To upgrade their DNA «switches,» Wong and his colleagues steered clear of transcription factors and instead switched human
kidney cell genes on and off using scissorlike enzymes that selectively cut out snippets of DNA.
Not exact matches
«New
gene editing technique turns human pluripotent stem
cells into a model system for polycystic
kidney disease.»
The researchers inserted the
genes for the 25 subtypes into human
kidney cells (an easier feat than working with real taste
cells).
«This is the first study to show the actual
cell behaviors caused by mutations in
genes causally linked to polycystic
kidney disease, an important new step in the path towards treatment,» said Dr. Robert L. Bacallao, associate professor of medicine at the IU School of Medicine in Indianapolis.
Using
cell models and genetically engineered mice, the authors then could reproduce
kidney disease changes upon expression of APOL1
gene variants, but the disease required the presence suPAR.
Derived mostly from human embryonic
kidney 293T (HEK293T) and HeLa
cell lines, EdiGene Knockout (KO) Cell Lysates have been optimized through the use of genome editing technology and validated at the genomic level through PCR and Sanger - sequencing techniques to ensure the accuracy and knockout of the target g
cell lines, EdiGene Knockout (KO)
Cell Lysates have been optimized through the use of genome editing technology and validated at the genomic level through PCR and Sanger - sequencing techniques to ensure the accuracy and knockout of the target g
Cell Lysates have been optimized through the use of genome editing technology and validated at the genomic level through PCR and Sanger - sequencing techniques to ensure the accuracy and knockout of the target
gene.
«Sickle
cell gene linked to elevated risk of developing
kidney failure.»
Similarly, carriers in the Jackson study of one copy of the
genes that cause sickle -
cell disease — a useful trait against malaria in Africa — appear to be more at risk for
kidney disease.
AFRICAN GREEN MONKEY
CELL: An African green monkey kidney cell expressing the gene c - src, imaged using Bessel beam plane illuminat
CELL: An African green monkey
kidney cell expressing the gene c - src, imaged using Bessel beam plane illuminat
cell expressing the
gene c - src, imaged using Bessel beam plane illumination.
The team found deep conservation of certain processes that likely reflects similar underlying regulatory processes between mouse and man, but there were also significant differences in
gene expression during
kidney development, as well as in the timing, scale, organization, and molecular profile of key
cell types and
cell structures.
«Having a supply of these
cells could be a starting point to grow functional organs in the laboratory as well as a way to begin applying
cell therapy to
kidneys with malfunctioning
genes.»
«We provide a proof - of - principle for how to make and maintain unlimited numbers of precursor
kidney cells,» says Juan Carlos Izpisua Belmonte, professor in Salk's
Gene Expression Laboratory.
«Mutations in
gene essential for
cell regulation cause
kidney cancer in children.»
Mutations in a
gene that helps regulate when
genes are switched on and off in
cells have been found to cause rare cases of Wilms tumour, the most common
kidney cancer occurring in children.
By transferring the
gene for melanopsin into human embryonic
kidney cells, synthetic biologist Martin Fussenegger of the Swiss Federal Institute of Technology in Zurich and colleagues made these
cells light - sensitive as well.
«This data allows classification of all human protein - coding
genes into those coding for house - hold functions (present in all
cells) and those that are tissue - specific
genes with highly specialized expression in particular organs and tissues, such as
kidney, liver, brain, heart, pancreas.
$ 1.8 M Supports Cancer Drug Discovery on Commonly Mutated
Gene New Brunswick Patch — April 5, 2016 Behavioral Scientist Shares Insights about FDA's Proposed Rule on Banning Tanning Bed Use among Minors News-Medical.net - March 19, 2016 Intervention Program Reduces Caregiver Distress during Hospitalization of Pediatric Stem
Cell Transplant Patients News-Medical.net - March 9, 2016 Exploring Genomic Pathways in the Development of Ovarian Cancer GMNews.com - March 2, 2016 Differences in Type of Small Protein may further Elucidate Lung Cancer Risk in African Americans ScienceDaily.com - March 2, 2016 Study Looks at Post-Treatment Resources for Prostate Cancer Patients Transitioning to Survivorship News-Medical.net - February 11, 2016 Drawing the Line on Tanning Bed Use by Teens ScienceDaily.com - December 21, 2015 What Rutgers Study Uncovered about E-Cigarette Use NJBiz.com - December 9, 2015 Identification of Barrier that Prevents Progression of Benign
Kidney Tumors to Malignant Disease MedicalNewsToday.com - November, 24, 2015 What is the Color of the Lung Cancer Ribbon?
Aug 8, 2008 Two New Predisposition
Genes For Breast, Thyroid And
Kidney Cancers Could Lead to More Accurate Diagnosis and Earlier Detection of These Cancers Charis Eng, MD, PhD, Sondra J and Stephen R Hardis Endowed Chair of Cancer Genomic Medicine and Chair, GMI, and her team published in the Aug 8, 2008 issue of the American Journal of Human Genetics that germline mutations in SDHB and SDHD, which play key roles in the mitochondria (the
cell's power houses), predispose to Cowden and Cowden - like syndromes.
However, because mature
cells in the stomach, pancreas, liver, and
kidney all activate the same
genes and go through the same process when they begin to divide again, the findings could mean that cancer initiation is much more similar across organs than scientists have thought.
The Hopkins scientists report that the loss of a single
gene in
kidney cancer
cells causes them to stop making mitochondria, the tiny powerhouses of the
cell that consume oxygen to generate energy.
This is a
gene that scientists can look for to find out if it — and the
gene it now partners — made it into the
kidney cell's DNA.
So the scientists inserted the taste
genes into human
kidney cells that were growing in dishes.
The SNP is in the
gene encoding claudin 14 (CLDN14), a protein expressed in the
kidney and one of a family of membrane proteins that regulate the passage of ions and small solutes between
cells.
Our biological studies suggest that a critically reduced amount of this protein alters
cell shape, migration, proliferation, and
gene expression to the detriment of brain, heart, and
kidney development.
How do
kidney cells activate the EPO
gene in response to oxygen deficiency?
``... several animal studies indicate serious health risks associated with GM food consumption including infertility, immune dysregulation, accelerated aging, dysregulation of
genes associated with cholesterol synthesis, insulin regulation,
cell signaling, and protein formation, and changes in the liver,
kidney, spleen and gastrointestinal system.»