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Yusuke Okuno

Showing results (201-210 of 222) with videos related to

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The New England Journal of Medicine|July 2, 2015
Somatic Mutations and Clonal Hematopoiesis in Aplastic AnemiaTetsuichi Yoshizato, Bogdan Dumitriu, Kohei Hosokawa, et al.
American Journal of Hematology|February 6, 2023
Germline and somatic RUNX1 variants in a pediatric bone marrow failure cohortAyako Yamamori, Motoharu Hamada, Hideki Muramatsu, et al.
Nature Communications|July 4, 2015
Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcomaMasafumi Seki, Riki Nishimura, Kenichi Yoshida, et al.
The Journal of Investigative Dermatology|August 5, 2017
Biallelic Mutations in KDSR Disrupt Ceramide Synthesis and Result in a Spectrum of Keratinization Disorders Associated with ThrombocytopeniaTakuya Takeichi, Antonio Torrelo, John Y W Lee, et al.
Blood|September 20, 2013
BCOR and BCORL1 mutations in myelodysplastic syndromes and related disordersFrederik Damm, Virginie Chesnais, Yasunobu Nagata, et al.
British Journal of Haematology|November 27, 2014
Loss of function mutations in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan anaemiaRuNan Wang, Kenichi Yoshida, Tsutomu Toki, et al.
Nature Genetics|July 9, 2013
Somatic SETBP1 mutations in myeloid malignanciesHideki Makishima, Kenichi Yoshida, Nhu Nguyen, et al.
The Journal of Allergy and Clinical Immunology|July 19, 2016
Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome-like immunodeficiencyYuki Tsujita, Kanako Mitsui-Sekinaka, Kohsuke Imai, et al.
Nature Genetics|September 24, 2013
The landscape of somatic mutations in Down syndrome-related myeloid disordersKenichi Yoshida, Tsutomu Toki, Yusuke Okuno, et al.
Scientific Reports|August 26, 2022
Whole-exome analysis of 177 pediatric patients with undiagnosed diseasesKotaro Narita, Hideki Muramatsu, Satoshi Narumi, et al.
Pageof 23

Showing results (201-210 of 222) with videos related to

Sort By:
Pageof 23
The New England Journal of Medicine|July 2, 2015
Somatic Mutations and Clonal Hematopoiesis in Aplastic AnemiaTetsuichi Yoshizato, Bogdan Dumitriu, Kohei Hosokawa, et al.
American Journal of Hematology|February 6, 2023
Germline and somatic RUNX1 variants in a pediatric bone marrow failure cohortAyako Yamamori, Motoharu Hamada, Hideki Muramatsu, et al.
Nature Communications|July 4, 2015
Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcomaMasafumi Seki, Riki Nishimura, Kenichi Yoshida, et al.
The Journal of Investigative Dermatology|August 5, 2017
Biallelic Mutations in KDSR Disrupt Ceramide Synthesis and Result in a Spectrum of Keratinization Disorders Associated with ThrombocytopeniaTakuya Takeichi, Antonio Torrelo, John Y W Lee, et al.
Blood|September 20, 2013
BCOR and BCORL1 mutations in myelodysplastic syndromes and related disordersFrederik Damm, Virginie Chesnais, Yasunobu Nagata, et al.
British Journal of Haematology|November 27, 2014
Loss of function mutations in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan anaemiaRuNan Wang, Kenichi Yoshida, Tsutomu Toki, et al.
Nature Genetics|July 9, 2013
Somatic SETBP1 mutations in myeloid malignanciesHideki Makishima, Kenichi Yoshida, Nhu Nguyen, et al.
The Journal of Allergy and Clinical Immunology|July 19, 2016
Phosphatase and tensin homolog (PTEN) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome-like immunodeficiencyYuki Tsujita, Kanako Mitsui-Sekinaka, Kohsuke Imai, et al.
Nature Genetics|September 24, 2013
The landscape of somatic mutations in Down syndrome-related myeloid disordersKenichi Yoshida, Tsutomu Toki, Yusuke Okuno, et al.
Scientific Reports|August 26, 2022
Whole-exome analysis of 177 pediatric patients with undiagnosed diseasesKotaro Narita, Hideki Muramatsu, Satoshi Narumi, et al.
Pageof 23