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Copy Number Variations and Gene Mutations Identified by Multiplex Ligation-Dependent Probe Amplification in Romanian Chronic Lymphocytic Leukemia Patients.
- Published in:
- Journal of Personalized Medicine, 2023, v. 13, n. 8, p. 1239, doi. 10.3390/jpm13081239
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- Article
Association of TLR4 Rs4986791 Polymorphism and TLR9 Haplotypes with Acute Myeloid Leukemia Susceptibility: A Case-Control Study of Adult Patients.
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- Journal of Personalized Medicine, 2022, v. 12, n. 3, p. 409, doi. 10.3390/jpm12030409
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- Article
TET2 rs1548483 SNP Associating with Susceptibility to Molecularly Annotated Polycythemia Vera and Primary Myelofibrosis.
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- Journal of Personalized Medicine, 2020, v. 10, n. 4, p. 259, doi. 10.3390/jpm10040259
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- Article
Glutathione S-transferase (GSTM1, GSTT1) gene polymorphisms, maternal gestational weight gain, bioimpedance factors and their relationship with birth weight: a cross-sectional study in Romanian mothers and their newborns.
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- Romanian Journal of Morphology & Embryology, 2017, v. 58, n. 4, p. 1285
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- Article
TERT rs2853669 as a predictor for overall survival in patients with acute myeloid leukaemia.
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- 2022
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- Publication type:
- journal article
The Genetic Landscape of Myelodysplastic Neoplasm Progression to Acute Myeloid Leukemia.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 6, p. 5734, doi. 10.3390/ijms24065734
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- Article
From Descriptive to Functional Genomics of Leukemias Focusing on Genome Engineering Techniques.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 18, p. 10065, doi. 10.3390/ijms221810065
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- Article
Association Analysis of TP53 rs1042522, MDM2 rs2279744, rs3730485, MDM4 rs4245739 Variants and Acute Myeloid Leukemia Susceptibility, Risk Stratification Scores, and Clinical Features: An Exploratory Study.
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- Journal of Clinical Medicine, 2020, v. 9, n. 6, p. 1672, doi. 10.3390/jcm9061672
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- Article
Modelling the Effects of MCM7 Variants, Somatic Mutations, and Clinical Features on Acute Myeloid Leukemia Susceptibility and Prognosis.
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- Journal of Clinical Medicine, 2020, v. 9, n. 1, p. 158, doi. 10.3390/jcm9010158
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- Publication type:
- Article
Pathogenic Biallelic Mutations in ECHS1 in a Case with Short-Chain Enoyl-CoA Hydratase (SCEH) Deficiency-Case Report and Literature Review.
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- International Journal of Environmental Research & Public Health, 2022, v. 19, n. 4, p. 2088, doi. 10.3390/ijerph19042088
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- Publication type:
- Article
Cytokine TGF-β1, TNF-α, IFN-γ and IL-6 Gene Polymorphisms and Localization of Premalignant Gastric Lesions in Immunohistochemically H. pylori-negative Patients.
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- International Journal of Medical Sciences, 2021, v. 18, n. 12, p. 2743, doi. 10.7150/ijms.60517
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- Publication type:
- Article
Cytokine rs361525, rs1800750, rs1800629, rs1800896, rs1800872, rs1800795, rs1800470, and rs2430561 SNPs in relation with prognostic factors in acute myeloid leukemia.
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- Cancer Medicine, 2019, v. 8, n. 12, p. 5492, doi. 10.1002/cam4.2424
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- Article
MC4R and ENPP1 gene polymorphisms and their implication in maternal and neonatal risk for obesity.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-47402-2
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- Publication type:
- Article
Significant Associations between AXIN1 rs1805105, rs12921862, rs370681 Haplotypes and Variant Genotypes of AXIN2 rs2240308 with Risk of Congenital Heart Defects.
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- International Journal of Environmental Research & Public Health, 2020, v. 17, n. 20, p. 7671, doi. 10.3390/ijerph17207671
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- Article
MECOM, HBS1L-MYB, THRB-RARB, JAK2, and TERT polymorphisms defining the genetic predisposition to myeloproliferative neoplasms: A study on 939 patients.
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- American Journal of Hematology, 2018, v. 93, n. 1, p. 100, doi. 10.1002/ajh.24946
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- Article
An Update on the Genetic Aspects in Congenital Ventricular Septal Defect.
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- Acta Marisiensis. Seria Medica, 2020, v. 66, n. 2, p. 43, doi. 10.2478/amma-2020-0012
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- Article
Genetic Investigation and Clinical Aspects in a Romanian Treacher Collins Syndrome Family - A Case Report.
