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index medicus (11) 11
atherosclerosis (7) 7
humans (7) 7
cardiac & cardiovascular systems (4) 4
coronary heart disease (4) 4
gene expression (4) 4
research (4) 4
risk factors (4) 4
biochemistry (3) 3
cells, cultured (3) 3
cholesterol (3) 3
chromosomes, human, pair 9 - genetics (3) 3
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genetic aspects (3) 3
genetics (3) 3
genomics (3) 3
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mutation (3) 3
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polymorphism, single nucleotide (3) 3
proteins (3) 3
9p21.3 (2) 2
abridged index medicus (2) 2
alleles (2) 2
animals (2) 2
atherosclerosis - genetics (2) 2
beer (2) 2
cardiology (2) 2
cardiovascular disease (2) 2
care and treatment (2) 2
case-control studies (2) 2
cdkn2a و cdkn2b (2) 2
cell proliferation (2) 2
chemistry (2) 2
compositions or test papers therefor (2) 2
condition-responsive control in microbiological orenzymological processes (2) 2
coronary artery disease - genetics (2) 2
coronary artery disease - metabolism (2) 2
dehydrogenases (2) 2
enzymology (2) 2
gene-expression (2) 2
genetic disorders (2) 2
genetic variation (2) 2
genetics & heredity (2) 2
genotype & phenotype (2) 2
hearing impairment (2) 2
heart attacks (2) 2
interferon (2) 2
investigating or analysing materials by determining theirchemical or physical properties (2) 2
measuring (2) 2
measuring or testing processes involving enzymes, nucleicacids or microorganisms (2) 2
medicine (2) 2
metabolism (2) 2
metallurgy (2) 2
microbiology (2) 2
mutation or genetic engineering (2) 2
mutations (2) 2
myocardial-infarction (2) 2
pathology (2) 2
patients (2) 2
peripheral vascular disease (2) 2
phosphorylation (2) 2
physics (2) 2
processes of preparing such compositions (2) 2
single nucleotide polymorphisms (2) 2
spirits (2) 2
studies (2) 2
testing (2) 2
tgf-beta (2) 2
transcription factors - genetics (2) 2
urine (2) 2
vinegar (2) 2
wine (2) 2
الخلايا العضلية الملساء (2) 2
القطعة رقم پ21.3 على كروموسوم رقم 9 (2) 2
مرض الشرايين التاجية (2) 2
موضع خطر (2) 2
3 untranslated region (1) 1
3' untranslated regions (1) 1
3'untranslated region (1) 1
9p21.3 cad risk locus (1) 1
abdominal aortic-aneurysm (1) 1
adenosine triphosphate - metabolism (1) 1
adolescent (1) 1
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aged, 80 and over (1) 1
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PLoS ONE, ISSN 1932-6203, 2014, Volume 9, Issue 9, p. e106294
Journal Article
Genetics in Medicine, ISSN 1098-3600, 04/2018, Volume 20, Issue 5, pp. 536 - 544
Purpose: Hearing loss is more prevalent in the Saudi Arabian population than in other populations; however, the full range of genetic etiologies in this... 
Saudi Arabia | OTOF | prelingual profound hearing loss | genetic testing | PENDRED-SYNDROME | IMPAIRMENT | NEUROPATHY | USHER-SYNDROME | FAMILIES | GENETICS & HEREDITY | DEAFNESS | AUDITORY PERFORMANCE | MUTATIONS | CONSANGUINITY | MYOSIN VIIA GENE | Hearing impairment | Population | Original
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2013, Volume 61, Issue 2, pp. 143 - 147
Journal Article
Clinical Chemistry, ISSN 0009-9147, 05/2018, Volume 64, Issue 5, pp. 870 - 872
Within the central nervous system (CNS), serine has an important role as an excitatory neurotransmitter (as D-serine, and also as a precursor for glycine), as... 
