The researchers focused on a process — known as «homeostatic scaling down» — that has been well -
studied in lab neurons but not before in living animals.
Not exact matches
To
study how the fruit fly
neurons responded to external temperature, Yadlapalli worked with Chang Jiang, a postdoctoral researcher
in the
labs of Pramod Reddy and Edgar Meyhofer of the U-M Department of Mechanical Engineering.
Europe came through: Last year, Cory received a European Molecular Biology Organization (EMBO) Installation Grant for his
lab in mitochondrial biogenesis, and Gülayşe won a Marie Curie International Reintegration Grant from the European Commission to
study how single genes can yield different protein products
in neurons.
In a 2016 study, for example, Dokholyan's lab found evidence that «trimer» structures made of just three copies of the SOD1 protein are toxic to the type of neuron affected in AL
In a 2016
study, for example, Dokholyan's
lab found evidence that «trimer» structures made of just three copies of the SOD1 protein are toxic to the type of
neuron affected
in AL
in ALS.
For the new
study, Dokholyan's team, including lead author Cheng Zhu, PhD, a postdoctoral researcher
in his
lab, conducted complicated experiments to compare how trimers affect
neurons to how larger fibrils affect
neurons.
For example, animal
studies have shown that
neurons derived
in the
lab from human embryonic stem cells improve Parkinson's symptoms; however, any residual stem cells associated with those
neurons could form masses of unwanted cells.
In a recent study published in the Journal of Neuroscience, Michele Noonan, a University of Texas neuroscience graduate student in the lab of Amelia Eisch, shows that a lack of neurogenesis, or birth of new neurons, in the adult rat can actually cause drug addictio
In a recent
study published
in the Journal of Neuroscience, Michele Noonan, a University of Texas neuroscience graduate student in the lab of Amelia Eisch, shows that a lack of neurogenesis, or birth of new neurons, in the adult rat can actually cause drug addictio
in the Journal of Neuroscience, Michele Noonan, a University of Texas neuroscience graduate student
in the lab of Amelia Eisch, shows that a lack of neurogenesis, or birth of new neurons, in the adult rat can actually cause drug addictio
in the
lab of Amelia Eisch, shows that a lack of neurogenesis, or birth of new
neurons,
in the adult rat can actually cause drug addictio
in the adult rat can actually cause drug addiction.
The
study's lead author, Toni - Lee Sterley, a postdoctoral associate
in Bains»
lab said, «What was remarkable was that CRH
neurons from the partners, who were not themselves exposed to an actual stress, showed changes that were identical to those we measured
in the stressed mice.»
The
study also includes three co-first authors: Qingjian Han from Ji's group who discovered SHANK3
in sensory
neurons and pain defects
in SHANK3 mutant mice; Yong Ho Kim, an electrophysiologist
in Ji's group who found diminished TRPV1 function
in SHANK3 mutant mice; and Xiaoming Wang from Jiang's
lab who generated SHANK3 mutant mice.
But recent
studies in both humans and
lab mice have suggested that motor
neurons in the brain — the upper motor
neurons — may be involved
in disease progression, although the extent and significance of this involvement has remained unknown.
«That suggests these
neurons are providing a copy of the motor command directly to the auditory system,» said David M. Schneider, Ph.D., co-lead author of the
study and a postdoctoral fellow
in Mooney's
lab.
This week
in the JCI, a
study conducted by David Engblom's
lab at Linköping University
in Sweden has demonstrated that the aversive effects of inflammatory pain are driven by prostaglandin signaling specifically on serotonin - producing
neurons in the brainstem.
Now, a preclinical
study, from the
lab of Olivier Berton, PhD, an assistant professor
in the department of Psychiatry,
in collaboration with Sheryl Beck, PhD, a professor
in the department of Anesthesiology at Children's Hospital of Philadelphia, found that bullying and other social stresses triggered symptoms of depression
in mice by activating GABA
neurons,
in a never - before - seen direct relationship between social stimuli and this neural circuitry.
In another study of mice injected with GDF11, postdoc Lida Katsimpardi and others in the lab of Harvard neuroscientist Lee Rubin found that GDF11 also encourages growth of new blood vessels and olfactory neurons in the mouse brai
In another
study of mice injected with GDF11, postdoc Lida Katsimpardi and others
in the lab of Harvard neuroscientist Lee Rubin found that GDF11 also encourages growth of new blood vessels and olfactory neurons in the mouse brai
in the
lab of Harvard neuroscientist Lee Rubin found that GDF11 also encourages growth of new blood vessels and olfactory
neurons in the mouse brai
in the mouse brain.
