Keywords: حذف; Immunodeficiency; Foals; DNA-PKcs; Deletion; Fragment analysis;
مقالات ISI حذف (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: حذف; MDD; major depressive disorder; WGS; whole-genome sequencing; CNV; copy number variation; SNV; single nucleotide variant; INDEL; small insertion and deletion; Major depressive disorder; Healthy controls; Paired-end reads; Deletion; Chromosome; Mexican-Ame
Keywords: حذف; Arabidopsis; Heavy ion irradiation; Mutation; Mutant sector; Deletion;
Keywords: حذف; Occlusion; Trajectory continuity; Accretion; Deletion;
Keywords: حذف; BEN; bendamustine; CI; combination index; CLB; chlorambucil; CLL; chronic lymphocytic leukemia; Cyclo; cyclophosphamide; dADO; deoxyadenosine; Del; deletion; DHE; dihydroethidium; DiOC6; 3,3â²-dihexyloxacarbocyanine iodide; DMSO; dimethyl sulfoxide; DR;
Keywords: حذف; ACE; angiotensin-converting enzyme; Ang; angiotensin; D; deletion; EtBr; ethidium bromide; HCEFS; high constant electric field strength; HVPS; high-voltage power supply; I; insertion; LCEFS; low constant electric field strength; ME; microchip electrophore
Keywords: حذف; Malaria; Rapid diagnostic tests; Pfhrp2; Deletion; Variation;
Keywords: حذف; Phylogenetics; Distance methods; Invariant sites; Insertion; Deletion; Gaps as missing data;
Keywords: حذف; aneuploidy; deletion; duplication; dosage balance; buffering; compensation
Keywords: حذف; chromosome; deletion; prenatal diagnosis; ultrasound
Keywords: حذف; Duchenne muscular dystrophy; Deletion; Duplication; Egypt; MLPA; Sequencing
Keywords: حذف; Antidepressant; copy number; deletion; duplication; pharmacogenetic; pharmacogenomic; rare genetic variation;
Keywords: حذف; TFBM; transcription factor binding motif(s); gfp; green fluorescent protein; Del; deletion; ED; evolutionary distance; Pita; Allele mining; Promoter mining; Core promoter; Transcription factor binding sites;
Keywords: حذف; DMD; DMD gene; Deletion; Carrier detection;
Keywords: حذف; Ovarian cancer; Next generation sequencing; Targeted therapy; Mutation; Deletion; Gene fusion;
Keywords: حذف; ADHD; Deletion; Copy number variation; Epistasis; CNV; MYT-1;
Keywords: حذف; Autosomal recessive spastic ataxia of Charlevoix–Saguenay (ARSACS); Inherited peripheral neuropathy (IPN); Nonsense mutation; Deletion
Keywords: حذف; Spastic paraplegia 28 (SPG28); Autosomal recessive; DDHD1; Frameshift; Stop gain; Deletion
Keywords: حذف; Combinatorics; Deletion; Insertion; k-match; Match section; Sequence alignment
A natural “GA” insertion mutation in the sequence encoding the 3â²UTR of CXCL12/SDF-1α: Identification, characterization, and functional impact on mRNA splicing
Keywords: حذف; 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
KCNQ2 encephalopathy: A case due to a de novo deletion
Keywords: حذف; KCNQ2 encephalopathy; Deletion; EEG; Genetic; Neonatal-onset epilepsy;
Frequency of SMN1 exon 7 deletion in patients with spinal muscular atrophy in Kashmir
Keywords: حذف; Kashmir; Spinal muscular atrophy; Survival motor neuron; Deletion;
The first instance of HPR-deleted ISAV detection in eviscerated, fresh salmon at a Chinese entry-exit port
Keywords: حذف; Infectious salmon anemia virus; Highly polymorphic region; Deletion; Fresh salmon; Chinese entry-exit port;
Antiviral resistance due to deletion in the neuraminidase gene and defective interfering-like viral polymerase basic 2 RNA of influenza A virus subtype H3N2
