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Kwang Min Sohn

Showing results (1-10 of 7) with videos related to

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Therapeutic Drug Monitoring|June 17, 2006
Sequence-based CYP2D6 genotyping in the Korean populationSoo-Youn Lee, Kwang Min Sohn, Ji Young Ryu, et al.
Headache|July 20, 2007
Association between a polymorphism in the lymphotoxin-a promoter region and migraineKyung-A Lee, Soo Yeon Jang, Kwang-Min Sohn, et al.
Clinical Chemistry|November 25, 2003
Haplotype structure of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene and its relationship to serum total bilirubin concentration in a male Korean populationChang-Seok Ki, Kyung-A Lee, Soo-Youn Lee, et al.
Journal of Gastroenterology|June 4, 2004
Novel interleukin 1beta polymorphism increased the risk of gastric cancer in a Korean populationKyung-A Lee, Chang-Seok Ki, Hye-Jin Kim, et al.
Journal of Korean Medical Science|June 29, 2007
Distinct linkage disequilibrium (LD) runs of single nucleotide polymorphisms and microsatellite markers; implications for use of mixed marker haplotypes in LD-based mappingKyung-A Lee, Kwang-Min Sohn, Seung-Hee Cho, et al.
Journal of Human Genetics|August 31, 2002
A novel missense mutation (I344K) in the SPG4gene in a Korean family with autosomal-dominant hereditary spastic paraplegiaChang-Seok Ki, Won Yong Lee, Do Hoon Han, et al.
American Journal of Human Genetics|August 19, 2007
Mutations in PRPS1, which encodes the phosphoribosyl pyrophosphate synthetase enzyme critical for nucleotide biosynthesis, cause hereditary peripheral neuropathy with hearing loss and optic neuropathy (cmtx5)Hee-Jin Kim, Kwang-Min Sohn, Michael E Shy, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Therapeutic Drug Monitoring|June 17, 2006
Sequence-based CYP2D6 genotyping in the Korean populationSoo-Youn Lee, Kwang Min Sohn, Ji Young Ryu, et al.
Headache|July 20, 2007
Association between a polymorphism in the lymphotoxin-a promoter region and migraineKyung-A Lee, Soo Yeon Jang, Kwang-Min Sohn, et al.
Clinical Chemistry|November 25, 2003
Haplotype structure of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene and its relationship to serum total bilirubin concentration in a male Korean populationChang-Seok Ki, Kyung-A Lee, Soo-Youn Lee, et al.
Journal of Gastroenterology|June 4, 2004
Novel interleukin 1beta polymorphism increased the risk of gastric cancer in a Korean populationKyung-A Lee, Chang-Seok Ki, Hye-Jin Kim, et al.
Journal of Korean Medical Science|June 29, 2007
Distinct linkage disequilibrium (LD) runs of single nucleotide polymorphisms and microsatellite markers; implications for use of mixed marker haplotypes in LD-based mappingKyung-A Lee, Kwang-Min Sohn, Seung-Hee Cho, et al.
Journal of Human Genetics|August 31, 2002
A novel missense mutation (I344K) in the SPG4gene in a Korean family with autosomal-dominant hereditary spastic paraplegiaChang-Seok Ki, Won Yong Lee, Do Hoon Han, et al.
American Journal of Human Genetics|August 19, 2007
Mutations in PRPS1, which encodes the phosphoribosyl pyrophosphate synthetase enzyme critical for nucleotide biosynthesis, cause hereditary peripheral neuropathy with hearing loss and optic neuropathy (cmtx5)Hee-Jin Kim, Kwang-Min Sohn, Michael E Shy, et al.
Pageof 1