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Yusuke Okuno

Showing results (191-200 of 222) with videos related to

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Human Mutation|September 13, 2019
A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in IndiaFrank X Donovan, Avani Solanki, Minako Mori, et al.
Experimental Hematology|March 17, 2019
KLF1 mutation E325K induces cell cycle arrest in erythroid cells differentiated from congenital dyserythropoietic anemia patient-specific induced pluripotent stem cellsHiroshi Kohara, Taiju Utsugisawa, Chika Sakamoto, et al.
British Journal of Haematology|July 30, 2016
Whole-exome sequencing reveals the spectrum of gene mutations and the clonal evolution patterns in paediatric acute myeloid leukaemiaNorio Shiba, Kenichi Yoshida, Yuichi Shiraishi, et al.
Haematologica|April 3, 2020
Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patientsMinako Mori, Asuka Hira, Kenichi Yoshida, et al.
Nature Genetics|June 26, 2013
Integrated molecular analysis of clear-cell renal cell carcinomaYusuke Sato, Tetsuichi Yoshizato, Yuichi Shiraishi, et al.
Haematologica|February 23, 2019
Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patientsMinako Mori, Asuka Hira, Kenichi Yoshida, et al.
The Journal of Allergy and Clinical Immunology|December 13, 2016
Abnormal hematopoiesis and autoimmunity in human subjects with germline IKZF1 mutationsAkihiro Hoshino, Satoshi Okada, Kenichi Yoshida, et al.
Nature Genetics|April 2, 2014
Genomic and molecular characterization of esophageal squamous cell carcinomaDe-Chen Lin, Jia-Jie Hao, Yasunobu Nagata, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 20, 2017
Clinical utility of next-generation sequencing for inherited bone marrow failure syndromesHideki Muramatsu, Yusuke Okuno, Kenichi Yoshida, et al.
Cancer Research|August 1, 2021
Mathematical Modeling and Mutational Analysis Reveal Optimal Therapy to Prevent Malignant Transformation in Grade II IDH-Mutant GliomasKosuke Aoki, Hiromichi Suzuki, Takashi Yamamoto, et al.
Pageof 23

Showing results (191-200 of 222) with videos related to

Sort By:
Pageof 23
Human Mutation|September 13, 2019
A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in IndiaFrank X Donovan, Avani Solanki, Minako Mori, et al.
Experimental Hematology|March 17, 2019
KLF1 mutation E325K induces cell cycle arrest in erythroid cells differentiated from congenital dyserythropoietic anemia patient-specific induced pluripotent stem cellsHiroshi Kohara, Taiju Utsugisawa, Chika Sakamoto, et al.
British Journal of Haematology|July 30, 2016
Whole-exome sequencing reveals the spectrum of gene mutations and the clonal evolution patterns in paediatric acute myeloid leukaemiaNorio Shiba, Kenichi Yoshida, Yuichi Shiraishi, et al.
Haematologica|April 3, 2020
Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patientsMinako Mori, Asuka Hira, Kenichi Yoshida, et al.
Nature Genetics|June 26, 2013
Integrated molecular analysis of clear-cell renal cell carcinomaYusuke Sato, Tetsuichi Yoshizato, Yuichi Shiraishi, et al.
Haematologica|February 23, 2019
Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patientsMinako Mori, Asuka Hira, Kenichi Yoshida, et al.
The Journal of Allergy and Clinical Immunology|December 13, 2016
Abnormal hematopoiesis and autoimmunity in human subjects with germline IKZF1 mutationsAkihiro Hoshino, Satoshi Okada, Kenichi Yoshida, et al.
Nature Genetics|April 2, 2014
Genomic and molecular characterization of esophageal squamous cell carcinomaDe-Chen Lin, Jia-Jie Hao, Yasunobu Nagata, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 20, 2017
Clinical utility of next-generation sequencing for inherited bone marrow failure syndromesHideki Muramatsu, Yusuke Okuno, Kenichi Yoshida, et al.
Cancer Research|August 1, 2021
Mathematical Modeling and Mutational Analysis Reveal Optimal Therapy to Prevent Malignant Transformation in Grade II IDH-Mutant GliomasKosuke Aoki, Hiromichi Suzuki, Takashi Yamamoto, et al.
Pageof 23