Comprehensive characterization of the cis-regulatory code responsible for the spatio-temporal expression of olSix3.2 in the developing medaka forebrain

Por Conte, Ivan, Bovolenta, Paola
Publicado em 2007

miR-204 is required for lens and retinal development via Meis2 targeting

Por Conte, Ivan, Carrella, Sabrina, Avellino, Raffaella, Karali, Marianthi, Marco-Ferreres, Raquel, Bovolenta, Paola, Banfi, Sandro
Publicado em 2010

TGF-β Controls miR-181/ERK Regulatory Network during Retinal Axon Specification and Growth

Por Carrella, Sabrina, Barbato, Sara, D’Agostino, Ylenia, Salierno, Francesco Giuseppe, Manfredi, Anna, Banfi, Sandro, Conte, Ivan
Publicado no PLoS One (2015)

A trans-Regulatory Code for the Forebrain Expression of Six3.2 in the Medaka Fish

Por Beccari, Leonardo, Marco-Ferreres, Raquel, Tabanera, Noemi, Manfredi, Anna, Souren, Marcel, Wittbrodt, Beate, Conte, Ivan, Wittbrodt, Jochen, Bovolenta, Paola
Publicado no J Biol Chem (2015)

miR-204 Targeting of Ankrd13A Controls Both Mesenchymal Neural Crest and Lens Cell Migration

Por Avellino, Raffaella, Carrella, Sabrina, Pirozzi, Marinella, Risolino, Maurizio, Salierno, Francesco Giuseppe, Franco, Paola, Stoppelli, Patrizia, Verde, Pasquale, Banfi, Sandro, Conte, Ivan
Publicado em 2013

The impairment of HCCS leads to MLS syndrome by activating a non-canonical cell death pathway in the brain and eyes

Por Indrieri, Alessia, Conte, Ivan, Chesi, Giancarlo, Romano, Alessia, Quartararo, Jade, Tatè, Rosarita, Ghezzi, Daniele, Zeviani, Massimo, Goffrini, Paola, Ferrero, Ileana, Bovolenta, Paola, Franco, Brunella
Publicado em 2013

The impairment of HCCS leads to MLS syndrome by activating a non-canonical cell death pathway in the brain and eyes

Por Indrieri, Alessia, Conte, Ivan, Chesi, Giancarlo, Romano, Alessia, Quartararo, Jade, Tatè, Rosarita, Ghezzi, Daniele, Zeviani, Massimo, Goffrini, Paola, Ferrero, Ileana, Bovolenta, Paola, Franco, Brunella
Publicado em 2014

miR‐181a/b control the assembly of visual circuitry by regulating retinal axon specification and growth

Por Carrella, Sabrina, D'Agostino, Ylenia, Barbato, Sara, Huber‐Reggi, Sabina P., Salierno, Francesco G., Manfredi, Anna, Neuhauss, Stephan C.F., Banfi, Sandro, Conte, Ivan
Publicado no Dev Neurobiol (2015)

Identification and Characterization of FGF2-Dependent mRNA: microRNA Networks During Lens Fiber Cell Differentiation

Por Wolf, Louise, Gao, Chun S., Gueta, Karen, Xie, Qing, Chevallier, Tiphaine, Podduturi, Nikhil R., Sun, Jian, Conte, Ivan, Zelenka, Peggy S., Ashery-Padan, Ruth, Zavadil, Jiri, Cvekl, Ales
Publicado em 2013

Mutations in COX7B Cause Microphthalmia with Linear Skin Lesions, an Unconventional Mitochondrial Disease

Por Indrieri, Alessia, van Rahden, Vanessa Alexandra, Tiranti, Valeria, Morleo, Manuela, Iaconis, Daniela, Tammaro, Roberta, D’Amato, Ilaria, Conte, Ivan, Maystadt, Isabelle, Demuth, Stephanie, Zvulunov, Alex, Kutsche, Kerstin, Zeviani, Massimo, Franco, Brunella
Publicado em 2012

The <it>ADAMTS18 </it>gene is responsible for autosomal recessive early onset severe retinal dystrophy

Por Peluso Ivana, Conte Ivan, Testa Francesco, Dharmalingam Gopuraja, Pizzo Mariateresa, Collin Rob WJ, Meola Nicola, Barbato Sara, Mutarelli Margherita, Ziviello Carmela, Barbarulo Anna Maria, Nigro Vincenzo, Melone Mariarosa AB, Simonelli Francesca, Banfi Sandro
Publicado em 2013-01-01

The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy

Por Peluso, Ivana, Conte, Ivan, Testa, Francesco, Dharmalingam, Gopuraja, Pizzo, Mariateresa, Collin, Rob WJ, Meola, Nicola, Barbato, Sara, Mutarelli, Margherita, Ziviello, Carmela, Barbarulo, Anna Maria, Nigro, Vincenzo, Melone, Mariarosa AB, Simonelli, Francesca, Banfi, Sandro
Publicado em 2013

The combination of transcriptomics and informatics identifies pathways targeted by miR-204 during neurogenesis and axon guidance

Por Conte, Ivan, Merella, Stefania, Garcia-Manteiga, Jose Manuel, Migliore, Chiara, Lazarevic, Dejan, Carrella, Sabrina, Marco-Ferreres, Raquel, Avellino, Raffaella, Davidson, Nathan Paul, Emmett, Warren, Sanges, Remo, Bockett, Nicholas, Van Heel, David, Meroni, Germana, Bovolenta, Paola, Stupka, Elia, Banfi, Sandro
Publicado em 2014

Pax6 Regulates Gene Expression in the Vertebrate Lens through miR-204

Por Shaham, Ohad, Gueta, Karen, Mor, Eyal, Oren-Giladi, Pazit, Grinberg, Dina, Xie, Qing, Cvekl, Ales, Shomron, Noam, Davis, Noa, Keydar-Prizant, Maya, Raviv, Shaul, Pasmanik-Chor, Metsada, Bell, Rachel E., Levy, Carmit, Avellino, Raffaella, Banfi, Sandro, Conte, Ivan, Ashery-Padan, Ruth
Publicado em 2013

MiR-204 is responsible for inherited retinal dystrophy associated with ocular coloboma

Por Conte, Ivan, Hadfield, Kristen D., Barbato, Sara, Carrella, Sabrina, Pizzo, Mariateresa, Bhat, Rajeshwari S., Carissimo, Annamaria, Karali, Marianthi, Porter, Louise F., Urquhart, Jill, Hateley, Sofie, O’Sullivan, James, Manson, Forbes D. C., Neuhauss, Stephan C. F., Banfi, Sandro, Black, Graeme C. M.
Publicado no Proc Natl Acad Sci U S A (2015)

Recessive Mutations in SLC38A8 Cause Foveal Hypoplasia and Optic Nerve Misrouting without Albinism

Por Poulter, James A., Al-Araimi, Musallam, Conte, Ivan, van Genderen, Maria M., Sheridan, Eamonn, Carr, Ian M., Parry, David A., Shires, Mike, Carrella, Sabrina, Bradbury, John, Khan, Kamron, Lakeman, Phillis, Sergouniotis, Panagiotis I., Webster, Andrew R., Moore, Anthony T., Pal, Bishwanath, Mohamed, Moin D., Venkataramana, Anandula, Ramprasad, Vedam, Shetty, Rohit, Saktivel, Murugan, Kumaramanickavel, Govindasamy, Tan, Alex, Mackey, David A., Hewitt, Alex W., Banfi, Sandro, Ali, Manir, Inglehearn, Chris F., Toomes, Carmel
Publicado em 2013