瑞鸿网词典双语例句Hemophilia is caused by a hereditary lack of one of the clotting factors.血友病就是因为遗传上缺乏一种凝血胶原引起的.
The primary types of hemolytic anemia are genetic or acquired. What is the most common cause of hemolytic anemia? The most common intrinsic causes of hemolytic anemia are thalassemia and sickle cell disease. Autoimmune disorders are believed to be the most common extrinsic cause. Other hemolysis ...
Are somatic mutations the same as acquired mutations? How is an embryo different than a somatic cell? Are imprinted genes autosomal? Do somatic cells reproduce asexually? Is achondroplasia autosomal recessive? Is the law of segregation used for diploid somatic cells? Are meristems cells diploid?
In patients, mutations in samhd1, among other genes, have been associated with the rare hereditary autoimmune disease Aicardi-Goutières Syndrome (AGS) [23]. Due to the enzymatic functions of the genes involved in AGS, it has been hypothesized that aberrant nucleic acids, most likely DNA, trigg...
Impaired insulin- stimulated expression of the glycogen synthase gene in skeletal muscle of type 2 diabetic patients is acquired rather than inherited. J Clin Endocrinol Metab 2000; 85:1584 –1590. 115. Lofman M, Yki-Jarvinen H, Parkkonen M et al. Increased concentrations of glyco- gen ...
Scientists used the gene-editing tool to repair a mutation that leads to hereditary blindness. But the treatment shocked the cells, with half of them unable to repair the damage inflicted to their DNA. CRISPR-editing embryos is thus still a distant reality. “At this point, it’s too ...
2197 Hemophilia B is characterized by structural and functional defects in coagulation factor IX (FIX) caused by mutations in the F9 gene. Various mutations (nonsense, missense, etc.) are known to be associated with the disease, including a synonymous V107V mutation reported recently by Knobe ...
(rs1853021,rs1800769,rs3798220,rs10455872)inmodulating VTEsusceptibility.FivehundredandsixteenpatientswithVTEwithouthereditaryand acquiredthrombophiliaand1117healthycontrolsubjects,comparableforageandsex, wereinvestigated.LPAKIV-2polymorphism,rs3798220andrs10455872SNPsweregeno- typedbyTaqMantechnology.Concerningrs185...