Results 121 to 130 of about 3,144 (163)

At the nucleus of cancer: how the nuclear envelope controls tumor progression. [PDF]

MedComm (2020)
Paganelli F, Poli A, Truocchio S, Martelli AM, Palumbo C, Lattanzi G, Chiarini F.   +6 more
europepmc   +1 more source

Human iPSC-Derived Muscle Cells as a New Model for Investigation of EDMD1 Pathogenesis. [PDF]

Int J Mol Sci
Lisowska M, Rowińska M, Suszyńska A, Bearzi C, Łaczmańska I, Hanusek J, Kunik A, Dzianisava V, Rzepecki R, Machowska M, Piekarowicz K.   +10 more
europepmc   +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

Mechanosensitive nuclear checkpoint: nuclear envelope as a sensor of chromosomal instability and driver of cell fate. [PDF]

Mechanobiol Med
Ji C, Chen J, Wei F.
europepmc   +1 more source

The nucleus as a mechanobiological hub in muscle aging. [PDF]

Nucleus
Esen O, Battey E, Stroud MJ, Kirby TJ.
europepmc   +1 more source

Membrane curvature elastic stress triggers recruitment of PML-II onto the inner nuclear membrane. [PDF]

Mol Biol Cell
McPhee M, Salsman J, Newman AA, Voutsina N, Crosby AH, Dellaire G, Ridgway ND.   +6 more
europepmc   +1 more source

Emerin preserves stem cell survival through maintenance of centrosome and nuclear lamina structure.

Development
Jones SD, Miller JEB, Amos MM, Hernández JM, Piaszynski KM, Geyer PK.   +5 more
europepmc   +1 more source

Dissociation of Emerin for from Barrier-to-autointegration Factor is Regulated through Mitotic Phosphorylation of Emerin in a Xenopus Egg Cell-free System

Dissociation of Emerin for from Barrier-to-autointegration Factor is Regulated through Mitotic Phosphorylation of Emerin in a Xenopus Egg Cell-free System
openaire  

Emerin in health and disease [PDF]

Seminars in Cell and Developmental Biology, 2014
Emery-Dreifuss muscular dystrophy (EDMD) is caused by mutations in the genes encoding emerin, lamins A and C and FHL1. Additional EDMD-like syndromes are caused by mutations in nesprins and LUMA. This review will specifically focus on emerin function and the current thinking for how loss or mutations in emerin cause EDMD.
James Holaska
exaly   +3 more sources