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List of works by Christelle Arrondel

A homozygous missense mutation in the ciliary gene TTC21B causes familial FSGS

scientific article

A large tandem duplication within the COL4A5 gene is responsible for the high prevalence of Alport syndrome in French Polynesia

scientific article published in June 2004

A murine model of Denys-Drash syndrome reveals novel transcriptional targets of WT1 in podocytes.

scientific article published on January 2010

Alport syndrome associated with diffuse leiomyomatosis: COL4A5‐COL4A6 deletion associated with a mild form of Alport nephropathy

scientific article published on 01 January 2002

COL4A3/COL4A4 mutations: from familial hematuria to autosomal-dominant or recessive Alport syndrome

scientific article published on June 2002

Discovery of microvascular miRNAs using public gene expression data: miR-145 is expressed in pericytes and is a regulator of Fli1

scientific article published in 2009

Fetal renin-angiotensin-system blockade syndrome: renal lesions

scientific article published on 30 January 2014

INF2 mutations in Charcot-Marie-Tooth disease with glomerulopathy

scientific article

Loss-of-function mutations in WDR73 are responsible for microcephaly and steroid-resistant nephrotic syndrome: Galloway-Mowat syndrome

scientific article

Molecular fingerprinting of the podocyte reveals novel gene and protein regulatory networks

article

Mutation-dependent recessive inheritance of NPHS2-associated steroid-resistant nephrotic syndrome

article published in 2014

Mutations in sphingosine-1-phosphate lyase cause nephrosis with ichthyosis and adrenal insufficiency

scientific article published on 06 February 2017

Mutations in theCOL4A4 and COL4A3 genes cause familial benign hematuria

article

Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis.

scientific article

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