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Human Molecular Genetics|May 8, 2013
APP/PS1 mice overexpressing SREBP-2 exhibit combined Aβ accumulation and tau pathology underlying Alzheimer's diseaseElisabet Barbero-Camps, Anna Fernández, Laura Martínez, et al.Human Molecular Genetics|April 13, 2013
Analysis of TFAP2A mutations in Branchio-Oculo-Facial Syndrome indicates functional complexity within the AP-2α DNA-binding domainHong Li, Ryan Sheridan, Trevor WilliamsHuman Molecular Genetics|April 16, 2013
De-repression of FOXO3a death axis by microRNA-132 and -212 causes neuronal apoptosis in Alzheimer's diseaseHon-Kit Andus Wong, Tatiana Veremeyko, Nehal Patel, et al.Human Molecular Genetics|February 19, 2013
Mutations in NEK8 link multiple organ dysplasia with altered Hippo signalling and increased c-MYC expressionValeska Frank, Sandra Habbig, Malte P Bartram, et al.Human Molecular Genetics|February 20, 2013
Connexin 43 is involved in the generation of human-induced pluripotent stem cellsQiong Ke, Li Li, Bing Cai, et al.Human Molecular Genetics|February 21, 2013
Behavioural and functional characterization of Kv10.1 (Eag1) knockout miceRoser Ufartes, Tomasz Schneider, Lena Sünke Mortensen, et al.Human Molecular Genetics|February 23, 2013
Gata3 antagonizes cancer progression in Pten-deficient prostatesAlana H T Nguyen, Mathieu Tremblay, Katharina Haigh, et al.Human Molecular Genetics|May 23, 2013
A Y328C missense mutation in spermine synthase causes a mild form of Snyder-Robinson syndromeZhe Zhang, Joy Norris, Vera Kalscheuer, et al.Human Molecular Genetics|May 28, 2013
The functional genetic link of NLGN4X knockdown and neurodevelopment in neural stem cellsLingling Shi, Xiao Chang, Peilin Zhang, et al.Human Molecular Genetics|May 18, 2013
ALS-associated mutations in FUS disrupt the axonal distribution and function of SMNEwout J N Groen, Katsumi Fumoto, Anna M Blokhuis, et al.Pageof 1,196