Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Gustincich, S."'
Autor:
Gustincich, S., Batalov, S., Beisel, K. W., Bono, H., Carninci, P., Fletcher, C. F., Grimmond, S., Hirokawa, N., Jarvis, E. D., Jegla, T., Kawasawa, Y., Lemieux, J., Miki, H., Raviola, E., Teasdale, R. D., Tominaga, N., Yagi, K., Zimmer, A., Arakawa, T., Waki, K., Kawai, J., Hayashizaki, Y., Okazaki, Y.
We analyzed the mouse Representative Transcript and Protein Set for molecules involved in brain function.We found full-length cDNAs of many known brain genes and discovered new members of known brain gene families, including Family 3 G-protein couple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2ebbc46f623e2e1a87f5c795a2ffdd5
https://europepmc.org/articles/PMC403671/
https://europepmc.org/articles/PMC403671/
Autor:
Raffaella Calligaris, Gilberto Pizzolato, Sara Finaurini, Piero Carninci, Lucia Antonutti, Remo Sanges, Maria Bertuzzi, Gianni Pezzoli, Dave Tang, Mauro Catalan, Stefano Goldwurm, Stefano Gustincich, Paolo Manganotti, Francesca Persichetti, Christina Vlachouli
Minisatellites, also called variable number of tandem repeats (VNTRs), are a class of repetitive elements that may affect gene expression at multiple levels and have been correlated to disease. Their identification and role as expression quantitative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e0ddb1d9bf67777d6477e203c293610
http://hdl.handle.net/20.500.11767/110181
http://hdl.handle.net/20.500.11767/110181
Autor:
Francesca Fasolo, Remo Sanges, Piero Carninci, Francesca Persichetti, Flavio Mignone, Silvia Zucchelli, Claudio Santoro, Laura Patrucco, Clelia Peano, Carlotta Bon, Diego Cotella, Stefano Gustincich, Massimiliano Volpe, Daniele Sblattero
Publikováno v:
The FASEB Journal
Transposable elements (TEs) compose about half of the mammalian genome and, as embedded sequences, up to 40% of long noncoding RNA (lncRNA) transcripts. Embedded TEs may represent functional domains within lncRNAs, providing a structured RNA platform
Autor:
Paolo Ascenzi, Stefano Espinoza, Mauro Giacca, Margherita Francescatto, Roberta Russo, Daniela Cesselli, Lorena Zentilin, Francesca Persichetti, Marta Codrich, Giampiero Leanza, Stefano Gustincich, Silvia Zucchelli, Maria Bertuzzi, Antonio Paolo Beltrami
Publikováno v:
Cell Death & Disease
Hemoglobin (Hb) is the major protein in erythrocytes and carries oxygen (O2) throughout the body. Recently, Hb has been found synthesized in atypical sites, including the brain. Hb is highly expressed in A9 dopaminergic (DA) neurons of the substantia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::963d0574c7b6ced5d3ea1d12865108cf
http://hdl.handle.net/20.500.11767/48752
http://hdl.handle.net/20.500.11767/48752
Autor:
Luisa Iommarini, Ada Funaro, Stefano Gustincich, Anna Maria Porcelli, Giovanni Stevanin, Alessandro Brussino, Paola Roncaglia, Anna Bartoletti Stella, H Krmac, Giuseppe Gasparre, Cecilia Mancini, Francesca Maltecca, Claudia Cagnoli, Giorgio Casari, Isabelle Le Ber, Sylvie Forlani, Nicola Lo Buono, Maria Antonietta Calvaruso, Alfredo Brusco, Elena Gazzano, Alexandra Durr, Alexis Brice, Dario Ghigo
Publikováno v:
BMC Medical Genomics
BMC Medical Genomics, 2013, 6 (1), pp.22. ⟨10.1186/1755-8794-6-22⟩
BMC Medical Genomics, BioMed Central, 2013, 6 (1), pp.22. ⟨10.1186/1755-8794-6-22⟩
