- A case of Pfeiffer syndrome with c833_834GC>TG (Cys278Leu) mutation in the FGFR2 gene
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Lee MY, Jeon GW, Jung JM, Sin JB
- KMID: 2073610
- Korean J Pediatr.
- 2010 Jul;53(7):774-777.
- doi: 10.3345/kjp.2010.53.7.774
Pfeiffer syndrome is a rare autosomal dominant disorder characterized by coronal craniosynostosis, brachycephaly, mid-facial hypoplasia, and broad and deviated thumbs and great toes. Pfeiffer syndrome occurs in approximately 1:100,000 live... -
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- Myeloid and lymphoid neoplasm with eosinophilia and abnormalities of PDGFRB presenting as congestive heart failure and hypereosinophilia
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Kwon JW, Kwon JH, Her AY
- KMID: 2387653
- Allergy Asthma Respir Dis.
- 2017 Jul;5(4):232-236.
- doi: 10.4168/aard.2017.5.4.232
Hypereosinophilic syndrome (HES) is a heterogeneous disorder characterized by persistent hypereosinophilia with the evidence of organ dysfunction caused by eosinophilic involvement. HES can be induced by various secondary causes, including... -
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- Microarray Analysis of Gene Expression During Differentiation of Human Mesenchymal Stem Cells Treated with Vitamin E in vitro into Osteoblasts
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Ahn KH, Jung HK, Jung SE, Yi KW, Park HT, Shin JH, Kim YT, Hur JY, Kim SH, Kim T
- KMID: 2300157
- Korean J Bone Metab.
- 2011 May;18(1):23-32.
OBJECTIVE: Supplementation with vitamin E is able to protect bone against free radical-induced elevation of bone-resorbing cytokines. We examined gene expression by microarray analysis during the differentiation of human mesenchymal... -
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- Fibroblast Growth Factor Receptor 1 Overexpression Is Associated with Poor Survival in Patients with Resected Muscle Invasive Urothelial Carcinoma
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Lim S, Koh MJ, Jeong HJ, Cho NH, Choi YD, Cho DY, Lee HY, Rha SY
- KMID: 2374112
- Yonsei Med J.
- 2016 Jul;57(4):831-839.
- doi: 10.3349/ymj.2016.57.4.831
PURPOSE: To examine the usefulness of various receptor tyrosine kinase expressions as prognostic markers and therapeutic targets in muscle invasive urothelial cancer (UC) patients. MATERIALS AND METHODS: We retrospectively analyzed the... -
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