Chaolan L. Pan
Shanghai, China
Last Updated: 09/26/2026
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Found 52 publications
Overlapping Xp21.2 duplications define an X-linked hypotrichosis simplex and implicate TAB3 dosage sensitivity.
Journal: American journal of human genetics
Published: August 18, 2026
Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort.
Journal: The British journal of dermatology
Published: May 08, 2026
Overlapping Xq13.3 duplications define an X-linked hypotrichosis simplex and implicate TAB3 dosage sensitivity.
Journal: American journal of human genetics
Published: April 03, 2026
Platelet-Derived Extracellular Vesicles Alleviate Psoriatic Inflammation via Mitochondrial Transfer to Macrophages.
Journal: Experimental dermatology
Published: February 18, 2025
First successful treatment of epidermolytic Ichthyosis with Vunakizumab: A Case Report.
Journal: Frontiers in immunology
Published: February 10, 2025
Spongiotic psoriasiform dermatitis with dual features of eczema and psoriasis: Janus kinase inhibition as a potential therapeutic option.
Journal: Clinical and experimental dermatology
Published: December 21, 2024
Ultra-high gene transfection efficiency in suspension cells mediated by highly branched-linear poly(β-amino ester)s.
Journal: Journal of controlled release : official journal of the Controlled Release Society
Published: October 31, 2024
Effective therapy with simvastatin compound ointment in palmoplantar keratoderma induced by lanosterol synthase (LSS) gene variants.
Journal: The British journal of dermatology
Published: September 29, 2024
Successfully treated with siltuximab and prednisone in a 7-year-old girl with DOCK8-deficiency presenting as recurrent wart-like lesions: a case report.
Journal: Frontiers in immunology
Published: April 18, 2024
First Case of Superficial Epidermolytic Ichthyosis Successfully Treated by Dupilumab.
Journal: Dermatitis : contact, atopic, occupational, drug
Published: March 15, 2024
A novel missense pathogenic variant in the CYLD gene in a Chinese family with multiple familial trichoepithelioma.
Journal: International journal of dermatology
Published: February 19, 2024
Chromosome 8 inversion mutation in congenital generalized hypertrichosis: localization of precise breakpoints.
Journal: The British journal of dermatology
Published: January 08, 2024
Last Updated: 09/26/2026