(Q73694533)

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

6 November 2019

title

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

1 reference

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6 November 2019

1

1 reference

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6 November 2019

author name string

Jaworski A

series ordinal

2

1 reference

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

6 November 2019

Connors TD

series ordinal

3

1 reference

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6 November 2019

Wells RD

series ordinal

4

1 reference

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

6 November 2019

language of work or name

English

0 references

publication date

27 February 2001

1 reference

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

Journal of Biological Chemistry

6 November 2019

published in

1 reference

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

6 November 2019

volume

276

1 reference

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

6 November 2019

issue

21

1 reference

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

6 November 2019

page(s)

18597-18604

1 reference

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

The molecular biology of polycystic kidney disease

6 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Autosomal dominant polycystic kidney disease: clues to pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Molecular genetics and mechanism of autosomal dominant polycystic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

A dominant mutation in the Ikaros gene leads to rapid development of leukemia and lymphoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Strong homophilic interactions of the Ig-like domains of polycystin-1, the protein product of an autosomal dominant polycystic kidney disease gene, PKD1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

The role of the polycystins in kidney development

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

PKD1 interacts with PKD2 through a probable coiled-coil domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Loss of heterozygosity in polycystic kidney disease with a missense mutation in the repeated region of PKD1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

The molecular basis of focal cyst formation in human autosomal dominant polycystic kidney disease type I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Loss of the polycystic kidney disease (PKD1) region of chromosome 16p13 in renal cyst cells supports a loss-of-function model for cyst pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

An unusual pattern of mutation in the duplicated portion of PKD1 is revealed by use of a novel strategy for mutation detection

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Gene conversion is a likely cause of mutation in PKD1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

DNA structural transitions within the PKD1 gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

DNA: Structure and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

H-DNA and related structures.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Tandem repeats finder: a program to analyze DNA sequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Multistranded DNA structures

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

A dominant negative allele of the Escherichia coli uvrD gene encoding DNA helicase II. A biochemical and genetic characterization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Mutations in uvrD induce the SOS response in Escherichia coli

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Intramolecular triplex formation of the purine.purine.pyrimidine type

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Studies on the ability of minor groove binders to induce supercoiling in DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Production of positively supercoiled DNA by netropsin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

The interaction of intercalators and groove-binding agents with DNA triple-helical structures: the influence of ligand structure, DNA backbone modifications and sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Drug binding to higher ordered DNA structures: netropsin complexation with a nucleic acid triple helix

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Influence of drug binding on DNA flexibility: a normal mode analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Flexible DNA: genetically unstable CTG.CAG and CGG.CCG from human hereditary neuromuscular disease genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Left-handed DNA in restriction fragments and a recombinant plasmid

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

21 January 2018

Left-handed DNA in vivo.

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Tetracycline promoter mutations decrease non-B DNA structural transitions, negative linking differences and deletions in recombinant plasmids in Escherichia coli.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Intramolecular DNA triplexes in supercoiled plasmids

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

The intrinsically unstable life of DNA triplet repeats associated with human hereditary disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Left-handed Z-DNA: structure and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Unambiguous demonstration of triple-helix-directed gene modification

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Mutagenesis in mammalian cells induced by triple helix formation and transcription-coupled repair

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Roles of topoisomerases in maintaining steady-state DNA supercoiling in Escherichia coli

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Conformational and thermodynamic properties of supercoiled DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Equilibrium distributions of topological states in circular DNA: interplay of supercoiling and knotting

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Simplification of DNA Topology Below Equilibrium Values by Type II Topoisomerases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Transcription-driven supercoiling of DNA: direct biochemical evidence from in vitro studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Transcription-induced hypersupercoiling of plasmid DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Supercoiling of the DNA template during transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Characterization of the Escherichia coli damage-independent UvrBC endonuclease activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

A model for a umuDC-dependent prokaryotic DNA damage checkpoint

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

The importance of repairing stalled replication forks

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

RecQ and RecJ process blocked replication forks prior to the resumption of replication in UV-irradiated Escherichia coli

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Mutation Detection in the Repeated Part of the PKD1 Gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Novel and recurrent mutations in the PKD1 (Polycystic Kidney disease) gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

Mutational analysis within the 3′ region of the PKD1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074/JBC.M100845200

21 January 2018

Identifiers

DOI

10.1074/JBC.M100845200

1 reference

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

6 November 2019

1 reference