CONTE, IVAN
CONTE, IVAN
DIPARTIMENTO DI BIOLOGIA
CARNITINE BIOSYNTHESIS IN CNS
2004 Monfregola, J; Cevenini, Armando; Conte, I; D’Urso, M; Ursini, Mv
Apoptosome independent caspase 9 activation underlies Microphthalmia with linear skin defects (MLS) syndrome.
2011 Indrieri, A.; Conte, I.; Chesi, G.; Ghezzi, D.; Quartararo, J.; Ferrero, I.; Tate, R.; Goffrini, P.; Zeviani, M.; Bovolenta, P.; Franco, Brunella
Down regulation of Hccs in medaka recapitulates the phenotype observed in Microphthalmia with linear skin lesions (MLS) syndrome.
2009 A., Indrieri; Conte, Ivan; G., Chesi; P., Bovolenta; Franco, Brunella
Funcional characterization of the TMLH gene: promoter analysis, in situ hybridization, identification and mapping of alternative splicing variants
2007 J., Monfregola; G., Napolitano; I., Conte; Cevenini, Armando; C., Migliaccio; M., D'Urso; M. V., Ursini; Napolitano, Gennaro; Conte, Ivan
The impairment of HCCS leads to MLS syndrome by activating a non-canonical cell death pathway in the brain and eyes.
2013 A., Indrieri; I., Conte; G., Chesi; Romano, Alessia; J., Quartararo; R., Tatè; D., Ghezzi; M., Zeviani; P., Goffrini; I., Ferrero; P., Bovolenta; Franco, Brunella; Conte, Ivan
Mutations in COX7B cause Microphthalmia with linear skin lesions, an unconventional mitochondrial disease.
2012 A., Indrieri; V., van Rahden; V., Tiranti; M., Morleo; D., Iaconis; R., Tammaro; I., D’Amato; I., Conte; I., Maystadt; S., Demuth; A., Zvulunov; K., Kutsche; M., Zeviani; Franco, Brunella; Conte, Ivan
MiR-211 is essential for adult cone photoreceptor maintenance and visual function
2017 Barbato, Sara; Marrocco, Elena; Intartaglia, Daniela; Pizzo, Mariateresa; Asteriti, Sabrina; Naso, Federica; Falanga, Danila; Bhat, Rajeshwari S.; Meola, Nicola; Carissimo, Annamaria; Karali, Marianthi; Prosser, Haydn M.; Cangiano, Lorenzo; Surace, Enrico Maria; Banfi, Sandro; Conte, Ivan; Conte, Ivan
TGF-β controls MIR-181/ERK regulatory network during retinal axon specification and growth
2015 Carrella, S.; Barbato, S.; D'Agostino, Y.; Salierno, F. G.; Manfredi, A.; Banfi, S.; Conte, I.
MiR-204 is responsible for inherited retinal dystrophy associated with ocular coloboma
2015 Conte, I.; Hadfield, K. D.; Barbato, S.; Carrella, S.; Pizzo, M.; Bhat, R. S.; Carissimo, A.; Karali, M.; Porter, L. F.; Urquhart, J.; Hateley, S.; O'Sullivan, J.; Manson, F. D. C.; Neuhauss, S. C. F.; Banfi, S.; Black, G. C. M.
miR-181a/b control the assembly of visual circuitry by regulating retinal axon specification and growth
2015 Carrella, S.; D'Agostino, Y.; Barbato, S.; Huber-Reggi, S. P.; Salierno, F. G.; Manfredi, A.; Neuhauss, S. C. F.; Banfi, S.; Conte, I.
The combination of transcriptomics and informatics identifies pathways targeted by miR-204 during neurogenesis and axon guidance
2014 Conte, I.; Merella, S.; Garcia-Manteiga, J. M.; Migliore, C.; Lazarevic, D.; Carrella, S.; Marco-Ferreres, R.; Avellino, R.; Davidson, N. P.; Emmett, W.; Sanges, R.; Bockett, N.; Van Heel, D.; Meroni, G.; Bovolenta, P.; Stupka, E.; Banfi, S.
miR-204 Targeting of Ankrd13A Controls Both Mesenchymal Neural Crest and Lens Cell Migration
2013 Avellino, R.; Carrella, S.; Pirozzi, M.; Risolino, M.; Salierno, F. G.; Franco, P.; Stoppelli, P.; Verde, P.; Banfi, S.; Conte, I.
