Answer:A. Codominance
Explanation:
This is a type of genetic inheritance where neither of the genes is dominant over another. Thus both pair of the gene are expressed on the same LOCUS equally with none masking another. Therefore an individual receive both allele of a heterozygous gene, and have equal phenotypic expression
An example is the AB blood group in man, where both allele present on the same locus are fully expressed with no one dominant over another.
Incomplete dominance refers to a blend of alleles where one does not have full dominance over another another, therefore gives a new phenotypic expression different from both alleles.
e.g pink flower allele in four o'clock flower.
Answer:
Around 25-30 gigatons.
Explanation:
Although natural processes do produce much more carbon dioxide than humans, its a delicate balance and all of that carbon dioxide is absorbed back. However, when humans arrived, they disrupted that balance, and even with the relatively small amount it is creating big problems.
Answer:
False
Explanation:
Prophase is the first phase of mitosis, the chromosomes are visible in this stage. The chromosomes are distinct but they are not shortened.
Answer:
Answer explained
Explanation:
a. Overexpression of Axl receptor tyroxine kinase correlates with the decresed patient's overall survival and hence it's inhibition is under process.
AXL TKI BMS777607 treatment increased AXL protein levels after 24 h as observed by Western blot and flow cytometry analysis. Mechanistically, this inhibition-induced AXL cell surface accumulation was neither associated with epigenetic modifications, nor altered transcriptional and translational regulation. Hence this later increased the glycosylated protien abundance in kinase dead mutant. The kinase function blockaging resulted in impaired internalisation which finally incresed the level of proliferation.
An alternative technique may exist in linkage of Axl Tkl to a degradation machinery recruitment unit .
b. Mendelian disorders like cystic fibrosis results from error in the given DNA sequence which can be autosomal dominant and recessive both and also X or Y linked. Mutated gene results in the Mendelian disorders. Whereas in cancer there can be mutation or proliferation of the given cells in a specific area. In cancer cells there is 2.5 times more the mRNA present while 6.2times the DNA and hence the detection and diagnosis automatically becomes difficult as in Mendelian disorders only single sequence needs to be studied at a time .
Answer:
karyoninesis
(that's what I think you asking)
