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Journal of Human Genetics|August 16, 2002
Confirmation of genetic homogeneity of nonsyndromic low-frequency sensorineural hearing loss by linkage analysis and a DFNA6/14 mutation in a Japanese familyKazuki Komatsu, Nobukatsu Nakamura, Mohsen Ghadami, et al.Biochemistry and Molecular Biology Education : a Bimonthly Publication of the International Union of Biochemistry and Molecular Biology|August 13, 2025
ABCC11 Earwax Trait and Genotype Are Suitable Tools for Introductory Labs to Learn Genetics and Molecular TechniquesTohru Ohta, Rie Takai, Akiko Yoshida, et al.Journal of Neurosurgery|January 28, 2004
Direct repair of a blisterlike aneurysm on the internal carotid artery with vascular closure staple clips. Technical noteToshiharu Yanagisawa, Kazuo Mizoi, Taku Sugawara, et al.Journal of Human Genetics|August 31, 2002
A catalog of 106 single-nucleotide polymorphisms (SNPs) and 11 other types of variations in genes for transforming growth factor-beta1 (TGF-beta1) and its signaling pathwayYukio Watanabe, Akira Kinoshita, Takahiro Yamada, et al.American Journal of Medical Genetics. Part A|June 10, 2003
Inv dup del(4)(:p14 --> p16.3::p16.3 --> qter) with manifestations of partial duplication 4p and Wolf-Hirschhorn syndromeYuki Kondoh, Takaya Toma, Hirofumi Ohashi, et al.Journal of Human Genetics|March 28, 2002
Nonaka myopathy is caused by mutations in the UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase gene (GNE)Tomohiko Kayashima, Hidenori Matsuo, Akira Satoh, et al.Gene|May 30, 2002
The gene TSGA14, adjacent to the imprinted gene MEST, escapes genomic imprintingTakahiro Yamada, Tomohiko Kayashima, Kentaro Yamasaki, et al.Cancer Genomics & Proteomics|June 22, 2022
Requirement of CLIC4 Expression in Human Colorectal Cancer Cells for Sensitivity to Growth Inhibition by FucoxanthinolReo Yokoyama, Ayumi Kushibiki, Shiori Yamada, et al.Journal of Human Genetics|January 24, 2006
Expression of the Snurf-Snrpn IC transcript in the oocyte and its putative role in the imprinting establishment of the mouse 7C imprinting domainChristophe K Mapendano, Tatsuya Kishino, Kazumi Miyazaki, et al.Human Biology|July 27, 2018
A Novel Association between the 27-bp Deletion and 538G>A Mutation in the ABCC11 GeneYusuke S Hori, Aiko Yamada, Norifumi Matsuda, et al.Pageof 8