Single-nucleotide polymorphisms can cause different structural folds of mRNA. - Wikidata - awgldk - TriplyDB

Single-nucleotide polymorphisms can cause different structural folds of mRNA.

Single-nucleotide polymorphisms can cause different structural folds of mRNA.

http://www.wikidata.org/entity/Q30727714

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Limb-girdle muscular dystrophy type 2H associated with mutation in TRIM32, a putative E3-ubiquitin-ligase gene SERKAL syndrome: an autosomal-recessive disorder caused by a loss-of-function mutation in WNT4 Splicing in action: assessing disease causing sequence changes No influence of the P-glycoprotein polymorphisms MDR1 G2677T/A and C3435T on the virological and immunological response in treatment naïve HIV-positive patients Evidence for selection on synonymous mutations affecting stability of mRNA secondary structure in mammals Association of Common Variants in MMPs with Periodontitis Risk A Variant of GJD2, Encoding for Connexin 36, Alters the Function of Insulin Producing β-Cells Alternative CHRNB4 3'-UTRs mediate the allelic effects of SNP rs1948 on gene expression RNAsnp: efficient detection of local RNA secondary structure changes induced by SNPs.Design of a bioactive small molecule that targets r(AUUCU) repeats in spinocerebellar ataxia 10 Schizophrenia genes, gene expression, and neuropathology: on the matter of their convergence Codon bias and the folding dynamics of the cystic fibrosis transmembrane conductance regulator.The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration ALDH1A2 (RALDH2) genetic variation in human congenital heart disease.Nucleotide sequence analyses of the MRP1 gene in four populations suggest negative selection on its coding region.Identification and analysis of single nucleotide polymorphisms (SNPs) in the mosquito Anopheles funestus, malaria vector.Conflicting selection pressures on synonymous codon use in yeast suggest selection on mRNA secondary structures The impact of the nucleosome code on protein-coding sequence evolution in yeast C-Reactive protein gene variants are associated with postoperative C-reactive protein levels after coronary artery bypass surgery.Polymorphic variation in TIRAP is not associated with susceptibility to childhood TB but may determine susceptibility to TBM in some ethnic groups Polymorphisms in DNA repair genes and MDR1 and the risk for non-Hodgkin lymphoma.Laying a solid foundation for Manhattan--'setting the functional basis for the post-GWAS era'.Search for informative polymorphisms in candidate genes: clock genes and circadian behaviour in blue tits Association analysis of retinoic acid receptor beta (RARbeta) gene with high myopia in Chinese subjects.Polymorphisms in estrogen receptors predict the risk of male infertility: a meta-analysis ABCB1/MDR1 gene polymorphisms as a prognostic factor in colorectal cancer.The association between Toll-like receptor 2 single-nucleotide polymorphisms and hepatocellular carcinoma susceptibility Mutational analysis of class III receptor tyrosine kinases (C-KIT, C-FMS, FLT3) in idiopathic myelofibrosis.Associations between estrogen receptor-beta polymorphisms and endometriosis risk: a meta-analysis Sounds of silence: synonymous nucleotides as a key to biological regulation and complexity.Polymorphisms of estrogen receptors and risk of depression: therapeutic implications.Engineering microorganisms based on molecular evolutionary analysis: a succinate production case study Use of a simplified nomogram to individualize digoxin dosing versus standard dosing practices in patients with heart failure.Risk for premenstrual dysphoric disorder is associated with genetic variation in ESR1, the estrogen receptor alpha gene.Association of PPARγ2 polymorphisms with carcass and meat quality traits in a Pietrain x Jinhua F2 population A silent exonic SNP in kdm3a affects nucleic acids structure but does not regulate experimental autoimmune encephalomyelitis.Antidepressant drug discovery in the postgenomic era.Clinical relevance of multiple single-nucleotide polymorphisms in Pneumocystis jirovecii Pneumonia: development of a multiplex PCR-single-base-extension methodology.ProMMP-2: TIMP-1 complexes identified in plasma of healthy individuals Genomic variants in exons and introns: identifying the splicing spoilers.

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P2860

Single-nucleotide polymorphisms can cause different structural folds of mRNA.

http://www.wikidata.org/entity/Q30727714

description

1999 nî lūn-bûn

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1999 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

1999 թվականի հուլիսին հրատարակված գիտական հոդված

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1999年の論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

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1999年论文

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name

Single-nucleotide polymorphisms can cause different structural folds of mRNA.

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Single-nucleotide polymorphisms can cause different structural folds of mRNA.

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type

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Single-nucleotide polymorphisms can cause different structural folds of mRNA.

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Single-nucleotide polymorphisms can cause different structural folds of mRNA.

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Single-nucleotide polymorphisms can cause different structural folds of mRNA.

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Single-nucleotide polymorphisms can cause different structural folds of mRNA.

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Proceedings of the National Academy of Sciences of the United States of America

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Single-nucleotide polymorphisms can cause different structural folds of mRNA.

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J P Basilion

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L X Shen

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V P Stanton

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P2860

Conserved terminal hairpin sequences of histone mRNA precursors are not involved in duplex formation with the U7 RNA but act as a target site for a distinct processing factor

A conserved helical element is essential for internal initiation of translation of hepatitis C virus RNA

The structure of an RNA pseudoknot that causes efficient frameshifting in mouse mammary tumor virus

Structure and dynamics of the iron responsive element RNA: implications for binding of the RNA by iron regulatory binding proteins

Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei

Specificity of ribonucleoprotein interaction determined by RNA folding during complex formulation

Identification of the iron-responsive element for the translational regulation of human ferritin mRNA

An inhibitor of the Tat/TAR RNA interaction that effectively suppresses HIV-1 replication

Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome

Modified deoxyoligonucleotides stable to exonuclease degradation in serum.

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single-nucleotide polymorphism

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