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 Ray

Showing results (541-550 of 566) with videos related to

Pageof 57
Sort By:
BMC Genomics|April 30, 2015
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M SyndromeChristian R Marshall, Sandra A Farrell, Donna Cushing, et al.
Journal of Studies on Alcohol and Drugs|March 24, 2026
Behaviors and Norms Regarding Sexual Violence and Alcohol Use: How Do Service Members and College Students CompareKristen H Walter, Laura D Crocker, Travis N Ray, et al.
Human Genetics|September 30, 2005
The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitisMichele D Bishop, Steven D Freedman, Julian Zielenski, et al.
Science (New York, N.Y.)|July 1, 2017
ELABELA deficiency promotes preeclampsia and cardiovascular malformations in miceLena Ho, Marie van Dijk, Sam Tan Jian Chye, et al.
Cell Stem Cell|September 22, 2015
ELABELA Is an Endogenous Growth Factor that Sustains hESC Self-Renewal via the PI3K/AKT PathwayLena Ho, Shawn Y X Tan, Sheena Wee, et al.
Stem Cell Reports|June 8, 2017
Long-Term Culture of Self-renewing Pancreatic Progenitors Derived from Human Pluripotent Stem CellsJamie Trott, Ee Kim Tan, Sheena Ong, et al.
EMBO Molecular Medicine|July 2, 2017
Orkambi® and amplifier co-therapy improves function from a rare <i>CFTR</i> mutation in gene-edited cells and patient tissueSteven V Molinski, Saumel Ahmadi, Wan Ip, et al.
Annals of the American Thoracic Society|October 15, 2025
Pulmonary Artery Size on CT Associates with Mean Pulmonary Artery Pressure and MortalityTyler J Couch, Gerald J Beck, Erika B Rozenzweig, et al.
Neurology. Genetics|December 14, 2016
Clinical and genetic study of hereditary spastic paraplegia in CanadaNicolas Chrestian, Nicolas Dupré, Ziv Gan-Or, et al.
Nature Genetics|July 26, 2017
PRDM15 safeguards naive pluripotency by transcriptionally regulating WNT and MAPK-ERK signalingSlim Mzoughi, Jingxian Zhang, Delphine Hequet, et al.
Pageof 57

Showing results (541-550 of 566) with videos related to

Sort By:
Pageof 57
BMC Genomics|April 30, 2015
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M SyndromeChristian R Marshall, Sandra A Farrell, Donna Cushing, et al.
Journal of Studies on Alcohol and Drugs|March 24, 2026
Behaviors and Norms Regarding Sexual Violence and Alcohol Use: How Do Service Members and College Students CompareKristen H Walter, Laura D Crocker, Travis N Ray, et al.
Human Genetics|September 30, 2005
The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitisMichele D Bishop, Steven D Freedman, Julian Zielenski, et al.
Science (New York, N.Y.)|July 1, 2017
ELABELA deficiency promotes preeclampsia and cardiovascular malformations in miceLena Ho, Marie van Dijk, Sam Tan Jian Chye, et al.
Cell Stem Cell|September 22, 2015
ELABELA Is an Endogenous Growth Factor that Sustains hESC Self-Renewal via the PI3K/AKT PathwayLena Ho, Shawn Y X Tan, Sheena Wee, et al.
Stem Cell Reports|June 8, 2017
Long-Term Culture of Self-renewing Pancreatic Progenitors Derived from Human Pluripotent Stem CellsJamie Trott, Ee Kim Tan, Sheena Ong, et al.
EMBO Molecular Medicine|July 2, 2017
Orkambi® and amplifier co-therapy improves function from a rare <i>CFTR</i> mutation in gene-edited cells and patient tissueSteven V Molinski, Saumel Ahmadi, Wan Ip, et al.
Annals of the American Thoracic Society|October 15, 2025
Pulmonary Artery Size on CT Associates with Mean Pulmonary Artery Pressure and MortalityTyler J Couch, Gerald J Beck, Erika B Rozenzweig, et al.
Neurology. Genetics|December 14, 2016
Clinical and genetic study of hereditary spastic paraplegia in CanadaNicolas Chrestian, Nicolas Dupré, Ziv Gan-Or, et al.
Nature Genetics|July 26, 2017
PRDM15 safeguards naive pluripotency by transcriptionally regulating WNT and MAPK-ERK signalingSlim Mzoughi, Jingxian Zhang, Delphine Hequet, et al.
Pageof 57