Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients

scientific article published on 10 December 2009

Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.2353/JMOLDX.2010.090063
P932PMC publication ID2797722
P698PubMed publication ID20007843
P5875ResearchGate publication ID40685599

P50authorJan LubińskiQ11718282
Dagmara DymerskaQ114456268
Ryszard SłomskiQ18670230
Tomasz ByrskiQ58345332
Grzegorz KurzawskiQ59543960
Andrzej PlawskiQ80706496
Jacek GronwaldQ91084015
Tomasz HuzarskiQ97187823
Janina SuchyQ114456208
Józef KładnyQ114456211
Pablo Serrano-FernándezQ114456240
P2093author name stringRodney J Scott
Krzysztof Kaklewski
P2860cites workIdentification of deletion mutations and three new genes at the familial polyposis locusQ24294229
Mutations predisposing to hereditary nonpolyposis colorectal cancerQ28235642
Identification and characterization of the familial adenomatous polyposis coli geneQ29620382
SNP genotyping using the Sequenom MassARRAY iPLEX platformQ33402982
Genetic susceptibility to non-polyposis colorectal cancerQ33764029
Cancer risk in mutation carriers of DNA-mismatch-repair genesQ34502900
Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rateQ34728026
Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.Q34732921
Lynch syndrome genesQ36246487
Recurrent APC gene mutations in Polish FAP familiesQ42221964
Germline MSH2 and MLH1 mutational spectrum in HNPCC families from Poland and the Baltic StatesQ43075069
High-throughput gene sequencing assay development for hereditary nonpolyposis colon cancer.Q54692672
Frequency and nature of hMSH6 germline mutations in Polish patients with colorectal, endometrial and ovarian cancersQ61945791
Germline MSH2 and MLH1 mutational spectrum including large rearrangements in HNPCC families from Poland (update study)Q61945792
Family studies in cancer of the colon and rectumQ67448119
Hereditary colorectal cancerQ68309682
Familial aggregation of tumors in the three-year experience of a population-based colorectal cancer registryQ69648588
DNA isolation by a rapid method from human blood samples: effects of MgCl2, EDTA, storage time, and temperature on DNA yield and qualityQ72689207
Hereditary colorectal cancerQ73088287
APC gene mutations causing familial adenomatous polyposis in Polish patientsQ82706701
P433issue1
P921main subjectLynch syndromeQ783644
P304page(s)82-90
P577publication date2009-12-10
P1433published inThe Journal of Molecular DiagnosticsQ7743603
P1476titleCombined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients
P478volume12

Reverse relations

cites work (P2860)
Q36552174DNA and RNA analyses in detection of genetic predisposition to cancer
Q46738228Fast diagnostic test for the identification of an increased genetic predisposition to colon cancer (exemplified on a DNA test for recurrent mutations of the gene MMR).
Q58562100Heterogenous loss of mismatch repair (MMR) protein expression: a challenge for immunohistochemical interpretation and microsatellite instability (MSI) evaluation
Q47664722Immunohistochemical null-phenotype for mismatch repair proteins in colonic carcinoma associated with concurrent MLH1 hypermethylation and MSH2 somatic mutations.
Q45956204Lynch syndrome mutations shared by the Baltic States and Poland.

Search more.