Zobrazeno 1 - 10 of 19 pro vyhledávání: '"Sun-Wha Park"'
1
Akademický článek
Dysbiotic Vaginal Microbiota Induces Preterm Birth Cascade via Pathogenic Molecules in the Vagina
Autor: AbuZar Ansari, Young-Ah You, Gain Lee, Soo Min Kim, Sun Wha Park, Young Min Hur, Young Ju Kim
Publikováno v: Metabolites, Vol 14, Iss 1, p 45 (2024)
Dysbiotic vaginal microbiota (DVM) disturb the vaginal environment, including pH, metabolite, protein, and cytokine profiles. This study investigated the impact of DVM on the vaginal environment in 40 Korean pregnant women and identified predictable
Externí odkaz: https://doaj.org/article/72d27da8756c45cb82120d0f88c9ce44
Zobrazit plný text záznamu
4
Sensitivity study of the Yfiler® PLUS PCR Amplification Kit in forensic casework samples
Autor: Dong Sub Lee, Ju Yeon Jung, Sun Wha Park, Si Keun Lim, Kyoung Sook Kim, Yang Han Lee
Publikováno v: Analytical Science and Technology. 29:43-48
A variety of Y-STR analysis kits have been developed and used in the forensic field. Prior to the forensic application of a new kit, laboratory validation and sensitivity tests are essential processes in selecting suitable alternatives and for assuri
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1a820f5449a1816697fd7e32e04f2e96
https://doi.org/10.5806/ast.2016.29.1.43
Zobrazit plný text záznamu
6
Akademický článek
Development of a Y-STR 12-plex PCR system and haplotype analysis in a Korean population.
Autor: SUN WHA PARK1, CHOON HONG HWANG2, EUN MIN CHO1, JI HWAN PARK1, BYUNG OK CHOI3, KI WHA CHUNG1 kwchung@kongju.ac.kr
Publikováno v: Journal of Genetics. Dec2009, Vol. 88 Issue 3, p353-358. 8p. 3 Charts, 2 Graphs.
Zobrazit plný text záznamu
7
Compound heterozygous mutations of TYMP as underlying causes of mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)
Autor: Ki Wha Chung, Jung Hee Hwang, Byung Suk Yoon, Ha-Neul Jeong, Hye Jin Kim, Bum Chun Suh, Ji Hoon Park, Sun Wha Park, Byung-Ok Choi
Publikováno v: Molecular Medicine Reports. 8:17-22
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE), an autosomal recessive multiorgan disease, frequently associated with mutations in the thymidine phosphorylase (TYMP) gene. TYMP encodes thymidine phosphorylase (TP), which has an essenti
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51302736120cf906913e2bba81572866
https://doi.org/10.3892/mmr.2013.1479
Zobrazit plný text záznamu
8
Compound mutations of PEO1 and TYMP in a progressive external ophthalmoplegia patient with incomplete mitochondrial neurogastrointestinal encephalomyopathy phenotype
Autor: Byung-Ok Choi, Ki Wha Chung, Il-Nam Sunwoo, Jung Hee Hwang, Sun Wha Park, Khriezhanuo Nakhro, Eun Min Cho, Seung Min Kim
Publikováno v: Genes & Genomics. 33:431-437
The Mendelian inherited progressive external ophthalmoplegia (PEO) and mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) are genetically heterogeneous mitochondrial diseases caused by nuclear-mitochondrial intergenomic defects. The PEO1 a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::19ae199d4c06f43d1839cf6a3b24124d
https://doi.org/10.1007/s13258-011-0089-y
Zobrazit plný text záznamu
9
A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14
Autor: Byung Ok Choi, Sumaria Kanwal, Sang Beom Kim, Heasoo Koo, Jeong Hyun Yoo, Jong-Won Kim, Song Ja Kim, Sung Hee Kang, Ki Wha Chung, Young Chul Choi, Kyoung Gyu Choi, Stephan Züchner, Young Se Hyun, Kee Duk Park, Sun Wha Park
Publikováno v: Human Mutation. 32:669-677
Both peripheral neuropathy and distal myopathy are well-established inherited neuromuscular disorders characterized by progressive weakness and atrophy of the distal limb muscles. A complex phenotype of peripheral neuropathy, myopathy, hoarseness, an
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::990050e14fd6bdeea87b9d955236f8c7
https://doi.org/10.1002/humu.21488
Zobrazit plný text záznamu
10
Inheritance of Charcot–Marie–Tooth disease 1A with rare nonrecurrent genomic rearrangement
Autor: Jung Hee Hwang, Nam Keun Kim, Byung-Ok Choi, Young Se Hyun, Sun Wha Park, Hyeon Jeong Jeon, Ki Wha Chung
Publikováno v: neurogenetics. 12:51-58
Rare copy number variations by the nonrecurrent rearrangements involving PMP22 have been recently suggested to be associated with CMT1A peripheral neuropathy. As a mechanism of the nonrecurrent rearrangement, replication-based fork stalling template
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::863c6109bb24bf17f62085453dfc38bf
https://doi.org/10.1007/s10048-010-0272-3
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje