Search Results - "Chuong, Ho Quoc"
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Spectrum of HBB gene mutations among 696 β–thalassemia patients and carriers in Southern Vietnam
Published in Molecular biology reports (01-04-2022)“…Background Thalassemias are common inherited blood disorders that have been extensively studied in Asia. Thus far, data on mutations of the HBB gene in…”
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Liquid biopsy uncovers distinct patterns of DNA methylation and copy number changes in NSCLC patients with different EGFR-TKI resistant mutations
Published in Scientific reports (12-08-2021)“…Targeted therapy with tyrosine kinase inhibitors (TKI) provides survival benefits to a majority of patients with non-small cell lung cancer (NSCLC). However,…”
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A Simple, Rapid, and Cost-Effective PCR Procedure for Detection of NUDT15 Gene Variants in Vietnamese Patients with Acute Lymphoblastic Leukemia
Published in Journal of laboratory physicians (01-12-2023)“…Abstract Objective The NUDT15 variants impact thiopurine dose selection in acute lymphoblastic leukemia patients. The ability to rapidly detect variants is…”
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Ultra-Deep Sequencing of Plasma-Circulating DNA for the Detection of Tumor- Derived Mutations in Patients with Nonmetastatic Colorectal Cancer
Published in Cancer investigation (21-04-2022)“…Identification of tumor-derived mutation (TDM) in liquid biopsies (LB), especially in early-stage patients, faces several challenges, including low…”
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Molecular characteristics of young‐onset colorectal cancer in Vietnamese patients
Published in Asia-Pacific journal of clinical oncology (01-12-2022)“…Background Colorectal cancer (CRC) is one of the most common cancer globally. Understanding the genetic characteristics of CRC is essential for appropriate…”
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Pre-gestational diabetes mellitus, gestational diabetes mellitus, and its association with the MTHFR C677T polymorphism
Published in Medicine (Baltimore) (12-07-2024)“…Gestational diabetes mellitus (GDM) is a common condition during pregnancy and is associated with an increased risk of pre-eclampsia. The…”
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Spectrum of WAS gene mutations in Vietnamese patients with Wiskott-Aldrich syndrome
Published in Pediatrics international (01-01-2024)“…WAS gene mutational analysis is crucial to establish a definite diagnosis of Wiskott-Aldrich syndrome (WAS). Data on the genetic background of WAS in…”
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Spectrum mutations of PRF1, UNC13D, STX11, and STXBP2 genes in Vietnamese patients with hemophagocytic lymphohistiocytosis
Published in International journal of laboratory hematology (01-12-2021)“…Introduction The prevalence of gene mutations in hemophagocytic lymphohistiocytosis (HLH) varied between studies. Thus far, data on the genetic background of…”
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Clinical and Hematological Relevance of JAK2V617F, CALR, and MPL Mutations in Vietnamese Patients with Essential Thrombocythemia
Published in Asian Pacific journal of cancer prevention : APJCP (01-09-2019)“…Background: The picture of Vietnamese patients with essential thrombocythemia (ET) remains mostly undetermined. Our study intended to determine the frequency…”
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