D. Martinet

Discipline

Histoire (1)

Type de document

Articles (12) Colloques et conférences (1)

Co-auteur

Date

Source

Mot-clé

analyse (8) gène (8) Analysis (8) Deletion (6) Cases (5) Human beings (5) Cases (5) enfant (4) adulte (4) Phenotype (4) Genes (4) Obesity (4) Growth (4) Chromosomes (4) Body mass index (4) Number (4) Growth (4) adulte (4) nourisson (3) spectacle (3) région (3) cartographie (cartes) (3) effet (3) ADN (3) maladie (3) jeune (3) Strategy (3) Population (3) Expression (3) DNA (3)

Documents écrit par D. Martinet (13) | parle de D. Martinet (0)

A single epidermal stem cell strategy for safe ex vivo gene therapy.
A. Rochat et al. (2015)
A New CRB1 Rat Mutation Links Müller Glial Cells to Retinal Telangiectasia.
M. Zhao et al. (2015)
Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity.
R.G. Walters et al. (2013)
Presence of an oligodendroglioma-like component in newly diagnosed glioblastoma identifies a pathogenetically heterogeneous subgroup and lacks prognostic value: central pathology review of the EORTC_26981/NCIC_CE.3 trial.
M.E. Hegi et al. (2012)
Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats.
P. Stankiewicz et al. (2012)
Subtelomeric deletion of chromosome 10p15.3: clinical findings and molecular cytogenetic characterization.
C. DeScipio et al. (2012)
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
F. Zufferey et al. (2012)
Network-guided analysis of genes with altered somatic copy number and gene expression reveals pathways commonly perturbed in metastatic melanoma.
A. Valsesia et al. (2011)
High-level transgene expression by homologous recombination-mediated gene transfer.
M. Grandjean et al. (2011)
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
S. Jacquemont et al. (2011)
16q24.1 microdeletion in a premature newborn: Usefulness of array-based comparative genomic hybridization in persistent pulmonary hypertension of the newborn.
F. Zufferey et al. (2011)
A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.
R.G. Walters et al. (4 févr. 2010)
Fast generation of high producer cho cell lines by an iterative transfection process
P.A. Girod et al. (2006)