Social behaviors can be assessed with computer vision
in mouse models of disease in a home cage environment T. HANANIA, P. KABITZKE, M. MAZELLA, I. FILIPOV, V. ALEXANDROV, D. BRUNNER... Abstract / Posters
Not exact matches
He conducted his postdoctoral research at Brigham and Women's Hospital / Harvard Medical School, where he researched the role
of the Wnt signaling pathway
in mouse models of kidney
disease, and was part
of a team that discovered a stem cell subtype responsible for solid organ fibrosis.
«It would be interesting to
model some
of these
diseases in mice and see if supplementing NMN provides any benefit to their behavior or memory.»
Gene therapy delivered to a specific part
of the brain reverses symptoms
of depression
in a
mouse model of the
disease — potentially laying the groundwork for a new approach to treating severe cases
of human depression
in which drugs are ineffective.
These findings allowed researchers to create a chimera virus: a
mouse virus with a human viral gene that can be used to test molecules that inhibit human LANA protein
in an animal
model of disease, treating not only human herpes virus infection but also its associated cancers.
Researchers from Instituto de Medicina Molecular (iMM) Lisboa have created a chimera virus that allows the study
of molecules to treat cancers caused by human herpes virus infection
in mice models of disease.
The behavioral tests used here
modeled one dimension
of the
disease — an inability to experience pleasure from normal activities — but not others, such as stress and anxiety, and probably tap into different brain mechanisms
in mice than
in humans, he says.
By directly manipulating a portion
of the prion protein - coding gene, Whitehead Institute researchers have created
mouse models of two neurodegenerative
diseases that are fatal
in humans.
We demonstrated that DENV serotype 2 (DENV2)-- specific human monoclonal antibody (HMAb) 2D22 is therapeutic
in a
mouse model of antibody - enhanced severe dengue
disease.
The new research investigated the effectiveness
of MSC therapy
in a
mouse model of chronic inflammatory lung
disease, which reflects some
of the essential features
of diseases such as COPD and cystic fibrosis.
Specifically, the Mount Sinai study was designed to test whether pharmacological compounds designed to block the function
of XPO1 / CRM1 could stop
disease progression
in mouse models that exhibit some
of the characteristics
of MS. Researchers found that two chemical agents (called KPT - 276 and KPT - 350) prevented XPO1 / CRM1 from shuttling cargo out
of the nucleus
of nerve cells, which protected them from free radicals and structural damage.
A drug that acts like a growth - promoting protein
in the brain reduces degeneration and motor deficits associated with Huntington's
disease in two
mouse models of the disorder, according to a study appearing November 27
in the Journal
of Neuroscience.
The UT Southwestern group had previously used CRISPR - Cas9, the original gene - editing system, to correct the Duchenne defect
in a
mouse model of the
disease and
in human cells.
The scientists then tested three new mTOR inhibitors currently under development (pp242, AZD8055 and INK128)
in combination with the chemotherapies AraC, Etoposide and Cisplatin to see how they affected laboratory lines
of leukemia cells and
mouse models of the
disease.
«The compounds identified
in this study, when administered orally, both reduced the inflammation that is a hallmark
of multiple sclerosis and protected against the nerve cell damage seen
in mouse models of the
disease,» said Jeffery Haines, PhD, a post-doctoral fellow at Mount Sinai and the study's lead author.
«This is the first time a compound targeting Gaucher
disease has been tested in a mouse model of Parkinson's disease and was shown to be effective,» said the study's senior author, Marie - Francoise Chesselet, the Charles H. Markham Professor of Neurology at UCLA and director of the UCLA Center for the Study of Parkinson's D
disease has been tested
in a
mouse model of Parkinson's
disease and was shown to be effective,» said the study's senior author, Marie - Francoise Chesselet, the Charles H. Markham Professor of Neurology at UCLA and director of the UCLA Center for the Study of Parkinson's D
disease and was shown to be effective,» said the study's senior author, Marie - Francoise Chesselet, the Charles H. Markham Professor
of Neurology at UCLA and director
of the UCLA Center for the Study
of Parkinson's
DiseaseDisease.
