日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Clinical and molecular spectrum of inherited epidermolysis bullosa in a Thai cohort: A 12-year retrospective study

泰国人群中遗传性大疱性表皮松解症的临床和分子谱:一项为期12年的回顾性研究

Supsrisunjai, Chavalit; Tirachaimongkol, Nuanjutha; Bunnag, Thareena; Sengtae, Nuttaporn; Tongsima, Sissades; Ngamphiw, Chumpol; Komkhong, Wanchanida; Kootiratrakarn, Tanawatt; Wessagowit, Vesarat; Kantaputra, Piranit

Disseminated Autochthonous Dermal Leishmaniasis Caused by Leishmania siamensis (PCM2 Trang) in a Patient from Central Thailand Infected with Human Immunodeficiency Virus

泰国中部一名感染人类免疫缺陷病毒的患者发生由暹罗利什曼原虫(PCM2 Trang株)引起的播散性本土皮肤利什曼病

Supsrisunjai, Chavalit; Kootiratrakarn, Tanawatt; Puangpet, Pailin; Bunnag, Thareena; Chaowalit, Prapaipit; Wessagowit, Vesarat

Normal and abnormal mechanisms of gene splicing and relevance to inherited skin diseases

基因剪接的正常和异常机制及其与遗传性皮肤病的相关性

Wessagowit, Vesarat; Nalla, Vijay K; Rogan, Peter K; McGrath, John A

Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome

kindlin-1(秀丽隐杆线虫肌动蛋白-细胞外基质连接蛋白UNC-112的人类同源物)的缺失会导致金德勒综合征。

Siegel, Dawn H; Ashton, Gabrielle H S; Penagos, Homero G; Lee, James V; Feiler, Heidi S; Wilhelmsen, Kirk C; South, Andrew P; Smith, Frances J D; Prescott, Alan R; Wessagowit, Vesarat; Oyama, Noritaka; Akiyama, Masashi; Al Aboud, Daifullah; Al Aboud, Khalid; Al Githami, Ahmad; Al Hawsawi, Khalid; Al Ismaily, Abla; Al-Suwaid, Raouf; Atherton, David J; Caputo, Ruggero; Fine, Jo-David; Frieden, Ilona J; Fuchs, Elaine; Haber, Richard M; Harada, Takashi; Kitajima, Yasuo; Mallory, Susan B; Ogawa, Hideoki; Sahin, Sedef; Shimizu, Hiroshi; Suga, Yasushi; Tadini, Gianluca; Tsuchiya, Kikuo; Wiebe, Colin B; Wojnarowska, Fenella; Zaghloul, Adel B; Hamada, Takahiro; Mallipeddi, Rajeev; Eady, Robin A J; McLean, W H Irwin; McGrath, John A; Epstein, Ervin H