The gaps help to
regulate signaling in the brain, and the bridges are the «connection across a synapse [that] is the release key that fits into a very specific lock to initiate the next step.»
Not exact matches
A number of individual genes have been linked to suicide, such as those involved
in the
brain's response to mood - lifting serotonin, and a
signalling molecule called
brain - derived neurotrophic factor (BDNF), which
regulates the
brain's response to stress.
Latest research from the National Centre for Biological Sciences (NCBS, Bangalore), now shows that maintaining Calcium balance
in cells is also needed for another purpose — it may be
regulating the levels of an important
signalling molecule called dopamine
in the
brain.
What was especially «exciting» about this finding, he says, is that these variations were near a neural highway that previous studies have shown helps
regulate life span
in worms and flies, and that stopping chemical
signals from this
brain pathway extends the life span of mice.
It was originally investigated
in 1995 by pharmacologist Franco Borsini and a team of researchers at Boehringer Ingelheim Italia
in Milan as an antidepressant because of its ability to
regulate neurotransmitters — the
brain's chemical -
signaling molecules.
These include a family of
signaling molecules called protocaderins, which
regulate neuronal development and short - range interactions between neurons, and a family of transcription factors called zinc fingers, which are mainly expressed
in embryonic and nervous tissues and are thought to play roles
in brain development.
In a study being published in the journal Neuron, researchers show that the signal molecule TGF - beta acts as a time signal that regulates the nerve stem cells» potential at different stages of the brain's development — knowledge that may be significant for future pharmaceutical developmen
In a study being published
in the journal Neuron, researchers show that the signal molecule TGF - beta acts as a time signal that regulates the nerve stem cells» potential at different stages of the brain's development — knowledge that may be significant for future pharmaceutical developmen
in the journal Neuron, researchers show that the
signal molecule TGF - beta acts as a time
signal that
regulates the nerve stem cells» potential at different stages of the
brain's development — knowledge that may be significant for future pharmaceutical development.
UCLA researchers looked at levels of these neurotransmitters — glutamate and gamma - aminobutyric acid, known as GABA —
in a
brain region called the insula, which integrates
signals from higher
brain regions to
regulate emotion, thinking and physical functions such as blood pressure and perspiration.
A neurosurgical procedure
in which an implanted neurostimulator delivers electrical
signals to specific areas of the
brain to help
regulate abnormal
signals, DBS is currently only approved
in the U.S. for the treatment of Parkinson's disease and essential tremor.
The resulting rhythmic
signals produced by this transfer of cations are what support the synchronous contraction of our heart muscles and neuronal firing
in parts of the
brain, like the thalamus, which helps
regulate our sleep - wake cycle, or circadian rhythm.
BREATHLESS Nerve endings
in the lungs send
signals — triggered by force - detecting proteins — to the
brain and spinal cord that help
regulate breathing.
For example, the scientists identified a deletion
in one gene called «stargazin» that is required for
regulating the transmission of
signals between neurons
in the
brain.
When the researchers looked at
brain size, they found that for fighters who had increasing levels of tau over time, there was a 7 percent decline
in the volume of their thalamus, which is located
in the center of the
brain and
regulates sleep, consciousness, alertness, cognitive function and language while also sending sensory and movement
signals to other portions of the
brain.
January 4, 2006 Chemical
signaling helps
regulate sensory map formation
in the
brain Researchers from the University of Chicago have uncovered an important mechanism used by the developing
brain to pattern nerve connections
in the part of the
brain that interprets visual
signals.
Corollary studies focused on the mechanisms that
regulate brain endocannabinoid
signaling have provided critical
in vivo evidence of an «on demand,» activity - dependent nature of endocannabinoid influence.
In humans, low levels of hydrogen sulfide serve as a signaling molecule that helps regulate physiological processes in the brain, heart and other organ
In humans, low levels of hydrogen sulfide serve as a
signaling molecule that helps
regulate physiological processes
in the brain, heart and other organ
in the
brain, heart and other organs.
In the new study, Song and colleagues discovered that this hippocampal PV interneuron -
signaling is
regulated by a GABA circuit coming from the medial septum, a cluster of neurons near the front of the
brain.
In terms of pathogenic mechanisms of PD, given that miR - 181a is selectively up - regulated in nigrostriatal DA neurons of the PD brain [13], our current findings suggest that this up - regulation in miR - 181a may contribute to the ongoing mDA axonal degeneration by inhibiting BMP - Smad signalling in viv
In terms of pathogenic mechanisms of PD, given that miR - 181a is selectively up -
regulated in nigrostriatal DA neurons of the PD brain [13], our current findings suggest that this up - regulation in miR - 181a may contribute to the ongoing mDA axonal degeneration by inhibiting BMP - Smad signalling in viv
in nigrostriatal DA neurons of the PD
brain [13], our current findings suggest that this up - regulation
in miR - 181a may contribute to the ongoing mDA axonal degeneration by inhibiting BMP - Smad signalling in viv
in miR - 181a may contribute to the ongoing mDA axonal degeneration by inhibiting BMP - Smad
signalling in viv
in vivo.
