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Regulatory Region SNP

Known as: Single Nucleotide Polymorphism in Regulatory Sequences, rSNP 
Single Nucleotide Polymorphism in Regulatory Sequences (Regulatory Region SNP) consists of a variation at an appreciable frequency between… Expand
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Abstract Here, we present the updated rSNPBase 3.0 database (http://rsnp3.psych.ac.cn), which provides human SNP-related… Expand
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2016
2016
Transcription factor binding specificity is crucial for proper target gene regulation. Motif discovery algorithms identify the… Expand
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Highly Cited
2015
Highly Cited
2015
MOTIVATION Genome-wide association studies revealed that most disease-associated single nucleotide polymorphisms (SNPs) are… Expand
Review
2013
Review
2013
Single nucleotide polymorphisms (SNPs) represent to the genetics variant most common founded in the human genome. These… Expand
2011
2011
We have proposed the RSi Research Cloud (RSi-Cloud), which enables integration of robot services with internet services. Until… Expand
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Highly Cited
2010
Highly Cited
2010
Motivation: Determining the functional impact of non-coding disease-associated single nucleotide polymorphisms (SNPs) identified… Expand
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Highly Cited
2010
Highly Cited
2010
Motivation: Determining the functional impact of non-coding disease-associated single nucleotide polymorphisms (SNPs) identified… Expand
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Review
2008
Review
2008
The most common form of genetic variation, single nucleotide polymorphisms or SNPs, can affect the way an individual responds to… Expand
Highly Cited
2006
Highly Cited
2006
We describe a pathogenetic mechanism underlying a variant form of the inherited blood disorder α thalassemia. Association studies… Expand
Review
2006
Review
2006
  • P. Buckland
  • Biochimica et biophysica acta
  • 2006
  • Corpus ID: 34552854
The search for the genetic variations underlying all human phenotypes is in its infancy but must be one of the long term goals of… Expand