Marie Virtanen

Establishment and Utility of SwedAD: A Nationwide Swedish Registry for Patients with Atopic Dermatitis Receiving Systemic Pharmacotherapy

Alsterholm, Mikael; Svedbom, Axel; Anderson, Chris D.; Sommar, Lena Holm et al.

Ingår i Acta Dermato-Venereologica, 2023

• DOI för Establishment and Utility of SwedAD: A Nationwide Swedish Registry for Patients with Atopic Dermatitis Receiving Systemic Pharmacotherapy
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Exploration of novel candidate genes involved in epidermal keratinocyte differentiation and skin barrier repair in man

Zhang, Hanqing; Weström, Simone; Kappelin, Per; Virtanen, Marie et al.

Ingår i Differentiation, s. 19-27, 2021

• DOI för Exploration of novel candidate genes involved in epidermal keratinocyte differentiation and skin barrier repair in man

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

Zhang, Hanqian; Ericsson, Maja; Weström, Simone; Vahlquist, Anders et al.

Ingår i Experimental dermatology, s. 1164-1171, 2019

• DOI för Patients with congenital ichthyosis and TGM1 mutations overexpress other ARCI genes in the skin: Part of a barrier repair response?
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Quantitative image analysis of protein expression and colocalisation in skin sections

Zhang, Hanqian; Ericsson, Maja; Virtanen, Marie; Weström, Simone et al.

Ingår i Experimental dermatology, s. 196-199, 2018

• DOI för Quantitative image analysis of protein expression and colocalisation in skin sections

CARD14-associated papulosquamous eruption: A spectrum including features of psoriasis and pityriasis rubra pilaris

Craiglow, Brittany G.; Boyden, Lynn M.; Hu, Ronghua; Virtanen, Marie et al.

Ingår i The Journal of American Academy of Dermatology, s. 487-494, 2018

• DOI för CARD14-associated papulosquamous eruption: A spectrum including features of psoriasis and pityriasis rubra pilaris

Establishment and Utility of SwedAD: A Nationwide Swedish Registry for Patients with Atopic Dermatitis Receiving Systemic Pharmacotherapy

Alsterholm, Mikael; Svedbom, Axel; Anderson, Chris D.; Sommar, Lena Holm et al.

Ingår i Acta Dermato-Venereologica, 2023

• DOI för Establishment and Utility of SwedAD: A Nationwide Swedish Registry for Patients with Atopic Dermatitis Receiving Systemic Pharmacotherapy
• Ladda ner fulltext (pdf) av Establishment and Utility of SwedAD: A Nationwide Swedish Registry for Patients with Atopic Dermatitis Receiving Systemic Pharmacotherapy

Exploration of novel candidate genes involved in epidermal keratinocyte differentiation and skin barrier repair in man

Zhang, Hanqing; Weström, Simone; Kappelin, Per; Virtanen, Marie et al.

Ingår i Differentiation, s. 19-27, 2021

• DOI för Exploration of novel candidate genes involved in epidermal keratinocyte differentiation and skin barrier repair in man

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

Zhang, Hanqian; Ericsson, Maja; Weström, Simone; Vahlquist, Anders et al.

Ingår i Experimental dermatology, s. 1164-1171, 2019

• DOI för Patients with congenital ichthyosis and TGM1 mutations overexpress other ARCI genes in the skin: Part of a barrier repair response?
• Ladda ner fulltext (pdf) av Patients with congenital ichthyosis and TGM1 mutations overexpress other ARCI genes in the skin: Part of a barrier repair response?

Quantitative image analysis of protein expression and colocalisation in skin sections

Zhang, Hanqian; Ericsson, Maja; Virtanen, Marie; Weström, Simone et al.

Ingår i Experimental dermatology, s. 196-199, 2018

• DOI för Quantitative image analysis of protein expression and colocalisation in skin sections

CARD14-associated papulosquamous eruption: A spectrum including features of psoriasis and pityriasis rubra pilaris

Craiglow, Brittany G.; Boyden, Lynn M.; Hu, Ronghua; Virtanen, Marie et al.

