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Daneshyari Genetics Journas Latest Articles

Genetics Research Articles

Research paperNutrition modulates Fto and Irx3 gene transcript levels, but does not alter their DNA methylation profiles in rat white adipose tissues
Fulltext Access 5 Pages 2017
Whole genome sequencing and annotation of halophilic Salinicoccus sp. BAB 3246 isolated from the coastal region of Gujarat
Fulltext Access 5 Pages 2017
No evidence of disease activity (NEDA) in MS should include CSF biology - Towards a 'Disease-Free Status Score'
Fulltext Access 5 Pages 2017
Transcriptome profiling of Elettaria cardamomum (L.) Maton (small cardamom)
Fulltext Access 5 Pages 2017
Comparison of SHOX and associated elements duplications distribution between patients (Lėri-Weill dyschondrosteosis/idiopathic short stature) and population sample
Fulltext Access 5 Pages 2017
Research papermiRNA-146a, miRNA-155 and JNK expression levels in peripheral blood mononuclear cells according to grade of knee osteoarthritis
Fulltext Access 5 Pages 2017
Common variation of the CYP17 gene in Iraqi women with endometriosis disease
Fulltext Access 5 Pages 2017
The association between OPG rs3102735 gene polymorphism, microembolic signal and stroke severity in acute ischemic stroke patients
Fulltext Access 5 Pages 2017
Validation of aspirin response-related transcripts in patients with coronary artery disease and preliminary investigation on CMTM5 function
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Intraspecies comparative genomics of three strains of Orientia tsutsugamushi with different antibiotic sensitivity
Fulltext Access 5 Pages 2017
The +4259A>C polymorphism of TIM-3 but not -1637C>T polymorphism of TIM-1 is associated with Multiple sclerosis in Isfahan population
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Genome sequences of 12 isolates of the EU1 lineage of Phytophthora ramorum, a fungus-like pathogen that causes extensive damage and mortality to a wide range of trees and other plants
Fulltext Access 5 Pages 2017
Mannose-Binding Lectin (MBL) gene polymorphisms in susceptibility to pulmonary tuberculosis among the Lur population of Lorestan Province of Iran
Fulltext Access 5 Pages 2017
Ecotropic Viral Integration Site 5 (EVI5) variants are associated with multiple sclerosis in Iranian population
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Association study of the vesicular monoamine transporter 1 (VMAT1) gene with autism in an Iranian population
Fulltext Access 5 Pages 2017
Review articleClassifying PML risk with disease modifying therapies
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Prevalence and genetic analysis of α- and β-thalassemia in Baise region, a multi-ethnic region in southern China
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Association of a Vascular Endothelial Growth Factor genetic variant with Serum VEGF level in subjects with Metabolic Syndrome
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Characterization of soluble N-ethylmaleimide-sensitive factor attachment protein receptor gene STX18 variations for possible roles in congenital heart diseases
Fulltext Access 5 Pages 2017
Evaluation of MicroRNA-210 and Protein tyrosine phosphatase, non-receptor type 2 in Pre-eclampsia
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Draft genome sequence of Thalassobius gelatinovorus CECT 4357T, a roseobacter with the potential ability to degrade polycyclic aromatic hydrocarbons
Fulltext Access 5 Pages 2017
Hospitalization length survey and relation with distribution of LasA protease and type III secretion system encoding-genes in multi-drug resistant Pseudomonas aeruginosa isolates from burn wounds in southwest of Iran
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Complex karyotype involving six chromosomes, with one dicentric and three yet unreported acquired chromosomal aberrations in a case of splenic marginal zone lymphoma
Fulltext Access 5 Pages 2017
Heat stress-induced activation of a Trichoderma harzianum PIL superfamily gene
Fulltext Access 5 Pages 2017
Identification of serotypes and virulence markers (stx) of Escherichia coli isolated from patients with diarrhea in Shiraz, Iran
Fulltext Access 5 Pages 2017
WITHDRAWN: CREM variant rs17583959 conferred susceptibility to T1D risk in the Tunisian families
Fulltext Access 5 Pages 2017
Computational study of some amoebicidal phytochemicals against heat shock protein of Naegleria fowleri
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Association of CDKAL1 gene rs7756992 A/G polymorphism with type 2 diabetes mellitus and diabetic nephropathy in the Egyptian population
Fulltext Access 5 Pages 2017
Mitochondrial genomes of two Babesia taxa from sheep in China as a foundation for population genetic and epidemiological investigations
Fulltext Access 5 Pages 2017
First identification and phylogenetic analysis of equine hepacivirus in Korea
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Orientia tsutsugamushi infection in rodents in Anhui Province of China
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15 year fulminant hepatitis B follow-up in Belgium: Viral evolution and signature of demographic change
