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Iscience|April 10, 2023
INPP5D modulates TREM2 loss-of-function phenotypes in a β-amyloidosis mouse modelAkihiro Iguchi, Sho Takatori, Shingo Kimura, et al.
British Journal of Haematology|September 15, 2025
Differential transcript level of ANKRD26 and clinical phenotype among the ANKRD26 variants in the Japanese registry for congenital thrombocytopeniaAtsushi Sakamoto, Toru Uchiyama, Kazuhiko Nakabayashi, et al.
Cancer Medicine|August 10, 2013
IKZF1 deletion is associated with a poor outcome in pediatric B-cell precursor acute lymphoblastic leukemia in JapanDaisuke Asai, Toshihiko Imamura, So-ichi Suenobu, et al.
Frontiers in Immunology|August 28, 2020
Hematopoietic Cell Transplantation for Chronic Granulomatous Disease in JapanMasakatsu Yanagimachi, Koji Kato, Akihiro Iguchi, et al.
American Journal of Human Genetics|February 26, 2013
ACTN1 mutations cause congenital macrothrombocytopeniaShinji Kunishima, Yusuke Okuno, Kenichi Yoshida, et al.
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