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- Acta Marisiensis. Seria Medica, 2019, v. 65, n. 4, p. 157, doi. 10.2478/amma-2019-0026
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- Publication type:
- Article
Antibody Protection against Long-Term Memory Loss Induced by Monomeric C-Reactive Protein in a Mouse Model of Dementia.
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- Biomedicines, 2021, v. 9, n. 7, p. 828, doi. 10.3390/biomedicines9070828
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- Article
Detecţia mozaicului în diagnosticul prenatal prin tehnicile MLPA şi QF-PCR.
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- Ginecologia.ro, 2019, p. 66
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- Publication type:
- Article
From Six Gene Polymorphisms of the Antioxidant System, Only GPX Pro198Leu and GSTP1 Ile105Val Modulate the Risk of Acute Myeloid Leukemia.
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- Oxidative Medicine & Cellular Longevity, 2015, v. 2015, p. 1, doi. 10.1155/2016/2536705
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- Publication type:
- Article
The CAT-262 C>T, MnSOD Ala16Val, GPX1 Pro198Leu Polymorphisms Related to Oxidative Stress and the Presence of Gastric Lesions.
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- Journal of Gastrointestinal & Liver Diseases, 2018, v. 27, n. 4, p. 371, doi. 10.15403/jgld.2014.1121.274.cat
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- Publication type:
- Article
The Influence of GPX1 Pro198Leu, CAT C262T and MnSOD Ala16Val Gene Polymorphisms on Susceptibility for Non-Hodgkin Lymphoma and Overall Survival Rate at Five Years from Diagnosis.
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- Acta Medica Marisiensis, 2019, v. 65, n. 1, p. 25, doi. 10.2478/amma-2019-0005
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- Publication type:
- Article
Development, Applications, Benefits, Challenges and Limitations of the New Genome Engineering Technique. An Update Study.
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- Acta Medica Marisiensis, 2017, v. 63, n. 1, p. 4, doi. 10.1515/amma-2017-0007
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- Publication type:
- Article
Deep Venous Thrombosis Associated With Inferior Vena Cava Abnormalities And Hypoplastic Kidney In Siblings.
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- Acta Medica Marisiensis, 2016, v. 62, n. 2, p. 266, doi. 10.1515/amma-2016-0011
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- Publication type:
- Article
Study on Changes of the Urea, Serum Creatinine and Glomerular Protein Permeability, after General Anesthesia with Sevoflurane.
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- Acta Medica Marisiensis, 2015, v. 61, n. 3, p. 176, doi. 10.1515/amma-2015-0053
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- Publication type:
- Article
Pitt-Hopkins Syndrome: Clinical and Molecular Findings of a 5-Year-Old Patient.
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- Genes, 2020, v. 11, n. 6, p. 596, doi. 10.3390/genes11060596
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- Article
Presence of copy number aberrations and clinical prognostic factors in patients with acute myeloid leukemia: an analysis of effect modification - Authors’ reply.
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- Polish Archives of Internal Medicine, 2020, v. 130, n. 4, p. 347, doi. 10.20452/pamw.15327
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- Article
Presence of copy number aberration and clinical prognostic factors in patients with acute myeloid leukemia: an analysis of effect modification.
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- Polish Archives of Internal Medicine, 2019, v. 129, n. 12, p. 898, doi. 10.20452/pamw.15093
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- Publication type:
- Article
The Role of DNA Repair (XPC , XPD , XPF , and XPG) Gene Polymorphisms in the Development of Myeloproliferative Neoplasms.
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- Medicina (1010660X), 2024, v. 60, n. 3, p. 506, doi. 10.3390/medicina60030506
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- Publication type:
- Article
Evaluation of the Copy Number Variants and Single-Nucleotide Polymorphisms of ABCA3 in Newborns with Respiratory Distress Syndrome—A Pilot Study.
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- Medicina (1010660X), 2024, v. 60, n. 3, p. 419, doi. 10.3390/medicina60030419
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- Article
Analysis of Mutational Status of IGHV , and Cytokine Polymorphisms as Prognostic Factors in Chronic Lymphocytic Leukemia: The Romanian Experience.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 3, p. 1799, doi. 10.3390/ijms25031799
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- Publication type:
- Article
Descriptive and Functional Genomics in Neonatal Respiratory Distress Syndrome: From Lung Development to Targeted Therapies.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 1, p. 649, doi. 10.3390/ijms25010649
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- Publication type:
- Article