The 2nd International Workshop ‘Novel Therapeutic Strategies in Cancer' in St-Petersburg

Por Tentler, D, Garabadgiu, A V, Barlev, N A
Publicado em 2013

A microdeletion in 19q13.2 associated with mental retardation, skeletal malformations, and Diamond-Blackfan anaemia suggests a novel contiguous gene syndrome

Por Tentler, D., Gustavsson, P., Elinder, G., Eklof, O., Gordon, L., Mandel, A., Dahl, N.
Publicado em 2000

Genome-wide analyses of human perisylvian cerebral cortical patterning

Por Abrahams, B. S., Tentler, D., Perederiy, J. V., Oldham, M. C., Coppola, G., Geschwind, D. H.
Publicado em 2007

Assignment of the locus for ichthyosis prematurity syndrome to chromosome 9q33.3–34.13

Por Klar, J, Gedde-Dahl, T, Larsson, M, Pigg, M, Carlsson, B, Tentler, D, Vahlquist, A, Dahl, N
Publicado em 2004

KMTase Set7/9 is a critical regulator of E2F1 activity upon genotoxic stress

Por Lezina, L, Aksenova, V, Ivanova, T, Purmessur, N, Antonov, A V, Tentler, D, Fedorova, O, Garabadgiu, A V, Talianidis, I, Melino, G, Barlev, N A
Publicado no Cell Death Differ (2014)

Discovery of Novel Isatin-Based p53 Inducers

Por Davidovich, P., Aksenova, V., Petrova, V., Tentler, D., Orlova, D., Smirnov, S., Gurzhiy, V., Okorokov, A. L., Garabadzhiu, A., Melino, G., Barlev, N., Tribulovich, V.
Publicado no ACS Med Chem Lett (2015)

miR-16 and miR-26a target checkpoint kinases Wee1 and Chk1 in response to p53 activation by genotoxic stress

Por Lezina, L, Purmessur, N, Antonov, A V, Ivanova, T, Karpova, E, Krishan, K, Ivan, M, Aksenova, V, Tentler, D, Garabadgiu, A V, Melino, G, Barlev, N A
Publicado em 2013

Identification of microdeletions spanning the Diamond-Blackfan anemia locus on 19q13 and evidence for genetic heterogeneity.

Por Gustavsson, P, Garelli, E, Draptchinskaia, N, Ball, S, Willig, T N, Tentler, D, Dianzani, I, Punnett, H H, Shafer, F E, Cario, H, Ramenghi, U, Glomstein, A, Pfeiffer, R A, Goringe, A, Olivieri, N F, Smibert, E, Tchernia, G, Elinder, G, Dahl, N
Publicado em 1998