Pages that link to "Q39459426"
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The following pages link to Richie Soong (Q39459426):
Displaying 50 items.
- Human genetics and genomics a decade after the release of the draft sequence of the human genome (Q21245451) (← links)
- Immunotherapy in the treatment of non-small cell lung cancer (Q27000382) (← links)
- Patients with colorectal tumors with microsatellite instability and large deletions in HSP110 T17 have improved response to 5-fluorouracil–based chemotherapy. (Q27852842) (← links)
- Detection of BRAF V600E mutation by pyrosequencing (Q28277357) (← links)
- GBSA: a comprehensive software for analysing whole genome bisulfite sequencing data. (Q30583255) (← links)
- Clonal characterization of sporadic cribriform-morular variant of papillary thyroid carcinoma by laser microdissection-based APC mutation analysis (Q33306292) (← links)
- Distribution of gemcitabine pathway genotypes in ethnic Asians and their association with outcome in non-small cell lung cancer patients (Q33379914) (← links)
- Genetic factors associated with intestinal metaplasia in a high risk Singapore-Chinese population: a cohort study (Q33509913) (← links)
- Comprehensive profiling of DNA methylation in colorectal cancer reveals subgroups with distinct clinicopathological and molecular features (Q33584274) (← links)
- Insights into the genetic structure and diversity of 38 South Asian Indians from deep whole-genome sequencing (Q33617748) (← links)
- Whole-genome reconstruction and mutational signatures in gastric cancer. (Q33751188) (← links)
- Increased drug resistance is associated with reduced glucose levels and an enhanced glycolysis phenotype. (Q33842748) (← links)
- Transposon mutagenesis identifies genes driving hepatocellular carcinoma in a chronic hepatitis B mouse model (Q34038257) (← links)
- Clinical potential of DNA methylation in gastric cancer: a meta-analysis (Q34257393) (← links)
- Gene discovery in familial cancer syndromes by exome sequencing: prospects for the elucidation of familial colorectal cancer type X. (Q34269998) (← links)
- Elevated expression of Runx2 as a key parameter in the etiology of osteosarcoma. (Q34308600) (← links)
- Localized sclerotic bone response demonstrated reduced nanomechanical creep properties. (Q34467626) (← links)
- Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation (Q34495057) (← links)
- Studying the epigenome using next generation sequencing (Q34631495) (← links)
- Implications of dihydropyrimidine dehydrogenase on 5-fluorouracil pharmacogenetics and pharmacogenomics. (Q34775315) (← links)
- Association of the IL-1B +3954 C/T polymorphism with the risk of gastric cancer in a population in Western China. (Q35002799) (← links)
- DNA methylation subgroups and the CpG island methylator phenotype in gastric cancer: a comprehensive profiling approach. (Q35132907) (← links)
- Advances and challenges in fluoropyrimidine pharmacogenomics and pharmacogenetics. (Q36317002) (← links)
- Epigenome-wide association of DNA methylation markers in peripheral blood from Indian Asians and Europeans with incident type 2 diabetes: a nested case-control study (Q36496178) (← links)
- Deep whole-genome sequencing of 100 southeast Asian Malays (Q36524738) (← links)
- Correlation of aldo-ketoreductase (AKR) 1C3 genetic variant with doxorubicin pharmacodynamics in Asian breast cancer patients. (Q36948123) (← links)
- The expression of RUNX3 in colorectal cancer is associated with disease stage and patient outcome. (Q37123524) (← links)
- TRARESA: a tissue microarray-based hospital system for biomarker validation and discovery. (Q37208515) (← links)
- A multicenter blinded study to evaluate KRAS mutation testing methodologies in the clinical setting (Q37396252) (← links)
- Ethnic differences in survival outcome in patients with advanced stage non-small cell lung cancer: results of a meta-analysis of randomized controlled trials. (Q37870656) (← links)
- Exome sequencing: dual role as a discovery and diagnostic tool (Q37978583) (← links)
- Technological advances in DNA sequence enrichment and sequencing for germline genetic diagnosis (Q37988576) (← links)
- Exome versus transcriptome sequencing in identifying coding region variants (Q37999069) (← links)
- Differences in outcome and toxicity between Asian and caucasian patients with lung cancer treated with systemic therapy. (Q38003669) (← links)
- Targeting ROS1 with anaplastic lymphoma kinase inhibitors: a promising therapeutic strategy for a newly defined molecular subset of non-small-cell lung cancer. (Q38052420) (← links)
- Use of intraoperative cell-salvage for autologous blood transfusions in metastatic spine tumour surgery: a systematic review. (Q38175259) (← links)
- RUNX3 inactivation by frequent promoter hypermethylation and protein mislocalization constitute an early event in breast cancer progression. (Q38293760) (← links)
- Patz1 regulates embryonic stem cell identity. (Q38481414) (← links)
- Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity (Q38779718) (← links)
- RUNX3 downregulation in human lung adenocarcinoma is independent of p53, EGFR or KRAS status. (Q39325857) (← links)
- Pharmacologic synergy between dual phosphoinositide-3-kinase and mammalian target of rapamycin inhibition and 5-fluorouracil in PIK3CA mutant gastric cancer cells. (Q39396274) (← links)
- Clinical and therapeutic relevance of PIM1 kinase in gastric cancer (Q39459093) (← links)
- MicroRNA-130b regulates the tumour suppressor RUNX3 in gastric cancer (Q39736530) (← links)
- An improved quality control for bisulfite-PCR-based DNA methylation analysis: cycle threshold value (Q39947562) (← links)
- Identification of potentially useful combinations of epidermal growth factor receptor tyrosine kinase antagonists with conventional cytotoxic agents using median effect analysis (Q40238246) (← links)
- E1A-F is overexpressed early in human colorectal neoplasia and associated with cyclooxygenase-2 and matrix metalloproteinase-7. (Q40440769) (← links)
- Simultaneous detection of variable number tandem repeats, single nucleotide polymorphisms, and allelic imbalance in the thymidylate synthase gene enhancer region using denaturing high-performance liquid chromatography (Q40502197) (← links)
- RUNX3 protein is overexpressed in human basal cell carcinomas (Q42496689) (← links)
- CD133 expression predicts for non-response to chemotherapy in colorectal cancer (Q43191501) (← links)
- Correlation between epidermal growth factor receptor mutations and expression of female hormone receptors in East-Asian lung adenocarcinomas. (Q43252127) (← links)