Profilo personale

Nicoletta Rossi

Le informazioni pubblicate in questa pagina sono gestite in completa autonomia da NICOLETTA ROSSI il/la quale se ne assume ogni responsabilità

Prodotti della ricerca

Patrizia Calandra1, Nicoletta Rossi 1, Richard J. L. F. Lemmers 2, Emanuela Teveroni 1, Mauro Monforte 3, Giorgio Tasca3 , Enzo Ricci 3, Fabiola Moretti1 , Silvère M. van der Maarel2 , Giancarlo Deidda1 .

Methylation of the Region Distal to the D4Z4 Array is Lower Than Predicted in FSHD1

(2019) 26th Annual FSHD International Research Congress, June 19-20, 2019
Bret A. Moore1, Brian C. Leonard2, Lionel Sebbag1, Sydney G. Edwards1, Ann Cooper1, Denise M. Imai3, 4, Luis Santos4, Christopher Reilly3, Stephen M. Griffey3, Lynette Bower5, David Clary5, 6, Michel J. Roux 7,8,9,10,11, Hamid Meziane7,8,9,10,11, Ewan Straiton Jeremy Mason Yann Herault Ann M. Flenniken12,14, Lauryl M.J. Nutter12,13, Zorana Berberovic12,14, Celeste Owen12,14, Susan Newbigging12,14, Hibret Adissu12,14, Mohammed Eskandarian12,14, Chih-Wei Hsu15, Sowmya Kalaga15, Uchechukwu Udensi15, Chinwe Asomugha15, Ritu Bohat16, Juan J. Gallegos16, John R. Seavitt16, Jason D. Heaney16, Arthur L. Beaudet16, Mary E. Dickinson15,16, Monica J. Justice12,13,16, Vivek Philip17, Vivek Kumar 17, Karen L. Svenson17, Robert E. Braun17, Sara Wells4, Heather Cater4, Michelle Stewart4, Sharon Clementson-Mobbs4, Russell Joynson4, Xiang Gao18, Tomohiro Suzuki19, Shigeharu Wakana 19, Damian Smedley20, J. K Seong21, Glauco Tocchini-Valentini22, Mark Moore23, Colin Fletcher24, Natasha Karp25, Ramiro Ram...

Identification of genes required for eye development by high-throughput screening of mouse knockouts

Bret A. Moore1, Brian C. Leonard2, Lionel Sebbag1, Sydney G. Edwards1, Ann Cooper1, Denise M. Imai3, 4, Luis Santos4, Christopher Reilly3, Stephen M. Griffey3, Lynette Bower5, David Clary5, 6, Michel J. Roux 7,8,9,10,11, Hamid Meziane7,8,9,10,11, Ewan Straiton Jeremy Mason Yann Herault Ann M. Flenniken12,14, Lauryl M.J. Nutter12,13, Zorana Berberovic12,14, Celeste Owen12,14, Susan Newbigging12,14, Hibret Adissu12,14, Mohammed Eskandarian12,14, Chih-Wei Hsu15, Sowmya Kalaga15, Uchechukwu Udensi15, Chinwe Asomugha15, Ritu Bohat16, Juan J. Gallegos16, John R. Seavitt16, Jason D. Heaney16, Arthur L. Beaudet16, Mary E. Dickinson15,16, Monica J. Justice12,13,16, Vivek Philip17, Vivek Kumar 17, Karen L. Svenson17, Robert E. Braun17, Sara Wells4, Heather Cater4, Michelle Stewart4, Sharon Clementson-Mobbs4, (2018) in Communications biology
Rozman J.; Rathkolb B.; Oestereicher M.A.; Schutt C.; Ravindranath A.C.; Leuchtenberger S.; Sharma S.; Kistler M.; Willershauser M.; Brommage R.; Meehan T.F.; Mason J.; Haselimashhadi H.; Aguilar-Pimentel A.; Becker L.; Treise I.; Moreth K.; Garrett L.; Holter S.M.; Zimprich A.; Marschall S.; Amarie O.V.; Calzada-Wack J.; Neff F.; Brachthauser L.; Lengger C.; Stoeger C.; Zapf L.; Cho Y.-L.; Da Silva-Buttkus P.; Kraiger M.J.; Mayer-Kuckuk P.; Gampe K.K.; Wu M.; Conte N.; Warren J.; Chen C.-K.; Tudose I.; Relac M.; Matthews P.; Cater H.L.; Natukunda H.P.; Cleak J.; Teboul L.M.; Clementson-Mobbs S.; Szoke-Kovacs Z.; Walling A.P.; Johnson S.J.; Codner G.F.; Fiegel T.; Ring N.; Westerberg H.; Greenaway S.; Sneddon D.; Morgan H.; Loeffler J.; Stewart M.E.; Ramirez-Solis R.; Bradley A.; Skarnes W.C.; Steel K.P.; Maguire S.A.; Dench J.; Lafont D.; Vancollie V.E.; Pearson S.A.; Gates A.S.; Sanderson M.; Shannon C.; Anthony L.F.E.; Sumowski M.T.; McLaren R.S.B.; Doe B.; Wardle-Jones H.; Griffith...

Identification of genetic elements in metabolism by high-throughput mouse phenotyping

(2018) in Nature communications
Patrizia Calandra1, Nicoletta Rossi 1, Richard J. L. F. Lemmers 2, Emanuela Teveroni 1, Mauro Monforte 3, Enzo Ricci 3, Fabiola Moretti 1, Silvère M. van der Maarel 2, Giancarlo Deidda 1.

