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MBOAT7 rs641738 variant in metabolic-dysfunction- associated fatty liver disease and cardiovascular risk.
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- Medicine & Pharmacy Reports: Clujul Medical, 2023, v. 96, n. 1, p. 41, doi. 10.15386/mpr-2504
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- Publication type:
- 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
Prevalence of Azole-Resistant Aspergillus Section Fumigati Strains Isolated from Romanian Vineyard Soil Samples.
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- Antibiotics (2079-6382), 2023, v. 12, n. 12, p. 1695, doi. 10.3390/antibiotics12121695
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- Publication type:
- Article
Long-Lasting Enhanced Cytokine Responses Following SARS-CoV-2 BNT162b2 mRNA Vaccination.
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- Vaccines, 2024, v. 12, n. 7, p. 736, doi. 10.3390/vaccines12070736
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- Publication type:
- Article
Skeletal Abnormalities and VDR1 Gene Polymorphisms in Mucopolysaccharidosis Patients.
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- Pharmacogenomics & Personalized Medicine, 2021, v. 14, p. 349, doi. 10.2147/PGPM.S295241
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- Publication type:
- Article
CALR versus JAK2 mutated essential thrombocythaemia - a report on 141 patients.
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- British Journal of Haematology, 2015, v. 168, n. 1, p. 151, doi. 10.1111/bjh.13076
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- Publication type:
- Article
The relationship between factor V Leiden, prothrombin G20210A, and MTHFR mutations and the first major thrombotic episode in polycythemia vera and essential thrombocythemia.
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- Annals of Hematology, 2014, v. 93, n. 2, p. 203, doi. 10.1007/s00277-013-1838-6
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- Publication type:
- Article
The G allele of the JAK2 rs10974944 SNP, part of JAK2 46/1 haplotype, is strongly associated with JAK2 V617F-positive myeloproliferative neoplasms.
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- Annals of Hematology, 2010, v. 89, n. 10, p. 979, doi. 10.1007/s00277-010-0960-y
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- Publication type:
- Article
Genomic study via chromosomal microarray analysis in a group of Romanian patients with obesity and developmental disability/intellectual disability.
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- Journal of Pediatric Endocrinology & Metabolism, 2019, v. 32, n. 7, p. 667, doi. 10.1515/jpem-2018-0439
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- Publication type:
- Article
The c.301_302delAG PROP1 gene mutation in Romanian patients with multiple pituitary hormone deficiency.
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- Journal of Pediatric Endocrinology & Metabolism, 2015, v. 28, n. 9/10, p. 993, doi. 10.1515/jpem-2014-0289
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- Publication type:
- Article
Association of 276G>T adiponectin gene polymorphism to plasma adiponectin and albuminuria in type 2 diabetic patients.
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- International Urology & Nephrology, 2012, v. 44, n. 6, p. 1771, doi. 10.1007/s11255-011-0118-4
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- Article
Sex-Specific Differences in Cytokine Production Capacity in Patients with Gout Compared to Controls.
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- Gout, Urate, & Crystal Deposition Disease, 2024, v. 2, n. 2, p. 133, doi. 10.3390/gucdd2020012
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- Article
Urate‐induced immune programming: Consequences for gouty arthritis and hyperuricemia.
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- Immunological Reviews, 2020, v. 294, n. 1, p. 92, doi. 10.1111/imr.12833
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- Article
HFE Gene C282Y, H63D and S65C Mutations Frequency in the Transylvania Region, Romania.
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- Journal of Gastrointestinal & Liver Diseases, 2012, v. 21, n. 2, p. 177
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- Publication type:
- Article
Homozygous G320V Mutation in the HJV Gene Causing Juvenile Hereditary Haemochromatosis Type A. A Case Report.
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- Journal of Gastrointestinal & Liver Diseases, 2010, v. 19, n. 2, p. 191
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- Publication type:
- Article
No association between the STAT5b rs6503691 (C>T) SNP and myeloproliferative neoplasms.
