Pages that link to "Q33343446"
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The following pages link to Novel roles for MLH3 deficiency and TLE6-like amplification in DNA mismatch repair-deficient gastrointestinal tumorigenesis and progression. (Q33343446):
Displaying 19 items.
- Animal models of colorectal cancer (Q27009170) (← links)
- Genetic mechanisms in Apc-mediated mammary tumorigenesis (Q33406237) (← links)
- Animal models of gastrointestinal and liver diseases. New mouse models for studying dietary prevention of colorectal cancer (Q34001641) (← links)
- Msh6 protects mature B cells from lymphoma by preserving genomic stability (Q34254602) (← links)
- Mouse models of inherited cancer syndromes (Q34447472) (← links)
- Induction of olfaction and cancer-related genes in mice fed a high-fat diet as assessed through the mode-of-action by network identification analysis (Q34650169) (← links)
- Biochemical characterization of MLH3 missense mutations does not reveal an apparent role of MLH3 in Lynch syndrome (Q34926104) (← links)
- Mismatch repair gene MLH3 Pro844Leu and Thr942Ile polymorphisms and the susceptibility to cervical carcinoma and HPV infection: a case-control study in a Chinese population (Q35156069) (← links)
- miR-23a promotes the transition from indolent to invasive colorectal cancer (Q36837231) (← links)
- Loss of Rb1 in the gastrointestinal tract of Apc1638N mice promotes tumors of the cecum and proximal colon. (Q36926836) (← links)
- Epigenetic repression of DNA mismatch repair by inflammation and hypoxia in inflammatory bowel disease-associated colorectal cancer (Q37357503) (← links)
- Pharmacological inhibition of polycomb repressive complex-2 activity induces apoptosis in human colon cancer stem cells (Q37431211) (← links)
- RUNX3 is multifunctional in carcinogenesis of multiple solid tumors (Q37720402) (← links)
- Stable expression of MutLγ in human cells reveals no specific response to mismatched DNA, but distinct recruitment to damage sites. (Q39148893) (← links)
- Inhibition of colorectal cancer genomic copy number alterations and chromosomal fragile site tumor suppressor FHIT and WWOX deletions by DNA mismatch repair (Q42700921) (← links)
- Alternative splicing within the Wnt signaling pathway: role in cancer development. (Q53211105) (← links)
- A frameshift mutation in exon 19 of MLH1 in a Chinese Lynch syndrome family: a pedigree study (Q61810176) (← links)
- Identification of a novel germline frameshift mutation p.D300fs of PMS1 in a patient with hepatocellular carcinoma: A case report and literature review (Q89448254) (← links)
- Somatic genetic aberrations in benign breast disease and the risk of subsequent breast cancer (Q96608949) (← links)