«Of mice and men — are mice
relevant models for human disease?»
Not exact matches
In 2009, he established the Center
for Human Disease Modeling at Duke University, which aims to facilitate collaboration across disciplines and to develop physiologically relevant, scalable tools to study variation among human patient gen
Human Disease Modeling at Duke University, which aims to facilitate collaboration across disciplines and to develop physiologically
relevant, scalable tools to study variation among
human patient gen
human patient genomes.
«New therapies
for ALS are urgently needed — and our creation of
human models using iPS cell technology will hopefully deepen our understanding of how the
disease develops — and lead to
relevant therapies
for patients,» said Senior Investigator Steve Finkbeiner, MD, PhD, who leads ALS research at Gladstone.
To build upon the encouraging early discoveries, Helmsley renewed and expanded its Crohn's funding
for the Institute in 2013 to begin new work with three major aims: 1) continue studies of individual genes to determine how genetic differences between Crohn's patients and healthy individuals contribute to the
disease; 2) evaluate promising small molecules in
disease -
relevant studies and prioritize insights from genetics to help develop novel therapeutics; and 3) begin basic experimentation in animal
models with Crohn's
disease to provide the data necessary to begin testing new therapies in
humans.
Here we tested whether
human NSCs could be reprogrammed into iPS cells utilizing a similar strategy as described above since they represent a more clinically
relevant source of cells
for basic studies and
modeling human disease.
«Using an animal
model that's
relevant to
human disease, Fouchier and Kawaoka have shown that relatively few mutations may be required
for an influenza virus to evolve into astrain that can pass effectively between individuals and cause serious illness.
Recently, mouse neural stem cells (NSCs) have been shown capable of reprogramming into a pluripotent state by forced expression of Oct3 / 4 and Klf4; however it has been unknown whether this same strategy could apply to
human NSCs, which would result in more
relevant pluripotent stem cells
for modeling human disease.