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ACTA2 - actin alpha 2, smooth muscle. Synonym (s): ACTSA. Previous symbol (s) and name (s): actin, alpha 2, smooth muscle, aorta. Type: gene with protein product. Chromosomal location: 10q23.31. OMIM: 102620.
10 Μαρ 2015 · Individuals with ACTA2 mutations present with both type A and type B aortic dissections at significantly younger ages than individuals enrolled in the International Registry of Acute Aortic Dissection (IRAD) study 22 and are likely to report a family history of thoracic aortic disease.
The findings provide support for a common effect of genes coding for cell adhesion ... nor did they indicate whether such mutations also cause ADHD in adults. A first systematic ... Zametkin A, et al. The diagnosis of childhood hyperactivity. A US–U.K. cross-national study of DSM-III and ICD-9. J Child Psychol Psychiatry. 1988;29:289–300 ...
12 Απρ 2020 · In the current study, we set out to explore the contribution of common genetic variants to the risk of ADHD across the lifespan by conducting GWAS-MAs separately for children and adults with ...
The ACTA2 gene provides instructions for making a protein called smooth muscle alpha (α)-2 actin, which is part of the actin protein family. Learn about this gene and related health conditions.
16 Αυγ 2018 · The 21st century has witnessed the discovery of ADHD-associated rare and common genetic variants and resolved that its genetic architecture involves a spectrum of genetic variation in terms of frequencies and effect sizes.
what is the difference between acta2 mutations & multisystemic smooth muscle dysfunction syndrome (msmds)? Many mutations in the ACTA2 gene have been found to date in patients with familial thoracic aortic aneurysms (dilatations and tears of the largest vessel in the body).
