Further, geneticdeletion of the SPTLC2 gene preserved cardiac function following MI.
2
Neither Ab depletion of IFN-gamma nor geneticdeletion of IFN-gamma impaired early DVT resolution.
3
Results: Mice with geneticdeletion of Nur77 exhibited increased susceptibility to diet-induced obesity and insulin resistance.
4
Here, we explored the role of RIP3 geneticdeletion in in vivo and in vitro PD models.
5
These results were supported by geneticdeletion of Gal-3 in both MCT and Sugen Hypoxia rat models.
1
Hearing thresholds in patients with a complete monosomy Xp were about 10 dB worse compared with those in patients with a partialmonosomy Xp.
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.
6
First, we constructed a recombinant which contains both a G2R deletionmutation and an A18R temperature-sensitive mutation and found that this recombinant was viable.
7
In MD, a recurrent P799L mutation was identified in nine subjects, as well as 10 novel mutations including F471del, the first deletionmutation of TRPV4.
8
To date, only four nonsense or small deletionmutations have been reported.
9
Likewise, deletionmutations disrupting the apoE-NS5A interaction resulted in blockade of HCV production.
10
MtDNA deletionmutations were identified in skeletal muscles of all patients.
11
Six showed insertional mutation, and three showed deletionmutations.
12
Deletionmutations in these two genes in animal models mark the progression from adenoma to carcinoma.
13
Only five deletionmutations yielded lethal phenotypes, and these were colinear, spanning a 56-amino-acid region within domain II.
14
We constructed and characterized in-frame deletionmutations in several FrzS domains to determine their roles in protein localization.
15
We report identification of a novel small deletionsmutation in the RUNX2 gene in a Chinese family with CCD.
16
In addition, two heterozygous deletionmutations and five heterozygous duplication mutations within PARK2 were identified in PD subjects and controls.