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Daneshyari Genetics Journas Latest Articles

Genetics Research Articles

OCA2 rs4778137 polymorphism predicts survival of breast cancer patients receiving neoadjuvant chemotherapy
Fulltext Access 5 Pages 2018
Pig PON1: Expression and promoter methylation
Fulltext Access 5 Pages 2018
Vitamin D receptor Fok1 polymorphism and its relationship with premenstrual syndrome
Fulltext Access 5 Pages 2018
A study of CAG repeat instability of HTT gene following spermatogenesis, by single sperm analysis
Fulltext Access 5 Pages 2018
C677T and A1298C polymorphisms of Methylenetetrahydrofolate reductase (MTHFR) gene: Effect and risk to develop chronic myeloid leukemia: A study on Syrian patients
Fulltext Access 5 Pages 2018
The occurrence of blaTEM, blaSHV and blaOXA genotypes in Extended-Spectrum β-Lactamase (ESBL)-producing Pseudomonas aeruginosa strains in Southwest of Iran
Fulltext Access 5 Pages 2018
Identification and functional analysis of a novel mutation in the PAX3 gene associated with Waardenburg syndrome type I
Fulltext Access 5 Pages 2018
The impacts of nineteen mutations on the enzymatic activity of USP26
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Association between FASN gene polymorphisms ultrasound carcass traits and intramuscular fat in Qinchuan cattle
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Genetic contribution of SUN5 mutations to acephalic spermatozoa in Fujian China
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Whole exome sequencing identifies a novel mutation (c.333 + 2T > C) of TNNI3K in a Chinese family with dilated cardiomyopathy and cardiac conduction disease
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Maternal and neonatal irisin precursor gene FNDC5 polymorphism is associated with preterm birth
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Phylogenetic analysis of two goat-origin PCV2 isolates in China
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Association of the XRCC1 Arg194Trp and Arg399Gln polymorphisms with depression and hopelessness levels in individuals exposed to sour gas
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Maturity Onset Diabetes of the Young (MODY) in Tunisia: Low frequencies of GCK and HNF1A mutations
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TDRD6 is associated with oligoasthenoteratozoospermia by sequencing the patient from a consanguineous family
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Biallelic UNC80 mutations caused infantile hypotonia with psychomotor retardation and characteristic facies 2 in two Chinese patients with variable phenotypes
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New bifunctional restriction-modification enzyme AloI isoschizomer (PcoI): Bioinformatics analysis, purification and activity confirmation
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Two cases of complex balanced autosomal translocations associated with severe oligozoospermia
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A functional promoter polymorphism in interleukin 12B gene is associated with an increased risk of ovarian endometriosis
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The effects of Capn1 gene inactivation on the differential expression of genes in skeletal muscle
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Synergistic defects of novo FAS and homozygous UNC13D leading to autoimmune lymphoproliferative syndrome-like disease: A 10-year-old Chinese boy case report
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Human Leukocyte Antigen class II polymorphisms among Croatian patients with type 1 diabetes and autoimmune polyglandular syndrome type 3 variant
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Genetic variants within 17q12 are associated with the risk of cervical cancer in the Han Chinese population
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A Next Generation Sequencing custom gene panel as first line diagnostic tool for atypical cases of syndromic obesity: Application in a case of Alström syndrome
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Worldwide prevalence of familial multiple sclerosis: A systematic review and meta-analysis
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Developmental expression of the slurp-like1/ly2.3/ly97.3 and slurp-like2/ly2.2/ly97.2 genes during zebrafish early embryogenesis
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Validation of Cameriere's medical-legal age estimation method using seconds premolars in a Portuguese population
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The association between iceA and vacA allelic gene variations of Helicobacter pylori strains and gastric disorders
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A novel compound heterozygote mutation in the ARSB gene in a patient with Maroteaux-Lamy syndrome and its Insilico evaluation
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Quantitative assessment of HR and NHEJ activities via CRISPR/Cas9-induced oligodeoxynucleotide-mediated DSB repair
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A de novo 921 Kb microdeletion at 11q13.1 including neurexin 2 in a boy with developmental delay, deficits in speech and language without autistic behaviors
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Marking of definitive HSC precursors in E7.5-E8.5 embryos using an Abcg2-CreER lineage-tracing mouse model
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Construction of pOGOduet - An inducible, bicistronic vector for synthesis of recombinant proteins in Corynebacterium glutamicum
