Showing results (1211-1220 of 3,506) with videos related to
Sort By:
Pageof 351
Journal of Human Genetics|September 24, 2005
Mutations of syntaxin 11 and SNAP23 genes as causes of familial hemophagocytic lymphohistiocytosis were not found in Japanese peopleKen Yamamoto, Eiichi Ishii, Hisanori Horiuchi, et al.Journal of Human Genetics|September 13, 2005
Androgenic correlates of genetic variation in the gene encoding 5alpha-reductase type 1Justine A Ellis, Sianna Panagiotopoulos, Aysel Akdeniz, et al.Journal of Human Genetics|September 13, 2005
A model of prediction system for adverse cardiovascular reactions by calcineurin inhibitors among patients with renal transplants using gene-based single-nucleotide polymorphismsTaisei Mushiroda, Susumu Saito, Yukiko Tanaka, et al.Journal of Human Genetics|September 15, 2005
Estrogen receptor alpha gene relationship with peak bone mass and body mass index in Chinese nuclear familiesWei-Xia Jian, Yan-Jun Yang, Ji-Rong Long, et al.Journal of Human Genetics|December 17, 2004
Association study using combination analysis of SNP and STRP markers: CD14 promoter polymorphism and IgE level in Taiwanese asthma childrenJiu-Yao Wang, Ling-Mei Wang, Cherry Guan-Ju Lin, et al.Journal of Human Genetics|December 14, 2004
Haplotype-based analysis of alpha 2A, 2B, and 2C adrenergic receptor genes captures information on common functional loci at each geneInna Belfer, Beata Buzas, Heather Hipp, et al.Journal of Human Genetics|January 7, 2005
mtDNA/nDNA ratio in 14484 LHON mitochondrial mutation carriersTomoki Nishioka, Augustinus Soemantri, Takafumi IshidaJournal of Human Genetics|May 29, 2004
Identification and evaluation of 55 genetic variations in the BRCA1 and the BRCA2 genes of patients from 50 Japanese breast cancer familiesMasanori Kawahara, Masato Sakayori, Kazuko Shiraishi, et al.Journal of Human Genetics|June 5, 2004
Association between genetic variation in the gene for death-associated protein-3 (DAP3) and adult asthmaTomomitsu Hirota, Kazuhiko Obara, Akira Matsuda, et al.Journal of Human Genetics|March 8, 2005
Post-zygotic de novo trinucleotide repeat expansion at spinocerebellar ataxia type 7 locus: evidence from an Indian familyUma Mittal, Sanghamitra Roy, Satish Jain, et al.Pageof 351