Search Results - "Teo, S.M."
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Recurrent Fusion Genes in Gastric Cancer: CLDN18-ARHGAP26 Induces Loss of Epithelial Integrity
Published in Cell reports (Cambridge) (14-07-2015)“…Genome rearrangements, a hallmark of cancer, can result in gene fusions with oncogenic properties. Using DNA paired-end-tag (DNA-PET) whole-genome sequencing,…”
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TP53 intron 1 hotspot rearrangements are specific to sporadic osteosarcoma and can cause Li-Fraumeni syndrome
Published in Oncotarget (10-04-2015)“…Somatic mutations of TP53 are among the most common in cancer and germline mutations of TP53 (usually missense) can cause Li-Fraumeni syndrome (LFS). Recently,…”
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3
Molecular insights into evolution, mutations and receptor-binding specificity of influenza A and B viruses from outpatients and hospitalized patients in Singapore
Published in International journal of infectious diseases (01-01-2020)“…•Singapore influenza A and B virus strains from 2012-2015 are mainly part of the global influenza virus circulation and evolution.•Several amino acid sites…”
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Elucidating the genomic architecture of Asian EGFR-mutant lung adenocarcinoma through multi-region exome sequencing
Published in Nature communications (15-01-2018)“…EGFR -mutant lung adenocarcinomas (LUAD) display diverse clinical trajectories and are characterized by rapid but short-lived responses to EGFR tyrosine kinase…”
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A common BIM deletion polymorphism mediates intrinsic resistance and inferior responses to tyrosine kinase inhibitors in cancer
Published in Nature medicine (01-04-2012)“…Intrinsic resistance to tyrosine kinase inhibitor (TKI) drugs is limiting the progress of targeted cancer therapies. The efficacy of TKIs relies on their…”
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An integrative model of pathway convergence in genetically heterogeneous blast crisis chronic myeloid leukemia
Published in Blood (25-06-2020)“…Targeted therapies against the BCR-ABL1 kinase have revolutionized treatment of chronic phase (CP) chronic myeloid leukemia (CML). In contrast, management of…”
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Integrative Profiling of T790M-Negative EGFR-Mutated NSCLC Reveals Pervasive Lineage Transition and Therapeutic Opportunities
Published in Clinical cancer research (01-11-2021)“…Despite the established role of EGFR tyrosine kinase inhibitors (TKIs) in -mutated NSCLC, drug resistance inevitably ensues, with a paucity of treatment…”
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Priapism mimic: penile metastasis from hepatocellular carcinoma
Published in BMJ case reports (21-03-2022)“…We describe the case of a metastatic penile tumour of hepatocellular origin treated with surgical resection…”
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Perioperative anticoagulation and open distal corpora cavernosa shunt in the management of a case of stuttering idiopathic persistent childhood ischaemic priapism
Published in Asian journal of urology (01-10-2021)“…Childhood priapism is a rare entity and there is currently no consensus regarding its contemporary management. The use of perioperative anticoagulation and…”
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10
The role of intravesical prostatic protrusion (IPP) in the evaluation and treatment of bladder outlet obstruction (BOO)
Published in Neurourology and urodynamics (01-04-2016)“…Aims Intravesical prostatic protrusion (IPP) may be an underutilized modality for the assessment of bladder outlet obstruction (BOO). Pressure flow studies or…”
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Whole-genome sequencing of asian lung cancers: second-hand smoke unlikely to be responsible for higher incidence of lung cancer among Asian never-smokers
Published in Cancer research (Chicago, Ill.) (01-11-2014)“…Asian nonsmoking populations have a higher incidence of lung cancer compared with their European counterparts. There is a long-standing hypothesis that the…”
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Detection of chromosomal breakpoints in patients with developmental delay and speech disorders
Published in PloS one (06-03-2014)“…Delineating candidate genes at the chromosomal breakpoint regions in the apparently balanced chromosome rearrangements (ABCR) has been shown to be more…”
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Systems consequences of amplicon formation in human breast cancer
Published in Genome research (01-10-2014)“…Chromosomal structural variations play an important role in determining the transcriptional landscape of human breast cancers. To assess the nature of these…”
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14
Comprehensive long-span paired-end-tag mapping reveals characteristic patterns of structural variations in epithelial cancer genomes
Published in Genome research (01-05-2011)“…Somatic genome rearrangements are thought to play important roles in cancer development. We optimized a long-span paired-end-tag (PET) sequencing approach…”
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Comparison of patient survival between various subgroups among renal transplant patients: A single center experience
Published in Transplantation proceedings (01-09-2004)“…To compare patient graft survival between various subgroups among renal transplant patients. A retrospective analysis of all renal transplant patients from…”
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Functional Analysis of the CML Blast Crisis Transcriptome and Epigenome Using Crispr-CAS9 and Pharmacologic Approaches
Published in Blood (03-12-2015)“…Current models of CML blast crisis (BC) propose that expression of BCR-ABL results in genomic instability and the acquisition of genetic alterations that…”
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The Genomic and Epigenomic Landscapes of Blast Crisis Transformation in Chronic Myeloid Leukemia
Published in Blood (03-12-2015)“…The transition from chronic phase (CP) to blast crisis (BC) chronic myeloid leukemia (CML) is characterized by reprogramming of the CML transcriptome (Radich…”
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Abstract A1-25: Intratumor heterogeneity in never-smoker Asian EGFR mutant lung adenocarcinoma
Published in Cancer research (Chicago, Ill.) (15-11-2015)“…Abstract Lung cancer has the highest cancer associated mortality rate in many countries across the world. In contrast to western populations, approximately…”
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Abstract B2-54: Intratumor heterogeneity in never-smoker Asian EGFR mutant lung adenocarcinoma
Published in Cancer research (Chicago, Ill.) (15-11-2015)“…Abstract Lung cancer has the highest cancer associated mortality rate in many countries across the world. In contrast to western populations, approximately…”
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Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: variable phenotypic expression in three affected sisters from Mexican ancestry
Published in Renal failure (01-02-2015)“…Familial hypomagnesemia with hypercalciuria and nephrocalcinosis is a rare autosomal recessive renal disease caused by mutations in genes for the tight…”
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