X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (14) 14
index medicus (14) 14
female (11) 11
male (10) 10
phenotype (8) 8
methotrexate (7) 7
middle aged (7) 7
rheumatoid arthritis (7) 7
adult (5) 5
aged (5) 5
child (5) 5
pharmacology & pharmacy (5) 5
serbia (5) 5
arthritis, rheumatoid - genetics (4) 4
biology (4) 4
child, preschool (4) 4
genetic aspects (4) 4
genotype (4) 4
oncology (4) 4
pharmacogenetics (4) 4
polymorphism (4) 4
tumor proteins (4) 4
aged, 80 and over (3) 3
arthritis, rheumatoid - diagnosis (3) 3
arthritis, rheumatoid - drug therapy (3) 3
arthritis, rheumatoid - enzymology (3) 3
biomedicine (3) 3
cancer (3) 3
dentistry (3) 3
diagnosis (3) 3
expression (3) 3
gene frequency (3) 3
gene mutations (3) 3
genes (3) 3
genetic homozygosity (3) 3
genetic polymorphism (3) 3
genetic predisposition to disease (3) 3
genetic research (3) 3
genetics & heredity (3) 3
homozygote (3) 3
immunohistochemistry (3) 3
lung neoplasms - genetics (3) 3
lung neoplasms - pathology (3) 3
medicine, general & internal (3) 3
methotrexate - adverse effects (3) 3
modifying antirheumatic drugs (3) 3
musculoskeletal diseases (3) 3
mutation (3) 3
oral squamous cell carcinoma (3) 3
pediatrics (3) 3
polymerase chain reaction (3) 3
polymorphism, genetic (3) 3
prognosis (3) 3
risk factors (3) 3
risk-factors (3) 3
severity of illness index (3) 3
acute lymphoblastic-leukemia (2) 2
adolescent (2) 2
age (2) 2
analysis (2) 2
analysis of variance (2) 2
antirheumatic agents - adverse effects (2) 2
association (2) 2
biomedicine general (2) 2
cancer research (2) 2
carcinoma (2) 2
carcinoma, squamous cell - genetics (2) 2
case-control studies (2) 2
chi-square distribution (2) 2
children (2) 2
chromosome origin (2) 2
deletions (2) 2
dhfr (2) 2
disability evaluation (2) 2
dna, neoplasm - analysis (2) 2
drug therapy (2) 2
duplications (2) 2
efficacy (2) 2
enzymes (2) 2
genetics (2) 2
hemic and lymphatic diseases (2) 2
hrc-test (2) 2
identification (2) 2
immunology (2) 2
immunophenotype (2) 2
immunophenotyping (2) 2
imprinting (2) 2
infant (2) 2
logistic models (2) 2
lung cancer (2) 2
management (2) 2
medicine (2) 2
medicine, research & experimental (2) 2
mthfr (2) 2
myelodysplastic syndromes - genetics (2) 2
neural-tube defects (2) 2
p53 (2) 2
p53 mutations (2) 2
pathology (2) 2
pcr (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


European Journal of Clinical Pharmacology, ISSN 0031-6970, 3/2013, Volume 69, Issue 3, pp. 377 - 383
Gamma-glutamyl hydrolase (GGH), cyclin D1 (CCND1) and thymidylate synthase (TS) genes encode enzymes that are involved in methotrexate (MTX) action. In a group... 
Biomedicine | Pharmacology/Toxicology | Methotrexate | Rheumatoid arthritis | Genetic polymorphism | MODIFYING ANTIRHEUMATIC DRUGS | REDUCED FOLATE CARRIER | G870A POLYMORPHISM | COMMON POLYMORPHISMS | RHEUMATOID-ARTHRITIS PATIENTS | ACUTE LYMPHOBLASTIC-LEUKEMIA | CANCER SUSCEPTIBILITY | FUNCTIONAL-ANALYSIS | PHARMACOLOGY & PHARMACY | REDUCTASE GENES | THYMIDYLATE-SYNTHASE | Bone Marrow Diseases - enzymology | Multivariate Analysis | Humans | Methotrexate - pharmacokinetics | Middle Aged | gamma-Glutamyl Hydrolase - metabolism | Male | Young Adult | Arthritis, Rheumatoid - drug therapy | Aged, 80 and over | Antirheumatic Agents - adverse effects | Adult | Female | Odds Ratio | gamma-Glutamyl Hydrolase - genetics | Arthritis, Rheumatoid - diagnosis | Bone Marrow - drug effects | Severity of Illness Index | Genetic Predisposition to Disease | Pharmacogenetics | Bone Marrow Diseases - chemically induced | Gene Frequency | Risk Factors | Thymidylate Synthase - metabolism | Arthritis, Rheumatoid - enzymology | Logistic Models | Chi-Square Distribution | Thymidylate Synthase - genetics | Bone Marrow Diseases - genetics | Polymorphism, Genetic | Methotrexate - adverse effects | Arthritis, Rheumatoid - genetics | Phenotype | Analysis of Variance | Cyclin D1 - genetics | Antirheumatic Agents - pharmacokinetics | Aged | Rheumatoid factor | Complications and side effects | Enzymes | Genes | Hydrolases | Genetic aspects | Universities and colleges | Bone marrow | Genotype & phenotype | Drug therapy | Toxicity | Patients | Index Medicus
Journal Article
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
Genetika, ISSN 0534-0012, 2016, Volume 48, Issue 2, pp. 707 - 716
Retinopathy of prematurity (ROP) is a vascular proliferative disorder of retina, that causes visual impairment in premature children. Beside well known risk... 
