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List of works by Cécile Jeanpierre

11p15.5-specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesis.

scientific article

A highly polymorphic probe on 11p15.5: L22.5.2 (D11S774).

scientific article

A study of new NEK8 mutations in patients with severe renal cystic hypodysplasia and ciliopathy-associated defects.

scientific article

Antioncogenes: models for tumors in children

scientific article published in January 1991

Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract

scientific article published on 01 April 2019

Changes in WT1 splicing are associated with a specific gene expression profile in Wilms' tumour

scientific article published in August 2002

Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13. Subdivision of the WAGR complex region.

scientific article published on May 1989

Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis

article

Chromosomal assignment of the uromodulin gene (UMOD) to 16p13.11

scientific article

Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19

scientific article

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

scientific article published on July 1990

Control of the Wnt pathways by nephrocystin-4 is required for morphogenesis of the zebrafish pronephros

scientific article published on 15 April 2011

Correlations of allelic imbalance of chromosome 14 with adverse prognostic parameters in 148 renal cell carcinomas

scientific article published on 01 December 1996

DCDC2 Mutations Cause Neonatal Sclerosing Cholangitis

scientific journal article

Deducing the stage of origin of Wilms' tumours from a developmental series of Wt1-mutant mice

scientific article

FGF9 and FGF20 maintain the stemness of nephron progenitors in mice and man.

scientific article

Frequent overexpression of cyclin D2/cyclin-dependent kinase 4 in Wilms' tumor

scientific article published on 01 April 2005

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

scientific article

Gonad development in Drash and Frasier syndromes depends on WT1 mutations

scientific article published on 01 March 2003

High cyclin E staining index in blastemal, stromal or epithelial cells is correlated with tumor aggressiveness in patients with nephroblastoma

scientific article

Identification of human mutations in TRAF3IP1 in patients with nephronophthisis and retinal degeneration.

scientific article

Integrin Alpha 8 Recessive Mutations Are Responsible for Bilateral Renal Agenesis in Humans

Integrin alpha 8 recessive mutations are responsible for bilateral renal agenesis in humans

scientific article

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

scientific article

Management of Wilms tumors in Drash and Frasier syndromes.

scientific article published in January 2009

Molecular cytogenetic anomalies and phenotype alterations in a newly established cell line from Wilms tumor with diffuse anaplasia.

scientific article

Nephrocystins play a crucial role in renal epithelial morphogenesis via the regulation of Wnt/PCP components Dishevelled and Rho GTPases.

scientific article published on 16 November 2012

Novel NEK8 Mutations Cause Severe Syndromic Renal Cystic Dysplasia through YAP Dysregulation

scientific article

Novel perspectives for investigating congenital anomalies of the kidney and urinary tract (CAKUT)

scientific article published on 01 December 2011

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

scientific article

Profiling of differential gene expression in Wilms tumor by cDNA expression array.

scientific article published on December 2001

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

scientific article published on 13 April 2011

Severe prenatal renal anomalies associated with mutations in HNF1B or PAX2 genes.

scientific article published on 28 March 2013

Sex reversal and diaphragmatic hernia in phenotypicaly female sibs with normal XY chromosomes.

scientific article published in April 2000

Small glomeruli in WAGR (Wilms Tumor, Aniridia, Genitourinary Anomalies and Mental Retardation) syndrome

scientific article published in June 2007

Software and database for the analysis of mutations in the human WT1 gene

scientific article published in January 1998

Spectrum of hSNF5/INI1 somatic mutations in human cancer and genotype-phenotype correlations

scientific article published on 01 December 1999

Surgical management and genotype/phenotype correlations in WT1 gene–related diseases (drash, frasier syndromes)

article

Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract

scientific article published on 31 May 2017

The copy number variation landscape of congenital anomalies of the kidney and urinary tract

scientific article published on 21 December 2018

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

scientific article published in September 2009

WT1 splicing alterations in Wilms' tumors

scientific article published on 01 October 2000

Whole-exome sequencing identifies mutations of TBC1D1 encoding a Rab-GTPase-activating protein in patients with congenital anomalies of the kidneys and urinary tract (CAKUT).

scientific article published on 16 November 2015

Wilms' tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomas

scientific article

[FGF9 and FGF20 maintain the stemness of nephron progenitors during kidney development]

scientific article published on 27 March 2013

[Genetics and nephrotic syndrome]

scientific article published on 01 January 1998

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