[Antioncogenes: models for tumors in children]C Junien, I Henry, C Jeanpierre, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Chromosomal assignment of the uromodulin gene (UMOD) to 16p13.11C Jeanpierre, S A Whitmore, E Austruy, et al.
Genomics|July 1, 1990
Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumorC Jeanpierre, C Antignac, C Beroud, et al.
Journal of Pediatric Surgery|February 20, 2003
Surgical management and genotype/phenotype correlations in WT1 gene-related diseases (Drash, Frasier syndromes)F Auber, S Lortat-Jacob, S Sarnacki, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 29, 2000
WT1 splicing alterations in Wilms' tumorsD Baudry, M Hamelin, M O Cabanis, et al.
Genomics|March 1, 1993
Physical and genetic mapping of the dipeptidase gene DPEP1 to 16q24.3E Austruy, C Jeanpierre, C Antignac, et al.
Genes, Chromosomes & Cancer|December 1, 1995
Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesisE Austruy, S Candon, I Henry, et al.
Human Molecular Genetics|November 11, 1999
Spectrum of hSNF5/INI1 somatic mutations in human cancer and genotype-phenotype correlationsN Sévenet, A Lellouch-Tubiana, D Schofield, et al.
Cancer Research|June 15, 1993
Isolation of kidney complementary DNAs down-expressed in Wilms' tumor by a subtractive hybridization approachE Austruy, M Cohen-Salmon, C Antignac, et al.
Genomics|August 1, 1992
11p15.5-specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesisA Puech, L Ahnine, H J Lüdecke, et al.
Pageof 3