「Clinical significance of RAS pathway alterations in pediatric acute myeloid leukemia」の関連論文
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原発性膠芽腫におけるTERTプロモーター領域遺伝子変異の臨床的・病理学的意義
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Detection of subclonal SETBP1 and JAK3 mutations in juvenile myelomonocytic leukemia using droplet digital PCR
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Phosphorylated proteome analysis of a novel germline ABL1 mutation causing an autosomal dominant syndrome with ventricular septal defect
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Germline and somatic RUNX1 variants in a pediatric bone marrow failure cohort
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SMAD4発現保持とRUNX3発現喪失は膵管癌予後不良因子となる
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膠芽腫におけるPIK3CA遺伝子変異の臨床的意義についての考察
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Low ETV1 mRNA expression is associated with recurrence in gastrointestinal stromal tumors
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Clinical efficacy of osimertinib in EGFR-mutant non-small cell lung cancer with distant metastasis
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Rare Genetic Variants in the Gene Encoding Histone Lysine Demethylase 4C (KDM4C) and Their Contributions to Susceptibility to Schizophrenia and Autism Spectrum Disorder
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肺腺癌における新しい活性化KRAS遺伝子変異の検討
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Novel Prognostic Implications of Methylated RNA and Demethylases in Resected HCC and Background Liver Tissue
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Quantitative monitoring of circulating tumor DNA in patients with advanced pancreatic cancer undergoing chemotherapy
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Genetic analysis of pheochromocytoma and paraganglioma complicating cyanotic congenital heart disease
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Integrated genetic and epigenetic analysis revealed heterogeneity of acute lymphoblastic leukemia in Down syndrome
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肝細胞癌に対するレンバニチブ療法の臨床効果に及ぼすNOS3遺伝子多型の影響
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Prognostic value of somatic mutations at remission in acute myeloid leukemia
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Whole-exome analysis of 177 pediatric patients with undiagnosed diseases
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Large-scale clinico-genomic profile of non-small cell lung cancer with KRAS G12C : Results from LC-SCRUM-Asia study
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TP53遺伝子変異がp53経路の遺伝子発現に及ぼす影響に関するがん種横断的研究
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Successful treatment of a novel type I interferonopathy due to a de novo PSMB9 gene mutation with a Janus kinase inhibitor
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Rare single-nucleotide DAB1 variants and their contribution to Schizophrenia and autism spectrum disorder susceptibility
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頭頸部扁平上皮癌における遺伝子変異と蛋白表現型によるp53機能分類
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大腸癌におけるARID1A遺伝子変異の及ぼす影響および間質細胞のPD-L1発現との関連
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髄膜腫の解剖学的発生部位、病理診断に基づく遺伝子解析研究
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ジュベール症候群関連疾患の臨床遺伝学的解析
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転移または再発乳癌の末梢血循環DNA変異解析の検討
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Clinical diagnostic value of telomere length measurement in inherited bone marrow failure syndromes
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Expression of programmed cell death ligand-1 by immune cells in the microenvironment is a favorable prognostic factor for primary diffuse large B-cell lymphoma of the central nervous system
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Frequent intragenic microdeletions of elastin in familial supravalvular aortic stenosis
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FLI1遺伝子マイクロサテライト多型と全身性強皮症との関連の検討
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視床高悪性度神経膠腫摘出例におけるヒストン変異およびTERT promoter変異と生存予後に関する研究
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“その他の医原性免疫不全関連リンパ増殖性疾患”の臨床的特徴及び遺伝子変異解析についての研究
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Investigation for a novel therapeutic target in acute myeloid leukemia with monosomy 7
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癌患者ゲノミクスデータ解析を基盤とした乳癌幹細胞性維持機構の解明
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悪性リンパ腫における血中循環細胞外遊離DNAを用いたゲノム解析に関する研究
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大腸癌の抗EGFR抗体薬感受性に関与するDNAメチル化異常と遺伝子発現の関連性
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【令和2年度若手研究者表彰奨学金 受賞記念講演要旨】Association of aberrant ASNS imprinting with asparaginase sensitivity and chromosomal abnormality in childhood BCP-ALL
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複数の遺伝子変異が関与する遺伝性難聴症例の解析
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非小細胞肺がん患者におけるオシメルチニブ有害事象とSTAT3, CYP3A5, ABCG2遺伝子多型との関連
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神経線維腫症2型の臨床的・遺伝的背景の解析
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Investigation of therapeutic target of DNMT3A-mutant acute myeloid leukemia
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日本人高度蛋白尿患者に対する包括的遺伝子診断
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再発難治性白血病に対する個別化医療を目指した患者特異的治療標的の同定
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Clinicopathologic Analysis of Primary Adrenal Diffuse Large B-Cell Lymphoma : A Reappraisal of 23 Japanese Patients Based on EBV Association and PD-L1 Expression in Tumor Cells
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Investigation of OLIG2 as a candidate gene for schizophrenia and autism spectrum disorder
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BRCAnessに基づく遺伝性乳がん原因遺伝子の病原性変異評価法の開発
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子宮内膜癌におけるPPP2R1A遺伝子変異の意義の検討
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膵癌における腫瘍浸潤リンパ球と患者の生存に関連した三次リンパ組織の統合分析
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H3F3A mutant allele specific imbalance in an aggressive subtype of diffuse midline glioma, H3 K27M-mutant
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Extracellular miRNAs as Predictive Biomarkers for Glypican-3-Derived Peptide Vaccine Therapy Response in Ovarian Clear Cell Carcinoma