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Norisato Mitsutake

Showing results (101-110 of 108) with videos related to

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Journal of Translational Medicine|March 24, 2011
MiRNA-205 modulates cellular invasion and migration via regulating zinc finger E-box binding homeobox 2 expression in esophageal squamous cell carcinoma cellsKayoko Matsushima, Hajime Isomoto, Naoyuki Yamaguchi, et al.
Human Molecular Genetics|March 31, 2010
The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in ChernobylMeiko Takahashi, Vladimir A Saenko, Tatiana I Rogounovitch, et al.
Nature Genetics|April 3, 2012
Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repairYuka Nakazawa, Kensaku Sasaki, Norisato Mitsutake, et al.
Thyroid : Official Journal of the American Thyroid Association|January 7, 2015
The common genetic variant rs944289 on chromosome 14q13.3 associates with risk of both malignant and benign thyroid tumors in the Japanese populationTatiana I Rogounovitch, Andrey Bychkov, Meiko Takahashi, et al.
Cell|March 7, 2020
Ubiquitination of DNA Damage-Stalled RNAPII Promotes Transcription-Coupled RepairYuka Nakazawa, Yuichiro Hara, Yasuyoshi Oka, et al.
American Journal of Human Genetics|April 30, 2013
Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemiaKazuya Kashiyama, Yuka Nakazawa, Daniela T Pilz, et al.
The Lancet. Oncology|October 2, 2025
Genetic modification of the AJCC classification of papillary thyroid cancer: an international, multicentre, retrospective cohort studyMingzhao Xing, Shuhuang Lin, Aarti Mathur, et al.
Science Advances|December 23, 2020
Digenic mutations in <i>ALDH2</i> and <i>ADH5</i> impair formaldehyde clearance and cause a multisystem disorder, AMeD syndromeYasuyoshi Oka, Motoharu Hamada, Yuka Nakazawa, et al.
Pageof 11

Showing results (101-110 of 108) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 108 results.
Journal of Translational Medicine|March 24, 2011
MiRNA-205 modulates cellular invasion and migration via regulating zinc finger E-box binding homeobox 2 expression in esophageal squamous cell carcinoma cellsKayoko Matsushima, Hajime Isomoto, Naoyuki Yamaguchi, et al.
Human Molecular Genetics|March 31, 2010
The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in ChernobylMeiko Takahashi, Vladimir A Saenko, Tatiana I Rogounovitch, et al.
Nature Genetics|April 3, 2012
Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repairYuka Nakazawa, Kensaku Sasaki, Norisato Mitsutake, et al.
Thyroid : Official Journal of the American Thyroid Association|January 7, 2015
The common genetic variant rs944289 on chromosome 14q13.3 associates with risk of both malignant and benign thyroid tumors in the Japanese populationTatiana I Rogounovitch, Andrey Bychkov, Meiko Takahashi, et al.
Cell|March 7, 2020
Ubiquitination of DNA Damage-Stalled RNAPII Promotes Transcription-Coupled RepairYuka Nakazawa, Yuichiro Hara, Yasuyoshi Oka, et al.
American Journal of Human Genetics|April 30, 2013
Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemiaKazuya Kashiyama, Yuka Nakazawa, Daniela T Pilz, et al.
The Lancet. Oncology|October 2, 2025
Genetic modification of the AJCC classification of papillary thyroid cancer: an international, multicentre, retrospective cohort studyMingzhao Xing, Shuhuang Lin, Aarti Mathur, et al.
Science Advances|December 23, 2020
Digenic mutations in <i>ALDH2</i> and <i>ADH5</i> impair formaldehyde clearance and cause a multisystem disorder, AMeD syndromeYasuyoshi Oka, Motoharu Hamada, Yuka Nakazawa, et al.
Pageof 11