Zobrazeno 1 - 10
of 111
pro vyhledávání: '"Maurice A.M. van Steensel"'
Autor:
Yanshan Liu, Siddharth Banka, Yingzhi Huang, Jonathan Hardman-Smart, Derek Pye, Antonio Torrelo, Glenda M. Beaman, Marcelo G. Kazanietz, Martin J. Baker, Carlo Ferrazzano, Chenfu Shi, Gisela Orozco, Stephen Eyre, Michel van Geel, Anette Bygum, Judith Fischer, Zosia Miedzybrodzka, Faris Abuzahra, Albert Rübben, Sara Cuvertino, Jamie M. Ellingford, Miriam J. Smith, D. Gareth Evans, Lizelotte J.M.T. Weppner-Parren, Maurice A.M. van Steensel, Iskander H. Chaudhary, D. Chas Mangham, John T. Lear, Ralf Paus, Jorge Frank, William G. Newman, Xue Zhang
Publikováno v:
British Journal of Dermatology, 187(6), 948-961. Wiley
Background Bazex–Dupré–Christol syndrome (BDCS; MIM301845) is a rare X-linked dominant genodermatosis characterized by follicular atrophoderma, congenital hypotrichosis and multiple basal cell carcinomas (BCCs). Previous studies have linked BDCS
Publikováno v:
Experimental Dermatology. 30:1471-1476
Cutibacterium acnes (also known as Propionibacterium acnes) has long been implicated in the pathogenesis of acne, inspiring both therapeutic and personal care approaches aiming to control the disease by controlling the bacterium. The purported associ
Autor:
Yanshan Liu, Siddharth Banka, Yingzhi Huang, Jonathan Hardman-Smart, Derek Pye, Antonio Torrelo, Glenda M. Beaman, Marcelo G. Kazanietz, Martin J Baker, Carlo Ferrazzano, Chenfu Shi, Gisela Orozco, Stephen Eyre, Michel van Geel, Anette Bygum, Judith Fischer, Zosia Miedzybrodzka, Faris Abuzahra, Albert Rübben, Sara Cuvertino, Jamie M. Ellingford, Miriam J. Smith, D. Gareth Evans, Lizelotte J.M.T Weppner-Parren, Maurice A.M. van Steensel, Iskander H. Chaudhary, D. Chas Mangham, John T. Lear, Ralf Paus, Jorge Frank, William G. Newman, Xue Zhang
BackgroundBazex-Dupré-Christol syndrome (BDCS; MIM301845) is a rare X-linked dominant genodermatosis characterized by follicular atrophoderma, congenital hypotrichosis and multiple basal cell carcinomas (BCCs). Previous studies have linked BDCS to a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f771ae001418a78ce8b7b617e700c3ed
https://doi.org/10.1101/2022.02.12.22270762
https://doi.org/10.1101/2022.02.12.22270762
Autor:
Marlon R. Schneider, Xinhong Lim, Ewan A. Langan, Maurice A.M. van Steensel, Klaus Göbel, Ralf Paus, R. Clayton, David M. Ansell, Mauro Picardo, Ivo J. H. M. de Vos
Publikováno v:
Biological Reviews. 95:592-624
The nervous system communicates with peripheral tissues through nerve fibres and the systemic release of hypothalamic and pituitary neurohormones. Communication between the nervous system and the largest human organ, skin, has traditionally received
Publikováno v:
Imaging Technologies and Transdermal Delivery in Skin Disorders
Autor:
Yee Kiat Heng, Helen Smith, Simon Biing Ming Lee, Aloysius Chow, Jing Wen Kong, Maurice A.M. van Steensel, Sok Huang Teo
Publikováno v:
Acta dermato-venereologica. 101(9)
Most teledermatology studies focus on patients' satisfaction; fewer focus on the experiences of healthcare professionals. This qualitative study explored healthcare professionals' perceptions of teledermatology used for linking public primary care cl
Publikováno v:
International journal of dermatologyReferences. 60(11)
Poikiloderma is a skin condition that combines atrophy, telangiectasia, and macular pigment changes (hypo- as well as hyperpigmentation). It is often mistaken for mottled pigmentation by general practitioners or nondermatology specialists. Poikiloder
Autor:
Julian L. Goggi, Thomas J. Carney, Nicole C. Syder, Jason Taslim, Ivo J. H. M. de Vos, Sheena Li Ming Ong, Arnette Shi Wei Wong, Maurice A.M. van Steensel
Publikováno v:
Biology Open
article-version (VoR) Version of Record
Biology Open, Vol 9, Iss 12 (2020)
Open Biology, 9(12):054270. COMPANY OF BIOLOGISTS LTD
article-version (VoR) Version of Record
Biology Open, Vol 9, Iss 12 (2020)
Open Biology, 9(12):054270. COMPANY OF BIOLOGISTS LTD
Frank-Ter Haar syndrome (FTHS, MIM #249420) is a rare skeletal dysplasia within the defective collagen remodelling spectrum (DECORS), which is characterised by craniofacial abnormalities, skeletal malformations and fibrotic soft tissues changes inclu
Comedonal acne is a common skin disease characterized by cystic dilation of the hair follicle junctional zone. While the molecular mechanisms of acne pathogenesis are not well understood, an emerging hypothesis holds that imbalances in key signalling
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0973b5ac70094985c35b80abccad52b4
https://doi.org/10.21203/rs.3.rs-84554/v1
https://doi.org/10.21203/rs.3.rs-84554/v1
Autor:
Michel van Geel, Maurice A.M. van Steensel, Jos L. V. Broers, Ahmad Albuloushi, Jennifer A. Easton, Barry J. Coull, Vincent Oji, Gladys H. M. R. Brouns, Miriam A.F. Kamps, Patricia Martin
Publikováno v:
Experimental Dermatology, 28(10), 1106-1113. Wiley
Erythrokeratodermia variabilis et progressiva (EKV-P) is caused by mutations in either the GJB3 (Cx31) or GJB4 genes (Cx30.3). We identified a rare GJB3 missense mutation, c.134G>A (p.G45E), in two unrelated patients and investigated its cellular cha