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A 8-year retrospective cohort study comparing Interferon-β formulations for relapsing‐remitting multiple sclerosis
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Vaccinia Related Kinase 2 (VRK2) expression in neurological disorders: schizophrenia, epilepsy and multiple sclerosis
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Treatment for paraneoplastic neuromyelitis optica spectrum disorder (NMOsd): Probable effects of tocilizumab for both cancer and NMOsd
Fulltext Access 5 Pages 2018
Reply to Tsivgoulis and colleagues comments
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A complex phenotype in a family with a pathogenic SOX3 missense variant
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The use of satellite data to measure ultraviolet-B penetrance and its potential association with age of multiple sclerosis onset
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Matching-adjusted comparisons demonstrate better clinical outcomes with SC peginterferon beta-1a every two weeks than with SC interferon beta-1a three times per week
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Refactory Trigeminal Neuralgia successfully treated by combination therapy (Pregabalin plus Lamotrigine)
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Intrathecal K free light chain synthesis in multiple sclerosis at clinical onset associates with local IgG production and improves the diagnostic value of cerebrospinal fluid examination
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The significance role of regulatory T cells in the persistence of infections by intracellular bacteria
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Detection of a novel RNA virus with hepatitis E virus-like non-structural genome organization in amphibian, agile frog (Rana dalmatina) tadpoles
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HomBlocks: A multiple-alignment construction pipeline for organelle phylogenomics based on locally collinear block searching
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Draft genome sequence of Geobacillus yumthangensis AYN2 sp. nov., a denitrifying and sulfur reducing thermophilic bacterium isolated from the hot springs of Sikkim
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Genetic diversity analysis of Leptadenia pyrotechnica in Jodhpur region of India
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Unreported combination of rearrangements in a childhood B-cell acute lymphoblastic leukemia case: Coexistence of translocation t(8;14) and monoallelic loss of tumor suppressor gene TP53
Fulltext Access 5 Pages 2018
Computational analysis of non-synonymous SNPs in bovine Mx1 gene
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3D-3D facial superimposition between monozygotic twins: A novel morphological approach to the assessment of differences due to environmental factors
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Characterization and cryopreservation of Amur leopard cats (Prionailurus bengalensis euptilurus) semen collected by urethral catheterization
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Production and purification of IgY antibodies from chicken egg yolk
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Effect of vitamin A deficiency on thymosin-β4 and CD4 concentrations
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Impact of Apo E gene polymorphism on HCV therapy related outcome in a cohort of HCV Egyptian patients
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DMH4, a VEGFR2 inhibitor, effectively suppresses growth and invasion of lung cancer cells
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Proliferation of Toxoplasma gondii (RH strain) is inhibited by the combination of pravastatin and simvastatin with low concentrations of conventional drugs used in toxoplasmosis
Fulltext Access 5 Pages 2018
Caveolin-1 rs4730751 gene polymorphism in kidney allograft recipients
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Relationship between MTHFR gene polymorphisms (C677T and A1298C) and chronic lymphocytic leukemia in the Turkish population
Fulltext Access 5 Pages 2018
Response to “XPA is primarily cytoplasmic but is transported into the nucleus upon UV damage”
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FAN1 protects against repeat expansions in a Fragile X mouse model
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The use of the M-Vac® wet-vacuum system as a method for DNA recovery
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The influence of alcohol content variation in UK packaged beers on the uncertainty of calculations using the Widmark equation
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Use of ultrasonographic fetometry for the estimation of days to kidding in dairy does
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Applying 3D prints to reconstructing postmortem craniofacial features damaged by devastating head injuries
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The deceleration of a spherical projectile passing through porcine organs at laboratory temperature (16 °C) and core body temperature (37 °C)
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Involuntary sterilization among HIV-positive Garifuna women from Honduras seeking asylum in the United States: Two case reports
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What do clinicians understand about deaths reportable to the coroner - Use of clinical scenarios to enhance learning
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Does the serotonin receptor gene (rs6313 and rs6314) polymorphism have a role in suicidal attempts?
