X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (17) 17
index medicus (17) 17
female (13) 13
male (13) 13
middle aged (8) 8
genetic aspects (6) 6
oncology (6) 6
phenotype (6) 6
adult (5) 5
aged (5) 5
methotrexate (5) 5
rheumatoid arthritis (5) 5
serbia (5) 5
analysis (4) 4
arthritis, rheumatoid - genetics (4) 4
biology (4) 4
biomedicine (4) 4
cancer (4) 4
child (4) 4
child, preschool (4) 4
gene frequency (4) 4
genetic predisposition to disease (4) 4
genetic research (4) 4
genetics & heredity (4) 4
immunology (4) 4
immunophenotyping (4) 4
lung neoplasms - genetics (4) 4
mutation (4) 4
pcr (4) 4
polymorphism, genetic (4) 4
prognosis (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
cancer research (3) 3
deletions (3) 3
gene mutations (3) 3
genetic polymorphism (3) 3
genotype (3) 3
immunohistochemistry (3) 3
infant (3) 3
lung neoplasms - pathology (3) 3
methotrexate - adverse effects (3) 3
pediatrics (3) 3
pharmacogenetics (3) 3
pharmacology & pharmacy (3) 3
polymerase chain reaction (3) 3
risk factors (3) 3
severity of illness index (3) 3
tumors (3) 3
acute lymphoblastic-leukemia (2) 2
analysis of variance (2) 2
antirheumatic agents - adverse effects (2) 2
association (2) 2
azoospermia (2) 2
biomedicine general (2) 2
carcinoma (2) 2
case-control studies (2) 2
cdh13 (2) 2
chi-square distribution (2) 2
chromosome deletion (2) 2
chromosome origin (2) 2
dhfr (2) 2
diagnosis (2) 2
disability evaluation (2) 2
dna mutational analysis (2) 2
duplications (2) 2
efficacy (2) 2
enzymes (2) 2
expression (2) 2
genes (2) 2
genetic association studies (2) 2
genetic testing (2) 2
genetics (2) 2
hemic and lymphatic diseases (2) 2
human genetics (2) 2
identification (2) 2
immunophenotype (2) 2
imprinting (2) 2
infertility (2) 2
leukemia (2) 2
logistic models (2) 2
lung cancer (2) 2
medical colleges (2) 2
medicine, general & internal (2) 2
methylation (2) 2
mgmt (2) 2
microfertilization (2) 2
modifying antirheumatic drugs (2) 2
mthfr (2) 2
musculoskeletal diseases (2) 2
myelodysplastic syndromes - genetics (2) 2
neoplasm staging (2) 2
oligospermia (2) 2
p53 mutations (2) 2
pathology (2) 2
polymorphism (2) 2
polymorphism, single nucleotide (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
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
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 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
Nastava i vaspitanje, ISSN 0547-3330, 2016, Volume 65, Issue 2, pp. 439 - 449
The aim of this research was to compare knowledge retention and course satisfaction among the students who attended a combined teaching course (traditional... 
educational technologies | combined learning | e-learning
Journal Article
Clinical and Experimental Rheumatology, ISSN 0392-856X, 2012, Volume 30, Issue 2, pp. 178 - 183
Journal Article
Journal Article
Clinical Lung Cancer, ISSN 1525-7304, 2012, Volume 13, Issue 4, pp. 297 - 303
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
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
Srpski Arhiv za Celokupno Lekarstvo, ISSN 0370-8179, 2008, Volume 136, Issue 3-4, pp. 126 - 130
Introduction Y chromosome microdeletions are the second most frequent genetic cause of male infertility after Klinefelter's syndrome. Objective The aim of the... 
Azoospermia | Infertility | Microfertilization | PCR | Y chromosome | Oligospermia | microfertilization | oligospermia | azoospermia | infertility
Journal Article
No results were found for your search.

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