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Archives of Biological Sciences, ISSN 0354-4664, 2014, Volume 66, Issue 3, pp. 1055 - 1059
Myelodysplastic syndromes (MDS) are clonal hematologic stem cell disorders with an as yet unknown molecular pathology. Genetic instability has been proposed as... 
657DEL5 | MDS | NBS1 mutations | Nibrin | CELLS | COMPLEX | PROTEIN | NIJMEGEN BREAKAGE SYNDROME | DNA-DAMAGE RESPONSE | REPAIR | TELOMERE DYSFUNCTION | 657del5 | BIOLOGY | nibrin | ATAXIA-TELANGIECTASIA | APLASTIC-ANEMIA | ASSOCIATION
Journal Article
Journal of Medical Biochemistry, ISSN 1452-8258, 7/2010, Volume 29, Issue 3, pp. 135 - 138
The most widespread diseases of modern man have a polygenic basis, including genetic predisposition and factors in the external environment. Such is the case... 
atherosclerosis | trombofilija | genski polimorfizmi | thrombophilia | ateroskleroza | gene polymorphisms | RISK | ABDOMINAL AORTIC-ANEURYSMS | BIOCHEMISTRY & MOLECULAR BIOLOGY
Journal Article
Clinical and Experimental Rheumatology, ISSN 0392-856X, 2012, Volume 30, Issue 2, pp. 178 - 183
Journal Article
Archives of Medical Science, ISSN 1734-1922, 12/2010, Volume 6, Issue 6, pp. 854 - 859
Introduction: Assuming that spina bifida (SB) is a genetically controlled disease, the aim of our study was to evaluate the degree of genetic homozygosity and... 
Spina bifida | Genetic homozygosity | Genetic variability | genetic homozygosity | MEDICINE, GENERAL & INTERNAL | spina bifida | NEURAL-TUBE DEFECTS | genetic variability | Basic Research
Journal Article
Journal of Medical Biochemistry, ISSN 1452-8258, 2014, Volume 33, Issue 1, pp. 3 - 7
Molecular genetic testing is part of modern medical practice. DNA tests are an essential part of diagnostics and genetic counseling in single gene diseases,... 
Molecular genetics | Test | Genetic counselling | Methods | molecular genetics | genetic counselling | HOMOCYSTEINE | test | GENOTYPE | methods | BIOCHEMISTRY & MOLECULAR BIOLOGY | THROMBOPHILIA | GENOMIC MEDICINE
Journal Article
Archives of Biological Sciences, ISSN 0354-4664, 2012, Volume 64, Issue 2, pp. 787 - 792
Duchenne and Becker muscular dystrophy (DMD/BMD) are severe X-linked neuromuscular disorders caused by mutations in the dystrophin gene. Our aim was to... 
SYBR | green | Real-time PCR | Duchenne/Becker muscular dystrophy | carrier detection | ΔΔCt method | DIAGNOSIS | DUPLICATIONS | SYBR (R) Green | DMD/BMD | DMD GENE | IDENTIFICATION | FEMALE CARRIERS | Delta Delta Ct method | POLYMERASE-CHAIN-REACTION | BIOLOGY | DUCHENNE MUSCULAR-DYSTROPHY | DELETIONS | SYBR® Green
Journal Article
Archives of Biological Sciences, ISSN 0354-4664, 2011, Volume 63, Issue 3, pp. 649 - 653
Myelodysplastic syndromes (MDS) are rare in children and only a few studies have analyzed their molecular mechanisms. The NPM1 gene encodes for nucleophosmin... 
Nucleophosmin | Children | NPM1 mutation | Myelodysplastic syndromes | PROGNOSTIC IMPLICATIONS | AML | NUCLEOPHOSMIN MUTATIONS | NES MOTIF | STABILITY | ACUTE MYELOGENOUS LEUKEMIA | ACUTE MYELOID-LEUKEMIA | PREVALENCE | nucleophosmin | NORMAL KARYOTYPE | children | BIOLOGY | AGE
Journal Article
Archives of Biological Sciences, ISSN 0354-4664, 2010, Volume 62, Issue 4, pp. 957 - 965
Balkan endemic nephropathy (BEN) was recognized as a distinct entity more than 50 years ago, but the exact environmental and genetic causes of the disease... 
RAS system | ACE I/D | Balkan endemic nephropathy | AT1R A1166C | Candidate gene polymorphism | II TYPE-1 RECEPTOR | candidate gene polymorphism | DIABETIC-NEPHROPATHY | ARISTOLOCHIC ACID | INSERTION-DELETION POLYMORPHISM | RENIN-ANGIOTENSIN SYSTEM | COAL DEPOSITS | DISEASE | BIOLOGY | CONVERTING-ENZYME GENE | A1166C POLYMORPHISM | BULGARIAN PATIENTS
Journal Article
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