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

Debra S Regier

Showing results (21-30 of 38) with videos related to

Pageof 4
Sort By:
Proceedings of the National Academy of Sciences of the United States of America|May 17, 2005
Diacylglycerol kinase iota regulates Ras guanyl-releasing protein 3 and inhibits Rap1 signalingDebra S Regier, Jared Higbee, Katrina M Lund, et al.
Obstetrics and Gynecology|January 25, 2013
Management of reproductive health in Cowden syndrome complicated by endometrial polyps and breast cancerAsli Kalin, Melissa A Merideth, Debra S Regier, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 11, 2021
Pediatric medical genetics house call: Telemedicine for the next generation of patients and providersAndrea J Cohen, Natasha Shur, Danielle Starin, et al.
Science (New York, N.Y.)|February 3, 2007
Targeting of diacylglycerol degradation to M1 muscarinic receptors by beta-arrestinsChristopher D Nelson, Stephen J Perry, Debra S Regier, et al.
American Journal of Medical Genetics. Part A|January 28, 2023
The past, present, and future of child growth monitoring: A review and primer for clinical geneticsNatasha Shur, Annie Tigranyan, Carrie Daymont, et al.
Translational Science of Rare Diseases|May 23, 2022
The Rare Disease Research Scholars Program: A training curriculum for clinical researchers with mixed methods evaluation studyDebra S Regier, Jennifer A Weaver, Nancy Cheng, et al.
Molecular Genetics and Metabolism|April 10, 2025
Recruitment through empathy and education: The role of the clinical experience on workforce developmentRishisree Achanta, Ashley Cannon, Shayla R Goldberg, et al.
American Journal of Medical Genetics. Part A|October 14, 2020
Rapid deployment of a telemedicine care model for genetics and metabolism during COVID-19Natasha Shur, Shireen M Atabaki, Monisha S Kisling, et al.
Molecular Genetics and Metabolism Reports|December 21, 2016
Diagnosis of LCHAD/TFP deficiency in an at risk newborn using umbilical cord blood acylcarnitine analysisDonna B Raval, Kristina P Cusmano-Ozog, Omar Ayyub, et al.
JIMD Reports|December 26, 2024
Mitochondrial trifunctional protein deficiency caused by a deep intronic deletion leading to aberrant splicingThomas Cassini, Sarah Silverstein, Molly Behan, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
Proceedings of the National Academy of Sciences of the United States of America|May 17, 2005
Diacylglycerol kinase iota regulates Ras guanyl-releasing protein 3 and inhibits Rap1 signalingDebra S Regier, Jared Higbee, Katrina M Lund, et al.
Obstetrics and Gynecology|January 25, 2013
Management of reproductive health in Cowden syndrome complicated by endometrial polyps and breast cancerAsli Kalin, Melissa A Merideth, Debra S Regier, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 11, 2021
Pediatric medical genetics house call: Telemedicine for the next generation of patients and providersAndrea J Cohen, Natasha Shur, Danielle Starin, et al.
Science (New York, N.Y.)|February 3, 2007
Targeting of diacylglycerol degradation to M1 muscarinic receptors by beta-arrestinsChristopher D Nelson, Stephen J Perry, Debra S Regier, et al.
American Journal of Medical Genetics. Part A|January 28, 2023
The past, present, and future of child growth monitoring: A review and primer for clinical geneticsNatasha Shur, Annie Tigranyan, Carrie Daymont, et al.
Translational Science of Rare Diseases|May 23, 2022
The Rare Disease Research Scholars Program: A training curriculum for clinical researchers with mixed methods evaluation studyDebra S Regier, Jennifer A Weaver, Nancy Cheng, et al.
Molecular Genetics and Metabolism|April 10, 2025
Recruitment through empathy and education: The role of the clinical experience on workforce developmentRishisree Achanta, Ashley Cannon, Shayla R Goldberg, et al.
American Journal of Medical Genetics. Part A|October 14, 2020
Rapid deployment of a telemedicine care model for genetics and metabolism during COVID-19Natasha Shur, Shireen M Atabaki, Monisha S Kisling, et al.
Molecular Genetics and Metabolism Reports|December 21, 2016
Diagnosis of LCHAD/TFP deficiency in an at risk newborn using umbilical cord blood acylcarnitine analysisDonna B Raval, Kristina P Cusmano-Ozog, Omar Ayyub, et al.
JIMD Reports|December 26, 2024
Mitochondrial trifunctional protein deficiency caused by a deep intronic deletion leading to aberrant splicingThomas Cassini, Sarah Silverstein, Molly Behan, et al.
Pageof 4