慶應義塾大学 · 医学
Hideyuki Hayashi教授の研究室は、がんの個別化医療を推進するため、がんゲノム解析を基盤とした診断・予後予測の研究を展開しています。特に、パニックステート(膵がん)を対象とした標的シーケンシングによるドライバー遺伝子変異の同定や、MSI-H/dMMR状態のPCR法と次世代シーケンシング(NGS)の臨床的整合性の検証が主な研究テーマです。また、臨床応用に即した遺伝子診断プロトコルの構築や、治療反応のバイオマーカーの同定にも注力しています。
Figures are computed from collected data and may differ slightly.
The number of mutated driver genes assessed using a targeted deep sequencing assay was a promising prognostic biomarker for pancreatic cancer.
Various malignancies exhibit high microsatellite instability (MSI-H) or mismatch repair deficiency (dMMR). The MSI-IVD kit, a polymerase chain reaction (PCR)-based method, was the first tumor-agnostic companion diagnostic to detect MSI status in MSI-H solid tumors. Recently, next-generation sequencing (NGS), which can also detect MSI-H/dMMR, has been made clinically available; however, its real-world concordance with PCR-based testing of MSI-H/dMMR remains to be investigated. The co-primary end
Precision medicine is a promising strategy for cancer treatment. In this study, we developed an in-house clinical sequencing system to perform a comprehensive cancer genomic profiling test as a clinical examination and analyzed the utility of this system. Genomic DNA was extracted from tumor tissues and peripheral blood cells collected from 161 patients with different stages and types of cancer. A comprehensive targeted amplicon exome sequencing for 160 cancer-related genes was performed using n
When carefully managed, FOLFIRINOX is acceptably safe and efficacious in Japanese patients with unresectable pancreatic cancer.
Journal Article Multiple fixed drug eruption caused by acetaminophen Get access H. Hayashi, H. Hayashi Department of Dermatology, Hokkaido University Graduate School of Medicine, Kita‐ku, Sapporo 060‐8638, Japan Search for other works by this author on: Oxford Academic Google Scholar T. Shimizu, T. Shimizu Department of Dermatology, Hokkaido University Graduate School of Medicine, Kita‐ku, Sapporo 060‐8638, Japan Search for other works by this author on: Oxford Academic Google Scholar H. Shimizu
The reaction of Escherichia coli aspartate aminotransferase (AspAT) with L-erythro-3-hydroxyaspartate (HOAsp) produces an intense absorption at 494 nm (epsilon = 13,650 M-1 cm-1), which is ascribed to the quinonoid intermediate. However, when Tyr70 of AspAT has been replaced by Phe, the enzyme shows only a faint absorption at 494 nm (epsilon = 522 M-1 cm-1) on the reaction with HOAsp. This indicates the involvement of the hydroxy group of Tyr70 in stabilizing the quinonoid intermediate formed fr
Journal Article Epidermotropic metastatic malignant melanoma with a pedunculated appearance Get access H. Hayashi, H. Hayashi Department of Dermatology, Hokkaido University Graduate School of Medicine, N15, W7, Sapporo 060‐8638, Japan Search for other works by this author on: Oxford Academic Google Scholar T. Kawashima, T. Kawashima Department of Dermatology, Hokkaido University Graduate School of Medicine, N15, W7, Sapporo 060‐8638, Japan Search for other works by this author on: Oxford Academi
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