Výsledky vyhledávání - "Maria E Pueyo"

Transforming Growth Factor-β1 Production Is Correlated With Genetically Determined ACE Expression in Congenic Rats

Autor: M. Challah, Maria E. Pueyo, Michel Marre, Marie-Paule Jacob, Liliane Louedec, Roger Gaertner, Monique Philippe, Jean-Baptiste Michel, Dominique Gauguier

Publikováno v: Diabetes. 53:1111-1118

Genetic background appears to modulate the development of diabetic vascular complications. In particular, polymorphisms in the ACE gene have been associated with diabetic nephropathy and, in some studies, macrovascular complications. However, the lin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::245e3f271dddac848dff36e3ea895f0f
https://doi.org/10.2337/diabetes.53.4.1111

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The bioavailability and postprandial utilisation of sweet lupin (Lupinus albus)-flour protein is similar to that of purified soyabean protein in human subjects: a study using intrinsically 15N-labelled proteins

Autor: Sylvain Mahé, Maria E Pueyo, François Mariotti, Daniel Tomé

Publikováno v: British Journal of Nutrition. 87:315-323

Sweet lupin (Lupinus albus ), a protein-rich legume devoid of anti-nutritional factors, is considered to have a high potential for protein nutrition in man. Results concerning the nutritional value of lupin protein are, however, conflicting in animal

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a19e41cad8e33cee52ae1db2628f1e73
https://doi.org/10.1079/bjnbjn2002526

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Autor: François Mariotti, Maria E. Pueyo, Daniel Tomé, Sylvain Mahé

Publikováno v: British Journal of Nutrition. 87:315-323

Sweet lupin (Lupinus albus), a protein-rich legume devoid of anti-nutritional factors, is considered to have a high potential for protein nutrition in man. Results concerning the nutritional value of lupin protein are, however, conflicting in animals

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::783f4cc2bd9c44de4c630ceee3682b55
https://doi.org/10.1079/bjn2002526

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Endothelium-independent conversion of angiotensin I by vascular smooth muscle cells

Autor: Maria E. Pueyo, Jean-Baptiste Michel, Christophe Boixel, Olivier Meilhac, Florence Coulet, Walter Gonzalez

Publikováno v: Cell and Tissue Research. 303:227-234

The conversion of angiotensin I (AT-I) to angiotensin II (AT-II) by angiotensin I-converting enzyme (ACE) is a key step in the action of angiotensins. ACE is constitutively expressed in endothelial cells, but can also be detected at low levels in smo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::158d0b6678cb8ecfd5c220193a22ed63
https://doi.org/10.1007/s004410000309

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Regulation of Vascular Endothelial Growth Factor Expression by cAMP in Rat Aortic Smooth Muscle Cells

Autor: Jean-Baptiste Michel, Maria E. Pueyo, Gisela D'Angelo, Yan Chen

Publikováno v: Experimental Cell Research
Experimental Cell Research, Elsevier, 1998, 238 (2), pp.354-358. ⟨10.1006/excr.1997.3864⟩
Experimental Cell Research, 1998, 238 (2), pp.354-358. ⟨10.1006/excr.1997.3864⟩

International audience; Vascular endothelial growth factor (VEGF) is an endothelial cell mitogen which stimulates angiogenesis. VEGF is regulated by multiple factors such as hypoxia, phorbol esters, and growth factors. However, data concerning the ex

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2bb2e977cb4f94bffcc1b7ecf09fba8
https://doi.org/10.1006/excr.1997.3864

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Clinical Phenotypes, Insulin Secretion, and Insulin Sensitivity in Kindreds With Maternally Inherited Diabetes and Deafness Due to Mitochondrial tRNALeu(UUR) Gene Mutation

Autor: Jeppe Sturis, Philippe Froguel, Jean Fiet, Maria E. Pueyo, Maria M. Byrne, Jean-Jacques Robert, Gilberto Velho, Philippe Passa, Hélène Blanché, Nathalie Vionnet, Kenneth S. Polonsky, Karine Clément

Publikováno v: Scopus-Elsevier

An A-to-G transition in the mitochondrial tRNALeu(UUR) gene at base pair 3243 has been shown to be associated with the maternally transmitted clinical phenotype of NIDDM and sensorineural hearing loss in white and Japanese pedigrees. We have detected

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fffbe50e3cf43e27260ac275d2d4412
https://doi.org/10.2337/diab.45.4.478

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A Method for Obtaining Monodispersed Cells from Isolated Porcine Islets of Langerhans

Autor: M N Gangnerau, Sylviane Darquy, Gérard Reach, Vincent Poitout, S. Di Maria, Arbet-Engels C, Maria E. Pueyo

Publikováno v: Scopus-Elsevier

Micro or macroencapsulation of islets of Langerhans have been proposed as a bioartificial pancreas. Encapsulation of dispersed single cells instead of porcine islets should improve the oxygenation of encapsulated tissue. The aim of this work was, the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73827603abad1c252103189c167965ad
https://doi.org/10.1177/039139889501800108

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Arginine-Induced Insulin Release in Glucokinase-Deficient Subjects

Autor: Maria E. Pueyo, Karine Clément, Jean-Jacques Robert, Philippe Passa, Philippe Froguel, Martine Vaxillaire, Gilberto Velho

Publikováno v: Scopus-Elsevier

OBJECTIVE In eight glucokinase (GCK)-deficient subjects, we have investigated insulin secretion rates (ISRs) in response to intravenous arginine. Impairment in the enzymatic activity of mutant GCK leads to a reduced glycolytic flux in β-cells. This

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e8a57fe135e3b754d3b5ac2d4962d83
https://doi.org/10.2337/diacare.17.9.1015

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Insulin secretory abnormalities in subjects with hyperglycemia due to glucokinase mutations

Autor: Maria E. Pueyo, Nathalie Vionnet, Graeme I. Bell, Philippe Passa, J. Takeda, David M. Cohen, Karine Clément, Markus Stoffel, Maria M. Byrne, Jeppe Sturis

Publikováno v: Journal of Clinical Investigation. 93:1120-1130

Pancreatic beta-cell function was studied in six subjects with mutations in the enzyme glucokinase (GCK) who were found to have elevated fasting and postprandial glucose levels in comparison to six normoglycemic controls. Insulin secretion rates (ISR

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::139f35861ad325b88222a29a62905f5c
https://doi.org/10.1172/jci117064

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Deletion of the donor splice site of intron 4 in the glucokinase gene causes maturity-onset diabetes of the young

Autor: Maria E. Pueyo, F. Sun, Corinne Antignac, M. Vaxillaire, Suzanne Lesage, Gilberto Velho, Ph. Passa, Bertrand Knebelmann, Habib Zouali, David M. Cohen

Publikováno v: Journal of Clinical Investigation. 92:1174-1180

Missense and nonsense mutations in the glucokinase gene have recently been shown to result in maturity-onset diabetes of the young (MODY), a subtype of non-insulin-dependent diabetes mellitus with early age of onset. Glucokinase catalyzes the formati

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50ae513d0b4027397c1f0a3a6d2379a8
https://doi.org/10.1172/jci116687

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