Autor: "Acquaviva, M" - OpacWWW

Skocz do pozycji: 1.

Tytuł:: Transcriptome analysis defines myocardium gene signatures in children with ToF and ASD and reveals disease-specific molecular reprogramming in response to surgery with cardiopulmonary bypass.
Autorzy:: Raggi F; Laboratory of Molecular Biology, IRCSS Istituto Giannina Gaslini, Padiglione 2, L.go G.Gaslini 5, 16147, Genova, Italy.
Cangelosi D; Laboratory of Molecular Biology, IRCSS Istituto Giannina Gaslini, Padiglione 2, L.go G.Gaslini 5, 16147, Genova, Italy.
Becherini P; Laboratory of Molecular Biology, IRCSS Istituto Giannina Gaslini, Padiglione 2, L.go G.Gaslini 5, 16147, Genova, Italy.; Department of Internal Medicine, University of Genova, Genova, Italy.
Blengio F; Laboratory of Molecular Biology, IRCSS Istituto Giannina Gaslini, Padiglione 2, L.go G.Gaslini 5, 16147, Genova, Italy.; INSERM U955 Equipe 16, Creteil, France.
Morini M; Laboratory of Molecular Biology, IRCSS Istituto Giannina Gaslini, Padiglione 2, L.go G.Gaslini 5, 16147, Genova, Italy.
Acquaviva M; Laboratory of Molecular Biology, IRCSS Istituto Giannina Gaslini, Padiglione 2, L.go G.Gaslini 5, 16147, Genova, Italy.; Immunobiology of Neurological Disorders Unit, Institute of Experimental Neurology INSPE, Ospedale San Raffaele, Milano, Italy.
Belli ML; Laboratory of Molecular Biology, IRCSS Istituto Giannina Gaslini, Padiglione 2, L.go G.Gaslini 5, 16147, Genova, Italy.; Cytomorphology Laboratory, Heamo-Onco-TMO Department, IRCSS Istituto Giannina Gaslini, Genova, Italy.
Panizzon G; Department of Cardiology, IRCSS Istituto Giannina Gaslini, Genova, Italy.
Cervo G; Department of Cardiology, IRCSS Istituto Giannina Gaslini, Genova, Italy.
Varesio L; Laboratory of Molecular Biology, IRCSS Istituto Giannina Gaslini, Padiglione 2, L.go G.Gaslini 5, 16147, Genova, Italy.
Eva A; Laboratory of Molecular Biology, IRCSS Istituto Giannina Gaslini, Padiglione 2, L.go G.Gaslini 5, 16147, Genova, Italy.
Bosco MC; Laboratory of Molecular Biology, IRCSS Istituto Giannina Gaslini, Padiglione 2, L.go G.Gaslini 5, 16147, Genova, Italy. .; Pokaż więcej
Źródło:: Journal of translational medicine [J Transl Med] 2020 Jan 10; Vol. 18 (1), pp. 21. Date of Electronic Publication: 2020 Jan 10.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Heart Septal Defects, Atrial*/genetics
Myocardium*/metabolism
Tetralogy of Fallot*
Cardiopulmonary Bypass ; Child ; Gene Expression Profiling ; Humans

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Skocz do pozycji: 2.

