Zobrazeno 1 - 10
of 83
pro vyhledávání: '"A. C Ottolenghi"'
Autor:
F. Habarou, A. Brassier, M. Rio, D. Chrétien, S. Monnot, V. Barbier, R. Barouki, J.P. Bonnefont, N. Boddaert, B. Chadefaux-Vekemans, L. Le Moyec, J. Bastin, C. Ottolenghi, P. de Lonlay
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 2, Iss C, Pp 25-31 (2015)
Pyruvate carboxylase (PC) is a biotin-containing mitochondrial enzyme that catalyzes the conversion of pyruvate to oxaloacetate, thereby being involved in gluconeogenesis and in energy production through replenishment of the tricarboxylic acid (TCA)
Externí odkaz:
https://doaj.org/article/6948171860ed4d01b7b2deed66d05db1
Publikováno v:
Néphrologie & Thérapeutique. 18:394-395
Autor:
A. Hadchouel, D. Drummond, C. Pontoizeau, M. Hurtado-Nedelec, J. El Benna, E. Gachelin, C. Perisson, C. Vigier, M. Schiff, F. Lacaille, T.J. Molina, L. Berteloot, S. Renolleau, C. Ottolenghi, J.M. Tréluyer, J. De Blic, C. Delacourt
Publikováno v:
Revue des Maladies Respiratoires Actualités. 14:46
Autor:
P. Laforêt, Fanny Mochel, A. Buch, Rosaline Quinlivan, J. Vissing, Karen Lindhardt Madsen, C. Ottolenghi, Nanna S. Poulsen, Stéphane N. Hatem, D. Raaschou-Pedersen, Mads Godtfeldt Stemmerik, M. Atencio, Claude Jardel
Publikováno v:
Neuromuscular Disorders. 28:S113-S114
Autor:
G. Contu, V. Mazza, Annibale Volpe, C. Ottolenghi, Mariangela Pati, Antonino Forabosco, I. Di Monte
Publikováno v:
Prenatal Diagnosis. 24:677-684
Objectives The aim of this study was to establish the accuracy of fetal gender assignment by sonography in the biometrical range of 18 to 29 mm of biparietal diameter (BPD). Methods Transvaginal and/or transabdominal sonography was used to detect the
Autor:
Antonino Forabosco, Annibale Volpe, Francesco Rivasi, V. Mazza, I. Di Monte, F. Baldassari, C. Ottolenghi
Publikováno v:
Prenatal Diagnosis. 23:716-721
Objectives We present a case of early prenatal diagnosis of recurrent 46,XY partial gonadal dysgenesis, by combining early genetic and sonographic evaluations. Methods The conceptus of a mother with a first child affected by 46,XY gonadal dysgenesis
Autor:
M. Ricchetti, Tony Sourisseau, Jeannette Soria, Mehdi Touat, Christopher J. Lord, Ken A. Olaussen, Anne Lombès, C. Ottolenghi, D. Enot, Gérard Pierron, A. Thompson, Alan Ashworth, Sophie Postel-Vinay, Frédéric Bouillaud, Ludovic Bigot, Faraz K. Mardakheh, Nicolas Dorvault, Clément Pontoizeau, Luc Friboulet, Alain Sarasin
Publikováno v:
Journal of Clinical Oncology. 35:e23159-e23159
e23159 Background: ERCC1 (Excision Repair Cross-Complementation group 1) deficiency is the most frequent DNA repair defect in non-small cell lung cancers (NSCLC), making this enzyme an attractive therapeutic target for synthetic lethal (SL) approache
Publikováno v:
Fetal and Pediatric Pathology. 19:415-423
Deletions of the distal short arm of chromosome 9 have been reported in association with gonadal dysgenesis and XY sex reversal. These findings suggest that this region harbors at least one gene that might be involved in sexual development. Recent st
Publikováno v:
European Journal of Human Genetics. 8:167-173
Accumulating evidence suggests that haploinsufficiency of a dosage-sensitive gene(s) in human chromosome 9p24.3 is responsible for the failure of testicular development and feminisation in XY patients with monosomy for 9p. We have used molecular cyto
Autor:
C. Ottolenghi, B Tassinari, A Lodi, E. Morsiani, Puviani Ac, S Ganzerli, Paolo Pazzi, Daniele Ricci
Publikováno v:
The International Journal of Artificial Organs. 22:778-785
Various three-dimensional configurations, such as polyester tissue and woven-nonwoven, hydrophilic polyester fabric, either collagen-coated or uncoated, were investigated as potential scaffold for hepatocyte culture, in view of their use in bioreacto