Answer:
The code for heredity is carried on genes in each organism's DNA. Explanation; Genes are portions of the genome that codes for a protein or an RNA, Hereditary information that is contained in nucleotide sequence of DNA.
Explanation:
Numerous degenerative neurological conditions, most notably Parkinson's disease, have been linked to an excessive buildup of alpha synuclein (a-syn) in the brain. Intraneuronal inclusions, often known as Lewy bodies, are neuropathological characteristics seen in Parkinson's disease, Lewy body dementia, and other synucleopathies. The aggregation of a-syn is their main structural component. A-syn accumulation, aggregation, and ensuing Lewy body formation can be attributed to a variety of biological processes. These include genetic changes in parkin, synuclein, or the deubiquitinating enzyme ubiquitin C-terminal hydrolase (UCH-L1), which results in less efficient removal of a-syn via the ubiquitin proteasomal pathway (UPP). Additionally, environmental variables and an age-related decline in antioxidant defense mechanisms that heighten oxidative stress and can have an impact on the formation or clearance of a-syn are intracellular insults.
We focused on changes in the aggregation and clearance of a-syn as impacted by the UPP and the oxidative stress pathways in our dynamic models of a-syn processing in both normal and various disease states. A free radical profile similar to that observed in vivo after exposure to the neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine is produced during simulation of enhanced oxidative stress (MPTP). To replicate the kinetics of a-syn that correlates to the neuropathology reported for the sporadic and hereditary types of Parkinson's disease, different model parameters of oxidative stress, UPP failure, or both routes are used. With the use of this in silico model, it is possible to evaluate the kinetics of pathway elements and more accurately identify and validate key pharmaceutical targets.
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Atom, molecule, cell, tissue, organ, and organ system
It should be 50/50 if the male would be Rr for heterogenous male red and the female rr for homogenous for white.
Answer:
Meiosis is a type of cell division that reduces the number of chromosomes in the parent cell by half and produces four gamete cells. ... The process results in four daughter cells that are haploid, which means they contain half the number of chromosomes of the diploid parent cell.
Explanation:
Unlike in mitosis, the daughter cells produced during meiosis are genetically diverse. Homologous chromosomes exchange bits of DNA to create genetically unique, hybrid chromosomes destined for each daughter cell
