Pkd1 unusual DNA conformations are recognized by nucleotide excision repair (Q73694533)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11279140%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

Pkd1 unusual DNA conformations are recognized by nucleotide excision repair (English)

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6 November 2019

1

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6 November 2019

author name string

Jaworski A

series ordinal

2

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6 November 2019

Connors TD

series ordinal

3

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6 November 2019

Wells RD

series ordinal

4

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6 November 2019

language of work or name

English

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publication date

27 February 2001

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Journal of Biological Chemistry

6 November 2019

published in

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6 November 2019

volume

276

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6 November 2019

issue

21

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6 November 2019

page(s)

18597-18604

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The molecular biology of polycystic kidney disease

6 November 2019

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Analysis of the genomic sequence for the autosomal dominant polycystic kidney disease (PKD1) gene predicts the presence of a leucine-rich repeat. The American PKD1 Consortium (APKD1 Consortium)

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Gene conversion is a likely cause of mutation in PKD1.

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Role of the Escherichia coli nucleotide excision repair proteins in DNA replication

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Tandem repeats finder: a program to analyze DNA sequences

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Differential DNA secondary structure-mediated deletion mutation in the leading and lagging strands

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Multistranded DNA structures

21 January 2018

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The B- to Z-DNA equilibrium in vivo is perturbed by biological processes

21 January 2018

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An intramolecular triplex in the human gamma-globin 5'-flanking region is altered by point mutations associated with hereditary persistence of fetal hemoglobin

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uvrD mutations enhance tandem repeat deletion in the Escherichia coli chromosome via SOS induction of the RecF recombination pathway

21 January 2018

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Relationship between Escherichia coli growth and deletions of CTG.CAG triplet repeats in plasmids.

21 January 2018

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Cloning, characterization and properties of plasmids containing CGG triplet repeats from the FMR-1 gene

21 January 2018

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Stability of a CTG/CAG trinucleotide repeat in yeast is dependent on its orientation in the genome

21 January 2018

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Stability of the human fragile X (CGG)(n) triplet repeat array in Saccharomyces cerevisiae deficient in aspects of DNA metabolism

21 January 2018

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The high-resolution crystal structure of a 24-kDa gyrase B fragment from E. coli complexed with one of the most potent coumarin inhibitors, clorobiocin

21 January 2018

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Studies on the binding of actinomycin D to DNA and DNA model polymers

21 January 2018

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Crystal structure of the 2:1 complex between d(GAAGCTTC) and the anticancer drug actinomycin D

21 January 2018

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Drug-DNA sequence-dependent interactions analysed by electric linear dichroism

21 January 2018

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Intramolecular triplex formation of the purine.purine.pyrimidine type

21 January 2018

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Interaction of drugs with Z-DNA: cooperative binding of actinomycin D or actinomine to the left-handed forms of poly(dG-dC).poly(dG-dC) and poly(dG-m5dC).poly(dG-m5dC) reverses the conformation of the helix

21 January 2018

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The effect of intercalating drugs on the kinetics of the B to Z transition of poly(dG-dC).

21 January 2018

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Binding of an antitumor drug to DNA, Netropsin and C-G-C-G-A-A-T-T-BrC-G-C-G

21 January 2018

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Molecular structure of the netropsin-d(CGCGATATCGCG) complex: DNA conformation in an alternating AT segment

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Direct evidence for the effect of transcription on local DNA supercoiling in vivo

21 January 2018

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Transcription-induced hypersupercoiling of plasmid DNA.

21 January 2018

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Supercoiling of the DNA template during transcription

21 January 2018

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21 January 2018

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The importance of repairing stalled replication forks

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21 January 2018

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Nucleotide excision repair affects the stability of long transcribed (CTG*CAG) tracts in an orientation-dependent manner in Escherichia coli

21 January 2018

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Mismatch repair in Escherichia coli enhances instability of (CTG)n triplet repeats from human hereditary diseases

21 January 2018

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21 January 2018

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Identification of mutations in the repeated part of the autosomal dominant polycystic kidney disease type 1 gene, PKD1, by long-range PCR.

21 January 2018

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Mutation detection in the repeated part of the PKD1 gene

21 January 2018

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Mutation detection of PKD1 identifies a novel mutation common to three families with aneurysms and/or very-early-onset disease

21 January 2018

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DGGE screening of PKD1 gene reveals novel mutations in a large cohort of 146 unrelated patients

21 January 2018

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Identification of mutations in the duplicated region of the polycystic kidney disease 1 gene (PKD1) by a novel approach

21 January 2018

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Three novel mutations of the PKD1 gene in Italian families with autosomal dominant polycystic kidney disease

21 January 2018

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A stable, nonsense mutation associated with a case of infantile onset polycystic kidney disease 1 (PKD1).

21 January 2018

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Novel and recurrent mutations in the PKD1 (polycystic kidney disease) gene

21 January 2018

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Autosomal dominant polycystic kidney disease (ADPKD) in an Italian family carrying a novel nonsense mutation and two missense changes in exons 44 and 45 of the PKD1 Gene

21 January 2018

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A novel nonsense mutation in the PKD1 gene (C3817T) is associated with autosomal dominant polycystic kidney disease (ADPKD) in a large three-generation Italian family

21 January 2018

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Human gene mutations. Gene symbol: PKD1. Disease: Polycystic kidney disease.

21 January 2018

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Detection of a novel nonsense mutation and an intragenic polymorphism in the PKD1 gene of a Cypriot family with autosomal dominant polycystic kidney disease

21 January 2018

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Mutational analysis within the 3′ region of the PKD1 gene

21 January 2018

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Recurrence of the PKD1 nonsense mutation Q4041X in Spanish, Italian, and British families

21 January 2018

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A novel splice-acceptor site mutation (IVS13-2A>T) of polycystic kidney disease 1 (PKD1) gene resulting in an RNA processing defect with a 74-nucleotide deletion in exon 14 of the mRNA transcript

21 January 2018

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Splicing mutations of the polycystic kidney disease 1 (PKD1) gene induced by intronic deletion

21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.M100845200

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11279140%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference