Exam 11: Genome Alterations - Mutation and Epigenetics
Exam 1: A Perspective on Human Genetics60 Questions
Exam 2: Cells and Cell Division60 Questions
Exam 3: Transmission of Genes from Generation to Generation60 Questions
Exam 4: Pedigree Analysis in Human Genetics60 Questions
Exam 5: The Inheritance of Complex Traits60 Questions
Exam 6: Cytogenetics - Karyotypes and Chromosome Aberrations60 Questions
Exam 7: Development and Sex Determination60 Questions
Exam 8: The Structure - Replication - and Chromosomal Organization of DNA60 Questions
Exam 9: Gene Expression and Gene Regulation60 Questions
Exam 10: From Proteins to Phenotypes60 Questions
Exam 11: Genome Alterations - Mutation and Epigenetics60 Questions
Exam 12: Genes and Cancer60 Questions
Exam 13: An Introduction to Genetic Technology60 Questions
Exam 14: Biotechnology and Society60 Questions
Exam 15: Genomes and Genomics60 Questions
Exam 16: Reproductive Technology - Genetic Testing - and Gene Therapy60 Questions
Exam 17: Genes and The Immune System60 Questions
Exam 18: Genetics of Behavior60 Questions
Exam 19: Population Genetics and Human Evolution60 Questions
Select questions type
When ____ is incorporated into DNA or RNA during synthesis,it will create a(n)____.
(Multiple Choice)
4.9/5
(42)
People with cystic fibrosis display a single phenotype for the disorder.
(True/False)
4.8/5
(39)
Tris-BP was banned after the discovery that the chemical caused cancer in test animals and was ____________________ through the ____________________ by those wearing treated clothing.
(Short Answer)
4.7/5
(32)
Nonsense mutations change termination codons into amino acid codons.
(True/False)
4.9/5
(42)
When the number of trinucleotide repeats in a gene is significantly above normal,it can produce a mutant phenotype.
(True/False)
4.9/5
(38)
Distinguish between sense and nonsense mutations and describe the characteristics of a protein affected by each type of mutation.
(Essay)
4.8/5
(42)
A mutation of an autosomal recessive trait can remain undetected for generations.
(True/False)
4.8/5
(35)
A form of mutation associated with the expansion in copy number of a nucleotide triplet in or near a gene is called a(n)____________________.
(Short Answer)
4.8/5
(35)
Several genetic disorders,including Fanconi anemia and ataxia telangiectasia,are caused by mutations in ____.
(Multiple Choice)
4.9/5
(41)
Explain what might occur when purine or pyrimidine bases in nucleotides undergo tautomeric shifts.
(Essay)
4.8/5
(33)
Beckwith-Wiedemann syndrome results from abnormalities of ____________________.
(Short Answer)
4.8/5
(38)
Mutagenic chemicals that ____ and are incorporated into DNA or RNA during synthesis are called base analogs.
(Multiple Choice)
4.8/5
(39)
The ability of DNA polymerase to repair its own nucleotide mismatches is called ____________________.
(Short Answer)
4.9/5
(32)
____________________ are mutations involving the increase of the number of repeat sequences in genes.
(Short Answer)
4.8/5
(38)
Nucleotide substitutions are mutations that alter the ____________________,but not the ____________________,of nucleotides in a DNA molecule.
(Short Answer)
4.7/5
(38)
Showing 41 - 60 of 60
Filters
- Essay(0)
- Multiple Choice(0)
- Short Answer(0)
- True False(0)
- Matching(0)