Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Arnaud, Galichet"'
Autor:
William V.J. Hariton, Katja Schulze, Siavash Rahimi, Taravat Shojaeian, Laurence Feldmeyer, Roman Schwob, Andrew M. Overmiller, Beyza S. Sayar, Luca Borradori, Mỹ G. Mahoney, Arnaud Galichet, Eliane J. Müller
Publikováno v:
iScience, Vol 26, Iss 12, Pp 108568- (2023)
Summary: Stem cells (SCs) are critical to maintain tissue homeostasis. However, it is currently not known whether signaling through cell junctions protects quiescent epithelial SC reservoirs from depletion during disease-inflicted damage. Using the a
Externí odkaz:
https://doaj.org/article/f8c4ec496e3c410ab9492b5aed9727df
Autor:
Dominik P. Waluk, Gila Zur, Ronnie Kaufmann, Monika M. Welle, Vidhya Jagannathan, Cord Drögemüller, Eliane J. Müller, Tosso Leeb, Arnaud Galichet
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 6, Iss 9, Pp 2949-2954 (2016)
X-linked hypohidrotic ectodermal dysplasia (XLHED) caused by variants in the EDA gene represents the most common ectodermal dysplasia in humans. We investigated three male mixed-breed dogs with an ectodermal dysplasia phenotype characterized by marke
Externí odkaz:
https://doaj.org/article/b680d225afd34ca4a3b9d353afdfe54c
Autor:
Leonardo Murgiano, Dominik P. Waluk, Rachel Towers, Natalie Wiedemar, Joëlle Dietrich, Vidhya Jagannathan, Michaela Drögemüller, Pierre Balmer, Tom Druet, Arnaud Galichet, M. Cecilia Penedo, Eliane J. Müller, Petra Roosje, Monika M. Welle, Tosso Leeb
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 6, Iss 9, Pp 2963-2970 (2016)
We investigated a family of horses exhibiting irregular vertical stripes in their hair coat texture along the neck, back, hindquarters, and upper legs. This phenotype is termed “brindle” by horse breeders. We propose the term “brindle 1 (BR1)
Externí odkaz:
https://doaj.org/article/7e53b415bac24ae1b0b9f45106fe7f69
Autor:
Anina Bauer, Dominik P Waluk, Arnaud Galichet, Katrin Timm, Vidhya Jagannathan, Beyza S Sayar, Dominique J Wiener, Elisabeth Dietschi, Eliane J Müller, Petra Roosje, Monika M Welle, Tosso Leeb
Publikováno v:
PLoS Genetics, Vol 13, Iss 3, p e1006651 (2017)
Ichthyoses are a heterogeneous group of inherited cornification disorders characterized by generalized dry skin, scaling and/or hyperkeratosis. Ichthyosis vulgaris is the most common form of ichthyosis in humans and caused by genetic variants in the
Externí odkaz:
https://doaj.org/article/7a2c6c4a24fc4a2181d596809ad75188
Autor:
Pierre Balmer, Anina Bauer, Shashikant Pujar, Kelly M McGarvey, Monika Welle, Arnaud Galichet, Eliane J Müller, Kim D Pruitt, Tosso Leeb, Vidhya Jagannathan
Publikováno v:
PLoS ONE, Vol 12, Iss 8, p e0180359 (2017)
Keratins represent a large protein family with essential structural and functional roles in epithelial cells of skin, hair follicles, and other organs. During evolution the genes encoding keratins have undergone multiple rounds of duplication and hum
Externí odkaz:
https://doaj.org/article/fbd6ad78bc464dc290ccb474f76ff090
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0119809 (2015)
The majority of pemphigus vulgaris (PV) patients suffer from a live-threatening loss of intercellular adhesion between keratinocytes (acantholysis). The disease is caused by auto-antibodies that bind to desmosomal cadherins desmoglein (Dsg) 3 or Dsg3
Externí odkaz:
https://doaj.org/article/1947dbc44d254bf582948d4ce2ad676d
Autor:
Pierre Balmer, Petra Roosje, William V.J. Hariton, Eliane J. Müller, Beyza S. Sayar, Vidhya Jagannathan, Arnaud Galichet, Tosso Leeb
Publikováno v:
The Journal of Cell Biology
Balmer, Pierre; Hariton, William V. J.; Sayar, Beyza; Jagannathan, Vidhya; Galichet, Arnaud; Leeb, Tosso; Roosje, Petra; Müller, Eliane J. (2021). SUV39H2 epigenetic silencing controls fate conversion of epidermal stem and progenitor cells. Journal of cell biology, 220(4) Rockefeller Institute Press 10.1083/jcb.201908178
Balmer, Pierre; Hariton, William V. J.; Sayar, Beyza; Jagannathan, Vidhya; Galichet, Arnaud; Leeb, Tosso; Roosje, Petra; Müller, Eliane J. (2021). SUV39H2 epigenetic silencing controls fate conversion of epidermal stem and progenitor cells. Journal of cell biology, 220(4) Rockefeller Institute Press 10.1083/jcb.201908178
Balmer et al. identify a new player in the complex network of epigenetic modifiers safeguarding stem and progenitor cell pools in stratified epithelia. SUV39H2, an enzyme introducing repressive methyl marks on chromatin, governs the master switch of
Autor:
Vidhya Jagannathan, Jeanette Bannoehr, Philippe Plattet, Regula Hauswirth, Cord Drögemüller, Michaela Drögemüller, Dominique J Wiener, Marcus Doherr, Marta Owczarek-Lipska, Arnaud Galichet, Monika M Welle, Katarina Tengvall, Kerstin Bergvall, Hannes Lohi, Silvia Rüfenacht, Monika Linek, Manon Paradis, Eliane J Müller, Petra Roosje, Tosso Leeb
Publikováno v:
PLoS Genetics, Vol 9, Iss 10, p e1003848 (2013)
Hereditary nasal parakeratosis (HNPK), an inherited monogenic autosomal recessive skin disorder, leads to crusts and fissures on the nasal planum of Labrador Retrievers. We performed a genome-wide association study (GWAS) using 13 HNPK cases and 23 c
Externí odkaz:
https://doaj.org/article/3d8a63b89ffb4466b2f4cfe3cd64012b
Autor:
Beyza S. Sayar, Pierre Balmer, Eliane J. Müller, William V.J. Hariton, Petra Roosje, Arnaud Galichet, Dominique J Wiener, Auxanne K Fellay
Publikováno v:
Experimental Dermatology. 28:350-354
FAM83G/Fam83g genetic variants have been described in dogs, mice and recently also in humans. They are associated with palmoplantar keratoderma and altered hair or coat phenotype, reported as wooly phenotype in mice. FAM83G/Fam83g is an unexplored ef
Autor:
My G. Mahoney, Eliane J. Müller, Andrew M. Overmiller, Luca Borradori, Bs. Sayar, W.V. Hariton, Arnaud Galichet, Katja Schulze
Publikováno v:
Journal of Investigative Dermatology. 141:S204