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Annals of Human Biology|September 20, 2012
Haplotypic association of ADAM33 (T+1, S+1 and V - 3) gene variants in genetic susceptibility to asthma in Indian populationPriya Tripathi, Shally Awasthi, Rajendra Prasad, et al.
Human Molecular Genetics|March 6, 2007
Lafora disease proteins malin and laforin are recruited to aggresomes in response to proteasomal impairmentShuchi Mittal, Deepti Dubey, Kazuhiro Yamakawa, et al.
Neurobiology of Disease|January 9, 2017
Loss of laforin or malin results in increased Drp1 level and concomitant mitochondrial fragmentation in Lafora disease mouse modelsMamta Upadhyay, Saloni Agarwal, Pratibha Bhadauriya, et al.
Biochemical and Biophysical Research Communications|June 24, 2015
Lafora disease proteins laforin and malin negatively regulate the HIPK2-p53 cell death pathwayMamta Upadhyay, Smriti Gupta, Pratibha Bhadauriya, et al.
Human Molecular Genetics|October 4, 2011
Dysfunctions in endosomal-lysosomal and autophagy pathways underlie neuropathology in a mouse model for Lafora diseaseRajat Puri, Toshimitsu Suzuki, Kazuhiro Yamakawa, et al.
Journal of Human Genetics|December 24, 2010
Association of ADAM33 gene polymorphisms with asthma in Indian childrenShally Awasthi, Priya Tripathi, Subramaniam Ganesh, et al.
Molecular Neurobiology|April 22, 2025
Inactivation of Laforin Phosphatase and Increased Glucose Uptake Underlie Glycogen Synthase-Mediated Neuronal Survival Under Oxidative StressAkanksha Onkar, Deepashree Sheshadri, Kamali Nagarajan, et al.
CNS & Neurological Disorders Drug Targets|November 16, 2018
Extending Arms of Insulin Resistance from Diabetes to Alzheimer's Disease: Identification of Potential Therapeutic TargetsSmriti Gupta, Nitin Kumar Singhal, Subramaniam Ganesh, et al.
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