Large-scale methylation analysis in facioscapulohumeral muscular dystrophy (FSHD)

(2018) FSH Society Facioscapulohumeral Muscular Dystrophy [FSHD] 2018 International Research Congress & Research Planning Meetings, las vegas NV USA, June 8-9, 2018
Meehan T.F.; Conte N.; West D.B.; Jacobsen J.O.; Mason J.; Warren J.; Chen C.-K.; Tudose I.; Relac M.; Matthews P.; Karp N.; Santos L.; Fiegel T.; Ring N.; Westerberg H.; Greenaway S.; Sneddon D.; Morgan H.; Codner G.F.; Stewart M.E.; Brown J.; Horner N.; International Mouse Phenotyping Consortium; Haendel M.; Washington N.; Mungall C.J.; Reynolds C.L.; Gallegos J.; Gailus-Durner V.; Sorg T.; Pavlovic G.; Bower L.R.; Moore M.; Morse I.; Gao X.; Tocchini-Valentini G.P.; Obata Y.; Cho S.Y.; Seong J.K.; Seavitt J.; Beaudet A.L.; Dickinson M.E.; Herault Y.; Wurst W.; De Angelis M.H.; Kent Lloyd K.C.; Flenniken A.M.; Nutter L.M.J.; Newbigging S.; McKerlie C.; Justice M.J.; Murray S.A.; Svenson K.L.; Braun R.E.; White J.K.; Bradley A.; Flicek P.; Wells S.; Skarnes W.C.; Adams D.J.; Parkinson H.; Mallon A.-M.; Brown S.D.M.; Smedley D.

Disease model discovery from 3,328 gene knockouts by the International Mouse Phenotyping Consortium

(2017) in Nature genetics (Print)
Bowl M.R.; Simon M.M.; Ingham N.J.; Greenaway S.; Santos L.; Cater H.; Taylor S.; Mason J.; Kurbatova N.; Pearson S.; Bower L.R.; Clary D.A.; Meziane H.; Reilly P.; Minowa O.; Kelsey L.; Allen S.; Clementson-Mobbs S.; Codner G.; Fray M.; Gardiner W.; Joynson R.; Kenyon J.; Loeffler J.; Nell B.; Parker A.; Quwailid D.; Stewart M.; Walling A.; Zaman R.; Chen C.-K.; Conte N.; Matthews P.; Relac M.; Tudose I.; Warren J.; Le Marchand E.; El Amri A.; El Fertak L.; Ennah H.; Ali-Hadji D.; Ayadi A.; Wattenhofer-Donze M.; Moulaert D.; Jacquot S.; Andre P.; Birling M.-C.; Pavlovic G.; Lalanne V.; Lux A.; Riet F.; Mittelhaeuser C.; Bour R.; Guimond A.; Bam'Hamed C.; Leblanc S.; Vasseur L.; Selloum M.; Sorg T.; Ayabe S.; Furuse T.; Kaneda H.; Kobayashi K.; Masuya H.; Miura I.; Obata Y.; Suzuki T.; Tamura M.; Tanaka N.; Yamada I.; Yoshiki A.; Berberovic Z.; Bubshait M.; Cabezas J.; Carroll T.; Clark G.; Clarke S.; Creighton A.; Danisment O.; Eskandarian M.; Feugas P.; Gertsenstein M.; Guo R.; Hunte...

A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction

(2017) in Nature communications
de Angelis MH, Nicholson G, Selloum M, White JK, Morgan H, Ramirez-Solis R, Sorg T, Wells S, Fuchs H, Fray M, Adams DJ, Adams NC, Adler T, Aguilar-Pimentel A, Ali-Hadji D, Amann G, André P, Atkins S, Auburtin A, Ayadi A, Becker J, Becker L, Bedu E, Bekeredjian R, Birling MC, Blake A, Bottomley J, Bowl MR, Brault V, Busch DH, Bussell JN, Calzada-Wack J, Cater H, Champy MF, Charles P, Chevalier C, Chiani F, Codner GF, Combe R, Cox R, Dalloneau E, Dierich A, Di Fenza A, Doe B, Duchon A, Eickelberg O, Esapa CT, Fertak LE, Feigel T, Emelyanova I, Estabel J, Favor J, Flenniken A, Gambadoro A, Garrett L, Gates H, Gerdin AK, Gkoutos G, Greenaway S, Glasl L, Goetz P, Da Cruz IG, Götz A, Graw J, Guimond A, Hans W, Hicks G, Hölter SM, Höfler H, Hancock JM, Hoehndorf R, Hough T, Houghton R, Hurt A, Ivandic B, Jacobs H, Jacquot S, Jones N, Karp NA, Katus HA, Kitchen S, Klein-Rodewald T, Klingenspor M, Klopstock T, Lalanne V, Leblanc S, Lengger C, le Marchand E, Ludwig T, Lux A, McKerlie C, Maie...

Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics

(2015) in Nature genetics (Print)
Glauco P. Tocchini-Valentini and the Members of EMMA - INFRAFRONTIER - IMPC Monterotondo

EMMA - INFRAFRONTIER - IMPC Monterotondo Mouse Clinic (MMC)

(2014) 2014 IMPC Annual Meeting, Barcellona, 11 - 13 novembre
Putti S.1; Calandra P.; Rossi N.; Scarabino D.; Deidda G.; Tocchini-Valentini G.P.

Highly efficient, in vivo optimized, archaeal endonuclease for controlled RNA splicing in mammalian cells

(2013) in The FASEB journal
Gates, Hilary; Mallon, Ann-Marie; Brown, Steve D. M.

High-throughput mouse phenotyping

(2011) in Methods (S. Diego Calif. Print)
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