G. Merla

Discipline

Anthropologie biologique (4) Psychologie (1)

Type de document

Articles (11) Recensions (1)

Co-auteur

Date

Source

Mot-clé

Genes (7) gène (6) spectacle (5) puits (4) région (4) Phenotype (4) Transcription (4) Transcription (4) Cases (3) Patients (3) Mice (3) Human beings (3) Expression (3) Example (3) Cases (3) Regions (3) Patients (3) roman (3) risque (2) protéine (2) association (2) architecture (2) cartographie (cartes) (2) évolution (2) ADN (2) maladie (2) adulte (2) cancer (2) Deletion (2) Cancer (2)

Documents écrit par G. Merla (11) | parle de G. Merla (0)

FOXI3 pathogenic variants cause one form of craniofacial microsomia.
K. Mao et al. (11 avr. 2023)
MYC-containing amplicons in acute myeloid leukemia: genomic structures, evolution, and transcriptional consequences.
L'Abbate A. et al.
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition).
D.J. Klionsky et al.
BRF1 mutations alter RNA polymerase III-dependent transcription and cause neurodevelopmental anomalies.
G. Borck et al. (2015)
The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome.
M.R. Sailani et al. (2013)
A fish-specific transposable element shapes the repertoire of p53 target genes in zebrafish.
L. Micale et al. (2012)
The E3-Ubiquitin Ligase TRIM50 Interacts with HDAC6 and p62, and Promotes the Sequestration and Clearance of Ubiquitinated Proteins into the Aggresome.
C. Fusco et al. (2012)
Using transcription modules to identify expression clusters perturbed in Williams-Beuren syndrome.
C.N. Henrichsen et al. (2011)
Mutation spectrum of MLL2 in a cohort of Kabuki syndrome patients.
L. Micale et al. (2011)
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
S. Jacquemont et al. (2011)
Williams-Beuren syndrome TRIM50 encodes an E3 ubiquitin ligase.
L. Micale et al. (2008)