Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Muriel Cario‐Andre"'
Autor:
Yvon Gauthier, Sebastien Lepreux, Muriel Cario‐Andre, Jérome Rambert, Adrien Dakdaki, Marie‐Edith Lafon, Redouane Abouqal, Laila Benzekri
Publikováno v:
Pigment Cell & Melanoma Research. 36:78-85
Segmental vitiligo (SV) is a unilateral subtype of vitiligo which is clinically characterized by a cutaneous depigmentation and histologically by a melanocyte loss from the epidermis and hair follicle reservoirs. To date, its pathogenesis remains a m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::396043bf7749af0ce0c4ce313ba95d34
https://doi.org/10.1111/pcmr.13064
https://doi.org/10.1111/pcmr.13064
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
BackgroundSegmental vitiligo (SV) is a subset of vitiligo typically characterized by its unilateral distribution. The pathogenesis of SV remains unclear, and until now the two main patterns proposed for SV have lacked biological support. This calls f
Externí odkaz:
https://doaj.org/article/3328b28522944c528df8c5f442093550
Autor:
Muriel, Cario-Andre
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 1489
During a long time, immunofluorescence has been neglected to benefit of molecular biology especially genetics, transcriptomics, and proteomics analyses. These techniques give good results on cell culture but for organs that are made of numerous cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8f2ea7b2f6bf16cb67dd62462ed39718
https://pubmed.ncbi.nlm.nih.gov/27734366
https://pubmed.ncbi.nlm.nih.gov/27734366
Autor:
Muriel, Cario-Andre, Sebastien, Lepreux, Catherine, Pain, Carine, Nizard, Emmanuelle, Noblesse, Alain, Taïeb
Publikováno v:
Journal of cutaneous pathology. 31(6)
Senile lentigo (SL) is a common component of photoaged skin. It is characterized by hyperpigmented macules which affect chronically irradiated skin mostly after 50 years of age. This study was undertaken to assess the basic morphology of SL on dorsum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dc92c16d4011df03b98af605f67395df
https://pubmed.ncbi.nlm.nih.gov/15186432
https://pubmed.ncbi.nlm.nih.gov/15186432
Autor:
Hamid Reza Rezvani, Frédéric Mazurier, Fanny Morice-Picard, Thomas Jouary, Muriel Cario-André, Cécile Ged, Hubert de Verneuil, Alain Taïeb
Publikováno v:
Dermatologica Sinica, Vol 28, Iss 3, Pp 93-101 (2010)
Xeroderma pigmentosum (XP) type C is a rare autosomal recessive disorder that occurs because of inactivation of the xeroderma pigmentosum group C (XPC) protein, which is an important DNA damage recognition protein involved in DNA nucleotide excision
Externí odkaz:
https://doaj.org/article/eeadbef10f9046348190b25cc0ff6250