Zobrazeno 1 - 10 of 570 pro vyhledávání: '"Varrone S."'
2
A-Kinase-Anchor-Protein 121 amplifica selettivamente la traduzione di segnali cAMP dipendenti sul mitocondrio ed inibisce l?apoptosi
Autor: Carlucci A., Affaitati A., de Cristofaro T., Cardone L., Garbi C., Varrone S., Avvedimento V. E, Feliciello A.
Publikováno v: Giornate Scientifiche delle facoltà di Medicina e Chirurgia, Farmacia, Medicina Veterinaria ed Agraria, Portici, 2002
info:cnr-pdr/source/autori:Carlucci A., Affaitati A., de Cristofaro T.,Cardone L., Garbi C., Varrone S., Avvedimento V. E, Feliciello A./congresso_nome:Giornate Scientifiche delle facoltà di Medicina e Chirurgia, Farmacia, Medicina Veterinaria ed Agraria/congresso_luogo:Portici/congresso_data:2002/anno:2002/pagina_da:/pagina_a:/intervallo_pagine
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::00116e30fff25d61468ab3b4de82dfc5
http://www.cnr.it/prodotto/i/107733
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3
Increased DNA damage in polyglutamine diseases
Autor: Affaitati A., Giuliano P., de Cristofaro T., Varrone S.
Publikováno v: Molecular mechanisms of neurodegeneration, Milano, 2003
info:cnr-pdr/source/autori:Affaitati A., Giuliano P., de Cristofaro T. and Varrone S./congresso_nome:Molecular mechanisms of neurodegeneration/congresso_luogo:Milano/congresso_data:2003/anno:2003/pagina_da:/pagina_a:/intervallo_pagine
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::5c196bfd91037a8dae85b218dda79606
http://www.cnr.it/prodotto/i/107749
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7
Friedreich's disease. A linkage study in southern and central Italy
Autor: Francesca Cavalcanti, Cocozza, S., Filla, A., Michele, G., Pianese, L., Porcellini, A., Monticelli, A., Pandolfo, M., Banfi, S., Varrone, S.
Publikováno v: Scopus-Elsevier
Europe PubMed Central
ResearcherID
We studied linkage and linkage disequilibrium between the genetic locus of Friedreich's disease (FRDA) and two maker loci (D9S15 and D9S5) of chromosome 9q13-q21.1 in 49 subjects from 12 families in southern and central Italy. No recombination event
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::656cc939c9fd0d412fb4c68bb0b8b25b
http://hdl.handle.net/11588/340897
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8
A PILOT-STUDY FOR NEONATAL SCREENING OF CONGENITAL ADRENAL-HYPERPLASIA DUE TO 21-HYDROXYLASE AND 11-BETA-HYDROXYLASE DEFICIENCY IN CAMPANIA REGION
Autor: Valentino R, Tommaselli AP, Rossi R, Lombardi G, Varrone S.
Publikováno v: Journal of endocrinological investigation (Online) 13 (1990): 221–225.
info:cnr-pdr/source/autori:Valentino R, Tommaselli AP, Rossi R, Lombardi G, Varrone S./titolo:A PILOT-STUDY FOR NEONATAL SCREENING OF CONGENITAL ADRENAL-HYPERPLASIA DUE TO 21-HYDROXYLASE AND 11-BETA-HYDROXYLASE DEFICIENCY IN CAMPANIA REGION/doi:/rivista:Journal of endocrinological investigation (Online)/anno:1990/pagina_da:221/pagina_a:225/intervallo_pagine:221–225/volume:13
A neonatal screening for both 21-hydroxylase and 11-beta-hydroxylase deficiencies, responsible for congenital adrenal hyperplasia (CAH), has been conducted in Campania Region, Southern Italy. In 4380 neonates, aged 2-10 days, capillary blood from a h
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::00326097d66a05adf3082da063c52f8f
https://publications.cnr.it/doc/233117
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10
Akademický článek
Effects of Thyroid Hormones on the Multiple Molecular Forms of Mitochondrial Malate-Dehydrogenase.
Autor: Varrone, S., Consiglio, E., Covelli, I.
Publikováno v: Hormone Research; 1970, Vol. 1 Issue 3, p148-163, 16p
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