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

M Nolan

Showing results (1071-1080 of 1,093) with videos related to

Pageof 110
Sort By:
Diabetic Medicine : a Journal of the British Diabetic Association|February 3, 2019
An Irish National Diabetes in Pregnancy Audit: aiming for best outcomes for women with diabetesA M Egan, M J Brassill, E Brosnan, et al.
Molecular Therapy. Methods & Clinical Development|December 17, 2024
mRNA vaccines encoding membrane-anchored RBDs of SARS-CoV-2 mutants induce strong humoral responses and can overcome immune imprintingHareth A Al-Wassiti, Stewart A Fabb, Samantha L Grimley, et al.
Emerging Infectious Diseases|March 23, 2023
Adeno-Associated Virus 2 and Human Adenovirus F41 in Wastewater during Outbreak of Severe Acute Hepatitis in Children, IrelandNiamh A Martin, Gabriel Gonzalez, Liam J Reynolds, et al.
JAMA Network Open|January 29, 2026
Universal Newborn Screening for Congenital Cytomegalovirus Using Dried Blood Spot SpecimensNorma P Tavakoli, Virginia Sack, Andrew S Handel, et al.
BMJ Open Respiratory Research|January 6, 2026
Singing for lung health following completion of pulmonary rehabilitation: feasibility of a randomised controlled trialAdam Lewis, Peter Jung, Parris Williams, et al.
The Journal of Clinical Investigation|March 12, 2014
Dominant β-catenin mutations cause intellectual disability with recognizable syndromic featuresValter Tucci, Tjitske Kleefstra, Andrea Hardy, et al.
Genetica|December 29, 2004
Towards a mutant map of the mouse--new models of neurological, behavioural, deafness, bone, renal and blood disordersSohaila Rastan, Tertius Hough, Amy Kierman, et al.
Studies in Mycology|March 25, 2020
101 <i>Dothideomycetes</i> genomes: A test case for predicting lifestyles and emergence of pathogensS Haridas, R Albert, M Binder, et al.
Nature Genetics|August 10, 2000
A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouseP M Nolan, J Peters, M Strivens, et al.
American Journal of Human Genetics|May 31, 2016
Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic EncephalopathyMarianna Madeo, Michelle Stewart, Yuyang Sun, et al.
Pageof 110

Showing results (1071-1080 of 1,093) with videos related to

Sort By:
Pageof 110
Diabetic Medicine : a Journal of the British Diabetic Association|February 3, 2019
An Irish National Diabetes in Pregnancy Audit: aiming for best outcomes for women with diabetesA M Egan, M J Brassill, E Brosnan, et al.
Molecular Therapy. Methods & Clinical Development|December 17, 2024
mRNA vaccines encoding membrane-anchored RBDs of SARS-CoV-2 mutants induce strong humoral responses and can overcome immune imprintingHareth A Al-Wassiti, Stewart A Fabb, Samantha L Grimley, et al.
Emerging Infectious Diseases|March 23, 2023
Adeno-Associated Virus 2 and Human Adenovirus F41 in Wastewater during Outbreak of Severe Acute Hepatitis in Children, IrelandNiamh A Martin, Gabriel Gonzalez, Liam J Reynolds, et al.
JAMA Network Open|January 29, 2026
Universal Newborn Screening for Congenital Cytomegalovirus Using Dried Blood Spot SpecimensNorma P Tavakoli, Virginia Sack, Andrew S Handel, et al.
BMJ Open Respiratory Research|January 6, 2026
Singing for lung health following completion of pulmonary rehabilitation: feasibility of a randomised controlled trialAdam Lewis, Peter Jung, Parris Williams, et al.
The Journal of Clinical Investigation|March 12, 2014
Dominant β-catenin mutations cause intellectual disability with recognizable syndromic featuresValter Tucci, Tjitske Kleefstra, Andrea Hardy, et al.
Genetica|December 29, 2004
Towards a mutant map of the mouse--new models of neurological, behavioural, deafness, bone, renal and blood disordersSohaila Rastan, Tertius Hough, Amy Kierman, et al.
Studies in Mycology|March 25, 2020
101 <i>Dothideomycetes</i> genomes: A test case for predicting lifestyles and emergence of pathogensS Haridas, R Albert, M Binder, et al.
Nature Genetics|August 10, 2000
A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouseP M Nolan, J Peters, M Strivens, et al.
American Journal of Human Genetics|May 31, 2016
Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic EncephalopathyMarianna Madeo, Michelle Stewart, Yuyang Sun, et al.
Pageof 110