Keywords: هوموسیگوت; Hypercholesterolaemia; Homozygote; Compound heterozygote; Lipoprotein apheresis
مقالات ISI هوموسیگوت (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.
Nonsyndromic Peripheral Pulmonary Artery Stenosis Is Associated With Homozygosity of RNF213 p.Arg4810Lys Regardless of Co-occurrence of Moyamoya Disease
Keywords: هوموسیگوت; homozygote; Moyamoya disease; peripheral pulmonary arterial stenosis; pulmonary hypertension; MMD; Moyamoya disease; MRA; magnetic resonance angiography; PAH; pulmonary arterial hypertension; PPAS; peripheral pulmonary arterial stenosis;
Cross-resistance patterns to ACCase-inhibitors in American sloughgrass (Beckmannia syzigachne Steud.) homozygous for specific ACCase mutations
Keywords: هوموسیگوت; Beckmannia syzigachne; ACCase gene; Cross-resistance; Mutation; Homozygote
Familial hypercholesterolemia/autosomal dominant hypercholesterolemia: Molecular defects, the LDL-C continuum, and gradients of phenotypic severity
Keywords: هوموسیگوت; Autosomal dominant; Autosomal recessive; Familial hypercholesterolemia; Genotype; Heterozygote; Heterozygous; Homozygote; Homozygous; LDL-C level; Lipid-lowering therapy; Monogenic; Phenotype; Statins;
Familial hypercholesterolemia and estimation of US patients eligible for low-density lipoprotein apheresis after maximally tolerated lipid-lowering therapy
Keywords: هوموسیگوت; Apheresis; Cardiovascular disease; Coronary artery disease; Familial hypercholesterolemia; Heterozygote; Heterozygous; Homozygote; Homozygous; LDL-C level; Maximally tolerated lipid-lowering therapy
Impacto clÃnico de la cuantificación de la carga mutacional de JAK2V617F en pacientes con neoplasias mieloproliferativas crónicas Ph negativas clásicas
Keywords: هوموسیگوت; Janus Quinasa; Neoplasias mieloproliferativas; Cromosoma Filadelfia; Homocigoto; Diagnóstico; Leucocitosis; Esplenomegalia; Trombosis; Pronóstico; Janus Kinase; Myeloproliferative disorders; Philadelphia chromosome; Homozygote; Diagnosis; Leukocytosis;
The human caveolin 1 gene upstream purine complex and neurodegeneration—A common signature
Keywords: هوموسیگوت; Multiple sclerosis; Alzheimer's disease; Caveolin 1; Neurodegenerative; Homozygote; Purine complex
Hypertrophic cardiomyopathy in the Amish community — What we may learn from it
Keywords: هوموسیگوت; MYBPC3; Homozygote; Heterozygous carrier; Medical home; Cardiac death
Familial Hypercholesterolemia: Screening, diagnosis and management of pediatric and adult patients: Clinical guidance from the National Lipid Association Expert Panel on Familial Hypercholesterolemia
Keywords: هوموسیگوت; Familial hypercholesterolemia; LDL receptor; Apheresis; Cascade screening; Heterozygous; Heterozygote; Homozygous; Homozygote
Familial Hypercholesterolemia: Screening, diagnosis and management of pediatric and adult patients : Clinical guidance from the National Lipid Association Expert Panel on Familial Hypercholesterolemia
Keywords: هوموسیگوت; Familial hypercholesterolemia; LDL receptor; Apheresis; Cascade screening; Heterozygous; Heterozygote; Homozygous; Homozygote
Harmful recessive effects on fertility detected by absence of homozygous haplotypes
Keywords: هوموسیگوت; genomics; lethal recessive; haplotype; homozygote;
Effect of human leukocyte antigen homozygosity on rubella vaccine–induced humoral and cell-mediated immune responses
Keywords: هوموسیگوت; HLA antigens; Homozygote; Rubella virus; Measles-mumps-rubella vaccine; Immunity
Skew in the human caveolin 1 gene upstream purine complex homozygote haplotype compartment in multiple sclerosis
Keywords: هوموسیگوت; Multiple sclerosis; Caveolin 1; Haplotype; Homozygote; Purine complex;
Rodzina obciÄ
żona talasemiÄ
β - opis przypadku
Keywords: هوموسیگوت; talasemia β; dziecko; homozygota; mutacja IVS-I-6(T>C); β-thalassemia; child; homozygote; mutation IVS-I-6(T>C);
Novel homozygous mutation of the caveolin-3 gene in rippling muscle disease with extraocular muscle paresis
Keywords: هوموسیگوت; Rippling muscle disease; Caveolin-3; Homozygote; Extraocular muscle; Limb-girdle muscular dystrophy 1C
16q-linked autosomal dominant cerebellar ataxia: A clinical and genetic study
Keywords: هوموسیگوت; 16q-linked ADCA; Puratrophin-1 gene; Heterozygote; Homozygote; Haplotype analysis