MEDICAL LABORATORY TECHNOLOGY | Genetic disorders | DNA microarrays | Seizures (Medicine) | Serine | Hearing loss | Plasma | Dehydrogenases | Congenital diseases | Congenital defects | Vitamin B | Congenital anomalies | Nervous system | Microcephaly | Hearing impairment
Journal Article
Cell Reports, ISSN 2211-1247, 05/2014, Volume 7, Issue 3, pp. 834 - 847
Journal Article
Circulation, ISSN 0009-7322, 11/2015, Volume 132, Issue 21, pp. 1969 - 1978
BACKGROUND—The mechanism whereby the 9p21.3 locus confers risk for coronary artery disease remains incompletely understood. Risk alleles are associated with... 
atherosclerosis | molecular biology | smooth muscle cells | coronary disease | genetics | CARDIAC & CARDIOVASCULAR SYSTEMS | TGF-BETA | MYOCARDIAL-INFARCTION | CARDIAC MYOCYTES | CYCLE ARREST | CHROMOSOME 9P21 | ANGIOTENSIN-II | SKELETAL-MUSCLE | GENE-EXPRESSION | TEF-1 | PERIPHERAL VASCULAR DISEASE | MICE | Humans | Middle Aged | Male | Gene Knockdown Techniques | Muscle Proteins - biosynthesis | Young Adult | Chromosomes, Human, Pair 9 - genetics | Cyclin-Dependent Kinase Inhibitor p16 - biosynthesis | Adult | Female | Muscle Proteins - antagonists & inhibitors | Muscle Proteins - physiology | Genes, Reporter | Recombinant Proteins - metabolism | DNA-Binding Proteins - physiology | Transcription Factors - physiology | DNA-Binding Proteins - antagonists & inhibitors | Cells, Cultured | Transforming Growth Factor beta - physiology | Transcription Factors - antagonists & inhibitors | Transcription Factors - biosynthesis | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Muscle, Smooth, Vascular - cytology | Genes, p16 | Muscle Proteins - genetics | Coronary Disease - genetics | Adolescent | Alleles | Polymorphism, Single Nucleotide | Aorta - cytology | DNA-Binding Proteins - biosynthesis | Care and treatment | Research | Single nucleotide polymorphisms | Molecular biology | Gene expression | Coronary heart disease
Journal Article
Clinical Chemistry, ISSN 0009-9147, 12/2018, Volume 64, Issue 12, pp. 1785 - 1787
Journal Article
Clinical Chemistry, ISSN 0009-9147, 08/2018, Volume 64, Issue 8, pp. 1260 - 1269
Plasma insulin-like growth factor-I (IGF-I)4 concentration was also decreased at <25 ng/mL (reference interval, 50-286). The SLC7A7 gene product is the y+L... 
LYSINURIC PROTEIN INTOLERANCE | SLC7A7 | MEDICAL LABORATORY TECHNOLOGY | Urine | Proteins | Dehydrogenases | Hyperammonemia | Diarrhea | Growth hormones | Amino acids | Insulin-like growth factors | Mutation | Metabolism | Patients
Journal Article
Journal of Taibah University Medical Sciences, ISSN 1658-3612, 06/2017, Volume 12, Issue 3, pp. 199 - 204
يعتبرالموضع الخطر للقطعة رقم پ21.3 على كروموسوم رقم ٩ أول موضع يوصف لارتباطه بزيادة خطر الإصابة بالحوادث ذات الصلة بأمراض الشرايين التاجية، وعدد من الظواهر... 
Smooth muscle cell | مرض الشرايين التاجية | القطعة رقم پ21.3 على كروموسوم رقم 9 | Risk locus | الخلايا العضلية الملساء | موضع خطر | CDKN2A and CDKN2B | Coronary artery disease | CDKN2A و CDKN2B | 9p21.3 | Physiological aspects | Genetic aspects | Research | Single nucleotide polymorphisms | Coronary heart disease | Risk factors
Journal Article
Journal of Taibah University Medical Sciences, ISSN 1658-3612, 06/2017, Volume 12, Issue 3, pp. 199 - 204
يعتبرالموضع الخطر للقطعة رقم پ21.3 على كروموسوم رقم ٩ أول موضع يوصف لارتباطه بزيادة خطر الإصابة بالحوادث ذات الصلة بأمراض الشرايين التاجية، وعدد من الظواهر... 
الخلايا العضلية الملساء | موضع خطر | مرض الشرايين التاجية | CDKN2A و CDKN2B | القطعة رقم پ21.3 على كروموسوم رقم 9
Journal Article
Circulation Research, ISSN 0009-7330, 09/2015, Volume 117, Issue 8, pp. 671 - 683
RATIONALE:Inflammation impairs macrophage cholesterol clearance from vascular tissues and promotes atherosclerosis. Inflammatory macrophages suppress... 
