Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Roberta, Galavotti"'
Autor:
Cristina Tecchio, Angelo Andreini, Claudio Costantini, Alberto Zamò, Donata de Sabata, Fiorenza Aprili, Roberta Galavotti, Emanuele Guardalben, Fabio Benedetti
Publikováno v:
Hematology Reports, Vol 9, Iss 4 (2018)
The prognosis of patients affected by myelofibrosis (MF) is usually dismal and allogeneic hematopoietic stem cell transplantation (HSCT) remains the only cure. The number of HSCTs in MF patients has recently increased. However, a major obstacle is st
Externí odkaz:
https://doaj.org/article/ac444d9f52934852ab829116789a9ffc
Autor:
Angelo Andreini, Emanuele Guardalben, Donata de Sabata, Fiorenza Aprili, Claudio Costantini, Alberto Zamò, Cristina Tecchio, Fabio Benedetti, Roberta Galavotti
Publikováno v:
Hematology Reports
Hematology Reports, Vol 9, Iss 4 (2018)
Hematology Reports, Vol 9, Iss 4 (2018)
The prognosis of patients affected by myelofibrosis (MF) is usually dismal and allogeneic hematopoietic stem cell transplantation (HSCT) remains the only cure. The number of HSCTs in MF patients has recently increased. However, a major obstacle is st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08166c9fb445ae2fae849bfe112e401e
http://hdl.handle.net/2318/1671208
http://hdl.handle.net/2318/1671208
Autor:
Roberta Galavotti, Simone Cesaro, Paola De Filippi, Claudia Cagioni, Ada Zaccaron, Marco Zecca, Cesare Danesino, Chiara Cugno, Anna Leszl, Geertruy te Kronnie, Silvia Bresolin, Svetlana Donska, Annamaria Di Meglio, Fiorenza Aprili
Publikováno v:
International Journal of Hematology. 99:208-212
A twin pair affected by juvenile myelomonocytic leukemia (JMML) with the same somatic PTPN11 mutation and abnormal chromosome 7 in bone marrow samples but distinct prognostic gene expression signatures, received a matched-unrelated donor and matched-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37cc8c1f451e5c5b7201f9418dc6f2ac
https://doi.org/10.1007/s12185-013-1489-3
https://doi.org/10.1007/s12185-013-1489-3
Autor:
Heiko, Witt, Miklos Sahin Toth, Olfert, Landt, Jian Min Chen, Thilo, Kahne, Drenth, Joost P. H., Zoltan, Kukor, Edit, Szepessy, Walter, Halangk, Stefan, Dahm, Klaus, Rohde, Hans Ulrich Schulz, Cedric Le Marechal, Nejat, Akar, Ammann, Rudolf W., Kaspar, Truninger, Mario, Bargetzi, Eesh, Bhatia, Carlo, Castellani, Giulia Martina Cavestro, Milos, Cerny, DESTRO-BISOL, Giovanni, Spedini, Gabriella, Hans, Eiberg, Jansen, Jan B. M. J., Monika, Koudova, Eva, Rausova, Milan, Macek, Macek Jr, M., Nuria, Malats, Real, Francisco X., Hans Jurgen Menzel, Pedro, Moral, Roberta, Galavotti, Pier Franco Pignatti, Olga, Rickards, Julius, Spicak, Narcis Octavian Zarnescu, Wolfgang, Bock, Gress, Thomas M., Helmut, Friess, Johann, Ockenga, Hartmut, Schmidt, Roland, Pfutzer, Matthias, Lohr, Peter, Simon, Frank Ulrich Weiss, Lerch, Markus M., Niels, Teich, Volker, Keim, Thomas, Berg, Bertram, Wiedenmann, Werner, Luck, David Alexander Groneberg, Michael, Becker, Thomas, Keil, Andreas, Kage, Jana, Bernardova, Markus, Braun, Claudia, Guldner, Juliane, Halangk, Jonas, Rosendahl, Ulrike, Witt, Matthias, Treiber, Renate, Nickel, Claude, Ferec
Publikováno v:
Nature Genetics, 38, 6, pp. 668-73
Recercat. Dipósit de la Recerca de Catalunya
instname
Nature Genetics, 38, 668-73
Karolinska Institutet
Recercat. Dipósit de la Recerca de Catalunya
instname
Nature Genetics, 38, 668-73
Karolinska Institutet
Chronic pancreatitis is a common inflammatory disease of the pancreas. Mutations in the genes encoding cationic trypsinogen (PRSS1) and the pancreatic secretory trypsin inhibitor (SPINK1) are associated with chronic pancreatitis. Because increased pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c84ef25b3b8f04b9a05573390b501145
https://doi.org/10.1038/ng1797
https://doi.org/10.1038/ng1797
