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Journal of Clinical Immunology
|
September 27, 2015
Late-Onset Combined Immunodeficiency with a Novel IL2RG Mutation and Probable Revertant Somatic Mosaicism
Yusuke Okuno, Akihiro Hoshino, Hideki Muramatsu, et al.
Blood
|
June 26, 2025
Association of Epstein-Barr virus genomic alterations with human pathologies
Htet Thiri Khine, Yoshitaka Sato, Motoharu Hamada, et al.
The Journal of Allergy and Clinical Immunology
|
March 17, 2021
Successful treatment of a novel type I interferonopathy due to a de novo PSMB9 gene mutation with a Janus kinase inhibitor
Shinsuke Kataoka, Nozomu Kawashima, Yusuke Okuno, et al.
The Journal of Allergy and Clinical Immunology
|
November 16, 2016
Haploinsufficiency of TNFAIP3 (A20) by germline mutation is involved in autoimmune lymphoproliferative syndrome
Masatoshi Takagi, Shohei Ogata, Hiroo Ueno, et al.
Cell Transplantation
|
December 20, 2022
Clinical Impact of Melphalan Pharmacokinetics on Transplantation Outcomes in Children Undergoing Hematopoietic Stem Cell Transplantation
Ryo Maemura, Manabu Wakamatsu, Kana Matsumoto, et al.
Cancer Research
|
August 22, 2019
Pathogenic Epigenetic Consequences of Genetic Alterations in IDH-Wild-Type Diffuse Astrocytic Gliomas
Fumiharu Ohka, Keiko Shinjo, Shoichi Deguchi, et al.
Blood Advances
|
October 25, 2019
Transcriptome analysis offers a comprehensive illustration of the genetic background of pediatric acute myeloid leukemia
Norio Shiba, Kenichi Yoshida, Yusuke Hara, et al.
Blood
|
February 14, 2018
Integrated molecular profiling of juvenile myelomonocytic leukemia
Norihiro Murakami, Yusuke Okuno, Kenichi Yoshida, et al.
The Journal of Experimental Medicine
|
October 20, 2018
Gain-of-function <i>IKBKB</i> mutation causes human combined immune deficiency
Chelisa Cardinez, Bahar Miraghazadeh, Kay Tanita, et al.
Haematologica
|
December 3, 2016
Exome sequencing identified <i>RPS15A</i> as a novel causative gene for Diamond-Blackfan anemia
Fumika Ikeda, Kenichi Yoshida, Tsutomu Toki, et al.
Page
of 23
Search research articles
Search
Showing results (181-190 of 222) with videos related to
Sort By:
Page
of 23
Journal of Clinical Immunology
|
September 27, 2015
Late-Onset Combined Immunodeficiency with a Novel IL2RG Mutation and Probable Revertant Somatic Mosaicism
Yusuke Okuno, Akihiro Hoshino, Hideki Muramatsu, et al.
Blood
|
June 26, 2025
Association of Epstein-Barr virus genomic alterations with human pathologies
Htet Thiri Khine, Yoshitaka Sato, Motoharu Hamada, et al.
The Journal of Allergy and Clinical Immunology
|
March 17, 2021
Successful treatment of a novel type I interferonopathy due to a de novo PSMB9 gene mutation with a Janus kinase inhibitor
Shinsuke Kataoka, Nozomu Kawashima, Yusuke Okuno, et al.
The Journal of Allergy and Clinical Immunology
|
November 16, 2016
Haploinsufficiency of TNFAIP3 (A20) by germline mutation is involved in autoimmune lymphoproliferative syndrome
Masatoshi Takagi, Shohei Ogata, Hiroo Ueno, et al.
Cell Transplantation
|
December 20, 2022
Clinical Impact of Melphalan Pharmacokinetics on Transplantation Outcomes in Children Undergoing Hematopoietic Stem Cell Transplantation
Ryo Maemura, Manabu Wakamatsu, Kana Matsumoto, et al.
Cancer Research
|
August 22, 2019
Pathogenic Epigenetic Consequences of Genetic Alterations in IDH-Wild-Type Diffuse Astrocytic Gliomas
Fumiharu Ohka, Keiko Shinjo, Shoichi Deguchi, et al.
Blood Advances
|
October 25, 2019
Transcriptome analysis offers a comprehensive illustration of the genetic background of pediatric acute myeloid leukemia
Norio Shiba, Kenichi Yoshida, Yusuke Hara, et al.
Blood
|
February 14, 2018
Integrated molecular profiling of juvenile myelomonocytic leukemia
Norihiro Murakami, Yusuke Okuno, Kenichi Yoshida, et al.
The Journal of Experimental Medicine
|
October 20, 2018
Gain-of-function <i>IKBKB</i> mutation causes human combined immune deficiency
Chelisa Cardinez, Bahar Miraghazadeh, Kay Tanita, et al.
Haematologica
|
December 3, 2016
Exome sequencing identified <i>RPS15A</i> as a novel causative gene for Diamond-Blackfan anemia
Fumika Ikeda, Kenichi Yoshida, Tsutomu Toki, et al.
Page
of 23