4a/b polymorphism | Retinopathy of prematurity | SNP | T-786C polymorphism | ENOS gene | AGRONOMY | RISK-FACTORS | VARIANTS | eNOS gene | GENETICS & HEREDITY | GROWTH-FACTOR | ASSOCIATION | retinopathy of prematurity
Journal Article
TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE, ISSN 0040-8727, 04/2019, Volume 247, Issue 4, pp. 259 - 264
Early-onset neonatal sepsis (EOS) is diagnosed during the first 7 days of neonatal life and is the major cause of morbidity and mortality among preterm... 
C-REACTIVE PROTEIN | MORTALITY | MEDICINE, RESEARCH & EXPERIMENTAL | DIAGNOSIS | INFECTIONS | preterm infants | SUSCEPTIBILITY | PROCALCITONIN | gene polymorphism | INTERLEUKIN-6 | interleukin 6 | MEDICINE, GENERAL & INTERNAL | BIRTH-WEIGHT INFANTS | tumor necrosis factor alpha | SEPTIC SHOCK | early onset sepsis | EXPRESSION
Journal Article
Expert Opinion on Drug Metabolism & Toxicology, ISSN 1742-5255, 03/2019, Volume 15, Issue 3, pp. 253 - 257
Background: Methotrexate (MTX), a folate analogue, is the most commonly used disease-modifying drug in the treatment of rheumatoid arthritis (RA). However,... 
DHFR | toxicity | methotrexate | genetic polymorphism | rheumatoid arthritis | pharmacogenetics | EFFICACY | GENOTYPE | BIOCHEMISTRY & MOLECULAR BIOLOGY | POOR RESPONSE | DISEASE | RESISTANCE | PHARMACOLOGY & PHARMACY | TOXICOLOGY | Index Medicus
Journal Article
JOURNAL OF PHARMACY AND PHARMACEUTICAL SCIENCES, ISSN 1482-1826, 04/2019, Volume 22, Issue 1, pp. 142 - 149
Purpose: Treatment of Ischemic stroke (IS) in acute phase is based on the use of thrombolytic rt-PA therapy. We aimed to determine whether different alleles... 
SYSTEMATIC ANALYSIS | GLOBAL BURDEN | HEART | RISK-FACTORS | PLASMINOGEN-ACTIVATOR | GENOTYPE | CARDIOVASCULAR-DISEASE | PHARMACOLOGY & PHARMACY | 4G/5G POLYMORPHISM | ANGIOTENSIN-CONVERTING ENZYME | HEALTH-CARE PROFESSIONALS
Journal Article
Archives of Biological Sciences, ISSN 0354-4664, 2014, Volume 66, Issue 2, pp. 729 - 734
The effect of 5,10-methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphism on serum lipid profiles is controversial. We randomly selected 530... 
Schoolchildren | MTHFR gene | MTHFR 677T allele | Lipid levels | Atherosclerosis | Polymorphism | atherosclerosis | schoolchildren | lipid levels | polymorphism
Journal Article
Genetika, ISSN 0534-0012, 2016, Volume 48, Issue 1, pp. 395 - 408
A folate analogue methotrexate (MTX) is the most commonly used disease-modifying drug in the treatment of rheumatoid arthritis. However, the clinical response... 
MTHFR | MTHFD1 | RFC1 | Methotrexate | Rheumatoid arthritis | Genetic polymorphism | methotrexate | genetic polymorphism | rheumatoid arthritis
Journal Article
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
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 Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.