Cargando…

Correction: p53-Independent Cell Cycle and Erythroid Differentiation Defects in Murine Embryonic Stem Cells Haploinsufficient for Diamond Blackfan Anemia-Proteins: RPS19 versus RPL5

Detalles Bibliográficos
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2014
Materias:	Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4005761/ http://dx.doi.org/10.1371/journal.pone.0096689

Ejemplares similares

p53-Independent Cell Cycle and Erythroid Differentiation Defects in Murine Embryonic Stem Cells Haploinsufficient for Diamond Blackfan Anemia-Proteins: RPS19 versus RPL5
por: Singh, Sharon A., et al.
Publicado: (2014)

Defects of protein production in erythroid cells revealed in a zebrafish Diamond–Blackfan anemia model for mutation in RPS19
por: Zhang, Y, et al.
Publicado: (2014)

Diamond–Blackfan anemia RPL35A: a case report
por: Noel, Colin Byron
Publicado: (2019)

Rpl5-Inducible Mouse Model for Studying Diamond-Blackfan Anemia
por: Kazerounian, Shideh, et al.
Publicado: (2019)

Transcriptome analysis of Rpl11-deficient zebrafish model of Diamond-Blackfan Anemia
por: Zhang, Zhaojun, et al.
Publicado: (2014)

Molecular basis of Diamond–Blackfan anemia: structure and function analysis of RPS19
por: Gregory, Lynn A., et al.
Publicado: (2007)

Targeted Resequencing and Analysis of the Diamond-Blackfan Anemia Disease Locus RPS19
por: Martinez Barrio, Alvaro, et al.
Publicado: (2009)

Recurring mutations in RPL15 are linked to hydrops fetalis and treatment independence in Diamond-Blackfan anemia
por: Wlodarski, Marcin W., et al.
Publicado: (2018)

Adult-Onset Diamond-Blackfan Anemia with RPL11 Gene Variation Case Report
por: Mars-Holt, Evida, et al.
Publicado: (2022)

An RPS19-edited model for Diamond-Blackfan anemia reveals TP53-dependent impairment of hematopoietic stem cell activity
por: Bhoopalan, Senthil Velan, et al.
Publicado: (2023)

Mutations in RPS19 may affect ribosome function and biogenesis in Diamond Blackfan anemia
por: Hiregange, Disha‐Gajanan, et al.
Publicado: (2022)

The nuclear gene rpl18 regulates erythroid maturation via JAK2-STAT3 signaling in zebrafish model of Diamond–Blackfan anemia
por: Chen, Cheng, et al.
Publicado: (2020)

Whole exome sequencing in the differential diagnosis of Diamond-Blackfan anemia: Clinical and molecular study of three patients with novel RPL5 and mosaic RPS19 mutations
por: Errichiello, Edoardo, et al.
Publicado: (2017)

Diamond-Blackfan anemia caused by chromosome 1p22 deletion encompassing RPL5
por: Tominaga, Makiko, et al.
Publicado: (2019)

Transcriptome Analysis of the Zebrafish Model of Diamond-Blackfan Anemia from RPS19 Deficiency via p53-Dependent and -Independent Pathways
por: Jia, Qiong, et al.
Publicado: (2013)

Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes
por: Watkins-Chow, Dawn E., et al.
Publicado: (2013)

Systematic transcriptome analysis of the zebrafish model of diamond-blackfan anemia induced by RPS24 deficiency
por: Song, Binfeng, et al.
Publicado: (2014)

Computational Studies of the Structural Basis of Human RPS19 Mutations Associated With Diamond-Blackfan Anemia
por: An, Ke, et al.
Publicado: (2021)

Hemin Augments Growth and Hemoglobinization of Erythroid Precursors from Patients with Diamond-Blackfan Anemia
por: Fibach, Eitan, et al.
Publicado: (2012)

Correction: Transcriptome Analysis of the Zebrafish Model of Diamond-Blackfan Anemia from RPS19 Deficiency via p53-Dependent and -Independent Pathways
por: Jia, Qiong, et al.
Publicado: (2013)

Correction: Transcriptome Analysis of the Zebrafish Model of Diamond-Blackfan Anemia from RPS19 Deficiency via p53-Dependent and -Independent Pathways
por: Jia, Qiong, et al.
Publicado: (2013)

Correction: Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes
por: Watkins-Chow, Dawn E., et al.
Publicado: (2015)

Identification of a novel RPS26 nonsense mutation in a Chinese Diamond-Blackfan Anemia patient
por: Shi, Xiaodong, et al.
Publicado: (2019)

Diamond–Blackfan anemia with mutation in RPS19: A case report and an overview of published pieces of literature
por: Jahan, Dilshad, et al.
Publicado: (2020)

Bochdalek hernia with Diamond-Blackfan anemia associated with RPS19 gene mutation: A case report
por: Yoo, Ye Seul, et al.
Publicado: (2019)

Proerythroblast Cells of Diamond-Blackfan Anemia Patients With RPS19 and CECR1 Mutations Have Similar Transcriptomic Signature
por: Karaosmanoglu, Beren, et al.
Publicado: (2021)

Genotype-phenotype association and variant characterization in Diamond Blackfan anemia caused by pathogenic variants in RPL35A
por: Gianferante, D. Matthew, et al.
Publicado: (2020)

Eltrombopag Improves Erythroid Differentiation in a Human Induced Pluripotent Stem Cell Model of Diamond Blackfan Anemia
por: Qanash, Husam, et al.
Publicado: (2021)

A new murine Rpl5 (uL18) mutation provides a unique model of variably penetrant Diamond-Blackfan anemia
por: Yu, Lei, et al.
Publicado: (2021)

Assessment of hematopoietic failure due to Rpl11 deficiency in a zebrafish model of Diamond-Blackfan anemia by deep sequencing
por: Zhang, Zhaojun, et al.
Publicado: (2013)

HEATR3 variants impair nuclear import of uL18 (RPL5) and drive Diamond-Blackfan anemia
por: O’Donohue, Marie-Françoise, et al.
Publicado: (2022)

An update on the pathogenesis and diagnosis of Diamond–Blackfan anemia
por: Da Costa, Lydie, et al.
Publicado: (2018)

Emerging Therapeutic Approaches for Diamond Blackfan Anemia
por: Aspesi, Anna, et al.
Publicado: (2018)

Shock in the Setting of Diamond-Blackfan Anemia Relapse
por: Haddaden, Metri, et al.
Publicado: (2021)

Adult-onset Diamond-Blackfan anemia with a novel mutation in the exon 5 of RPL11: too late and too rare
por: Flores Ballester, Elena, et al.
Publicado: (2015)

Transcriptome analysis reveals a ribosome constituents disorder involved in the RPL5 downregulated zebrafish model of Diamond-Blackfan anemia
por: Wan, Yang, et al.
Publicado: (2016)

Variable Clinical Features in a Large Family With Diamond Blackfan Anemia Caused by a Pathogenic Missense Mutation in RPS19
por: Cole, Sarah, et al.
Publicado: (2022)

Altered translation of GATA1 in Diamond-Blackfan anemia
por: Ludwig, Leif S., et al.
Publicado: (2014)

Diamond Blackfan Anemia: Genetics, Pathogenesis, Diagnosis and Treatment
por: Engidaye, Getabalew, et al.
Publicado: (2019)

PSAT224 Endocrine Manifestations in Diamond Blackfan Anemia
por: Shah, Anvay, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_gq8ilv49at9qai7o3t2hpq7hum