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

Michelle Webb

Showing results (41-50 of 48) with videos related to

Pageof 5
Sort By:
You have reached the last page of results.This site can display upto 48 results.
BMJ Open|May 20, 2021
Our journey, our story: a study protocol for the evaluation of a co-design framework to improve services for Aboriginal youth mental health and well-beingMichael Wright, Alex Brown, Patricia Dudgeon, et al.
Journal of Affective Disorders|December 16, 2003
Burden of dysthymia and comorbid illness in adults in a Canadian primary care setting: high rates of psychiatric illness in the offspringBarbara Bell, Lori Chalklin, Michael Mills, et al.
American Journal of Medical Genetics. Part A|April 6, 2022
High prevalence of deleterious mutations in concomitant nonsyndromic cleft and outflow tract heart defectsNaikhoba C O Munabi, Shady Mikhail, Omar Toubat, et al.
BMC Medical Education|June 16, 2026
Teaching at scale: a mixed-methods study of team-based learning analytics to enable early support in medical educationElizabeth Sheader, Lisa Donlan, Connor Allen, et al.
Plos Pathogens|October 3, 2015
Phospho-dependent Regulation of SAMHD1 Oligomerisation Couples Catalysis and RestrictionLaurence H Arnold, Harriet C T Groom, Simone Kunzelmann, et al.
Plos Medicine|November 2, 2006
Atypical haemolytic uraemic syndrome associated with a hybrid complement geneJulian P Venables, Lisa Strain, Danny Routledge, et al.
Human Mutation|July 4, 2012
A guide for functional analysis of BRCA1 variants of uncertain significanceGaël A Millot, Marcelo A Carvalho, Sandrine M Caputo, et al.
Nature|November 8, 2011
HIV-1 restriction factor SAMHD1 is a deoxynucleoside triphosphate triphosphohydrolaseDavid C Goldstone, Valerie Ennis-Adeniran, Joseph J Hedden, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
BMJ Open|May 20, 2021
Our journey, our story: a study protocol for the evaluation of a co-design framework to improve services for Aboriginal youth mental health and well-beingMichael Wright, Alex Brown, Patricia Dudgeon, et al.
Journal of Affective Disorders|December 16, 2003
Burden of dysthymia and comorbid illness in adults in a Canadian primary care setting: high rates of psychiatric illness in the offspringBarbara Bell, Lori Chalklin, Michael Mills, et al.
American Journal of Medical Genetics. Part A|April 6, 2022
High prevalence of deleterious mutations in concomitant nonsyndromic cleft and outflow tract heart defectsNaikhoba C O Munabi, Shady Mikhail, Omar Toubat, et al.
BMC Medical Education|June 16, 2026
Teaching at scale: a mixed-methods study of team-based learning analytics to enable early support in medical educationElizabeth Sheader, Lisa Donlan, Connor Allen, et al.
Plos Pathogens|October 3, 2015
Phospho-dependent Regulation of SAMHD1 Oligomerisation Couples Catalysis and RestrictionLaurence H Arnold, Harriet C T Groom, Simone Kunzelmann, et al.
Plos Medicine|November 2, 2006
Atypical haemolytic uraemic syndrome associated with a hybrid complement geneJulian P Venables, Lisa Strain, Danny Routledge, et al.
Human Mutation|July 4, 2012
A guide for functional analysis of BRCA1 variants of uncertain significanceGaël A Millot, Marcelo A Carvalho, Sandrine M Caputo, et al.
Nature|November 8, 2011
HIV-1 restriction factor SAMHD1 is a deoxynucleoside triphosphate triphosphohydrolaseDavid C Goldstone, Valerie Ennis-Adeniran, Joseph J Hedden, et al.
Pageof 5