An optimized procedure for the design and evaluation of Ecotilling assays (Q30484692)

17 November 2017

An optimized procedure for the design and evaluation of Ecotilling assays (English)

1 reference

17 November 2017

3

1 reference

17 November 2017

2

Anita Brandstätter

1 reference

17 November 2017

PMCID

2586031

language of work or name

English

0 references

publication date

30 October 2008

1 reference

17 November 2017

1 reference

17 November 2017

9

1 reference

17 November 2017

510

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2164-9-510

17 November 2017

0 references

cites work

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MiRSNPs or MiR-polymorphisms, new players in microRNA mediated regulation of the cell: Introducing microRNA pharmacogenomics

20 June 2018

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The impact of next-generation sequencing technology on genetics

20 June 2018

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Singleton SNPs in the human genome and implications for genome-wide association studies

20 June 2018

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JASPAR, the open access database of transcription factor-binding profiles: new content and tools in the 2008 update

20 June 2018

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Genome-wide association studies in aging-related processes such as diabetes mellitus, atherosclerosis and cancer

20 June 2018

1 reference

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Genomewide association analysis of coronary artery disease

20 June 2018

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Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

20 June 2018

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A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

20 June 2018

1 reference

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Medical sequencing at the extremes of human body mass

20 June 2018

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Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.

20 June 2018

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PolymiRTS Database: linking polymorphisms in microRNA target sites with complex traits

20 June 2018

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ESPERR: learning strong and weak signals in genomic sequence alignments to identify functional elements

20 June 2018

1 reference

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The potential of electrophoretic mobility shift assays for clinical mutation detection

20 June 2018

1 reference

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High-throughput discovery of rare human nucleotide polymorphisms by Ecotilling

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586031

Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels

20 June 2018

1 reference

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MPromDb: an integrated resource for annotation and visualization of mammalian gene promoters and ChIP-chip experimental data

20 June 2018

1 reference

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EPD in its twentieth year: towards complete promoter coverage of selected model organisms

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586031

TRANSFAC and its module TRANSCompel: transcriptional gene regulation in eukaryotes

20 June 2018

1 reference

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Automated band mapping in electrophoretic gel images using background information

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586031

MatInspector and beyond: promoter analysis based on transcription factor binding sites

20 June 2018

1 reference

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Rare variant hypothesis for multifactorial inheritance: susceptibility to colorectal adenomas as a model

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586031

Systematic discovery of regulatory motifs in human promoters and 3' UTRs by comparison of several mammals

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586031

Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586031

Assessing computational tools for the discovery of transcription factor binding sites

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586031

Multiple rare variants in different genes account for multifactorial inherited susceptibility to colorectal adenomas

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586031

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586031

Quantitative genetic variation: a post-modern view

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586031

Efficient discovery of DNA polymorphisms in natural populations by Ecotilling.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586031

Prediction of mammalian microRNA targets

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586031

Large-scale discovery of induced point mutations with high-throughput TILLING.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586031

High-throughput screening for induced point mutations.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586031

Mutation detection using a novel plant endonuclease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586031

A novel method to develop highly specific models for regulatory units detects a new LTR in GenBank which contains a functional promoter.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586031

Studies of association of variants near the HHEX, CDKN2A/B, and IGF2BP2 genes with type 2 diabetes and impaired insulin release in 10,705 Danish subjects: validation and extension of genome-wide association studies.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586031

An optimized ecotilling protocol for polyploids or pooled samples using a capillary electrophoresis system.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586031

Analysis of TP53 gene mutations in human lung cancer: comparison of capillary electrophoresis single strand conformation polymorphism assay with denaturing gradient gel electrophoresis and direct sequencing.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2586031

Polymorphic Polymorphic MicroRNA-Target Interactions: A Novel Source of Phenotypic Variation

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18973671

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Endonucleolytic mutation analysis by internal labeling (EMAIL)

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18973671

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2164-9-510

1 reference

PMCID

2586031

Dimensions Publication ID

17 November 2017

0 references

1 reference

17 November 2017

1 reference

PMCID

2586031