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Articles by Chaolan Pan
Overlapping Xp21.2 duplications define an X-linked hypotrichosis simplex and implicate TAB3 dosage sensitivity
Main text (The American Journal of Human Genetics 113, 1719–1735; August 6, 2026) In the originally published version of this article, the cytogenetic band designation “Xq13.3” was incorrect. The correct designation is “Xp21.2.” The designation has now been corrected throughout the main text and supplemental information, including in the article title. The genomic coordinates and duplication breakpoint information reported in the article are correct and remain unchanged.
Overlapping Xq13.3 duplications define an X-linked hypotrichosis simplex and implicate TAB3 dosage sensitivity
Keywords X-linked hypotrichosis simplex structural variant tandem duplication TAB3 anti-inflammatory therapy copy-number variant Get full text access Log in, subscribe or purchase for full access. References 1. Doolan, B.J. ∙ Rayinda, T. ∙ Chiu, F.P. ... A review of genotrichoses and hair pathology associated with inherited skin diseases Br. J. Dermatol. 2023; 189:154-160 2. Hayashi, R. ∙ Shimomura, Y. Update of recent findings in genetic hair disorders J. Dermatol. 2022; 49:55-67 3. Peled, A. ∙ Samuelov, L.
A novel missense pathogenic variant in the CYLD gene in a Chinese family with multiple familial trichoepithelioma
Department of Dermatology, The Children's Hospital of Fudan University, Shanghai, China Department of Dermatology, Anhui University of Science and Technology First Affiliated Hospital, Anhu, China These authors contributed equally to the work.
ADAM17 variant causes hair loss via ubiquitin ligase TRIM47 mediated degradation
ResearchDermatologyGenetics Open Access | 10.1172/jci.insight.177588 JCI Insight. https://doi.org/10.1172/jci.insight.177588. Copyright © 2024, Wang et al. This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. View PDF Abstract Hypotrichosis is a genetic disorder which characterized by a diffuse and progressive loss of scalp and/or body hair.
Pharmaceuticals | Free Full-Text | A Carbon 21 Steroidal Glycoside with Pregnane Skeleton from Cynanchum atratum Bunge Promotes Megakaryocytic and Erythroid Differentiation in Erythroleukemia HEL Cells through Regulating Platelet-Derived Growth Factor Rec
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Exploring Th17‐related inflammation in AP1B1‐associated KIDAR syndrome and potential therapeutic implications of secukinumab
DATA AVAILABILITY STATEMENT The data that support the findings of this study are available from the corresponding author upon reasonable request.
Successful treatment of cutaneous protothecosis with fluconazole: A case report and epidemiology study of Prototheca infection in China
1 INTRODUCTION Prototheca is ubiquitous in nature,1 but protothecosis is a rare infection caused by prototheca.
RESEARCH LETTER Fuying Chen, Fuying Chen Department of Dermatology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China Institute of Dermatology, Shanghai Jiaotong University School of Medicine, Shanghai, China contributed equally to this work.
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