Search filters

List of works by Melanie Parisot

ADAR1 mediated regulation of neural crest derived melanocytes and Schwann cell development

scientific article published on 10 January 2020

Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome

scientific article published on 03 September 2019

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

scientific article

Mild B-cell lymphocytosis in patients with a CARD11 C49Y mutation

scientific article

Mutations in the adaptor-binding domain and associated linker region of p110δ cause Activated PI3K-δ Syndrome 1 (APDS1).

scientific article published on 20 April 2017

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

scientific article published on 13 April 2011

Utility of whole exome sequencing for the early diagnosis of pediatric-onset cerebellar atrophy associated with developmental delay in an inbred population

scientific article published on 4 May 2016

Paulina is supported by:

About Paulina

Help