Zobrazeno 1 - 10
of 217
pro vyhledávání: '"Eul‐Ju Seo"'
Autor:
Daehyun Chu, Miyoung Kim, Young-Uk Cho, Sang-Hyun Hwang, Seongsoo Jang, Eul-Ju Seo, Chan-Jeoung Park, Han-Seung Park, Jung-Hee Lee, Sung Han Kang, Hyery Kim, Kyung-Nam Koh, Ho Joon Im
Publikováno v:
HemaSphere, Vol 7, p e58008b2 (2023)
Externí odkaz:
https://doaj.org/article/64e7fc9adf834610b682cf90e167c3f9
Autor:
Donghyun Kim, Eul-Ju Seo, Yun Sun Song, Chong Hyun Suh, Jong Won Kim, Dong Joon Kim, Dae Chul Suh
Publikováno v:
Neurointervention, Vol 14, Iss 2, Pp 91-98 (2019)
Purpose Hereditary hemorrhagic telangiectasia (HHT), a rare genetic vascular disorder, has been rarely reported in South Korea. We investigated the current prevalence and presenting patterns of genetically confirmed HHT in South Korea. Materials and
Externí odkaz:
https://doaj.org/article/139e1316d78a4131a76de7feb4dda81a
Autor:
Eun-Ji Choi, Young-Uk Cho, Eun-Hye Hur, Seongsoo Jang, Nayoung Kim, Han-Seung Park, Jung-Hee Lee, Kyoo-Hyung Lee, Si-Hwan Kim, Sang-Hyun Hwang, Eul-Ju Seo, Chan-Jeoung Park, Je-Hwan Lee
Publikováno v:
Haematologica, Vol 107, Iss 2 (2021)
DDX41 mutations are associated with hematologic malignancies including myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML), but the incidence in idiopathic cytopenia of undetermined significance (ICUS) is unknown. We investigated the inci
Externí odkaz:
https://doaj.org/article/40d74261a7ac4518839a280e5511bb3d
Publikováno v:
Journal of Ophthalmology, Vol 2021 (2021)
Purpose. Retinitis pigmentosa (RP) shows great diversity between genotypes and phenotypes, and it is important to identify the causative genes. This study aimed to analyze the molecular profiles, associated ocular characteristics, and progression of
Externí odkaz:
https://doaj.org/article/e382cfee407048b59d83478385897eb1
Autor:
Seongjun So, Yeonmi Lee, Jiwan Choi, Seoon Kang, Ji-Yoon Lee, Julie Hwang, Joosung Shin, James R Dutton, Eul-Ju Seo, Beom Hee Lee, Chong Jai Kim, Shoukhrat Mitalipov, Soo Jin Oh, Eunju Kang
Publikováno v:
PLoS ONE, Vol 15, Iss 5, p e0233057 (2020)
Poor survival of human pluripotent stem cells (hPSCs) following freezing, thawing, or passaging hinders the maintenance and differentiation of stem cells. Rho-associated kinases (ROCKs) play a crucial role in hPSC survival. To date, a typical ROCK in
Externí odkaz:
https://doaj.org/article/7a20225a742d4ddd8bcbbb45190f4ce2
Autor:
Yeonhwa Song, Jin-Sun Kim, Se-Hyuk Kim, Yoon Kyung Park, Eunsil Yu, Ki-Hun Kim, Eul-Ju Seo, Heung-Bum Oh, Han Chu Lee, Kang Mo Kim, Haeng Ran Seo
Publikováno v:
Journal of Experimental & Clinical Cancer Research, Vol 37, Iss 1, Pp 1-13 (2018)
Abstract Background Hepatocellular carcinoma (HCC) is one of the most common malignant tumors worldwide and has poor prognosis. Specially, patients with HCC usually have poor tolerance of systemic chemotherapy, because HCCs develop from chronically d
Externí odkaz:
https://doaj.org/article/fa10a60671f847108d40127210cb18b6
Autor:
Yoon-Myung Kim, Ja Hyang Cho, Eungu Kang, Gu-Hwan Kim, Eul-Ju Seo, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 21, Iss 1, Pp 15-20 (2016)
PurposeWilliams-Beuren syndrome (WBS) is caused by a hemizygous microdeletion of chromosome 7q11.23 and is characterized by global cognitive impairment, dysmorphic facial features, and supravalvular aortic stenosis. Endocrine dysfunctions have been r
Externí odkaz:
https://doaj.org/article/d59c030eed464175bc6c4bbf274c95f4
Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay
Autor:
Go Hun Seo, Ja Hye Kim, Ja Hyang Cho, Gu-Hwan Kim, Eul-Ju Seo, Beom Hee Lee, Jin-Ho Choi, Han-Wook Yoo
Publikováno v:
Korean Journal of Pediatrics, Vol 59, Iss 1, Pp 16-23 (2016)
PurposeThe 1p36 deletion syndrome is a microdeletion syndrome characterized by developmental delays/intellectual disability, craniofacial dysmorphism, and other congenital anomalies. To date, many cases of this syndrome have been reported worldwide.
Externí odkaz:
https://doaj.org/article/e29d256000404232915951353fbcd025
Autor:
Go Hun Seo, Eungu Kang, Ja Hyang Cho, Beom Hee Lee, Jin-Ho Choi, Gu-Hwan Kim, Eul-Ju Seo, Han-Wook Yoo
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 20, Iss 2, Pp 110-113 (2015)
Turner syndrome is one of the most common chromosomal disorders. It is caused by numerical or structural abnormalities of the X chromosome and results in short stature and gonadal dysgenesis. The short stature arises from haploinsufficiency of the SH
Externí odkaz:
https://doaj.org/article/e47ae07928964c919bc8e73a91b50ad1
Autor:
Yoon-Myung Kim, In-Hee Choi, Jun Suk Kim, Ja Hye Kim, Ja Hyang Cho, Beom Hee Lee, Gu-Hwan Kim, Jin-Ho Choi, Eul-Ju Seo, Han-Wook Yoo
Publikováno v:
Korean Journal of Pediatrics, Vol 59, Iss Suppl 1, Pp S25-S28 (2016)
Phelan-McDermid syndrome is a rare genetic disorder caused by the terminal or interstitial deletion of the chromosome 22q13.3. Patients with this syndrome usually have global developmental delay, hypotonia, and speech delays. Several putative genes s
Externí odkaz:
https://doaj.org/article/1c2f55f8a7084d579de8039500998543