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Sheau-Chiou Chao

Associate Professor

  • 1492 Citations
  • 17 h-Index
19942019
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Personal profile

Education

  • 國立成功大學學士後醫學系學士

Research Interests

  • 皮膚學
  • 皮膚外科
  • 小兒皮膚科
  • 分子生物學
  • 美容醫學

Fingerprint Dive into the research topics where Sheau-Chiou Chao is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 8 Similar Profiles
Mutation Medicine & Life Sciences
Genes Medicine & Life Sciences
Taiwan Medicine & Life Sciences
Skin Medicine & Life Sciences
Benign Familial Pemphigus Medicine & Life Sciences
Missense Mutation Medicine & Life Sciences
Epidermolysis Bullosa Simplex Medicine & Life Sciences
Palmoplantar Keratoderma Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Projects 2001 2008

毛孔角化症之致病基因位置的研究

Chao, S.

07-08-01 → 08-07-31

Project: Research project

黑色素生成相關基因及蛋白?′﹞筐??(PAR-2)在肝斑病灶的表現情形，並評估與不同種類淡斑劑療效的相關性

Chao, S.

06-08-01 → 07-07-31

Project: Research project

在Hailey-Hailey disease患者的重建表皮上，類固醇、cyclosporine、tacrolimus、蛋白??抑制劑及維他命A酸等化合物對凝血?■楖`素、細胞橋小體及黏連分子表現的影響

Chao, S.

05-08-01 → 06-07-31

Project: Research project

播散型表淺性日光性汗孔角化症之基因確認

Chao, S.

04-08-01 → 05-07-31

Project: Research project

比較細胞凋亡相關蛋白及TGF-beta2 在角質棘皮瘤、鱗狀上皮細胞癌及正常皮膚之表現情形

Chao, S.

03-08-01 → 04-07-31

Project: Research project

Research Output 1994 2019

Scleritis and anterior uveitis may herald the development of an epibulbar tumor in patients with extranodal Rosai-Dorfman disease: A case report

Lee, Y. K., Chao, S-C., Lee, C-N. & Hung, J-H., 2019 Jul 10, In : BMC Ophthalmology. 19, 1, 144.

Research output: Contribution to journal › Article

Open Access
Sinus Histiocytosis
Scleritis
Anterior Uveitis
Neoplasms
Eye Manifestations
1 Citation (Scopus)

Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in WNT10A

Hsu, T. C., Lee, J. Y. Y., Hsu, M. M. L. & Chao, S-C., 2018 Apr 1, In : Journal of Dermatology. 45, 4, p. 475-478 4 p.

Research output: Contribution to journal › Article

Missense Mutation
Ectodermal Dysplasia
Mutation
Tooth Abnormalities
Hypotrichosis

Cerebrotendinous xanthomatosis-a case report with novel compound heterozygous mutation of CYP27A1 gene

Yuan, J., Sung, P-S., Lee, Y-Y. & Chao, S-C., 2018 Dec 1, In : Dermatologica Sinica. 36, 4, p. 200-202 3 p.

Research output: Contribution to journal › Article

Cerebrotendinous Xanthomatosis
Xanthomatosis
Mutation
Exons
Cholestanetriol 26-Monooxygenase

Generalized Dowling-Degos disease with an initiation codon mutation of KRT5 mutation

Hsieh, F. N., Chao, S-C. & Lee, Y-Y., 2018 Jun 1, In : Dermatologica Sinica. 36, 2, p. 103-104 2 p.

Research output: Contribution to journal › Letter

Initiator Codon
Mutation
Dowling-Degos Disease

A novel mutation of the RNA-specific adenosine deaminase 1 gene in a Taiwanese patient with dyschromatosis symmetrica hereditaria and Becker's nevus-like lesion

Chen, Y. C., Chao, S-C., Yang, M. H. & Yang, C-C., 2016 Jun 1, In : Dermatologica Sinica. 34, 2, p. 110-111 2 p.

Research output: Contribution to journal › Letter

Adenosine Deaminase
Nevus
RNA
Mutation
Genes