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

P Kirk

Showing results (191-200 of 269) with videos related to

Pageof 27
Sort By:
Molecular Genetics & Genomic Medicine|October 1, 2024
Deep Sequencing and Phenotyping in an Australian Tuberous Sclerosis Complex "No Mutations Identified" CohortClara W T Chung, Adam M Bournazos, Lok Chi Denise Chan, et al.
ACS Energy Letters|May 6, 2026
The Strategic Role of 2D Nanomaterials in Grid ModernizationMatthew Glasscott, James D Burgess, Peter Byrley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 16, 2022
Correspondence on "Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)" by Gregg et alSarah Righetti, Lisa Dive, Alison D Archibald, et al.
Circulation Research|February 18, 2006
Quantitative trait loci modifying cardiac atrial septal morphology and risk of patent foramen ovale in the mouseEdwin P Kirk, Changbaig Hyun, Peter C Thomson, et al.
American Journal of Physiology. Endocrinology and Metabolism|October 22, 2002
Sexual dimorphism is associated with decreased expression of processed myostatin in malesChristopher D McMahon, Ljiljana Popovic, Ferenc Jeanplong, et al.
Journal of the American College of Cardiology|June 12, 2003
Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndromeDavid A Elliott, Edwin P Kirk, Thomas Yeoh, et al.
Annals of the Academy of Medicine, Singapore|April 15, 2021
Psychosocial impact of the COVID-19 pandemic on paediatric healthcare workersAngela H P Kirk, Shu Ling Chong, Kai Qian Kam, et al.
Circulation|October 6, 2009
Cardiac T2* magnetic resonance for prediction of cardiac complications in thalassemia majorP Kirk, M Roughton, J B Porter, et al.
International Journal of Cardiology|December 20, 2016
The promises and challenges of exome sequencing in familial, non-syndromic congenital heart diseaseGillian M Blue, David Humphreys, Justin Szot, et al.
American Journal of Medical Genetics. Part A|November 2, 2011
Somatic mutations in NKX2–5, GATA4, and HAND1 are not a common cause of tetralogy of Fallot or hypoplastic left heartGiorgia Esposito, Tanya L Butler, Gillian M Blue, et al.
Pageof 27

Showing results (191-200 of 269) with videos related to

Sort By:
Pageof 27
Molecular Genetics & Genomic Medicine|October 1, 2024
Deep Sequencing and Phenotyping in an Australian Tuberous Sclerosis Complex "No Mutations Identified" CohortClara W T Chung, Adam M Bournazos, Lok Chi Denise Chan, et al.
ACS Energy Letters|May 6, 2026
The Strategic Role of 2D Nanomaterials in Grid ModernizationMatthew Glasscott, James D Burgess, Peter Byrley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 16, 2022
Correspondence on "Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)" by Gregg et alSarah Righetti, Lisa Dive, Alison D Archibald, et al.
Circulation Research|February 18, 2006
Quantitative trait loci modifying cardiac atrial septal morphology and risk of patent foramen ovale in the mouseEdwin P Kirk, Changbaig Hyun, Peter C Thomson, et al.
American Journal of Physiology. Endocrinology and Metabolism|October 22, 2002
Sexual dimorphism is associated with decreased expression of processed myostatin in malesChristopher D McMahon, Ljiljana Popovic, Ferenc Jeanplong, et al.
Journal of the American College of Cardiology|June 12, 2003
Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndromeDavid A Elliott, Edwin P Kirk, Thomas Yeoh, et al.
Annals of the Academy of Medicine, Singapore|April 15, 2021
Psychosocial impact of the COVID-19 pandemic on paediatric healthcare workersAngela H P Kirk, Shu Ling Chong, Kai Qian Kam, et al.
Circulation|October 6, 2009
Cardiac T2* magnetic resonance for prediction of cardiac complications in thalassemia majorP Kirk, M Roughton, J B Porter, et al.
International Journal of Cardiology|December 20, 2016
The promises and challenges of exome sequencing in familial, non-syndromic congenital heart diseaseGillian M Blue, David Humphreys, Justin Szot, et al.
American Journal of Medical Genetics. Part A|November 2, 2011
Somatic mutations in NKX2–5, GATA4, and HAND1 are not a common cause of tetralogy of Fallot or hypoplastic left heartGiorgia Esposito, Tanya L Butler, Gillian M Blue, et al.
Pageof 27