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Genomic and transcriptomic landscape of conjunctival melanoma.
Published in:
PLoS Genetics, 2020, v. 16, n. 12, p. 1, doi. 10.1371/journal.pgen.1009201
By:
- Cisarova, Katarina;
- Folcher, Marc;
- El Zaoui, Ikram;
- Pescini-Gobert, Rosanna;
- Peter, Virginie G.;
- Royer-Bertrand, Beryl;
- Zografos, Leonidas;
- Schalenbourg, Ann;
- Nicolas, Michael;
- Rimoldi, Donata;
- Leyvraz, Serge;
- Riggi, Nicolò;
- Moulin, Alexandre P.;
- Rivolta, Carlo
Publication type:
Article
Immunohistochemical detection of sphingosine-1-phosphate receptor 1 and 5 in human multiple sclerosis lesions.
Published in:
Neuropathology & Applied Neurobiology, 2014, v. 40, n. 5, p. 564, doi. 10.1111/nan.12048
By:
- Brana, Corinne;
- Frossard, Marie José;
- Pescini Gobert, Rosanna;
- Martinier, Nicolas;
- Boschert, Ursula;
- Seabrook, Timothy J.
Publication type:
Article
Heterozygous deletions of noncoding parts of the PRPF31 gene cause retinitis pigmentosa via reduced gene expression.
Published in:
Molecular Vision, 2021, v. 27, p. 107
By:
- Ruberto, Francesco Paolo;
- Balzano, Sara;
- Namburi, Prasanthi;
- Kimchi, Adva;
- Pescini-Gobert, Rosanna;
- Obolensky, Alexey;
- Banin, Eyal;
- Ben-Yosef, Tamar;
- Sharon, Dror;
- Rivolta, Carlo
Publication type:
Article
A New CRB1 Rat Mutation Links Müller Glial Cells to Retinal Telangiectasia.
Published in:
Journal of Neuroscience, 2015, v. 35, n. 15, p. 6093, doi. 10.1523/JNEUROSCI.3412-14.2015
By:
- Min Zhao;
- Andrieu-Soler, Charlotte;
- Kowalczuk, Laura;
- Cortés, María Paz;
- Berdugo, Marianne;
- Dernigoghossian, Marilyn;
- Halili, Francisco;
- Jeanny, Jean-Claude;
- Goldenberg, Brigitte;
- Savoldelli, Michèle;
- Sanharawi, Mohamed El;
- Naud, Marie-Christine;
- van Ijcken, Wilfred;
- Pescini-Gobert, Rosanna;
- Martinet, Danielle;
- Maass, Alejandro;
- Wijnholds, Jan;
- Crisanti, Patricia;
- Rivolta, Carlo;
- Behar-Cohen, Francine
Publication type:
Article

Found: 4

Genomic and transcriptomic landscape of conjunctival melanoma.

Immunohistochemical detection of sphingosine-1-phosphate receptor 1 and 5 in human multiple sclerosis lesions.

Heterozygous deletions of noncoding parts of the PRPF31 gene cause retinitis pigmentosa via reduced gene expression.

A New CRB1 Rat Mutation Links Müller Glial Cells to Retinal Telangiectasia.