Shushant Jain

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