Keywords: جهش ژنتیکی; Gastric stromal tumor; Risk; Recurrence; Treatment measures; Genetic mutation; Immunohistochemical assay;
مقالات ISI جهش ژنتیکی (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: جهش ژنتیکی; Early life; Malnutrition; Neurodevelopment; Neuropsychiatric disorders; Genetic mutation; Epigenetics; Precision nutrition;
Keywords: جهش ژنتیکی; Cost-effectiveness; Metastatic colorectal cancer; Precision medicine; Genetic mutation; Epidermal growth factor receptor;
Keywords: جهش ژنتیکی; Melanoma; Genetic mutation; Treatment;
Keywords: جهش ژنتیکی; Breast cancer; Young women; Hereditary cancer; Early-onset; Genetic mutation;
Keywords: جهش ژنتیکی; Muscular dystrophy; Genetic mutation; Polymorphism; Progression; Risk factors; Onset;
Keywords: جهش ژنتیکی; Wilson disease; Hereditary hemochromatosis; Genetic mutation; Biological function; Genotypes and phenotypes; WD; Wilson disease; HH; Hereditary hemochromatosis; TGN; trans-Golgi network; ATP7B; ATPase; Cu + transporting; beta polypeptide; HFE; hemochrom
Keywords: جهش ژنتیکی; Chemotherapy; genetic mutation; neoadjuvant treatment; palliative care; pancreas cancer; pancreatic ductal adenocarcinoma; surgery
Keywords: جهش ژنتیکی; Meta-heuristics; Discrete shuffled frog leaping algorithm; Knapsack problem; Genetic mutation
Keywords: جهش ژنتیکی; Inherited disorder; DNA testing; Genetic mutation;
Keywords: جهش ژنتیکی; AHR; aryl hydrocarbon receptor; AIP; aryl hydrocarbon receptor interacting protein; BMP-4; bone morphogenetic protein 4; CDK; cyclin-dependent kinases; CDKN1A; cyclin-dependent kinase inhibitor 1A; CDKN1B; cyclin-dependent kinase inhibitor 1B; CDKN2A; cyc
Keywords: جهش ژنتیکی; LncRNAs; Graphene oxide; Chemical modification; Genetic mutation; Caenorhabditis elegans
Accuracy of the cobas EGFR Mutation Assay in Non-small-cell Lung Cancer Compared With Three Laboratory-developed Tests
Keywords: جهش ژنتیکی; Genetic mutation; In vitro diagnostics; Laboratory test; Tissue section; Tyrosine kinase inhibitor;
Evidence of multiple mechanisms of alphacypermethrin and deltamethrin resistance in ticks Rhipicephalus microplus in Benin, West Africa
Keywords: جهش ژنتیکی; Enzymatic; Genetic mutation; Esterases; Oxidases; Glutathion-S-transferases;
Zika virus: The transboundary pathogen from mosquito and updates
Keywords: جهش ژنتیکی; Zika virus; Epidemiology; Genetic mutation; Microcephaly; Molecular pathogenesis; Prevention;
CRISPR-Cas9; an efficient tool for precise plant genome editing
Keywords: جهش ژنتیکی; Genetic mutation; Genetic engineering; Homologous recombination; DNA; Transcription;
The frequency of mutations in the ATP7B gene in Russia
Keywords: جهش ژنتیکی; Genetic mutation; ATP7B; Wilson's disease;
Autosomal Recessive Cerebellar Ataxia type 1 mimicking multiple sclerosis: A report of two siblings with a novel mutation in SYNE1 gene in a Saudi family
Keywords: جهش ژنتیکی; Autosomal Recessive Cerebellar Ataxia type 1; Genetic mutation; Multiple sclerosis; White matter disease; SYNE1;
Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis
Keywords: جهش ژنتیکی; Amyotrophic lateral sclerosis; Matrin-3; Nuclear matrix protein and DNA/RNA binding protein; French-Canadian population; Genetic mutation;
Perfil clÃnico y pronóstico de las miocardiopatÃas causadas por mutaciones en el gen de la troponina T
Keywords: جهش ژنتیکی; MiocardiopatÃa; Genética; Mutación génica; Troponina; Hipertrofia; Insuficiencia cardiaca; Muerte súbita; Cardiomyopathy; Genetics; Genetic mutation; Troponin; Hypertrophy; Heart failure; Sudden death; DAI; desfibrilador automático implantable; GMM;
