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

The Syphilis Pandemic Prior to Penicillin: Origin, Health Issues, Cultural Representation and Ethical Challenges

青霉素问世前的梅毒大流行:起源、健康问题、文化表征和伦理挑战

Ekselius, Lisa; Gerdin, Bengt; Vahlquist, Anders

Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients

对224例患者的大型队列中鉴定的ALOX12B或ALOXE3突变进行荟萃分析

Hotz, Alrun; Kopp, Julia; Bourrat, Emmanuelle; Oji, Vinzenz; Komlosi, Katalin; Giehl, Kathrin; Bouadjar, Bakar; Bygum, Anette; Tantcheva-Poor, Iliana; Hellström Pigg, Maritta; Has, Cristina; Yang, Zhou; Irvine, Alan D; Betz, Regina C; Zambruno, Giovanna; Tadini, Gianluca; Süßmuth, Kira; Gruber, Robert; Schmuth, Matthias; Mazereeuw-Hautier, Juliette; Jonca, Natalie; Guez, Sophie; Brena, Michela; Hernandez-Martin, Angela; van den Akker, Peter; Bolling, Maria C; Hannula-Jouppi, Katariina; Zimmer, Andreas D; Alter, Svenja; Vahlquist, Anders; Fischer, Judith

Ichthyosis: A Road Model for Skin Research

鱼鳞病:皮肤研究的路线图

Vahlquist, Anders; Törmä, Hans

Patients with congenital ichthyosis and TGM1 mutations overexpress other ARCI genes in the skin: Part of a barrier repair response?

患有先天性鱼鳞病和 TGM1 基因突变的患者皮肤中其他 ARCI 基因过度表达:这是屏障修复反应的一部分吗?

Zhang, Hanqian; Ericsson, Maja; Weström, Simone; Vahlquist, Anders; Virtanen, Marie; Törmä, Hans

Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment

遗传性非综合征型鱼鳞病:病理生理学、诊断和治疗的最新进展

Vahlquist, Anders; Fischer, Judith; Törmä, Hans

Revertant mosaicism repairs skin lesions in a patient with keratitis-ichthyosis-deafness syndrome by second-site mutations in connexin 26

回复镶嵌现象通过连接蛋白 26 的第二位点突变修复角膜炎-鱼鳞病-耳聋综合征患者的皮肤病变

Sanna Gudmundsson, Maria Wilbe, Sara Ekvall, Adam Ameur, Nicola Cahill, Ludmil B Alexandrov, Marie Virtanen, Maritta Hellström Pigg, Anders Vahlquist, Hans Törmä, Marie-Louise Bondeson

Oral liarozole in the treatment of patients with moderate/severe lamellar ichthyosis: results of a randomized, double-blind, multinational, placebo-controlled phase II/III trial

口服利阿唑治疗中重度板层状鱼鳞病患者:一项随机、双盲、多中心、安慰剂对照的II/III期试验结果

Vahlquist, A; Blockhuys, S; Steijlen, P; van Rossem, K; Didona, B; Blanco, D; Traupe, H

Filaggrin genotype determines functional and molecular alterations in skin of patients with atopic dermatitis and ichthyosis vulgaris

丝聚蛋白基因型决定特应性皮炎和寻常型鱼鳞病患者皮肤的功能和分子改变

Winge, Mårten C G; Hoppe, Torborg; Berne, Berit; Vahlquist, Anders; Nordenskjöld, Magnus; Bradley, Maria; Törmä, Hans

Strong Maternal Khoisan Contribution to the South African Coloured Population: A Case of Gender-Biased Admixture

南非有色人种中科伊桑族母系血统的显著贡献:一个性别偏向性混血案例

Morange, Pierre-Emmanuel; Bezemer, Irene; Saut, Noémie; Bare, Lance; Burgos, Gwenaelle; Brocheton, Jessy; Durand, Hervé; Biron-Andreani, Christine; Schved, Jean-Francois; Pernod, Gilles; Galan, Pilar; Drouet, Ludovic; Zelenika, Diana; Germain, Marine; Nicaud, Viviane; Heath, Simon; Ninio, Ewa; Delluc, Aurélien; Münzel, Thomas; Zeller, Tanja; Brand-Herrmann, Stefan-Martin; Alessi, Marie-Christine; Tiret, Laurence; Lathrop, Mark; Cambien, François; Blankenberg, Stefan; Emmerich, Joseph; Trégouët, David-Alexandre; Rosendaal, Frits R; Bungartz, Kathryn D; Williamson, Robin E; Doherty, Leana; Sheen, Mee Rie; Vlachos, Adrianna; Choesmel, Valerie; O'Donohue, Marie-Françoise; Clinton, Catherine; Schneider, Hal E; Sieff, Colin A; Newburger, Peter E; Ball, Sarah E; Niewiadomska, Edyta; Matysiak, Michal; Glader, Bertil; Arceci, Robert J; Farrar, Jason E; Atsidaftos, Eva; Lipton, Jeffrey M; Gleizes, Pierre-Emmanuel; Gazda, Hanna T; Morange, Pierre-Emmanuel; Bezemer, Irene; Saut, Noémie; Bare, Lance; Burgos, Gwenaelle; Brocheton, Jessy; Durand, Hervé; Biron-Andreani, Christine; Schved, Jean-Francois; Pernod, Gilles; Galan, Pilar; Drouet, Ludovic; Zelenika, Diana; Germain, Marine; Nicaud, Viviane; Heath, Simon; Ninio, Ewa; Delluc, Aurélien; Münzel, Thomas; Zeller, Tanja; Brand-Herrmann, Stefan-Martin; Alessi, Marie-Christine; Tiret, Laurence; Lathrop, Mark; Cambien, François; Blankenberg, Stefan; Emmerich, Joseph; Trégouët, David-Alexandre; Rosendaal, Frits R; Dahlqvist, Johanna; Klar, Joakim; Tiwari, Neha; Schuster, Jens; Törmä, Hans; Badhai, Jitendra; Pujol, Ramon; van Steensel, Maurice AM; Brinkhuizen, Tjinta; Gijezen, Lieke; Chaves, Antonio; Tadini, Gianluca; Vahlquist, Anders; Dahl, Niklas; Garber, Kathryn B; Froyen, Guy; Quintana-Murci, Lluis; Harmant, Christine; Quach, Hélène; Balanovsky, Oleg; Zaporozhchenko, Valery; Bormans, Connie; van Helden, Paul D; Hoal, Eileen G; Behar, Doron M

A single-nucleotide deletion in the POMP 5' UTR causes a transcriptional switch and altered epidermal proteasome distribution in KLICK genodermatosis

在KLICK基因皮肤病中,POMP 5' UTR中的单核苷酸缺失导致转录转换和表皮蛋白酶体分布改变。

Dahlqvist, Johanna; Klar, Joakim; Tiwari, Neha; Schuster, Jens; Törmä, Hans; Badhai, Jitendra; Pujol, Ramon; van Steensel, Maurice A M; Brinkhuizen, Tjinta; Gijezen, Lieke; Chaves, Antonio; Tadini, Gianluca; Vahlquist, Anders; Dahl, Niklas