Such methods include cell fusion, microencapsulation and macroencapsulation, and recombinant DNA technology (
including gene deletion, gene doubling, introducing a foreign gene, and changing the positions of genes when achieved by recombinant DNA technology).»
Not exact matches
My background has
included: PCR,
gene synthesis, cloning, codon optimization, site - directed mutagenesis, chromosomal
gene integration /
deletion, albumin fusion, fermentation using NBS BioFlo3000, SDS - PAGE, Coomassie staining, and Western blotting.
In this study, the researchers found that conditional
deletion of Sox2 — the
gene encoding the SOX2 stem cell transcription factor — and the associated dampening of astrocyte reactivity appear to promote functional recovery,
including behavioral recovery, after traumatic brain injury, said Dr. Zhang, a W.W. Caruth, Jr..
A very rare form of a thalassemia is due to a
deletion of a larger area of chromosome 16
including the a globin
genes.
Future posts will
include non-homologous end joining, using CRISPR for
gene activation, creating
deletions using CRISPR - Cas tools, validation, and more.
«In 100 percent of small - cell lung cancers, there is a
deletion in this region of chromosome 3, very often
including the HYAL2
gene,» he said.
Forms of variation
include single DNA base pair alterations, duplications or
deletions of
genes or sets of
genes, and translocations, a chromosomal rearrangement in which a segment of genetic material from one chromosome becomes heritably linked to another chromosome.
Using our own data and publically available data from array comparative genomic hybridization (aCGH), we identified a minimal
deletion for the cardiomyopathy associated with del1p36 that
included only the terminal 14 exons of the transcription factor PRDM16 (PR domain containing 16), a
gene that had previously been shown to direct brown fat determination and differentiation.
For each mouse line, Lexicon provided not only the mouse strain itself, but also detailed, objective data on the impact of the specific
gene deletion on the mouse's phenotype, which
includes appearance, health, fitness, behavior, ability to reproduce, and radiological and microscopic data.
Known and novel independent prognostic markers were identified in our cohort of proteasome inhibitor and IMiD - treated patients with long follow - up,
including events with context - specific prognostic value, such as
deletions of the PRDM1
gene.
For each mouse line, Deltagen provided the mouse strain, but also detailed, objective data on the impact of the specific
gene deletion on the mouse's phenotype, which
includes appearance, health, fitness, behavior, ability to reproduce, and radiological and microscopic data.
They also described the
gene's size and genetic
deletions associated with disease,
including a very large
deletion of the
gene coding for dystrophin found in a patient with mild disease.
CEA, which segregates in several herding breeds with Collie ancestry, was mapped to a large region of CFA37 that
included over 40
genes [92]; subsequently the fact that the disorder segregates in multiple, closely related breeds was used to reduce the size of the critical disease - associated region and pinpoint the causal mutation to a 7.8 kb intronic
deletion in the NHEJ1
gene, which spans a highly conserved binding domain to which several developmentally important
genes bind [91].