Tytuł:: Assessment of copy number variations in 120 patients with Poland syndrome.
Autorzy:: Vaccari CM; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DiNOGMI), University of Genoa, Genoa, Italy.
Tassano E; Medical Genetics Unit, Istituto Giannina Gaslini, Genoa, Italy.
Torre M; Pediatric Surgery Unit and Airway Team, Istituto Giannina Gaslini, Genoa, Italy.
Gimelli S; Department of Genetic Medicine and Development, Geneva University Medical School, Geneva, Switzerland.
Divizia MT; Medical Genetics Unit, Istituto Giannina Gaslini, Genoa, Italy.
Romanini MV; Plastic and Reconstructive Surgery, Pediatric Surgery Unit, Istituto Giannina Gaslini, Genoa, Italy.
Bossi S; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DiNOGMI), University of Genoa, Genoa, Italy.
Musante I; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DiNOGMI), University of Genoa, Genoa, Italy.
Valle M; Radiology Unit, Istituto Giannina Gaslini, Genoa, Italy.
Senes F; Reconstructive Microsurgery and Hand Surgery Unit, Istituto Giannina Gaslini, Genoa, Italy.
Catena N; Reconstructive Microsurgery and Hand Surgery Unit, Istituto Giannina Gaslini, Genoa, Italy.
Bedeschi MF; Medical Genetics Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Baban A; Medical Genetics Unit, Istituto Giannina Gaslini, Genoa, Italy.; Present Address: Department of Pediatric Cardiology and Cardiac Surgery, Bambino Gesù Children's Hospital, Rome, Italy.
Calevo MG; U.O.S.D. Epidemiology and Biostatistics, Istituto Giannina Gaslini, Genoa, Italy.
Acquaviva M; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DiNOGMI), University of Genoa, Genoa, Italy.
Lerone M; Medical Genetics Unit, Istituto Giannina Gaslini, Genoa, Italy.
Ravazzolo R; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DiNOGMI), University of Genoa, Genoa, Italy.; Medical Genetics Unit, Istituto Giannina Gaslini, Genoa, Italy.; Medical Genetics Unit, Istituto Giannina Gaslini, via G. Gaslini 5, 16148, Genoa, Italy.
Puliti A; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DiNOGMI), University of Genoa, Genoa, Italy. .; Medical Genetics Unit, Istituto Giannina Gaslini, Genoa, Italy. .; Medical Genetics Unit, Istituto Giannina Gaslini, via G. Gaslini 5, 16148, Genoa, Italy. .; Pokaż więcej
Źródło:: BMC medical genetics [BMC Med Genet] 2016 Nov 25; Vol. 17 (1), pp. 89. Date of Electronic Publication: 2016 Nov 25.
Typ publikacji:: Journal Article
MeSH Terms:: DNA Copy Number Variations*
Gene Regulatory Networks*
Comparative Genomic Hybridization/*methods
Karyotyping/*methods
Poland Syndrome/*genetics
Chromosome Duplication ; Female ; Genetic Predisposition to Disease ; Humans ; Male ; Sequence Deletion

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Skocz do pozycji: 3.

Tytuł:: Design of a multi-signature ensemble classifier predicting neuroblastoma patients' outcome.
Autorzy:: Cornero A; Laboratory of Molecular Biology, G. Gaslini Institute, Genoa 16147, Italy.
Acquaviva M
Fardin P
Versteeg R
Schramm A
Eva A
Bosco MC
Blengio F
Barzaghi S
Varesio L; Pokaż więcej
Źródło:: BMC bioinformatics [BMC Bioinformatics] 2012 Mar 28; Vol. 13 Suppl 4, pp. S13. Date of Electronic Publication: 2012 Mar 28.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Algorithms*
Gene Expression Profiling*
Neuroblastoma/*genetics
Neuroblastoma/*therapy
Humans ; Infant ; Neural Networks, Computer ; Neuroblastoma/diagnosis ; Neuroblastoma/mortality ; Prognosis ; Risk Assessment ; Treatment Outcome

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Skocz do pozycji: 4.

Tytuł:: Identification of multiple hypoxia signatures in neuroblastoma cell lines by l1-l2 regularization and data reduction.
Autorzy:: Fardin P; Laboratory of Molecular Biology, Gaslini Institute, 16147 Genoa, Italy. />Cornero A
Barla A
Mosci S
Acquaviva M
Rosasco L
Gambini C
Verri A
Varesio L; Pokaż więcej
Źródło:: Journal of biomedicine & biotechnology [J Biomed Biotechnol] 2010; Vol. 2010, pp. 878709. Date of Electronic Publication: 2010 Jun 28.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Cell Hypoxia*/genetics
Cell Hypoxia*/physiology
Gene Expression Profiling/*methods
Gene Expression Regulation, Neoplastic/*genetics
Neuroblastoma/*metabolism
Algorithms ; Cell Line, Tumor ; Cluster Analysis ; Computational Biology/methods ; Humans ; Oligonucleotide Array Sequence Analysis ; Principal Component Analysis ; Reproducibility of Results

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Skocz do pozycji: 5.

