Anders Vahlquist
Overview
Explore the profile of Anders Vahlquist including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
60
Citations
1089
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Ekselius L, Gerdin B, Vahlquist A
Acta Derm Venereol
. 2024 Mar;
104:adv34879.
PMID: 38436430
Syphilis is currently a treatable disease, with a low incidence in most developed countries, although the prevalence has increased recently, especially among men-who-have-sex-with-men. In many of the least developed countries,...
2.
Zhang H, Westrom S, Kappelin P, Virtanen M, Vahlquist A, Torma H
Differentiation
. 2021 May;
119:19-27.
PMID: 34029921
A proper skin barrier function requires constant formation of stratum corneum, i.e. the outermost layer of epidermis composed of terminally differentiated keratinocytes. The complex process of converting proliferative basal keratinocytes...
3.
Hotz A, Kopp J, Bourrat E, Oji V, Komlosi K, Giehl K, et al.
Genes (Basel)
. 2021 Jan;
12(1).
PMID: 33435499
The autosomal recessive congenital ichthyoses (ARCI) are a nonsyndromic group of cornification disorders that includes lamellar ichthyosis, congenital ichthyosiform erythroderma, and harlequin ichthyosis. To date mutations in ten genes have...
4.
Vahlquist A, Larko O
Acta Derm Venereol
. 2020 Dec;
100(19):adv00351.
PMID: 33330943
No abstract available.
5.
Vahlquist A, Torma H
Acta Derm Venereol
. 2020 Mar;
100(7):adv00097.
PMID: 32147743
The understanding of monogenetic disorders of cornification, including the group of diseases called ichthyoses, has expanded greatly in recent years. Studies of the aetiology of more than 50 types of...
6.
Zhang H, Ericsson M, Westrom S, Vahlquist A, Virtanen M, Torma H
Exp Dermatol
. 2018 Oct;
28(10):1164-1171.
PMID: 30372788
Autosomal recessive congenital ichthyosis (ARCI) is a group of monogenic skin disorders caused by mutations in any of at least 12 different genes, many of which are involved in the...
7.
8.
Zhang H, Ericsson M, Virtanen M, Westrom S, Wahlby C, Vahlquist A, et al.
Exp Dermatol
. 2017 Nov;
27(2):196-199.
PMID: 29094393
Immunofluorescence (IF) and in situ proximity ligation assay (isPLA) are techniques that are used for in situ protein expression and colocalisation analysis, respectively. However, an efficient quantitative method to analyse...
9.
Vahlquist A, Fischer J, Torma H
Am J Clin Dermatol
. 2017 Aug;
19(1):51-66.
PMID: 28815464
Hereditary ichthyoses are due to mutations on one or both alleles of more than 30 different genes, mainly expressed in the upper epidermis. Syndromic as well as nonsyndromic forms of...
10.
Gudmundsson S, Wilbe M, Ekvall S, Ameur A, Cahill N, Alexandrov L, et al.
Hum Mol Genet
. 2017 Feb;
26(6):1070-1077.
PMID: 28158657
Revertant mosaicism (RM) is a naturally occurring phenomenon where the pathogenic effect of a germline mutation is corrected by a second somatic event. Development of healthy-looking skin due to RM...