Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Matilde Caruso"'
Autor:
Paul R. J. Ames, Alessia Arcaro, Matilde Caruso, Maria Graf, Vincenzo Marottoli, Fabrizio Gentile
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 23, p 14641 (2022)
We evaluated the relevance of plasma homocysteine (HC) and the TT genotype of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism (rs1801133) in sickle cell disease (SCD) and associated vaso-occlusive crisis (VOC) and ischemic stroke (
Externí odkaz:
https://doaj.org/article/137a237b870242b8a2f53dfb43197df7
Autor:
Mira Merashli MD, Alessia Arcaro MSc, Maria Graf MD, Matilde Caruso MD, Paul R. J. Ames MD, MSc, PhD, Fabrizio Gentile MD, PhD
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 27 (2021)
The relationship between antiphospholipid antibodies (aPL) and sickle cell disease (SCD) has never been systematically addressed. Our aim was to evaluate potential links between SCD and aPL in all age groups. EMBASE/PubMed was screened from inception
Externí odkaz:
https://doaj.org/article/c7e8f28ee6b5417abdf1a778d3d6dfec
Autor:
Giovanna D'Andrea, Matilde Caruso, Luigi Iannaccone, Paul R.J. Ames, Fabrizio Gentile, Maurizio Margaglione, Vincenzo Marottoli
The aim of the study was to compare age at first venous thromboembolism (VTE), plasma homocysteine and activated partial thromboplastin time ratio (aPTTr) amongst unprovoked VTE patients with the methylentetrahydrofolate reductase (MTHFR) C667T genot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f127edbf3d30d4f2e19b41df91fefd07
http://hdl.handle.net/11695/100426
http://hdl.handle.net/11695/100426
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis
Clinical and Applied Thrombosis/Hemostasis, Vol 27 (2021)
Clinical and Applied Thrombosis/Hemostasis, Vol 27 (2021)
The relationship between antiphospholipid antibodies (aPL) and sickle cell disease (SCD) has never been systematically addressed. Our aim was to evaluate potential links between SCD and aPL in all age groups. EMBASE/PubMed was screened from inception
Autor:
Giovanni Vigliotta, Matilde Caruso, Claudia Miele, Francesco Oriente, Maria Alessandra Maitan, Gerolama Condorelli, Francesco Beguinot, Alessandra Trencia, Stefania Santopietro, Pietro Formisano
Publikováno v:
Diabetes
On the basis of the recommendation of the American Diabetes Association’s Panel on Ethical Scientific Programs (ESP), the American Diabetes Association, the publisher of Diabetes, is issuing this expression of concern to alert readers to questions
Autor:
Francesco Beguinot, Francesca Fiory, Matilde Caruso, Francesco Oriente, Domenico Accili, Brunella Capaldo, A Oliva, Gerolama Condorelli, Pietro Formisano, Gabriele Riccardi, Claudia Miele
Publikováno v:
Diabetes
On the basis of the recommendation of the American Diabetes Association’s Panel on Ethical Scientific Programs (ESP), the American Diabetes Association, the publisher of Diabetes, is issuing this expression of concern to alert readers to questions
Autor:
Francesco Oriente, A Oliva, Brunella Capaldo, Gerolama Condorelli, Domenico Accili, Francesco Beguinot, Claudia Miele, Pietro Formisano, Matilde Caruso, Francesca Fiory, Gabriele Riccardi
Publikováno v:
Diabetes (N.Y.N.Y.) 49 (2000): 1194–1202.
