Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Bethan Lemley"'
Autor:
Cheng Cui, Bishwanath Chatterjee, Deanne Francis, Qing Yu, Jovenal T. SanAgustin, Richard Francis, Terry Tansey, Charisse Henry, Baolin Wang, Bethan Lemley, Gregory J. Pazour, Cecilia W. Lo
Publikováno v:
Disease Models & Mechanisms, Vol 4, Iss 1, Pp 43-56 (2011)
SUMMARY Meckel-Gruber syndrome (MKS) is a recessive disorder resulting in multiple birth defects that are associated with mutations affecting ciliogenesis. We recovered a mouse mutant with a mutation in the Mks1 gene (Mks1del64-323) that caused a 260
Externí odkaz:
https://doaj.org/article/bf8f8da5e4e4498ebca37febe1fe095f
Autor:
Michael L O'Byrne, Lihai Song, Jing Huang, Bethan Lemley, David Goldberg, Monique M Gardner, Chitra Ravishankar, Jonathan J Rome, Andrew C Glatz
Publikováno v:
American Heart Journal. 263:35-45
Publikováno v:
Cardiology in the young.
First-year cardiology fellows must quickly learn basic competency in echocardiography during fellowship orientation. This educational process was disrupted in 2020 due to the coronavirus pandemic, as our hands-on echocardiography teaching transitione
Autor:
Bethan Lemley, Kiona Allen
Publikováno v:
Circulation. Cardiovascular quality and outcomes. 15(4)
Autor:
Bethan Lemley, Catherine W. Gillespie, Tyler Bradley-Hewitt, Twalib Aliku, Andrea Dantin, Craig Sable, Peter Lwabi, Michelle Ploutz, Andrea Beaton
Publikováno v:
Cardiology in the Young. 27:82-89
IntroductionRheumatic heart disease causes substantial morbidity in children in low-income countries. School-based echocardiographic screening has been suggested as a means to identify children with latent disease; however, little is known about the
Autor:
Cheng Cui, Richard Francis, Deanne Francis, Terry Tansey, Jovenal T. SanAgustin, Charisse Henry, Bishwanath Chatterjee, Gregory J. Pazour, Cecilia W. Lo, Baolin Wang, Qing Yu, Bethan Lemley
Publikováno v:
Disease Models & Mechanisms
Disease Models & Mechanisms, Vol 4, Iss 1, Pp 43-56 (2011)
Disease Models & Mechanisms, Vol 4, Iss 1, Pp 43-56 (2011)
SUMMARY Meckel-Gruber syndrome (MKS) is a recessive disorder resulting in multiple birth defects that are associated with mutations affecting ciliogenesis. We recovered a mouse mutant with a mutation in the Mks1 gene (Mks1del64-323) that caused a 260