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Cancer Reports (Hoboken, N.J.)|September 23, 2021
Genetic features of B-cell lymphoblastic lymphoma with TCF3-PBX1Ryota Shirai, Tomoo Osumi, Aiko Sato-Otsubo, et al.
Blood Advances|September 17, 2021
Association of allele-specific methylation of the ASNS gene with asparaginase sensitivity and prognosis in T-ALLKoshi Akahane, Shunsuke Kimura, Kunio Miyake, et al.
Endocrine Journal|August 4, 2017
Next generation sequencing-based mutation screening of 86 patients with idiopathic short statureAtsushi Hattori, Yuko Katoh-Fukui, Akie Nakamura, et al.
Journal of Diabetes Investigation|November 27, 2016
Nucleotide substitutions in CD101, the human homolog of a diabetes susceptibility gene in non-obese diabetic mouse, in patients with type 1 diabetesMisako Okuno, Yoshihito Kasahara, Masafumi Onodera, et al.
Human Molecular Genetics|February 13, 2018
Loss-of-function and gain-of-function mutations in PPP3CA cause two distinct disordersTakeshi Mizuguchi, Mitsuko Nakashima, Mitsuhiro Kato, et al.
Blood Advances|January 10, 2022
Genome-wide DNA methylation analysis in pediatric acute myeloid leukemiaGenki Yamato, Tomoko Kawai, Norio Shiba, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 10, 2014
Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutationsToshiyuki Maeda, Ken Higashimoto, Kosuke Jozaki, et al.
Rheumatology (Oxford, England)|February 6, 2024
Comparison of retention of biologics in Japanese patients with elderly-onset rheumatoid arthritis-the ANSWER cohort studySadao Jinno, Akira Onishi, Shuhei Hattori, et al.
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