Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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"Genes and alleles are the same thing."
Please explain in detail why this is false and a misconception.
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- Part A One result of X-linkage is a crisscross pattern of inheritance in which sons express recessive genes of their fathers and daughters express recessive genes of their mothers. O True O False Submit Provide Feedback Request Answer Copyright © 2023 Pearson Education Inc. All rights reserved. | Terms of Use | Privacy Policy | Permissions | Contact Us | View?assignment ProblemID=10436487&offset=next MacBook Pro P Pearson or tyne URL Next >arrow_forwardDoes that mean if someone is a carrier the genotype will be Fh/fh? Because Fh is the diseased allele and fh is the wildtype or how will is it going to be. I am not sure how to answer it.arrow_forwardDuchenne’s muscular dystrophy (DMD) is an X-linked disease that causes progressive muscle weakness and is often fatal. “XD” represents the wild type allele, and “Xd,” the mutant allele. Jonah is XDXd Y and his brother Pete is Xd Y. Jonah and Pete BOTH have DMD of equal severity and phenotypes. You might have thought Jonah’s DMD would be less severe given his genotype. To better understand the situation, you investigate Jonah’s Xist chromosome region in his defective muscle cells. Which of the following is consistent with his phenotype? (Select all that apply.) The Xd-containing chromosome is inactive in defective muscle cells. The XD-containing chromosome has a methylated Xist promoter. The XD-containing chromosome has an unmethylated Xist promoter. The Xd-containing chromosome is active in defective muscle cells.arrow_forward
- Select all the characteristics that make sickle-cell disease a good candidate to study genetic diseases. (Check all that apply.) Check All That Apply It is easily identifiable by a physical characteristic.It is easily identifiable by a physical characteristic. It results from a single change in a single gene.It results from a single change in a single gene. It can be influenced by the environment.It can be influenced by the environment. The sickle-cell inheritance pattern is not influenced by other genes.The sickle-cell inheritance pattern is not influenced by other genes.arrow_forwardPlease explain why Huntington’s Disease is a dominant allele, but its occurrence is very low in the population.arrow_forwardC:/Users/korea/Downloads/RNA%20in%20cancer.pdf 田 Edge as your default browser? Set as default Genetics 2 Final Exam Word Insert Design Layout References Mailings Review View Help O Tell me what you want to do (B 10 , 嘴A:ニ.=-元, A A Aa- * 倍 AaBbCcD AaBbCcDe AaBbC AaBbCcDc A a Normal U - abs X2 x A-型,A.A@ - No Spac. Heading 1 Heading 2 Font Paragraph Styles primarily on just seven or eight nucleotides at the 5' end of the miRNA (ca the 'seed region').. Q3: what actually happened if Splicing factor mutated? Give an example and describes the outcome. W 5 words LEEnglish (United States) CHIMZ PolylA) site terized, with implications for tumorigenesis. mRNA export factors generally facilitate use of distal cleav- age and polyadenylation sites, leading to long 3' UTR isoform expression. This requires both the ATY SUO (-3 CSTF2 CHOCI DET receptor NXF1 and cleavage factor Im complex 68 kDa subunit (CFIM68), which cooperate to facilitate nuclear export LUZP4 TREX Cleavage stimulation factor EM prt…arrow_forward
- Sickle cell anemia is a genetic disease most common in those of African ancestry that results from the mutation of a single basepair. This mutation results in a change to the hemoglobin protein. In this experiment, “S” will represent the normal allele and “s” thesickle allele. They are codominant alleles. Therefore, SS is normal, Ss is not fatal but mildly symptomatic, and ss is debilitating,painful, and often fatal. After hundreds or even thousands of generations, both alleles are still common in those of African ancestry. How would you explain this?arrow_forwardThe questions below all refer to the following pedigree. The locus for allele D/d determines how cilia function within the body. Mutations at this allele cause abnormal ciliary function, resulting in a clinical disorder characterized by frequent respiratory infections (including in the ears, sinuses, and lungs), as well as infertility. In the pedigree, black circles/squares represent individuals affected by the disorder. White circles/squares represent unaffected individuals. Remember, if a trait is rare in a population (such as this one), we assume individuals marrying into the family are NOT carriers unless the information provided indicates otherwise. A1 A2 II B1 B2 B3 B4. B5 B6_ II C1. C2 C3. C4. C5 IV D1. D2, D4 . D5 Individuals C2 and C3 are considering having additional children. However, having already had a child with this disorder, they visit a genetic counselor to determine what the probability is that their future child would have the disorder. If C2 and C3 have another…arrow_forward
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