Because transthyretin is made in part by the choroid plexus, it can be used as an immunohistochemical marker for choroid plexus papillomas as well as carcinomas.
32.
Preliminary data suggest that these CSF-lymph connections form around the time that the CSF secretory capacity of the choroid plexus is developing ( in utero ).
33.
Because transthyretin is made in part by the choroid plexus, it can be used as an immunohistochemical marker for choroid plexus papillomas as well as carcinomas.
34.
The choroidal fissure, in this sense, is the narrow cleft along the medial wall of the lateral ventricle, where the choroid plexus is attached at the margins.
35.
Along the inner surface of both ventricles, the ventricular wall remains thin, and a choroid plexus develops, releasing CSF . The CSF quickly fills the neural canal.
36.
In the case of prolactin and leptin, there is evidence of active uptake at the choroid plexus from the blood into the cerebrospinal fluid ( CSF ).
37.
Once destruction of the brain is complete, the cerebellum, midbrain, thalami, basal ganglia, choroid plexus, and portions of the occipital lobes typically remain preserved to varying degrees.
38.
When the choroid plexus is removed, a cleft-like opening is left along the medial wall of the temporal horn; this cleft constitutes the lower part of the choroidal fissure.
39.
Generally, leptin is thought to enter the brain at the choroid plexus, where the intense expression of a form of leptin receptor molecule could act as a transport mechanism.
40.
Other factors that contribute of the migration are slit proteins ( produced at the choroid plexus ) and their gradient ( generated by the flow of cerebrospinal fluid ).