Keywords: حذف; Influenza; Antiviral; Resistance; H3N2; Deletion; Defective interfering viral RNA;
Identification of CDAN1, C15ORF41 and SEC23B mutations in Chinese patients affected by congenital dyserythropoietic anemia
Keywords: حذف; CDA; congenital dyserythropoietic anaemias; PolyPhen; Polymorphism Phenotyping v2; SIFT; Sorting Intolerant From Tolerant; MAF; minor allele frequency; Provean; Protein Variation Effect Analyzer; ExAC; Exome Aggregation Consortium; SNP; single nucleotide
Development of an Sce-I mutagenesis system for Burkholderia cepacia complex strains
Keywords: حذف; Bacterial genetics; Burkholderia; Cepacia; Cenocepacia; Deletion; Mutagenesis;
Prenatal diagnosis of a case with SEA-HPFH deletion thalassemia with whole HBB gene deletion
Keywords: حذف; β-Thalassemia; Deletion; Hereditary persistence of fetal hemoglobinemia (HPFH);
The c.305del3 in IL-2 gene in Homonoidea theoretically affects IL-2/IL-2Rα interaction as well as lymphocyte homeostasis
Keywords: حذف; Interleukin-2; Ancestor; Molecular dynamics simulation; Modeling; Deletion; Lymphocyte homeostasis;
A novel BRCA1 gene deletion detection in human breast carcinoma MCF-7 cells through FRET between quantum dots and silver nanoclusters
Keywords: حذف; Deletion; Fluorescence; Nanobiosensor; Nanoclusters; Quantum dots; Mutations;
KatG plays an important role in Aeromonas hydrophila survival in fish macrophages and escape for further infection
Keywords: حذف; A. hydrophila; Aeromonas hydrophila; bp; base pair(s); C. jejuni; Campylobacter jejuni; Cm; chloramphenicol; DMSO; dimethyl sulphoxide; E. coli; Escherichia coli; FCS; foetal calf serum; F. tularensis; Francisella tularensis; H2O2; hydrogen peroxide; LB;
Pitfalls in molecular diagnosis of Friedreich ataxia
Keywords: حذف; Friedreich ataxia; FXN gene; Aluseq; Deletion; TP-PCR; Diagnosis;
4-bp insertion/deletion polymorphism within the promoter of EGLN2 gene is associated with susceptibility to cancer in Asian population: Evidence from a meta-analysis
Keywords: حذف; EGLN2; Cancer; Polymorphism; Deletion; Insertion; Meta-analysis;
Determination of complete sequence information of the human ABO blood group orthologous gene in pigs and breed difference in blood type frequencies
Keywords: حذف; EAA; Erythrocyte antigen A; KNP; Korean Native Pig; AGH; American Guinea Hog; EDTA; ethylenediaminetetraacetic acid; SDS; sodium dodecyl sulfate; IACUC; Institutional Animal Care and Use Committee; DMSO; dimethyl sulfoxide; SINE; short interspersed nuclea
Copy number variations of SCN5A in Brugada syndrome
Keywords: حذف; Brugada syndrome; Copy number variation; Deletion; Duplication; Multiplex ligation-dependent probe amplification; SCN5A;
Heterodimer formation by Oct4 and Smad3 differentially regulates epithelial-to-mesenchymal transition-associated factors in breast cancer progression
Keywords: حذف; BCa; Breast cancer; BLAST; Basic Local Alignment Search Tool; CCL5; -C-C motif ligand 5; CCR5; -C-C chemokine receptor type 5; ChIP; Chromatin immunoprecipitation; Co-IP; Co-immunoprecipitation; CSCs; Cancer stem cells; CXCL13; -CXC chemokine ligand
Effects of cytochrome P450 single nucleotide polymorphisms on methadone metabolism and pharmacodynamics
Keywords: حذف; ADH; alcohol dehydrogenase; CDC; Centers for Disease Control and Prevention; CYP; cytochrome P450; del; deletion; EDDP; 2-ethyl-1,5-dimethyl-3,3-diphenylpyrrolidine; EM; extensive metabolizer; EMDP; 2-ethyl-5-methyl-3,3-diphenyl-1-pyrroline; FDA; Food and
