New remote - control technology may offer biologists a powerful way to do
this with cells and genes.
Not exact matches
I won't reveal yet who my favorites are, but I will say that these young scientist - founders came up
with very creative solutions for preventing infections in some common surgeries, tackling resistance in targeted antibody drugs, improving
gene vectors for
cell therapies, helping the vision - impaired «see» faces
and better read their environments, imaging hard - to - see spots in the lungs
and other organs, improving genetic risk analysis,
and expediting the logistical operations of hospitals.
The companies» R&D will focus on on a
gene mutation present in a wide swath of patients
with ALS, a degenerative nervous system disease that eats away at nerve
cells and weakens muscles.
Essentially the model reproduces the inner workings of all of the proteins within the organism
and allows scientists to see everything from how
cells interact
with each other to the functions of
genes in a larger context that had not been previously understood.
His research has spanned hematopoiesis,
gene therapy, stem
cell biology, genomics
and cancer, consistently focusing on bringing the very latest research advances to patients
with heretofore incurable diseases.
With major clinical successes in areas such as CAR - T,
gene therapy, immune - oncology,
cell therapy
and gene editing, many see 2017 as the year that biotech really came of age.
Risk Versus Reward: The Value of
Cell Therapy for Patients and Investors Source: Streetwise Reports (4/25/18) The cell therapy space, encompassing disruptive new treatment including stem cell therapy, immunotherapy and gene editing, has begun to mature, with a handful of product approvals and others in late - stage developm
Cell Therapy for Patients
and Investors Source: Streetwise Reports (4/25/18) The
cell therapy space, encompassing disruptive new treatment including stem cell therapy, immunotherapy and gene editing, has begun to mature, with a handful of product approvals and others in late - stage developm
cell therapy space, encompassing disruptive new treatment including stem
cell therapy, immunotherapy and gene editing, has begun to mature, with a handful of product approvals and others in late - stage developm
cell therapy, immunotherapy
and gene editing, has begun to mature,
with a handful of product approvals
and others in late - stage development.
The
cell therapy space, encompassing disruptive new treatment including stem
cell therapy, immunotherapy
and gene editing, has begun to mature,
with a handful of product approvals
and others in late - stage development.
To quote Ayala
and Kiger's textbook, Modern Genetics: «There is no way of knowing whether a given
gene will mutate in a particular
cell or in a particular generation,» because the mutations «are unoriented
with respect to adaptation.»
Mutations are indeed not, so far as we know, selected by any overall purpose favoring evolution; but this is compatible
with there being short - run
and very naive purposes, desires, or feelings in the atoms
and molecules constituting the
genes, as well as in every
cell and every metazoan
with a nervous system.
iPS
cells tend to age prematurely
and die; they are also created
with cancer - causing
genes, which could make them dangerous to use therapeutically.
The strict definition of celiac disease — positive antibodies to gliadin, intestinal endomysium,
and tissue transglutaminase, together
with the presence of HLA - DQ2 or HLA - DQ8
genes and an intestinal biopsy that shows at least 20 - 25 CD3
cells per 100 epithelial
cells — will account for about 75 - 80 % of all those sensitive to gluten.
And 1 in 13 African American infants are born
with the sickle
cell trait, meaning they carry the sickle
cell gene, although they don't have SCD.
A person has SCT when they have a
gene for healthy blood
and a
gene for blood
with sickle
cell.
Gene Expression in Cumulus
Cells and Correlation
with Pregnancy Outcome in Women.
All animal
cells are made up of two genomes, the nuclear genome
with 10,000 s of protein coding
genes and the mitochondrial genome
with 13 protein - encoding
genes.
McCallion's strategy to make sense of all this data looks at the active
genes in
cells affected by a disease, groups of
genes that interact
with one another, their vulnerability to mutation
and information from past scientific studies to filter more than a thousand
gene candidates for disease risk down to just a handful within any one implicated region.
The study, led by Dr Len Stephens
and Dr Phill Hawkins
and published today in the journal Molecular
Cell, reveals why loss of the PTEN
gene has such an impact on many people
with prostate cancer, as well as in some breast cancers.
Genetic variations most strongly associated
with high scores were found near the GATA2
gene — involved in the development of inner ear hair
cells and the inferior colliculus.
Those made
with iPS
cells, by contrast, tend to accumulate mutations
and suffer abnormal patterns of
gene activation.
Their brains differed in the activity of over a hundred
genes that provide
cells with energy, influence chemical communications in the brain
and strengthen the connection between nerve
cells.
An in - depth genetic analysis, performed
with the participation of graduate students Tal Lupo
and Lihee Asaf, pointed to a
gene called WNT5B, which was revealed to be the factor prompting stem
cells to differentiate into lymphatic
cells.
They made these clones by a process called automatic parthenogenesis: The egg is formed normally (
with half the species» usual number of chromosomes), then fertilized by the «polar body,» a
cell that is created during oogenesis
and contains the same
gene copies as the egg, resulting in the shark having half the genetic variation of its mother.
Fluorescence - activated sorting is then used to identify
and retrieve from this mix only those
cells that display strong reporter
gene expression, which represent the
cells with the most active enhancers.
