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David J Cutler

Showing results (81-90 of 142) with videos related to

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Clinical Epigenetics|March 25, 2023
Longitudinal DNA methylation profiling of the rectal mucosa identifies cell-specific signatures of disease status, severity and clinical outcomes in ulcerative colitis cell-specific DNA methylation signatures of UCSuresh Venkateswaran, Hari K Somineni, Jason D Matthews, et al.
Frontiers in Neurology|August 1, 2022
Novel Missense <i>CNTNAP2</i> Variant Identified in Two Consanguineous Pakistani Families With Developmental Delay, Epilepsy, Intellectual Disability, and Aggressive BehaviorNoor Badshah, Kari A Mattison, Sohail Ahmad, et al.
Human Molecular Genetics|February 20, 2009
Origins, distribution and expression of the Duarte-2 (D2) allele of galactose-1-phosphate uridylyltransferaseAmanda E Carney, Rebecca D Sanders, Kerry R Garza, et al.
Inflammatory Bowel Diseases|May 18, 2021
Site- and Taxa-Specific Disease-Associated Oral Microbial Structures Distinguish Inflammatory Bowel DiseasesHari K Somineni, Jordan H Weitzner, Suresh Venkateswaran, et al.
Cellular and Molecular Gastroenterology and Hepatology|July 16, 2021
Ileal Derived Organoids From Crohn's Disease Patients Show Unique Transcriptomic and Secretomic SignaturesBarbara Joanna Niklinska-Schirtz, Suresh Venkateswaran, Murugadas Anbazhagan, et al.
Genetics|September 1, 2017
Testing Two Evolutionary Theories of Human Aging with DNA Methylation DataChloe Robins, Allan F McRae, Joseph E Powell, et al.
Frontiers in Aging Neuroscience|January 23, 2023
Evaluation of AQP4 functional variants and its association with fragile X-associated tremor/ataxia syndromeAndrea Elias-Mas, Miriam Potrony, Jaume Bague, et al.
G3 (Bethesda, Md.)|February 16, 2022
Methylation quantitative trait loci are largely consistent across disease states in Crohn's diseaseSuresh Venkateswaran, Hari K Somineni, Varun Kilaru, et al.
Medrxiv : the Preprint Server for Health Sciences|May 18, 2026
Modeling rare coding variation on chromosome X provides insight into the genetics and differential sex prevalence of autism spectrum disorderF Kyle Satterstrom, Kiana Jodeiry, Behrang Mahjani, et al.
G3 (Bethesda, Md.)|November 17, 2017
Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart DefectsBenjamin L Rambo-Martin, Jennifer G Mulle, David J Cutler, et al.
Pageof 15

Showing results (81-90 of 142) with videos related to

Sort By:
Pageof 15
Clinical Epigenetics|March 25, 2023
Longitudinal DNA methylation profiling of the rectal mucosa identifies cell-specific signatures of disease status, severity and clinical outcomes in ulcerative colitis cell-specific DNA methylation signatures of UCSuresh Venkateswaran, Hari K Somineni, Jason D Matthews, et al.
Frontiers in Neurology|August 1, 2022
Novel Missense <i>CNTNAP2</i> Variant Identified in Two Consanguineous Pakistani Families With Developmental Delay, Epilepsy, Intellectual Disability, and Aggressive BehaviorNoor Badshah, Kari A Mattison, Sohail Ahmad, et al.
Human Molecular Genetics|February 20, 2009
Origins, distribution and expression of the Duarte-2 (D2) allele of galactose-1-phosphate uridylyltransferaseAmanda E Carney, Rebecca D Sanders, Kerry R Garza, et al.
Inflammatory Bowel Diseases|May 18, 2021
Site- and Taxa-Specific Disease-Associated Oral Microbial Structures Distinguish Inflammatory Bowel DiseasesHari K Somineni, Jordan H Weitzner, Suresh Venkateswaran, et al.
Cellular and Molecular Gastroenterology and Hepatology|July 16, 2021
Ileal Derived Organoids From Crohn's Disease Patients Show Unique Transcriptomic and Secretomic SignaturesBarbara Joanna Niklinska-Schirtz, Suresh Venkateswaran, Murugadas Anbazhagan, et al.
Genetics|September 1, 2017
Testing Two Evolutionary Theories of Human Aging with DNA Methylation DataChloe Robins, Allan F McRae, Joseph E Powell, et al.
Frontiers in Aging Neuroscience|January 23, 2023
Evaluation of AQP4 functional variants and its association with fragile X-associated tremor/ataxia syndromeAndrea Elias-Mas, Miriam Potrony, Jaume Bague, et al.
G3 (Bethesda, Md.)|February 16, 2022
Methylation quantitative trait loci are largely consistent across disease states in Crohn's diseaseSuresh Venkateswaran, Hari K Somineni, Varun Kilaru, et al.
Medrxiv : the Preprint Server for Health Sciences|May 18, 2026
Modeling rare coding variation on chromosome X provides insight into the genetics and differential sex prevalence of autism spectrum disorderF Kyle Satterstrom, Kiana Jodeiry, Behrang Mahjani, et al.
G3 (Bethesda, Md.)|November 17, 2017
Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart DefectsBenjamin L Rambo-Martin, Jennifer G Mulle, David J Cutler, et al.
Pageof 15