Now Perry and Holmes have built up a detailed picture
of how this happens through experiments
in mice with prion
disease, a
model of neurodegeneration.
In the study, exosomes, which are generated by all cells and are naturally present in blood, were modified as «iExosomes,» capable of delivering small RNA to specifically target mutant KRAS, resulting in disease suppression and increased overall survival in mouse model
In the study, exosomes, which are generated by all cells and are naturally present
in blood, were modified as «iExosomes,» capable of delivering small RNA to specifically target mutant KRAS, resulting in disease suppression and increased overall survival in mouse model
in blood, were modified as «iExosomes,» capable
of delivering small RNA to specifically target mutant KRAS, resulting
in disease suppression and increased overall survival in mouse model
in disease suppression and increased overall survival
in mouse model
in mouse models.
Most importantly, these cells protected
mice from developing diabetes
in a
model of disease, having the critical ability to produce insulin
in response to changes
in glucose levels.
«This
mouse model also will be useful
in studies to further investigate impact
of the omega - 3 omega - 6 ratio
in disease prevention and treatment.»
Recently research published
in Cancer Discovery showed that changing the schedules
of drug administration can improve outcomes leading to more complete responses
in mouse models of the
disease.
Blocking this inflammation after radiation therapy brought a significant improvement
in survival
in a
mouse model of the
disease.
«Gut microbes promote motor deficits
in a
mouse model of Parkinson's
disease.»
Antibiotic treatment reduced motor deficits and molecular hallmarks
of Parkinson's
disease in a
mouse model, whereas transplantation
of gut microbes from patients with Parkinson's
disease exacerbated symptoms
in these
mice.
She and her colleagues will be exploring the role
of YY1 further, using clinical samples as well as
mouse models, to look at the protein
in diseases like lupus to deepen their understanding
of how autoimmunity could result from the «escape»
of immune genes from X chromosome inactivation.
This was observed
in human ovarian cancer cells grown
in culture, and then
in mouse models of the
disease.
Desgrosellier said the team will follow up with
mouse models containing tumor fragments from patients to better reflect the diversity
of cell types present
in human
disease.
Using CRISPR / Cas9, the Hamon Center team was able to correct the genetic defect
in a
mouse model of DMD and thus prevent the development
of features
of the
disease, which
in boys causes progressive muscle weakness and degeneration, often along with breathing and heart complications.
Most animal studies
of the
disease are conducted with laboratory
mice that have been genetically engineered and bred to
model ALS, but for this research, investigators used rats with ALS because they more accurately portray the
disease's variable course
in humans.
The prevention
of dilated cardiomyopathy
in a
mouse model by feeding a high - fat diet signals an advance
in the understanding
of the mechanisms involved
in heart
disease and has implications for the future development
of treatments for this condition.
«This research project is a prime example
of how
mouse models can help us to better understand cancer
diseases in human beings,» says Sabine Harlander.
In Remodeling of the Mononuclear Phagocyte Network Underlies Chronic Inflammation and Disease Progression in Heart Failure: Critical Importance of the Cardiosplenic Axis, Prabhu and colleagues showed that immune cells that are stored in the spleen were intricately involved in the heart failure that follows a heart attack, or infarction, in a mouse - model syste
In Remodeling
of the Mononuclear Phagocyte Network Underlies Chronic Inflammation and
Disease Progression
in Heart Failure: Critical Importance of the Cardiosplenic Axis, Prabhu and colleagues showed that immune cells that are stored in the spleen were intricately involved in the heart failure that follows a heart attack, or infarction, in a mouse - model syste
in Heart Failure: Critical Importance
of the Cardiosplenic Axis, Prabhu and colleagues showed that immune cells that are stored
in the spleen were intricately involved in the heart failure that follows a heart attack, or infarction, in a mouse - model syste
in the spleen were intricately involved
in the heart failure that follows a heart attack, or infarction, in a mouse - model syste
in the heart failure that follows a heart attack, or infarction,
in a mouse - model syste
in a
mouse -
model system.
This molecule, Del - 1, is the same regulatory protein that has been found to prevent inflammation and bone loss
in a
mouse model of gum
disease.
