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RUNX1 gene expression in Egyptian acute myeloid leukemia patients: may it have therapeutic implications?


Etoposide-induced DNA damage in a chromosomal breakpoint of RUNX1 gene is independent of RUNX1 expression

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10.19746/j.cnki.issn.1009-2137.2021.05.007

[Clinical Characteristics of Acute Myeloid Leukemia Patients with RUNX1 Gene Mutation].



Transcriptional Regulation of RUNX1: An Informatics Analysis



A novel RUNX1 exon 3 - 7 deletion causing a familial platelet disorder.


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10.1016/j.cancergen.2021.02.004

A novel case of intrachromosomal amplification and insertion of RUNX1 on derivative chromosome 2 in pediatric AML.



Two faces of RUNX3 in myeloid transformation.



Immunonano-Lipocarrier-Mediated Liver Sinusoidal Endothelial Cell-Specific RUNX1 Inhibition Impedes Immune Cell Infiltration and Hepatic Inflammation in Murine Model of NASH



Characterization of the Platelet Phenotype Caused by a Germline RUNX1 Variant in a CRISPR/Cas9-Generated Murine Model.


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10.19746/j.cnki.issn.1009-2137.2021.01.028

[Characteristic of 8p11 Myeloproliferative Syndrome with Rare Phenotype].


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10.3760/cma.j.issn.0253-2727.2021.01.009

[Clinical features and prognosis of ETV6-RUNX1-positive childhood B-precursor acute lymphocyte leukemia].



Germline RUNX1 variation and predisposition to childhood acute lymphoblastic leukemia.



Familial Leukemia Associated with Thrombocytopenia



The correction of ETV6/RUNX1 translocation in acute lymphocytic leukemia cells: a new gene targeting system by homologous recombination mechanism



Protective Effect and Mechanisms of New Gelatin on Chemotherapy-Induced Hematopoietic Injury Zebrafish Model


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10.24287/1726-1708-2018-17-4-51-56

Случай редкой наследственной тромбоцитопении с предрасположенностью к развитию острого миелоидного лейкоза у детей-близнецов



Etv6/Runx1 Fusion Gene Abrogation Decreases The Oncogenic Potencial Of Tumour Cells In A Preclinical Model Of Acute Lymphoblastic Leukaemia



Myeloid/Lymphoid Neoplasm With FGFR1 Rearrangement Accompanying RUNX1 and NOTCH1 Gene Mutations



Isolated Bone Marrow Non-Langerhans Cell Histiocytosis Preceding RUNX1-Mutated Acute Myeloid Leukemia: Case Report and Literature Review.



Identification of a novel long non-coding RNA within RUNX1 intron 5



Genetic Signature of Acute Lymphoblastic Leukemia and Netherton Syndrome Co-incidence—First Report in the Literature



Human parvovirus B19‐associated encephalopathy with hereditary spherocytosis



A novel germline RUNX1 mutation with co-occurrence of somatic alterations in a case of myeloid neoplasm with familial thrombocytopenia: first report from India


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