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1 - 25 of 75 results for author:"Rocchi M." in Literature citations

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Lack of TIR8/SIGIRR triggers progression of chronic lymphocytic leukemia in mouse models.

Bertilaccio M.T., Simonetti G., Dagklis A., Rocchi M., Rodriguez T.V., Apollonio B., Mantovani A., Ponzoni M., Ghia P., Garlanda C. et al.

Blood 118:660-669(2011) · Mapped (10)

HS1 has a central role in the trafficking and homing of leukemic B cells.

Scielzo C., Bertilaccio M.T., Simonetti G., Dagklis A., ten Hacken E., Fazi C., Muzio M., Caiolfa V., Kitamura D., Restuccia U. et al.

Blood 116:3537-3546(2010) · Mapped (11)

CBFA2T2 and C20orf112: two novel fusion partners of RUNX1 in acute myeloid leukemia.

Guastadisegni M.C., Lonoce A., Impera L., Di Terlizzi F., Fugazza G., Aliano S., Grasso R., Cluzeau T., Raynaud S., Rocchi M. et al.

Leukemia 24:1516-1519(2010) · Mapped (6)

Genetic modulation of the Let-7 microRNA binding to KRAS 3'-untranslated region and survival of metastatic colorectal cancer patients treated with salvage cetuximab-irinotecan.

Graziano F., Canestrari E., Loupakis F., Ruzzo A., Galluccio N., Santini D., Rocchi M., Vincenzi B., Salvatore L., Cremolini C. et al.

Pharmacogenomics J. 10:458-464(2010) · Mapped (10)

Genome sequence, comparative analysis, and population genetics of the domestic horse.

Wade C.M., Giulotto E., Sigurdsson S., Zoli M., Gnerre S., Imsland F., Lear T.L., Adelson D.L., Bailey E., Bellone R.R. et al.

Science 326:865-867(2009) · UniProtKB (22,397)

DDX11L: a novel transcript family emerging from human subtelomeric regions.

Costa V., Casamassimi A., Roberto R., Gianfrancesco F., Matarazzo M.R., D'Urso M., D'Esposito M., Rocchi M., Ciccodicola A.

BMC Genomics 10:250-250(2009) · UniProtKB (7)

The rest repression of the neurosecretory phenotype is negatively modulated by BHC80, a protein of the BRAF/HDAC complex.

Klajn A., Ferrai C., Stucchi L., Prada I., Podini P., Baba T., Rocchi M., Meldolesi J., D'Alessandro R.

J. Neurosci. 29:6296-6307(2009) · Mapped (3)

A novel fusion 5'AFF3/3'BCL2 originated from a t(2;18)(q11.2;q21.33) translocation in follicular lymphoma.

Impera L., Albano F., Lo Cunsolo C., Funes S., Iuzzolino P., Laveder F., Panagopoulos I., Rocchi M., Storlazzi C.T.

Oncogene 27:6187-6190(2008) · Mapped (8)

Efficacy of LL-37 and granulocyte colony-stimulating factor in a neutropenic murine sepsis due to Pseudomonas aeruginosa.

Cirioni O., Ghiselli R., Tomasinsig L., Orlando F., Silvestri C., Skerlavaj B., Riva A., Rocchi M., Saba V., Zanetti M. et al.

Shock 30:443-448(2008) · Mapped (4)

CYP3 phylogenomics: evidence for positive selection of CYP3A4 and CYP3A7.

Qiu H., Taudien S., Herlyn H., Schmitz J., Zhou Y., Chen G., Roberto R., Rocchi M., Platzer M., Wojnowski L.

Pharmacogenet. Genomics 18:53-66(2008) · UniProtKB (18)

Upregulation of the SOX5 by promoter swapping with the P2RY8 gene in primary splenic follicular lymphoma.

Storlazzi C.T., Albano F., Lo Cunsolo C., Doglioni C., Guastadisegni M.C., Impera L., Lonoce A., Funes S., Macri E., Iuzzolino P. et al.

Leukemia 21:2221-2225(2007) · Mapped (7)

Evolutionary and biomedical insights from the rhesus macaque genome.

Gibbs R.A., Rogers J., Katze M.G., Bumgarner R., Weinstock G.M., Mardis E.R., Remington K.A., Strausberg R.L., Venter J.C., Wilson R.K. et al.

Science 316:222-234(2007) · UniProtKB (35,178)

Heterochromatin protein 1 interacts with 5'UTR of transposable element ZAM in a sequence-specific fashion.

