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Showing results (201-210 of 566) with videos related to

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Bioinformatics (Oxford, England)|December 10, 2014
Identification of deleterious synonymous variants in human genomesOrion J Buske, AshokKumar Manickaraj, Seema Mital, et al.
Inorganic Chemistry|March 22, 2007
Syntheses, crystal structures, and magnetic properties of metal-organic hybrid materials of Cu(II): effect of a long chain dicarboxylate backbone, and counteranion in their structural diversityA K Ghosh, D Ghoshal, E Zangrando, et al.
Molecular and Cellular Biology|January 1, 1990
Molecular and functional analysis of the muscle-specific promoter region of the Duchenne muscular dystrophy geneH J Klamut, S B Gangopadhyay, R G Worton, et al.
Indian Journal of Dermatology, Venereology and Leprology|February 3, 2017
Vdrl-sero-survey in Sirmur District of Himachal PradeshS K Bagchi, Subhash Chakraborty, A Das, et al.
Cureus|August 7, 2024
Hypertension and Device-Based Therapies for Resistant Hypertension: An Up-to-Date ReviewOluwaremilekun Tolu-Akinnawo, David N Ray, Tiwalade Awosanya, et al.
American Journal of Medical Genetics|May 30, 1998
FGFR2 mutation associated with clinical manifestations consistent with Antley-Bixler syndromeK Chun, J Siegel-Bartelt, D Chitayat, et al.
Bioinformatics (Oxford, England)|June 6, 2013
Identification of deleterious synonymous variants in human genomesOrion J Buske, AshokKumar Manickaraj, Seema Mital, et al.
European Journal of Human Genetics : EJHG|April 6, 2017
Severe neurodegeneration, progressive cerebral volume loss and diffuse hypomyelination associated with a homozygous frameshift mutation in CSTBAlan O'Brien, Christian R Marshall, Susan Blaser, et al.
Clinical Pediatrics|September 7, 2025
Relationship Between Household Social Risk and Symptoms of Depression and Anxiety in Adolescents: A Retrospective Cohort StudyDeepak Palakshappa, Kristin N Ray, Kelsey Schweiberger, et al.
The EMBO Journal|December 1, 1991
Molecular analysis of X-autosome translocations in females with Duchenne muscular dystrophyS E Bodrug, J J Holden, P N Ray, et al.
Pageof 57

Showing results (201-210 of 566) with videos related to

Sort By:
Pageof 57
Bioinformatics (Oxford, England)|December 10, 2014
Identification of deleterious synonymous variants in human genomesOrion J Buske, AshokKumar Manickaraj, Seema Mital, et al.
Inorganic Chemistry|March 22, 2007
Syntheses, crystal structures, and magnetic properties of metal-organic hybrid materials of Cu(II): effect of a long chain dicarboxylate backbone, and counteranion in their structural diversityA K Ghosh, D Ghoshal, E Zangrando, et al.
Molecular and Cellular Biology|January 1, 1990
Molecular and functional analysis of the muscle-specific promoter region of the Duchenne muscular dystrophy geneH J Klamut, S B Gangopadhyay, R G Worton, et al.
Indian Journal of Dermatology, Venereology and Leprology|February 3, 2017
Vdrl-sero-survey in Sirmur District of Himachal PradeshS K Bagchi, Subhash Chakraborty, A Das, et al.
Cureus|August 7, 2024
Hypertension and Device-Based Therapies for Resistant Hypertension: An Up-to-Date ReviewOluwaremilekun Tolu-Akinnawo, David N Ray, Tiwalade Awosanya, et al.
American Journal of Medical Genetics|May 30, 1998
FGFR2 mutation associated with clinical manifestations consistent with Antley-Bixler syndromeK Chun, J Siegel-Bartelt, D Chitayat, et al.
Bioinformatics (Oxford, England)|June 6, 2013
Identification of deleterious synonymous variants in human genomesOrion J Buske, AshokKumar Manickaraj, Seema Mital, et al.
European Journal of Human Genetics : EJHG|April 6, 2017
Severe neurodegeneration, progressive cerebral volume loss and diffuse hypomyelination associated with a homozygous frameshift mutation in CSTBAlan O'Brien, Christian R Marshall, Susan Blaser, et al.
Clinical Pediatrics|September 7, 2025
Relationship Between Household Social Risk and Symptoms of Depression and Anxiety in Adolescents: A Retrospective Cohort StudyDeepak Palakshappa, Kristin N Ray, Kelsey Schweiberger, et al.
The EMBO Journal|December 1, 1991
Molecular analysis of X-autosome translocations in females with Duchenne muscular dystrophyS E Bodrug, J J Holden, P N Ray, et al.
Pageof 57