Keywords: جهش; Ecological information; Mutation; Synergy; Ecosystem stability; Discrete-event systemFSM, finite state machine; SLS, soil-like substrate; SLSAE, SLS-based artificial ecosystem; ODEs, ordinary differential equations
مقالات ISI جهش (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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.
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; Environmental mutagens; DNA damage; DNA replication; Mutation; Polymerase; Replisome
Keywords: جهش; Menkes disease; Genotype–phenotype; Treatment; Mutation
Pathological hemichannels associated with human Cx26 mutations causing Keratitis-Ichthyosis-Deafness syndrome
Keywords: جهش; Connexin; Mutation; Genetic disease; Channel; Epidermis;
A natural “GA” insertion mutation in the sequence encoding the 3â²UTR of CXCL12/SDF-1α: Identification, characterization, and functional impact on mRNA splicing
Keywords: جهش; aa; amino acid(s); AREs; AU-rich elements; ARMS; amplification refractory mutation system; bp; base pair(s); cDNA; DNA complementary to RNA; cpm; counts per minute; CXCL; C-X-C motif chemokine ligand; CXCR; C-X-C chemokine receptor; d; deoxyribo; DMSO; di
An integro-PDE model with variable motility
Keywords: جهش; Nonlocal; Reaction-diffusion equation; Mutation; Mathematical ecology;
Fibronectin Glomerulopathy Caused by the Y973C Mutation in Fibronectin: A Case Report and Literature Review
Keywords: جهش; fibronectins; nephrotic syndrome; mutation;
Anti-MOG antibody encephalitis mimicking neurological deterioration in a case of Rett syndrome with MECP2 mutation
Keywords: جهش; Anti-MOG antibody encephalitis; Rett syndrome; MECP2; Mutation; MRI;
Targeted next generation sequencing identified a novel mutation in MYO7A causing Usher syndrome type 1 in an Iranian consanguineous pedigree
Keywords: جهش; Usher syndrome; MYO7A; Mutation; Targeted next generation sequencing;
Report of two unrelated families with Jalili syndrome and a novel nonsense heterozygous mutation in CNNM4 gene
Keywords: جهش; Jalili syndrome; Cone-rod dystrophy; Amelogenesis imperfecta; CNNM4; Mutation;
Clinical and molecular characteristics of colombian patients with mucopolysaccharidosis IVA, and description of a new galns gene mutation
Keywords: جهش; Mucopolysaccharidosis IVA; Morquio syndrome; GALNS; Lysosomal storage disorder; Mutation;
Speech and language delay in a patient with WDR4 mutations
Keywords: جهش; WDR4; Primordial dwarfism (PD); Mutation; Whole-exome sequencing;
Dialysis as a Treatment Option for a Patient With Normal Kidney Function and Familial Tumoral Calcinosis Due to a Compound Heterozygous FGF23 Mutation
Keywords: جهش; Case report; fibroblast growth factor 23 (FGF-23); FGF23 mutation; hemodialysis; hyperphosphatemia; genetic disease; metabolic disorder; mutation; tumoral calcinosis; extra-osseous calcifications;
Identification and functional analysis of a novel mutation in the PAX3 gene associated with Waardenburg syndrome type I
Keywords: جهش; WS1; Waardenburg syndrome type 1; PAX3; Paired box gene 3; NCC; Neural crest cells; MITF; The Microphthalmia-Associated Transcription Factor; WS3; Waardenburg syndrome type 3; HRCT; The high-resolution computed tomography; MRI; Magnetic resonance imaging;
Computational analysis of non-synonymous SNPs in bovine Mx1 gene
Keywords: جهش; Bovine; Gene; Mutation; SNP;
Clinical characteristics and outcomes of patients with BRCA1 or RAD51C methylated versus mutated ovarian carcinoma
Keywords: جهش; Ovarian carcinoma; Methylation; Homologous recombination; Mutation;
SCN5A mutation type and topology are associated with the risk of ventricular arrhythmia by sodium channel blockers
Keywords: جهش; Brugada syndrome; SCN5A; Mutation; Ajmaline; PVC; Arrhythmia;
