Answer:
Granulosa cells
Explanation:
Foliculogenesis is a dynamic and complex process through which the follicle goes through many stages of development in a short period (approximately 60 days in humans and some chimpanzees).
The stages classification is based on morphological changes such as follicular size or diameter, the number of follicular cell layers, etcetera. These classifications might vary among authors but could be denominated as:
- De Graaf follicles (This is the one shown in the image)
Through each stage, there are certain modifications in the oocyte, follicular cells, and connective tissue. As the oocyte grows, the follicular cells might reach a size twice or three times bigger than the ones of the primordial follicles. Their shape also changes and they adopt an aspect of stratified epithelium. Their cytoplasm gets a granulous aspect, after what these cells receive the name of <u><em>granulous cells</em></u>. The De Graaf follicle characterizes for having a space named follicular antro that displaces the oocyte to one of the sides.
The oocyte at this point gets surrounded by <u>zona pellucida</u> and <u>corona radiata </u>.
The follicular antro (The highlighted structure) separates the oocyte from the externally located <u>granulosa cells</u> or follicular cells.
Answer:
Scanning Electron Microscopes
Explanation:
Answer:
D. The tubes allow water and nutrients to be transported throughout
the plant.
Explanation:
option D supports the description of the cells. The long , vertical tubes transport water and nutrients and are most likely xylem and phloem vessels.
option A is wrong since, chloroplasts inside the cell helps in absorbing sunlight.
option C is also wrong, because water loss is controlled by the stomata in the leaves and they are not long tubes.
option B could possibly be right but option D is better suited.
Answer:
The correct answer is CHLOROPHYLL
Answer:
The below options will complete the question
Select one:
a. Gap repair synthesis
b. Mismatch repair
c. Direct repair
d. Nucleotide excision repair
Our answer is surely A.
a. Gap repair synthesis
Explanation:
Alleles of gene B differ by 6 bps and are seeming close to each other among the 1123 bp within the particular gene, favouring the gap repair synthesis.
In the gap repair synthesis, a double stranded break is formed at a homologous chromosome with a small part of the gene or the 6 bps of the recessive allele
being digested away.
Strand invasion and a D-loop formation is followed by the new region being occupied by the dominant B allele to yielding dominant B allele in both chromosomes.
The gap repair synthesis allows the 6bps to be converted to the dominant B from the recessive b when in proximity/being close together.
