Sickle-cell anemia (SCA) is adiseasethat links biochemistry, pathology,naturalselection,populationgenetics,gene expression, andgenomics. Although the disease has existed for thousands of years, it wasn't until 1910 that thesymptomcomplex featuring anemia, recurrent fevers, and bouts of horrificpain, ...
The double helix of DNA is made up of billions of pieces of genetic information. What Dr. Collins is saying is, out of all that, it's just one error in the DNA code -- a "T" that should have been an "A" -- that causes sickle cell anemia. Fix that error, and you cure the ...
百度试题 题目在PUBMED数据库中检索镰刀状细胞贫血(sickle cell anemia)的遗传学(Medical Genetics)的相关信息可以进入哪个界面?() 相关知识点: 试题来源: 解析 Clinical QueriesJournal DatabaseAdvanced Search 反馈 收藏
Key Words: Sickle cell anemia, infant mortality, pre-reproductive mortality, Indian tribes, malaria, sickle cell crisis management, remedial hope for sickle cell patients.D ParmarEgyptian Journal of Medical Human GeneticsParmar D. Sickle cell anaemia: review and remedial hope. Egypt J Med Hum ...
Solovieff, N.et al. Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5′ olfactory receptor gene cluster.Blood115, 1815–22 (2010). ArticleCASGoogle Scholar Leonardo, F. C.et al. Reduced rate of sickle-related complications in Brazilia...
1982, Biochemical Genetics The association of sickle cell anemia with heterozygous and homozygous α‐thalassemia‐2: In vitro HB chain synthesis 1979, American Journal of Hematology Prenatal Diagnosis of Sickle-Cell Anemia and Alpha G-Philadelphia: Study of a Fetus Also at Risk for Hb S/β...
在PUBMED数据库中检索镰刀状细胞贫血(sickle cell anemia)的遗传学(Medical Genetics)的相关信息可以进入哪个界面?() A.Single Citation MatcherB.Advanced SearchC.Journal DatabaseD.Clinical Queries 点击查看答案&解析手机看题 你可能感兴趣的试题 多项选择题 检索表达式中通配符号含义正确的有() A.?——表示任意...
Sickle Cell Anemia Sickle cellis a homogenous geneticanemiacaused when an abnormal gene (hemoglobin S or HbS) causes the substitution of the amino acidvaline, for another, glutamicacid (Amundsen et al., 1984). The sickle gene protects heterogeneous carriers (HbC) fromP. falciparumin malaria ende...
Discovering the genetics underlying foetal haemoglobin production in adults. Br J Haematol. 2009;145:455–67. Google Scholar Hebbel RP. Ischemia-reperfusion injury in sickle cell anemia: relationship to acute chest syndrome, endothelial dysfunction, arterial vasculopathy, and inflammatory pain. Hematol/...
Genetics and public health in the 21st century. New York (NY): Oxford University Press, 2000: 431–46 Chapter Google Scholar Gaston MH, Verter JI, Woods G, et al. Prophylaxis with oral penicillin in children with sickle cell anemia: a randomized trial. N Engl J Med 1986; 314: 1593–...