Zobrazeno 1 - 10 of 23 pro vyhledávání: '"Han Sol Bae"'
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Akademický článek
Blood-testis barrier integrity depends on Pin1 expression in Sertoli cells
Autor: Rabia Islam, Heein Yoon, Bong-soo Kim, Han-sol Bae, Hye-rim Shin, Woo-Jin Kim, Won-joon Yoon, Yun-Sil Lee, Kyung Mi Woo, Jeong-Hwa Baek, Hyun-Mo Ryoo
Publikováno v: Scientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
Abstract The conformation and function of a subset of serine and threonine-phosphorylated proteins are regulated by the prolyl isomerase Pin1 through isomerization of phosphorylated Ser/Thr-Pro bonds. Pin1 is intensely expressed in Sertoli cells, but
Externí odkaz: https://doaj.org/article/c70b3e12080e47299670d20625366f94
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2
Occurrence and Risk Factors for Macular Edema in Patients with Juvenile Idiopathic Arthritis-Associated Uveitis
Autor: Christoph Tappeiner, Kai Rothaus, Arnd Heiligenhaus, Han Sol Bae, Karoline Walscheid
Publikováno v: Journal of Clinical Medicine
Journal of Clinical Medicine, Vol 10, Iss 4513, p 4513 (2021)
Tappeiner, Christoph; Bae, Han Sol; Rothaus, Kai; Walscheid, Karoline; Heiligenhaus, Arnd (2021). Occurrence and Risk Factors for Macular Edema in Patients with Juvenile Idiopathic Arthritis-Associated Uveitis. Journal of clinical medicine, 10(19) MDPI 10.3390/jcm10194513
Volume 10
Issue 19
Purpose: To analyze occurrence and risk factors for macular edema (ME) in juvenile idiopathic arthritis-associated uveitis (JIA-U). Methods: Retrospective analysis of patients with JIA-U at a tertiary referral uveitis center between 2000 and 2019. Ep
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a89e6989d3761b8984166c585e71eaf4
https://pubmed.ncbi.nlm.nih.gov/34640527
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3
Peptidyl‐prolyl cis–trans isomerase NIMA interacting 1 regulates skeletal muscle fusion through structural modification of Smad3 in the linker region
Autor: Yun-Sil Lee, Bongsoo Kim, Kyung Mi Woo, Heein Yoon, Hyun-Mo Ryoo, Han-Sol Bae, Rabia Islam, Jeong-Hwa Baek, Won-Joon Yoon, Hye-Rim Shin
Publikováno v: Journal of Cellular Physiology
Myoblast fusion is critical for muscle growth, regeneration, and repair. We previously reported that the enzyme peptidyl-prolyl cis-trans isomerase NIMA interacting 1 (Pin1) is involved in osteoclast fusion. The objective of this study was to investi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eaa27e1d5d223b72278d8466b83959e7
http://europepmc.org/articles/PMC6686165
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4
A novel RUNX2 mutation in exon 8, G462X, in a patient with Cleidocranial Dysplasia
Autor: Yu-Jin Jung, Han-Sol Bae, Seung-Hak Baek, Hyun-Mo Ryoo
Publikováno v: Journal of Cellular Biochemistry. 119:1152-1162
To identify a novel mutation of Runx2 gene in Cleidocranial Dysplasia (CCD) patients and to characterize the functional consequences of this mutation. The subjects consisted of 12 Korean CCD patients. After oral epithelial cells were collected using
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2751f950690339da939946e705e8c7c4
https://doi.org/10.1002/jcb.26283
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5
An HDAC Inhibitor, Entinostat/MS-275, Partially Prevents Delayed Cranial Suture Closure in Heterozygous Runx2 Null Mice
Autor: Hyun-Mo Ryoo, Seoae Cho, Kang-Young Choi, Young-Dan Cho, Rabia Islam, Han-Sol Bae, Seung-Hak Baek, Jin-Muk Lim, Jeong-Hwa Baek, Won-Joon Yoon, Minseok Seo, Kyung Mi Woo, Yun-Sil Lee, Bongsoo Kim, Hye-Rim Shin, Hong-Gee Kim
Publikováno v: Journal of Bone and Mineral Research. 32:951-961
Cleidocranial dysplasia (CCD) is an autosomal dominant skeletal disorder caused by mutations in RUNX2, coding a key transcription factor of early osteogenesis. CCD patients suffer from developmental defects in cranial bones. Despite numerous investig
