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

David Watkins

Showing results (171-180 of 208) with videos related to

Pageof 21
Sort By:
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 20, 2019
MRI Tumor Regression Grade and Circulating Tumor DNA as Complementary Tools to Assess Response and Guide Therapy Adaptation in Rectal CancerShelize Khakoo, Paul David Carter, Gina Brown, et al.
American Journal of Human Genetics|July 2, 2021
Shifting landscapes of human MTHFR missense-variant effectsJochen Weile, Nishka Kishore, Song Sun, et al.
Nature Communications|January 11, 2022
Mutations in Hcfc1 and Ronin result in an inborn error of cobalamin metabolism and ribosomopathyTiffany Chern, Annita Achilleos, Xuefei Tong, et al.
Frontiers in Oncology|October 5, 2020
Diagnostic Accuracy and Safety of Coaxial System in Oncology Patients Treated in a Specialist Cancer Center With Prospective Validation Within Clinical Trial DataKhurum Khan, Reyes Gonzalez-Exposito, David Cunningham, et al.
American Journal of Medical Genetics. Part A|February 2, 2022
Probing the functional consequence and clinical relevance of CD320 p.E88del, a variant in the transcobalamin receptor geneFaith Pangilinan, David Watkins, David Bernard, et al.
American Journal of Human Genetics|September 10, 2013
An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1Hung-Chun Yu, Jennifer L Sloan, Gunter Scharer, et al.
Lancet (London, England)|November 24, 2024
Halving premature death and improving quality of life at all ages: cross-country analyses of past trends and future directionsOle F Norheim, Angela Y Chang, Sarah Bolongaita, et al.
Clinical Epigenetics|April 20, 2022
Epimutations in both the TESK2 and MMACHC promoters in the Epi-cblC inherited disorder of intracellular metabolism of vitamin B<sub>12</sub>Abderrahim Oussalah, Youssef Siblini, Sébastien Hergalant, et al.
Journal of the American Heart Association|March 28, 2023
American Heart Association's Children's Strategically Focused Research Network ExperienceCraig Sable, Jennifer S Li, Martin Tristani-Firouzi, et al.
Nature Genetics|August 28, 2012
Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolismDavid Coelho, Jaeseung C Kim, Isabelle R Miousse, et al.
Pageof 21

Showing results (171-180 of 208) with videos related to

Sort By:
Pageof 21
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 20, 2019
MRI Tumor Regression Grade and Circulating Tumor DNA as Complementary Tools to Assess Response and Guide Therapy Adaptation in Rectal CancerShelize Khakoo, Paul David Carter, Gina Brown, et al.
American Journal of Human Genetics|July 2, 2021
Shifting landscapes of human MTHFR missense-variant effectsJochen Weile, Nishka Kishore, Song Sun, et al.
Nature Communications|January 11, 2022
Mutations in Hcfc1 and Ronin result in an inborn error of cobalamin metabolism and ribosomopathyTiffany Chern, Annita Achilleos, Xuefei Tong, et al.
Frontiers in Oncology|October 5, 2020
Diagnostic Accuracy and Safety of Coaxial System in Oncology Patients Treated in a Specialist Cancer Center With Prospective Validation Within Clinical Trial DataKhurum Khan, Reyes Gonzalez-Exposito, David Cunningham, et al.
American Journal of Medical Genetics. Part A|February 2, 2022
Probing the functional consequence and clinical relevance of CD320 p.E88del, a variant in the transcobalamin receptor geneFaith Pangilinan, David Watkins, David Bernard, et al.
American Journal of Human Genetics|September 10, 2013
An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1Hung-Chun Yu, Jennifer L Sloan, Gunter Scharer, et al.
Lancet (London, England)|November 24, 2024
Halving premature death and improving quality of life at all ages: cross-country analyses of past trends and future directionsOle F Norheim, Angela Y Chang, Sarah Bolongaita, et al.
Clinical Epigenetics|April 20, 2022
Epimutations in both the TESK2 and MMACHC promoters in the Epi-cblC inherited disorder of intracellular metabolism of vitamin B<sub>12</sub>Abderrahim Oussalah, Youssef Siblini, Sébastien Hergalant, et al.
Journal of the American Heart Association|March 28, 2023
American Heart Association's Children's Strategically Focused Research Network ExperienceCraig Sable, Jennifer S Li, Martin Tristani-Firouzi, et al.
Nature Genetics|August 28, 2012
Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolismDavid Coelho, Jaeseung C Kim, Isabelle R Miousse, et al.
Pageof 21