Search Results - "TEO, Audrey S. M"
-
1
OPTIMA: sensitive and accurate whole-genome alignment of error-prone genomic maps by combinatorial indexing and technology-agnostic statistical analysis
Published in Gigascience (19-01-2016)“…Resolution of complex repeat structures and rearrangements in the assembly and analysis of large eukaryotic genomes is often aided by a combination of…”
Get full text
Journal Article -
2
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…”
Get full text
Journal Article -
3
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…”
Get full text
Journal Article -
4
Long span DNA paired-end-tag (DNA-PET) sequencing strategy for the interrogation of genomic structural mutations and fusion-point-guided reconstruction of amplicons
Published in PloS one (28-09-2012)“…Structural variations (SVs) contribute significantly to the variability of the human genome and extensive genomic rearrangements are a hallmark of cancer…”
Get full text
Journal Article -
5
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…”
Get full text
Journal Article -
6
Single-molecule optical genome mapping of a human HapMap and a colorectal cancer cell line
Published in Gigascience (29-12-2015)“…Next-generation sequencing (NGS) technologies have changed our understanding of the variability of the human genome. However, the identification of genome…”
Get full text
Journal Article -
7
Whole-genome reconstruction and mutational signatures in gastric cancer
Published in Genome biology (01-01-2012)“…BACKGROUND: Gastric cancer is the second highest cause of global cancer mortality. To explore the complete repertoire of somatic alterations in gastric cancer,…”
Get full text
Journal Article -
8
Specific profiles of house dust mite sensitization in children with asthma and in children with eczema
Published in Pediatric allergy and immunology (01-06-2010)“…Shek LP, Chong AR, Soh SE, Cheong N, Teo ASM, Yi FC, Giam YC, Chua KY, Van Bever HP. Specific profiles of house dust mite sensitization in children with asthma…”
Get full text
Journal Article -
9
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…”
Get full text
Journal Article -
10
De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development
Published in Nature genetics (01-02-2017)“…Jeanne Amiel, Bernd Wollnik, Bruno Reversade and colleagues report de novo missense mutations in SMCHD1 in patients with Bosma arhinia microphthalmia syndrome…”
Get full text
Journal Article -
11
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…”
Get full text
Journal Article -
12
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,…”
Get full text
Journal Article -
13
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…”
Get full text
Journal Article -
14
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…”
Get more information
Journal Article -
15
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…”
Get full text
Journal Article -
16
Integrative genomic analyses of European intrahepatic cholangiocarcinoma: Novel ROS1 fusion gene and PBX1 as prognostic marker
Published in Clinical and translational medicine (01-06-2024)“…Background Cholangiocarcinoma (CCA) is a fatal cancer of the bile duct with a poor prognosis owing to limited therapeutic options. The incidence of…”
Get full text
Journal Article -
17
Novel mutations in ndh in isoniazid-resistant Mycobacterium tuberculosis isolates
Published in Antimicrobial agents and chemotherapy (01-07-2001)“…Novel mutations in NADH dehydrogenase (ndh) were detected in 8 of 84 (9.5%) isoniazid (INH)-resistant isolates (T110A [n = 1], R268H [n = 7]), but not in 22…”
Get full text
Journal Article -
18
Expression of the Blomia tropicalis paramyosin Blo t 11 and its immunodominant peptide in insect cells
Published in Biotechnology and applied biochemistry (01-07-2006)“…Blo t 11, a dust‐mite (Blomia tropicalis) paramyosin, is an allergen with significant IgE reactivity that has potential as a diagnostic/therapeutic reagent for…”
Get full text
Journal Article -
19
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…”
Get full text
Journal Article -
20
Novel Mutations in ndh in Isoniazid-Resistant Mycobacterium tuberculosisIsolates
Published in Antimicrobial Agents and Chemotherapy (01-07-2001)“…Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
Get full text
Journal Article