Keywords: جهش ژنی; H.pylori; Helicobactor pylori; PPI; Proton pump inhibitor; TBRI; Theodor Bilharz Research Institute; DNA; Deoxy-ribonucleic acid; PCR; Polymerase chain reaction; 16S rRNA; 16 S ribosomal ribonucleic acid; dNTPs; Deoxynucleotide Triphosphates; SPSS; Statis
مقالات ISI جهش ژنی (ترجمه نشده)
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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 ژنی; Left ventricular noncompaction; Genetics; Noncompaction cardiomyopathy; Gene mutations;
Keywords: جهش ژنی; Congenital hypothyroidism; Gene mutations; Next-generation sequencing; China;
Keywords: جهش ژنی; Molecular genetic testing; Next generation sequencing; Prognosis; Myelodysplastic syndromes; International Prognostic Scoring System; Gene mutations;
Keywords: جهش ژنی; Cancer; Gene mutations; Carcinogenesis;
Keywords: جهش ژنی; Acute myeloid leukemia; Biomarkers; Gene mutations; DNA methylation; Protein expression;
Keywords: جهش ژنی; Methylmalonic aciduria; Homocystinuria; Early onset; Gene mutations; Outcome;
Keywords: جهش ژنی; Hereditary pancreatitis; Children; Gene mutations; Chronic pancreatitis;
Keywords: جهش ژنی; Zebrafish; Next generation sequencing; Gene mutations; TALEN; CRISPR/Cas9
Keywords: جهش ژنی; Small cell lung cancer; Gene mutations; Therapy; Immunotherapy; Neuroendocrine;
Keywords: جهش ژنی; Gene mutations; Chronic lymphocytic leukemia; Biology and prognosis;
Keywords: جهش ژنی; Lung cancer; Smoking cessation; Cancer prevention; Targeted therapy; Immunotherapy; Screening; Pathology; Staging; Surgery; Adjuvant chemotherapy; Radiotherapy; Gene mutations; Master protocols; Biomarkers; Value of therapy;
Keywords: جهش ژنی; Lung cancer; Gene mutations; Tumor models; Patient-derived xenografts; Biomarkers;
Keywords: جهش ژنی; MDS; Genomic profiling; Epigenetics; Cytogenetics; Gene Mutations;
Keywords: جهش ژنی; extracellular matrix; glaucoma; trabecular meshwork; intraocular pressure; gene mutations; animal models; perfusion culture;
Keywords: جهش ژنی; Hyperinsulinism; Hypoglycemia; PET scan; 18F-DOPA; Gene mutations
Keywords: جهش ژنی; Acute myeloid leukemia; Gene mutations; Allogeneic hematopoietic stem cell transplantation;
Keywords: جهش ژنی; Subclinical congenital hypothyroidism; Dual oxidase 2 gene (DUOX2); Gene mutations; Next-generation sequencing; Chinese population
Keywords: جهش ژنی; Coronary artery disease; Transforming growth factor beta; Gene mutations; Atherosclerosis
Keywords: جهش ژنی; Neurotoxins; Gene mutations; Mercury; Arsenic; Lead; Selenium; MPV17-related hepatocerebral mitochondrial DNA depletion syndrome; Anthropocene
Mutation screening of the GLIS3 gene in a cohort of 592 Chinese patients with congenital hypothyroidism
Keywords: جهش ژنی; Congenital hypothyroidism; GLIS3; Gene mutations; China; Next-generation sequencing;
Extranodal NK/T-cell lymphoma: Updates in biology and management strategies
Keywords: جهش ژنی; NK/T-cell lymphoma; Gene mutations; Chemotherapy; Radiotherapy;
Featured structure-activity relationships for some tri- and tetrachlorobiphenyls in human CYP2E1-activated mutagenicity - Impact of the extent of ortho-chlorination
Keywords: جهش ژنی; Noncoplanar polychlorinated biphenyls; CYP2E1; Micronuclei; Centromere protein B; Gene mutations; V79â¯cells;
Exome sequencing analysis reveals homozygous GJB2 gene mutation in a Mexican family with profound hearing loss
Keywords: جهش ژنی; GJB2 gene; Hypoacusia; Gene mutations; Connexins; Homozygous; Gene GJB2; Hipoacusia; Mutaciones génicas; Conexinas; Homocigoto;
Analysis of a panel of druggable gene mutations and of ALK and PD-L1 expression in a series of thymic epithelial tumors (TETs)
Keywords: جهش ژنی; Thymoma; Thymic carcinoma; Gene mutations; c-KIT; PD-L1;
Next-generation sequencing analysis of TSHR in 384 Chinese subclinical congenital hypothyroidism (CH) and CH patients
Keywords: جهش ژنی; Subclinical congenital hypothyroidism; TSH receptor gene (TSHR); Gene mutations; Next-generation sequencing; Chinese population;
NF-κB activation in chronic lymphocytic leukemia: A point of convergence of external triggers and intrinsic lesions
Keywords: جهش ژنی; Chronic lymphocytic leukemia; NF-κB; Microenvironment; Gene mutations;
Congenital Aniridia and the Ocular Surface
Keywords: جهش ژنی; aniridia; aniridia-associated keratopathy; congenital aniridia; gene mutations; haplo-insufficiency; iris; Pax6 gene;
Two novel compound heterozygous families with a trimutation in the GJB2 gene causing sensorineural hearing loss
Keywords: جهش ژنی; GJB2 gene; Hypoacusia; Gene mutations; Connexins
Multidrug-resistant and heteroresistant Mycobacterium tuberculosis and associated gene mutations in Ethiopia
Keywords: جهش ژنی; Multidrug-resistant tuberculosis; Heteroresistance; Gene mutations; Ethiopia
Hairy cell leukaemia-variant: Disease features and treatment
Keywords: جهش ژنی; Hairy cell leukaemia variant; TP53; MAP2K1; Gene mutations; Immunophenotype; Diagnosis; Treatment;
Sex-dichotomous effects of functional COMT genetic variations on cognitive functions disappear after menopause in both health and schizophrenia
Keywords: جهش ژنی; Cognition; Gene mutations; Haplotypes; Executive functions; Psychiatry; Hormonal status;
Particular distribution of the GJB2/GJB6 gene mutations in Mexican population with hearing impairment
Keywords: جهش ژنی; GJB2 gene; GJB6 gene; Hypoacusia; Gene mutations; Connexins
Gene mutations in small-cell lung cancer (SCLC): Results of a panel of 6 genes in a cohort of Italian patients
Keywords: جهش ژنی; SCLC; Gene mutations; EGFR; c-MET; BRAF; KRAS; PDGFRa; c-KIT
Genetic basis of Brugada syndrome
Keywords: جهش ژنی; Brugada syndrome; Gene mutations; SCN5A; Overlap syndrome
Chronic myelomonocytic leukemia: Myelodysplastic or myeloproliferative?
