Cmmb 413 - Study guides, Class notes & Summaries

CMMB 413 Final Exam Review Actual Questions and Answers Solved 100%

CMMB 413 (MT 1) Question and answers rated A+ 2024 mRNA start codon: - correct answer AUG ____% of DNA encodes protein. - correct answer 1.5 Mitochondrial DNA is ____kb and encodes ____ genes. - correct answer 16, 37 Maternally-Inherited Diabetes and Deafness is caused by mutations which reduce ____ activities. - correct answer tRNA Unique (single-copy) DNA in humans: ____% - correct answer 50 Clustered tandem repeats - correct answer 10-15 Dispersed repetitive family ...

Types of DNA Variation - single nucleotide variant (SNV) - small nucleotide insertion/deletion - dynamic mutations - microsatellite - copy number variation (CNV) Single Nucleotide Variants (SNVs) - most common type of sequence variation - >3 000 000 per person - can be benign or disease causing Initiation Codon (Start Codon) AUG (methionine) Stop Codons UGA, UAA, UAG

CMMB 413 Final Exam 2024 Update| Questions with Correct Answers| Guaranteed Success Define and describe cancer uncontrolled growth from the multistep accumulation of errors (ie. a genetic process) in genes involved in cell growth (ie control it) ie cell replication and cell death the first step can be inherited natural aging mechanism, cause of most "old age" deaths define neoplasia new growth define hyperplasia too much growth, looks like accumulation of normal looking cells on t...

Define and describe cancer uncontrolled growth from the multistep accumulation of errors (ie. a genetic process) in genes involved in cell growth (ie control it) ie cell replication and cell death the first step can be inherited natural aging mechanism, cause of most "old age" deaths define neoplasia new growth define hyperplasia too much growth, looks like accumulation of normal looking cells on top of each other

CMMB 413: MT 2Underlying mechanism of abnormal chromosome segregation: - correct answer Nondisjunction Underlying mechanism of recurrent chromosome syndromes: - correct answer Recombination at segmental duplications Underlying mechanism of idiopathic chromosome abnormalities: - correct answer Sporadic, variable breakpoints Spontaneous/de novo. Sometimes of unknown origin. - correct answer Idiopathic Underlying mechanism of unbalanced familial abnormalities (heritable): - correct...

CMMB 413 Final Exam Actual Questions and Answers with complete solution Types of DNA Variation - answer- single nucleotide variant (SNV) - small nucleotide insertion/deletion - dynamic mutations - microsatellite - copy number variation (CNV) Single Nucleotide Variants (SNVs) - answer- most common type of sequence variation - >3 000 000 per person - can be benign or disease causing Initiation Codon (Start Codon) - answerAUG (methionine) Stop Codons - answerUGA, UAA, UAG 20 - answer...

CMMB 413 (MT 1)mRNA start codon: - correct answer AUG ____% of DNA encodes protein. - correct answer 1.5 Mitochondrial DNA is ____kb and encodes ____ genes. - correct answer 16, 37 Maternally-Inherited Diabetes and Deafness is caused by mutations which reduce ____ activities. - correct answer tRNA Unique (single-copy) DNA in humans: ____% - correct answer 50 Clustered tandem repeats - correct answer 10-15 Dispersed repetitive family of genes consisting of >10% of the g...

CMMB 413 Final Exam Review Actual Questions and Answers Solved 100% Types of DNA Variation - answer- single nucleotide variant (SNV) - small nucleotide insertion/deletion - dynamic mutations - microsatellite - copy number variation (CNV) Single Nucleotide Variants (SNVs) - answer- most common type of sequence variation - >3 000 000 per person - can be benign or disease causing Initiation Codon (Start Codon) - answerAUG (methionine) Stop Codons - answerUGA, UAA, UAG 20 - answernumb...

CMMB 413 Final Exam Actual Questions and Answers with complete solution Types of DNA Variation - answer- single nucleotide variant (SNV) - small nucleotide insertion/deletion - dynamic mutations - microsatellite - copy number variation (CNV) Single Nucleotide Variants (SNVs) - answer- most common type of sequence variation - >3 000 000 per person - can be benign or disease causing Initiation Codon (Start Codon) - answerAUG (methionine) Stop Codons - answerUGA, UAA, UAG 20 - answer...