ZOLLO, MASSIMO

ZOLLO, MASSIMO  

Dipartimento di Medicina molecolare e Biotecnologie mediche  

Mostra records
Risultati 1 - 20 di 153 (tempo di esecuzione: 0.09 secondi).
Titolo Data di pubblicazione Autore(i) File
8th International Congress of the NDPKinase/Nm23/awd Family-From Basic Science to Clinical Application- 1-gen-2010 Zollo, Massimo
A critical evaluation of biochemical activities reported for the nucleoside diphosphate kinase/Nm23/Awd family proteins: opportunities and missteps in understanding their biological functions. 1-gen-2011 Steeg, Ps; Zollo, Massimo; Wieland, T.
A mammalian homolog of the Drosophila retinal degeneration B gene: implications for the evolution of phototransduction mechanisms. 1-gen-1997 Rubboli, F; Bulfone, A; Bogni, S; Marchitiello, A; Zollo, Massimo; Borsani, G; Ballabio, Andrea; Banfi, S.
A mammalian homologue of the Drosophila retinal degeneration B gene: implications for the evolution of phototransduction mechanisms. 1-gen-1997 Rubboli, F; Zollo, Massimo
A manual high-throughput M13 DNA preparation 1-gen-1994 Zollo, Massimo; Chen, E. Y.
A method for point mutation analysis that links SSCP and dye primer fluorescent sequencing 1-gen-1998 Chiarelli, I; Zollo, Massimo
A method to direct sequence cosmid LAWRIST16 clones. 1-gen-1997 Repetto, M; Zollo, Massimo
A method to direct sequence cosmid LAWRIST16 clones. 1-gen-1997 Repetto, M; Ballabio, Andrea; Zollo, Massimo
A new candidate region for the positional cloning of the XLP gene 1-gen-1998 A., Bolino; L., Yi; M., Seri; R., Cusano; R., Cinti; A., Coffey; R., Brooksbank; G., Howell; D., Bentley; Jr, Davis; A., Lanyi; D., Huang; M., Stark; M., Creaven; L., Bjrkhaug; F., Heitzmann; J., Lamartine; S., Gaudi; Bs, Sylla; Gm, Lenoir; E., Castagnola; R., Giacchino; G., Porta; Franco, Brunella; Zollo, Massimo; J., Sumegi; G., Romeo
A Structurally Simple Vaccine Candidate Reduces Progression and Dissemination of Triple-Negative Breast Cancer 1-gen-2020 Amedei, A.; Asadzadeh, F.; Papi, F.; Vannucchi, M. G.; Ferrucci, V.; Bermejo, I. A.; Fragai, M.; De Almeida, C. V.; Cerofolini, L.; Giuntini, S.; Bombaci, M.; Pesce, E.; Niccolai, E.; Natali, F.; Guarini, E.; Gabel, F.; Traini, C.; Catarinicchia, S.; Ricci, F.; Orzalesi, L.; Berti, F.; Corzana, F.; Zollo, M.; Grifantini, R.; Nativi, C.
