Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Julie Deuquet"'
Autor:
Jérôme Bürgi, Béatrice Kunz, Laurence Abrami, Julie Deuquet, Alessandra Piersigilli, Sabine Scholl-Bürgi, Ekkehart Lausch, Sheila Unger, Andrea Superti-Furga, Paolo Bonaldo, F. Gisou van der Goot
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-10 (2017)
Hyaline fibromatosis syndrome (HFS) is a hereditary disease characterized by nodular cutaneous lesions and joint pain. Here Bürgiet al. show that CMG2/ANTXR2 regulates collagen VI abundance, with loss-of-function mutations promoting collagen VI accu
Externí odkaz:
https://doaj.org/article/4a3ba698348d47b29640ed06c5b22c1a
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0119864 (2015)
ANTXR 1 and 2, also known as TEM8 and CMG2, are two type I membrane proteins, which have been extensively studied for their role as anthrax toxin receptors, but with a still elusive physiological function. Here we have analyzed the importance of N-gl
Externí odkaz:
https://doaj.org/article/248dd73085b544ce91d1cea798f34b56
Autor:
Sheila Unger, F. Gisou van der Goot, Ekkehart Lausch, Béatrice Kunz, Paolo Bonaldo, Sabine Scholl-Bürgi, Andrea Superti-Furga, Jérôme Bürgi, Julie Deuquet, Alessandra Piersigilli, Laurence Abrami
Publikováno v:
Nature communications, vol. 8, pp. 15861
Nature Communications, Vol 8, Iss 1, Pp 1-10 (2017)
Nature Communications
Nature Communications, Vol 8, Iss 1, Pp 1-10 (2017)
Nature Communications
Loss-of-function mutations in capillary morphogenesis gene 2 (CMG2/ANTXR2), a transmembrane surface protein, cause hyaline fibromatosis syndrome (HFS), a severe genetic disorder that is characterized by large subcutaneous nodules, gingival hypertroph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81e83e8ff5da1b92fa04294c960e80bd
https://serval.unil.ch/resource/serval:BIB_D06F5FC5430F.P002/REF.pdf
https://serval.unil.ch/resource/serval:BIB_D06F5FC5430F.P002/REF.pdf
Publikováno v:
The EMBO Journal. 31:3-13
Capillary morphogenesis gene 2 (CMG2) is a type I membrane protein involved in the homeostasis of the extracellular matrix. While it shares interesting similarities with integrins, its exact molecular role is unknown. The interest and knowledge about
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28d98ef779d7b8a46bc99597b5162754
https://doi.org/10.1038/emboj.2011.442
https://doi.org/10.1038/emboj.2011.442
Autor:
Suzanne Salvi, Luisa Bonafé, Dariusz Rokicki, Asvin K. K. Lakkaraju, Nicolas Guex, Françoise Gisou van der Goot, Laurence Abrami, John A. Martignetti, Julie Deuquet, Maria Celeste M. Ramirez, Andrea Superti-Furga, Ekkehart Lausch
Publikováno v:
Embo Molecular Medicine, vol. 3, no. 4, pp. 208-221
EMBO Molecular Medicine
EMBO molecular medicine
EMBO Molecular Medicine
EMBO molecular medicine
Hyaline Fibromatosis Syndrome (HIS) is a human genetic disease caused by mutations in the anthrax toxin receptor 2 (or cmg2) gene, which encodes a membrane protein thought to be involved in the homeostasis of the extracellular matrix. Little is known
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f3c197ed9d196b3cd09bec11567db37
https://doi.org/10.1002/emmm.201100124
https://doi.org/10.1002/emmm.201100124
Autor:
Analisa DiFeo, F. Gisou van der Goot, John A. Martignetti, Maria Celeste M. Ramirez, Julie Deuquet, Laurence Abrami
Publikováno v:
Human mutation. 30(4)
Systemic hyalinosis is an autosomal recessive disease that encompasses two allelic syndromes, infantile systemic hyalinosis (ISH) and juvenile hyaline fibromatosis (JHF), which are caused by mutations in the CMG2 gene. Here we have analyzed the cellu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8d453163cebdde345ac535f38a63026
https://pubmed.ncbi.nlm.nih.gov/19191226
https://pubmed.ncbi.nlm.nih.gov/19191226
Autor:
Anna Bafico, Julie Deuquet, Béatrice Kunz, F. Gisou van der Goot, Gary Davidson, Laurence Abrami
Publikováno v:
Cellular microbiology. 10(12)
To exert its activity, anthrax toxin must be endocytosed and its enzymatic toxic subunits delivered to the cytoplasm. It has been proposed that, in addition to the anthrax toxin receptors (ATRs), lipoprotein-receptor-related protein 6 (LRP6), known f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0001b04aa81b568243160253a2ba6ff5
https://pubmed.ncbi.nlm.nih.gov/18717822
https://pubmed.ncbi.nlm.nih.gov/18717822
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 3, p e0119864 (2015)
PLoS ONE, Vol 10, Iss 3, p e0119864 (2015)
ANTXR 1 and 2, also known as TEM8 and CMG2, are two type I membrane proteins, which have been extensively studied for their role as anthrax toxin receptors, but with a still elusive physiological function. Here we have analyzed the importance of N-gl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f29ed87b10153d286775125015a9e89
https://doi.org/10.1371/journal.pone.0119864
https://doi.org/10.1371/journal.pone.0119864