Non-coding RNAs in the development of sensory organs and related diseases
2013 Conte, I.; Banfi, S.; Bovolenta, P.
Sox2-mediated differential activation of Six3.2 contributes to forebrain patterning
2012 Beccari, L.; Conte, I.; Cisneros, E.; Bovolenta, P.
Vax2 regulates retinoic acid distribution and cone opsin expression in the vertebrate eye
2011 Alfano, G.; Conte, I.; Caramico, T.; Avellino, R.; Arno', Barbara; Pizzo, M. T.; Tanimoto, N.; Beck, S. C.; Huber, G.; Dolle, P.; Seeliger, M. W.; Banfi, S.
MiR-204 is required for lens and retinal development via Meis2 targeting
2010 Conte, I.; Carrella, S.; Avellino, R.; Karali, M.; Marco-Ferreres, R.; Bovolenta, P.; Banfi, S.
Identification and expression analysis of novel Jakmip1 transcripts
2007 Costa, V.; Conte, I.; Ziviello, C.; Casamassimi, A.; Alfano, G.; Banfi, S.; Ciccodicola, A.
Comprehensive characterization of the cis-regulatory code responsible for the spatio-temporal expression of olSix3.2 in the developing medaka forebrain
2007 Conte, I.; Bovolenta, P.
Mapping of MRX81 in Xp11.2-Xq12 suggests the presence of a new gene involved in nonspecific X-linked mental retardation
2003 Annunziata, Ida; Lanzara, Carmela; Conte, Ivan; Zullo, Alberto; Ventruto, Valerio; Rinaldi, Maria Michela; D'Urso, Michele; Casari, Giorgio; Ciccodicola, Alfredo; Miano, Maria Giuseppina
Identification and characterisation of the retinitis pigmentosa 1-like1 gene (RP1L1): A novel candidate for retinal degenerations
2003 Conte, I.; Lestingi, M.; den Hollander, A.; Alfano, G.; Ziviello, C.; Pugliese, M.; Circolo, D.; Caccioppoli, C.; Ciccodicola, A.; Banfi, S.
Titolo | Tipologia | Data di pubblicazione | Autore(i) | File |
---|---|---|---|---|
CARNITINE BIOSYNTHESIS IN CNS | 4.2 Abstract in Atti di convegno | 2004 | Monfregola, J; Cevenini, Armando; Conte, I; D’Urso, M; Ursini, Mv | |
Apoptosome independent caspase 9 activation underlies Microphthalmia with linear skin defects (MLS) syndrome. | 4.1 Articoli in Atti di convegno | 2011 | Indrieri, A.; Conte, I.; Chesi, G.; Ghezzi, D.; Quartararo, J.; Ferrero, I.; Tate, R.; Goffrini, P.; Zeviani, M.; Bovolenta, P.; Franco, Brunella | |
Down regulation of Hccs in medaka recapitulates the phenotype observed in Microphthalmia with linear skin lesions (MLS) syndrome. | 4.1 Articoli in Atti di convegno | 2009 | A., Indrieri; Conte, Ivan; G., Chesi; P., Bovolenta; Franco, Brunella | |
Funcional characterization of the TMLH gene: promoter analysis, in situ hybridization, identification and mapping of alternative splicing variants | 1.1 Articolo in rivista | 2007 | J., Monfregola; G., Napolitano; I., Conte; Cevenini, Armando; C., Migliaccio; M., D'Urso; M. V., Ursini; Napolitano, Gennaro; Conte, Ivan | |
The impairment of HCCS leads to MLS syndrome by activating a non-canonical cell death pathway in the brain and eyes. | 1.1 Articolo in rivista | 2013 | A., Indrieri; I., Conte; G., Chesi; Romano, Alessia; J., Quartararo; R., Tatè; D., Ghezzi; M., Zeviani; P., Goffrini; I., Ferrero; P., Bovolenta; Franco, Brunella; Conte, Ivan | |
Mutations in COX7B cause Microphthalmia with linear skin lesions, an unconventional mitochondrial disease. | 1.1 Articolo in rivista | 2012 | A., Indrieri; V., van Rahden; V., Tiranti; M., Morleo; D., Iaconis; R., Tammaro; I., D’Amato; I., Conte; I., Maystadt; S., Demuth; A., Zvulunov; K., Kutsche; M., Zeviani; Franco, Brunella; Conte, Ivan | |
MiR-211 is essential for adult cone photoreceptor maintenance and visual function | 1.1 Articolo in rivista | 2017 | Barbato, Sara; Marrocco, Elena; Intartaglia, Daniela; Pizzo, Mariateresa; Asteriti, Sabrina; Naso, Federica; Falanga, Danila; Bhat, Rajeshwari S.; Meola, Nicola; Carissimo, Annamaria; Karali, Marianthi; Prosser, Haydn M.; Cangiano, Lorenzo; Surace, Enrico Maria; Banfi, Sandro; Conte, Ivan; Conte, Ivan | |
