田村豪良 (Takeaki Tamura) - マイポータル

基本情報

所属: 日本大学医学部医学科助教

研究者番号: 01001891
J-GLOBAL ID: 202401015023356573
researchmap会員ID: R000068421

研究分野

ライフサイエンス / 血液、腫瘍内科学 /

論文

Genomic copy number analysis using droplet digital PCR: A simple method with EvaGreen single-color fluorescent design.

Tamura T., Imaizumi T., Shimojima Yamamoto K., Yamamoto T.

Methods in Molecular Biology 1794 293-304 2024年
Clonal hematopoiesis without malignant transformation lasting over 2 years in a 9-year-old boy, following treatment for acute lymphocytic leukemia.

Yagasaki H., Shimozawa K., Kanezawa K., Tamura T., Kamiyama M., Yamamoto T., Morioka I.

Journal of Pediatric Hematology and Oncology 46(6) e453-456 2024年
Reciprocal chromosome translocation t(3;4)(q27;q31.2) with deletion of 3q27 and reduced FBXW7 expression in a patient with developmental delay, hypotonia and seizures.

Tamura T., Shimojima Yamamoto K., Tohyama J., Morioka I., Kanno H., Yamamoto T.

Journal of Human Genetics 69(12) 639-44 2024年
【今月の症例】4歳男児，急性リンパ芽球性白血病

山口喬, 青木亮二, 中原衣里菜, 伊東正剛, 田村豪良, 金澤剛二, 下澤克宜, 森岡一朗, 岡田真広, 宮崎治

小児科臨床 77(3) 369-371 2024年
Breakpoint analysis for cytogenetically balanced translocation revealed unexpected complex structural abnormalities and suggested the position effect for MEF2C.

Tamura T, Shimojima Yamamoto K, Imaizumi T, Yamamoto H, Miyamoto Y, Yagasaki H, Morioka I, Kanno H, Yamamoto T

American Journal of Medical Genetics Part A 191(6) 1632-1638 2023年筆頭著者
Identification of small-sized intrachromosomal segments at the ends of INV-DUP-DEL patterns.

Shimojima Yamamoto K, Tamura T, Okamoto N, Nishi E, Noguchi A, Takahashi I, Sawaishi Y, Shimizu M, Kanno H, Minakuchi Y …

Journal of Human Genetics 68(11) 751-757 2023年
Interstitial microdeletions of 3q26.2q26.31 in two patients with neurodevelopmental delay and distinctive features.

Tamura T, Yamamoto-Shimojima K, Shiihara T, Sakazume S, Okamoto N, Yagasaki H, Morioka I, Kanno H, Yamamoto T

American Journal of Medical Genetics Part A 191(1) 400-407 2023年筆頭著者
Long-read sequence analysis for clustered genomic copy number aberrations revealed architectures of intricately intertwined rearrangements.

Tamura T, Yamamoto-Shimojima K, Okamoto N, Yagasaki H, Morioka I, Kanno H, Minakuchi Y, Toyoda A, Yamamoto T

American Journal of Medical Genetics Part A 191(1) 112-119 2023年筆頭著者
A Filipino infant with severe neutropenia owing to SRP54 mutations was successfully treated with ethnically mismatched cord blood transplantation from a Japanese cord blood bank.

Tamura T, Yagasaki H, Nakahara E, Ito M, Ueno M, Kanezawa K, Hirai M, Morioka I

Annals of Hematology 100(11) 2859-2860 2021年筆頭著者