Search Results - "VAHLQUIST, Anders"

Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment by Vahlquist, Anders, Fischer, Judith, Törmä, Hans

“…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…”
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The Syphilis Pandemic Prior to Penicillin: Origin, Health Issues, Cultural Representation and Ethical Challenges by Ekselius, Lisa, Gerdin, Bengt, Vahlquist, Anders

“…Syphilis is currently a treatable disease, with a low incidence in most developed countries, although the prevalence has increased recently, especially among…”
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Obituary: Annamari Ranki by Peltonen, Sirkku, Vahlquist, Anders, Lindberg, Magnus, Larkö, Olle

“…Obituary…”
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Ichthyosis: A Road Model for Skin Research by Vahlquist, Anders, Törmä, Hans

“…The understanding of monogenetic disorders of cornification, including the group of diseases called ichthyoses, has expanded greatly in recent years. Studies…”
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The Times They Are A-changin by Vahlquist, A

“…Abstract is missing (Editorial)…”
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The Editorial Office of ActaDV Appears in a New Costume by Vahlquist, Anders, Larkö, Olle

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The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB by Fine, Jo-David, MD, MPH, FRCP, Eady, Robin A.J., DSc, FRCP, FMedSci, Bauer, Eugene A., MD, Bauer, Johann W., MD, Bruckner-Tuderman, Leena, MD, PhD, Heagerty, Adrian, MD, FRCP, Hintner, Helmut, MD, Hovnanian, Alain, MD, PhD, Jonkman, Marcel F., MD, PhD, Leigh, Irene, MD, FRCP, FMedSci, McGrath, John A., MD, FRCP, Mellerio, Jemima E., MD, FRCP, Murrell, Dedee F., MD, Shimizu, Hiroshi, MD, PhD, Uitto, Jouni, MD, PhD, Vahlquist, Anders, MD, PhD, Woodley, David, MD, Zambruno, Giovanna, MD

“…Background Since publication in 2000 of the Second International Consensus Report on Diagnosis and Classification of Epidermolysis Bullosa, many advances have…”
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Changes in Editorial Board of Acta Dermato-Venereologica by Schmidtchen, A, Vahlquist, A

“…Abstract is missing (Editorial)…”
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Interactions between FATP4 and ichthyin in epidermal lipid processing may provide clues to the pathogenesis of autosomal recessive congenital ichthyosis by Li, Hao, Vahlquist, Anders, Törmä, Hans

“…Abstract Background Autosomal recessive congenital ichthyosis (ARCI) is caused by mutations in ≥10 different genes, of which transglutaminase-1 (TGM1)…”
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Mutations in the Fatty Acid Transport Protein 4 Gene Cause the Ichthyosis Prematurity Syndrome by Klar, Joakim, Schweiger, Martina, Zimmerman, Robert, Zechner, Rudolf, Li, Hao, Törmä, Hans, Vahlquist, Anders, Bouadjar, Bakar, Dahl, Niklas, Fischer, Judith

“…Ichthyosis prematurity syndrome (IPS) is an autosomal-recessive disorder characterized by premature birth and neonatal asphyxia, followed by a lifelong…”
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Genotypic and Clinical Spectrum of Self-Improving Collodion Ichthyosis: ALOX12B, ALOXE3, and TGM1 Mutations in Scandinavian Patients by Vahlquist, Anders, Bygum, Anette, Gånemo, Agneta, Virtanen, Marie, Hellström-Pigg, Maritta, Strauss, Gitte, Brandrup, Flemming, Fischer, Judith

“…Infants born with autosomal recessive congenital ichthyosis (ARCI) are often encapsulated in a collodion membrane, which shows a lamellar or erythrodermic type…”
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Chemical Chaperones Protect Epidermolysis Bullosa Simplex Keratinocytes from Heat Stress–Induced Keratin Aggregation: Involvement of Heat Shock Proteins and MAP Kinases by Chamcheu, Jean Christopher, Navsaria, Harshad, Pihl-Lundin, Inger, Liovic, Mirjana, Vahlquist, Anders, Törmä, Hans

“…Epidermolysis bullosa simplex (EBS) is a blistering skin disease caused by mutations in keratin genes (KRT5 or KRT14), with no existing therapies. Aggregates…”
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Filaggrin genotype determines functional and molecular alterations in skin of patients with atopic dermatitis and ichthyosis vulgaris by Winge, Mårten C G, Hoppe, Torborg, Berne, Berit, Vahlquist, Anders, Nordenskjöld, Magnus, Bradley, Maria, Törmä, Hans

“…Several common genetic and environmental disease mechanisms are important for the pathophysiology behind atopic dermatitis (AD). Filaggrin (FLG)…”
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Quantitative image analysis of protein expression and colocalisation in skin sections by Zhang, Hanqian, Ericsson, Maja, Virtanen, Marie, Weström, Simone, Wählby, Carolina, Vahlquist, Anders, Törmä, Hans

“…Immunofluorescence (IF) and in situ proximity ligation assay (isPLA) are techniques that are used for in situ protein expression and colocalisation analysis,…”
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A Single-Nucleotide Deletion in the POMP 5′ UTR Causes a Transcriptional Switch and Altered Epidermal Proteasome Distribution in KLICK Genodermatosis by 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

“…KLICK syndrome is a rare autosomal-recessive skin disorder characterized by palmoplantar keratoderma, linear hyperkeratotic papules, and ichthyosiform scaling…”
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Keratinocyte differentiation induced by calcium, phorbol ester or interferon-γ elicits distinct changes in the retinoid signalling pathways by Karlsson, Teresa, Vahlquist, Anders, Törmä, Hans

“…Abstract Background Retinoids influence keratinocyte proliferation and differentiation via binding to nuclear retinoic acid receptors (RARα, -γ) and retinoid X…”
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The involvement of cytochrome p450 (CYP) 26 in the retinoic acid metabolism of human epidermal keratinocytes by Pavez Loriè, Elizabeth, Li, Hao, Vahlquist, Anders, Törmä, Hans

“…All-trans retinoic acid (RA) levels are controlled by enzymes of the vitamin A metabolism (RDH16, RalDH2, and LRAT) and RA catabolism (CYP26 and CYP2S1). Here,…”
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Both all-trans retinoic acid and cytochrome P450 (CYP26) inhibitors affect the expression of vitamin A metabolizing enzymes and retinoid biomarkers in organotypic epidermis by Pavez Loriè, Elizabeth, Chamcheu, Jean Christopher, Vahlquist, Anders, Törmä, Hans

“…The biosynthesis of retinoic acid (RA) from retinol is controlled by several enzymes, e.g. dehydrogenases (RalDH2, RoDH-4) and retinol-esterifying enzyme…”
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Characterization of immortalized human epidermolysis bullosa simplex (KRT5) cell lines: Trimethylamine N-oxide protects the keratin cytoskeleton against disruptive stress condition by Chamcheu, Jean Christopher, Lorié, Elizabeth Pavez, Akgul, Baki, Bannbers, Elin, Virtanen, Marie, Gammon, Luke, Moustakas, Aristidis, Navsaria, Harshad, Vahlquist, Anders, Törmä, Hans

“…Abstract Background Epidermolysis bullosa simplex (EBS) is an autosomal inherited mechano-bullous disease, characterized by intraepidermal blistering and skin…”
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Epidermolysis Bullosa Care in Scandinavia by Vahlquist, Anders, MD, PhD, Tasanen, Kaisa, MD, PhD

“…The recessive forms of epidermolysis bullosa (EB) are common in Scandinavia, especially in the northern parts of Norway and Sweden. The daily care of EB in…”
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