Targeted disruption of the ribosomal protein S19 gene is lethal prior to implantation. - Wikidata - awgldk - TriplyDB

Targeted disruption of the ribosomal protein S19 gene is lethal prior to implantation.

Targeted disruption of the ribosomal protein S19 gene is lethal prior to implantation.

http://www.wikidata.org/entity/Q37424374

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Impaired ribosome biogenesis in Diamond-Blackfan anemia The role of human ribosomal proteins in the maturation of rRNA and ribosome production Ectopic mineralization in the middle ear and chronic otitis media with effusion caused by RPL38 deficiency in the Tail-short (Ts) mouse.Guarding the 'translation apparatus': defective ribosome biogenesis and the p53 signaling pathway Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes Molecular basis of Diamond Blackfan anemia: structure and function analysis of RPS19 Specific Role for Yeast Homologs of the Diamond Blackfan Anemia-associated Rps19 Protein in Ribosome Synthesis.Regulatory Roles of Rpl22 in Hematopoiesis: An Old Dog with New Tricks Inhibition of MDM2-mediated p53 ubiquitination and degradation by ribosomal protein L5 Crucial role of Bysl in mammalian preimplantation development as an integral factor for 40S ribosome biogenesis RACK1 depletion in a mouse model causes lethality, pigmentation deficits and reduction in protein synthesis efficiency RPLP1, a crucial ribosomal protein for embryonic development of the nervous system Loss of the mouse ortholog of the shwachman-diamond syndrome gene (Sbds) results in early embryonic lethality EMG1 is essential for mouse pre-implantation embryo development The ribosomal protein Rpl22 controls ribosome composition by directly repressing expression of its own paralog, Rpl22l1 The ribosomal protein L32-2 (RPL32-2) of S. pombe exhibits a novel extraribosomal function by acting as a potential transcriptional regulator.Ribosomal protein gene knockdown causes developmental defects in zebrafish.Clusters of basic amino acids contribute to RNA binding and nucleolar localization of ribosomal protein L22 Visualization of the spatial arrangement of nuclear organization using three-dimensional fluorescence in situ hybridization in early mouse embryos: A new "EASI-FISH chamber glass" for mammalian embryos.The role of the innate immune response regulatory gene ABCF1 in mammalian embryogenesis and development The ribosome filter redux.The emerging importance of ribosomal dysfunction in the pathogenesis of hematologic disorders.Ribosomal proteins and human diseases: pathogenesis, molecular mechanisms, and therapeutic implications Ribosomopathies: mechanisms of disease.Ribosomal proteins: functions beyond the ribosome Genetics of ribosomal proteins: "curiouser and curiouser"Dysregulation of RNA polymerase I transcription during disease.Untangling the phenotypic heterogeneity of Diamond Blackfan anemia.Animal models of Diamond Blackfan anemia.Reduced ribosomal protein gene dosage and p53 activation in low-risk myelodysplastic syndrome.Establishing Rps6 hemizygous mice as a model for studying how ribosomal protein haploinsufficiency impairs erythropoiesis.Proteomic Profile of Mabuya sp. (Squamata: Scincidae) Ovary and Placenta During Gestation.Inactivation of ribosomal protein L22 promotes transformation by induction of the stemness factor, Lin28B.Development of Soft Tissue Sarcomas in Ribosomal Proteins L5 and S24 Heterozygous Mice.The p53 pathway in hematopoiesis: lessons from mouse models, implications for humans.Recent insights into the pathogenesis of Diamond-Blackfan anaemia.Diamond-Blackfan anemia, ribosome and erythropoiesis.Feedback regulation of c-Myc by ribosomal protein L11 A Novel Mutation of Ribosomal Protein S19 Gene in a Chinese Child with Diamond-Blackfan Anemia Pathophysiology and management of inherited bone marrow failure syndromes.

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P2860

Targeted disruption of the ribosomal protein S19 gene is lethal prior to implantation.

http://www.wikidata.org/entity/Q37424374

description

article científic

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article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on May 2004

@en

vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Targeted disruption of the ribosomal protein S19 gene is lethal prior to implantation.

@en

Targeted disruption of the ribosomal protein S19 gene is lethal prior to implantation.

@nl

type

label

Targeted disruption of the ribosomal protein S19 gene is lethal prior to implantation.

@en

Targeted disruption of the ribosomal protein S19 gene is lethal prior to implantation.

@nl

prefLabel

Targeted disruption of the ribosomal protein S19 gene is lethal prior to implantation.

@en

Targeted disruption of the ribosomal protein S19 gene is lethal prior to implantation.

@nl

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MCB.24.9.4032-4037.2004

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Molecular and Cellular Biology

P1476

Targeted disruption of the ribosomal protein S19 gene is lethal prior to implantation.

@en

P2093

Andreas Ooka

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

Edward J Davey

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Erik Forsberg

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Hans Matsson

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Isao Hamaguchi

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Natalia Draptchinskaia

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Niklas Dahl

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Per Levéen

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

Stefan Karlsson

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P2860

Fibroblast growth factor-2 interacts with free ribosomal protein S19

Structure and function of ribosomal protein S4 genes on the human and mouse sex chromosomes

Altered cellular responses by varying expression of a ribosomal protein gene: sequential coordination of enhancement and suppression of ribosomal protein S3a gene expression induces apoptosis

Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome

Identification of receptor-binding sites of monocyte chemotactic S19 ribosomal protein dimer

Mutations in ribosomal protein S19 gene and diamond blackfan anemia: wide variations in phenotypic expression

Truncating ribosomal protein S19 mutations and variable clinical expression in Diamond-Blackfan anemia

Evidence for linkage of familial Diamond-Blackfan anemia to chromosome 8p23.3-p22 and for non-19q non-8p disease

Ullrich-Turner syndrome is not caused by haploinsufficiency of RPS4X

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

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4032-4037

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scholarly article

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10.1128/MCB.24.9.4032-4037.2004

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2004-05-01T00:00:00Z

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8620062

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15082795

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387766

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