Zobrazeno 1 - 10 of 64 pro vyhledávání: '"Haing-Woon Baik"'
1
Akademický článek
Acute dural venous sinus thrombosis in a child with idiopathic steroid-dependent nephrotic syndrome: a case report
Autor: Se Jin Park, Haing-Woon Baik, Myung Hyun Cho, Ju Hyung Kang
Publikováno v: Childhood Kidney Diseases, Vol 26, Iss 2, Pp 101-106 (2022)
Nephrotic syndrome (NS) is a hypercoagulable state in which children are at risk of venous thromboembolism. A higher risk has been reported in children with steroid-resistant NS than in those with steroid-sensitive NS. The mortality rate of cerebral
Externí odkaz: https://doaj.org/article/0b6f6faffe7e43528374487dfed504d6
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2
Data from Selenium Regulates Cyclooxygenase-2 and Extracellular Signal-Regulated Kinase Signaling Pathways by Activating AMP-Activated Protein Kinase in Colon Cancer Cells
Autor: Ock Jin Park, Joohun Ha, Seong-Kyu Lee, Haing Woon Baik, Young-Joon Surh, Young Min Kim, Jin-Taek Hwang
Epidemiologic and experimental evidences indicate that selenium, an essential trace element, can reduce the risk of a variety of cancers. Protection against certain types of cancers, particularly colorectal cancers, is closely associated with pathway
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::528645836ece35f130b7de97e9119362
https://doi.org/10.1158/0008-5472.c.6495230
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6
Genetic analysis of the Gitelman syndrome coexisting with Osteogenesis imperfecta
Autor: Hye-Jeong Ahn, Ju Hyung Kang, Ju Young Kim, Haing-Woon Baik, Se Jin Park
Publikováno v: Clinica Chimica Acta. 518:116-122
Gitelman syndrome (GS) is an autosomal recessive disorder caused by loss-of-function mutations in SLC12A3, which encodes the Na-Cl cotransporter (NCC). Osteogenesis imperfecta (OI) is an autosomal dominant disorder caused by the inheritance of mutati
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b3e6affd8e17c01756fb1fdf97debc3
https://doi.org/10.1016/j.cca.2021.03.018
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7
Akademický článek
Exendin-4 Protects Against Sulfonylurea-Induced β-Cell Apoptosis
Autor: Ju-Young Kim, Dong-Mee Lim, Hyung-Seo Park, Chan-Il Moon, Kyung-Jin Choi, Seong-Kyu Lee, Haing-Woon Baik, Keun-Young Park, Byung-Joon Kim
Publikováno v: Journal of Pharmacological Sciences, Vol 118, Iss 1, Pp 65-74 (2012)
Sulfonylurea is one of the commonly used anti-diabetic drugs that stimulate insulin secretion from β-cells. Despite their glucose lowering effects in type 2 diabetes mellitus, long-term treatment brought on secondary failure characterized by β-cell
Externí odkaz: https://doaj.org/article/3e8613daa9944238a7651a143a9b9071
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8
Akademický článek
17Beta-estradiol Stimulates Glucose Uptake Through Estrogen Receptor and AMP-activated Protein Kinase Activation in C2C12 Myotubes (Korean J Obes 2016;25:190-6)
Autor: Ki-Ho Lee, Kyung-Jin Jo, Ju-Young Kim, Haing-Woon Baik, Seong-Kyu Lee
Publikováno v: Journal of Obesity & Metabolic Syndrome, Vol 26, Iss 1, Pp 78-79 (2017)
Obesity and obesity-related disease are becoming serious global issues. The incidence of obesity and type 2 diabetes has increased in children and adolescents. Type 2 diabetes is a chronic disease that is difficult to treat, and the accurate assessme
Externí odkaz: https://doaj.org/article/95d4560d8f3341afaca6bf98f88dce91
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9
Molecular diagnosis of McArdle disease using whole-exome sequencing
Autor: Jun Hyung Park, Seong-Kyu Lee, Sunghoon Lee, Jin-Soon Park, Ju Hyung Kang, Haing-Woon Baik
Publikováno v: Experimental and Therapeutic Medicine
Whole-exome sequencing (WES) analysis has been used recently as a diagnostic tool for finding molecular defects. In the present study, researchers attempted to analyze molecular defects through WES in a 13-year-old female patient who had not been dia
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fe93fa54de7bd13f61d053c7ad3f9a7
http://europepmc.org/articles/PMC8343624
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