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  2. Canine degenerative myelopathy - Wikipedia

    en.wikipedia.org/wiki/Canine_degenerative_myelopathy

    A dog with degenerative myelopathy often stands with its legs close together and may not correct an unusual foot position due to a lack of conscious proprioception. Canine degenerative myelopathy, also known as chronic degenerative radiculomyelopathy, is an incurable, progressive disease of the canine spinal cord that is similar in many ways to amyotrophic lateral sclerosis (ALS).

  3. Missense mutation - Wikipedia

    en.wikipedia.org/wiki/Missense_mutation

    Missense mutation is a type of nonsynonymous substitution in a DNA sequence. Two other types of nonsynonymous substitution are the nonsense mutations , in which a codon is changed to a premature stop codon that results in truncation of the resulting protein , and the nonstop mutations , in which a stop codon erasement results in a longer ...

  4. Nonsynonymous substitution - Wikipedia

    en.wikipedia.org/wiki/Nonsynonymous_substitution

    There are several common types of nonsynonymous substitutions. [3]Missense mutations are nonsynonymous substitutions that arise from point mutations, mutations in a single nucleotide that result in the substitution of a different amino acid, resulting in a change to the protein encoded.

  5. Sudden acquired retinal degeneration syndrome - Wikipedia

    en.wikipedia.org/wiki/Sudden_acquired_retinal...

    Despite similar symptoms and blood test results to Cushing's disease, evaluation of dogs with SARDS did not reveal any tumors in the pituitary or adrenal glands, [9] and recent work has indicated significant differences in the clinical and laboratory test parameters between the two diseases. [10]

  6. Frameshift mutation - Wikipedia

    en.wikipedia.org/wiki/Frameshift_mutation

    Experiments can be run to determine the frequency of the frameshift mutation by adding or removing a pre-set number of nucleotides. Experiments have been run by adding four basepairs, called the +4 experiments, but a team from Emory University looked at the difference in frequency of the mutation by both adding and deleting a base pair. It was ...

  7. Amino acid replacement - Wikipedia

    en.wikipedia.org/wiki/Amino_acid_replacement

    Amino acid replacement is a change from one amino acid to a different amino acid in a protein due to point mutation in the corresponding DNA sequence. It is caused by nonsynonymous missense mutation which changes the codon sequence to code other amino acid instead of the original.

  8. Point mutation - Wikipedia

    en.wikipedia.org/wiki/Point_mutation

    Missense mutations code for a different amino acid. A missense mutation changes a codon so that a different protein is created, a non-synonymous change. [4] Conservative mutations result in an amino acid change. However, the properties of the amino acid remain the same (e.g., hydrophobic, hydrophilic, etc.).

  9. Mutation rate - Wikipedia

    en.wikipedia.org/wiki/Mutation_rate

    Recently reported estimates of the human genome-wide mutation rate. The human germline mutation rate is approximately 0.5×10 −9 per basepair per year. [1]In genetics, the mutation rate is the frequency of new mutations in a single gene, nucleotide sequence, or organism over time. [2]