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Four cases showed a CTNNB1 mutation and one an APC germlinemutation.
2
Testing for MEN1 germlinemutation is possible in a research setting.
3
The confirmation of a germlinemutation always requires a comparison with healthy tissue.
4
The secondary aim was to see association of germlinemutation in histopathologically proven patients.
5
Heterozygous carriers of an ATM germlinemutation have an increased susceptibility for breast cancer.
1
We report the first family with a dominantly inheritedmutation of the nebulin gene (NEB).
2
Impact: Our finding is the first instance of a plausible candidate high penetrance inheritedmutation predisposing to NPC.
3
We describe the genetic findings, phenotypic variability, and recessive inheritance of an often dominantly inheritedmutation as notable elements in their case.
4
The secondary mutation may involve a substantial loss of chromosomal material and thus lead to identification of the site of the inheritedmutation.
5
We have studied three families with congenital onset, each with a dominantly inheritedmutation in a C-terminal exon of the ryanodine receptor 1.
1
The BC1 plants inheritedvariant extra R chromosomes or fragments from allotetraploid as revealed by GISH and AFLP analysis.
1
Twelve patients carrying BRCA1 germ-linemutation were included in the study.
2
The study includes 778 women carrying a BRCA1 germ-linemutation belonging to 403 families.
3
The present mutation is the 19th nucleotide substitution identified as a germ-linemutation at this locus and the second mutation generating a stop codon.
4
Options available for germ-linemutation carriers, in addition to cancer screening, include prophylactic colectomy as well as prophylactic total abdominal hysterectomy and bilateral salpingo-oophorectomy.
5
The germ-linemutation (G382D) of the human MUTYH gene is therefore likely to be responsible for the occurrence of a mutator phenotype in these patients.
Использование термина germline variant на английском
1
Non-tumoural tissue was sequenced to exclude germlinevariants in cases where available.
2
Hypothesis: Germlinevariants of double-strand break repair genes are markers of DTC risk.
3
Other possible AURKA germlinevariants were screened by sequencing 10 of the familial cases.
4
Background: During the process of tumor profiling, there is the potential to detect germlinevariants.
5
However, the putative contribution of common NOS3 germlinevariants to breast cancer risk remained unknown.
6
Objective: To determine the risks of breast cancer associated with germlinevariants in cancer predisposition genes.
7
Additionally, nine FAP-PTC patients had rare germlinevariants in genes that were previously associated with thyroid carcinoma.
8
Two ETV6 germlinevariants gave rise to both AML and ALL, with lineage-specific genetic lesions in the leukemia genomes.
9
However, the relevance of germlinevariants in other genes from multigene hereditary cancer testing panels is not well defined.
10
We identified two germlinevariants that are predictive of poor patient outcomes by Cox regression, controlling for eleven covariates.
11
Data were processed through an analytical pipeline to search for rare germlinevariants in known or novel CRC predisposing genes.
12
Second is a case illustrating the potential for tumor sequencing to suggest germlinevariants associated with a hereditary cancer syndrome.
13
In this study, we investigated the contribution of rare germlinevariants to risk of malignant pediatric astrocytoma on a population level.
14
Results: We discovered 72 rare deleterious germlinevariants in 56 genes shared by all three individuals.
15
Previous studies have mostly focused on the roles of somatic mutations in tumorigenesis, but how germlinevariants act is largely unknown.
16
Results: In total, 32 germlinevariants in 23 genes were identified and confirmed by Sanger sequencing.