Showing results (191-200 of 230) with videos related to

Sort By:
Pageof 23
Human Molecular Genetics|February 28, 2006
Multiple candidate gene analysis identifies alpha-synuclein as a susceptibility gene for sporadic Parkinson's diseaseIkuko Mizuta, Wataru Satake, Yuko Nakabayashi, et al.
Psychiatric Genetics|March 12, 2013
Genome-wide association study of schizophrenia using microsatellite markers in the Japanese populationHiroki Shibata, Ken Yamamoto, Zhu Sun, et al.
Clinical Epigenetics|May 19, 2017
Genetic heterogeneity of patients with suspected Silver-Russell syndrome: genome-wide copy number analysis in 82 patients without imprinting defectsTakanobu Inoue, Akie Nakamura, Tomoko Fuke, et al.
Frontiers in Immunology|October 20, 2018
Reference Grade Characterization of Polymorphisms in Full-Length HLA Class I and II Genes With Short-Read Sequencing on the ION PGM System and Long-Reads Generated by Single Molecule, Real-Time Sequencing on the PacBio PlatformShingo Suzuki, Swati Ranade, Ken Osaki, et al.
The Tokai Journal of Experimental and Clinical Medicine|February 15, 2011
Fine mapping of a psoriasis-susceptibility locus within the HLA class II region by using microsatellite markers in an association study of Japanese cases and controlsTomotaka Mabuchi, Akira Oka, Mariko Iizuka, et al.
Brain & Development|March 31, 2009
Comprehensive genetic analyses of PLP1 in patients with Pelizaeus-Merzbacher disease applied by array-CGH and fiber-FISH analyses identified new mutations and variable sizes of duplicationsKeiko Shimojima, Takehiko Inoue, Ai Hoshino, et al.
Scientific Reports|March 14, 2020
Autologous cord blood cell therapy for neonatal hypoxic-ischaemic encephalopathy: a pilot study for feasibility and safetyMasahiro Tsuji, Mariko Sawada, Shinichi Watabe, et al.
European Journal of Human Genetics : EJHG|May 28, 2020
Clinical and genetic characterization of nephropathy in patients with nail-patella syndromeYutaka Harita, Seiya Urae, Riki Akashio, et al.
American Journal of Medical Genetics. Part A|September 4, 2021
Medical, welfare, and educational challenges and psychological distress in parents caring for an individual with 22q11.2 deletion syndrome: A cross-sectional survey in JapanRyo Morishima, Yousuke Kumakura, Satoshi Usami, et al.
Cancer Gene Therapy|April 15, 2024
Inhibition of the galactosyltransferase C1GALT1 reduces osteosarcoma cell proliferation by interfering with ERK signaling and cell cycle progressionKentaro Watanabe, Keiji Tasaka, Hideto Ogata, et al.
Pageof 23