Genetics | 3'untranslated region | Macrophages | Coronary artery disease | Cholesterol | Atherosclerosis | atherosclerosis | coronary artery disease | MEF2 | CARDIAC & CARDIOVASCULAR SYSTEMS | NECROSIS-FACTOR-ALPHA | PROLIFERATION | IDENTIFICATION | KLF2 | REGULATORY FACTOR-2 | macrophages | genetics | 3 untranslated region | GENE-EXPRESSION | cholesterol | PERIPHERAL VASCULAR DISEASE | DIFFERENTIATION | HEMATOLOGY | NF-KAPPA-B | POLARIZATION | Apolipoproteins E - deficiency | Atherosclerosis - genetics | Humans | Middle Aged | Male | Protective Factors | Inflammation - metabolism | Aged, 80 and over | 3' Untranslated Regions | Odds Ratio | Disease Models, Animal | Genetic Predisposition to Disease | Coronary Artery Disease - metabolism | Risk Factors | Coronary Artery Disease - prevention & control | Atherosclerosis - metabolism | Macrophage Activation | Mice, Knockout | Polymorphism, Genetic | Radiography | Macrophages - metabolism | Phenotype | Coronary Artery Disease - genetics | MEF2 Transcription Factors - metabolism | Inflammation - prevention & control | Kruppel-Like Transcription Factors - genetics | Transcription Factors - deficiency | ATP Binding Cassette Transporter 1 - metabolism | Case-Control Studies | Transfection | Kruppel-Like Transcription Factors - metabolism | Receptors, LDL - deficiency | Female | Nuclear Proteins - genetics | Promoter Regions, Genetic | Receptors, LDL - genetics | Mice, Inbred C57BL | Cells, Cultured | Nuclear Proteins - metabolism | Transcription Factors - genetics | Cholesterol - metabolism | Transcription Factors - metabolism | Carrier Proteins - genetics | Homozygote | Coronary Artery Disease - diagnostic imaging | Animals | Carrier Proteins - metabolism | Apolipoproteins E - genetics | Inflammation - genetics | Aged | Atherosclerosis - prevention & control
Journal Article
Journal of Taibah University Medical Sciences, ISSN 1658-3612, 09/2015, Volume 10, Issue 3, pp. 266 - 270
تتفاعل العوامل البيئية والصحية والجينية لتتسبب في ظهور أمراض القلب التاجية. وتعتبر أمراض القلب التاجية من الأسباب الرئيسة للوفيات حول العالم. وتشمل العوامل... 
أمراض القلب التاجية | GWAS | التصلب العصيدي | Atherosclerosis | CAD | الكولسترول | SNPs | بروتين شحمي | دراسات الارتباط على مستوى الجينوم | Lipoprotiens | Cholesterol
Journal Article
Journal of Molecular Diagnostics, The, ISSN 1525-1578, 2016, Volume 18, Issue 6, pp. 882 - 889
Diagnostic next-generation sequencing (NGS)-based gene panels are increasingly used for prevalent disorders with genetic and clinical heterogeneity. Clinical... 
Pathology
Journal Article
Journal of Taibah University Medical Sciences, ISSN 1658-3612, 09/2015, Volume 10, Issue 3, p. 266
O*O*UOs.O[sup.1]U Os.UO[sup.1]UOs.UU Os.UO[umlaut]UO[bar]UO[c] UOs.UO[micro]O-UO[c] UOs.UO[logical not]UUUO[c] UO*O*O[sup.3]O[umlaut]O[umlaut] UU... 
Genetic variation | Genetic aspects | Lipid metabolism | Coronary heart disease | Health aspects | Risk factors
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 01/2013, Volume 61, Issue 2, p. 143
Because post-transcriptional mechanisms modulate levels of p16 (encoded by CDKN2A) and p15 (encoded by CDKN2B), we tested whether interferon-[gamma] regulates... 
Genetic disorders | Genetic aspects | Universities and colleges | Biological response modifiers | Coronary heart disease | Risk factors | Interferon gamma | Endothelium | Interferon | Heart attacks | Cloning | Cardiovascular disease | Kinases | Gene expression | Proteins | Studies | Genotype & phenotype | Hypotheses | Rodents | Atherosclerosis | Binding sites
Journal Article
Journal of Taibah University Medical Sciences, ISSN 1658-3612, 12/2015, Volume 10, Issue 4, pp. 509 - 511
Journal Article