Detalhe da pesquisa
1.
Arabidopsis thaliana FANCD2 Promotes Meiotic Crossover Formation.
Plant Cell
; 30(2): 415-428, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29352063
2.
Gain- and Loss-of-Function Mutations in the Breast Cancer Gene GATA3 Result in Differential Drug Sensitivity.
PLoS Genet
; 12(9): e1006279, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27588951
3.
A thesaurus of genetic variation for interrogation of repetitive genomic regions.
Nucleic Acids Res
; 43(10): e68, 2015 May 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-25820428
4.
A reversible gene trap collection empowers haploid genetics in human cells.
Nat Methods
; 10(10): 965-71, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24161985
5.
Targeting a cell state common to triple-negative breast cancers.
Mol Syst Biol
; 11(1): 789, 2015 Feb 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-25699542
6.
TOPS: a versatile software tool for statistical analysis and visualization of combinatorial gene-gene and gene-drug interaction screens.
BMC Bioinformatics
; 15: 98, 2014 Apr 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-24712852
7.
Characterizing the functional consequences of haploinsufficiency of NELF-A (WHSC2) and SLBP identifies novel cellular phenotypes in Wolf-Hirschhorn syndrome.
Hum Mol Genet
; 21(10): 2181-93, 2012 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22328085
8.
A chemical-genetic screen reveals a mechanism of resistance to PI3K inhibitors in cancer.
Nat Chem Biol
; 7(11): 787-93, 2011 Sep 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-21946274
9.
Mutations in Cullin 4B result in a human syndrome associated with increased camptothecin-induced topoisomerase I-dependent DNA breaks.
Hum Mol Genet
; 19(7): 1324-34, 2010 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20064923
10.
A novel plant gene essential for meiosis is related to the human CtIP and the yeast COM1/SAE2 gene.
EMBO J
; 26(24): 5061-70, 2007 Dec 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-18007598
11.
MEK inhibitors block growth of lung tumours with mutations in ataxia-telangiectasia mutated.
Nat Commun
; 7: 13701, 2016 12 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27922010
12.
Meier-Gorlin syndrome and Wolf-Hirschhorn syndrome: two developmental disorders highlighting the importance of efficient DNA replication for normal development and neurogenesis.
DNA Repair (Amst)
; 12(8): 637-44, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23706772
13.
CUL4B-deficiency in humans: understanding the clinical consequences of impaired Cullin 4-RING E3 ubiquitin ligase function.
Mech Ageing Dev
; 132(8-9): 366-73, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21352845
14.
Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome.
Nat Genet
; 43(4): 350-5, 2011 Feb 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-21358633
15.
Human DNA damage response and repair deficiency syndromes: linking genomic instability and cell cycle checkpoint proficiency.
DNA Repair (Amst)
; 8(9): 1139-52, 2009 Sep 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-19473885
16.
UVB and caffeine: inhibiting the DNA damage response to protect against the adverse effects of UVB.
J Invest Dermatol
; 129(7): 1611-3, 2009 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-19521409
17.
Expression of the ubiquitin variant ubR48 decreases proteolytic activity in Arabidopsis and induces cell death.
Planta
; 223(4): 684-97, 2006 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-16200408
18.
The Arabidopsis thaliana MND1 homologue plays a key role in meiotic homologous pairing, synapsis and recombination.
J Cell Sci
; 119(Pt 12): 2486-96, 2006 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-16763194