「Molecular pathways for development of multiple subtypes of intraductal papillary mucinous neoplasm of the pancreas」の関連論文
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胆管内乳頭状腫瘍(IPNB)は臨床病理学的徴候および分子異常と関連した2つのTypeに分けられる
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Integrated genomic/epigenomic analysis of sub-types and their cellular origin in clear cell ovarian carcinomas
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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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混合型十二指腸乳頭部癌における臨床病理学的特徴と遺伝学的変化
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Genetic analysis of pheochromocytoma and paraganglioma complicating cyanotic congenital heart disease
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Imaging features of localized IDH wild-type histologically diffuse astrocytomas: a single-institution case series
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悪性胸膜中皮腫における統合的ゲノム解析
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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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神経線維腫症2型の臨床的・遺伝的背景の解析
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膵管内乳頭粘液性腫瘍由来浸潤癌と通常型膵癌の差異の検討
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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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マルチリージョンシークエンスを用いた腫瘍内不均一性と腫瘍進化の過程の解析
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Mutations in SAM syndrome and palmoplantar keratoderma patients suggest genotype/phenotype correlations in DSG1 mutations
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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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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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Integrated genetic and epigenetic analysis revealed heterogeneity of acute lymphoblastic leukemia in Down syndrome
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A heterozygous SERPINB7 mutation is a possible modifying factor for epidermolytic palmoplantar keratoderma
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Quantitative monitoring of circulating tumor DNA in patients with advanced pancreatic cancer undergoing chemotherapy
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Integrated diagnosis based on transcriptome analysis in suspected pediatric sarcomas
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Clinical significance of RAS pathway alterations in pediatric acute myeloid leukemia
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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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Clinicopathological and molecular characteristics of endometrial neuroendocrine carcinomas reveal preexisting endometrial carcinoma origin
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Gene expression profiling using targeted RNA-sequencing to elucidate the progression from histologically normal lung tissues to non-invasive lesions in invasive lung adenocarcinoma
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Germline and somatic RUNX1 variants in a pediatric bone marrow failure cohort
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リスク因子別にみた表在型食道扁平上皮癌のゲノム変化の特徴
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肺腺癌におけるOvarian cancer immuno-reactive antigen domain containing 2 (OCIAD2) 発現の臨床病理学的意義および機能解析
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Ependymoma-like tumors with mesenchymal differentiation harboring C11orf95-NCOA1/2 or -RELA fusion: a hitherto unclassified tumor related to ependymoma
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Studies on TP53 gene mutations in canine histiocytic sarcoma
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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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日本におけるイヌの消化管上皮性腫瘍の発生動向と病理発生解明に関する研究
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胃癌におけるSWI/SNF複合体異常及び免疫回避機構関連因子の検討
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膵神経内分泌腫瘍におけるクロマチンリモデリング因子異常と腫瘍進展・予後との関連
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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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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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Whole-exome analysis of 177 pediatric patients with undiagnosed diseases
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H3F3A mutant allele specific imbalance in an aggressive subtype of diffuse midline glioma, H3 K27M-mutant
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Novel Prognostic Implications of Methylated RNA and Demethylases in Resected HCC and Background Liver Tissue
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Low ETV1 mRNA expression is associated with recurrence in gastrointestinal stromal tumors
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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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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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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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Is a specific T classification needed for extrahepatic intraductal papillary neoplasm of the bile duct (IPNB) type 2 associated with invasive carcinoma?
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胃底腺型胃癌の内視鏡治療および網羅的遺伝子発現解析の検討
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Updated allele frequencies of SERPINB7 founder mutations in Asian patients with Nagashima-type palmoplantar keratosis/keratoderma
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胃の神経内分泌細胞癌と混合型神経内分泌腫瘍における臨床病理学的検討およびエクソーム解析
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同時性多発大腸癌の臨床病理・分子学的解析
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消化管神経内分泌腫瘍におけるO6-methylguanine DNA methyltransferase とglucose transporter 2 の発現検討
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Histiocytic and dendritic cell neoplasms: Reappraisal of a Japanese series based on t(14;18) and neoplastic PD-L1 expression
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大腸鋸歯状腺腫の内視鏡及び網羅的遺伝子発現解析による検討