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Sampathkumar Rangasamy

Showing results (11-20 of 26) with videos related to

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Experimental Eye Research|May 8, 2020
Transcriptomics analysis of pericytes from retinas of diabetic animals reveals novel genes and molecular pathways relevant to blood-retinal barrier alterations in diabetic retinopathySampathkumar Rangasamy, Finny Monickaraj, Christophe Legendre, et al.
Diabetes|July 2, 2008
A common nonsynonymous single nucleotide polymorphism in the SLC30A8 gene determines ZnT8 autoantibody specificity in type 1 diabetesJanet M Wenzlau, Yu Liu, Liping Yu, et al.
Journal of Diabetes and Its Complications|March 25, 2017
Association of increased levels of MCP-1 and cathepsin-D in young onset type 2 diabetes patients (T2DM-Y) with severity of diabetic retinopathySruthi Reddy, Anandakumar Amutha, Ramachandran Rajalakshmi, et al.
Clinical Genetics|May 8, 2024
FGF12 copy number variant associated with epileptic encephalopathyAnna Abraham, Keri Ramsey, Newell Belnap, et al.
Scientific Reports|May 25, 2021
Improved methods for RNAseq-based alternative splicing analysisRebecca F Halperin, Apurva Hegde, Jessica D Lang, et al.
Seminars in Pediatric Neurology|July 3, 2018
Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test resultsBrittany Gerald, Keri Ramsey, Newell Belnap, et al.
Rare (Amsterdam, Netherlands)|May 21, 2024
Snyder-Robinson syndrome presenting with learning disability, epilepsy, and osteoporosis: a novel <i>SMS</i> gene variantMegumi Leung, Meredith Sanchez-Castillo, Newell Belnap, et al.
Investigative Ophthalmology & Visual Science|June 20, 2015
A De Novo Mutation in TEAD1 Causes Non-X-Linked Aicardi SyndromeIsabelle Schrauwen, Szabolcs Szelinger, Ashley L Siniard, et al.
Human Genetics|November 22, 2019
Compound heterozygous mutations in SNAP29 is associated with Pelizaeus-Merzbacher-like disorder (PMLD)Lorida Llaci, Keri Ramsey, Newell Belnap, et al.
F1000Research|July 1, 2017
Case Report: Novel mutations in <i>TBC1D24</i> are associated with autosomal dominant tonic-clonic and myoclonic epilepsy and recessive Parkinsonism, psychosis, and intellectual disabilityErika Banuelos, Keri Ramsey, Newell Belnap, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Experimental Eye Research|May 8, 2020
Transcriptomics analysis of pericytes from retinas of diabetic animals reveals novel genes and molecular pathways relevant to blood-retinal barrier alterations in diabetic retinopathySampathkumar Rangasamy, Finny Monickaraj, Christophe Legendre, et al.
Diabetes|July 2, 2008
A common nonsynonymous single nucleotide polymorphism in the SLC30A8 gene determines ZnT8 autoantibody specificity in type 1 diabetesJanet M Wenzlau, Yu Liu, Liping Yu, et al.
Journal of Diabetes and Its Complications|March 25, 2017
Association of increased levels of MCP-1 and cathepsin-D in young onset type 2 diabetes patients (T2DM-Y) with severity of diabetic retinopathySruthi Reddy, Anandakumar Amutha, Ramachandran Rajalakshmi, et al.
Clinical Genetics|May 8, 2024
FGF12 copy number variant associated with epileptic encephalopathyAnna Abraham, Keri Ramsey, Newell Belnap, et al.
Scientific Reports|May 25, 2021
Improved methods for RNAseq-based alternative splicing analysisRebecca F Halperin, Apurva Hegde, Jessica D Lang, et al.
Seminars in Pediatric Neurology|July 3, 2018
Neonatal epileptic encephalopathy caused by de novo GNAO1 mutation misdiagnosed as atypical Rett syndrome: Cautions in interpretation of genomic test resultsBrittany Gerald, Keri Ramsey, Newell Belnap, et al.
Rare (Amsterdam, Netherlands)|May 21, 2024
Snyder-Robinson syndrome presenting with learning disability, epilepsy, and osteoporosis: a novel <i>SMS</i> gene variantMegumi Leung, Meredith Sanchez-Castillo, Newell Belnap, et al.
Investigative Ophthalmology & Visual Science|June 20, 2015
A De Novo Mutation in TEAD1 Causes Non-X-Linked Aicardi SyndromeIsabelle Schrauwen, Szabolcs Szelinger, Ashley L Siniard, et al.
Human Genetics|November 22, 2019
Compound heterozygous mutations in SNAP29 is associated with Pelizaeus-Merzbacher-like disorder (PMLD)Lorida Llaci, Keri Ramsey, Newell Belnap, et al.
F1000Research|July 1, 2017
Case Report: Novel mutations in <i>TBC1D24</i> are associated with autosomal dominant tonic-clonic and myoclonic epilepsy and recessive Parkinsonism, psychosis, and intellectual disabilityErika Banuelos, Keri Ramsey, Newell Belnap, et al.
Pageof 3