Results 141 to 150 of about 3,036 (198)

Detection of Nuclear Blebbing and DNA Leakage in Mammalian Cells by Immunofluorescence. [PDF]

J Vis Exp
DiCintio AJ, Joudeh LA, Waldman AS.
europepmc   +1 more source

Relationships between nuclear lamins and telomere biology in progeroid laminopathies and cancer

, 2015
R. James Turner
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

Clinical and metabolic consequences of a historic pathogenic lamin A/C founder variant. [PDF]

Sci Rep
Wong LY, Torfs T, Vanherle SJV, Janssen J, Claes GRF, Stroeks SLVM, Willemars MMA, Schianchi F, Kapsokalyvas D, Weltjens E, Swinnen A, Strzelecka A, Krapels IPC, Heymans SRB, Glatz J, van den Wijngaard A, Brunner HG, Broers J, Luiken JFP, Hoes MF, Verdonschot JAJ, Nabben M.   +21 more
europepmc   +1 more source

Interplay between microtubule interactome, myonuclei mechanotransduction, and positioning in myopathies. [PDF]

Nucleus
Castellano L, Caillol D, Streichenberger N, Gache V.   +3 more
europepmc   +1 more source

1P044 Molecular basis of conformational dynamics and enzymatical maturation process of nuclear lamin A related to onset of laminopathies(01B. Protein : Structure & Function,Poster,The 52nd Annual Meeting of the Biophysical Society of Japan(BSJ2014))

, 2014
Mai Tsunoda, M. Mio, Toshihiko Sugiki, Kazuhiro Mio   +3 more
openalex   +2 more sources

Comprehensive genetic screening of 70 severe adolescent idiopathic scoliosis probands reveals novel pathogenic variants and syndromic associations. [PDF]

Front Med (Lausanne)
Horbacz M, Koczkowska M, Rocławski M, Ceynowa M, Madanecki P, Sarkisyan D, Mieczkowski J, Śledzińska K, Dumanski JP, Pankowski R, Piotrowski A.   +10 more
europepmc   +1 more source

[Laminopathies--interdisciplinary problem].

Kardiologia polska, 2008
Zofia T, Bilińska, Anna, Fidziańska
openaire   +1 more source

NPPA-Associated Atrial Dilated Cardiomyopathy: Genotypic and Phenotypic Insights From an Ultrarare Inherited Disorder. [PDF]

JACC Case Rep
Forleo C, Dicorato MM, Carella MC, Basile P, Dentamaro I, Santobuono VE, Guaricci AI, Resta N, Ciccone MM, Arbustini E.   +9 more
europepmc   +1 more source