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RNA expression analysis of efflux pump genes in clinical isolates of multidrug-resistant and extensively drug-resistant Mycobacterium tuberculosis in South Korea
Fulltext Access 5 Pages 2017
Porcine kobuvirus 1 in healthy and diarrheic pigs: Genetic detection and characterization of virus and co-infection with rotavirus A
Fulltext Access 5 Pages 2017
Functional characteristics of a novel SMAD4 mutation from thoracic aortic aneurysms (TAA)
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Research paperCorrelation between RNA-Seq and microarrays results using TCGA data
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Heterogeneous recombination among Hepatitis B virus genotypes
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Occult hepatitis B virus infection in Greek patients with congenital bleeding disorders
Fulltext Access 5 Pages 2017
A variant on chromosome 2p13.3 is associated with atopic dermatitis in Chinese Han population
Fulltext Access 5 Pages 2017
A66G and C524T polymorphisms of methionine synthase reductase gene are linked to the development of acyanotic congenital heart diseases in Egyptian children
Fulltext Access 5 Pages 2017
Prevalence, molecular epidemiology, and zoonotic potential of Entamoeba spp. in nonhuman primates in China
Fulltext Access 5 Pages 2017
Large-scale amplicon sequencing of the SP3D gene responsible for fruit-yield heterosis in tomato
Fulltext Access 5 Pages 2017
A DNA barcoding approach for identifying species in Amazonian traditional medicine: The case of Piri-Piri
Fulltext Access 5 Pages 2017
Clinical outcomes and predictive factors related to good outcomes in plasma exchange in severe attack of NMOSD and long extensive transverse myelitis: Case series and review of the literature
Fulltext Access 5 Pages 2017
Disruption of NNAT, NAP1L5 and MKRN3 DNA methylation and transcription in rabbit parthenogenetic fetuses
Fulltext Access 5 Pages 2017
Association of mitochondrial DNA 10398 A/G polymorphism with attention deficit and hyperactivity disorder in Korean children
Fulltext Access 5 Pages 2017
Genetic characterization of the glycoprotein G of Chandipura viruses in India with emphasis on an outbreak of 2015
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Novel functional polymorphism in IGF-1 gene associated with multiple sclerosis: A new insight to MS
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Brucella suis biovar 2 multi locus sequence type ST16 in wild boars (Sus scrofa) from Abruzzi region, Italy. Introduction from Central-Eastern Europe?
Fulltext Access 5 Pages 2017
Human papillomavirus type 16 lineage analysis based on E6 region in cervical samples of Iranian women
Fulltext Access 5 Pages 2017
Intronic variants of SLC26A4 gene enhance splicing efficiency in hybrid minigene assay
Fulltext Access 5 Pages 2017
Research paperThe long non-coding RNA MIAT regulates zinc finger E-box binding homeobox 1 expression by sponging miR-150 and promoteing cell invasion in non-small-cell lung cancer
Fulltext Access 5 Pages 2017
Evaluation of the relationship between CD36 and MARCO single-nucleotide polymorphisms and susceptibility to carotid atherosclerosis in a Chinese Han population
Fulltext Access 5 Pages 2017
GSA: Genome Sequence Archive*
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The effect of Fampridine-SR on cognitive fatigue in a randomized double-blind crossover trial in patients with MS
Fulltext Access 6 Pages 2017
People with MS are less physically active than healthy controls but as active as those with other chronic diseases: An updated meta-analysis
Fulltext Access 6 Pages 2017
The association between FOXP3 gene variations and autism: True or false positive?
Fulltext Access 6 Pages 2017
Construction of pDUO: A bicistronic shuttle vector series for dual expression of recombinant proteins
Fulltext Access 6 Pages 2017
Horizontal transfer of chromosomal markers mediated by the large conjugative plasmid pXO16 from Bacillus thuringiensis serovar israelensis
Fulltext Access 6 Pages 2017
Characterization of pHeBE7, an IncFII-type virulence-resistance plasmid carrying blaCTX-M-98b, blaTEM-1, and rmtB genes, detected in Escherichia coli from a chicken isolate in China
Fulltext Access 6 Pages 2017
Novel toxins from type II toxin-antitoxin systems with acetyltransferase activity
Fulltext Access 6 Pages 2017
Reprint of “An integrated dual strategy to control Fusarium graminearum sensu stricto by the biocontrol agent Streptomyces sp. RC 87B under field conditions”
Fulltext Access 6 Pages 2017
Development of cpSSR markers for analysis of genetic diversity in Gladiolus cultivars
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An integrated dual strategy to control Fusarium graminearum sensu stricto by the biocontrol agent Streptomyces sp. RC 87B under field conditions
Fulltext Access 6 Pages 2017
Association of serum gamma-glutamyltransferase and C-reactive proteins with neuromyelitis optica and multiple sclerosis
Fulltext Access 6 Pages 2017
Response to: S. Sega-Jazbec et al.: “Management of infusion related reactions associated with alemtuzumab in patients with multiple sclerosis” Multiple Sclerosis and Related Disorders 2017
