Not exact matches
In experiments on cell cultures, both of these inhibitors succeeded in breaking various forms of the TKI resistance: including forms
caused by
additional mutations of the gene Bcr - Abl as well as those
caused by large quantities of the protein Gab2.
Eight
additional affected children in six unrelated families were found to also have disease -
causing mutations in this gene.
The researchers considered two possible explanations: Disease suppression might be the result of one or two
additional substitutions on the same gene that buffer the harmful effect of the
mutation; or suppression may be
caused by numerous small substitutions throughout the genome that form an aggregate «shield.»
«Smoking can
cause new
mutations among cancer survivors that can lead to secondary and
additional primary cancers.
Velculescu cautions that medical practice may not change much until
additional studies validate their findings, and there are ongoing clinical trials studying the removal of fallopian tubes instead of ovaries in women with cancer -
causing, hereditary BRCA1 and BRCA2
mutations.
Geneticist Richard Sturm of the University of Queensland in Brisbane, Australia, an author of one of the papers says that someday scientists may find
additional mutations that
cause blue eyes but for now, the signs point to a single change.
In some patients, the cancer cells carrying the T790 - M
mutation acquired an
additional EGFR
mutation not seen before, labeled C797S, which blocked the AZD9291 from docking to the tumor cells, and
causing the disease to advance.
Additional experiments with cultured cells suggested that the
mutation interferes with one of the enzymes that breaks down the APP protein and
causes a 40 % reduction in β amyloid formation, Stefansson and colleagues report online today in Nature.
[69,72] In gastrointestinal stromal tumors (GIST), secondary resistance to KIT inhibition is
caused primarily by development of
additional KIT
mutations.
Thus the search is on is to discover
additional cancer -
causing genes «downstream» of TET
mutations that drive uncontrolled cell division in either context.
Additional in vitro and in vivo studies are needed to determine the
cause of the specificity of JAK2V617F for myeloid diseases, as second
mutations, host modifiers, differential cytokine receptor expression, and other factors may influence the ultimate phenotype of hematopoietic progenitors that acquire the JAK2V617F
mutation.
When done improperly, the process can
cause you to breathe in
additional, possibly large doses of mercury vapor — a big problem if you have the MTHFR gene
mutation and intestinal permeability (an excess of mercury exposure all at once can overburden your detox pathways).
That caution was subsequently validated by
additional research that completely excluded the Phosducin gene and led to identification of gene and
mutation causing Type A PRA.