Vahlquist, Anders
Anders Vahlquist Swedish researcher
Vahlquist, Anders, 1947-
VIAF ID: 280847704 (Personal)
Permalink: http://viaf.org/viaf/280847704
Preferred Forms
- 100 0 _ ‡a Anders Vahlquist ‡c Swedish researcher
- 100 1 _ ‡a Vahlquist, Anders
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- 100 1 _ ‡a Vahlquist, Anders
- 100 1 _ ‡a Vahlquist, Anders
- 100 1 _ ‡a Vahlquist, Anders
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- 100 1 _ ‡a Vahlquist, Anders, ‡d 1947-
4xx's: Alternate Name Forms (4)
Works
Title | Sources |
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13-cis-retinoic acid competitively inhibits 3 alpha-hydroxysteroid oxidation by retinol dehydrogenase RoDH-4: a mechanism for its anti-androgenic effects in sebaceous glands? | |
[The Berzelius symposium on genetic dermatoses: cutaneous gene therapy--potential treatment of severe skin diseases] | |
Both all-trans retinoic acid and cytochrome P450 | |
[Burdensome rules for clinical trials are not in proportion to benefits for the patient] | |
Characterization of immortalized human epidermolysis bullosa simplex (KRT5) cell lines: trimethylamine N-oxide protects the keratin cytoskeleton against disruptive stress condition | |
Chemical and metabolic studies on the vitamin A transporting protein complex | |
Chemical chaperones protect epidermolysis bullosa simplex keratinocytes from heat stress-induced keratin aggregation : involvement of heat shock proteins and MAP kinases | |
The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB | |
The clinical spectrum of congenital ichthyosis in Sweden: a review of 127 cases. | |
Congenital ichthyosis: an overview of current and emerging therapies | |
Connexin 26 (GJB2) mutations in two Swedish patients with atypical Vohwinkel (mutilating keratoderma plus deafness) and KID syndrome both extensively treated with acitretin. | |
Dermatologi, venereologi | |
Differential effects of UV irradiation on nuclear retinoid receptor levels in cultured keratinocytes and melanocytes | |
Epidermolysis bullosa care in Scandinavia | |
The expression of epidermal lipoxygenases and transglutaminase-1 is perturbed by NIPAL4 mutations: indications of a common metabolic pathway essential for skin barrier homeostasis | |
Expression of retinoid-regulated genes in lamellar ichthyosis vs. healthy control epidermis: changes after oral treatment with liarozole | |
Filaggrin genotype determines functional and molecular alterations in skin of patients with atopic dermatitis and ichthyosis vulgaris | |
Five new homozygous mutations in the KIND1 gene in Kindler syndrome. | |
From the melanoma incidence in Australia to the role of essential fatty acids in acne | |
Generalized and naevoid epidermolytic ichthyosis in Denmark: clinical and mutational findings | |
Genotype-phenotype correlations emerging from the identification of missense mutations in MBTPS2. | |
Genotypic and clinical spectrum of self-improving collodion ichthyosis: ALOX12B, ALOXE3, and TGM1 mutations in Scandinavian patients | |
Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita | |
Ichthyin/NIPAL4 localizes to keratins and desmosomes in epidermis and Ichthyin mutations affect epidermal lipid metabolism. | |
Immunofluorescence localization of nuclear retinoid receptors in psoriasis versus normal human skin | |
Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment. | |
The involvement of cytochrome p450 (CYP) 26 in the retinoic acid metabolism of human epidermal keratinocytes | |
Keratinocyte differentiation induced by calcium, phorbol ester or interferon-gamma elicits distinct changes in the retinoid signalling pathways | |
Keratins 2 and 4/13 in reconstituted human skin are reciprocally regulated by retinoids binding to nuclear receptor RARalpha | |
L'acupuncture n'a pas un effet spécifique d'un point sur le psoriasis | |
Management of congenital ichthyoses : European guidelines of care : part one | |
Moving towards open access: high-quality research and publication is essential, but visibility of the work is critical | |
Mutations in the fatty acid transport protein 4 gene cause the ichthyosis prematurity syndrome | |
A New Look for ActaDV with More Rapid Publication. | |
News and views from the editor | |
Novel point mutation in the STS gene in a patient with X-linked recessive ichthyosis. | |
Oral alitretinoin in congenital ichthyosis: a pilot study shows variable effects and a risk of central hypothyroidism | |
Palmoplantar keratoderma of the Gamborg-Nielsen type is caused by mutations in the SLURP1 gene and represents a variant of Mal de Meleda | |
Pleomorphic ichthyosis: proposed name for a heterogeneous group of congenital ichthyoses with phenotypic shifting and mild residual scaling | |
Quality of life in adults with congenital ichthyosis | |
Quantitative image analysis of protein expression and colocalisation in skin sections. | |
Recurrent pyoderma gangrenosum and cystic acne associated with leucocyte adhesion deficiency due to novel mutations in ITGB2: successful treatment with infliximab and adalimumab | |
Retinoids and carotenoids in dermatology | |
Revertant mosaicism repairs skin lesions in a patient with keratitis-ichthyosis-deafness syndrome by second-site mutations in connexin 26. | |
Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009. | |
A single-nucleotide deletion in the POMP 5' UTR causes a transcriptional switch and altered epidermal proteasome distribution in KLICK genodermatosis | |
Sjögren-larsson syndrome: a study of clinical symptoms and dermatological treatment in 34 Swedish patients | |
Splice site and deletion mutations in keratin (KRT1 and KRT10) genes: unusual phenotypic alterations in Scandinavian patients with epidermolytic hyperkeratosis | |
Sweat gland morphology and periglandular innervation in essential palmar hyperhidrosis before and after treatment with intradermal botulinum toxin |