Studies of individual
neurons in dishes of cultured
neurons and
in brain slices by co-first author Robert E. Stanley, a graduate student
in the
lab, revealed that
neurons in the mutant mice had decreased numbers of dendritic spines, an important part of the synapses that
neurons use to communicate with one another.
In a study published in the journal Neuron, co-first authors Christian Burgess, PhD, a postdoctoral fellow; Rohan Ramesh, a graduate student, and colleagues in Andermann's lab recorded images of brain activity in mice across different states of hunger and satiet
In a
study published
in the journal Neuron, co-first authors Christian Burgess, PhD, a postdoctoral fellow; Rohan Ramesh, a graduate student, and colleagues in Andermann's lab recorded images of brain activity in mice across different states of hunger and satiet
in the journal
Neuron, co-first authors Christian Burgess, PhD, a postdoctoral fellow; Rohan Ramesh, a graduate student, and colleagues
in Andermann's lab recorded images of brain activity in mice across different states of hunger and satiet
in Andermann's
lab recorded images of brain activity
in mice across different states of hunger and satiet
in mice across different states of hunger and satiety.
Researchers from Hiroki Taniguchi's
lab at the Max Planck Florida Institute for Neuroscience (MPFI) published a
study in eNeuro
in May 2017 showing for the first time that a unique type of inhibitory interneuron called chandelier cells — which are implicated
in several diseases affecting the brain such as schizophrenia and epilepsy — seem to develop their connections differently than other types of
neurons.
As a graduate student
in James Townsel's
lab, he
studied the regulation and function of choline receptors, which are responsible for the transport of cholinergic
neurons.
Previous
studies from George's
lab had shown that nicotine activates certain «reward»
neurons in the brain — giving positive reinforcement to keep smoking.
Indeed, after many years of
studies on mirror
neurons and their functioning we are shifting our
lab research to the
study of the control mechanisms
in the brain for mirror
neurons.
The combination of signals — microRNAs miR - 9 and miR - 124 plus transcription factors ISL1 and LHX3 — tells the cell to fold up the genetic instructions for making skin and unfurl the instructions for making motor
neurons, according to Yoo and the
study's co-first authors, Daniel G. Abernathy and Matthew J. McCoy, doctoral students
in Yoo's
lab; and Woo Kyung Kim, PhD, a postdoctoral research associate.
In a study published today (Aug. 4, 2016) in Cell Reports, senior author Chapman, first author Bomba - Warczak and colleagues present clear evidence that toxin is moving between neurons in a lab dis
In a
study published today (Aug. 4, 2016)
in Cell Reports, senior author Chapman, first author Bomba - Warczak and colleagues present clear evidence that toxin is moving between neurons in a lab dis
in Cell Reports, senior author Chapman, first author Bomba - Warczak and colleagues present clear evidence that toxin is moving between
neurons in a lab dis
in a
lab dish.
The technique makes it possible to
study motor
neurons of the human central nervous system
in the
lab.
These manipulations, belonging to optogenetics — a technique extensively
studied in Yizhar's
lab — enabled the researchers to activate only those amygdala
neurons that interact with the cortex, and then to map out the cortical
neurons that receive input from these light - sensitive
neurons.
This is achieved by
neurons in a very old part of the brain, the brainstem, according to a
study by Carmen Birchmeier's
lab at the Max Delbrück Center for Molecular Medicine
in the Helmholtz Association (MDC).
Now,
in this
study, the Wernig
lab found that the BAM combination induces degeneration of
neurons that use the transmitter glutamate and, to a lesser extent, GABA.
In their study «D - Serine and Serine Racemase are Localized to Neurons in the Adult Mouse and Human Forebrain,» the lab utilized SR deficient (SR - / --RRB- mice, which have < 15 % of normal D - serine levels, to validate and optimize a D - serine immunohistochemical metho
In their
study «D - Serine and Serine Racemase are Localized to
Neurons in the Adult Mouse and Human Forebrain,» the lab utilized SR deficient (SR - / --RRB- mice, which have < 15 % of normal D - serine levels, to validate and optimize a D - serine immunohistochemical metho
in the Adult Mouse and Human Forebrain,» the
lab utilized SR deficient (SR - / --RRB- mice, which have < 15 % of normal D - serine levels, to validate and optimize a D - serine immunohistochemical method.