Allelic polymorphisms in the transcriptional regulatory region of human SEL1L. 1-gen-2001 Cattaneo, M; Zollo, Massimo
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 1-gen-2019 Salpietro1, Vincenzo; 3, 2; 140, ; Dixon4, Christine L.; 140, ; Guo5, Hui; 140, 6; Bello Stephanie Efthymiou 1, Oscar D.; 4, ; Maroofian1, Reza; Heimer7, Gali; 8, Lydie Burglen; 9, Stephanie Valence; Torti 10, Erin; Hacke11, Moritz; Rankin12, Julia; Tariq1, Huma; Colin13, Estelle; 14, ; Procaccio13, Vincent; 14, ; Striano2, Pasquale; 3, ; Mankad15, Kshitij; 4, Andreas Lieb; Chen16, Sharon; Pisani16, Laura; Bettencourt 17, Conceicao; 1, Roope Männikkö; Manole1, Andreea; Brusco 18, Alfredo; Grosso18, Enrico; Battista Ferrero19, Giovanni; Armstrong-Moron20, Judith; Gueden21, Sophie; Bar-Yosef7, Omer; Tzadok7, Michal; Monaghan10, Kristin G.; Santiago-Sim10, Teresa; Person10, Richard E.; Cho10, Megan T.; Willaert10, Rebecca; Yoo22, Yongjin; Chae23, Jong-Hee; Quan6, Yingting; Wu6, Huidan; Wang5, Tianyun; 6, ; Bernier24, Raphael A.; Xia6, Kun; Blesson25, Alyssa; Jain25, Mahim; Motazacker26, Mohammad M.; Jaeger27, Bregje; Schneider 28, Amy L.; Boysen28, Katja; Muir 29, Alison M.; Myers30, Candace T.; Gavrilova31, Ralitza H.; Gunderson31, Lauren; Schultz-Rogers 31, Laura; Klee31, Eric W.; Dyment32, David; Osmond32, Matthew; 34, 33; Parellada35, Mara; Llorente36, Cloe; Gonzalez-Peñas37, Javier; Carracedo38, Angel; 39, ; Van Haeringen40, Arie; Ruivenkamp40, Claudia; Nava41, Caroline; Heron41, Delphine; Nardello42, Rosaria; Iacomino43, Michele; Minetti2, Carlo; 3, ; Skabar44, Aldo; Fabretto44, Antonella; Study GroupMiquel Raspall-Chaure45, Synaps; Chez46, Michael; Tsai47, Anne; Fassi48, Emily; Shinawi48, Marwan; Constantino49, John N.; De Zorzi50, Rita; Fortuna 50, Sara; Kok51, Fernando; 52, ; Keren41, Boris; Bonneau13, Dominique; 14, ; Choi 22, Murim; Benzeev7, Bruria; Zara43, Federico; Mefford29, Heather C.; Scheffer28, Ingrid E.; Clayton-Smith53, Jill; 54, ; Macaya45, Alfons; Rothman4, James E.; 55, ; Eichler 5, Evan E.; 56, ; Kullmann 4 &, Dimitri M.; 1, Henry Houlden; Hanna1, SYNAPS Study Group Michael G.; Bugiardini1, Enrico; Hostettler1, Isabel; O’Callaghan1, Benjamin; Khan1, Alaa; Cortese1, Andrea; O’Connor1, Emer; Yau1, Wai Y.; Bourinaris1, Thomas; Kaiyrzhanov1, Rauan; Chelban1, Viorica; Madej1, Monika; Diana2, Maria C.; Vari2, Maria S.; Pedemonte2, Marina; Bruno2, Claudio; Balagura3, Ganna; Scala3, Marcello; Fiorillo3, Chiara; Nobili3, Lino; Malintan4, Nancy T.; Zanetti4, Maria N.; Krishnakumar4, Shyam S.; Lignani4, Gabriele; Jepson4, James E. C.; Broda43, Paolo; Baldassari43, Simona; Rossi43, Pia; Fruscione43, Floriana; Madia43, Francesca; Traverso43, Monica; De-Marco43, Patrizia; Pérez-Dueñas45, Belen; Munell45, Francina; Kriouile57, Yamna; El-Khorassani57, Mohamed; Karashova58, Blagovesta; Avdjieva58, Daniela; Kathom58, Hadil; Tincheva58, Radka; Van-Maldergem59, Lionel; Nachbauer60, Wolfgang; Boesch60, Sylvia; Gagliano61, Antonella; Amadori62, Elisabetta; Goraya63, Jatinder