Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Mijin, Oh"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-4 (2018)
Abstract Hereditary neuropathy with liability to pressure palsies (HNPP) is an autosomal dominant disorder mainly due to a deletion of chromosome 17p11.2 including PMP22 (PMP22 Del HNPP). The prevalence of HNPP is estimated to be 0.84 to 16 per 100,0
Externí odkaz:
https://doaj.org/article/7675c9a582414a019167cde5064c3ff4
Autor:
Dae-Yeon Cho, Mi-Young Lee, Young-Jun Kwon, Young Nam Kim, You-Jung Han, Hye-Sung Won, Hae-Jin Hu, Hyun Mee Ryu, Mijin Oh
Publikováno v:
Journal of Obstetrics and Gynaecology. 40:1090-1095
Clinical performance of the Momguard non-invasive prenatal test (NIPT) was evaluated in a cohort of Korean pregnant women. The foetal trisomies 21, 18 and 13 (T21, T18 and T13) were screened by low-coverage massive parallel sequencing in the maternal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dec158bcb8989f808b4d3933c4e038e0
https://doi.org/10.1080/01443615.2019.1680617
https://doi.org/10.1080/01443615.2019.1680617
Publikováno v:
Journal of Chitin and Chitosan. 24:84-89
Intestinal epithelial barrier plays an important role to regulate para-cellular transport of water, nutrients and ions and to defend against toxic agents and pathogens as a first barrier. Therefore, maintaining barrier integrity is required to enhanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5305b22276f732c3c1dfa84a3798b3d
https://doi.org/10.17642/jcc.24.2.2
https://doi.org/10.17642/jcc.24.2.2
Autor:
Hyun Ju Lee, Mi Ok Park, Seo Yoon Moon, Jeong Min Lee, Sangheon Lee, Dae-Yeon Cho, Mijin Oh, Dong Hee Seo, Hae-Jin Hu, Ki-Eun Hyeong, So-Young Kim
Publikováno v:
The Korean Journal of Blood Transfusion. 29:310-319
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8fb188c5030d584a1870d7cf97139e0a
https://doi.org/10.17945/kjbt.2018.29.3.310
https://doi.org/10.17945/kjbt.2018.29.3.310
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-4 (2018)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Hereditary neuropathy with liability to pressure palsies (HNPP) is an autosomal dominant disorder mainly due to a deletion of chromosome 17p11.2 including PMP22 (PMP22 Del HNPP). The prevalence of HNPP is estimated to be 0.84 to 16 per 100,000, but c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d14824f4b4a5eb75754c8d2d09c772c
http://link.springer.com/article/10.1186/s13023-018-0779-5
http://link.springer.com/article/10.1186/s13023-018-0779-5
Autor:
Sanghee Kim1, Mijin Oh2, Woongsic Jung1, Joonho Park3, Han-Gu Choi1, Seung Chul Shin4 biotech21@gmail.com
Publikováno v:
GigaScience. Mar2017, Vol. 6 Issue 3, p1-8. 8p.
Autor:
Mijin Oh, Namshin Kim, Seung-Won Lee, Soo-Jin Kwon, Seong-Han Sohn, Byung Ohg Ahn, Mina Jin, Won-Hyong Chung, Young-Joo Seol, Ki-Byung Lim, Dae-Jin Hyung, Keun Jin Choi, Seunghoon Baek, Beom-Seok Park, Won Byoung Chae, Goon-Bo Kim, Yoon-Jung Hwang, Hee-Ju Yu, Seongmun Jeong, Hee Chung, Jeong-Hwan Mun, Young-Min Jeong, Sang-Bong Choi
Publikováno v:
Theoretical and Applied Genetics. 129:1357-1372
This study presents a chromosome-scale draft genome sequence of radish that is assembled into nine chromosomal pseudomolecules. A comprehensive comparative genome analysis with the Brassica genomes provides genomic evidences on the evolution of the m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88bc36c8a92e8b107448fce96ec3a993
https://doi.org/10.1007/s00122-016-2708-0
https://doi.org/10.1007/s00122-016-2708-0
Publikováno v:
Journal of Genetic Medicine. 12:96-99
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67f72a9f7e6c703b466311d88e35f076
https://doi.org/10.5734/jgm.2015.12.2.96
https://doi.org/10.5734/jgm.2015.12.2.96
Publikováno v:
Journal of Laboratory Medicine and Quality Assurance. 37:214-218
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7544bcaf739ec60766a466e603ac9fbc
https://doi.org/10.15263/jlmqa.2015.37.4.214
https://doi.org/10.15263/jlmqa.2015.37.4.214
Autor:
Noelia Carrasquilla-Garcia, Anandkumar K. Surendrarao, Douglas R. Cook, Hee-Ju Yu, Brendan K. Riely, R. V. Penmetsa, Goon Bo Kim, Gang-Seob Lee, Deborah Chasman, Alireza Fotuhi Siahpirani, Sushmita Roy, Mijin Oh, Jeong-Hwan Mun, Sang Cheol Kim, Estíbaliz Larrainzar, Hyun Ju Hwang, Namshin Kim
Publikováno v:
Plant Physiology. 169:233-265
The legume-rhizobium symbiosis is initiated through the activation of the Nodulation (Nod) factor-signaling cascade, leading to a rapid reprogramming of host cell developmental pathways. In this work, we combine transcriptome sequencing with molecula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70641892e19b7c806056e945cee7931b
https://doi.org/10.1104/pp.15.00350
https://doi.org/10.1104/pp.15.00350