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A stable chromosomaldeletion in the ldhL gene was then constructed in L. plantarum by a two-step homologous recombination process.
2
In one, however, the mother has a chromosomaldeletion that can cause DiGeorge syndrome, which is marked by heart, neuromuscular and cognitive problems.
3
The HPV16 integration event gave rise to a short chromosomaldeletion limited to the local FRA3B region within 3p14.2.
4
These chromosomaldeletions are closely related to hepatitis B virus (HBV) infection.
5
Additional chromosomaldeletions were found in several chromosomal arms.
1
The results are consistent with a dominant negative mechanism for the deletionmutation.
2
We describe a kindred with GT in which the affected individuals have a unique inversion- deletionmutation in the gene for GPIIIa.
3
Replacement of Cys937 with Ala abolished the ability of the cloned EPEC intimin to complement the deletionmutation in DBS255.
4
A novel 12 bp deletionmutation (KHNG484-488) on KIT exon 9 was detected in a small intestinal GIST.
5
By sequencing the coding regions of CRYAB, we found in exon 3 a deletionmutation, 450delA, that is associated with cataract in this family.
1
A dual guide approach improved genedeletion efficacy in both cell types.
2
CHOP genedeletion in SCs decreased cell death in response to TNF-a.
3
Quantitative polymerase chain reaction indicated total WASP genedeletion in the proband.
4
Aromatase genedeletion in female mice exacerbates ischemic brain damage after stroke.
5
In addition, essential genes were predicted via single genedeletion studies.
Usage of deletion in English
1
We detected the presence of a recently described SDHB gene large deletion.
2
However, no base substitution or deletion was detected in the CPP3 patients.
3
Molecular investigations showed that one case had a 3' deletion of MLL.
4
Of note, the CriP-mediated Nrip1 deletion did not produce detectable off-target effects.
5
A dual guide approach improved gene deletion efficacy in both cell types.
6
Consistent with this, deletion of Mon1b causes similar defects in EE fusion.
7
In one family, a homozygous deletion of exon 4 could be demonstrated.
8
The deletion partially overlaps number of reported benign CNVs and pathogenic duplications.
9
This GT deletion is also characteristic for the recently identified p47-phox pseudogenes.
10
Haplotype analyses indicated that each recurrent deletion had a single common ancestor.
11
The deletion found in patient 2 probably arose from a similar misalignment.
12
Co-deletion was most common, but exon 2-specific homozygous deletion was also detected.
13
Coincidentally, a deletion of this region enhanced the IL-2-induced expression of beta-casein.
14
In contrast, Pten deletion in mouse organoids does not lead to folding.
15
To determine the role of TspA an isogenic deletion mutant was created.
16
Only 1 patient had no deletion but had an abnormal methylation pattern.