Search Results - "Ankathil, R"
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Clinical impact of ABCC1 and ABCC2 genotypes and haplotypes in mediating imatinib resistance among chronic myeloid leukaemia patients
Published in Journal of clinical pharmacy and therapeutics (01-12-2014)“…Summary What is known and objective The introduction and success of imatinib mesylate (IM) has brought about a paradigm shift in chronic myeloid leukaemia…”
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P0223 CYP3A4∗ 18 and CYP3A5∗ 3 gene polymorphisms and imatinib resistance in Malaysian patients with chronic myeloid leukaemia
Published in European journal of cancer (1990) (01-05-2014)“…Background Although imatinib mesylate (IM) has shown excellent efficacy as first-line therapy for treatment of chronic myeloid leukaemia (CML), resistance to…”
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OP0025 Genetic association of C480G polymorphism of SLC22A1 with clinical resistance to imatinib mesylate in Malaysian patients with chronic myeloid leukaemia
Published in European journal of cancer (1990) (01-05-2014)“…Background Despite imatinib mesylate (IM) being the gold standard drug for treatment of chronic myeloid leukaemia (CML), a significant proportion of CML…”
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The differential metabolite profiles of acute lymphoblastic leukaemic patients treated with 6-mercaptopurine using untargeted metabolomics approach
Published in Clinical biochemistry (01-04-2014)“…Acute lymphoblastic leukaemia (ALL) has posed challenges to the clinician due to variable patients' responses and late diagnosis. With the advance in…”
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Chromosomal abnormalities and reproductive outcome in Malaysian couples with miscarriages
Published in Singapore medical journal (01-10-2009)“…This study was done to determine the prevalence of chromosomal abnormalities and the subsequent reproductive outcome in couples who had two or more…”
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Somatic copy-neutral loss of heterozygosity and copy number abnormalities in Malaysian sporadic colorectal carcinoma patients
Published in Genetics and molecular research (07-02-2013)“…Colorectal cancer is one of the most common cancers in many countries, including Malaysia. The accumulation of genomic alterations is an important feature of…”
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Clinical manifestations in trisomy 9
Published in Indian journal of pediatrics (01-07-2009)“…Complete trisomy 9 is a lethal diagnosis and most fetuses diagnosed thus die prenatally or during the early postnatal period and majority of such cases have…”
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Germline BRCA1 mutation and survival analysis in familial breast cancer patients in Kerala; South India
Published in Journal of experimental & clinical cancer research (01-09-2007)“…Mutations in breast cancer susceptibility gene BRCA1 have been identified in breast or breast/ovarian cancer families from different ethnic background. We…”
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Two cases of isochromosome 18q syndrome
Published in Singapore medical journal (01-05-2007)“…Patients with isochromosome 18q, a rare cytogenetic abnormality, also reported as Edwards syndrome, is the second most common autosomal trisomy. However, the…”
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Cytogenetic and clinical profile of Down syndrome in Northeast Malaysia
Published in Singapore medical journal (01-06-2007)“…This study was designed to evaluate the karyotype pattern, clinical features and other systemic anomalies of patients with Down syndrome in Malaysia…”
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Two cases of deletion 5p syndrome: one with paternal involvement and another with atypical presentation
Published in Singapore medical journal (01-04-2008)“…We report two cases of deletion 5p or cri du chat syndrome (CdCS) with different presentations and risks of transmission: one case with paternal chromosome 5…”
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ABCB1 genetic variants in leukemias: current insights into treatment outcomes
Published in Pharmacogenomics and personalized medicine (01-01-2017)“…Despite improvements in treatment of different types of leukemia, not all patients respond optimally for a particular treatment. Some treatments will work…”
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Screening of dystrophin gene deletions in Malaysian patients with Duchenne muscular dystrophy
Published in Medical journal of Malaysia (01-03-2008)“…Duchenne Muscular Dystrophy (DMD) is an X-linked recessive genetic disorder characterized by rapidly progressive muscle weakness. The disease is caused by…”
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81P Genetic association of ABCG2 polymorphisms on triple-negative breast cancer susceptibility and prognosis
Published in ESMO open (01-05-2023)Get full text
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Deficient DNA repair capacity: a predisposing factor and high risk predictive marker in familial colorectal cancer
Published in Journal of experimental & clinical cancer research (01-03-1999)“…Even though colorectal cancer tends to aggregate in families, there is paucity of information on the genetic determinism for familial colorectal cancer (FCRC)…”
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DNA repair proficiency: a potential marker for identification of high risk members in breast cancer families
Published in Cancer letters (13-02-1998)“…Breast cancer is the single largest cancer and causes the high rate of cancer mortality among women. A positive family history of breast cancer is recognized…”
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Evaluating the Impact of MRP1 and MRP2 Polymorphisms on the Pharmacoresistance to Imatinib Treatment Among CML Patients
Published in Annals of oncology (01-11-2013)Get full text
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Predictive Molecular Markers of Imatinib Resistance and Prognosis in Chronic Myeloid Leukemia Patients
Published in Annals of oncology (01-11-2013)Get full text
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Molecular pathogenesis of chronic myelogenous leukaemia
Published in The National medical journal of India (01-09-1992)“…Chronic myelogenous leukaemia is a clonal neoplasm of the pluripotent haematopoietic stem cell which is characterized in most patients by a consistent…”
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