Shushant Jain Department of Clinical Genetics VU University Medical Center Biography Publications Institution JoVE Articles Shushant Jain has not added a biography. If you are Shushant Jain and would like to personalize this page please email our Author Liaison for assistance. Publications The Complete Automation of Cell Culture: Improvements for High-throughput and High-content Screening Journal of Biomolecular Screening. Sep, 2011 | Pubmed ID: 21775700 SFRS7-mediated Splicing of Tau Exon 10 is Directly Regulated by STOX1A in Glial Cells PloS One. 2011 | Pubmed ID: 21755018 From Single Genes to Gene Networks: High-throughput-high-content Screening for Neurological Disease Neuron. Oct, 2010 | Pubmed ID: 20955929 The Parkinson Disease-associated Leucine-rich Repeat Kinase 2 (LRRK2) is a Dimer That Undergoes Intramolecular Autophosphorylation The Journal of Biological Chemistry. Jun, 2008 | Pubmed ID: 18397888 Comprehensive Screening of a North American Parkinson's Disease Cohort for LRRK2 Mutation Neuro-degenerative Diseases. 2007 | Pubmed ID: 17622782 The R1441C Mutation of LRRK2 Disrupts GTP Hydrolysis Biochemical and Biophysical Research Communications. Jun, 2007 | Pubmed ID: 17442267 Analysis of IFT74 As a Candidate Gene for Chromosome 9p-linked ALS-FTD BMC Neurology. 2006 | Pubmed ID: 17166276 Kinase Activity is Required for the Toxic Effects of Mutant LRRK2/dardarin Neurobiology of Disease. Aug, 2006 | Pubmed ID: 16750377 Mutations in the Gene LRRK2 Encoding Dardarin (PARK8) Cause Familial Parkinson's Disease: Clinical, Pathological, Olfactory and Functional Imaging and Genetic Data Brain : a Journal of Neurology. Dec, 2005 | Pubmed ID: 16272164 Molecular Genetic Pathways in Parkinson's Disease: a Review Clinical Science (London, England : 1979). Oct, 2005 | Pubmed ID: 16171459 Clinical and Positron Emission Tomography of Parkinson's Disease Caused by LRRK2 Annals of Neurology. Mar, 2005 | Pubmed ID: 15732108 A Common LRRK2 Mutation in Idiopathic Parkinson's Disease Lancet. Jan 29-Feb 4, 2005 | Pubmed ID: 15680457 Genetic Screening for a Single Common LRRK2 Mutation in Familial Parkinson's Disease Lancet. Jan 29-Feb 4, 2005 | Pubmed ID: 15680455 Elevated Amyloid Beta Protein (Abeta42) and Late Onset Alzheimer's Disease Are Associated with Single Nucleotide Polymorphisms in the Urokinase-type Plasminogen Activator Gene Human Molecular Genetics. Feb, 2005 | Pubmed ID: 15615772 Cloning of the Gene Containing Mutations That Cause PARK8-linked Parkinson's Disease Neuron. Nov, 2004 | Pubmed ID: 15541308 Assessment of a DJ-1 (PARK7) Polymorphism in Finnish PD Neurology. Jun, 2004 | Pubmed ID: 15210917 Fine Mapping of the Alpha-T Catenin Gene to a Quantitative Trait Locus on Chromosome 10 in Late-onset Alzheimer's Disease Pedigrees Human Molecular Genetics. Dec, 2003 | Pubmed ID: 14559775 הקרנת תוכן גבוהה במחלות ניווניות Shushant Jain1, Ronald E. van Kesteren2, Peter Heutink1 1Department of Clinical Genetics, VU University Medical Center, 2Center for Neurogenomics and Cognitive Research, Neuroscience Campus Amsterdam JoVE 3452 Medicine
הקרנת תוכן גבוהה במחלות ניווניות Shushant Jain1, Ronald E. van Kesteren2, Peter Heutink1 1Department of Clinical Genetics, VU University Medical Center, 2Center for Neurogenomics and Cognitive Research, Neuroscience Campus Amsterdam JoVE 3452 Medicine