Clinical and Prognostic Profiles of Cardiomyopathies Caused by Mutations in the Troponin T Gene
Keywords: جهش ژنتیکی; Cardiomyopathy; Genetics; Genetic mutation; Troponin; Hypertrophy; Heart failure; Sudden death; MiocardiopatÃa; Genética; Mutación génica; Troponina; Hipertrofia; Insuficiencia cardiaca; Muerte súbita; DCM; dilated cardiomyopathy; HCM; hypertrophic c
Case report: A novel apolipoprotein A-I missense mutation apoA-I (Arg149Ser)Boston associated with decreased lecithin-cholesterol acyltransferase activation and cellular cholesterol efflux
Keywords: جهش ژنتیکی; HDL deficiency; Apolipoprotein A-I; Genetic mutation; Cellular cholesterol efflux; LCAT activity; CETP activity;
Place memory retention in Drosophila
Keywords: جهش ژنتیکی; Place memory; Memory phases; High temperature; Intermittent training; Genetic mutation; Drosophila
A novel RyR2 mutation in a 2-year-old baby presenting with atrial fibrillation, atrial flutter, and atrial ectopic tachycardia
Keywords: جهش ژنتیکی; AET; atrial ectopic tachycardia; AF; atrial fibrillation; AFL; atrial flutter; CASQ2; calsequestrin 2; CPVT; catecholaminergic polymorphic ventricular tachycardia; JTC; junctin; RyR2; cardiac ryanodine receptor 2; TRDN; triadin; Atrial arrhythmia; Catecho
Neurological dysfunction in a ball python (Python regius) colour morph and implications for welfare
Keywords: جهش ژنتیکی; animal welfare; artificial selection; ball python; captive reptiles; genetic mutation; heritable disorders
A novel ApoA-I truncation (ApoA-IMytilene) associated with decreased ApoA-I production
Keywords: جهش ژنتیکی; Genetic mutation; Apolipoprotein kinetics; HDL subpopulations; Cellular cholesterol efflux;
Effects of polymorphisms in translesion DNA synthesis genes on lung cancer risk and prognosis in Chinese men
Keywords: جهش ژنتیکی; Lung cancer; TLS pathway; Genetic mutation; Susceptibility; Survival; Men
R450H TSH receptor mutation in congenital hypothyroidism in Taiwanese children
Keywords: جهش ژنتیکی; CHT, congenital hypothyroidism; TSHR, thyroid stimulation hormone receptor; RFLP, restriction fragment length polymorphismCongenital hypothyroidism; TSH receptor; Genetic mutation
Blau syndrome, clinical and genetic aspects
Keywords: جهش ژنتیکی; Blau syndrome; Genetic mutation; NOD2; Uveitis; Camptodactyly; Autoinflammatory disease
Genetic Considerations for a Woman's Annual Gynaecological Examination
Keywords: جهش ژنتیکی; Genetic risk; genetic mutation; gynaecology; inheritance; family history; uterus; ovary; endometrial; vagina; colon; gastric; renal; breast; cardiac; thrombophilia; diabetes; epilepsy; uterine leiomyomata uteri; uterine leiomyomas; AD autosomal dominant;
Dysplastic Nevi
Keywords: جهش ژنتیکی; Dysplastic nevi; Melanoma; Genetic mutation; Cytologic atypia;
Pathology and Genetics of Pancreatic Neoplasms
Keywords: جهش ژنتیکی; Pancreatic cancer; Molecular pathology; Genetic alteration; Genetic mutation; Neoplasms; Molecular markers
Novel RPGR-ORF15 mutations in X-linked retinitis pigmentosa patients
Keywords: جهش ژنتیکی; Retinitis pigmentosa; Genetic mutation; Retina; RPGR
Genetic Testing of Patients With Long QT Syndrome
Keywords: جهش ژنتیکی; Síndrome de QT largo; Muerte súbita; Mutación genéticaLong QT syndrome; Sudden death; Genetic mutation
Estudio genético en el síndrome de QT largo en nuestro medio
