Peptide nucleic acid (PNA) probe-based analysis to detect filaggrin mutations in atopic dermatitis patients-Reference-Cited by-同舟云学术

Peptide nucleic acid (PNA) probe-based analysis to detect filaggrin mutations in atopic dermatitis patients

Published:2018-09-13 Issue:11 Volume:27 Page:1304-1308
ISSN:0906-6705
Container-title:Experimental Dermatology
language:en
Short-container-title:Exp Dermatol

Author:

Hwang Joonsung¹^ORCID,Lee Sangku¹,Kim Daehwan¹²,Han Goeun¹²,Soung Nak Kyun¹²,Cha-Molstad Hyunjoo¹,Lee Kyung Ho¹,Ryoo In Ja¹,Ahn Mi Ja¹,Kim Sung Tae³,Lee Min Jae³,Yoo Young Dong³,Lee Hee Gu⁴,Hong Jin Tae⁵^ORCID,Kim Hyunjung⁶,Choi Eung Ho⁷,Kim Soo-Chan⁸,Kwon Yong Tae³,Ahn Jong Seog¹²,Kim Bo Yeon¹²^ORCID

Affiliation:

1. Anticancer Agent Research Center; Korea Research Institute of Bioscience and Biotechnology (KRIBB); Cheongju Korea

2. Department of Biomolecular Science; University of Science & Technology (UST); Daejeon Korea

3. Department of Biomedical Sciences and Protein Metabolism Medical Research Center; College of Medicine; Seoul National University; Seoul Korea

4. Immunotherapy Convergence Research Center; Korea Research Institute of Bioscience and Biotechnology (KRIBB); Daejeon Korea

5. College of Pharmacy and Medical Research Center; Chungbuk National University; Cheongju Korea

6. Department of Dermatology; Seoul Medical Center; Seoul Korea

7. Department of Dermatology; Yonsei University Wonju College of Medicine; Wonju Korea

8. Department of Dermatology; Gangnam Severance Hospital; Yonsei University College of Medicine; Seoul Korea

Funder

R&D Convergence Program

Bio and Medical Technology Development Program

Basic Science Research Program

KRIBB Research Initiative Program

Publisher

Wiley

Subject

Dermatology,Molecular Biology,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/exd.13765/fullpdf

Reference26 articles.

1. Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis

2. Japanese-Specific Filaggrin Gene Mutations in Japanese Patients Suffering from Atopic Eczema and Asthma

3. FLGmutation p.Lys4021X in the C-terminal imperfect filaggrin repeat in Japanese patients with atopic eczema

4. Filaggrin Gene Defects and the Risk of Developing Allergic Disorders

5. Pyrrolidone carboxylic acid levels or caspase-14 expression in the corneocytes of lesional skin correlates with clinical severity, skin barrier function and lesional inflammation in atopic dermatitis

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