Answer:
Kinase-connected receptors or receptor tyro-sine kinases react for the most part to protein and chemical go between. A solitary trans membrane helix interfaces the extracellular restricting area to the intra-cellular space. e.g. insulin, development factors. The official of the ligand triggers the commencement of a few succession of occasions related with phosphorylation of proteins, this is called protein kinase course.
For instance, the official of development hormone to the receptor in the plasma layer causes dimerization (by the actuation of Janus kinase 2, JAK2) of the receptor (conformation change) that bring about auto-phosphorylation of tyro-sine buildups. The official of SH2-space (src homology) protein (Grb-2) to the phosphorylated tyro-sine buildups invigorates cell development through a course of protein phosphorylation.
a). RTKs are the trans-membrane receptors, which have a ligand restricting site on the extracellular area and tyro-sine authoritative on the intra-cellular space. In the event that it comes up short on the extracellular area, the ligand can't tie to the receptor site, so no cell reaction happens.
b). On the off chance that it does not have the intra-cellular space, the ligand can tie to the receptor site, the receptor can't impart signs tot eh intra-cellular area because of the absence of intra-cellular space.
Let 'C' denote the dominant trait of eye-crossing and 'c' denote the recessive trait of not being able to cross the eyes. The genotype of the father is heterozygous dominant for the trait of eye-crossing. This is denoted by 'Cc'. The mother is homozygous recessive for the trait of eye-crossing, denoted by 'cc'. The mating between the two will result in following genotypes: two of 'Cc' and two of 'cc'. Therefore the probability that the child will be able to cross his or her eyes is 0.5 or 50%.
Nuclear envelope is the answer
Answer:
A museum is a location that contains historical art and artifacts.
Explanation:
Joint hypermobility syndrome (JHS) and Ehlers-Danlos syndrome, hypermobility type (EDS-HT) are the tissue disorders which can be characterized by chronic pain, joint instability complications, and minor skin changes. During these, Fatigue and headache are the very common symptoms; though they can be diagnosed using specific criteria.
JHS/EDS-HT is a rare common condition that could not be diagnosed by most clinicians and pain specialists, resulting in interventions like symptomatic and non-satisfactory treatments, because there is a lack of reasonable pathophysiologic rationale.
Pain, fatigue, and headache in JHS/EDS are usually treated with the help of certain symptoms or on the basis of doctors’ experience.
<span>Therefore, in order to the cure of such symptoms, doctors suggest pathogenic mechanisms. The major aim of the re-writing of the natural history of JHS/EDS-HT is to raise awareness among clinical geneticists and specialists treating chronic pain conditions about pain and other complications of JHS/EDS-HT.</span>
