x
Filter:
Filters applied
- Melanoma
- wild typeRemove wild type filter
- Open AccessRemove Open Access filter
Author
- Al-Olabi, Lara1
- Atherton, David J1
- Aubert, Hélène1
- Bagazgoitia, Lorea1
- Barbarot, Sébastien1
- Borgogna, Cinzia1
- Bourrat, Emmanuelle1
- Calati, Federica1
- Chiaverini, Christine1
- Chong, W Kling1
- Davies, Kelli-Jo1
- Duffourd, Yannis1
- Gariglio, Marisa1
- Glover, Mary1
- Groesser, Leopold1
- Hadj-Rabia, Smail1
- Hamm, Henning1
- Happle, Rudolf1
- Harries, Sarah1
- Kinsler, Veronica A1
- Lacour, Jean-Philippe1
- Lanfredini, Simone1
- Mushtaq, Imran1
- O'Shaughnessy, Ryan1
- Olivero, Carlotta1
Keyword
- WT2
- actinic keratosis1
- AK1
- cutaneous squamous cell carcinoma1
- deoxyribonucleic acid1
- DNA1
- epidermodysplasia verruciformis1
- EV1
- hair follicle1
- HF1
- HPV1
- human papillomavirus1
- IFE1
- interfollicular epidermis1
- keratinocyte stem cell1
- KSC1
- phakomatosis pigmentovascularis1
- PPV1
- SCC1
- Sturge-Weber syndrome1
- SWS1
- TA1
- transcriptional activation1
Melanoma
2 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 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.