Keywords: غربالگری مولکولی; Molecular screening; Targeted therapies; Next-generation sequencing; Primary tumour; Metastases;
مقالات ISI غربالگری مولکولی (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: غربالگری مولکولی; Hemoglobinopathy; Next-generation sequencing; Molecular screening; Clinical genotyping;
Keywords: غربالگری مولکولی; Inherited retinal dystrophies; Retinitis pigmentosa; Macular dystrophy; Molecular screening; Leber congenital amaurosis; Vitelliform macular dystrophyDystrophies rétiniennes héréditaires; Rétinite pigmentaire; Dystrophie maculaire; Criblage moléculaire; A
Screening for vancomycin-resistant enterococci with Xpert® vanA/vanB: diagnostic accuracy and impact on infection control decision making
Keywords: غربالگری مولکولی; Infection control; molecular screening; PCR-based screening; selective culture; vanA; vancomycin-resistant enterococci;
Original ResearchSafety, tolerability and antitumour activity of LY2780301 (p70S6K/AKT inhibitor) in combination with gemcitabine in molecularly selected patients with advanced or metastatic cancer: a phase IB dose escalation study
Keywords: غربالگری مولکولی; LY2780301; Gemcitabine; PI3K/AKT/mTOR pathway; Dual p70S6K/AKT inhibition; PTEN; Molecular alterations; Phase I; Molecular screening; Drug development;
Myophosphorylase (PYGM) mutations determined by next generation sequencing in a cohort from Turkey with McArdle disease
Keywords: غربالگری مولکولی; Glycogenosis; Population specific; Novel mutation; Rare muscle disorders; Molecular screening; Genomics;
Characterization of additional vitamin D binding protein variants
Keywords: غربالگری مولکولی; DBP; vitamin D binding protein; DHPLC; denaturing high performance liquid chromatography; GC; group specific component; dbSNP; single nucleotide polymorphism database; 25OHD; 25-hydroxyvitamin D; LC-ESI-TOF-MS; liquid chromatography-electrospray ionizatio
Validation of the FAM19A4/mir124-2 DNA methylation test for both lavage- and brush-based self-samples to detect cervical (pre)cancer in HPV-positive women
Keywords: غربالگری مولکولی; Human papillomavirus; Self-sampling; Reflex test; Cervical cancer; Molecular screening; DNA methylation; HPV16/18 genotyping;
Morphostructural investigation of the female reproductive system and molecular evidence for Wolbachia in Balclutha brevis Lindberg 1954 (Hemiptera, Cicadellidae)
Keywords: غربالگری مولکولی; TEM; SEM; Histology; Molecular screening; Auchenorrhyncha; Entomopathogenic bacteria;
A case of long QT syndrome with triple gene abnormalities: Digenic mutations in KCNH2 and SCN5A and gene variant in KCNE1
Keywords: غربالگری مولکولی; ECG; electrocardiogram; LQTS; long QT syndrome; PAS; Per-Arnt-Sim; QTc; corrected QT interval; QTcb; QTc rectified using Bazett's formula; Digenic mutation; Compound mutation; KCNH2; SCN5A; KCNE1; molecular screening;
Factors influencing Dipylidium sp. infection in a free-ranging social carnivore, the spotted hyaena (Crocuta crocuta)
Keywords: غربالگری مولکولی; Spotted hyaena; Dipylidium; Molecular screening; Parasite infection; Grooming; Serengeti
Assessment of a clinical checklist in the diagnosis of fragile X syndrome in India
Keywords: غربالگری مولکولی; CGG expansion; Checklist; FMR1; FRAXA; Mental retardation; Molecular screening
Screening of High-Risk Families for Pancreatic Cancer
Keywords: غربالگری مولکولی; Endoscopic ultrasound; Familial pancreatic cancer; Hereditary pancreatitis; Molecular screening;
Mutation screening of the MECP2 gene in a large cohort of 613 fragile-X negative patients with mental retardation
Keywords: غربالگری مولکولی; Mental retardation; MECP2; Mutation; Polymorphism; Molecular screening
N- and C-terminal KCNE1 mutations cause distinct phenotypes of long QT syndrome
Keywords: غربالگری مولکولی; Long QT syndrome; KCNE1; Ion channels; Molecular screening; Electrophysiology