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The Genetics of Sickle Cell Disease (aka Sickle Cell Anemia)
The Genetics of Sickle Cell Disease (aka Sickle Cell Anemia)

... mutation responsible for this disease is one nucleotide out of ~3 billion that makes up human DNA. Yet it is enough to change the chemical properties of hemoglobin, the iron-protein complex within red blood cells that carries oxygen. There are approximately 280 million hemoglobin molecules in each R ...
Section 2: ß-Cell Genes: Functional Aspects
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... alleles for a trait occupy the same position on homologous chromosomes and thus govern the same trait. An inherited trait which is present even when inherited only from one parent. the form of the gene that shows up only when inherited from both parents. Requires both alleles to show the likelihood ...
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... multilayered; formed an antrum, or not yet; made a very large antrum, etc. The large corpus albicans will not be in these small-animal ovaries ...
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molecular genetics will make histopathologists redundant

... making. Their re-classification was begun by using microarrays. Perou et al.12 for example defined four subgroups (basal-like, Erb-B2 +, normal-breast-like, and luminal epithelial/ER+) of breast carcinoma; these correlated with overall survival and were significantly better at predicting survival th ...
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... X-linked Inheritance: affects genes on X chromosome  X-linked recessive: No father to son transmission.  Males with X-linked disorder always give X chromosome to daughters. Daughters are carriers.  X-linked recessive genes expressed in females if 2 copies of gene (on each X chromosome).  Y chro ...
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NEDD9

Neural precursor cell expressed developmentally down-regulated protein 9 (NEDD-9) is a protein that in humans is encoded by the NEDD9 gene. NEDD-9 is also known as enhancer of filamentation 1 (EF1), CRK-associated substrate-related protein (CAS-L), and Cas scaffolding protein family member 2 (CASS2). An important paralog of this gene is BCAR1.
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