We wanted to understand what types of differences are always there, what is causing them,
and what they mean,» says Juan Carlos Izpisua Belmonte, a professor in Salk's
Gene Expression Laboratory
and co-senior author,
with Kelly Frazer of the University of California, San Diego, on the new paper, which was published in
Cell Stem
Cell in April 2017.
Molecular characterization of the
cells that undergo
cell fate transition upon oncogenic Pik3ca expression demonstrated a profound oncogene - induced reprogramming of these newly formed
cells and identified
gene expression signatures, characteristic of the different
cell fate switches, which was predictive of the cancer
cell of origin, tumour type
and clinical outcomes in women
with breast cancers.
To see if the remaining 382
genes meet the minimum requirement for life, Venter's team will have to build a genome
with them
and drop it into a
cell.
The last piece of evidence together
with the fact that the parents do not carry the alterations suggest that the extra copies of
genes may have occurred either in the sperm or the egg, the parent's germ
cells,
and before or very early after fertilization.
ORDINARY
cells from people
with a genetic disease can be «fixed» by
gene therapy
and then reprogrammed to be stem
cells that will produce a limitless supply of defect - free
cells.
They also show that myomerger works
with another
gene, Tmem8c,
and its associated protein «myomaker» to fuse
cells that normally would not.
«As you look for methods to discern complex immune responses in human
cells, more
and more people look at what
genes are turned on
with infections or vaccination procedures.»
To find out, the researchers injected a cloned telomerase
gene into cultured
cells from retina, skin,
and blood vessels, all of which are associated
with degenerative, aging - related diseases.
In comparison
with African strains, infection by the Asian strain of Zika virus more potently affected the p53
gene and genes connected
with cells» responses to viral infection, such as interferons.
The results show — for the first time, Briggs thinks — that the bacterial genomes change
with depth: the micro-organisms at 554 metres carry more mutations in
genes that code for energy - related processes like
cell division
and biosynthesis of amino acids than are seen in their shallower counterparts.
The Porteus team started
with human stem
cells from the blood of patients
with sickle
cell disease, corrected the
gene mutation using CRISPR
and then concentrated the human stem
cells so that 90 percent carried the corrected sickle
cell gene.
The researchers — James Robl, a developmental biologist
and his colleagues at the University of Massachusetts at Amherst,
and Steve Stice at Advanced
Cell Technology in Worcester, Massachusetts — inserted a marker
gene fused
with a
gene for resistance to the chemical neomycin into a culture of connective tissue
cells called fibroblasts.
Base oxidation regulates
gene activity In cooperation
with colleagues at LMU, as well as researchers based in Berlin, Basel
and Utrecht, Carell
and his group have now shown, for the first time, that a standard base other than cytosine is also modified in embryonic stem
cells of mice.
The protein is now known to interact
with and control dozens of different
genes and proteins,
and it helps regulate the cycle of molecular events by which
cells grow
and reproduce.
Novel abnormalities in the FGFR
gene, called FGFR fusions, were identified in a spectrum of cancers,
and preliminary results
with cancer
cells harboring FGFR fusions suggested that some patients
with these cancers may benefit from treatment
with FGFR inhibitor drugs, according to data published in Cancer Discovery, a journal of the American Association for Cancer Research.
Vamsi Mootha, a mitochondrial biologist at Massachusetts General Hospital, his graduate student Isha Jain,
and their colleagues used a popular DNA - editing tool called CRISPR to knock out about 18,000 different
genes in human
cells that were altered to have the same problems as people
with mitochondrial diseases.
People
with the transthyretin amyloidosis have mutations in the DNA of the transthyretin
gene, which causes abnormal buildup
and deposits of a transport protein called transthyretin in nerve
and heart
cells.
Since patients (
and mice)
with Usher 1c also have balance problems caused by hair -
cell damage in the vestibular organs, the researchers also tested whether
gene therapy restored balance.
The virus, redesigned using sophisticated protein engineering techniques, works:
With its shield
and its adapter, these viral
gene shuttles efficiently infected tumor
cells in laboratory animals.
Lu's team will extract immune
cells called T
cells from the blood of the enrolled patients,
and then use CRISPR — Cas9 technology — which pairs a molecular guide able to identify specific genetic sequences on a chromosome
with an enzyme that can snip the chromosome at that spot — to knock out a
gene in the
cells.
It was unlikely that all 24
genes would be altered simultaneously in any one bacterium, so the cycle was repeated over
and over to increase the proportion of
cells with mutations in all 24
genes.
Biochemist Radhey Gupta of McMaster University in Canada proposes that a bacterium
and an archaean fused to form the first eukaryote, based on his analysis of a pair of slow - changing
genes found in what may be one of the oldest
cells with a nucleus, Giardia lamblia.
Women tend to be protected from diseases related to
genes on the X because female
cells randomly inactivate one of the X chromosomes,
and that leaves some
cells with a normal copy up
and running.
In the case of head
and neck squamous
cell carcinoma, for example, high stemness indices correlated
with mutations in the
gene NSD1.
They found similar changes in
gene expression in the same
genes with increased activity of glucose transporters in both the stem
cells and the fat
cells, Sen noted.
It found that
genes associated
with depression are involved in brain
cell development,
and that there was overlap between these genetic regions
and those linked to schizophrenia
and other mental illnesses.