info:cnr-pdr/source/autori:Caruso M, Miele C, Oliva A, Condorelli G, Oriente F, Riccardi G, Capaldo B, Fiory F, Accili D, Formisano P, Beguinot F./titolo:The IR1152 mutant insulin receptor selectively impairs insulin action in skeletal muscle but not in liver./doi:/rivista:Diabetes (N.Y.N.Y.)/anno:2000/pagina_da:1194/pagina_a:1202/intervallo_pagine:1194–1202/volume:49
Scopus-Elsevier
info:cnr-pdr/source/autori:Caruso M, Miele C, Oliva A, Condorelli G, Oriente F, Riccardi G, Capaldo B, Fiory F, Accili D, Formisano P, Beguinot F./titolo:The IR1152 mutant insulin receptor selectively impairs insulin action in skeletal muscle but not in liver./doi:/rivista:Diabetes (N.Y.N.Y.)/anno:2000/pagina_da:1194/pagina_a:1202/intervallo_pagine:1194–1202/volume:49
Scopus-Elsevier
In patients harboring the IR1152 mutant insulin receptor, hepatic glucose production was normally suppressed by insulin. Hepatocytes without the insulin receptor gene and expressing IR1152 (Hep(MUT)) also showed normal insulin suppression of glucose
Autor:
Francesco Oriente, Pietro Formisano, Giuseppe Bifulco, Claudia Miele, Gerolama Condorelli, Francesco Andreozzi, Matilde Caruso, Alessandra Maitan, Francesco Beguinot
Publikováno v:
The Journal of biological chemistry
274 (1999): 28637–28644.
info:cnr-pdr/source/autori:Caruso M, Miele C, Oriente F, Maitan A, Bifulco G, Andreozzi F, Condorelli G, Formisano P, Beguinot F./titolo:In L6 skeletal muscle cells, glucose induces cytosolic translocation of protein kinase C-alpha and trans-activates the insulin receptor kinase./doi:/rivista:The Journal of biological chemistry (Print)/anno:1999/pagina_da:28637/pagina_a:28644/intervallo_pagine:28637–28644/volume:274
274 (1999): 28637–28644.
info:cnr-pdr/source/autori:Caruso M, Miele C, Oriente F, Maitan A, Bifulco G, Andreozzi F, Condorelli G, Formisano P, Beguinot F./titolo:In L6 skeletal muscle cells, glucose induces cytosolic translocation of protein kinase C-alpha and trans-activates the insulin receptor kinase./doi:/rivista:The Journal of biological chemistry (Print)/anno:1999/pagina_da:28637/pagina_a:28644/intervallo_pagine:28637–28644/volume:274
In L6 skeletal muscle cells expressing human insulin receptors (L6(hIR)), exposure to 25 mM glucose for 3 min induced a rapid 3-fold increase in GLUT1 and GLUT4 membrane translocation and glucose uptake. The high glucose concentration also activated
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
Autor:
Francesco Oriente, Carlo G. Tocchetti, Matilde Caruso, Claudia Miele, Gabriele Riccardi, Gerolama Condorelli, Francesco Andreozzi, Francesco Beguinot, Pietro Formisano
Publikováno v:
Diabetologia (Berl.) 40 (1997): 421–429.
info:cnr-pdr/source/autori:Miele C, Formisano P, Condorelli G, Caruso M, Oriente F, Andreozzi F, Tocchetti CG, Riccardi G, Beguinot F./titolo:Abnormal glucose transport and GLUT1 cell-surface content in fibroblasts and skeletal muscle from NIDDM and obese subjects./doi:/rivista:Diabetologia (Berl.)/anno:1997/pagina_da:421/pagina_a:429/intervallo_pagine:421–429/volume:40
info:cnr-pdr/source/autori:Miele C, Formisano P, Condorelli G, Caruso M, Oriente F, Andreozzi F, Tocchetti CG, Riccardi G, Beguinot F./titolo:Abnormal glucose transport and GLUT1 cell-surface content in fibroblasts and skeletal muscle from NIDDM and obese subjects./doi:/rivista:Diabetologia (Berl.)/anno:1997/pagina_da:421/pagina_a:429/intervallo_pagine:421–429/volume:40
Glucose transport and GLUT1 expression were studied in fibroblasts from 7 lean and 5 obese non-insulin-dependent diabetic (NIDDM) subjects with at least 2 NIDDM first-degree relatives and from 12 lean and 5 obese non-diabetic subjects with no family