Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Elena, Chiticariu"'
Autor:
Hyun-Sook Park, Eirini Papanastasi, Gabriela Blanchard, Elena Chiticariu, Daniel Bachmann, Markus Plomann, Fanny Morice-Picard, Pierre Vabres, Asma Smahi, Marcel Huber, Christine Pich, Daniel Hohl
Publikováno v:
Communications Biology, Vol 4, Iss 1, Pp 1-13 (2021)
Park et al. characterise the interactome, localisation and function of Actin-Related Protein-Testis1 protein (ARP-T1), encoded by the ACTRT1 gene, associated with inherited basal cell cancer. They find that ARP-T1 is localised to the primary cilia ba
Externí odkaz:
https://doaj.org/article/a0f02e7c75a741a59d63e638f2446851
Autor:
Sabine Giroud, Elena Chiticariu-Durr
Publikováno v:
Revue Médicale Suisse. 16:624-628
Autor:
Elena Chiticariu, Daniel Hohl
Publikováno v:
Skin and the Heart ISBN: 9783030547783
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::210d0989cd18c82d5d61a40734fe014e
https://doi.org/10.1007/978-3-030-54779-0_6
https://doi.org/10.1007/978-3-030-54779-0_6
Autor:
Christine Pich, Asma Smahi, Daniel Hohl, Elena Chiticariu, Hyun-Sook Park, Gabriela Blanchard, Marcel Huber, Markus Plomann, Fanny Morice-Picard, Eirini Papanastasi, Pierre Vabres, Daniel Bachmann
Publikováno v:
Communications Biology
Communications Biology, Vol 4, Iss 1, Pp 1-13 (2021)
Communications biology, vol. 4, no. 1, pp. 544
Communications Biology, Vol 4, Iss 1, Pp 1-13 (2021)
Communications biology, vol. 4, no. 1, pp. 544
Actin-Related Protein-Testis1 (ARP-T1)/ACTRT1 gene mutations cause the Bazex-Dupré-Christol Syndrome (BDCS) characterized by follicular atrophoderma, hypotrichosis, and basal cell cancer. Here, we report an ARP-T1 interactome (PXD016557) that includ
Autor:
Pierre Vabres, Asma Smahi, Huyn-Sook Park, Marcel Huber, Fanny Morice-Picard, Daniel Bachmann, Daniel Hohl, Markus Plomann, Gabriela Blanchard, Eirini Papanastasi, Elena Chiticariu, Christine Pich
Actin-Related Protein-Testis1 (ARP-T1)/ ACTRT1 gene mutations cause the Bazex-Dupré-Christol Syndrome (BDCS) characterized by follicular atrophoderma, hypotrichosis and basal cell cancer. Here, we report an ARP-T1 interactome (PXD016557) involved in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e42be561c1c8c0994f0fdf4e47b01a61
https://doi.org/10.1101/2019.12.16.877498
https://doi.org/10.1101/2019.12.16.877498
Autor:
Elena Chiticariu, Daniel Hohl
Publikováno v:
The Journal of investigative dermatology. 140(6)
Netherton syndrome (NS) is a rare skin disorder involving the skin, hair, and immune system. Pathological manifestations are due to unopposed kallikrein peptidase activity because of a SPINK5 gene deficiency. In their article, Gouin et al. explore th
Publikováno v:
Nasza Dermatologia Online, Vol 4, Iss 4, Pp 462-462 (2013)
Externí odkaz:
https://doaj.org/article/a1179c0f2692456c9605e57910c2ce6e
Publikováno v:
Experimental Dermatology
Keratoacanthoma (KA) are common but exceptional benign tumors, often appearing on sun-exposed areas of light skinned people and showing spontaneous resolution. The goal of this study was to review existing literature, to point out the etiological com
Publikováno v:
Journal of Investigative Dermatology. 140:1662-1665.e1
Publikováno v:
Journal of Investigative Dermatology. 140:66-74.e4
CYLD is a deubiquitylase with tumor suppressor functions, first identified in patients with familial cylindromatosis. Despite many molecular mechanisms in which a function of CYLD was reported, affected patients only develop skin appendage tumors, an