TGF-β controls MIR-181/ERK regulatory network during retinal axon specification and growth | 1.1 Articolo in rivista | 2015 | Carrella, S.; Barbato, S.; D'Agostino, Y.; Salierno, F. G.; Manfredi, A.; Banfi, S.; Conte, I. | |
MiR-204 is responsible for inherited retinal dystrophy associated with ocular coloboma | 1.1 Articolo in rivista | 2015 | Conte, I.; Hadfield, K. D.; Barbato, S.; Carrella, S.; Pizzo, M.; Bhat, R. S.; Carissimo, A.; Karali, M.; Porter, L. F.; Urquhart, J.; Hateley, S.; O'Sullivan, J.; Manson, F. D. C.; Neuhauss, S. C. F.; Banfi, S.; Black, G. C. M. | |
miR-181a/b control the assembly of visual circuitry by regulating retinal axon specification and growth | 1.1 Articolo in rivista | 2015 | Carrella, S.; D'Agostino, Y.; Barbato, S.; Huber-Reggi, S. P.; Salierno, F. G.; Manfredi, A.; Neuhauss, S. C. F.; Banfi, S.; Conte, I. | |
The combination of transcriptomics and informatics identifies pathways targeted by miR-204 during neurogenesis and axon guidance | 1.1 Articolo in rivista | 2014 | Conte, I.; Merella, S.; Garcia-Manteiga, J. M.; Migliore, C.; Lazarevic, D.; Carrella, S.; Marco-Ferreres, R.; Avellino, R.; Davidson, N. P.; Emmett, W.; Sanges, R.; Bockett, N.; Van Heel, D.; Meroni, G.; Bovolenta, P.; Stupka, E.; Banfi, S. | |
miR-204 Targeting of Ankrd13A Controls Both Mesenchymal Neural Crest and Lens Cell Migration | 1.1 Articolo in rivista | 2013 | Avellino, R.; Carrella, S.; Pirozzi, M.; Risolino, M.; Salierno, F. G.; Franco, P.; Stoppelli, P.; Verde, P.; Banfi, S.; Conte, I. | |
Non-coding RNAs in the development of sensory organs and related diseases | 1.1 Articolo in rivista | 2013 | Conte, I.; Banfi, S.; Bovolenta, P. | |
Sox2-mediated differential activation of Six3.2 contributes to forebrain patterning | 1.1 Articolo in rivista | 2012 | Beccari, L.; Conte, I.; Cisneros, E.; Bovolenta, P. | |
Vax2 regulates retinoic acid distribution and cone opsin expression in the vertebrate eye | 1.1 Articolo in rivista | 2011 | Alfano, G.; Conte, I.; Caramico, T.; Avellino, R.; Arno', Barbara; Pizzo, M. T.; Tanimoto, N.; Beck, S. C.; Huber, G.; Dolle, P.; Seeliger, M. W.; Banfi, S. | |
MiR-204 is required for lens and retinal development via Meis2 targeting | 1.1 Articolo in rivista | 2010 | Conte, I.; Carrella, S.; Avellino, R.; Karali, M.; Marco-Ferreres, R.; Bovolenta, P.; Banfi, S. | |
Identification and expression analysis of novel Jakmip1 transcripts | 1.1 Articolo in rivista | 2007 | Costa, V.; Conte, I.; Ziviello, C.; Casamassimi, A.; Alfano, G.; Banfi, S.; Ciccodicola, A. | |
Comprehensive characterization of the cis-regulatory code responsible for the spatio-temporal expression of olSix3.2 in the developing medaka forebrain | 1.1 Articolo in rivista | 2007 | Conte, I.; Bovolenta, P. | |
Mapping of MRX81 in Xp11.2-Xq12 suggests the presence of a new gene involved in nonspecific X-linked mental retardation | 1.1 Articolo in rivista | 2003 | Annunziata, Ida; Lanzara, Carmela; Conte, Ivan; Zullo, Alberto; Ventruto, Valerio; Rinaldi, Maria Michela; D'Urso, Michele; Casari, Giorgio; Ciccodicola, Alfredo; Miano, Maria Giuseppina | |
Identification and characterisation of the retinitis pigmentosa 1-like1 gene (RP1L1): A novel candidate for retinal degenerations | 1.1 Articolo in rivista | 2003 | Conte, I.; Lestingi, M.; den Hollander, A.; Alfano, G.; Ziviello, C.; Pugliese, M.; Circolo, D.; Caccioppoli, C.; Ciccodicola, A.; Banfi, S. |