Fulltext Access 6 Pages 2017
Partial Vogt-Koyanagi-Harada syndrome as a differential diagnosis of optical neuritis
Fulltext Access 6 Pages 2017
Deconstructing the symbol digit modalities test in multiple sclerosis: The role of memory
Fulltext Access 6 Pages 2017
Human glutathione s-transferase enzyme gene variations and risk of multiple sclerosis in Iranian population cohort
Fulltext Access 6 Pages 2017
Multiple sclerosis: Association of gelatinase B/matrix metalloproteinase-9 with risk and clinical course the disease
Fulltext Access 6 Pages 2017
The impact of betaplus program on patient treatment satisfaction with interferon beta-1b in multiple sclerosis: Multicentric cross-sectional survey in the western Balkan countries
Fulltext Access 6 Pages 2017
Sequence analysis of the thrombospondin-related adhesive protein gene and heat shock protein 70 gene of Babesia gibsoni isolated from dogs in Nanjing, China
Fulltext Access 6 Pages 2017
Validity and reliability of the International Cooperative Ataxia Rating Scale (ICARS) and the Scale for the Assessment and Rating of Ataxia (SARA) in multiple sclerosis patients with ataxia
Fulltext Access 6 Pages 2017
Polysaccharides isolated from Hedyotis diffusa inhibits the aggressive phenotypes of laryngeal squamous carcinoma cells via inhibition of Bcl-2, MMP-2, and μPA
Fulltext Access 6 Pages 2017
Association of CnB 5I/5D promoter gene polymorphism and serum calcineurin levels in early onset of coronary artery disease of south Indian cohort
Fulltext Access 6 Pages 2017
Identification of pathogenic genes related to rheumatoid arthritis through integrated analysis of DNA methylation and gene expression profiling
Fulltext Access 6 Pages 2017
Effect of a single nucleotide polymorphism in the growth hormone secretagogue receptor (GHSR) gene on growth rate in pigs
Fulltext Access 6 Pages 2017
Association of common genetic variants in VEGFA with biliary atresia susceptibility in Northwestern Han Chinese
Fulltext Access 6 Pages 2017
Research paperSteroid sulfatase and filaggrin mutations in a boy with severe ichthyosis, elevated serum IgE level and moyamoya syndrome
Fulltext Access 6 Pages 2017
Genetic polymorphisms in CYP2A6 are associated with a risk of cigarette smoking and predispose to smoking at younger ages
Fulltext Access 6 Pages 2017
MicroRNA-181a and its target Smad 7 as potential biomarkers for tracking child acute lymphoblastic leukemia
Fulltext Access 6 Pages 2017
The nuclear protein-coding gene ANKRD23 negatively regulates myoblast differentiation
Fulltext Access 6 Pages 2017
Association of irisin and FNDC5 rs16835198 G > T gene polymorphism with type 2 diabetes mellitus and diabetic nephropathy. An Egyptian pilot study
Fulltext Access 6 Pages 2017
Beclin1 antagonizes LAPTM4B-mediated EGFR overactivation in gastric cancer cells
Fulltext Access 6 Pages 2017
Congenital adrenal hyperplasia due to 11-hydroxylase deficiency-Compound heterozygous mutations of a prevalent and two novel CYP11B1 mutations
Fulltext Access 6 Pages 2017
Structural annotation of Beta-1,4-N-acetyl galactosaminyltransferase 1 (B4GALNT1) causing Hereditary Spastic Paraplegia 26
Fulltext Access 6 Pages 2017
RDM16 and STA1 regulate differential usage of exon/intron in RNA directed DNA methylation pathway
Fulltext Access 6 Pages 2017
Influence of MTHFR C677T gene polymorphism in the development of cardiovascular disease in Egyptian patients with rheumatoid arthritis
Fulltext Access 6 Pages 2017
Predictive role of GSTP1-containing exosomes in chemotherapy-resistant breast cancer
Fulltext Access 6 Pages 2017
Intergenic variants may predispose to major depression disorder through regulation of long non-coding RNA expression
Fulltext Access 6 Pages 2017
A homozygous CEP135 mutation is associated with multiple morphological abnormalities of the sperm flagella (MMAF)
Fulltext Access 6 Pages 2017
MicroRNA-203a regulates fast muscle differentiation by targeting dmrt2a in zebrafish embryos
Fulltext Access 6 Pages 2017
EZH2-mediated α-actin methylation needs lncRNA TUG1, and promotes the cortex cytoskeleton formation in VSMCs
Fulltext Access 6 Pages 2017
Histone H3 lysine 4 methyltransferase KMT2D
Fulltext Access 6 Pages 2017
Association of donor and recipient SUMO4 rs237025 genetic variant with new-onset diabetes mellitus after liver transplantation in a Chinese population
Fulltext Access 6 Pages 2017
The human tRNA-modifying protein, TRIT1, forms amyloid fibers in vitro
Fulltext Access 6 Pages 2017
RNA polymerase III initiation on coligo DNA templates containing loops of variable sequence, size and nucleotide chemistry
Fulltext Access 6 Pages 2017
PAF53 is essential in mammalian cells: CRISPR/Cas9 fails to eliminate PAF53 expression
Fulltext Access 6 Pages 2017
ESR1 single nucleotide polymorphism rs1062577 (c.*3804T > A) alters the susceptibility of breast cancer risk in Iranian population
Fulltext Access 6 Pages 2017
Association of IRF5 polymorphisms with increased risk for systemic lupus erythematosus in population of Crete, a southern-eastern European Greek island
Fulltext Access 6 Pages 2017
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