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First author	Title	PubMed ID
Mancera E	High-resolution mapping of meiotic crossovers and non-crossovers in yeast.	18615017
Ganguly T	High throughput fluorescence-based conformation-sensitive gel electrophoresis (F-CSGE) identifies six unique BRCA2 mutations and an overall low incidence of BRCA2 mutations in high-risk BRCA1-negative breast cancer families.	9654203
Sands AT	High susceptibility to ultraviolet-induced carcinogenesis in mice lacking XPC.	7675084
Katagiri T	High proportion of missense mutations of the BRCA1 and BRCA2 genes in Japanese breast cancer families.	9609997
Goldsby RE	High incidence of epithelial cancers in mice deficient for DNA polymerase delta proofreading.	12429860
Morgan NV	High frequency of large intragenic deletions in the Fanconi anemia group A gene.	10521298
Wilson DM 3rd	Hex1: a new human Rad2 nuclease family member with homology to yeast exonuclease 1.	9685493
Rice G	Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndrome.	17357087
Bell DW	Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome.	10617473
Cheung VG	Heterozygous carriers of Nijmegen Breakage Syndrome have a distinct gene expression phenotype.	16809669
Wijker M	Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene.	10094191
Quaresima B	Hereditary nonpolyposis coloretal cancer: identification of novel germline mutations in two kindreds not fulfulling the Amsterdam criteria. Mutations in brief no. 203. Online.	10671064
Wehner M	Hereditary nonpolyposis colorectal cancer: pitfalls in deletion screening in MSH2 and MLH1 genes.	15870828
Wang Y	Hereditary nonpolyposis colorectal cancer: causative role of a germline missense mutation in the hMLH1 gene confirmed by the independent occurrence of the same somatic mutation in tumour tissue.	9272156
Wijnen J	Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations.	9311737
Wehner M	Hereditary nonpolyposis colorectal cancer (HNPCC): eight novel germline mutations in hMSH2 or hMLH1 genes.	9298827
Thompson E	Hereditary non-polyposis colorectal cancer and the role of hPMS2 and hEXO1 mutations.	14756672
Bisgaard ML	Hereditary non-polyposis colorectal cancer (HNPCC): phenotype-genotype correlation between patients with and without identified mutation.	12112654
Hadjisavvas A	Hereditary breast and ovarian cancer in Cyprus: identification of a founder BRCA2 mutation.	15172753
Felix CA	Hereditary and acquired p53 gene mutations in childhood acute lymphoblastic leukemia.	1737852
Guran S	Hereditary TP53 codon 292 and somatic P16INK4A codon 94 mutations in a Li-Fraumeni syndrome family.	10484981
Wang Y	Hepatopoietin interacts directly with COP9 signalosome and regulates AP-1 activity.	15304329
Lin-Marq N	Hepatitis B virus X protein interferes with cell viability through interaction with the p127-kDa UV-damaged DNA-binding protein.	11531405
Lee TH	Hepatitis B virus X protein interacts with a probable cellular DNA repair protein.	7815490
Leupin O	Hepatitis B virus X protein and simian virus 5 V protein exhibit similar UV-DDB1 binding properties to mediate distinct activities.	12743284

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