Anomalous rapid electrophoretic mobility of DNA containing triplet repeats associated with human disease genes.
about
Mapping of an origin of DNA replication in the promoter of fragile X gene FMR1Structural roles of CTG repeats in slippage expansion during DNA replicationLength-dependent energetics of (CTG)n and (CAG)n trinucleotide repeats.Molecular Correlates and Recent Advancements in the Diagnosis and Screening of FMR1-Related DisordersMolecular basis of genetic instability of triplet repeatsIntrinsic curvature associated with the coordinately regulated anthrax toxin gene promoters.Transcription increases the deletion frequency of long CTG.CAG triplet repeats from plasmids in Escherichia coli.Myotonic dystrophy: molecular windows on a complex etiology.The role of interruptions in polyQ in the pathology of SCA1.A high mobility group protein binds to long CAG repeat tracts and establishes their chromatin organization in Saccharomyces cerevisiae.Ethidium Bromide Modifies The Agarose Electrophoretic Mobility of CAG•CTG Alternative DNA Structures Generated by PCR.Improved single-strand DNA sizing accuracy in capillary electrophoresis.Structural analysis of slipped-strand DNA (S-DNA) formed in (CTG)n. (CAG)n repeats from the myotonic dystrophy locus.A theoretical model for the prediction of sequence-dependent nucleosome thermodynamic stability.Sequence-dependent DNA curvature and flexibility from scanning force microscopy images.Chemotherapeutic deletion of CTG repeats in lymphoblast cells from DM1 patients.Standardization of PCR amplification for fragile X trinucleotide repeat measurements.Trinucleotide repeat instability: genetic features and molecular mechanisms.FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome.Molecular dynamics studies of trinucleotide repeat DNA involved in neurodegenerative disorders.Flexible DNA: genetically unstable CTG.CAG and CGG.CCG from human hereditary neuromuscular disease genes.Cloning, characterization, and properties of seven triplet repeat DNA sequences.CTG triplet repeats from human hereditary diseases are dominant genetic expansion products in Escherichia coli.A crystallographic approach to DNA bending: prediction of nucleosome formation by DNA triple repeats and other repetitive sequences
P2860
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P2860
Anomalous rapid electrophoretic mobility of DNA containing triplet repeats associated with human disease genes.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年学术文章
@wuu
1995年学术文章
@zh
1995年学术文章
@zh-cn
1995年学术文章
@zh-hans
1995年学术文章
@zh-my
1995年学术文章
@zh-sg
1995年學術文章
@yue
1995年學術文章
@zh-hant
name
Anomalous rapid electrophoreti ...... ated with human disease genes.
@en
Anomalous rapid electrophoreti ...... ated with human disease genes.
@nl
type
label
Anomalous rapid electrophoreti ...... ated with human disease genes.
@en
Anomalous rapid electrophoreti ...... ated with human disease genes.
@nl
prefLabel
Anomalous rapid electrophoreti ...... ated with human disease genes.
@en
Anomalous rapid electrophoreti ...... ated with human disease genes.
@nl
P2093
P356
P1433
P1476
Anomalous rapid electrophoreti ...... ated with human disease genes.
@en
P2093
Chastain PD 2nd
Eichler EE
P304
16125-16131
P356
10.1021/BI00049A027
P407
P577
1995-12-01T00:00:00Z