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First reported <i>TRIB1</i> copy number loss in myelodysplastic syndrome (MDS) revealed by single nucleotide polymorphism array (SNP-array) with patient-matched control. [PDF]

Leuk Res Rep
Chi K, Song L.
europepmc   +1 more source

Applications and Challenges of Digital Health in Rheumatology

iNew Medicine, EarlyView.
Xiao‐Xiao Li, Xue‐Er Cheng, Ming‐Ming Zhang, Peng Wang, Hai‐Feng Pan   +4 more
wiley   +1 more source

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Single Nucleotide Polymorphisms

2006
The identification of DNA variation or gene mutations, which contributes to or determines a disease, has been a major research focus, as it describes the underlying inherited disease components. With the human genome being sequenced, the reference sequence is now at hand, facilitating the systematic identification of DNA variation and its subsequent ...
Ulrich Broeckel, Martin J. Hessner
  +7 more sources

Single-Nucleotide Polymorphism Mapping

2006
Single-nucleotide polymorphism (SNP) mapping is the easiest and most reliable way to map genes in Caenorhabditis elegans. SNPs are extremely dense and usually have no associated phenotype, making them ideal markers for mapping. SNP mapping has three steps.
M Wayne, Davis, Marc, Hammarlund
openaire   +2 more sources

Polymorphism and single nucleotide polymorphisms ( SNP s)

BJU International, 2013
Greg Shaw
openaire   +3 more sources

Inherently electroactive graphene oxide nanoplatelets as labels for single nucleotide polymorphism detection.

ACS Nano, 2012
Graphene materials are being widely used in electrochemistry due to their versatility and excellent properties as platforms for biosensing. However, no records show the use of inherent redox properties of graphene oxide as a label for detection. Here for
A. Bonanni, Chun Kiang Chua, Guanjia Zhao, Zdenek Sofer, M. Pumera   +4 more
semanticscholar   +1 more source

Hypertension and single nucleotide polymorphisms

Current Hypertension Reports, 2000
Hypertension is a common, complex disease phenotype that has been intensively studied to identify susceptibility loci in humans. Candidate genes continue to be uncovered via genetic analysis in model organisms through linkage analysis with families and/or sib-pairs and through association studies using sequence variants in genes that play a role in key
M J, Rieder, D A, Nickerson
openaire   +2 more sources