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Sickle-cell disease is one of the most common severe monogenicdisorders in the world.
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Recent breakthroughs in exome-sequencing technology have made possible the identification of many causal variants of monogenicdisorders.
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Currently according to the latest report of the international union of immunological societies, 37 separate monogenicdisorders were classified as autoinflammatory.
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The inherited disorders of hemoglobin, which include sickle cell disease and thalassemias, are the most common and widespread distributed monogenicdisorders.
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Inherited monogenicdisorders such as beta-hemoglobinopathies (BH) are fitting candidates for treatment via gene therapy by gene transfer or gene editing.
Использование термина monogenic disease на английском
1
In 50 cases, there was a causative mutation in a known monogenicdisease gene.
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Our findings corroborate PIGP as a monogenicdisease gene for developmental and epileptic encephalopathy.
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Neurodegenerative monogenicdiseases often affect tissues and organs beyond the nervous system.
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Several acute monogenicdiseases affect multiple body systems, causing death in childhood.
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Syndromic forms are in many cases due to chromosomal aberrations or monogenicdiseases.
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The inherited disorders of hemoglobin synthesis constitute the most common monogenicdiseases worldwide.
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Conclusions: Targeted sequencing of maternal plasma DNA for NIPD of monogenicdiseases is feasible.
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As these two diseases are monogenicdiseases, they make an attractive setting for gene therapy.
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These tests were expensive and targeted only at people with family histories of so-called monogenicdiseases.
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The present work demonstrates the feasibility of gene editing-based therapeutics toward monogenicdiseases such as CF.
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The detection platform can also be extended to analyze the mutational profiles of other monogenicdiseases.
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They expected to find maybe one person with a marker for one of those rare, monogenicdiseases.
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In the last decades the molecular basis of monogenicdiseases has been largely unraveled, although their treatment has often remained unsatisfactory.
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Retinal neurodegenerative diseases are especially attractive targets for gene replacement therapy, which appears to be clinically effective for several monogenicdiseases.
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Analyzing rare trophoblastic cells from Papanicolaou smears carrying the entire fetal genome provides an alternative method for noninvasive detection of monogenicdiseases.
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Gene therapy is a promising treatment option for monogenicdiseases, but success has been seen in only a handful of studies thus far.