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.

Part of Acta Dermato-Venereologica, 2023

• DOI for Establishment and Utility of SwedAD: A Nationwide Swedish Registry for Patients with Atopic Dermatitis Receiving Systemic Pharmacotherapy
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Palmoplantar keratoderma and digital clubbing in 2 sisters with hypertrophic osteoarthropathy

Eriksson, Daniel; Gyll, David; Virtanen, Marie; Dahl, Niklas et al.

Part of Jaad Case Reports, p. 133-136, 2023

• DOI for Palmoplantar keratoderma and digital clubbing in 2 sisters with hypertrophic osteoarthropathy
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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.

Part of Differentiation, p. 19-27, 2021

• DOI for 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.

Part of Experimental dermatology, p. 1164-1171, 2019

• DOI for 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.

Part of Experimental dermatology, p. 196-199, 2018

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

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.

Part of Acta Dermato-Venereologica, 2023

• DOI for Establishment and Utility of SwedAD: A Nationwide Swedish Registry for Patients with Atopic Dermatitis Receiving Systemic Pharmacotherapy
• Download full text (pdf) of Establishment and Utility of SwedAD: A Nationwide Swedish Registry for Patients with Atopic Dermatitis Receiving Systemic Pharmacotherapy

Palmoplantar keratoderma and digital clubbing in 2 sisters with hypertrophic osteoarthropathy

Eriksson, Daniel; Gyll, David; Virtanen, Marie; Dahl, Niklas et al.

Part of Jaad Case Reports, p. 133-136, 2023

• DOI for Palmoplantar keratoderma and digital clubbing in 2 sisters with hypertrophic osteoarthropathy
• Download full text (pdf) of Palmoplantar keratoderma and digital clubbing in 2 sisters with hypertrophic osteoarthropathy

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.

Part of Differentiation, p. 19-27, 2021

• DOI for 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.

Part of Experimental dermatology, p. 1164-1171, 2019

• DOI for Patients with congenital ichthyosis and TGM1 mutations overexpress other ARCI genes in the skin: Part of a barrier repair response?
• Download full text (pdf) of 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.

Part of Experimental dermatology, p. 196-199, 2018

• DOI for 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.

Part of The Journal of American Academy of Dermatology, p. 487-494, 2018

• DOI for 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.

Part of Human Molecular Genetics, p. 1070-1077, 2017

• DOI for 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.

Part of Journal of Investigative Dermatology, 2017

Ichthyosis patients with TGM1 mutations show aberrant transcriptomic expression

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

Part of 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.

Part of British Journal of Dermatology, p. 444-448, 2016

• DOI for 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.

Part of Acta Dermato-Venereologica, p. 932-+, 2016

• DOI for 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.

Part of 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.

Part of Acta Dermato-Venereologica, p. 1034-1035, 2015

• DOI for 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.

Part of Clincal and Experimental Dermatology, p. 30-34, 2014

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

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.

Part of Acta Dermato-Venereologica, p. 707-710, 2014

• DOI for 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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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.

Part of Journal of Investigative Dermatology, p. 1176-1176, 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.

Part of Journal of Investigative Dermatology, p. 1172-1172, 2014

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.

Part of 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.

Part of Human Mutation, p. 587-594, 2013

• DOI for 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.

Part of Acta Dermato-Venereologica, p. 309-313, 2013

• DOI for 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.

Part of British Journal of Dermatology, p. 263-272, 2011

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

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

Part of Experimental dermatology, p. 674-681, 2010

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

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.

Part of Journal of Investigative Dermatology, p. 438-443, 2010

• DOI for 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.

Part of 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.

Part of British Journal of Dermatology, p. 980-989, 2010

• DOI for 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

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.

Part of Journal of dermatological science (Amsterdam), p. 198-206, 2009

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