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- European Journal of Haematology, 2013, v. 90, n. 3, p. 257, doi. 10.1111/ejh.12040
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- Article
Possible association between -954G/C iNOS polymorphism in nasal polyposis. A case-control study in a population group of Northern Romania.
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- Romanian Journal of Rhinology, 2016, v. 6, n. 24, p. 197, doi. 10.1515/rjr-2016-0023
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- Publication type:
- Article
The Importance of Homozygous Polymorphisms of Methylenetetrahydrofolate ReducÃase Gene in Romanian Patients with Idiopathic Venous Thromboembolism.
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- 2013
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- Publication type:
- Journal Article
The Importance of Homozygous Polymorphisms of.
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- Balkan Medical Journal, 2013, v. 30, n. 2, p. 197, doi. 10.5152/balkanmedj.2013.7159
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- Article
The C677T Variant in the Methylenetetrahydrofolate Reductase Gene and Idiopathic Spontaneous Abortion in a Romanian Population Group.
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- Notulae Scientia Biologicae, 2012, v. 4, n. 1, p. 7, doi. 10.15835/nsb417259
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- Publication type:
- Article
Diagnostic Usefulness of MLPA Techniques for Recurrent Copy Number Variants Detection in Global Developmental Delay/Intellectual Disability.
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- 2021
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- Publication type:
- Case Study
Familial Essential Thrombocythemia Associated with MPL W515L Mutation in Father and JAK2 V617F Mutation in Daughter.
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- 2014
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- Publication type:
- Case Study
Genetic variants of Interleukin 1-Beta-511 C>T and cervical intraepithelial neoplasia.
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- Ginecologia.ro, 2016, v. 4, n. 13, p. 66
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- Publication type:
- Article
Genetic variants of Interleukin 1-Beta -511 C>T and cervical intraepithelial neoplasia.
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- Ginecologia.ro, 2016, v. 4, n. 12, p. 54
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- Publication type:
- Article
Molecular and Cytogenetic Analysis of Romanian Patients with Differences in Sex Development.
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- Diagnostics (2075-4418), 2021, v. 11, n. 11, p. 2107, doi. 10.3390/diagnostics11112107
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- Publication type:
- Article
Cholelithiasis in Patients with Gaucher Disease type 1: Risk Factors and the Role of ABCG5/ABCG8 Gene Variants.
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- Journal of Gastrointestinal & Liver Diseases, 2016, v. 25, n. 4, p. 447, doi. 10.15403/jgld.2014.1121.254.zim
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- Publication type:
- Article
TGF-β is elevated in hyperuricemic individuals and mediates urate-induced hyperinflammatory phenotype in human mononuclear cells.
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- Arthritis Research & Therapy, 2023, v. 25, n. 1, p. 1, doi. 10.1186/s13075-023-03001-1
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- Publication type:
- Article
Journey from theory to practice: Setting up a Huntington Disease service in Romania.
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- Cognitie, Creier, Comportament/Cognition, Brain, Behavior, 2017, v. 21, n. 3, p. 203, doi. 10.24193/cbb.2017.21.12
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- Publication type:
- Article
VEGF +936 C/T Genetic Polymorphism in Patients with Cervical Dysplasia.
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- Analytical Cellular Pathology: Cellular Oncology, 2016, p. 1, doi. 10.1155/2016/6074275
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- Publication type:
- Article
Non-Syndromic Hearing Loss in a Romanian Population: Carrier Status and Frequent Variants in the GJB2 Gene.
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- Genes, 2023, v. 14, n. 1, p. 69, doi. 10.3390/genes14010069
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- Publication type:
- Article
The XRCC1 Arg194Trp polymorphism is significantly associated with lung adenocarcinoma: a case-control study in an Eastern European Caucasian group.
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- OncoTargets & Therapy, 2015, v. 8, p. 3533, doi. 10.2147/OTT.S92361
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- Publication type:
- Article
Development of a Reliable PCR-RFLP Assay for Investigation of the JAK2 rs10974944 SNP, Which Might Predispose to the Acquisition of Somatic Mutation JAK2.
