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Human Heredity|September 17, 2005
Single-nucleotide polymorphisms and haplotype LD analysis of the 29-kb IGF2 region on chromosome 11p15.5 in the Korean populationHye-Ja Lee, Kwang-Joong Kim, Mi-Hyun Park, et al.Parasitology Research|July 4, 2012
Functional expression and characterization of an iron-containing superoxide dismutase of Acanthamoeba castellaniiJung-Yeon Kim, Byoung-Kuk Na, Kyoung-Ju Song, et al.European Journal of Protistology|February 7, 2021
Anteholosticha foissneri n. sp., a marine hypotrich ciliate (Ciliophora: Spirotrichea) from Vietnam: Morphology, morphogenesis, and molecular phylogenyJae-Ho Jung, Atef Omar, Mi-Hyun Park, et al.BMC Medical Genetics|July 20, 2013
Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean familiesHae-Mi Woo, Hong-Joon Park, Jeong-In Baek, et al.Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis|April 28, 2018
Utility of mitochondrial CO1 sequences for species discrimination of Spirotrichea ciliates (Protozoa, Ciliophora)Mi-Hyun Park, Jae-Ho Jung, Euna Jo, et al.Human Mutation|February 11, 2012
KMD: Korean Mutation Database for genes related to diseasesMi-Hyun Park, Soo Kyung Koo, Jin-Sung Lee, et al.Archives of Pharmacal Research|December 7, 2006
Cytotoxic and ACAT-inhibitory sesquiterpene lactones from the root of Ixeris dentata forma albifloraEun-Mi Ahn, Myun-Ho Bang, Myoung-Chong Song, et al.BMC Medical Genetics|April 29, 2014
Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencingHae-Mi Woo, Hong-Joon Park, Mi-Hyun Park, et al.Journal of Korean Medical Science|December 17, 2003
Preoperative anxiety and propofol requirement in conscious sedation for ovum retrievalJeong-Yeon Hong, Inn Soo Kang, Mi Kyoung Koong, et al.BMC Medical Genomics|September 5, 2024
Exploring novel MYH7 gene variants using in silico analyses in Korean patients with cardiomyopathyOc-Hee Kim, Jihyun Kim, Youngjun Kim, et al.Pageof 11