First description of a cefixime- and ciprofloxacin-resistant Neisseria gonorrhoeae isolate with mutations in key antimicrobial susceptibility-determining genes from the country of Georgia
Keywords: جهش; Antimicrobial; Georgia; gonorrhoea; mutation; Neisseria; resistance;
Quinolone-resistant phenotype of Flavobacterium columnare isolates harbouring point mutations both in gyrA and parC but not in gyrB or parE
Keywords: جهش; Antimicrobials; Flavobacterium columnare; Mutation; Quinolone; Resistance;
Identification and characterization of abamectin resistance in Tetranychus urticae Koch populations from greenhouses in Turkey
Keywords: جهش; Tetranychus urticae; Abamectin resistance; Detoxification enzymes; Mutation;
Inactivation of phoPQ genes attenuates Salmonella Gallinarum biovar Gallinarum to susceptible chickens
Keywords: جهش; Mutation; Virulence; Fowl typhoid; Adaptation; Chickens;
p.Q511L mutation of HNF1α in hepatocellular carcinoma suppresses the transcriptional activity and the anti-tumor effect of HNF1α
Keywords: جهش; HNF1α; HCC; Mutation; Transcription activity; Subcellular localization; Malignancy;
GRIN2A mutations in epilepsy-aphasia spectrum disorders
Keywords: جهش; Epilepsy; Aphasia; GRIN2A; Mutation; Electrical status epilepticus during sleep;
Clinical and functional studies of two novel variants in the LPL gene in subjects with severe hypertriglyceridemia
Keywords: جهش; LPL; Novel; Insertion; Mutation; LPL mass; LPL activity;
Nicotinic acetylcholine receptor subunit α6 associated with spinosad resistance in Rhyzopertha dominica (Coleoptera: Bostrichidae)
Keywords: جهش; Rhyzopertha dominica; Spinosad; Nicotinic acetylcholine receptor subunit α6; Mutation; Transcriptional expression;
A review on non-syndromic tooth agenesis associated with PAX9 mutations
Keywords: جهش; Hypodontia; Oligodontia; Mutation; PAX9;
Characterization of H9N2 avian influenza viruses from the Middle East demonstrates heterogeneity at amino acid position 226 in the hemagglutinin and potential for transmission to mammals
Keywords: جهش; Avian influenza virus; H9N2; Jordan; Next generation sequencing; Mutation; Hemagglutinin;
A mouse model of a novel missense mutation (Gly83Arg) in a Chinese kindred manifesting vitreous amyloidosis only
Keywords: جهش; Mouse model; Gly83Arg; Mutation; Vitreous; Amyloidosis; Transthyretin;
Genotype and clinical characteristics of congenital long QT syndrome in Thailand
Keywords: جهش; Long QT syndrome; Genetics; Mutation; Thailand; Children;
Enhanced production and antioxidant activity of endo-polysaccharides from Phellinus igniarius mutants screened by low power He-Ne laser and ultraviolet induction
Keywords: جهش; Phellinus igniarius; Mutation; Endo-polysaccharides; Physicochemical properties; Antioxidant activities;
HMGA2 and MED12 alterations frequently co-occur in uterine leiomyomas
Keywords: جهش; Leiomyoma; MED12; HMGA2; Mutation; Gene expression; Sequencing;
SETBP1 mutations in Chinese patients with acute myeloid leukemia and myelodysplastic syndrome
Keywords: جهش; AML; HRMA; Mutation; MDS; SETBP1;
Leber's hereditary optic neuropathy caused by a mutation in mitochondrial tRNAThr in eight Chinese pedigrees
Keywords: جهش; Leber's hereditary optic neuropathy (LHON); Mitochondrial DNA; tRNA; Mutation; Metabolism; Pathophysiology; Chinese;
Natural and targeted isovariants of the rice actin depolymerizing factor 2 can alter its functional and regulatory binding properties
Keywords: جهش; Actin depolymerizing factor 2; Isovariant; Mutation; Phosphorylation; Rice;
Germline DNA-repair Gene Mutations and Outcomes in Men with Metastatic Castration-resistant Prostate Cancer Receiving First-line Abiraterone and Enzalutamide
