Mutation of EMG1 causing Bowen-Conradi syndrome results in reduced cell proliferation rates concomitant with G2/M arrest and 18S rRNA processing delay.

Armistead, Joy; Hemming, Richard; Patel, Nehal; Triggs-Raine, Barbara

Armistead, Joy; Hemming, Richard; Patel, Nehal; Triggs-Raine, Barbara.

Afiliación

Armistead J; Department of Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, Manitoba, Canada ; Manitoba Institute of Child Health, Winnipeg, Manitoba, Canada.
Hemming R; Department of Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, Manitoba, Canada.
Patel N; Department of Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, Manitoba, Canada.
Triggs-Raine B; Department of Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, Manitoba, Canada ; Manitoba Institute of Child Health, Winnipeg, Manitoba, Canada.

BBA Clin ; 1: 33-43, 2014 Jun.

Article en En | MEDLINE | ID: mdl-26676230

Palabras clave

BCS, BowenConradi syndrome; BowenConradi syndrome; CPM, counts per minute; Cell proliferation; EMG1; EMG1, Essential for Mitotic Growth 1; IRES, internal ribosomal entry site.; Ribosome biogenesis; Ribosomopathy; SAM, S-adenosylmethionine; m1acp3-ψ, N1-methyl-N3-(3-amino-3-carboxypropyl) pseudouridine; rRNA; snoRNA, small nucleolar RNA

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: BBA Clin Año: 2014 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Países Bajos

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