Search research articles
Contact Us
Filters
Showing results (91-100 of 222) with videos related to
Page
of 23
Sort By:
Proceedings of the National Academy of Sciences of the United States of America
|
January 8, 2014
Mismatch repair protein hMSH2-hMSH6 recognizes mismatches and forms sliding clamps within a D-loop recombination intermediate
Masayoshi Honda, Yusuke Okuno, Sarah R Hengel, et al.
Haematologica
|
February 1, 2024
A retrospective analysis of gene fusions and treatment outcomes in pediatric acute megakaryoblastic leukemia without Down syndrome
Kyogo Suzuki, Asahito Hama, Yusuke Okuno, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
April 26, 2005
Combined effects of nifekalant and lidocaine on the spiral-type re-entry in a perfused 2-dimensional layer of rabbit ventricular myocardium
Mari Amino, Masatoshi Yamazaki, Harumichi Nakagawa, et al.
Nucleic Acids Research
|
March 9, 2013
An empirical Bayesian framework for somatic mutation detection from cancer genome sequencing data
Yuichi Shiraishi, Yusuke Sato, Kenichi Chiba, et al.
Brain & Development
|
September 13, 2017
Biallelic mutations in SZT2 cause a discernible clinical entity with epilepsy, developmental delay, macrocephaly and a dysmorphic corpus callosum
Yuji Nakamura, Yasuko Togawa, Yusuke Okuno, et al.
Bone Marrow Transplantation
|
June 10, 2021
Autoantibodies against the plakin family proteins as a novel marker for chronic graft-versus-host disease of the lung
Nozomu Kawashima, Eri Nishikawa, Atsunari Tsuchisaka, et al.
Frontiers in Immunology
|
February 12, 2019
A Syrian Refugee in Iraq Diagnosed as a Case of IL12RB1 Deficiency in Japan Using Dried Blood Spots
Lika'a Fasih Y Al-Kzayer, Ahmed K Yassin, Khalid Hama Salih, et al.
Human Genome Variation
|
October 25, 2019
A novel <i>CUL4B</i> splice site variant in a young male exhibiting less pronounced features
Yuji Nakamura, Yusuke Okuno, Hideki Muramatsu, et al.
Brain & Development
|
June 25, 2018
A patient with a GNAO1 mutation with decreased spontaneous movements, hypotonia, and dystonic features
Akihisa Okumura, Koichi Maruyama, Mami Shibata, et al.
Pediatric Blood & Cancer
|
November 30, 2024
Cord Blood Transplantation Using Myeloablative Conditioning for Pediatric Advanced Myelodysplastic Syndrome in AMeD Syndrome With a Novel ADH5 Variant
Yusuke Morishita, Motoharu Hamada, Suguru Uemura, et al.
Page
of 23
Search research articles
Search
Showing results (91-100 of 222) with videos related to
Sort By:
Page
of 23
Proceedings of the National Academy of Sciences of the United States of America
|
January 8, 2014
Mismatch repair protein hMSH2-hMSH6 recognizes mismatches and forms sliding clamps within a D-loop recombination intermediate
Masayoshi Honda, Yusuke Okuno, Sarah R Hengel, et al.
Haematologica
|
February 1, 2024
A retrospective analysis of gene fusions and treatment outcomes in pediatric acute megakaryoblastic leukemia without Down syndrome
Kyogo Suzuki, Asahito Hama, Yusuke Okuno, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society
|
April 26, 2005
Combined effects of nifekalant and lidocaine on the spiral-type re-entry in a perfused 2-dimensional layer of rabbit ventricular myocardium
Mari Amino, Masatoshi Yamazaki, Harumichi Nakagawa, et al.
Nucleic Acids Research
|
March 9, 2013
An empirical Bayesian framework for somatic mutation detection from cancer genome sequencing data
Yuichi Shiraishi, Yusuke Sato, Kenichi Chiba, et al.
Brain & Development
|
September 13, 2017
Biallelic mutations in SZT2 cause a discernible clinical entity with epilepsy, developmental delay, macrocephaly and a dysmorphic corpus callosum
Yuji Nakamura, Yasuko Togawa, Yusuke Okuno, et al.
Bone Marrow Transplantation
|
June 10, 2021
Autoantibodies against the plakin family proteins as a novel marker for chronic graft-versus-host disease of the lung
Nozomu Kawashima, Eri Nishikawa, Atsunari Tsuchisaka, et al.
Frontiers in Immunology
|
February 12, 2019
A Syrian Refugee in Iraq Diagnosed as a Case of IL12RB1 Deficiency in Japan Using Dried Blood Spots
Lika'a Fasih Y Al-Kzayer, Ahmed K Yassin, Khalid Hama Salih, et al.
Human Genome Variation
|
October 25, 2019
A novel <i>CUL4B</i> splice site variant in a young male exhibiting less pronounced features
Yuji Nakamura, Yusuke Okuno, Hideki Muramatsu, et al.
Brain & Development
|
June 25, 2018
A patient with a GNAO1 mutation with decreased spontaneous movements, hypotonia, and dystonic features
Akihisa Okumura, Koichi Maruyama, Mami Shibata, et al.
Pediatric Blood & Cancer
|
November 30, 2024
Cord Blood Transplantation Using Myeloablative Conditioning for Pediatric Advanced Myelodysplastic Syndrome in AMeD Syndrome With a Novel ADH5 Variant
Yusuke Morishita, Motoharu Hamada, Suguru Uemura, et al.
Page
of 23