Exam 11: Simple Inheritance and Meiosis
Exam 1: Process of Science117 Questions
Exam 2: Chemistry of Life114 Questions
Exam 3: Cell Structure and Function117 Questions
Exam 4: Nutrition, Enzymes, Metabolism108 Questions
Exam 5: Energy and Photosynthesis104 Questions
Exam 6: Dietary Energy and Cellular Respiration106 Questions
Exam 8: Genes to Proteins142 Questions
Exam 7: DNA Structure and Replication137 Questions
Exam 9: Cell Cycle and Cell Differentiation119 Questions
Exam 10: Mutations and Cancer171 Questions
Exam 11: Simple Inheritance and Meiosis117 Questions
Exam 12: Complex Inheritance124 Questions
Exam 13: Natural Selection and Adaptation99 Questions
Exam 14: Nonadaptive Evolution and Speciation74 Questions
Exam 15: Evidence for Evolution94 Questions
Exam 16: Life on Earth114 Questions
Exam 17: Prokaryotic Diversity97 Questions
Exam 18: Eukaryotic Diversity86 Questions
Exam 19: Human Evolution90 Questions
Exam 20: Population Ecology96 Questions
Exam 21: Community Ecology69 Questions
Exam 22: Ecosystem Ecology80 Questions
Exam 23: Sustainability88 Questions
Exam 24: Plant Growth and Reproduction97 Questions
Exam 25: Plant Physiology98 Questions
Exam 26: Overview of Physiology100 Questions
Exam 27: Digestive System96 Questions
Exam 28: Cardiovascular System99 Questions
Exam 29: Respiratory System92 Questions
Exam 30: Central Nervous System109 Questions
Exam 31: Reproductive System94 Questions
Exam 32: Immune System116 Questions
Exam 33: A Range of Biology279 Questions
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A diploid cell of baker's yeast has 32 chromosomes.How many chromosomes are in each of its haploid spores?
(Multiple Choice)
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In diploid organisms,having two homologues of each chromosome can be beneficial if one allele of a gene encodes a nonfunctional protein.Can haploid organisms avoid the negative effects of nonfunctional alleles?
(Multiple Choice)
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Use the following information for this question:
Phenylketonuria is considered to be an inborn error of metabolism.It is a recessive genetic condition in which the enzyme that breaks down the amino acid phenylalanine is defective or missing.Testing of all newborns allows this condition to be detected at birth.A special diet that severely minimizes phenylalanine (e.g. ,by avoiding diet sodas and most usual sources of protein)can treat the condition.
In this scenario,two carriers of both cystic fibrosis and phenylketonuria have a child.
What is the probability that the child will have cystic fibrosis and be a carrier for phenylketonuria?
(Multiple Choice)
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One of the mutations of the CFTR gene is the result of the deletion of three consecutive nucleotides.This leads to all of the following,EXCEPT
(Multiple Choice)
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Two normal individuals have a child who has cystic fibrosis,an autosomal recessive disease.How did this happen?
(Multiple Choice)
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If meiosis were to fail and a cell skipped meiosis I,so that meiosis II was the only meiotic division,how would you describe the resulting cells?
(Multiple Choice)
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How do the two alleles of the CFTR gene in a lung cell differ?
(Multiple Choice)
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How is the sequence of amino acids in a protein determined?
(Multiple Choice)
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Cystic fibrosis is the result of a nonfunctional protein that regulates
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