Ingår i The Journal of American Academy of Dermatology, s. 487-494, 2018

• DOI för CARD14-associated papulosquamous eruption: A spectrum including features of psoriasis and pityriasis rubra pilaris

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

Gudmundsson, Sanna; Wilbe, Maria; Ekvall, Sara; Ameur, Adam et al.

Ingår i Human Molecular Genetics, s. 1070-1077, 2017

• DOI för Revertant mosaicism repairs skin lesions in a patient with keratitis-ichthyosis-deafness syndrome by second-site mutations in connexin 26
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Proteins causing autosomal congenital recessive ichthyosis (ARCI) colocalize in differentiated primary keratinocytes and the interactions are altered in cells from patients with TGM1 mutations

Pettersson, M. H.; Zhang, Hanqian; Virtanen, Marie; Vahlquist, Anders et al.

Ingår i Journal of Investigative Dermatology, 2017

Ichthyosis patients with TGM1 mutations show aberrant transcriptomic expression

Zhang, Hanqian; Vahlquist, Anders; Virtanen, Marie; Törmä, Hans

Ingår i Journal of Investigative Dermatology, 2017

Whole-exome sequencing identifies novel autosomal recessive DSG1 mutations associated with mild SAM syndrome

Schlipf, N A; Vahlquist, Anders; Teigen, N; Virtanen, Marie et al.

Ingår i British Journal of Dermatology, s. 444-448, 2016

• DOI för Whole-exome sequencing identifies novel autosomal recessive DSG1 mutations associated with mild SAM syndrome

Spectrum of Autosomal Recessive Congenital Ichthyosis in Scandinavia: Clinical Characteristics and Novel and Recurrent Mutations in 132 Patients

Pigg, Maritta H.; Bygum, Anette; Ganemo, Agneta; Virtanen, Marie et al.

Ingår i Acta Dermato-Venereologica, s. 932-+, 2016

• DOI för Spectrum of Autosomal Recessive Congenital Ichthyosis in Scandinavia: Clinical Characteristics and Novel and Recurrent Mutations in 132 Patients

Quantitative analysis of immunofluorescence and in situ PLA staining using CellProfiler reveals impaired epidermal lipid processing pathway in ARCI patients with CYP4F22 mutations

Zhang, Hanqian; Virtanen, Marie; Weström, Simone; Bygum, A. et al.

Ingår i Journal of Investigative Dermatology, 2016

Reply to Nellen et al's Comment on the Classification of Clinical/genetic Variants of Mal de Meleda

Zhao, Linshu; Vahlquist, Anders; Virtanen, Marie; Wennerstrand, Lena et al.

Ingår i Acta Dermato-Venereologica, s. 1034-1035, 2015

• DOI för Reply to Nellen et al's Comment on the Classification of Clinical/genetic Variants of Mal de Meleda

A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by DSP mutations

Vahlquist, Anders; Virtanen, Marie; Hellström-Pigg, M.; Dragomir, Anca et al.

Ingår i Clincal and Experimental Dermatology, s. 30-34, 2014

• DOI för A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by DSP mutations

Ultrastructure of desmosomes as a diagnostic clue in a case of congenital skin fragility syndrome

Vahlquist, Anders; Virtanen, Marie; Hellström-Pigg, Maritta; Dragomir, Anca et al.

Ingår i Journal of Investigative Dermatology, s. 1172-1172, 2014

Ultrastructure of desmosomes as a diagnostic clue in a case of congenital skin fragility syndrome

Vahlquist, Anders; Virtanen, Marie; Hellström-Pigg, Maritta; Dragomir, Anca et al.

Ingår i Journal of Investigative Dermatology, s. 1176-1176, 2014

Palmoplantar Keratoderma of the Gamborg-Nielsen Type is Caused by Mutations in the SLURP1 Gene and Represents a Variant of Mal de Meleda

Zhao, Linshu; Vahlquist, Anders; Virtanen, Marie; Wennerstrand, Lena et al.