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Paraquat poisoning calls to the Malaysia National Poison Centre following its ban and subsequent restriction of the herbicide from 2004 to 2015
Fulltext Access 5 Pages 2018
Age estimation: Cameriere's open apices methodology accuracy on a southeast Brazilian sample
Fulltext Access 5 Pages 2018
Medico-legal investigation in an explicable case of congenital central hypoventilation syndrome due to a rare variant of the PHOX2B gene
Fulltext Access 5 Pages 2018
Stress2TF: a manually curated database of TF regulation in plant response to stress
Fulltext Access 5 Pages 2018
Alpha lipoic acid (ALA) effects on developmental competence of equine preantral follicles in short-term culture
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Production of live larvae following in vitro maturation of zebrafish oocytes
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Understanding direct neuronal reprogramming - from pioneer factors to 3D chromatin
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Additional features of Gillespie syndrome in two Brazilian siblings with a novel ITPR1 homozygous pathogenic variant
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Pakistan Genetic Mutation Database (PGMD); A centralized Pakistani mutome data source
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Atopic disorders in CHARGE syndrome: A retrospective study and literature review
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Refinement of the critical 7p22.1 deletion region: Haploinsufficiency of ACTB is the cause of the 7p22.1 microdeletion-related developmental disorders
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Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndrome
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Neonatal hyperinsulinemic hypoglycemia in a patient with 9p deletion syndrome
Fulltext Access 5 Pages 2018
Speech and language delay in a patient with WDR4 mutations
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Tuberculosis tubaria y peritoneal que simula carcinomatosis. Linfopenia con trombocitosis como auxiliar en el diagnóstico diferencial
Fulltext Access 5 Pages 2018
Diagnóstico prenatal del arco aórtico derecho, importancia de los planos de Yagel. Nuestra experiencia, descripción de 2 casos
Fulltext Access 5 Pages 2018
Papel de los espermatozoides en la transmisión de bacterias uropatógenas: Escherichia coli y Enterococcus faecalis
Fulltext Access 5 Pages 2018
Allele distribution and testing for association between an oxygen dependent degradation domain SNP in EPAS1 and pulmonary arterial pressures in yearling Angus cattle
Fulltext Access 5 Pages 2018
Genetic architecture of obesity and related metabolic traits - recent insights from isolated populations
Fulltext Access 5 Pages 2018
Insemination extender supplementation with bestatin and EDTA has no effect on rabbit reproductive performance
Fulltext Access 5 Pages 2018
p53 and K-ras mutations in lung tissues and sputum samples of individuals exposed to smoky coal emissions in Xuan Wei County, China
Fulltext Access 5 Pages 2018
Titanium dioxide nanoparticles: Toxicity and genotoxicity in Drosophila melanogaster (SMART eye-spot test and comet assay in neuroblasts)
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Using RNA-Seq with 11 marker genes to evaluate 1,4-dioxane compared with typical genotoxic and non-genotoxic rat hepatocarcinogens
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The presence of KRAS, PPP2R1A and ARID1A mutations in 101 Chinese samples with ovarian endometriosis
Fulltext Access 5 Pages 2018
A leukemic double-hit follicular lymphoma associated with a complex variant translocation, t(8;14;18)(q24;q32;q21), involving BCL2, MYC, and IGH
Fulltext Access 5 Pages 2018
Biallelic TP53 gain of function mutations in rapidly progressing solid tumors
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Primary aneurysmal bone cyst with a novel SPARC-USP6 translocation identified by next-generation sequencing
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Reprint of: Building a Safer and Faster CAR: Seatbelts, Airbags, and CRISPR
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Reproductive performance of lactating dairy cows after inducing ovulation using hCG in a five-day progesterone-based fixed-time AI protocol
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Histology confirms that macroscopic evaluation of ovaries is a valid method for the assessment of the reproductive status in wild boar
Fulltext Access 5 Pages 2018
Conceptus loss in Santa Inês ewes carrying twin pregnancies by natural mating or embryo transfer
Fulltext Access 5 Pages 2018
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