Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

N Robinson

Showing results (1071-1080 of 1,318) with videos related to

Pageof 132
Sort By:
European Journal of Human Genetics : EJHG|June 12, 2014
Missense variant in CCDC22 causes X-linked recessive intellectual disability with features of Ritscher-Schinzel/3C syndromeMateusz Kolanczyk, Peter Krawitz, Jochen Hecht, et al.
Bone Marrow Transplantation|October 20, 2009
CD3(+) and/or CD14(+) depletion from cord blood mononuclear cells before ex vivo expansion culture improves total nucleated cell and CD34(+) cell yieldsH Yang, S N Robinson, J Lu, et al.
Nature Protocols|November 13, 2015
Next-generation diagnostics and disease-gene discovery with the ExomiserDamian Smedley, Julius O B Jacobsen, Marten Jäger, et al.
The Journal of Nutrition|May 28, 2021
Single Nucleotide Polymorphisms in CD36 Are Associated with Macular Pigment among ChildrenRuyu Liu, Bridget A Hannon, Katie N Robinson, et al.
Clinical Cardiology|August 13, 2014
Total serum transforming growth factor-β1 is elevated in the entire spectrum of genetic aortic syndromesMathias Hillebrand, Nathalie Millot, Sara Sheikhzadeh, et al.
Teaching and Learning in Medicine|February 26, 2020
Helping Scholars Overcome Socioeconomic Barriers to Medical and Biomedical Careers: Creating a Pipeline InitiativeDeidra C Crews, Katherine L Wilson, Jungsan Sohn, et al.
BMJ Health & Care Informatics|May 8, 2021
User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosisAlanna Kulchak Rahm, Nephi A Walton, Lynn K Feldman, et al.
American Journal of Medical Genetics. Part A|September 19, 2025
An ITPR1 Variant in the IP3-ITPR1 Binding Pocket Associated With a Clinical Phenotype of Athetoid Cerebral PalsyThania Ordaz, Jagadish Chandrabose Sundaramurthi, Adam S Arterbery, et al.
The American Journal of Cardiology|January 8, 2011
Predictors of outcome of mitral valve prolapse in patients with the Marfan syndromeMeike Rybczynski, Hendrik Treede, Sara Sheikhzadeh, et al.
Cytotherapy|May 16, 2006
Ex vivo expanded umbilical cord blood T cells maintain naive phenotype and TCR diversityS Parmar, S N Robinson, K Komanduri, et al.
Pageof 132

Showing results (1071-1080 of 1,318) with videos related to

Sort By:
Pageof 132
European Journal of Human Genetics : EJHG|June 12, 2014
Missense variant in CCDC22 causes X-linked recessive intellectual disability with features of Ritscher-Schinzel/3C syndromeMateusz Kolanczyk, Peter Krawitz, Jochen Hecht, et al.
Bone Marrow Transplantation|October 20, 2009
CD3(+) and/or CD14(+) depletion from cord blood mononuclear cells before ex vivo expansion culture improves total nucleated cell and CD34(+) cell yieldsH Yang, S N Robinson, J Lu, et al.
Nature Protocols|November 13, 2015
Next-generation diagnostics and disease-gene discovery with the ExomiserDamian Smedley, Julius O B Jacobsen, Marten Jäger, et al.
The Journal of Nutrition|May 28, 2021
Single Nucleotide Polymorphisms in CD36 Are Associated with Macular Pigment among ChildrenRuyu Liu, Bridget A Hannon, Katie N Robinson, et al.
Clinical Cardiology|August 13, 2014
Total serum transforming growth factor-β1 is elevated in the entire spectrum of genetic aortic syndromesMathias Hillebrand, Nathalie Millot, Sara Sheikhzadeh, et al.
Teaching and Learning in Medicine|February 26, 2020
Helping Scholars Overcome Socioeconomic Barriers to Medical and Biomedical Careers: Creating a Pipeline InitiativeDeidra C Crews, Katherine L Wilson, Jungsan Sohn, et al.
BMJ Health & Care Informatics|May 8, 2021
User testing of a diagnostic decision support system with machine-assisted chart review to facilitate clinical genomic diagnosisAlanna Kulchak Rahm, Nephi A Walton, Lynn K Feldman, et al.
American Journal of Medical Genetics. Part A|September 19, 2025
An ITPR1 Variant in the IP3-ITPR1 Binding Pocket Associated With a Clinical Phenotype of Athetoid Cerebral PalsyThania Ordaz, Jagadish Chandrabose Sundaramurthi, Adam S Arterbery, et al.
The American Journal of Cardiology|January 8, 2011
Predictors of outcome of mitral valve prolapse in patients with the Marfan syndromeMeike Rybczynski, Hendrik Treede, Sara Sheikhzadeh, et al.
Cytotherapy|May 16, 2006
Ex vivo expanded umbilical cord blood T cells maintain naive phenotype and TCR diversityS Parmar, S N Robinson, K Komanduri, et al.
Pageof 132