Answer:
Answer is pterygopalatine ganglion
Explanation:
Parasympathetic ganglion are described as small terminal ganglia found within or near the organs they supply with nerves. they are also the autonomic ganglia of the parasympathetic nervous system.
Answer:
They emit steam and volcanic gases, such as sulfur dioxide and carbon dioxide. Fumaroles create pathways for rising heat, volcanic gas, and magma. Openings stemming down into the pool of magma. Cracks and fumaroles act like a window so scientists can get a glimpse of the gases inside volcanoes.
Explanation:
In water molecule the electrons between the oxygen and the hydrogen are shared, but the sharing is not equal. Oxygen pulls electrons slightly towards itself. Therefore, the electrons are more near the oxygen, making that part of molecule(oxygen part) slightly negative. Since the electrons are not near the hydrogen so, that part of the molecule is slightly positive.
Answer:
The C. elegans embryo is a powerful model system for studying the mechanics of metazoan cell division. Its primary advantage is that the architecture of the syncytial gonad makes it possible to use RNAi to generate oocytes whose cytoplasm is reproducibly (typically >95%) depleted of targeted essential gene products via a process that does not depend exclusively on intrinsic protein turnover. The depleted oocytes can then be analyzed as they attempt their first mitotic division following fertilization. Here we outline the characteristics that contribute to the usefulness of the C. elegans embryo for cell division studies. We provide a timeline for the first embryonic mitosis and highlight some of its key features. We also summarize some of the recent discoveries made using this system, particularly in the areas of nuclear envelope assembly/ dissassembly, centrosome dynamics, formation of the mitotic spindle, kinetochore assembly, chromosome segregation, and cytokinesis.
1. The C. elegans embryo as a system to study cell division
The C. elegans embryo is a powerful model system for studying the mechanics of metazoan cell division. Its primary advantage is that the syncytial gonad makes it possible to use RNA interference (RNAi) to generate oocytes whose cytoplasm is reproducibly (>95%) depleted of targeted essential gene products. Introduction of dsRNA rapidly catalyzes the destruction of the corresponding mRNA in many different systems. However, depletion of pre-existing protein is generally a slow process that depends on the half-life of the targeted protein. In contrast, in the C. elegans gonad, the protein present when the dsRNA is introduced is depleted by the continual packaging of maternal cytoplasm into oocytes (Figure 1). Since depletion relies on the rate of embryo production instead of protein half-life, the kinetics tend to be similar for different targets. By 36-48 hours after introduction of the dsRNA, newly formed oocytes are typically >95% depleted of the target protein.
Explanation:
The answer is adverse reactions
