Gene-rich chromosomal regions are preferentially localized in the lamin b deficient nuclear blebs of atypical progeria cells

Nucleus

Volumn 6, Issue 1, 2015, Pages 66-76

  Pfleghaar, Katrin Bercht ^b   Taimen, Pekka ^c   Butin Israeli, Veronika ^a   Shimi, Takeshi ^a   Langer Freitag, Sabine ^d   Markaki, Yolanda ^b   Goldman, Anne E ^a   Wehnert, Manfred ^e   Goldman, Robert D ^a  

^a NORTHWESTERN UNIVERSITY   (United States)

^b UNIVERSITY OF MUNICH   (Germany)

^c UNIVERSITY OF TURKU   (Finland)

^d TECHNICAL UNIVERSITY OF MUNICH   (Germany)

^e UNIVERSITY OF GREIFSWALD   (Germany)

Author keywords

Blebs; Chromatin organization; Lamins; Progeria; Transcription

Indexed keywords

HISTONE H3; LAMIN A; LAMIN B; PLASMID VECTOR; PROTEIN; PROTEIN P53; RNA POLYMERASE II; SKI INTERACTING PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; CELL NUCLEUS MEMBRANE; CHROMOSOME; CHROMOSOME 17; CHROMOSOME 18; CHROMOSOME 19; CHROMOSOME PAINTING; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; EUCHROMATIN; FIBROBLAST; FLUORESCENCE IN SITU HYBRIDIZATION; GENE EXPRESSION; HUMAN; HUMAN CELL; IMMUNOBLOTTING; IMMUNOFLUORESCENCE; LASER CAPTURE MICRODISSECTION; NUCLEAR LAMINA; NUCLEAR PORE COMPLEX; PROGERIA; TRANSCRIPTION REGULATION; CELL NUCLEUS; CHILD; DEFICIENCY; FEMALE; GENETIC TRANSCRIPTION; GENETICS; HUMAN CHROMOSOME; METABOLISM; MUTATION; PATHOLOGY;

CELL NUCLEUS; CHILD; CHROMOSOMES, HUMAN; FEMALE; HUMANS; LAMIN TYPE B; MUTATION; PROGERIA; TRANSCRIPTION, GENETIC;

EID: 84924271991     PISSN: 19491034     EISSN: 19491042     Source Type: Journal    
DOI: 10.1080/19491034.2015.1004256     Document Type: Article

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