Abbreviations: Aβ, amyloid β - peptide; AD, Alzheimer's disease; ALS, amyotrophic lateral sclerosis; Ambra1, activating molecule
in Beclin -1-
regulated autophagy; AMPK, AMP - activated protein kinase; APP, amyloid precursor protein; AR, androgen receptor; Atg, autophagy - related; AV, autophagic vacuole; Bcl, B - cell lymphoma; BH3, Bcl - 2 homology 3; CaMKKβ, Ca2 + - dependent protein kinase kinase β; CHMP2B, charged multivesicular body protein 2B; CMA, chaperone - mediated autophagy; 2 ′ 5 ′ ddA, 2 ′, 5 ′ - dideoxyadenosine; deptor, DEP - domain containing mTOR - interacting protein; DRPLA, dentatorubral pallidoluysian atrophy; 4E - BP1, translation initiation factor 4E - binding protein - 1; Epac, exchange protein directly activated by cAMP; ER, endoplasmic reticulum; ERK1 / 2, extracellular -
signal -
regulated kinase 1/2; ESCRT, endosomal sorting complex required for transport; FAD, familial AD; FDA, U.S. Food and Drug Administration; FIP200, focal adhesion kinase family - interacting protein of 200 kDa; FoxO3, forkhead box O3; FTD, frontotemporal dementia; FTD3, FTD linked to chromosome 3; GAP, GTPase - activating protein; GR, guanidine retinoid; GSK3, glycogen synthase kinase 3; HD, Huntington's disease; hiPSC, human induced pluripotent stem cell; hVps, mammalian vacuolar protein sorting homologue; IKK, inhibitor of nuclear factor κB kinase; IMPase, inositol monophosphatase; IP3R,
Ins (1,4,5) P3 receptor; I1R, imidazoline - 1 receptor; JNK1, c - Jun N - terminal kinase 1; LC3, light chain 3; LD, Lafora disease; L - NAME, NG - nitro - L - arginine methyl ester; LRRK2, leucine - rich repeat kinase 2; MIPS, myo - inositol -1-phosphate synthase; mLST8, mammalian lethal with SEC13 protein 8; MND, motor neuron disease; mTOR, mammalian target of rapamycin; mTORC, mTOR complex; MVB, multivesicular body; NAC, N - acetylcysteine; NBR1, neighbour of BRCA1 gene 1; NOS, nitric oxide synthase; p70S6K, ribosomal protein S6 kinase - 1; PD, Parkinson's disease; PDK1, phosphoinositide - dependent kinase 1; PE, phosphatidylethanolamine; PI3K, phosphoinositide 3 - kinase; PI3KC1a, class Ia PI3K; PI3KC3, class III PI3K; PI3KK, PI3K - related protein kinase; PINK1, PTEN - induced kinase 1; PKA, protein kinase A; PLC, phospholipase C; polyQ, polyglutamine; PS, presenilin; PTEN, phosphatase and tensin homologue deleted from chromosome 10; Rag, Ras - related GTP - binding protein; raptor, regulatory - associated protein of mTOR; Rheb, Ras homologue enriched
in brain; rictor, rapamycin - insensitive companion of mTOR; SBMA, spinobulbar muscular atrophy; SCA, spinocerebellar ataxia; SLC, solute carrier; SMER, small - molecule enhancer of rapamycin; SMIR, small - molecule inhibitor of rapamycin; SNARE, N - ethylmaleimide - sensitive factor - attachment protein receptor; SOD1, copper / zinc superoxide dismutase 1; TFEB, transcription factor EB; TOR, target of rapamycin; TSC, tuberous sclerosis complex; ULK1, UNC -51-like kinase 1; UVRAG, UV irradiation resistance - associated gene; VAMP, vesicle - associated membrane protein; v - ATPase, vacuolar H + - ATPase; Vps, vacuolar protein sorting
Researchers have found a new group of cells
in the retina that directly affect the biological clock by sending
signals to a region of the
brain which
regulates our daily (circadian) rhythms.
Delivery of circulating lipoproteins to specific neurons
in the Drosophila
brain regulates systemic insulin
signaling.
This
signaling helps the
brain regulate certain hormones
in the body that are responsible for waking us up and helping us fall asleep at night.