Ontology highlight
ABSTRACT:
INSTRUMENT(S): timsTOF Pro
ORGANISM(S): Homo Sapiens (human)
TISSUE(S): Cell Culture, Early Embryonic Cell
DISEASE(S): Cardiovascular System Disease
SUBMITTER: kyle brown
LAB HEAD: Lee Eckhardt
PROVIDER: PXD045092 | Pride | 2024-08-09
REPOSITORIES: Pride
Action | DRS | |||
---|---|---|---|---|
E317K2_analysis.tdf_bin | Other | |||
E317K3_analysis.tdf_bin | Other | |||
E317K4_analysis.tdf_bin | Other | |||
E317K_1_analysis.tdf_bin | Other | |||
N195K1analysis.tdf_bin | Other |
Items per page: 5 1 - 5 of 31 |
Anderson Corey L CL Brown Kyle A KA North Ryan J RJ Walters Janay K JK Kaska Sara T ST Wolff Mathew R MR Kamp Timothy J TJ Ge Ying Y Eckhardt Lee L LL
Journal of proteome research 20240508 6
Lamin A/C (LMNA) is an important component of nuclear lamina. Mutations cause arrhythmia, heart failure, and sudden cardiac death. While LMNA-associated cardiomyopathy typically has an aggressive course that responds poorly to conventional heart failure therapies, there is variability in severity and age of penetrance between and even within specific mutations, which is poorly understood at the cellular level. Further, this heterogeneity has not previously been captured to mimic the heterozygous ...[more]