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The New England Journal of Medicine
|
July 2, 2015
Somatic Mutations and Clonal Hematopoiesis in Aplastic Anemia
Tetsuichi 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 cohort
Ayako Yamamori, Motoharu Hamada, Hideki Muramatsu, et al.
Nature Communications
|
July 4, 2015
Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcoma
Masafumi 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 Thrombocytopenia
Takuya Takeichi, Antonio Torrelo, John Y W Lee, et al.
Blood
|
September 20, 2013
BCOR and BCORL1 mutations in myelodysplastic syndromes and related disorders
Frederik 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 anaemia
RuNan Wang, Kenichi Yoshida, Tsutomu Toki, et al.
Nature Genetics
|
July 9, 2013
Somatic SETBP1 mutations in myeloid malignancies
Hideki 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 immunodeficiency
Yuki Tsujita, Kanako Mitsui-Sekinaka, Kohsuke Imai, et al.
Nature Genetics
|
September 24, 2013
The landscape of somatic mutations in Down syndrome-related myeloid disorders
Kenichi Yoshida, Tsutomu Toki, Yusuke Okuno, et al.
Scientific Reports
|
August 26, 2022
Whole-exome analysis of 177 pediatric patients with undiagnosed diseases
Kotaro Narita, Hideki Muramatsu, Satoshi Narumi, et al.
Page
of 23
Search research articles
Search
Showing results (201-210 of 222) with videos related to
Sort By:
Page
of 23
The New England Journal of Medicine
|
July 2, 2015
Somatic Mutations and Clonal Hematopoiesis in Aplastic Anemia
Tetsuichi 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 cohort
Ayako Yamamori, Motoharu Hamada, Hideki Muramatsu, et al.
Nature Communications
|
July 4, 2015
Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcoma
Masafumi 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 Thrombocytopenia
Takuya Takeichi, Antonio Torrelo, John Y W Lee, et al.
Blood
|
September 20, 2013
BCOR and BCORL1 mutations in myelodysplastic syndromes and related disorders
Frederik 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 anaemia
RuNan Wang, Kenichi Yoshida, Tsutomu Toki, et al.
Nature Genetics
|
July 9, 2013
Somatic SETBP1 mutations in myeloid malignancies
Hideki 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 immunodeficiency
Yuki Tsujita, Kanako Mitsui-Sekinaka, Kohsuke Imai, et al.
Nature Genetics
|
September 24, 2013
The landscape of somatic mutations in Down syndrome-related myeloid disorders
Kenichi Yoshida, Tsutomu Toki, Yusuke Okuno, et al.
Scientific Reports
|
August 26, 2022
Whole-exome analysis of 177 pediatric patients with undiagnosed diseases
Kotaro Narita, Hideki Muramatsu, Satoshi Narumi, et al.
Page
of 23