Keywords: جهش; DNA repair; Germline; Mutation; Abiraterone; Enzalutamide;
Pulmonary artery hypertension in childhood: The transforming growth factor-β superfamily-related genes
Keywords: جهش; bone morphogenetic proteins; mutation; pulmonary hypertension;
A conserved residue of l-alanine dehydrogenase from Bacillus pseudofirmus, Lys-73, participates in the catalytic reaction through hydrogen bonding
Keywords: جهش; l-Alanine dehydrogenase; Catalytic activity; Hydrogen-bonding; Mutation;
Novel intracellular transport-refractory mutations in KCNH2 identified in patients with symptomatic long QT syndrome
Keywords: جهش; Long QT syndrome; KCNH2; Mutation; Patch-clamp; Immunofluorescence;
A two-year monitoring period of the genetic properties of clade 2.3.2.1c H5N1 viruses in Nigeria reveals the emergence and co-circulation of distinct genotypes
Keywords: جهش; HPAI; Full-genome sequencing; Co-circulation; Reassortment; Mutation; Evolution;
Rare targetable drivers (RTDs) in non-small cell lung cancer (NSCLC): Outcomes with immune check-point inhibitors (ICPi)
Keywords: جهش; ALK; anaplastic lymphoma kinase; BRAF; v-Raf murine sarcoma viral oncogene homolog B; cMET; tyrosine-protein kinase Met/hepatocyte growth factor receptor; CT; computer tomography; ECOG; PS Eastern Cooperative Oncology Group performance status; EGFR; epide
Genetic analysis of TIA1 gene in Chinese patients with amyotrophic lateral sclerosis
Keywords: جهش; Amyotrophic lateral sclerosis; TIA1; Mutation;
Improving transcriptional activity of human cytomegalovirus major immediate-early promoter by mutating NF-κB binding sites
Keywords: جهش; Transcriptional activity; Major immediate-early promoter; NF-κB binding site; Mutation; CMV; cytomegalovirus; MIEP; major immediate-early promoter; SELEX; systematic evolution of ligands by exponential enrichment; HCMV; human cytomegalovirus; CHO; Chines
Incomplete uptake of EGFR mutation testing and its impact on estimation of mutation prevalence in patients with non-squamous NSCLC: A population-based study in New Zealand
Keywords: جهش; CI; confidence interval; EGFR; epidermal growth factor receptor; NHI; National Health Index; NSCLC; non-small cell lung cancer; NZCR; New Zealand Cancer Registry; NZDep; New Zealand Deprivation Index; TKI; tyrosine kinase inhibitor; Non-small cell lung ca
Fourteen new mutations of BCKDHA, BCKDHB and DBT genes associated with maple syrup urine disease (MSUD) in Malaysian population
Keywords: جهش; Maple syrup urine disease; Autosomal recessive; Mutation; BCKDH; BCAAs; MSUD;
Apolipoprotein CII Amyloidosis Associated With p.Lys41Thr Mutation
Keywords: جهش; amyloidosis; apolipoprotein CII; kidney; mutation; p.Lys41Thr; proteomics;
Untying the gordion knot of targeting MET in cancer
Keywords: جهش; Amplification; Cancer; MET; Mutation; Targeted therapy;
Identification of a novel mutation (Ala66Thr) of SRY gene causes XY pure gonadal dysgenesis by affecting DNA binding activity and nuclear import
Keywords: جهش; AR; androgen receptor; CYP11A1; cytochrome P450 family 11 subfamily a member 1; CYP17A1; cytochrome P450 family 17 subfamily a member 1; DHH; desert hedgehog; DMRT1/2/3; doublesex and mab-3 related transcription factor 1/2/3; DSD; disorders of sex develop
Mutation in populations governed by a Galton-Watson branching process
Keywords: جهش; Mutation; Galton-Watson; Multitype branching process;
Diagnostic utility of histone H3.3 G34W, G34R, and G34V mutant-specific antibodies for giant cell tumors of bone
Keywords: جهش; Giant cell tumor of bone; H3F3A; Mutation; Immunohistochemistry; Denosumab;
Screening of GLE1 mutations in Chinese amyotrophic lateral sclerosis patients
Keywords: جهش; Amyotrophic lateral sclerosis; GLE1; Mutation;