Dissecting the transcriptional phenotype of ribosomal protein deficiency: implications for Diamond-Blackfan Anemia. - Wikidata - awgldk - TriplyDB

Dissecting the transcriptional phenotype of ribosomal protein deficiency: implications for Diamond-Blackfan Anemia.

Dissecting the transcriptional phenotype of ribosomal protein deficiency: implications for Diamond-Blackfan Anemia.

http://www.wikidata.org/entity/Q38994386

about

Ribosomopathies: Global process, tissue specific defects Ribosomopathies: how a common root can cause a tree of pathologies A novel ribosomopathy caused by dysfunction of RPL10 disrupts neurodevelopment and causes X-linked microcephaly in humans.Ribosomopathies and the paradox of cellular hypo- to hyperproliferation.Whole-genome RNAi screen highlights components of the endoplasmic reticulum/Golgi as a source of resistance to immunotoxin-mediated cytotoxicity The lysine residues within the human ribosomal protein S17 sequence naturally inserted into the viral nonstructural protein of a unique strain of hepatitis E virus are important for enhanced virus replication.Identification and fine mapping of nuclear and nucleolar localization signals within the human ribosomal protein S17.Immunophenotypic Profiling of Erythroid Progenitor-Derived Extracellular Vesicles in Diamond-Blackfan Anaemia: A New Diagnostic Strategy SBDS-Deficient Cells Have an Altered Homeostatic Equilibrium due to Translational Inefficiency Which Explains their Reduced Fitness and Provides a Logical Framework for Intervention.Alteration of heme metabolism in a cellular model of Diamond-Blackfan anemia.Probing the mechanisms underlying human diseases in making ribosomes.Lymphoblastoid cell lines from Diamond Blackfan anaemia patients exhibit a full ribosomal stress phenotype that is rescued by gene therapy.The Evolution of the Ribosomal Protein-MDM2-p53 Pathway.

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Dissecting the transcriptional phenotype of ribosomal protein deficiency: implications for Diamond-Blackfan Anemia.

http://www.wikidata.org/entity/Q38994386

description

2014 nî lūn-bûn

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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Dissecting the transcriptional ...... s for Diamond-Blackfan Anemia.

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Dissecting the transcriptional ...... s for Diamond-Blackfan Anemia.

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J.GENE.2014.04.077

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Dissecting the transcriptional ...... s for Diamond-Blackfan Anemia.

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Anna Aspesi

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Antonella Ronchi

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Claudio Santoro

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Elisa Pavesi

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Emilio Marengo

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Federica Avondo

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Hélène Moniz

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Ilenia Boria

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Irma Dianzani

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Lydie Da Costa

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P2860

Human RPS19, the gene mutated in Diamond-Blackfan anemia, encodes a ribosomal protein required for the maturation of 40S ribosomal subunits

ASC is a Bax adaptor and regulates the p53-Bax mitochondrial apoptosis pathway

Defective mitochondrial peroxiredoxin-3 results in sensitivity to oxidative stress in Fanconi anemia

Transcription factor GATA-1 regulates human HOXB2 gene expression in erythroid cells

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

The ribosomal basis of Diamond-Blackfan Anemia: mutation and database update

The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia

A rapid micropreparation technique for extraction of DNA-binding proteins from limiting numbers of mammalian cells

Transcriptional control of human p53-regulated genes

Ribosomal protein S19 deficiency leads to reduced proliferation and increased apoptosis but does not affect terminal erythroid differentiation in a cell line model of Diamond-Blackfan anemia.

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282-289

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10.1016/J.GENE.2014.04.077

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2

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Antonia Follenzi

Rossella Crescitelli

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2014-05-15T00:00:00Z

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