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- Acta Haematologica, 2010, v. 123, n. 2, p. 84, doi. 10.1159/000264954
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- Publication type:
- Article
Copy number variation analysis in 189 Romanian patients with global developmental delay/intellectual disability.
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- Italian Journal of Pediatrics, 2022, v. 48, n. 1, p. 1, doi. 10.1186/s13052-022-01397-1
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- Publication type:
- Article
Enhanced Innate and Acquired Immune Responses in Systemic Sclerosis Primary Peripheral Blood Mononuclear Cells (PBMCs).
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- International Journal of Molecular Sciences, 2023, v. 24, n. 19, p. 14438, doi. 10.3390/ijms241914438
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- Publication type:
- Article
XRCC3 THR241MET POLYMORPHISM IS NOT ASSOCIATED WITH LUNG CANCER RISK IN A ROMANIAN POPULATION.
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- Clujul Medical, 2016, v. 89, n. 1, p. 89, doi. 10.15386/cjmed-523
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- Publication type:
- Article
COMBINED GLUTATHIONE S TRANSFERASE M1/T1 NULL GENOTYPES IS ASSOCIATED WITH TYPE 2 DIABETES MELLITUS.
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- Clujul Medical, 2015, v. 88, n. 2, p. 159, doi. 10.15386/cjmed-436
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- Publication type:
- Article
THE ROLE OF OXIDATIVE STRESS AND VASCULAR INSUFFICIENCY IN PRIMARY OPEN ANGLE GLAUCOMA.
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- Clujul Medical, 2014, v. 87, n. 3, p. 143, doi. 10.15386/cjmed-295
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- Publication type:
- Article
GENETIC POLYMORPHISM OF GLUTATHIONE S TRANSFERASE AND LUNG CANCER RISK IN NORTHERN ROMANIA.
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- Clujul Medical, 2011, v. 84, n. 4, p. 520
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- Publication type:
- Article
ALPHA 1 ANTITRYPSIN DEFICIENCY AND LUNG CANCER RISK.
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- Clujul Medical, 2011, v. 84, n. 2, p. 20
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- Publication type:
- Article
POLIMORFISMUL APOPROTEINEI E LA PACIENŢII CU BOALĂGAUCHER TIP I.
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- Clujul Medical, 2009, v. 82, n. 4, p. 586
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- Publication type:
- Article
Gene variants of osteoprotegerin, estrogen-, calcitonin- and vitamin D-receptor genes and serum markers of bone metabolism in patients with Gaucher disease type 1.
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- 2018
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- Publication type:
- journal article
Clinical and genetic characteristics in a group of 45 patients with Turner syndrome (monocentric study).
- Published in:
- Therapeutics & Clinical Risk Management, 2017, v. 13, p. 613, doi. 10.2147/TCRM.S126301
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- Publication type:
- Article
The role of NOS2A -954G/C and vascular endothelial growth factor +936C/T polymorphisms in type 2 diabetes mellitus and diabetic nonproliferative retinopathy risk management.
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- 2015
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- Publication type:
- journal article
Cystathionine β-synthase 844ins68 Genetic Polymorphism in Spontaneous Abortion Susceptibility.
- Published in:
- Applied Medical Informatics, 2011, v. 29, n. 4, p. 34
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- Publication type:
- Article
The Analysis of Genetic Polymorphism. The Relationship between Interleukin - 4 Polymorphisms and Intraepithelial Cervical Neoplasia.
- Published in:
- Applied Medical Informatics, 2010, v. 27, n. 3, p. 43
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- Publication type:
- Article
METHYLENETETRAHYDROFOLATE REDUCTASE G1793A POLYMORPHISM AND MALE INFERTILITY IN A ROMANIAN POPULATION GROUP.
- Published in:
- Studia Universitatis Vasile Goldis Seria Stiintele Vietii (Life Sciences Series), 2010, v. 20, n. 1, p. 31
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- Publication type:
- Article
Relationship between VKORC1 single nucleotide polymorphism 1173C>T, bone mineral density & carotid intima-media thickness.
- Published in:
- Indian Journal of Medical Research, 2013, v. 137, n. 4, p. 734
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- Publication type:
- Article