Ribosomopathies: mechanisms of disease. - Test2 - elhamkhani - TriplyDB

Ribosomopathies: mechanisms of disease.

Ribosomopathies: mechanisms of disease.

http://www.wikidata.org/entity/Q34454066

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Regulatory Roles of Rpl22 in Hematopoiesis: An Old Dog with New Tricks Structural dynamics of the yeast Shwachman-Diamond syndrome protein (Sdo1) on the ribosome and its implication in the 60S subunit maturation GATA1 and PU.1 Bind to Ribosomal Protein Genes in Erythroid Cells: Implications for Ribosomopathies.Fungal Ribotoxins: A Review of Potential Biotechnological Applications.RP-MDM2-p53 Pathway: Linking Ribosomal Biogenesis and Tumor Surveillance.Rpl22 Loss Selectively Impairs αβ T Cell Development by Dysregulating Endoplasmic Reticulum Stress Signaling.Perturbation of RNA Polymerase I transcription machinery by ablation of HEATR1 triggers the RPL5/RPL11-MDM2-p53 ribosome biogenesis stress checkpoint pathway in human cells.The SSU processome interactome in Saccharomyces cerevisiae reveals novel protein subcomplexes.Molecular analysis and genotype-phenotype correlation of Diamond-Blackfan anemia.Structural Analysis Reveals Features of Ribosome Assembly Factor Nsa1/WDR74 Important for Localization and Interaction with Rix7/NVL2.The Roles of MDM2 and MDMX in Cancer.Further evidence for the involvement of in a Shwachman-Diamond-like syndrome and expansion of the phenotypic features

P2860

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P2860

Ribosomopathies: mechanisms of disease.

http://www.wikidata.org/entity/Q34454066

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2014 nî lūn-bûn

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2014 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

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2014 թվականի օգոստոսին հրատարակված գիտական հոդված

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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年論文

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2014年论文

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name

Ribosomopathies: mechanisms of disease.

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Ribosomopathies: mechanisms of disease.

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Ribosomopathies: mechanisms of disease.

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Ribosomopathies: mechanisms of disease.

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Ribosomopathies: mechanisms of disease.

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Ribosomopathies: mechanisms of disease.

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Ribosomopathies: mechanisms of disease.

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Ribosomopathies: mechanisms of disease.

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Ribosomopathies: mechanisms of disease.

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Clinical medicine insights. Blood disorders

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Ribosomopathies: mechanisms of disease.

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Hani Nakhoul

http://www.w3.org/2001/XMLSchema#string

Hua Lu

http://www.w3.org/2001/XMLSchema#string

Jiangwei Ke

http://www.w3.org/2001/XMLSchema#string

Shelya X Zeng

http://www.w3.org/2001/XMLSchema#string

Wenjuan Liao

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Xiang Zhou

http://www.w3.org/2001/XMLSchema#string

P2860

NOL11, implicated in the pathogenesis of North American Indian childhood cirrhosis, is required for pre-rRNA transcription and processing

Reduced transcription of TCOF1 in adult cells of Treacher Collins syndrome patients

The ribosome assembly factor Nep1 responsible for Bowen-Conradi syndrome is a pseudouridine-N1-specific methyltransferase

The Shwachman-Diamond SBDS protein localizes to the nucleolus

Uncoupling of GTP hydrolysis from eIF6 release on the ribosome causes Shwachman-Diamond syndrome

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

The human Shwachman-Diamond syndrome protein, SBDS, associates with ribosomal RNA

Identification of RPS14 as a 5q- syndrome gene by RNA interference screen

Impaired ribosome biogenesis in Diamond-Blackfan anemia

SBDS expression and localization at the mitotic spindle in human myeloid progenitors

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10.4137/CMBD.S16952

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7

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2014-08-14T00:00:00Z

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