ライフサイエンスコーパス: gene location

1 0 centimorgans, corresponding to the ANGPTL3 gene location.

2 esentative features from raw HM signals over gene locations.

3 ng that the dependence of synteny erosion on gene location along the centromere-telomere axis either

4 s between two ecotypes and identifying actin gene locations among yeast artificial chromosomes.

5 For each analysed SNP, gene location and >200 bp of surrounding annotated seque

6 Here we analyze the relationship between gene location and expression in Caenorhabditis elegans a

7 The distribution of gene location and gene expression in these sites indicat

8 For each analyzed SNP, gene location and over 200 bp of surrounding annotated s

9 d evolutionary analyses based on genome-wide gene location and protein sequence information.

10 on to the classical eukaryote rule of random gene location and provide paradigmatic exemplars with wh

11 mutations is dependent partially on mutation gene location and resulting efficiency of nonsense-media

12 model parameter estimates including disease-gene location and the age of the disease-predisposing mu

13 eats database that relates tandem repeats to gene locations and disease genes of the human genome.

14 ded into three groups according to their tau gene locations and effects on tau.

15 ion, bioinformatics has attempted to predict gene locations and functions in cyberspace prior to expe

16 lving tumor type and subtype, mutation type, gene location, and specific patient subpopulations targe

17 The human gene location at 2q21.1 was deduced from the map locatio

18 -modified RNAP was not detected at any virus gene location at 3 dpi and was detected at levels only s

19 ibutions that depend on the DNA copy number, gene location, cell doubling time, and the rates of tran

20 henotype and models phenotype differences as gene location changes.

21 selection for slow translation at particular gene locations, executed by suboptimal codon pairs.

22 Overlap in the gene locations for substance dependence and BMI suggests

23 Useful annotations include possible gene locations, homologies to known genes, and gene sign

24 ation, including SNP name, exact values, and gene location, if applicable.

25 -7 has been designated as IL-24 based on its gene location in the IL-10 locus and its mRNA expression

26 A gene location in the pericentromeric region of chromosom

27 signals and inserted individually into three gene locations in each of the two attenuated rHPIV1 back

28 In the search for the gene location of a monogenic disorder, multiplicity adju

29 fected to different extents depending on the gene location of the repeat expansion.

30 matics approach to define the structures and gene locations of the 71 members of the human SCAN domai

31 uman EAP as a probe, we identified the ENPEP gene location on human chromosome 4q25 by polymerase cha

32 SNP pleiotropic status was associated with gene location (p = 0.024; pleiotropic SNPs more often ex

33 equently both the intrinsic kinetics and the gene location play an important role in accounting for t

34 ing genomic, protein, DNA and RNA sequences, gene locations, RNA-editing sites, putative protein fami

35 n 2 strains can involve numerous chromosomal gene locations simultaneously, resulting in the transfer

36 tatus, little is known about the dynamics of gene location that accompany large-scale changes in gene

37 yzed, it was found that there was no general gene location that could be targeted to minimize or maxi

38 At present the STBMS1 locus is the only gene location that has been supported; however, others h

39 Here, we examine patterns in gene locations to infer large-scale features of bacteria

40 d replacement of a tetRA element in the fliA gene location using lambda-Red-mediated recombination.

41 osomal proteins, and the correlation of MRP3 gene locations with loci associated with disorders of en