Keywords: جهش ژنتیکی; Síndrome de QT largo; Muerte súbita; Mutación genéticaLong QT syndrome; Sudden death; Genetic mutation
Directed searching optimization algorithm for constrained optimization problems
Keywords: جهش ژنتیکی; Directed searching optimization algorithm; Constrained optimization problems; Position updating; Genetic mutation; Penalty function method
Pandemic (H1N1) 2009 virus revisited: An evolutionary retrospective
Keywords: جهش ژنتیکی; Influenza; Pandemic H1N1; Evolution; Genetic mutation; Genome reassortment; Phylodynamics
Solving 0–1 knapsack problem by a novel global harmony search algorithm
Keywords: جهش ژنتیکی; Novel global harmony search algorithm; 0–1 knapsack problems; Position updating; Genetic mutation
Canine inherited motor and sensory neuropathies: An updated classification in 22 breeds and comparison to Charcot-Marie-Tooth disease
Keywords: جهش ژنتیکی; Inherited motor and sensory neuropathy; Canine; Charcot-Marie-Tooth disease; Peripheral nervous system; Genetic mutation;
A family of hereditary long QT syndrome caused by Q738X HERG mutation
Keywords: جهش ژنتیکی; Genetic mutation; HERG channel; Long QT syndrome; Torsade de Pointes;
A novel global harmony search algorithm for reliability problems
Keywords: جهش ژنتیکی; Swarm intelligence; Particle swarm; Novel global harmony search algorithm; Reliability problems; Position updating; Genetic mutation
Novel global harmony search algorithm for unconstrained problems
Keywords: جهش ژنتیکی; Novel global harmony search algorithm; Position updating; Genetic mutation; Convergence; Stability; Harmony search algorithm
Costello syndrome H-Ras alleles regulate cortical development
Keywords: جهش ژنتیکی; Costello syndrome; H-Ras; Cortical development; In utero electroporation; Proliferation; Neurogenesis; Gliogenesis; Developmental disorder; Mental retardation; Genetic mutation
Allele-specific polymerase chain reaction diagnostic test for the functional MDR1 polymorphism in dogs
Keywords: جهش ژنتیکی; MDR1; P-glycoprotein; Multidrug transporter; Ivermectin; Genetic mutation
A low-cost telemetry system suitable for measuring mouse biopotentials
Keywords: جهش ژنتیکی; Electrocardiogram (ECG); Genetic mutation
Reshaping the folding energy landscape of human carbonic anhydrase II by a single point genetic mutation Pro237His
Keywords: جهش ژنتیکی; ANS; 8-anilino-1-naphthalene sulfonic acid; CA; carbonic anhydrase; GdnHCl; guanidine hydrochloride; HCA; human carbonic anhydrase; CD; circular dichroism; I320; intrinsic fluorescence intensity at 320Â nm; I365; intrinsic fluorescence intensity at 365Â n
Disruption of transforming growth factor β-Smad signaling pathway in head and neck squamous cell carcinoma as evidenced by mutations of SMAD2 and SMAD4
Keywords: جهش ژنتیکی; SMAD2; SMAD4; HNSCC; Genetic mutation; TGF-β receptorsTGFβ, Transforming growth factor-β; HNSCC, head and neck squamous cell carcinoma; TGFBRI, TGF-β type I receptor; TGFBRII, TGF-β type II receptor; LOH, loss of heterozygosity; ACVRIB, activin receptor t
Prise en charge chirurgicale d'un paragangliome préaortique : à  propos d'un cas
Keywords: جهش ژنتیکی; Paragangliome; Chirurgie; Histologie; Mutation génétique; Paraganglioma; Surgery; Histology; Genetic mutation;
Gliomas: advances in molecular analysis and characterization
Keywords: جهش ژنتیکی; Brain tumor; Malignant glioma; Glioblastoma multiforme; Brain cancer; Genetic mutation; Microarray; Gene expression profiling; Molecular profiling; EGFR; Granulin;