Ingår i Acta Dermato-Venereologica, s. 707-710, 2014

• DOI för Palmoplantar Keratoderma of the Gamborg-Nielsen Type is Caused by Mutations in the SLURP1 Gene and Represents a Variant of Mal de Meleda
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Detection of keratin filaments and aggregates in HeLa cells transfected with fluorescently tagged keratin 1 and 10 using a high content imaging assay

Törmä, Hans; Lindberg, Mikael; Li, Hao; Virtanen, Marie et al.

Ingår i Journal of Investigative Dermatology, 2013

Genotype-Phenotype Correlations Emerging from the Identification of Missense Mutations in MBTPS2

Bornholdt, Dorothea; Atkinson, T. Prescott; Bouadjar, Bakar; Catteau, Benoit et al.

Ingår i Human Mutation, s. 587-594, 2013

• DOI för Genotype-Phenotype Correlations Emerging from the Identification of Missense Mutations in MBTPS2

Generalized and Naevoid Epidermolytic Ichthyosis in Denmark: Clinical and Mutational Findings

Bygum, Anette; Virtanen, Marie; Brandrup, Flemming; Ganemo, Agneta et al.

Ingår i Acta Dermato-Venereologica, s. 309-313, 2013

• DOI för Generalized and Naevoid Epidermolytic Ichthyosis in Denmark: Clinical and Mutational Findings
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Immortalized keratinocytes derived from patients with epidermolytic ichthyosis reproduce the disease phenotype: A useful in vitro model for testing new treatments

Chamcheu, Jean Christopher; Pihl-Lundin, Inger; Eteti Mouyobo, Cedrique; Gester, Therese et al.

Ingår i British Journal of Dermatology, s. 263-272, 2011

• DOI för Immortalized keratinocytes derived from patients with epidermolytic ichthyosis reproduce the disease phenotype: A useful in vitro model for testing new treatments

Genotypic and clinical spectrum of self-improving collodion ichthyosis: ALOX12B, ALOXE3, and TGM1 mutations in Scandinavian patients

Vahlquist, Anders; Bygum, Anette; Gånemo, Agneta; Virtanen, Marie et al.

Ingår i Journal of Investigative Dermatology, s. 438-443, 2010

• DOI för Genotypic and clinical spectrum of self-improving collodion ichthyosis: ALOX12B, ALOXE3, and TGM1 mutations in Scandinavian patients

Immortalized keratinocytes from Epidermolytic Ichthyosis-patients reproduce the disease phenotype in vitro

Chamcheu, Jean Christopher; Virtanen, Marie; Moustakas, Aristidis; Navsaria, Harshad et al.

Ingår i Journal of Investigative Dermatology, 2010

Epidermolysis bullosa simplex due to KRT5 mutations: mutation-related differences in cellular fragility and the protective effects of trimethylamine N-oxide in cultured primary keratinocytes

Chamcheu, Jean Christopher; Virtanen, Marie; Navsaria, Harshad; Bowden, Paul E. et al.

Ingår i British Journal of Dermatology, s. 980-989, 2010

• DOI för Epidermolysis bullosa simplex due to KRT5 mutations: mutation-related differences in cellular fragility and the protective effects of trimethylamine N-oxide in cultured primary keratinocytes

Keratins 2 and 4/13 in reconstituted human skin are reciprocally regulated by retinoids binding to nuclear receptor RARα

Virtanen, Marie; Sirsjö, Allan; Vahlquist, Anders; Törmä, Hans

Ingår i Experimental dermatology, s. 674-681, 2010

• DOI för Keratins 2 and 4/13 in reconstituted human skin are reciprocally regulated by retinoids binding to nuclear receptor RARα

Characterization of immortalized human epidermolysis bullosa simplex (KRT5) cell lines: trimethylamine N-oxide protects the keratin cytoskeleton against disruptive stress condition

Chamcheu, Jean Christopher; Lorié, Elizabeth Pavez; Akgul, Baki; Bannbers, Elin et al.

Ingår i Journal of dermatological science (Amsterdam), s. 198-206, 2009

• DOI för Characterization of immortalized human epidermolysis bullosa simplex (KRT5) cell lines: trimethylamine N-oxide protects the keratin cytoskeleton against disruptive stress condition