REPAIRtoire - a database of DNA repair pathways

Welcome! Click here to login or here to register.

Home

Bujnicki Lab Homepage

Publications

FIRST PREVIOUS PAGE 92 of 153 NEXT LAST

Click on a column name to sort.

First author	Title	PubMed ID
Liu J	NEDD8 modification of CUL1 dissociates p120(CAND1), an inhibitor of CUL1-SKP1 binding and SCF ligases.	12504025
Kobayashi J	NBS1 localizes to gamma-H2AX foci through interaction with the FHA/BRCT domain.	12419185
Wang B	NBA1, a new player in the Brca1 A complex, is required for DNA damage resistance and checkpoint control.	19261749
Liu X	Myosin VIIa participates in opsin transport through the photoreceptor cilium.	10414956
Yoneda-Kato N	Myeloid leukemia factor 1 regulates p53 by suppressing COP1 via COP9 signalosome subunit 3.	15861129
Drotschmann K	Mutator phenotypes of yeast strains heterozygous for mutations in the MSH2 gene.	10077621
Drotschmann K	Mutator phenotypes of common polymorphisms and missense mutations in MSH2.	10469597
Siegel EC	Mutator gene of Escherichia coli B.	5338974
Zhou Q	Mutations/polymorphisms in the 55 kDa subunit of DNA polymerase epsilon in human colorectal cancer.	20065316
Nouspikel T	Mutations that disable the DNA repair gene XPG in a xeroderma pigmentosum group G patient.	7951246
Nichols AF	Mutations specific to the xeroderma pigmentosum group E Ddb- phenotype.	8798680
Byrd PJ	Mutations revealed by sequencing the 5' half of the gene for ataxia telangiectasia.	8789452
Nicolaides NC	Mutations of two PMS homologues in hereditary nonpolyposis colon cancer.	8072530
Palmbos PL	Mutations of the Yku80 C terminus and Xrs2 FHA domain specifically block yeast nonhomologous end joining.	16314503
Ishioka C	Mutations of the P53 gene, including an intronic point mutation, in colorectal tumors.	1647768
Savino M	Mutations of the Fanconi anemia group A gene (FAA) in Italian patients.	9399890
Miller CW	Mutations of the CHK2 gene are found in some osteosarcomas, but are rare in breast, lung, and ovarian tumors.	11746983
Takahashi H	Mutations of the BRCA2 gene in ovarian carcinomas.	8665505
Lamantea E	Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia.	12210792
Scartozzi M	Mutations of hMLH1 and hMSH2 in patients with suspected hereditary nonpolyposis colorectal cancer: correlation with microsatellite instability and abnormalities of mismatch repair protein expression.	11870161
Hiramoto T	Mutations of a novel human RAD54 homologue, RAD54B, in primary cancer.	10362364
Leach FS	Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer.	8261515
Papadopoulos N	Mutations of GTBP in genetically unstable cells.	7604266
Agostino A	Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO).	12707443
Broughton BC	Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy.	7920640

Welcome stranger! Click here to login or here to register.