Keywords: جهش ژنی; chronic myelomonocytic leukemia; prognostic score; gene mutations; ASXL1 gene mutation; demethylating agents
25-Hydroxyvitamin D-24-hydroxylase (CYP24A1): Its important role in the degradation of vitamin D
Keywords: جهش ژنی; CYP24A1; 25-Hydroxyvitamin D3; 1,25-Dihydroxyvitamin D3; Catabolism; Gene mutations; Idiopathic infantile hypercalcemia; CYP24A1 null-mouse; FGF-23
Hallazgos clínicos y genéticos en pacientes con deficiencia de biotinidasa detectados en el cribado neonatal o selectivo de sordera o de enfermedades metabólicas hereditarias
Keywords: جهش ژنی; Enfermedad metabólica hereditaria; Cribado neonatal; Sordera; Convulsiones sensibles a biotina; MutacionesInherited metabolic disorders; Newborn screening; Hearing loss; Biotin-sensitive seizures; Gene mutations
New genetic factors implicated in human GnRH-dependent precocious puberty: The role of kisspeptin system
Keywords: جهش ژنی; GnRH-dependent precocious puberty; Gene mutations; KISS1; KISS1R
Estudio genético del complejo enzimático succinato deshidrogenasa en los paragangliomas carotÃdeos. Implicaciones diagnósticas
Keywords: جهش ژنی; Paragangliomas carotÃdeos; Paragangliomas familiares; Paragangliomas múltiples; Paragangliomas malignos; Mutaciones genéticas; Complejo succinato deshidrogenasa; Carotid paragangliomas; Familial paragangliomas; Multiple paragangliomas; Malignant paraga
Interactions between oral contraceptive status and GSTM1 and GSTT1 deletions on insulin-like growth factor-1 (IGF-1) plasma levels in young healthy women
Keywords: جهش ژنی; Oral contraception; IGF-1; GSTM1; GSTT1; GSTP1; Gene mutations; Metabolism;
Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia
Keywords: جهش ژنی; Arrhythmia; Arrhythmogenic cardiomyopathy; Sudden death; Cell adhesion molecules; Gene mutations; Compound genotypes; ARVC/D; arrhythmogenic right ventricular cardiomyopathy/dysplasia; ECG; electrocardiogram; DHPLC; denaturing high-performance liquid chro
Mutations in Alpha-Actinin-2 Cause Hypertrophic Cardiomyopathy : A Genome-Wide Analysis
Keywords: جهش ژنی; α-actinin-2; gene mutations; hypertrophic cardiomyopathyACTN2, alpha-actinin-2; HCM, hypertrophic cardiomyopathy; ICD, implantable cardioverter-defibrillator; LOD, logarithm of odds ratio; LVH, left ventricular hypertrophy; PCR, polymerase chain reaction;
Pharmacogenetics in Heart Failure: How It Will Shape the Future
Keywords: جهش ژنی; Heart failure; Pharmacogenomics; Gene mutations; Genetics; Single nucleotide polymorphisms;
Skin cancer and solar UV radiation
Keywords: جهش ژنی; skin cancer; melanoma; incidence trends; UV radiation; DNA damage; gene mutations
Prognostic Implication of EGFR, KRAS, and TP53 Gene Mutations in a Large Cohort of Japanese Patients with Surgically Treated Lung Adenocarcinoma
Keywords: جهش ژنی; Lung cancer; EGFR; KRAS; TP53; Gene mutations
Genotoxic effects of radiofrequency electromagnetic fields
Keywords: جهش ژنی; Gene mutations; Cytogenetic effects; DNA fragmentation; Mechanisms of genotoxicity
Cytogenetics and Molecular Genetics of Acute Lymphoblastic Leukemia
Keywords: جهش ژنی; Acute lymphoblastic leukemia; Gene mutations; Chromosome aberrations; Human; Prognosis;
Hereditary retinopathies in the dog: Genetic fundamentals and genetic tests
Keywords: جهش ژنی; Dog; Gene mutations; Genetic tests; Retina; Retinitis pigmentosa; PRAAPR; Chien; Gène; Mutation; Rétine; Rétinite pigmentaire; Tests génétiques
Proximal and distal colorectal cancers show distinct gene-specific methylation profiles and clinical and molecular characteristics
Keywords: جهش ژنی; Colorectal cancer; DNA methylation; Microsatellite instability; Loss of heterozygosity; Gene mutations;