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1 mily members to establish genotype-phenotype cosegregation.
2 oncarriers to establish clinical and genetic cosegregation.
3 mmetric self-renewal and immortal DNA strand cosegregation.
4 mmetric self-renewal and immortal DNA strand cosegregation.
5 ly coupled by physical linkage and resulting cosegregation.
6 y is not possible without data demonstrating cosegregation.
7 tentially disease-causing gene variants with cosegregation, a novel hyperpolarization-activated cycli
10 Identification of a second mutant allele and cosegregation analysis confirmed correlation with the mu
13 t genomic sequencing and, where possible, by cosegregation analysis in the families of the index case
14 fied >500 seedling-lethal mutants, completed cosegregation analysis of the insertion and the lethal p
16 ed in an active Mutator (Mu) population, and cosegregation analysis revealed that it arose from a Mu3
18 nts were confirmed by Sanger sequencing, and cosegregation analysis was performed in families, follow
20 The authors were unable to determine through cosegregation analysis whether three other changes encou
23 MP guidelines is the lack of a definition of cosegregation as criteria for pathogenicity classificati
30 own inconsistent results; there is a lack of cosegregation in some pedigrees and an unexpectedly high
34 ese analyses reveal that immortal DNA strand cosegregation is also regulated by IMPDH and confirm the
35 al implicit precept that immortal DNA strand cosegregation is specific to cells undergoing asymmetric
36 its confounded effect on the pattern of gene cosegregation, it complicates linkage analysis and map c
39 erged that suggested at least some degree of cosegregation of ADHD and learning disabilities in famil
40 sk for DESR and cannot determine whether the cosegregation of ADHD in DESR within families is a resul
42 ed a second, ethnically distinct, family for cosegregation of disease with markers from the linked re
45 on suppression over large genomic tracts and cosegregation of genes of various functions, not necessa
46 latedness, and attempts are made to identify cosegregation of genetic markers and phenotypes within t
47 ons-sex concordance in sib pairs with HD and cosegregation of HD and LWD-impelled a test of the hypot
48 n bipolar affective disorder (BPAD) revealed cosegregation of high numbers of EvC and Bipolar I (BPI)
49 bsequent lineage restrictions, an unexpected cosegregation of lymphoid and myeloid gene expression an
51 In each of these families there is complete cosegregation of mood disorder with a segment of chromos
52 this phenomenon occurs involves preferential cosegregation of nonparental chromatids of both chromoso
53 eviously linked to schizophrenia through the cosegregation of oculocutaneous albinism with psychosis
58 regation, since deletion of clp1/flp1 causes cosegregation of sister chromatids, when sister kinetoch
60 1ADE2 inserted into a YAC were identified by cosegregation of the ADE2 gene with the URA3-marked YAC.
61 inkage analysis of F2(SxR) male rats detects cosegregation of the alpha1 Na,K-ATPase locus with salt-
62 n F2 and two backcross populations indicated cosegregation of the augmented orf107 and urf209 process
64 did the seeds of the F1 hybrids, indicating cosegregation of the genes for rosette size and the germ
66 forbold locus-specific haplotyping to detect cosegregation of the locus haplotype with the phenotype,
68 milial PA, whole-exome sequencing identified cosegregation of the PA phenotype with the heterozygous
69 integrated into the nuclear genome, (2) show cosegregation of the resistance phenotype with the intro
71 s can be combined with data from analysis of cosegregation of the UCVs with cancer, co-occurrence of
72 D is prevented by missing data demonstrating cosegregation of the variants and incomplete knowledge a
76 associated genes and the ability to test for cosegregation of variants with disease through extended
79 limits their number and immortal DNA strand cosegregation that limits their accumulation of mutation
86 s and emphasizes the importance of observing cosegregation with deafness in large families to confirm
87 subjects, and no evidence for association or cosegregation with disease in family-based analyses.
89 ino acid position in multiple pedigrees, and cosegregation with disease in these pedigrees provide ev
90 g studies because they provide a way to test cosegregation with disease of variants that are too rare
94 cluded from the EDA locus by the lack of its cosegregation with polymorphic markers flanking the EDA
98 med transmission of the PIEZO1 mutations and cosegregation with the disease phenotype in all affected
101 edicted to be damaging were investigated for cosegregation with the low HDL-C trait in the entire ext
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