Results 231 to 240 of about 22,553 (288)

Excess surface area of the nuclear lamina enables unhindered cell migration through constrictions. [PDF]

Sci Adv
McKee B, Abolghasemzade S, Wang TC, Harsh K, Kaur S, Blanchard R, Menon KB, Mohajeri M, Dickinson RB, Lele TP.   +9 more
europepmc   +1 more source

Dysfunctional cardiomyocyte signalling and heart disease. [PDF]

Curr Opin Cell Biol
Ridgway ZL, Li X.
europepmc   +1 more source

Lamin AC Cardiomyopathy, the Next Masquerader: Laminopathy Mimicking Cardiac Sarcoidosis. [PDF]

Cureus
Bashir H, Palmer C, Reddy A, Mazur W, OBrien T.   +4 more
europepmc   +1 more source

Genotype-phenotype insights of pediatric dilated cardiomyopathy. [PDF]

Front Pediatr
Dai Y, Wang Y, Fan Y, Han B.
europepmc   +1 more source

Disease pathogenicity in Hutchinson-Gilford progeria syndrome mice: insights from lung-associated alterations. [PDF]

Mol Med
Wang J, Guan Y, Wang Y, Tan J, Cao Z, Ding Y, Gao L, Fu H, Chen X, Lin J, Shen N, Fu X, Wang F, Mao J, Hu L.   +14 more
europepmc   +1 more source

Health-Related Physical Fitness in Women with Dunnigan Lipodystrophy with Mutation in LMNA Gene

, 2017
Luciana Zaranza Monteiro, Maria Cristina Foss‐Freitas, Júlio César Crescêncio, Lourenço Gallo Júnior, Fernanda Coelis, Francisco A. Pereira, Estela Cristina Carneseca, Renan Magalhães Montenegro, Milton Foss   +8 more
openalex   +1 more source

Downregulation of Nesprin1 by Runx2 deficiency is critical for the development of skeletal laminopathy-like pathology. [PDF]

Proc Natl Acad Sci U S A
Saito A, Nagayama K, Okada H, Onodera S, Aida N, Nakamura T, Sawada T, Hojo H, Kato S, Azuma T.   +9 more
europepmc   +1 more source

Clustering cell nuclei on microgrooves for disease diagnosis using deep learning. [PDF]

Sci Rep
Roellinger B, Thenier F, Leclech C, Coirault C, Angelini E, Barakat AI.   +5 more
europepmc   +1 more source

Major nuclear locales define nuclear genome organization and function beyond A and B compartments. [PDF]

Elife
Gholamalamdari O, van Schaik T, Wang Y, Kumar P, Zhang L, Zhang Y, Gonzalez GAH, Vouzas AE, Zhao PA, Gilbert DM, Ma J, van Steensel B, Belmont AS.   +12 more
europepmc   +1 more source

A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes

Genetics in Medicine, 2019
Joseph Park, M. Levin, C. Haggerty, Dustin N. Hartzel, R. Judy, R. Kember, N. Reza, M. Ritchie, A. Owens, S. Damrauer, D. Rader   +10 more
semanticscholar   +1 more source