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3796952a01bfcf6f2977f32156c49c6f
https://doi.org/10.1002/jbmr.3076
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6
Pin1-mediated Modification Prolongs the Nuclear Retention of β-Catenin in Wnt3a-induced Osteoblast Differentiation
Autor: Kyung Mi Woo, Han-Sol Bae, Won-Joon Yoon, Jeong-Hwa Baek, Hye-Rim Shin, Young-Dan Cho, Hyun-Mo Ryoo, Taegyung Lee, Rabia Islam, Bongsu Kim
Publikováno v: Journal of Biological Chemistry. 291:5555-5565
The canonical Wnt signaling pathway, in which β-catenin nuclear localization is a crucial step, plays an important role in osteoblast differentiation. Pin1, a prolyl isomerase, is also known as a key enzyme in osteogenesis. However, the role of Pin1
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76cc11ffb0ff57c379f9d8a2bc09854d
https://doi.org/10.1074/jbc.m115.698563
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7
Epigenetic Priming Confers Direct Cell Trans-Differentiation From Adipocyte to Osteoblast in a Transgene-Free State
Autor: Young Ku, Won-Joon Yoon, Kyung Mi Woo, Han-Sol Bae, Young-Dan Cho, Gene Lee, Joo-Cheol Park, Jeong-Hwa Baek, Dong-Seol Lee, Hyun-Mo Ryoo
Publikováno v: Journal of Cellular Physiology. 231:1484-1494
The bone marrow of healthy individuals is primarily composed of osteoblasts and hematopoietic cells, while that of osteoporosis patients has a larger portion of adipocytes. There is evidence that the epigenetic landscape can strongly influence cell d
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6f5e6c458e5a62238a29e0d40025509a
https://doi.org/10.1002/jcp.25183
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8
Characterization of dental phenotype in patients with cleidocranial dysplasia using longitudinal data
Autor: Yu-Jin Jung, Hyun-Mo Ryoo, Il-Sik Cho, Seung-Hak Baek, Sang-Woon Ha, Han-Sol Bae
Publikováno v: Angle Orthod
Objective: To investigate the characteristics of the dental phenotype in patients with cleidocranial dysplasia (CCD) using longitudinal data. Materials and Methods: Twelve unrelated Korean CCD patients were observed using a longitudinal series of rad
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0709af433625c075d1ced5cef49c61d3
https://europepmc.org/articles/PMC8191924/
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9
PIN1 is a new therapeutic target of craniosynostosis
Autor: Kang-Young Choi, Byung Soo Kim, Ho Il Yoon, Kyung Mi Woo, Hye-Rim Shin, Yong Seuk Lee, Han-Sol Bae, Young-Dan Cho, Hyun-Mo Ryoo, Jeong-Hwa Baek, Woojin Kim
Publikováno v: Human Molecular Genetics
Gain-of-function mutations in fibroblast growth factor receptors (FGFRs) cause congenital skeletal anomalies, including craniosynostosis (CS), which is characterized by the premature closure of craniofacial sutures. Apert syndrome (AS) is one of the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fd12672052dfdf3ff57029ff3438d62
https://pubmed.ncbi.nlm.nih.gov/30007339
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10
Blood-testis barrier integrity depends on Pin1 expression in Sertolicells
Autor: Yun-Sil Lee, Bongsoo Kim, Han-Sol Bae, Hye-Rim Shin, Kyung Mi Woo, Heein Yoon, Hyun-Mo Ryoo, Won-Joon Yoon, Rabia Islam, Woojin Kim, Jeong-Hwa Baek
Publikováno v: SCIENTIFIC REPORTS(7)
Scientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
Scientific Reports
The conformation and function of a subset of serine and threonine-phosphorylated proteins are regulated by the prolyl isomerase Pin1 through isomerization of phosphorylated Ser/Thr-Pro bonds. Pin1 is intensely expressed in Sertoli cells, but its func
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e25db901648c436792266ba6ad615bf0
http://open-repository.kisti.re.kr/cube/handle/open_repository/475544.do
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