Case reportDeletion of P2 promoter of GJB1 gene a cause of Charcot-Marie-Tooth disease
Keywords: حذف; Charcot-Marie-Tooth disease; X-linked; GJB1; Connexin 32; Deletion; P2 promoter; Schwann cell dysfunction;
Physiology and pathogenicity of cpdB deleted mutant of avian pathogenic Escherichia coli
Keywords: حذف; Avian pathogenic Escherichia coli (APEC); cpdB gene; Deletion; Physiology; Pathogenicity;
In vivo development of tigecycline resistance in Klebsiella pneumoniae owing to deletion of the ramR ribosomal binding site
Keywords: حذف; Klebsiella pneumoniae; Tigecycline resistance; Ribosomal binding site; Deletion; RamR translation;
Deletion of RDINK4/ARF enhancer: A novel mutation to “inactivate” the INK4-ARF locus
Keywords: حذف; RD enhancer; Deletion; The INK4-ARF locus; Cancer;
Autosomal dominant hypocalcemia due to a truncation in the C-tail of the calcium-sensing receptor
Keywords: حذف; Calcium-sensing receptor; Autosomal dominant hypocalcemia; Deletion; Activating mutation; Mutational analysis;
Impact of deletions and mutations in Hepatitis B virus envelope proteins on serological profile and clinical evolution
Keywords: حذف; Hepatitis B virus; Hepatocellular failure; preS/S variability; Deletion; Viral immune escape;
Deletion of NADH oxidase in Listeria monocytogenes promotes the bacterial infection of brain
Keywords: حذف; NADH oxidase; Deletion; Reactive oxygen species; Brain invasion; Inflammatory factors;
Associative role of TYMS6bpdel polymorphism and resulting hyperhomocysteinemia in the pathogenesis of preterm delivery and associated complications: A study from Northeast India
Keywords: حذف; PTD; preterm delivery; LBW; low birth weight; MTHFR; Methylene Tetrahydrofolate Reductase; TYMS; Thymidylate Synthase; IUD; intra uterine death; Del; deletion; Ins; insertion; MTHF; methylene tetrahydrofolate; UTI; urinary tract infection; UTR; untranslat
A novel Y chromosome microdeletion potentially associated with defective spermatogenesis identified by custom array comparative genome hybridization
Keywords: حذف; array CGH; deletion; male infertility; Y chromosome;
Superficial acral fibromyxoma: clinicopathological, immunohistochemical, and molecular study of 11 cases highlighting frequent Rb1 loss/deletions
Keywords: حذف; Superficial acral fibromyxoma; Digital fibromyxoma; Rb1; Deletion; Angiofibroma; Angiomyxoma;
Scanning indels in the 5q22.1 region and identification of the TMEM232 susceptibility gene that is associated with atopic dermatitis in the Chinese Han population
Keywords: حذف; AD; Atopic dermatitis; IHC; Immunohistochemistry; GWAS; Genome-wide association study; TMEM232; Transmembrane protein 232; SLC25A46; Solute carrier family 25 member 46; indels; Insertion and deletions; Atopic dermatitis; TMEM232; Deletion; Expression;
Effects of pyruvate kinase on the growth of Corynebacterium glutamicum and L-serine accumulation
Keywords: حذف; L-serine; Pyruvate kinase; Corynebacterium glutamicum; Mutation; Deletion;
Short communicationIdentification of a novel deletion in SURF1 gene: Heterogeneity in Leigh syndrome with COX deficiency
Keywords: حذف; Leigh syndrome; SURF1; COX deficiency; Deletion; Nonsense mutation;
Do the exome: A case of Williams-Beuren syndrome with severe epilepsy due to a truncating de novo variant in GABRA1
Keywords: حذف; Williams-Beuren syndrome; Deletion; GABRA1; De novo mutation; Epilepsy; Exome;