She works
in the
lab of Dr. Tiago Branco
studying how
neurons integrate synaptic signals.
«The physical symptoms that affect people with Parkinson's — including tremors and rigidity of movement — are caused by an imbalance between two types of medium spiny
neurons in the brain,» said Dr. Kreitzer, whose
lab studies how Parkinson's disease affects brain functions.
The
lab studies the pathways from sensory input to behavioral output by quantitative analysis of behavior under well - defined conditions, genetic manipulation of animals or individual neuronal cells, and calcium imaging from
neurons in living animals.
The Vetter
lab is
studying glaucoma at the molecular level to understand how genetics influence and determine the fate of
neurons in the retina and central nervous system.
However,
in a 2014
study, Dr. Sulzer's
lab demonstrated that dopamine
neurons (those affected by Parkinson's disease) are vulnerable because they have proteins on the cell surface that help the immune system recognize foreign substances.
For example, a
study conducted
in his own
lab found that forebrain assembloids generated from patients with Timothy syndrome — a genetic disease associated with autism and epilepsy, showed abnormal migration of GABAergic
neurons during the development of the cerebral cortex.
«It's really amazing that a change
in nutrient intake can have such dramatic influences on
neuron activity on such a short time scale,» said the
study's co-lead author Grant Kauwe, PhD, a postdoctoral research fellow
in the Haghighi
lab.
In fact, in one study, a dose of mercury sufficient to kill 1 percent of lab rats (lethal dose «LD01»), when combined with a dose of lead sufficient to kill 1 percent, killed 100 percent of the rats.13 A similar test involving mercury and aluminum in cultured neurons killed 60 percent of the cells when the two low - dose toxicants (LD01) were combined.14 Even antibiotics have been shown to enhance the uptake, retention and toxicity of mercury.14 Additionally, testosterone appears to aggravate mercury toxicity during development, while estrogen protects against it.15 This may explain why more boys than girls are diagnosed with autism spectrum disorders and attention deficit disorder
In fact,
in one study, a dose of mercury sufficient to kill 1 percent of lab rats (lethal dose «LD01»), when combined with a dose of lead sufficient to kill 1 percent, killed 100 percent of the rats.13 A similar test involving mercury and aluminum in cultured neurons killed 60 percent of the cells when the two low - dose toxicants (LD01) were combined.14 Even antibiotics have been shown to enhance the uptake, retention and toxicity of mercury.14 Additionally, testosterone appears to aggravate mercury toxicity during development, while estrogen protects against it.15 This may explain why more boys than girls are diagnosed with autism spectrum disorders and attention deficit disorder
in one
study, a dose of mercury sufficient to kill 1 percent of
lab rats (lethal dose «LD01»), when combined with a dose of lead sufficient to kill 1 percent, killed 100 percent of the rats.13 A similar test involving mercury and aluminum
in cultured neurons killed 60 percent of the cells when the two low - dose toxicants (LD01) were combined.14 Even antibiotics have been shown to enhance the uptake, retention and toxicity of mercury.14 Additionally, testosterone appears to aggravate mercury toxicity during development, while estrogen protects against it.15 This may explain why more boys than girls are diagnosed with autism spectrum disorders and attention deficit disorder
in cultured
neurons killed 60 percent of the cells when the two low - dose toxicants (LD01) were combined.14 Even antibiotics have been shown to enhance the uptake, retention and toxicity of mercury.14 Additionally, testosterone appears to aggravate mercury toxicity during development, while estrogen protects against it.15 This may explain why more boys than girls are diagnosed with autism spectrum disorders and attention deficit disorders.
In the lab I was studying why an excess of stress hormones had adverse consequences for health (in particular, damaging neurons), while with the baboons, I wanted to understand what social factors predicted who secreted more or less of those stress hormone
In the
lab I was
studying why an excess of stress hormones had adverse consequences for health (
in particular, damaging neurons), while with the baboons, I wanted to understand what social factors predicted who secreted more or less of those stress hormone
in particular, damaging
neurons), while with the baboons, I wanted to understand what social factors predicted who secreted more or less of those stress hormones.