Suggestions

Du même auteur

Homozygous Deletion in the Coding Sequence of the c-mer Gene in RCS Rats Unravels General Mechanisms of Physiological Cell Adhesion and Apoptosis

Archive ouverte | Nandrot, Emeline | CCSD

International audience. The RCS rat presents an autosomal recessive retinal pigment epithelium dystrophy characterized by the outer segments of photoreceptors being phagocytosis-deficient. A systematic genetic study...

Eight previously unidentified mutations found in the OA1 ocular albinism gene.

Archive ouverte | Mayeur, Hélène | CCSD

BACKGROUND: Ocular albinism type 1 (OA1) is an X-linked ocular disorder characterized by a severe reduction in visual acuity, nystagmus, hypopigmentation of the retinal pigmented epithelium, foveal hypoplasia, macromelanosomes in ...

Truncation of PITX2 differentially affects its activity on physiological targets.

Archive ouverte | Quentien, Marie-Hélène | CCSD

International audience. The bicoid-like transcription factor PITX2 has been previously described to interact with the pituitary-specific POU homeodomain factor POU1F1 (human ortholog of PIT-1) to achieve cell-specif...

Chargement des enrichissements...