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Journal of Human Genetics|March 4, 2000
Transduction of fibroblasts and CD34+ progenitors using a selectable retroviral vector containing cDNAs encoding arylsulfatase A and CD24A Tsutsudaasano, M Migita, K Takahashi, et al.Journal of Human Genetics|March 4, 2000
Isolation and characterization of a human cDNA encoding a protein homologous to the 7.2-kDa protein (subunit X) of bovine ubiquinol-cytochrome C reductaseH Akashi, H J Han, M Iizaka, et al.Journal of Human Genetics|March 4, 2000
Identification of two novel mutations of the carnitine/acylcarnitine translocase (CACT) gene in a patient with CACT deficiencyA Ogawa, S Yamamoto, M Kanazawa, et al.Journal of Human Genetics|May 17, 2001
A nucleotide variant in the promoter region of the interleukin-6 gene associated with decreased bone mineral densityN Ota, T Nakajima, I Nakazawa, et al.Journal of Human Genetics|May 17, 2001
Risk factor-gene interaction in carotid atherosclerosis: effect of gene polymorphisms of renin-angiotensin systemY Tabara, K Kohara, J Nakura, et al.Journal of Human Genetics|February 24, 2001
Non-homologous recombination between Alu and LINE-1 repeats caused a 430-kb deletion in the dystrophin gene: a novel source of genomic instabilityR Suminaga, Y Takeshima, K Yasuda, et al.Journal of Human Genetics|February 24, 2001
Two pathogenic point mutations exist in the authentic mitochondrial genome, not in the nuclear pseudogeneJ Akanuma, K Muraki, H Komaki, et al.Journal of Human Genetics|February 24, 2001
Association of bone mineral density with a dinucleotide repeat polymorphism at the calcitonin (CT) locusM Miyao, T Hosoi, M Emi, et al.Journal of Human Genetics|February 24, 2001
Haplotype analysis suggests that the two predominant mutations in Japanese patients with holocarboxylase synthetase deficiency are founder mutationsX Yang, Y Aoki, X Li, et al.Journal of Human Genetics|February 24, 2001
Construction of human-rodent hybrid cells containing single transferable fragments of human chromosome 10pY Murakami, H Uejima, H Fukuhara, et al.Pageof 351