MedMesh.i
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Serveur d'exploration sur la télématique - Checkpoint (PubMed)

Index « MedMesh.i » - entrée « Base Sequence »
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Attention, site généré par des moyens informatiques à partir de corpus bruts.
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Base Composition < Base Sequence < Bayes Theorem  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 5.
Ident.Authors (with country if any)Title
000166 (2014) Sara Duarte-Pereira [Portugal] ; Sarah S. Silva [Portugal] ; Luísa Azevedo [Portugal] ; Luísa Castro [Portugal] ; Ant Nio Amorim [Portugal] ; Raquel M. Silva [Portugal]NAMPT and NAPRT1: novel polymorphisms and distribution of variants between normal tissues and tumor samples.
000211 (2014) Renato Liguori [Italie] ; Sandro Quaranta [Italie] ; Rosanna Di Fiore [Italie] ; Ausilia Elce [Italie] ; Giuseppe Castaldo [Italie] ; Felice Amato [Italie]A novel polymorphism in the PAI-1 gene promoter enhances gene expression. A novel pro-thrombotic risk factor?
000272 (2012) Luzinete C B. Faria [Brésil] ; Andréa S L. Rocha ; João H. Kleinschmidt ; Márcio C. Silva-Filho ; Edson Bim ; Roberto H. Herai ; Michel E B. Yamagishi ; Reginaldo PalazzoIs a genome a codeword of an error-correcting code?
000307 (2011) Sara P. Garcia [Portugal] ; Armando J. PinhoMinimal absent words in four human genome assemblies.
000966 (????) Loredana M. Genovese [Italie] ; Filippo Geraci ; Marco PellegriniSpeedHap: an accurate heuristic for the single individual SNP haplotyping problem with many gaps, high reading error rate and low coverage.

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