Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Almerinda Cafieri"'
Autor:
Renata Auricchio, Emmanuel Van Obberghen, Francesco Oriente, Gerolama Condorelli, Almerinda Cafieri, Claudia Miele, Francesco Beguinot, Matilde Caruso, Dominique Sawka-Verhelle, Véronique Calleja, Pietro Formisano
Publikováno v:
The Journal of biological chemistry
274 (1999): 3094–3102.
info:cnr-pdr/source/autori:Miele C, Caruso M, Calleja V, Auricchio R, Oriente F, Formisano P, Condorelli G, Cafieri A, Sawka-Verhelle D, Van Obberghen E, Beguinot F./titolo:Differential role of insulin receptor substrate (IRS)-1 and IRS-2 in L6 skeletal muscle cells expressing the Arg1152--> Gln insulin receptor./doi:/rivista:The Journal of biological chemistry (Print)/anno:1999/pagina_da:3094/pagina_a:3102/intervallo_pagine:3094–3102/volume:274
274 (1999): 3094–3102.
info:cnr-pdr/source/autori:Miele C, Caruso M, Calleja V, Auricchio R, Oriente F, Formisano P, Condorelli G, Cafieri A, Sawka-Verhelle D, Van Obberghen E, Beguinot F./titolo:Differential role of insulin receptor substrate (IRS)-1 and IRS-2 in L6 skeletal muscle cells expressing the Arg1152--> Gln insulin receptor./doi:/rivista:The Journal of biological chemistry (Print)/anno:1999/pagina_da:3094/pagina_a:3102/intervallo_pagine:3094–3102/volume:274
In L6 muscle cells expressing the Arg1152 --> Gln insulin receptor (Mut), basal tyrosine phosphorylation of insulin receptor substrate (IRS)-1 was increased by 35% compared with wild-type cells (WT). Upon exposure to insulin, IRS-1 phosphorylation in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0edbec0f3584f6a8c86576e44147325d
https://doi.org/10.1074/jbc.274.5.3094
https://doi.org/10.1074/jbc.274.5.3094
Autor:
Francesco Beguinot, Paola Andalò, Claudia Miele, Francesco Oriente, Pietro Formisano, Almerinda Cafieri, Alessandra Trencia, Gerolama Condorelli, Giovanni Vigliotta, Matilde Caruso
Publikováno v:
Oncogene (Basingstoke, Online) 18 (1999): 4409–4415.
info:cnr-pdr/source/autori:Condorelli G, Vigliotta G, Cafieri A, Trencia A, Andalò P, Oriente F, Miele C, Caruso M, Formisano P, Beguinot F./titolo:PED%2FPEA-15: an anti-apoptotic molecule that regulates FAS%2FTNFR1-induced apoptosis./doi:/rivista:Oncogene (Basingstoke, Online)/anno:1999/pagina_da:4409/pagina_a:4415/intervallo_pagine:4409–4415/volume:18
info:cnr-pdr/source/autori:Condorelli G, Vigliotta G, Cafieri A, Trencia A, Andalò P, Oriente F, Miele C, Caruso M, Formisano P, Beguinot F./titolo:PED%2FPEA-15: an anti-apoptotic molecule that regulates FAS%2FTNFR1-induced apoptosis./doi:/rivista:Oncogene (Basingstoke, Online)/anno:1999/pagina_da:4409/pagina_a:4415/intervallo_pagine:4409–4415/volume:18
PED/PEA-15 is a recently cloned 15 kDa protein possessing a death effector domain (DED). In MCF-7 and HeLa cells, a fivefold overexpression of PED/PEA-15 blocked FasL and TNFalpha apoptotic effects. This effect of PED overexpression was blocked by in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57a58d7960dd6354840ef574f2d58dee
http://www.cnr.it/prodotto/i/255375
http://www.cnr.it/prodotto/i/255375
Autor:
Matilde Caruso, Mario Felice Tecce, Laura Beguinot, Gerolama Condorelli, Almerinda Cafieri, Giovanni Vigliotta, Pietro Formisano, Francesco Andreozzi, Francesco Beguinot, Carlo Iavarone, Carlo G. Tocchetti
We have used differential display to identify genes whose expression is altered in type 2 diabetes thus contributing to its pathogenesis. One mRNA is overexpressed in fibroblasts from type 2 diabetics compared with non‐diabetic individuals, as well
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edc70ddf25b106fd5410a5253dedb0e6
https://europepmc.org/articles/PMC1170721/
https://europepmc.org/articles/PMC1170721/