Perlman Syndrome: Overgrowth, Wilms Tumor Predisposition and DIS3L2.

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Perlman Syndrome: Overgrowth, Wilms Tumor Predisposition and DIS3L2.

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2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年學術文章

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2013年學術文章

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Perlman Syndrome: Overgrowth, Wilms Tumor Predisposition and DIS3L2.

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Perlman Syndrome: Overgrowth, Wilms Tumor Predisposition and DIS3L2.

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Perlman Syndrome: Overgrowth, Wilms Tumor Predisposition and DIS3L2.

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Perlman Syndrome: Overgrowth, Wilms Tumor Predisposition and DIS3L2.

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Perlman Syndrome: Overgrowth, Wilms Tumor Predisposition and DIS3L2.

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Perlman Syndrome: Overgrowth, Wilms Tumor Predisposition and DIS3L2.

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P1476

Perlman Syndrome: Overgrowth, Wilms Tumor Predisposition and DIS3L2.

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P2093

Dewi Astuti

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Eamonn R Maher

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Mark R Morris

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P2860

Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility

Human cell growth requires a functional cytoplasmic exosome, which is involved in various mRNA decay pathways

Human dis3p, which binds to either GTP- or GDP-Ran, complements Saccharomyces cerevisiae dis3

The human core exosome interacts with differentially localized processive RNases: hDIS3 and hDIS3L

Dis3-like 1: a novel exoribonuclease associated with the human exosome

Reconstitution, activities, and structure of the eukaryotic RNA exosome

Yeast exosome mutants accumulate 3'-extended polyadenylated forms of U4 small nuclear RNA and small nucleolar RNAs

Human Mps1 protein kinase is required for centrosome duplication and normal mitotic progression

The yeast exosome and human PM-Scl are related complexes of 3' --> 5' exonucleases

Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration

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scholarly article

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10.1002/J.1552-4876.2013.31358.X

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2013-04-09T00:00:00Z

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23576526

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