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- Al-Olabi, Lara1
- Asamaowei, Inemo E1
- Atherton, David J1
- Aubert, Hélène1
- Bagazgoitia, Lorea1
- Barbarot, Sébastien1
- Borgogna, Cinzia1
- Botchkarev, Vladimir A1
- Bourrat, Emmanuelle1
- Calati, Federica1
- Chiaverini, Christine1
- Chong, W Kling1
- Davies, Kelli-Jo1
- Duffourd, Yannis1
- Fessing, Michael Y1
- Gariglio, Marisa1
- Glover, Mary1
- Groesser, Leopold1
- Hadj-Rabia, Smail1
- Hamm, Henning1
- Happle, Rudolf1
- Harries, Sarah1
- Karakesisoglou, Iakowos1
- Kinsler, Veronica A1
- Lacour, Jean-Philippe1
Melanoma
3 Results
- Original Article Tumor BiologyOpen Access
HPV8 Field Cancerization in a Transgenic Mouse Model Is due to Lrig1+ Keratinocyte Stem Cell Expansion
Journal of Investigative DermatologyVol. 137Issue 10p2208–2216Published online: June 5, 2017- Simone Lanfredini
- Carlotta Olivero
- Cinzia Borgogna
- Federica Calati
- Kathryn Powell
- Kelli-Jo Davies
- and others
Cited in Scopus: 22β-Human papillomaviruses (HPVs) cause near ubiquitous latent skin infection within long-lived hair follicle (HF) keratinocyte stem cells. In patients with epidermodysplasia verruciformis, β-HPV viral replication is associated with skin keratosis and cutaneous squamous cell carcinoma. To determine the role of HF keratinocyte stem cells in β-HPV-induced skin carcinogenesis, we utilized a transgenic mouse model in which the keratin 14 promoter drives expression of the entire HPV8 early region (HPV8tg). - Original Article Keratinocytes/EpidermisOpen Access
p63 Transcription Factor Regulates Nuclear Shape and Expression of Nuclear Envelope-Associated Genes in Epidermal Keratinocytes
Journal of Investigative DermatologyVol. 137Issue 10p2157–2167Published online: June 5, 2017- Valentina Rapisarda
- Igor Malashchuk
- Inemo E. Asamaowei
- Krzysztof Poterlowicz
- Michael Y. Fessing
- Andrey A. Sharov
- and others
Cited in Scopus: 18The maintenance of a proper nuclear architecture and three-dimensional organization of the genes, enhancer elements, and transcription machinery plays an essential role in tissue development and regeneration. Here we show that in the developing skin, epidermal progenitor cells of mice lacking p63 transcription factor display alterations in the nuclear shape accompanied by a marked decrease in expression of several nuclear envelope-associated components (Lamin B1, Lamin A/C, Sun1, Nesprin-3, Plectin) compared with controls. - Original Article GeneticsOpen Access
Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis
Journal of Investigative DermatologyVol. 136Issue 4p770–778Published online: January 14, 2016- Anna C. Thomas
- Zhiqiang Zeng
- Jean-Baptiste Rivière
- Ryan O’Shaughnessy
- Lara Al-Olabi
- Judith St.-Onge
- and others
Cited in Scopus: 114Common birthmarks can be an indicator of underlying genetic disease but are often overlooked. Mongolian blue spots (dermal melanocytosis) are usually localized and transient, but they can be extensive, permanent, and associated with extracutaneous abnormalities. Co-occurrence with vascular birthmarks defines a subtype of phakomatosis pigmentovascularis, a group of syndromes associated with neurovascular, ophthalmological, overgrowth, and malignant complications. Here, we discover that extensive dermal melanocytosis and phakomatosis pigmentovascularis are associated with activating mutations in GNA11 and GNAQ, genes that encode Gα subunits of heterotrimeric G proteins.