María L. Arbonés
Instituto de Salud Carlos III(ES)Centre for Biomedical Network Research on Rare Diseases(ES)Instituto de Investigación de Enfermedades Raras(ES)Institut de Biologia Molecular de Barcelona(ES)
Publications by Year
Research Areas
Down syndrome and intellectual disability research, Genetics and Neurodevelopmental Disorders, Hearing, Cochlea, Tinnitus, Genetics, Signaling Pathways in Disease, Connexins and lens biology
Most-Cited Works
- → Lymphocyte homing and leukocyte rolling and migration are impaired in L-selectin-deficient mice(1994)827 cited
- → Sequential contribution of L- and P-selectin to leukocyte rolling in vivo.(1995)585 cited
- → Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus(1999)397 cited
- → Dyrk1A Haploinsufficiency Affects Viability and Causes Developmental Delay and Abnormal Brain Morphology in Mice(2002)339 cited
- → MicroRNA-199b targets the nuclear kinase Dyrk1a in an auto-amplification loop promoting calcineurin/NFAT signalling(2010)319 cited
- → MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss(2001)241 cited