Results 191 to 200 of about 18,044 (328)
Editorial: Nuclear morphology in development and disease
Tanmay P. Lele+4 more
doaj +1 more source
Heterogeneity of Nuclear Lamin A Mutations in Dunnigan-Type Familial Partial Lipodystrophy* [PDF]
Robert A. Hegele+3 more
openalex +1 more source
Twin‐arginine translocation D (TatD) homologs are found across all kingdoms, with debated roles in DNA degradation and protein quality control in unicellular organisms. We characterize TATDN1, the mammalian TatD orthologue, as a proteostatic stress‐responsive cytosolic protein dispensable for DNA degradation.
Gisel Barés+19 more
wiley +1 more source
Lamin A/C Gene Mutation Associated With Dilated Cardiomyopathy With Variable Skeletal Muscle Involvement [PDF]
Gary Brodsky+5 more
openalex +1 more source
Arrhythmogenic Cardiomyopathy: Towards Genotype Based Diagnoses and Management
To improve arrhythmogenic cardiomyopathy (ACM) patient care four pillars of ACM research are necessary. The first pillar to improve ACM is cohort studies in which the genotype‐specific natural history of disease is described, and subsequently genotype‐specific risk calculators can be developed, such as the DSP and PLN risk calculators.
Steven A. Muller+13 more
wiley +1 more source
Nuclear envelope proteins, mechanotransduction, and their contribution to breast cancer progression. [PDF]
Henretta S, Lammerding J.
europepmc +1 more source
Lamin A/C mutation in a woman and her two daughters with Dunnigan-type partial lipodystrophy and insulin resistance. [PDF]
Robert A. Hegele+2 more
openalex +1 more source