Minervini C.F., Marsano R.M., Casieri P., Fanti L., Caizzi R., Pimpinelli S., Rocchi M., Viggiano L.

Gene 393:1-10(2007) · Mapped (18)

SSADH variation in primates: intra- and interspecific data on a gene with a potential role in human cognitive functions.

Blasi P., Palmerio F., Aiello A., Rocchi M., Malaspina P., Novelletto A.

J. Mol. Evol. 63:54-68(2006) · Mapped (5)

A Ph-negative chronic myeloid leukemia with a complex BCR/ABL rearrangement and a t(6;9)(p21;q34.1).

Todoric-Zivanovic B., Marisavljevic D., Surace C., Cemerikic V., Markovic O., Krtolica K., Tatomirovic Z., Cikota B., Magic Z., Rocchi M.

Cancer Genet. Cytogenet. 166:180-185(2006) · Mapped (28)

Uridine diphosphate glucuronosyl transferase 1A1 promoter polymorphism predicts the risk of gastrointestinal toxicity and fatigue induced by irinotecan-based chemotherapy.

Massacesi C., Terrazzino S., Marcucci F., Rocchi M.B., Lippe P., Bisonni R., Lombardo M., Pilone A., Mattioli R., Leon A.

Cancer 106:1007-1016(2006) · Mapped (27)

Identification of a novel IGH-MMSET fusion transcript in a human myeloma cell line with the t(4;14)(p16.3;q32) chromosomal translocation.

Intini D., Fabris S., Storlazzi T., Otsuki T., Ciceri G., Verdelli D., Lombardi L., Rocchi M., Neri A.

Br. J. Haematol. 126:437-439(2004) · UniProtKB (1)

Neocentromeres in 15q24-26 map to duplicons which flanked an ancestral centromere in 15q25.

Ventura M., Mudge J.M., Palumbo V., Burn S., Blennow E., Pierluigi M., Giorda R., Zuffardi O., Archidiacono N., Jackson M.S. et al.

Genome Res. 13:2059-2068(2003) · UniProtKB (1)

Heterogeneous pattern of chromosomal breakpoints involving the MYC locus in multiple myeloma.

Fabris S., Storlazzi C.T., Baldini L., Nobili L., Lombardi L., Maiolo A.T., Rocchi M., Neri A.

Genes Chromosomes Cancer 37:261-269(2003) · Mapped (3)

Complex events in the evolution of the human pseudoautosomal region 2 (PAR2).

Charchar F.J., Svartman M., El-Mogharbel N., Ventura M., Kirby P., Matarazzo M.R., Ciccodicola A., Rocchi M., D'Esposito M., Graves J.A.

Genome Res. 13:281-286(2003) · UniProtKB (1)

Ultrastructural morphometrical and immunocytochemical analyses of hepatocyte nuclei from mice fed on genetically modified soybean.

Malatesta M., Caporaloni C., Gavaudan S., Rocchi M.B., Serafini S., Tiberi C., Gazzanelli G.

Cell Struct. Funct. 27:173-180(2002) · Mapped (7)

A human short-chain dehydrogenase/reductase gene: structure, chromosomal localization, tissue expression and subcellular localization of its product.

Pellegrini S., Censini S., Guidotti S., Iacopetti P., Rocchi M., Bianchi M., Covacci A., Gabrielli F.

Biochim. Biophys. Acta 1574:215-222(2002) · UniProtKB (1) · Mapped (2)

Divergent origins and concerted expansion of two segmental duplications on chromosome 16.

Eichler E.E., Johnson M.E., Alkan C., Tuzun E., Sahinalp C., Misceo D., Archidiacono N., Rocchi M.

J. Hered. 92:462-468(2001) · UniProtKB (1)

Assignment to chromosome 12q24.33, gene organization and splicing of the human KRAB/FPB containing zinc finger gene ZNF84.

Rosati M., Rocchi M., Storlazzi C.T., Grimaldi G.

Cytogenet. Cell Genet. 94:127-130(2001) · Mapped (1)

Human paralogs of KIAA0187 were created through independent pericentromeric-directed and chromosome-specific duplication mechanisms.

Crosier M., Viggiano L., Guy J., Misceo D., Stones R., Wei W., Hearn T., Ventura M., Archidiacono N., Rocchi M. et al.

Genome Res. 12:67-80(2002) · Mapped (1)

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