Tytuł:: Clinical features and molecular modelling of novel MPZ mutations in demyelinating and axonal neuropathies.
Autorzy:: Mandich P; Department of Neuroscience, Ophthalmology and Genetics, University of Genoa, Genoa, Italy. />Fossa P
Capponi S
Geroldi A
Acquaviva M
Gulli R
Ciotti P
Manganelli F
Grandis M
Bellone E; Pokaż więcej
Źródło:: European journal of human genetics : EJHG [Eur J Hum Genet] 2009 Sep; Vol. 17 (9), pp. 1129-34. Date of Electronic Publication: 2009 Mar 18.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Mutation*
Charcot-Marie-Tooth Disease/*genetics
Charcot-Marie-Tooth Disease/*pathology
Axons/pathology ; Charcot-Marie-Tooth Disease/classification ; DNA Mutational Analysis ; Demyelinating Diseases/genetics ; Demyelinating Diseases/pathology ; Frameshift Mutation ; Humans ; Mutation, Missense ; Myelin P0 Protein ; Peripheral Nervous System Diseases/genetics ; Peripheral Nervous System Diseases/pathology

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Skocz do pozycji: 6.

Tytuł:: Gap junction beta 1 (GJB1) gene mutations in Italian patients with X-linked Charcot-Marie-Tooth disease.
Autorzy:: Mandich P; Department of Neuroscience, Ophthalmology and Genetics, Section of Medical Genetics, University of Genova, c/o DIMI, Viale Benedetto XV, 6, 16132, Genova, Italy. .
Grandis M; Department of Neuroscience, Ophthalmology and Genetics, Section of Neurology and Neurological Rehabilitation, University of Genova, Genova, Italy.
Geroldi A; Department of Neuroscience, Ophthalmology and Genetics, Section of Medical Genetics, University of Genova, c/o DIMI, Viale Benedetto XV, 6, 16132, Genova, Italy.
Acquaviva M; Department of Neuroscience, Ophthalmology and Genetics, Section of Medical Genetics, University of Genova, c/o DIMI, Viale Benedetto XV, 6, 16132, Genova, Italy.
Varese A; Department of Neuroscience, Ophthalmology and Genetics, Section of Medical Genetics, University of Genova, c/o DIMI, Viale Benedetto XV, 6, 16132, Genova, Italy.
Gulli R; Department of Neuroscience, Ophthalmology and Genetics, Section of Medical Genetics, University of Genova, c/o DIMI, Viale Benedetto XV, 6, 16132, Genova, Italy.
Ciotti P; Department of Neuroscience, Ophthalmology and Genetics, Section of Medical Genetics, University of Genova, c/o DIMI, Viale Benedetto XV, 6, 16132, Genova, Italy.
Bellone E; Department of Neuroscience, Ophthalmology and Genetics, Section of Medical Genetics, University of Genova, c/o DIMI, Viale Benedetto XV, 6, 16132, Genova, Italy.; Pokaż więcej
Źródło:: Journal of human genetics [J Hum Genet] 2008; Vol. 53 (6), pp. 529-533. Date of Electronic Publication: 2008 Apr 01.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Mutation*
Charcot-Marie-Tooth Disease/*genetics
Connexins/*genetics
Genetic Diseases, X-Linked/*genetics
Base Sequence ; Cohort Studies ; DNA/genetics ; DNA Mutational Analysis ; Female ; Humans ; Italy ; Male ; Point Mutation ; Sequence Deletion ; Gap Junction beta-1 Protein

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