Parkinson’s disease is a brain disorder that may be caused by mutations in several genes that code for the production of alpha-synuclein. Individuals who have Parkinson’s disease exhibit symptoms such as uncontrollable tremors, difficulty walking, and loss of coordination. How might geneticists determine where the mutations that cause Parkinson’s disease are located? PCR analysis gene mapping DNA fingerprinting STR analysis

They could use SNPs(Single nucleotide polymorphisms) of DNA, which are an anaylysis of chromosomes using high tech laser magnification. This SNPing allows scientist to more closely view specific genes in chromosomes that cause certain traits. It allows for a greater genetic mapping and could also be used to see mutations, if you know which chromosome to look at.

IDK, just an idea, SNPs were used to look at different species trait exhibition, I thought it might work for this if used properly.

trachea, alveoli, lung capillaries, arteries

i believe the correct answer is the virus gets an envelope that contains host molecules when it leaves the host cell.

explanation:

during the bidding/release stage of a virus, it encapsulates itself with part of the membrane of the host cells in this case the cells of the monkey and is the reason as to why the scientist found the genetic material of the monkey on the viral cell surface.

further explanation

to understand this answer, we have to know the cycle a virus undergoes to replicate. a virus is basically a bunch of genetic material enclosed in a capsule and lacks any machinery or organelles to ensure their survival so they must enter a host cell in order to get the environment needed to survive. some viruses enter and lyse(destroy) the host cell after they have replicated and undergo the lytic cycle while some enter and leave the cell intact after replicating and these undergo a lysogenic cycle. to enter the cell, they undergo the first process called attachment by binding to specific receptors and co-receptors on the surface of the host cell. after attaching to the cell, they start the second phase called penetration where virus enters or is engulfed whole by the host cell through a process called endocytosis. it is the same process that a cell takes up materials it needs or pathogens around it. uncoating of the virus then happens after the virus has been engulfed and is the third stage. the virus then undergoes releasing of its genetic material in the host's matrix.   the materials then enter the nucleus and undergo biosynthesis by adding themselves in strands of rna being translated and then copies of the virus are produced in addition to the host genetic material. the material/newly formed viral material then undergoes assembly inside the host cell and form a capsule around them. the virus undergoes the last release/budding stage by binding to the host membrane and pushing outwards. in doing so when they tear away from the host membrane, they pick up the genetic material from the membrane of the host cell to form their envelope.

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level: high school