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Polymorphisms of apolipoprotein E and aneurysmal subarachnoid haemorrhage: A meta-analysisApolipoprotein C3 gene variants and the risk of coronary heart disease: A meta-analysisVitamin D receptor gene polymorphism in Egyptian pediatric acute lymphoblastic leukemia correlation with BMDGenetic association between inflammatory genes (IL-1α, CD14, LGALS2, PSMA6) and risk of ischemic stroke: A meta-analysisAssociation between microRNA-196a2 rs11614913, microRNA-146a rs2910164, and microRNA-423 rs6505162 polymorphisms and esophageal cancer risk: A meta-analysisMethylenetetrahydrofolate reductase gene C677T polymorphism and breast cancer risk: Evidence for genetic susceptibilityATM rs189037 (G > A) polymorphism and risk of lung cancer and head and neck cancer: A meta-analysisMetagenomics: A new horizon in cancer researchEpidemiology of prostate cancer in IndiaImpact of CYP2C9, VKORC1 and CYP4F2 genetic polymorphisms on maintenance warfarin dosage in Han-Chinese patients: A systematic review and meta-analysisUncoupling protein 2 gene polymorphisms in association with overweight and obesity susceptibility: A meta-analysisMarfan syndrome: An eyesight of syndromeAndrogen receptor gene polymorphism in zebra speciesInitial description of primate-specific cystine-knot Prometheus genes and differential gene expansions of D-dopachrome tautomerase genesDNA barcoding of Pentatomomorpha bugs (Hemiptera: Heteroptera) from Western Ghats of IndiaGenetic divergence in natural populations of bronze featherback, Notopterus notopterus (Osteoglossiformes: Notopteridae) from five Indian rivers, analyzed through mtDNA ATPase6/8 regionsInvestigating regulatory signatures of human autophagy related gene 5 (ATG5) through functional in silico analysisSLC34A2 gene compound heterozygous mutation identification in a patient with pulmonary alveolar microlithiasis and computational 3D protein structure prediction.Analysis of consequences of non-synonymous SNP in feed conversion ratio associated TGF-β receptor type 3 gene in chicken.Complete mitochondrial DNA genome of bonnethead shark, Sphyrna tiburo, and phylogenetic relationships among main superorders of modern elasmobranchsNucleotide polymorphisms and protein structure changes in the Fg16 gene of Fusarium graminearum sensu strictoA novel CHD7 mutation in a Chinese patient with CHARGE syndrome19q13.33→qter trisomy in a girl with intellectual impairment and seizuresSoutheast Asian mouth-brooding Betta fighting fish (Teleostei: Perciformes) species and their phylogenetic relationships based on mitochondrial COI and nuclear ITS1 DNA sequences and analyses.Assembly and variation analyses of Clarias batrachus mitogenome retrieved from WGS data and its phylogenetic relationship with other catfishes.Variants in motilin, somatostatin and their receptor genes and risk of biliary tract cancers and stones in Shanghai, ChinaAssociation between 5, 10-methylenetetrahydrofolate reductase (MTHFR) polymorphisms and congenital heart disease: A meta-analysisThe effect of citrulline and arginine supplementation on lactic acidemia in MELAS syndrome.C-reactive protein + 1059 G>C polymorphism in type 2 diabetes and coronary artery disease patients.The association between polymorphism of P53 codon 72 Arg/Pro and hepatocellular carcinoma susceptibility: evidence from a meta-analysis of 15 studies with 3704 cases.No detectable association of IGF2BP2 and SLC30A8 genes with type 2 diabetes in the population of Hyderabad, India.Appearance of leptin-HSP70 correlation, in type 2 diabetes.Genetic diversity within 5'upstream region of Toll-like receptor 8 gene reveals differentiation of riverine and swamp buffaloes.Identification and expression analysis of a novel intragenic EFNB1 mutation causing craniofrontonasal syndromeInvestigation of the monocyte diapedesis-related LFA-1 and JAM-A gene variants in Turkish coronary heart disease patientsA novel insertion-induced frameshift mutation of the androgen receptor gene in a patient with primary amenorrhea.Polymorphism analysis and new JAG1 gene mutations of Alagille syndrome in Mexican population.Current evidence on the four polymorphisms of VDR and breast cancer risk in Caucasian women.A 20 year history of clinical and genetic study of thyroid autoimmunity in a Tunisian multigenerational family: Evidence for gene interaction.Interstitial 12p deletion involving more than 40 genes in a patient with postnatal microcephaly, psychomotor delay, optic nerve atrophy, and facial dysmorphism.
P1433
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P1433
description
journal
@en
revista científica
@es
wetenschappelijk tijdschrift van Elsevier
@nl
wissenschaftliche Fachzeitschrift
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name
Meta gene
@ast
Meta gene
@en
Meta gene
@es
Meta gene
@nl
type
label
Meta gene
@ast
Meta gene
@en
Meta gene
@es
Meta gene
@nl
altLabel
Meta Gene
@en
prefLabel
Meta gene
@ast
Meta gene
@en
Meta gene
@es
Meta gene
@nl
P31
P3181
P1055
P1156
21100283722
P123
P1476
Meta gene
@en
P236
P3181
P571
2013-01-01T00:00:00Z