Found: 23
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Genotype TNF-α(-308) and Silicosis on Factory Workers in Vietnam in 2020.
- Published in:
- Inzynieria Mineralna, 2021, v. 48, n. 2, p. 459, doi. 10.29227/IM-2021-02-43
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- Article
Genetic analysis of 55 northern Vietnamese patients with Wilson disease: seven novel mutations in ATP7B.
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- Journal of Genetics, 2017, v. 96, n. 6, p. 933, doi. 10.1007/s12041-017-0857-9
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- Article
In silico validation revealed the role of SCN5A mutations and their genotype–phenotype correlations in Brugada syndrome.
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- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 12, p. 1, doi. 10.1002/mgg3.2263
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- Article
Mutation spectrum of retinoblastoma patients in Vietnam.
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- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 11, p. 1, doi. 10.1002/mgg3.2244
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- Publication type:
- Article
Association of the STAT4, CDKN1A, and IRF5 variants with risk of lupus nephritis and renal biopsy classification in patients in Vietnam.
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- Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 4, p. 1, doi. 10.1002/mgg3.1648
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- Article
Preventing AID, a physiological mutator, from deleterious activation: regulation of the genomic instability that is associated with antibody diversity.
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- International Immunology, 2010, v. 22, n. 4, p. 227, doi. 10.1093/intimm/dxq023
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- Article
Acromesomelic dysplasia Maroteaux‐type in patients from Vietnam.
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- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 8, p. 1420, doi. 10.1002/ajmg.a.61192
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- Article
Transformer vibration and noise monitoring system using internet of things.
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- IET Communications (Wiley-Blackwell), 2023, v. 17, n. 7, p. 815, doi. 10.1049/cmu2.12585
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- Publication type:
- Article
Experience of Autologous Immunotherapy for Non-Small Cell Lung Cancer Using Zoledronate-Actived Gammadelta T Cells.
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- Clinical Laboratory, 2024, v. 70, n. 1, p. 146, doi. 10.7754/Clin.Lab.2023.230663
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- Article
Oro-Dental Health and Primary Nephrotic Syndrome among Vietnamese Children.
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- Children, 2021, v. 8, n. 6, p. 1, doi. 10.3390/children8060494
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- Article
B cell–specific and stimulation-responsive enhancers derepress Aicda by overcoming the effects of silencers.
- Published in:
- Nature Immunology, 2010, v. 11, n. 2, p. 148, doi. 10.1038/ni.1829
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- Article
Targeted next‐generation sequencing determined a novel SGCG variant that is associated with limb‐girdle muscular dystrophy type 2C: A case report.
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- 2023
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- Publication type:
- Case Study
A case of self‐improving collodion ichthyosis in Vietnam.
- Published in:
- Pediatric Dermatology, 2020, v. 37, n. 3, p. 574, doi. 10.1111/pde.14128
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- Publication type:
- Article
A novel IGHMBP2 variant and clinical diversity in Vietnamese SMARD1 and CMT2S patients.
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- Frontiers in Pediatrics, 2024, p. 1, doi. 10.3389/fped.2024.1165492
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- Publication type:
- Article
The Plasma Levels of Protein Adiponectin (AdipoQ) and Meteorin-Like (Metrnl) in Newly Diagnosed Type 2 Diabetes Mellitus.
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- Diabetes, Metabolic Syndrome & Obesity: Targets & Therapy, 2024, v. 17, p. 2903, doi. 10.2147/DMSO.S471954
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- Publication type:
- Article
Feasibility of combining short tandem repeats (STRs) haplotyping with preimplantation genetic diagnosis (PGD) in screening for beta thalassemia.
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- PLoS ONE, 2022, v. 17, n. 12, p. 1, doi. 10.1371/journal.pone.0278539
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- Article
Mutation characteristic of 103 haemophilia A patients in Vietnam: Identification of novel mutations.
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- Haemophilia, 2019, v. 25, n. 4, p. e274, doi. 10.1111/hae.13738
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- Publication type:
- Article
Novel mutations in the SGCA gene in unrelated Vietnamese patients with limb-girdle muscular dystrophies disease.
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- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1248338
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- Publication type:
- Article
Merosin-deficient congenital muscular dystrophy type 1a: detection of LAMA2 variants in Vietnamese patients.
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- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1183663
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- Article
Relation between Single Nucleotide Polymorphism rs3738423 (C>T) of NPHS2 Gene and some Biochemical Parameters in Pediatrics Nephrotic Syndrome Patients.
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- Walailak Journal of Science & Technology, 2021, v. 18, n. 1, p. 1, doi. 10.48048/wjst.2021.6518
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- Article
BRCA1/2 Mutations in Vietnamese Patients with Hereditary Breast and Ovarian Cancer Syndrome.
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- Genes, 2022, v. 13, n. 2, p. 268, doi. 10.3390/genes13020268
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- Publication type:
- Article
Treatment outcomes of EGFR-TKI with or without locoregional brain therapy in advanced EGFR-mutant non-small cell lung cancer patients with brain metastases.
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- Contemporary Oncology / Współczesna Onkologia, 2023, v. 27, n. 2, p. 71, doi. 10.5114/wo.2023.129366
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- Article
Molecular Characterization and Genotype-Phenotype Correlation of G6PD Mutations in Five Ethnicities of Northern Vietnam.
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- Anemia (20901267), 2022, p. 1, doi. 10.1155/2022/2653089
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- Publication type:
- Article