Gatta Valentina
Gatta Valentina
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Male infertility: role of genetic background
A Ferlin, F Raicu, V Gatta, D Zuccarello, G Palka, C Foresta
Reproductive biomedicine online 14 (6), 734-745, 2007
Ascorbic acid and beta-carotene as modulators of oxidative damage.
R Cozzi, R Ricordy, T Aglitti, V Gatta, P Perticone, R De Salvia
Carcinogenesis 18 (1), 223-228, 1997
Use of the MLPA assay in the molecular diagnosis of gene copy number alterations in human genetic diseases
L Stuppia, I Antonucci, G Palka, V Gatta
International journal of molecular sciences 13 (3), 3245-3276, 2012
Valproic acid is neuroprotective in the rotenone rat model of Parkinson’s disease: involvement of α-synuclein
B Monti, V Gatta, F Piretti, SS Raffaelli, M Virgili, A Contestabile
Neurotoxicity research 17 (2), 130-141, 2010
Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA)
V Gatta, O Scarciolla, AR Gaspari, C Palka, MV De Angelis, A Di Muzio, ...
Human genetics 117 (1), 92-98, 2005
Epigenetics and male reproduction: the consequences of paternal lifestyle on fertility, embryo development, and children lifetime health
L Stuppia, M Franzago, P Ballerini, V Gatta, I Antonucci
Clinical epigenetics 7 (1), 1-15, 2015
Genetics of syndromic and nonsyndromic cleft lip and palate
L Stuppia, M Capogreco, G Marzo, D La Rovere, I Antonucci, V Gatta, ...
Journal of Craniofacial Surgery 22 (5), 1722-1726, 2011
C677T mutation in the 5, 10-MTHFR gene and risk of Down syndrome in Italy
L Stuppia, V Gatta, AR Gaspari, I Antonucci, E Morizio, G Calabrese, ...
European Journal of Human Genetics 10 (6), 388-390, 2002
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11
L Stuppia, V Gatta, G Calabrese, PG Franchi, E Morizio, C Bombieri, ...
Human genetics 102 (5), 566-570, 1998
The methylenetethrahydrofolate reductase (MTHFR) C677T polymorphism and male infertility in Italy
L Stuppia, V Gatta, O Scarciolla, A Colosimo, P Guanciali-Franchi, ...
Journal of endocrinological Investigation 26 (7), 620-622, 2003
Widening of a Y-chromosome interval-6 deletion transmitted from a father to his infertile son accounts for an oligozoospermia critical region distal to the RBM1 and DAZ genes.
L Stuppia, G Calabrese, PG Franchi, R Mingarelli, V Gatta, G Palka, ...
American journal of human genetics 59 (6), 1393, 1996
αVβ3-integrin routes herpes simplex virus to an entry pathway dependent on cholesterol-rich lipid rafts and dynamin2
T Gianni, V Gatta, G Campadelli-Fiume
Proceedings of the National Academy of Sciences 107 (51), 22260-22265, 2010
Inhibition of human tumor growth in mice by an oncolytic herpes simplex virus designed to target solely HER-2-positive cells
L Menotti, G Nicoletti, V Gatta, S Croci, L Landuzzi, C De Giovanni, ...
Proceedings of the National Academy of Sciences 106 (22), 9039-9044, 2009
Rethinking herpes simplex virus: the way to oncolytic agents
G Campadelli‐Fiume, C De Giovanni, V Gatta, P Nanni, PL Lollini, ...
Reviews in medical virology 21 (4), 213-226, 2011
Combination training in aging individuals modifies functional connectivity and cognition, and is potentially affected by dopamine-related genes
V Pieramico, R Esposito, F Sensi, F Cilli, D Mantini, PA Mattei, V Frazzini, ...
PLoS One 7 (8), e43901, 2012
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs
L Stuppia, I Antonucci, F Binni, A Brandi, N Grifone, A Colosimo, ...
European journal of human genetics 13 (8), 959-964, 2005
SHOX mutations detected by FISH and direct sequencing in patients with short stature
L Stuppia, G Calabrese, V Gatta, S Pintor, E Morizio, D Fantasia, ...
Journal of medical genetics 40 (2), e11-e11, 2003
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient
A Pizzuti, G Calabrese, M Bozzali, L Telvi, E Morizio, V Guida, V Gatta, ...
Investigative ophthalmology & visual science 43 (12), 3609-3612, 2002
Transcriptional regulation of the human FPR2/ALX gene: evidence of a heritable genetic variant that impairs promoter activity
F Simiele, A Recchiuti, D Mattoscio, A De Luca, E Cianci, S Franchi, ...
The FASEB Journal 26 (3), 1323-1333, 2012
A protective genetic variant for adverse environments? The role of childhood traumas and serotonin transporter gene on resilience and depressive severity in a high-risk population
V Carli, L Mandelli, L Zaninotto, A Roy, L Recchia, L Stoppia, V Gatta, ...
European Psychiatry 26 (8), 471-478, 2011
Il sistema al momento non pu eseguire l'operazione. Riprova pi tardi.
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