BMC Medical Genomics, 2013, 6 (1), pp.22. ⟨10.1186/1755-8794-6-22⟩
BMC Medical Genomics, BioMed Central, 2013, 6 (1), pp.22. ⟨10.1186/1755-8794-6-22⟩
Background SCA28 is an autosomal dominant ataxia associated with AFG3L2 gene mutations. We performed a whole genome expression profiling using lymphoblastoid cell lines (LCLs) from four SCA28 patients and six unrelated healthy controls matched for se
Autor:
Irma Dianzani, Rossella Crescitelli, Antonella Ronchi, Elisa Robotti, Stefano Gustincich, Lydie Da Costa, Elisa Pavesi, Emilio Marengo, Hélène Moniz, Paola Roncaglia, Anna Aspesi, Claudio Santoro, Narla Mohandas, Steven R. Ellis, Simone Merlin, Ugo Ramenghi, Ilenia Boria, Antonia Follenzi, Federica Avondo
Publikováno v:
Gene
Defects in genes encoding ribosomal proteins cause Diamond Blackfan Anemia (DBA), a red cell aplasia often associated with physical abnormalities. Other bone marrow failure syndromes have been attributed to defects in ribosomal components but the lin
Autor:
Silvia Zucchelli, Jessica Severin, Christina Vlachouli, Carsten O. Daub, Charles Plessy, Yoshihide Hayashizaki, Giovanni Pascarella, Stefano Gustincich, Anne Vassalli, Piero Carninci, Dejan Lazarevic, Claudia Carrieri, Boris Lenhard, Roberto Simone, Geoffrey J. Faulkner, Jun Kawai, Altuna Akalin, Nicolas Bertin, Peter Mombaerts
Publikováno v:
Genome Research
Plessy, C, Pascarella, G, Bertin, N, Akalin, A, Carrieri, C, Vassalli, A, Lazarevic, D, Severin, J, Vlachouli, C, Simone, R, Faulkner, G J, Kawai, J, Daub, C O, Zucchelli, S, Hayashizaki, Y, Mombaerts, P, Lenhard, B, Gustincich, S & Carninci, P 2012, ' Promoter architecture of mouse olfactory receptor genes ', Genome Research, vol. 22, no. 3, pp. 486-497 . https://doi.org/10.1101/gr.126201.111
Genome Research, vol. 22, no. 3, pp. 486-497
Web of Science
ResearcherID
Genome Research; Vol 22
Genome research
Plessy, C, Pascarella, G, Bertin, N, Akalin, A, Carrieri, C, Vassalli, A, Lazarevic, D, Severin, J, Vlachouli, C, Simone, R, Faulkner, G J, Kawai, J, Daub, C O, Zucchelli, S, Hayashizaki, Y, Mombaerts, P, Lenhard, B, Gustincich, S & Carninci, P 2012, ' Promoter architecture of mouse olfactory receptor genes ', Genome Research, vol. 22, no. 3, pp. 486-497 . https://doi.org/10.1101/gr.126201.111
Genome Research, vol. 22, no. 3, pp. 486-497
Web of Science
ResearcherID
Genome Research; Vol 22
Genome research
Odorous chemicals are detected by the mouse main olfactory epithelium (MOE) by about 1100 types of olfactory receptors (OR) expressed by olfactory sensory neurons (OSNs). Each mature OSN is thought to express only one allele of a single OR gene. Majo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce19820f256655a33407cb66746aa137
http://hdl.handle.net/11368/2769409
http://hdl.handle.net/11368/2769409
Autor:
Charles Plessy, Ana Maria Suzuki, Raffaella Calligaris, Salimullah, Piero Carninci, Dave Tang, Stefano Gustincich
Publikováno v:
Nucleic Acids Research
Nucleic Acids Research; Vol 41
Nucleic Acids Research; Vol 41
Template switching (TS) has been an inherent mechanism of reverse transcriptase, which has been exploited in several transcriptome analysis methods, such as CAGE, RNA-Seq and short RNA sequencing. TS is an attractive option, given the simplicity of t