D. Tentler

发表

A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans

R. Jonsson, A. Bolstad, A. Brookes, 2002, Nature Genetics.

Genome-wide analyses of human perisylvian cerebral cortical patterning

D. Geschwind, B. Abrahams, M. Oldham, 2007, Proceedings of the National Academy of Sciences.

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

D. Tentler, N. Dahl, A. Mandel, 2000, Journal of medical genetics.

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

M. Ivan, G. Melino, A. Antonov, 2013, Cell Death and Disease.

Novel isatin-derived molecules activate p53 via interference with Mdm2 to promote apoptosis

G. Melino, O. Demidov, P. Davidovich, 2018, Cell cycle.

Discovery of Novel Isatin-Based p53 Inducers.

G. Melino, P. Davidovich, N. Barlev, 2015, ACS medicinal chemistry letters.

A candidate region for Asperger syndrome defined by two 17p breakpoints

C. Gillberg, D. Tentler, M. Johansson, 2003, European Journal of Human Genetics.

A balanced reciprocal translocation t(5;7)(q14;q32) associated with autistic disorder: molecular analysis of the chromosome 7 breakpoint.

C. Gillberg, C. Betancur, E. Green, 2001, American journal of medical genetics.

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

G. Melino, A. Antonov, I. Talianidis, 2014, Cell Death and Differentiation.