Pages that link to "Q50239548"
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The following pages link to Yusuke Okuno (Q50239548):
Displaying 50 items.
- ACTN1 mutations cause congenital macrothrombocytopenia (Q24319165) (← links)
- Integrated molecular analysis of clear-cell renal cell carcinoma (Q27852382) (← links)
- Genomic and molecular characterization of esophageal squamous cell carcinoma (Q28657686) (← links)
- Loss of function mutations in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan anaemia. (Q29871483) (← links)
- An empirical Bayesian framework for somatic mutation detection from cancer genome sequencing data (Q30597080) (← links)
- Functional characterization of a novel GFI1B mutation causing congenital macrothrombocytopenia (Q33431782) (← links)
- Common Variable Immunodeficiency Caused by FANC Mutations (Q33441764) (← links)
- Clonal leukemic evolution in myelodysplastic syndromes with TET2 and IDH1/2 mutations (Q33558105) (← links)
- Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms (Q34655449) (← links)
- Mutations in the gene encoding the E2 conjugating enzyme UBE2T cause Fanconi anemia (Q35689795) (← links)
- Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcoma (Q35863493) (← links)
- Aberrant DNA Methylation Is Associated with a Poor Outcome in Juvenile Myelomonocytic Leukemia (Q35882742) (← links)
- Redox control of catalytic activities of membrane-associated protein tyrosine kinases. (Q35998123) (← links)
- Optical imaging of spiral waves: pharmacological modification of spiral-type excitations in a 2-dimensional layer of ventricular myocardium. (Q36286768) (← links)
- Profiling of somatic mutations in acute myeloid leukemia with FLT3-ITD at diagnosis and relapse (Q36322776) (← links)
- Paroxysmal nocturnal hemoglobinuria and telomere length predicts response to immunosuppressive therapy in pediatric aplastic anemia. (Q36337581) (← links)
- Somatic SETBP1 mutations in myeloid malignancies (Q37060418) (← links)
- BRCC3 mutations in myeloid neoplasms (Q37216363) (← links)
- Identification of Viruses in Cases of Pediatric Acute Encephalitis and Encephalopathy Using Next-Generation Sequencing (Q37254444) (← links)
- Novel and recurrent ATP2A2 mutations in Japanese patients with Darier's disease. (Q37507464) (← links)
- Variant ALDH2 is associated with accelerated progression of bone marrow failure in Japanese Fanconi anemia patients. (Q38267184) (← links)
- X-linked agammaglobulinemia associated with B-precursor acute lymphoblastic leukemia (Q38319601) (← links)
- Somatic mosaicism for a NRAS mutation associates with disparate clinical features in RAS-associated leukoproliferative disease: a report of two cases. (Q40186368) (← links)
- Whole-exome sequencing reveals the spectrum of gene mutations and the clonal evolution patterns in paediatric acute myeloid leukaemia. (Q40513597) (← links)
- Correlation of rabbit antithymocyte globulin serum levels and clinical outcomes in children who received hematopoietic stem cell transplantation from an alternative donor. (Q40929855) (← links)
- Fulminant adenovirus hepatitis after hematopoietic stem cell transplant: Retrospective real-time PCR analysis for adenovirus DNA in two cases (Q40972672) (← links)
- Late-Onset Combined Immunodeficiency with a Novel IL2RG Mutation and Probable Revertant Somatic Mosaicism. (Q40981154) (← links)
- Somatic Mutations and Clonal Hematopoiesis in Aplastic Anemia (Q41622816) (← links)
- Choreito formula for BK virus-associated hemorrhagic cystitis after allogeneic hematopoietic stem cell transplantation. (Q41637356) (← links)
- Comprehensive detection of viruses in pediatric patients with acute liver failure using next-generation sequencing (Q41921442) (← links)
- Clinical and genetic features of dyskeratosis congenita, cryptic dyskeratosis congenita, and Hoyeraal-Hreidarsson syndrome in Japan (Q41927518) (← links)
- Exome sequencing identified RPS15A as a novel causative gene for Diamond-Blackfan anemia (Q42361972) (← links)
- GATA2 and secondary mutations in familial myelodysplastic syndromes and pediatric myeloid malignancies. (Q42589188) (← links)
- Biallelic Mutations in KDSR Disrupt Ceramide Synthesis and Result in a Spectrum of Keratinization Disorders Associated with Thrombocytopenia (Q42679659) (← links)
- A PKC-mediated backup mechanism of the MXXCW motif-linked switch for initiating tyrosine kinase activities. (Q42805933) (← links)
- Somatic RHOA mutation in angioimmunoblastic T cell lymphoma. (Q42808195) (← links)
- Acute amiodarone promotes drift and early termination of spiral wave re-entry. (Q42949803) (← links)
- Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma (Q43491006) (← links)
- Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia (Q44998179) (← links)
- CD8 CD122 regulatory T cells contain clonally expanded cells with identical CDR3 sequences of the T-cell receptor β-chain. (Q45368373) (← links)
- Combined effects of nifekalant and lidocaine on the spiral-type re-entry in a perfused 2-dimensional layer of rabbit ventricular myocardium. (Q46453715) (← links)
- Moderate hypothermia increases the chance of spiral wave collision in favor of self-termination of ventricular tachycardia/fibrillation. (Q47878190) (← links)
- Biallelic mutations in SZT2 cause a discernible clinical entity with epilepsy, developmental delay, macrocephaly and a dysmorphic corpus callosum (Q48118505) (← links)
- Dynamics of clonal evolution in myelodysplastic syndromes (Q48139499) (← links)
- Development of clinical paroxysmal nocturnal haemoglobinuria in children with aplastic anaemia. (Q48232268) (← links)
- Clinical utility of next-generation sequencing for inherited bone marrow failure syndromes. (Q48335168) (← links)
- Germline IKAROS mutation associated with primary immunodeficiency that progressed to T-cell acute lymphoblastic leukemia (Q48343515) (← links)
- A novel IFIH1 mutation in the pincer domain underlies the clinical features of both Aicardi-Goutières and Singleton-Merten syndromes in a single patient. (Q48360159) (← links)
- Recurrent MYB rearrangement in blastic plasmacytoid dendritic cell neoplasm. (Q48361501) (← links)
- An infant with generalized pustular psoriasis and geographic tongue had a heterozygous IL36RN mutation and IgG2 deficiency. (Q49898813) (← links)