Showing results (41-50 of 1,718) with videos related to
Sort By:
Pageof 172
Alimentary Pharmacology & Therapeutics|September 26, 2007
Evidence of allelic heterogeneity for associations between the NOD2/CARD15 gene and ulcerative colitis among North IndiansG Juyal, D Amre, V Midha, et al.Neurogenetics|July 15, 2017
Characterization of SNPs in the dopamine-β-hydroxylase gene providing new insights into its structure-function relationshipToyanji Joseph Punchaichira, Sanjay Kumar Dey, Anirban Mukhopadhyay, et al.Psychiatric Genetics|September 15, 2020
The effect of rs1076560 (DRD2) and rs4680 (COMT) on tardive dyskinesia and cognition in schizophrenia subjectsToyanji Joseph Punchaichira, Prachi Kukshal, Triptish Bhatia, et al.Molecular Neurobiology|July 26, 2023
Effect of rs1108580 of DBH and rs1006737 of CACNA1C on Cognition and Tardive Dyskinesia in a North Indian Schizophrenia CohortToyanji Joseph Punchaichira, Prachi Kukshal, Triptish Bhatia, et al.Journal of Biosciences|June 25, 2021
Multiple allelic associations from genes involved in energy metabolism were identified in celiac diseaseSandilya Bhagavatula, Pratibha Banerjee, Ajit Sood, et al.Journal of Genetics|February 23, 2023
Celiac disease-associated loci show considerable genetic overlap with neuropsychiatric diseases but with limited transethnic applicabilityNidhi Sharma, Pratibha Banerjee, Ajit Sood, et al.Plos One|October 11, 2012
Potential of ayurgenomics approach in complex trait research: leads from a pilot study on rheumatoid arthritisRamesh C Juyal, Sapna Negi, Preeti Wakhode, et al.The Pharmacogenomics Journal|September 14, 2006
Genetic susceptibility to Tardive Dyskinesia in chronic schizophrenia subjects: V. Association of CYP1A2 1545 C>T polymorphismA K Tiwari, S N Deshpande, B Lerer, et al.Journal of Biosciences|April 3, 2002
Molecular genetics of schizophrenia: past, present and futureSuman Prasad, Prachi Semwal, Smita Deshpande, et al.Journal of Child Neurology|February 15, 2017
Validation of Polymerase Chain Reaction-Based Assay to Detect Actual Number of CGG Repeats in FMR1 Gene in Indian Fragile X Syndrome PatientsMadhumita Roy Chowdhury, Sandeepa Chauhan, Anjali Dabral, et al.Pageof 172