The team also showed that they could recover muscle growth and function
in mouse models of muscular dystrophy, a
disease with a known gene mutation.
But
in studies
of mouse models of the
disease, cyclodextrins, even when administered peripherally, have significantly impacted the neurological damage; it's not known how.
Using a combination
of cell - based and
mouse models, the researchers showed that the recently - evolved mycobacteria were more virulent, likely to cause more serious
disease in patients.
Once the microglia were mobilized
in mouse models of Alzheimer's
disease, the researchers observed a more than 60 percent reduction
in amyloid beta
in the brain.
By studying how these genes cause defects
in fly and
mouse models, we can improve our insights into the mechanisms related to human
disease,» said corresponding author and Dr. Hugo J. Bellen, professor
of neuroscience and molecular and human genetics at Baylor College
of Medicine and an investigator at the Howard Hughes Medical Institute.
The nanosponges also reduced
disease severity
in a live
mouse model of necrotizing fasciitis.
An international team
of researchers has shown that a new small - molecule drug can restore brain function and memory
in a
mouse model of Alzheimer's
disease.
Application
of sun protection factor 30 (SPF30) sunscreen prior to exposure to ultraviolet - B (UVB) light delayed melanoma onset
in a
mouse model of the
disease, according to data from a team at The Ohio State University Comprehensive Cancer Center Comprehensive Cancer Center — Arthur G. James Cancer Hospital and Richard J. Solove Research Institute.
Mouse embryonic stem cells, reported
in 1981 by Martin Evans, Matthew Kaufman, and Gail Martin, have allowed scientists to generate genetically customized strains
of mice that have revolutionized studies
of organismic development and immunity and have provided countless
models of human
disease.
In a
mouse model of Alzheimer's pathology, the scientists observed that trained microglia amplified the formation
of plaques even months after their immunological memory had been triggered, thus causing the
disease to become more severe.
In a novel animal study design that mimicked human clinical trials, researchers at University of California, San Diego School of Medicine report that long - term treatment using a small molecule drug that reduces activity of the brain's stress circuitry significantly reduces Alzheimer's disease (AD) neuropathology and prevents onset of cognitive impairment in a mouse model of the neurodegenerative conditio
In a novel animal study design that mimicked human clinical trials, researchers at University
of California, San Diego School
of Medicine report that long - term treatment using a small molecule drug that reduces activity
of the brain's stress circuitry significantly reduces Alzheimer's
disease (AD) neuropathology and prevents onset
of cognitive impairment
in a mouse model of the neurodegenerative conditio
in a
mouse model of the neurodegenerative condition.
Perlmutter researchers used a
mouse model of PDA, a
disease that is usually fatal
in patients within five years
of diagnosis.
In mouse models of disease, Yale researchers looked at the effects
of providing nutrients during infection and found opposing effects depending on whether the infections were bacterial or viral.
However, research at The University
of Manchester using higher doses
of Genistein Alygone
in the
mouse model of Sanfilippo
Disease has shown that this is effective
in reducing neurodegeneration2, 3.
In normal mice, stem cells (pink) express dystrophin (green) and are able to easily generate new muscle fibers, but in the disease model, there is no dystrophin and the stem cells lose their sense of direction and have trouble generating new muscle fiber
In normal
mice, stem cells (pink) express dystrophin (green) and are able to easily generate new muscle fibers, but
in the disease model, there is no dystrophin and the stem cells lose their sense of direction and have trouble generating new muscle fiber
in the
disease model, there is no dystrophin and the stem cells lose their sense
of direction and have trouble generating new muscle fibers.
Experiments
in mouse models of Parkinson's
disease and amyotrophic lateral sclerosis (ALS, or Lou Gehrig's
disease) have demonstrated that Nrf2 - based neural protection is primarily conferred by astrocytes, but how neurons might alert astrocytes to stressful conditions is poorly understood.
First author Antonio Di Meco and colleagues used a triple transgenic (3xTg)
mouse model that displays an AD - like phenotype, including cognitive decline, and Aβ and tau neuropathology characteristic
of the
disease in humans.