Give an example of a journal that is about genetic switches involving rna molecules. Give the author’s name the title of the study and the link to the journal
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- Choose a syndrome or disorder caused by a mutation. Write the cause, type, and efffect of this mutation.Give an example of a journal that is about genetic switches involving RNA molecules. Briefly describe the journal and include the objectives, methodology and the results. Then comment on what is the relevance of this journal that is also appealing to you. Provide the link to the journal.Using the diagram below describe the significance of DNA sequencing for identification of mutations.
- Give typing answer with explanation and conclusion The use of which type of endonuclease is more advantageous for genetic cloning: endonucleases generating blunt ends or sticky ends?Using the question in the image below, identify the locations of each mutation in strains 1, 2, and 3Follow these directions to access the entries for PTGS1 and PTGS2 in the “Gene” database at the NCBI Website:A. First, go to the NCBI homepage using the link on the lab webpage, or by going to: http://www.ncbi.nlm.nih.gov Select “Gene” from the database pulldown menu. Type “PTGS” in the search box, then click “Go.” Scan the results for the “Homo sapiens” entries. There should be one called “PTGS1” and one called “PTGS2.” Select each entry by clicking on its name, then read the paragraph under the “Summary” section for each entry. The drug Celebrex selectively inhibits PTGS2 while aspirin and other NSAID’s inhibit both PTGS1 and PTGS2 in the same way. Why do you think researchers wanted to discover a selective inhibitor to PTGS2? 2. Describe how studying 3-D structures of PTGS1 and PTGS2 could help researchers design a drug that binds to PTGS1, but not to PTGS2.
- Name a disease treated with a protein produced by genetically engineered microorganisms.Write the name of the term that describes the phrase. Two or more alternate forms or variations of a geneGive 1 example of syndrome or disorder caused by a mutation then write the cause, type, and effect of this mutation.