S.; Sultan64, Tipu; Kirmani65, Salman; Ibrahim66, Shahnaz; Jan66, Farida; Mine67, Jun; Banu68, Selina; Veggiotti69, Pierangelo; Zuccotti69, Gian V.; Ferrari70, Michel D.; Van Den Maagdenberg70, Arn M. J.; Verrotti71, Alberto; Marseglia72, Gian L.; Savasta72, Salvatore; Soler73, Miguel A.; Scuderi74, Carmela; Borgione74, Eugenia; Chimenz75, Roberto; Gitto75, Eloisa; Dipasquale75, Valeria; Sallemi75, Alessia; Fusco75, Monica; Cuppari75, Caterina; Cutrupi75, Maria C.; Ruggieri76, Martino; Cama77, Armando; Capra77, Valeria; Mencacci78, Niccolò E.; Boles79, Richard; Gupta80, Neerja; Kabra80, Madhulika; Papacostas81, Savvas; Zamba-Papanicolaou81, Eleni; Dardiotis82, Efthymios; Maqbool83, Shazia; Rana84, Nuzhat; Atawneh85, Osama; Lim86, Shen Y.; Shaikh87, Farooq; Koutsis88, George; Breza88, Marianthi; Coviello89, Domenico A.; Dauvilliers90, Yves A.; Alkhawaja91, Issam; Alkhawaja92, Mariam; Al-Mutairi93, Fuad; Stojkovic94, Tanya; Ferrucci, Veronica; Zollo, Massimo; Alkuraya96, Fowzan S.; Kinali97, Maria; Sherifa98, Hamed; Benrhouma99, Hanene; Turki99, Ilhem B. Y.; Tazir100, Meriem; Obeid101, Makram; Bakhtadze102, Sophia; Saadi103, Nebal W.; Zaki104, Maha S.; Triki105, Chahnez C.; Benfenati106, Fabio; Gustincich106, Stefano; Kara107, Majdi; Belcastro108, Vincenzo; Specchio109, Nicola; Capovilla110, Giuseppe; Karimiani111, Ehsan G.; Salih112, Ahmed M.; Okubadejo113, Njideka U.; Ojo113, Oluwadamilola O.; Oshinaike113, Olajumoke O.; Oguntunde113, Olapeju; Wahab114, Kolawole; Bello114, Abiodun H.; Abubakar115, Sanni; Obiabo116, Yahaya; Nwazor117, Ernest; Ekenze118, Oluchi; Williams119, Uduak; Iyagba120, Alagoma; Taiwo121, Lolade; Komolafe122, Morenikeji; Senkevich123, Konstantin; Shashkin124, Chingiz; Zharkynbekova125, Nazira; Koneyev126, Kairgali; Manizha127, Ganieva; Isrofilov127, Maksud; Guliyeva128, Ulviyya; Salayev129, Kamran; Khachatryan130, Samson; Rossi131, Salvatore; Silvestri131, Gabriella; Haridy132, Nourelhoda; Ramenghi133, Luca A.; Xiromerisiou134, Georgia; David135, Emanuele; Aguennouz136, Mhammed; Fidani137, Liana; Spanaki138 &, Cleanthe; Tucci139, Arianna
Amplification and overexpression of PRUNE in human sarcomas and breast carcinomas - a possible mechanism for altering the nm23-H1 activity 1-gen-2001 Forus, A; Zollo, Massimo
Amplification and overexpression of PRUNE in human sarcomas and breast carcinomas – a possible mechanism for altering the nm23-H1 activity. 1-gen-2001 Forus, A; D'Angelo, A; Henriksen, J; Merla, G; MAELANDSMO G., M; FLRENES V., A; Olivieri, S; Bjerkehagen, B; MEZAZEPEDA L., A; DEL VECCHIO BLANCO, F; Muller, C; Sanvito, F; Kononen, J; NESLAND J., M; Fodstad, ; Reymond, A; Kallioniemi, Op; Arrigoni, G; Ballabio, Andrea; Myklebost, O; AND ZOLLO, M.
