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Genes|April 3, 2021
Shukla-Vernon Syndrome: A Second Family with a Novel Variant in the BCORL1 GeneBabylakshmi Muthusamy, Anikha Bellad, Satish Chandra Girimaji, et al.Molecular Biotechnology|October 8, 2010
Human protein reference database and human proteinpedia as discovery resources for molecular biotechnologyRenu Goel, Babylakshmi Muthusamy, Akhilesh Pandey, et al.Current Protocols in Bioinformatics|March 19, 2013
Access guide to human proteinpediaBabylakshmi Muthusamy, Joji Kurian Thomas, T S Keshava Prasad, et al.Journal of Molecular Neuroscience : MN|May 14, 2020
A Novel Missense Variant in PHF6 Gene Causing Börjeson-Forssman-Lehman SyndromeAnikha Bellad, Aravind K Bandari, Akhilesh Pandey, et al.Molecular & Cellular Proteomics : MCP|February 23, 2005
A proteomic analysis of human hemodialysis fluidHenrik Molina, Jakob Bunkenborg, G Hanumanthu Reddy, et al.Omics : a Journal of Integrative Biology|July 10, 2023
Whole Exome Sequencing Reveals Novel Variants in Unexplained ErythrocytosisHarshit Khurana, Babylakshmi Muthusamy, Uday Yanamandra, et al.Acta Neurologica Belgica|June 28, 2023
Loss of function variants in L2HGDH gene causing L-2-hydroxyglutaric aciduriaAnikha Bellad, Vikram V Holla, Riyanka Kumari, et al.Frontiers in Psychiatry|June 6, 2020
A Novel LINS1 Truncating Mutation in Autosomal Recessive Nonsyndromic Intellectual DisabilityBabylakshmi Muthusamy, Anikha Bellad, Pramada Prasad, et al.Omics : a Journal of Integrative Biology|August 15, 2018
A Next-Generation Sequencing-Based Molecular Approach to Characterize a Tick Vector in Lyme DiseaseAnil K Madugundu, Babylakshmi Muthusamy, Sreelakshmi K Sreenivasamurthy, et al.Journal of Movement Disorders|June 13, 2023
KMT2B-Related Dystonia in Indian Patients With Literature Review and Emphasis on Asian CohortDebjyoti Dhar, Vikram V Holla, Riyanka Kumari, et al.Pageof 58