Autor:
Cristina Patuzzo, L. Pescollderung, Elisabetta Trabetti, Roberta Galavotti, Carmela Migliaccio, Giovanni Malerba, Attilio Boner, Pier Franco Pignatti
Publikováno v:
European Journal of Immunogenetics. 30:349-353
The literature contains conflicting reports on the association of common variants of the interleukin (IL)-4 receptor alpha (IL4RA) gene with atopic asthma. The purpose of the present study was to investigate the linkage and association of several gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83dc281284c271a61f5ec5d6ac7a3dc2
https://doi.org/10.1046/j.1365-2370.2003.00415.x
https://doi.org/10.1046/j.1365-2370.2003.00415.x
Autor:
Attilio Boner, Maria Camilla Lauciello, Elisabetta Trabetti, Pierfranco Pignatti, Silvia Venanzi, Giovanna Zanoni, L. C. Martinati, Giovanni Malerba, Roberta Galavotti, Lydia Pescollderungg
Publikováno v:
Clinical & Experimental Allergy. 31:1220-1224
Background Allergic asthma is a multifactorial disease for which there is a widely assessed, although poorly understood, genetic involvement. Genome-wide screens reported evidence for linkage of allergic asthma-related phenotypes to several chromosom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7bc9e10daa31eb0bce76599fb5feb65
https://doi.org/10.1046/j.1365-2222.2001.01132.x
https://doi.org/10.1046/j.1365-2222.2001.01132.x
Autor:
Lydia Pescollderungg, Francesca Belpinati, Roberta Galavotti, Giovanni Malerba, Luciano Xumerle, Elisabetta Trabetti, Attilio Boner, Pier Franco Pignatti
Publikováno v:
The Journal of allergy and clinical immunology. 128(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bc53ee47f768b71ba7e73e2539bffd5
https://pubmed.ncbi.nlm.nih.gov/21802127
https://pubmed.ncbi.nlm.nih.gov/21802127
Autor:
Lydia Pescollderungg, Cm Lindgren, Luciano Xumerle, Attilio Boner, Roberta Galavotti, P Kiviluoma, Tarja Laitinen, Pier Franco Pignatti, Giovanni Malerba, Elisabetta Trabetti, Juha Kere
Publikováno v:
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology. 37(1)
Summary Background Several genome scans have reported linkage of markers on chromosome 7p with asthma and related phenotypes in different populations. A fine mapping in Finnish and French-Canadian populations has associated the GPR154 gene (also know
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99ccb86437a52e00e3d0f04ad20af0db
https://pubmed.ncbi.nlm.nih.gov/17210045
https://pubmed.ncbi.nlm.nih.gov/17210045
Autor:
Maria Camilla Lauciello, Giovanna Zanoni, Michael B. Whalen, Lydia Pescollderungg, Roberta Galavotti, Attilio Boner, Giovanni Malerba, Laura C. Martinati, Pier Franco Pignatti, Elisabetta Trabetti, Cristina Patuzzo
Publikováno v:
The Journal of allergy and clinical immunology. 107(4)
Background: Genome and chromosome screens reported DNA markers on chromosome 14 linked to allergic asthma or intermediate phenotypes in several populations. Objective: We sought to perform a linkage study on chromosome 14 and a further association st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68f43c092c369b2c7e6930947c5eb081
https://pubmed.ncbi.nlm.nih.gov/11295654
https://pubmed.ncbi.nlm.nih.gov/11295654
Autor:
Elisabetta Trabetti, Attilio Boner, Laura C. Martinati, Maria Camilla Lauciello, Giovanni Malerba, Roberta Galavotti, Pier Franco Pignatti, R. O. Y. C. Levitt, Titia Scherpbier, Lydia Pescollderungg, Veronica Cusin, Giovanna Zanoni
Publikováno v:
Scopus-Elsevier
We investigated 116 Italian atopic families (560 individuals) for linkage with 13 DNA markers on chromosome 12. All the subjects were phenotyped for asthma, total serum IgE, bronchial hyperresponsiveness, skin-prick positivity to common aeroallergens
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3a07b55c77224faf484d1f22bc99157
http://hdl.handle.net/11562/301562
http://hdl.handle.net/11562/301562