Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Young Se Hyun"'
Autor:
Ha Yeun Song, Young Se Hyun, Seonmi Jo, Seung Hyun Jung, Hyun-Ju Hwang, Seong-Yong Kim, Hye Suck An
Publikováno v:
Mitochondrial DNA. Part B. Resources, Vol 2, Iss 2, Pp 785-786 (2017)
Parupeneus barberinus is a tropical/subtropical reef-dwelling marine fish belonging to the family Mullidae. Herein, we report the first sequencing and assembly of the complete mitochondrial genome of P. barberinus. The complete mitochondrial genome i
Externí odkaz:
https://doaj.org/article/ac16c817c47d42338ea89155dd4dda80
Autor:
Young Bin Hong, Jaesoon Joo, Young Se Hyun, Geon Kwak, Yu-Ri Choi, Ha Kyung Yeo, Dong Hwan Jwa, Eun Ja Kim, Won Min Mo, Soo Hyun Nam, Sung Min Kim, Jeong Hyun Yoo, Heasoo Koo, Hwan Tae Park, Ki Wha Chung, Byung-Ok Choi
Publikováno v:
PLoS Genetics, Vol 12, Iss 2, p e1005829 (2016)
Charcot-Marie-Tooth disease (CMT) is a heterogeneous group of peripheral neuropathies with diverse genetic causes. In this study, we identified p.I43N mutation in PMP2 from a family exhibiting autosomal dominant demyelinating CMT neuropathy by whole
Externí odkaz:
https://doaj.org/article/7d3a1c012e2d4792841fc3db70e1d610
Autor:
Ha Yeun, Song, Young Se, Hyun, Seonmi, Jo, Seung Hyun, Jung, Hyun-Ju, Hwang, Seong-Yong, Kim, Hye Suck, An
Publikováno v:
Mitochondrial DNA. Part B, Resources
article-version (VoR) Version of Record
article-version (VoR) Version of Record
Parupeneus barberinus is a tropical/subtropical reef-dwelling marine fish belonging to the family Mullidae. Herein, we report the first sequencing and assembly of the complete mitochondrial genome of P. barberinus. The complete mitochondrial genome i
Autor:
Ha Yeun, Song, Young Se, Hyun, Moongeun, Yoon, Jiyoung, Woo, Byung-Jin, Lim, Hyung June, Kim, Hye Suck, An
Publikováno v:
Mitochondrial DNA. Part B, Resources
article-version (VoR) Version of Record
article-version (VoR) Version of Record
Gymnogobius heptacanthus is a small intertidal species belonging to the family Gobiidae. Herein, we report the first sequencing and assembly of the complete mitochondrial genome of G. heptacanthus. The complete mitochondrial genome is 16,529 bp long
Autor:
Seonmi Jo, Yu Cheol Kim, Seung-Hyun Jung, Tae-Young Choi, Ilson Whang, Young Se Hyun, Ha Yeun Song
Publikováno v:
Experimental Neurobiology
Cephalopods have the most advanced nervous systems and intelligent behavior among all invertebrates. Their brains provide comparative insights for understanding the molecular and functional origins of the human brain. Although brain maps that contain
Publikováno v:
Genes & Genomics. 39:155-160
A small and air-breathing snail, Ellobium chinense (Ellobiidae), is a vulnerable species by International Union for Conservation of Nature (IUCN). To protect and manage habitat and population of E. chinense, microsatellite markers were developed usin
Autor:
Hyung Jun Park, Young Bin Hong, Young-Chul Choi, Jinho Lee, Eun Ja Kim, Ji-Su Lee, Won Min Mo, Soo Mi Ki, Hyo In Kim, Hye Jin Kim, Young Se Hyun, Hyun Dae Hong, Kisoo Nam, Sung Chul Jung, Sang-Beom Kim, Se Hoon Kim, Deok-Ho Kim, Ki-Wook Oh, Seung Hyun Kim, Jeong Hyun Yoo, Ji Eun Lee, Ki Wha Chung, Byung-Ok Choi
Publikováno v:
Annals of Neurology. 79:231-243
Publikováno v:
Legal medicine (Tokyo, Japan). 37
The unknown origin of DNA samples derived from crime scenes generates a considerable amount of uncertainty, as do unexpected short tandem repeat (STR) results caused by sample mix-ups, contamination, medical interventions, and transgender individuals
Autor:
Young Se Hyun, Il-Hun Kim, Ha Yeun Song, Daesik Park, Mamoru Toda, Tein-Shun Tsai, Hye Suck An
Publikováno v:
Genesgenomics. 40(7)
Unfortunately, one of the co-author's family name has been incorrectly published in the original online publication. The correct family name should be Tsai.
Autor:
Hye Jin Kim, Jinho Lee, Young Bin Hong, Heasoo Koo, Deok Ho Kim, Ki Wha Chung, Byung Ok Choi, Young Se Hyun, Alec S.T. Smith
Publikováno v:
Annals of Human Genetics. 79:460-469
Charcot-Marie-Tooth disease type 4H (CMT4H) is an autosomal recessive demyelinating subtype of peripheral enuropathies caused by mutations in the FGD4 gene. Most CMT4H patients are in consanguineous Mediterranean families characterized by early onset