ASAP1 promotes tumor cell motility and invasiveness, stimulates metastasis formation in vivo, and correlates with poor survival in colorectal cancer patients. 1-gen-2010 Müller, T.; Stein, U.; Poletti, A.; Garzia, L.; Rothley, M.; Plaumann, D.; Thiele, W.; Bauer, M.; Galasso, A.; Schlag, P.; Pankratz, M.; Zollo, Massimo; Sleeman, J. P.
Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination 1-gen-2019 Efthymiou, S.; Salpietro, V.; Malintan, N.; Poncelet, M.; Kriouile, Y.; Fortuna, S.; De Zorzi, R.; Payne, K.; Henderson, L. B.; Cortese, A.; Maddirevula, S.; Alhashmi, N.; Wiethoff, S.; Ryten, M.; Botia, J. A.; Provitera, V.; Schuelke, M.; Vandrovcova, J.; Walsh, L.; Torti, E.; Iodice, V.; Najafi, M.; Karimiani, E. G.; Maroofian, R.; Siquier-Pernet, K.; Boddaert, N.; De Lonlay, P.; Cantagrel, V.; Aguennouz, M.; El Khorassani, M.; Schmidts, M.; Alkuraya, F. S.; Edvardson, S.; Nolano, M.; Devaux, J.; Houlden, H.; Groppa, S.; Karashova, B. M.; Nachbauer, W.; Boesch, S.; Arning, L.; Timmann, D.; Cormand, B.; Perez-Duenas, B.; Goraya, J. S.; Sultan, T.; Mine, J.; Avdjieva, D.; Kathom, H.; Tincheva, R.; Banu, S.; Pineda-Marfa, M.; Veggiotti, P.; Ferrari, M. D.; Van Den Maagdenberg, A. M. J. M.; Verrotti, A.; Marseglia, G.; Savasta, S.; Garcia-Silva, M.; Ruiz, A. M.; Garavaglia, B.; Borgione, E.; Portaro, S.; Sanchez, B. M.; Boles, R.; Papacostas, S.; Vikelis, M.; Rothman, J.; Kullmann, D.; Papanicolaou, E. Z.; Dardiotis, E.; Maqbool, S.; Ibrahim, S.; Kirmani, S.; Rana, N. N.; Atawneh, O.; Lim, S. -Y.; Shaikh, F.; Koutsis, G.; Breza, M.; Mangano, S.; Scuderi, C.; Borgione, E.; Morello, G.; Stojkovic, T.; Zollo, M.; Heimer, G.; Dauvilliers, Y. A.; Minetti, C.; Al-Khawaja, I.; Al-Mutairi, F.; Hamed, S.; Pipis, M.; Bettencourt, C.; Rinaldi, S.
Biomarcatore per la rilevazione di cellule tumorali circolanti e relativi metodi e kit di rilevazione 1-gen-2011 Zollo, Massimo
CHARACTERIZATION OF A TRANSGENIC MOUSE MODEL OVEREXPRESSING H-PRUNE INTO EPIDERMIS 1-gen-2012 M ZOLLO
Cloning and functional analysis of SEL1L promoter region, a pancreas-specific gene. 1-gen-2001 Cattaneo, M; Zollo, Massimo
Common variants at 21q22.3 locus influence MX1 and TMPRSS2 gene expression and susceptibility to severe COVID-19 1-gen-2021 Andolfo, Immacolata; Russo, Roberta; Lasorsa, Vito Alessandro; Cantalupo, Sueva; Rosato, Barbara Eleni; Bonfiglio, Ferdinando; Frisso, Giulia; Abete, Pasquale; Cassese, Gian Marco; Servillo, Giuseppe; Esposito, Gabriella; Gentile, Ivan; Piscopo, Carmelo; Villani, Romolo; Fiorentino, Giuseppe; Cerino, Pellegrino; Buonerba, Carlo; Pierri, Biancamaria; Zollo, Massimo; Iolascon, Achille; Capasso, Mario