Sfoglia per SSD Settore BIO/18 - Genetica
14-3-3 proteins regulate exonuclease 1-dependent processing of stalled replication forks
2011 K. Engels, M. Giannattasio, M. Muzi-Falconi, M. Lopes, S. Ferrari
25 Years of thermomorphogenesis research: milestones and perspectives
2023 M. Quint, C. Delker, S. Balasubramanian, M. Balcerowicz, J.J. Casal, C.D.M. Castroverde, M. Chen, X. Chen, I. De Smet, C. Fankhauser, K.A. Franklin, K.J. Halliday, S. Hayes, D. Jiang, J. Jung, E. Kaiserli, S.V. Kumar, D. Maag, E. Oh, C. Park, S. Penfield, G. Perrella, S. Prat, R.S. Reis, P.A. Wigge, B.C. Willige, M. van Zanten
The 3' ends of the deletions of Spanish delta beta zero-thalassemia and black HPFH 1 and 2 lie within 17 kilobases
1987 C. Camaschella, A. Serra, G. Saglio, M. Baiget, N. Malgaretti, R. Mantovani, S. Ottolenghi
3d combo chrrna–dna–immunofish
2021 F. Marasca, A. Cortesi, B. Bodega
7q11.23 dosage-dependent dysregulation in human pluripotent stem cells affects transcriptional programs in disease-relevant lineages
2015 A. Adamo, S. Atashpaz, P. Germain, M. Zanella, G. D'Agostino, V. Albertin, J. Chenoweth, L. Micale, C. Fusco, C. Unger, B. Augello, O. Palumbo, B. Hamilton, M. Carella, E. Donti, G. Pruneri, A. Selicorni, E. Biamino, P. Prontera, R. Mckay, G. Merla, G. Testa
A blooming resolvase at chromosomal fragile sites
2013 A. Pellicioli, M. Muzi-Falconi
A CELL REPROGRAMMING-BASED APPROACH TO STUDY 7Q11.23 GENE DOSAGE IMBALANCES IN WILLIAMS BEUREN SYNDROME AND AUTISM SPECTRUM DISORDER
2015 S. Atashpazgargari
A conserved loop in polynucleotide phosphorylase (PNPase) essential for both RNA and ADP/phosphate binding
2014 T. Carzaniga, E. Mazzantini, M. Nardini, M.E. Regonesi, C. Greco, F. Briani, L. De Gioia, G. Dehò, P. Tortora
A database of annotated promoters of genes associated with common respiratory and related diseases
2012 R. Chowdhary, S.L. Tan, G. Pavesi, J. Jin, D. Dong, S.K. Mathur, A. Burkart, V. Narang, I. Glurich, B.A. Raby, S.T. Weiss, L. Wong, J.S. Liu, V.B. Bajic
A defective ABC transporter of the MRP family, responsible for the bean lpa1 mutation, affects the regulation of the phytic acid pathway, reduces seed myo-inositol and alters ABA sensitivity
2011 D. Panzeri, E. Cassani, E. Doria, G. Tagliabue, L. Forti, B. Campion, R. Bollini, C.A. Brearley, S.R. Pilu, E. Nielsen, F. Sparvoli
A dominant-negative MEC3 mutant uncovers new functions for the Rad17 complex and Tel1
2002 M. Giannattasio, E. Sommariva, R. Vercillo, F. Lippi Boncambi, G. Liberi, M. Foiani, P. Plevani, M. Muzi-Falconi
A functionally essential domain of RFX5 mediates activation of major histocompatibility complex class II promoters by promoting cooperative binding between RFX and NF-Y
2000 J. Villard, M. Peretti, K. Masternak, E. Barras, G. Caretti, R. Mantovani, W. Reith
A gene-trapping approch to study the correlation between Calmodulin and PCD in Arabidopsis thaliana
2003 A. De Francesco, M. Landoni, F. Foglia, C. Tonelli
A genetic approach to thermosensors identification in Pseudomonas aeruginosa
2012 F. Delvillani, C. Berens, C. Peano, L. Petiti, S. Ferrara, G. Dehò, G. Bertoni, F. Briani
A loss-of-function mutation in Calmodulin2 gene affects pollen germination in Arabidopsis thaliana
2010 M. Landoni, A. De Francesco, M. Galbiati, C. Tonelli
A maize anthocyanin transactivator induces pigmentation in hairy roots of dicotyledonous species
1998 F. Damiani, F. Paolocci, G. Consonni, F. Crea, C. Tonelli, S. Arcioni
A molecular study of a family with Greek hereditary persistence of fetal hemoglobin and beta-thalassemia
1984 B. Giglioni, C. Casini, R. Mantovani, S. Merli, P. Comi, S. Ottolenghi, G. Saglio, C. Camaschella, U. Mazza
A multi-nucleate male sterile mutant of maize with gametophytic expression
1997 M. Sari-Gorla, E. Gatti, M. Villa, M.E. Pè
A multivariate approach to the problem of QTL localization
2000 T. Calinski, Z. Kaczmarek, P. Krajewski, C. Frova, M. Sari-Gorla
A new p63-deficient mouse model or a fresh look at an old one?
2009 D. Aberdam, R. Mantovani
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