Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Ah-Ra Ko"'
Autor:
Sung Won Park, Seung-Tae Lee, Young Bae Sohn, Sung Yoon Cho, Se-Hwa Kim, Su Jin Kim, Chi Hwa Kim, Ah-Ra Ko, Kyung-Hoon Paik, Jong-Won Kim, Dong-Kyu Jin
Publikováno v:
Korean Journal of Pediatrics, Vol 55, Iss 10, Pp 388-392 (2012)
PurposeSingle-nucleotide polymorphism (SNP) markers within LIN28B have been reported to be related to the timing of pubertal growth. However, no study has investigated the frequency of genetic markers in girls with precocious puberty (PP) or early pu
Externí odkaz:
https://doaj.org/article/111aa7d8efde4bab98ca9e492b44daa3
Autor:
Ok Jeong Lee, Su-Jin Kim, Young Bae Sohn, Hyung-Doo Park, Soo-Youn Lee, Chi-Hwa Kim, Ah-Ra Ko, Yeon-Joo Yook, Su-Jin Lee, Sung Won Park, Se-Hwa Kim, Sung-Yoon Cho, Eun-Kyung Kwon, Sun Ju Han, Dong-Kyu Jin
Publikováno v:
Korean Journal of Pediatrics, Vol 55, Iss 3, Pp 88-92 (2012)
PurposeMucopolysaccharidosis type II (MPS II or Hunter syndrome) is a rare lysosomal storage disorder caused by iduronate-2-sulfatase (IDS) deficiency. MPS II causes a wide phenotypic spectrum of symptoms ranging from mild to severe. IDS activity, wh
Externí odkaz:
https://doaj.org/article/e1103987f64b4280aecf870c600b0834
Autor:
Seok-Ho Shin, Min-Ho Park, Jin-Ju Byeon, Byeong ill Lee, Yuri Park, Ah-ra Ko, Mi-ran Seong, Soyeon Lee, Mi Ra Kim, Jinwook Seo, Myung Eun Jung, Dong-Kyu Jin, Young G. Shin
Publikováno v:
Pharmaceutics, Vol 10, Iss 2, p 69 (2018)
Fabry disease is a rare lysosomal storage disorder resulting from the lack of α-Gal A gene activity. Globotriaosylceramide (GB3, ceramide trihexoside) is a novel endogenous biomarker which predicts the incidence of Fabry disease. At the early stage
Externí odkaz:
https://doaj.org/article/fe75ef9324dc4102a0549bb77a8fe849
Publikováno v:
Journal of Korea Planning Association. 57:124-137
Autor:
Ah-Ra Ko, Seung-Woo Yang
Publikováno v:
Korean Journal of Urban History. 30:37-98
Autor:
So-Yeon Lee, Joo-Hyun Seo, Dong-Kyu Jin, Sung Yoon Cho, Young Bae Sohn, Torayuki Okuyama, Mi-ran Seong, Mi Ra Kim, Ah-Ra Ko, Makoto Sakaguchi, Jung-Sun Kim, Takahiro Nakazawa, Motomichi Kosuga
Publikováno v:
Journal of Inherited Metabolic Disease. 41:1235-1246
Mucopolysaccharidosis II (MPS II) is caused by a deficiency of iduronate-2-sulfatase that results in accumulation of glycosaminoglycans (GAG), including heparan sulfate (HS), which is considered to contribute to neuropathology. We examined the effica
Autor:
Bonggil Hyun, Chang Ho Moon, Pung-Guk Jang, Keun-Hyung Choi, Seung Won Jung, Ah-Ra Ko, Se-Jong Ju, Min-Chul Jang, Kyoungsoon Shin
Publikováno v:
Ocean Science Journal. 51:333-342
Little is known regarding how harmful algal bloom species respond to different temperatures in terms of fatty acid production. This study examined the effects of temperature on the growth rates, cell volumes, and fatty acid concentrations and composi
Publikováno v:
Ocean Science Journal. 51:397-410
To track the diet of minke whale (Balaenoptera acutorostrata) in the East Sea (Japan Sea), a conjoint analysis of fatty acids and C and N stable isotopes was performed on blubber and skin from the whale and its potential prey. The total lipid content
Autor:
Su Jin Kim, Young Bae Sohn, Min Jung Kwak, Sung Yoon Cho, Dong-Kyu Jin, Jung-Sun Kim, Ah-Ra Ko, Malgorzata Przybylska, Seng H. Cheng, Nelson S. Yew, Sung Won Park
Publikováno v:
Molecular Genetics and Metabolism. 117:447-455
Mucolipidoses II and III (ML II and ML III) are lysosomal disorders in which the mannose 6-phosphate recognition marker is absent from lysosomal hydrolases and other glycoproteins due to mutations in GNPTAB, which encodes two of three subunits of the
Publikováno v:
Ocean and Polar Research. 38:35-46
To understand the diet of chaetognaths, the gut content and fatty acid trophic makers (FATMs) of Sagitta crassa and S. nagae, which are the most predominant species of chaetognath in the Yellow Sea, were analyzed. Gut contents of the two species exam