Banfi S - Search Results

1

Non-coding RNAs in the development of sensory organs and related diseases.

Conte I, Banfi S, Bovolenta P. Conte I, et al. Among authors: banfi s. Cell Mol Life Sci. 2013 Nov;70(21):4141-55. doi: 10.1007/s00018-013-1335-z. Epub 2013 Apr 16. Cell Mol Life Sci. 2013. PMID: 23588489 Review.

2

Vax2 inactivation in mouse determines alteration of the eye dorsal-ventral axis, misrouting of the optic fibres and eye coloboma.

Barbieri AM, Broccoli V, Bovolenta P, Alfano G, Marchitiello A, Mocchetti C, Crippa L, Bulfone A, Marigo V, Ballabio A, Banfi S. Barbieri AM, et al. Among authors: banfi s. Development. 2002 Feb;129(3):805-13. doi: 10.1242/dev.129.3.805. Development. 2002. PMID: 11830579

3

Characterization of MPP4, a gene highly expressed in photoreceptor cells, and mutation analysis in retinitis pigmentosa.

Conte I, Lestingi M, den Hollander A, Miano MG, Alfano G, Circolo D, Pugliese M, Testa F, Simonelli F, Rinaldi E, Baiget M, Banfi S, Ciccodicola A. Conte I, et al. Among authors: banfi s. Gene. 2002 Sep 4;297(1-2):33-8. doi: 10.1016/s0378-1119(02)00872-7. Gene. 2002. PMID: 12384283

4

Identification and characterisation of the retinitis pigmentosa 1-like1 gene (RP1L1): a novel candidate for retinal degenerations.

Conte I, Lestingi M, den Hollander A, Alfano G, Ziviello C, Pugliese M, Circolo D, Caccioppoli C, Ciccodicola A, Banfi S. Conte I, et al. Among authors: banfi s. Eur J Hum Genet. 2003 Feb;11(2):155-62. doi: 10.1038/sj.ejhg.5200942. Eur J Hum Genet. 2003. PMID: 12634863

5

Natural antisense transcripts associated with genes involved in eye development.

Alfano G, Vitiello C, Caccioppoli C, Caramico T, Carola A, Szego MJ, McInnes RR, Auricchio A, Banfi S. Alfano G, et al. Among authors: banfi s. Hum Mol Genet. 2005 Apr 1;14(7):913-23. doi: 10.1093/hmg/ddi084. Epub 2005 Feb 9. Hum Mol Genet. 2005. PMID: 15703187

6

Identification and expression analysis of novel Jakmip1 transcripts.

Costa V, Conte I, Ziviello C, Casamassimi A, Alfano G, Banfi S, Ciccodicola A. Costa V, et al. Among authors: banfi s. Gene. 2007 Nov 1;402(1-2):1-8. doi: 10.1016/j.gene.2007.07.001. Epub 2007 Jul 14. Gene. 2007. PMID: 17761393

7

Promiscuity of enhancer, coding and non-coding transcription functions in ultraconserved elements.

Licastro D, Gennarino VA, Petrera F, Sanges R, Banfi S, Stupka E. Licastro D, et al. Among authors: banfi s. BMC Genomics. 2010 Mar 4;11:151. doi: 10.1186/1471-2164-11-151. BMC Genomics. 2010. PMID: 20202189 Free PMC article.

8

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

Conte I, Carrella S, Avellino R, Karali M, Marco-Ferreres R, Bovolenta P, Banfi S. Conte I, et al. Among authors: banfi s. Proc Natl Acad Sci U S A. 2010 Aug 31;107(35):15491-6. doi: 10.1073/pnas.0914785107. Epub 2010 Aug 16. Proc Natl Acad Sci U S A. 2010. PMID: 20713703 Free PMC article.

9

Vax2 regulates retinoic acid distribution and cone opsin expression in the vertebrate eye.

Alfano G, Conte I, Caramico T, Avellino R, Arnò B, Pizzo MT, Tanimoto N, Beck SC, Huber G, Dollé P, Seeliger MW, Banfi S. Alfano G, et al. Among authors: banfi s. Development. 2011 Jan;138(2):261-71. doi: 10.1242/dev.051037. Epub 2010 Dec 9. Development. 2011. PMID: 21148184

10

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

Peluso I, Conte I, Testa F, Dharmalingam G, Pizzo M, Collin RW, Meola N, Barbato S, Mutarelli M, Ziviello C, Barbarulo AM, Nigro V, Melone MA; European Retinal Disease Consortium; Simonelli F, Banfi S. Peluso I, et al. Among authors: banfi s. Orphanet J Rare Dis. 2013 Jan 28;8:16. doi: 10.1186/1750-1172-8-16. Orphanet J Rare Dis. 2013. PMID: 23356391 Free PMC article.

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