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Journal of Human Genetics|June 6, 2019
Molecular genealogy of Tusi Lu's family reveals their paternal relationship with Jochi, Genghis Khan's eldest sonShao-Qing Wen, Hong-Bing Yao, Pan-Xin Du, et al.Journal of Human Genetics|June 4, 1998
Human autoimmune lymphoproliferative syndrome, a defect in the apoptosis-inducing Fas receptor: a lesson from the mouse modelS NagataJournal of Human Genetics|June 4, 1998
Identification by differential display of eight known genes induced during in vivo intimal hyperplasiaM Itoh, S Tsukada, T Orita, et al.Journal of Human Genetics|June 4, 1998
Expression analysis of two mutant human ornithine transcarbamylases in COS-7 cellsT Kogo, Y Satoh, M Kanazawa, et al.Journal of Human Genetics|June 11, 1998
Mutation and polymorphic marker analyses of 65K- and 67K-glutamate decarboxylase genes in two families with pyridoxine-dependent epilepsyS Kure, Y Sakata, S Miyabayashi, et al.Journal of Human Genetics|June 11, 1998
Novel germline mutations of hMSH2 in a patient with hereditary nonpolyposis colorectal cancer (HNPCC) and in a patient with six primary cancersS Okamura, K Koyama, Y Miyoshi, et al.Journal of Human Genetics|April 24, 2015
Human leukocyte antigen polymorphisms and personalized medicine for rheumatoid arthritisHiroshi Furukawa, Shomi Oka, Kota Shimada, et al.Journal of Human Genetics|August 5, 2016
Co-stimulatory CD28 and transcription factor NFKB1 gene variants affect idiopathic recurrent miscarriagesManeesh Kumar Misra, Bharti Singh, Aditi Mishra, et al.Journal of Human Genetics|August 5, 2016
Regulation of LOXL2 and SERPINH1 by antitumor microRNA-29a in lung cancer with idiopathic pulmonary fibrosisKazuto Kamikawaji, Naohiko Seki, Masaki Watanabe, et al.Journal of Human Genetics|May 22, 2023
Genome sequencing identifies coding and non-coding variants for non-syndromic hearing lossMemoona Ramzan, Duygu Duman, LeShon Chere Peart Hendricks, et al.Pageof 351