Pages that link to "Q37083952"
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The following pages link to Ribosomal and hematopoietic defects in induced pluripotent stem cells derived from Diamond Blackfan anemia patients. (Q37083952):
Displaying 44 items.
- Ribosomopathies: how a common root can cause a tree of pathologies (Q26781845) (← links)
- Induced pluripotent stem cells in hematology: current and future applications (Q27016090) (← links)
- Regulatory Roles of Rpl22 in Hematopoiesis: An Old Dog with New Tricks (Q28078535) (← links)
- Modeling Human Bone Marrow Failure Syndromes Using Pluripotent Stem Cells and Genome Engineering (Q28083303) (← links)
- Altered translation of GATA1 in Diamond-Blackfan anemia (Q33864534) (← links)
- Marrow failure: a window into ribosome biology (Q34431422) (← links)
- Ribosomal proteins: functions beyond the ribosome (Q34465473) (← links)
- p53-Independent cell cycle and erythroid differentiation defects in murine embryonic stem cells haploinsufficient for Diamond Blackfan anemia-proteins: RPS19 versus RPL5. (Q35099802) (← links)
- De novo generation of HSCs from somatic and pluripotent stem cell sources (Q35533599) (← links)
- Impaired Telomere Maintenance and Decreased Canonical WNT Signaling but Normal Ribosome Biogenesis in Induced Pluripotent Stem Cells from X-Linked Dyskeratosis Congenita Patients (Q35620795) (← links)
- Dysregulation of the Transforming Growth Factor β Pathway in Induced Pluripotent Stem Cells Generated from Patients with Diamond Blackfan Anemia. (Q35741406) (← links)
- Transcriptome analysis reveals a ribosome constituents disorder involved in the RPL5 downregulated zebrafish model of Diamond-Blackfan anemia (Q35951882) (← links)
- Efficient Recombinase-Mediated Cassette Exchange in hPSCs to Study the Hepatocyte Lineage Reveals AAVS1 Locus-Mediated Transgene Inhibition (Q36290454) (← links)
- Induction of multipotential hematopoietic progenitors from human pluripotent stem cells via respecification of lineage-restricted precursors (Q37462880) (← links)
- LiPS-A3S, a human genomic site for robust expression of inserted transgenes (Q37501610) (← links)
- Concise Review: Getting to the Core of Inherited Bone Marrow Failures. (Q37633372) (← links)
- Current status of pluripotent stem cells: moving the first therapies to the clinic. (Q38590664) (← links)
- From Genomics to Gene Therapy: Induced Pluripotent Stem Cells Meet Genome Editing (Q38592859) (← links)
- Osteosarcoma: Molecular Pathogenesis and iPSC Modeling (Q38653083) (← links)
- Molecular convergence in ex vivo models of Diamond-Blackfan anemia (Q38854631) (← links)
- Utilization of the AAVS1 safe harbor locus for hematopoietic specific transgene expression and gene knockdown in human ES cells (Q39015278) (← links)
- Ten years of iPSC: clinical potential and advances in vitro hematopoietic differentiation (Q39063423) (← links)
- Modeling Cancer with Pluripotent Stem Cells (Q39306963) (← links)
- Using induced human pluripotent stem cells to study Diamond-Blackfan anemia: an outlook on the clinical possibilities. (Q39873476) (← links)
- Immortalization of erythroid progenitors for in vitro large-scale red cell production (Q40111487) (← links)
- Drug discovery for Diamond-Blackfan anemia using reprogrammed hematopoietic progenitors (Q40343635) (← links)
- Lymphoblastoid cell lines from Diamond Blackfan anaemia patients exhibit a full ribosomal stress phenotype that is rescued by gene therapy (Q41696611) (← links)
- Proteolytic autodigestion: common tissue pathology in Shwachman-Diamond syndrome? (Q42724306) (← links)
- Bone marrow failure and developmental delay caused by mutations in poly(A)-specific ribonuclease (PARN). (Q47073215) (← links)
- Confounding in ex vivo models of Diamond-Blackfan anemia (Q48276800) (← links)
- Li-Fraumeni Syndrome Disease Model: A Platform to Develop Precision Cancer Therapy Targeting Oncogenic p53. (Q48690318) (← links)
- Perspective on Diamond-Blackfan anemia: lessons from a rare congenital bone marrow failure syndrome (Q49575039) (← links)
- Critical Diamond-Blackfan anemia due to ribosomal protein S19 missense mutation (Q51530791) (← links)
- Modeling Hematological Diseases and Cancer With Patient-Specific Induced Pluripotent Stem Cells (Q57490090) (← links)
- Emerging Therapeutic Approaches for Diamond Blackfan Anemia (Q58563105) (← links)
- Patient-Specific iPSC-Derived Endothelial Cells Provide Long-Term Phenotypic Correction of Hemophilia A (Q63359425) (← links)
- Diamond Blackfan Anemia: Genetics, Pathogenesis, Diagnosis and Treatment (Q64075943) (← links)
- Recent Updates on Induced Pluripotent Stem Cells in Hematological Disorders. (Q65002709) (← links)
- Emerging patent landscape for non-viral vectors used for gene therapy (Q89603279) (← links)
- Zebrafish Models of Diamond-Blackfan Anemia: A Tool for Understanding the Disease Pathogenesis and Drug Discovery (Q90632986) (← links)
- Guide snoRNAs: Drivers or Passengers in Human Disease? (Q90706174) (← links)
- Gene editing of PKLR gene in human hematopoietic progenitors through 5' and 3' UTR modified TALEN mRNA (Q90744990) (← links)
- Modeling blood diseases with human induced pluripotent stem cells (Q92570903) (← links)
- Pluripotent stem cell model of Shwachman-Diamond syndrome reveals apoptotic predisposition of hemoangiogenic progenitors (Q99248457) (← links)