Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Grant H. Young"'
Autor:
George Dialynas, Om K Shrestha, Jessica M Ponce, Monika Zwerger, Dylan A Thiemann, Grant H Young, Steven A Moore, Liping Yu, Jan Lammerding, Lori L Wallrath
Publikováno v:
PLoS Genetics, Vol 11, Iss 5, p e1005231 (2015)
Mutations in the human LMNA gene cause muscular dystrophy by mechanisms that are incompletely understood. The LMNA gene encodes A-type lamins, intermediate filaments that form a network underlying the inner nuclear membrane, providing structural supp
Externí odkaz:
https://doaj.org/article/4c60fc51ebc44279a70fea6f7284eab9
Autor:
Richard L. Amendola, Matthew P. Abdel, John J. Callaghan, Grant H. Young, David G. Lewallen, Devon D. Goetz
Publikováno v:
The Journal of Arthroplasty. 32:3480-3483
Background The authors and others have previously described the technique of cementing constrained liners into secure cementless acetabular shells and reported the short-term, average 3.9-year follow-up, using that technique. The purpose of the prese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::675874528cc3980f310fa2ac822e4bac
https://doi.org/10.1016/j.arth.2017.07.014
https://doi.org/10.1016/j.arth.2017.07.014
Autor:
Lori L. Wallrath, Shruti Bhide, Girish C. Melkani, Grant H. Young, Mastaneh Nikravesh, Maureen T. O'Connor, Sahaana Chandran, Adriana S. Trujillo, Diane E. Cryderman
Publikováno v:
Aging Cell
Summary Mutations in the human LMNA gene cause a collection of diseases known as laminopathies. These include myocardial diseases that exhibit age‐dependent penetrance of dysrhythmias and heart failure. The LMNA gene encodes A‐type lamins, interm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f471216a232685f03b503beef4cab95f
https://doi.org/10.1111/acel.12747
https://doi.org/10.1111/acel.12747
Autor:
Monika Zwerger, George Dialynas, Grant H. Young, Liping Yu, Jessica M. Ponce, Lori L. Wallrath, Steven A. Moore, Dylan A. Thiemann, Om K. Shrestha, Jan Lammerding
Publikováno v:
PLoS Genetics
PLoS Genetics, Vol 11, Iss 5, p e1005231 (2015)
PLoS Genetics, Vol 11, Iss 5, p e1005231 (2015)
Mutations in the human LMNA gene cause muscular dystrophy by mechanisms that are incompletely understood. The LMNA gene encodes A-type lamins, intermediate filaments that form a network underlying the inner nuclear membrane, providing structural supp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e00a4f5a89982d3032d093c8e64d54b8
https://pubmed.ncbi.nlm.nih.gov/25996830
https://pubmed.ncbi.nlm.nih.gov/25996830