Keywords: ناهمگونی فنوتیپی; Familial epilepsy; MTLE; Phenotypic heterogeneity;
مقالات ISI ناهمگونی فنوتیپی (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: ناهمگونی فنوتیپی; Overflow metabolism; Metabolite exchange; Warburg effect; Crabtree effect; Phenotypic heterogeneity; Exometabolome; Metabolite sensing;
Keywords: ناهمگونی فنوتیپی; clear cell hepatocellular carcinoma; phenotypic heterogeneity; glycogenosis; lipidosis; preneoplastic glycogenosis; progression; metabolic aberrations;
Keywords: ناهمگونی فنوتیپی; Antibiotics; Phenotypic heterogeneity; Antibacterial susceptibility; In vivo animal infection models; Single-cell level methods; Raman spectroscopy; Fluorescence;
Keywords: ناهمگونی فنوتیپی; Non–small-cell lung cancer; Cluster analysis; Phenotypic heterogeneity
Keywords: ناهمگونی فنوتیپی; Phenotypic heterogeneity; Single cell gene expression monitoring; Sinorhizobium meliloti; Exopolysaccharide biosynthesis; Quorum sensing;
Familial Hypertrophic Cardiomyopathy - Identification of cause and risk stratification through exome sequencing
Keywords: ناهمگونی فنوتیپی; HCM; Hypertrophic Cardiomyopathy; NGS; Next Generation Sequencing; OMIM; Online Mendelian Inheritance in Man; EPOCH-H; Epidemiology of Cardiomyopathy-Hypertrophic Cardiomyopathy; LV; Left Ventricular; NYHA; New York Heart Association; ECG; Electrocardiogr
Association of miR-149 polymorphism with onset age and severity in Charcot-Marie-Tooth disease type 1A
Keywords: ناهمگونی فنوتیپی; CMT1A; Association study; miR-149; Genetic modifier; Phenotypic heterogeneity;
Two novel mutations in the ABCG5 gene, c.144 -1G>A and c.1523 delC, in a Mexican family with sitosterolemia
Keywords: ناهمگونی فنوتیپی; Sitosterolemia; ABCG5 gene; c.144 -1G>A mutation; c.1523 delCmutation; First Mexican family with sitosterolemia; Phenotypic heterogeneity;
Implications of the diversity of class I HLA associations in psoriatic arthritis
Keywords: ناهمگونی فنوتیپی; MHC; Major histocompatibility complex; HLA; Human leukocyte antigen; TCR; T cell receptor; PCR; Polymerase chain reactions; Psoriatic arthritis; Genetic heterogeneity; HLA associations; Phenotypic heterogeneity; Adaptive immune response;
Exploring yale-brown obsessive-compulsive scale symptom structure in Iranian OCD patients using item-based factor analysis
Keywords: ناهمگونی فنوتیپی; Obsession; Compulsion; Symptom dimensions; Y-BOCS; Miscellaneous items; Phenotypic heterogeneity; Factors;
New mutations in the Notch3 gene in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL)
Keywords: ناهمگونی فنوتیپی; CADASIL; White matter lesions; NOTCH3 gene; Mutations; Phenotypic heterogeneity; Russian population;
Phenotypic heterogeneity in a large Thai slow-channel congenital myasthenic syndrome kinship
Keywords: ناهمگونی فنوتیپی; Slow-channel congenital myasthenic syndrome; Alpha subunit; Acetylcholine receptor; Phenotypic heterogeneity;
Pacientes con criterios clínicos de síndrome de Lynch con y sin mutación en genes reparadores del ADN (MLH1 y MSH2). Un reto para el clínico
Keywords: ناهمگونی فنوتیپی; Consejo genético; Cáncer colorrectal; Síndrome de Lynch; Cáncer hereditario; Heterogeneidad fenotípicaGenetic counseling; Colorectal cancer; Lynch syndrome; Hereditary cancer; Phenotypic heterogeneity
A novel dominant mutation in SIX1, affecting a highly conserved residue, result in only auditory defects in humans
Keywords: ناهمگونی فنوتیپی; Branchio-otic syndrome; Branchio-oto-renal syndrome; DFNA23; Hearing impairment; Phenotypic heterogeneity; Catweasel mouse; SIX1; Mutation
Bistable responses in bacterial genetic networks: Designs and dynamical consequences
Keywords: ناهمگونی فنوتیپی; AA, SpoIIAA; AB, SpoIIAB; lac, lactose; RR, response regulator; SHK, sensor histidine kinase; TCS, two-component system; TF, transcription factorBistability; Design principles; Dynamics; Phenotypic heterogeneity
Phenotypic heterogeneity, novel diagnostic markers, and target expression profiles in normal and neoplastic human mast cells
Keywords: ناهمگونی فنوتیپی; mast cells; phenotypic heterogeneity; systemic mastocytosis
On the origin of heterogeneity in (preservation) resistance of Bacillus spores: Input for a ‘systems’ analysis approach of bacterial spore outgrowth
Keywords: ناهمگونی فنوتیپی; Bacterial endospores; Sporulation and germination; Thermal resistance; Phenotypic heterogeneity; Food microbiology; Systems biology; Single cell analysis
Dystrophic epidermolysis bullosa phenotypes in a large consanguineous Tunisian family
Keywords: ناهمگونی فنوتیپی; Dystrophic epidermolysis bullosa; Phenotypic heterogeneity; Semidominant inheritance; Consanguinity
Alpha actin isoforms expression in human and rat adult cardiac conduction system
Keywords: ناهمگونی فنوتیپی; Actin isoforms; Human myocardium; Phenotypic heterogeneity; Ageing; Conductive system