An origin of DNA replication in the promoter region of the human fragile X mental retardation (FMR1) gene (Q35642112)

9 August 2017

title

An origin of DNA replication in the promoter region of the human fragile X mental retardation (FMR1) gene (English)

1 reference

9 August 2017

3

Walter Doerfler

1 reference

9 August 2017

5

Ellen Fanning

1 reference

9 August 2017

Steven J Gray

1

1 reference

9 August 2017

Jeannine Gerhardt

series ordinal

2

1 reference

9 August 2017

Lawrence E Small

series ordinal

4

1 reference

9 August 2017

language of work or name

English

0 references

publication date

13 November 2006

1 reference

Molecular and Cellular Biology

9 August 2017

published in

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9 August 2017

volume

27

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9 August 2017

issue

2

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9 August 2017

page(s)

426-437

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DNA replication: the unbearable lightness of origins

9 August 2017

cites work

1 reference

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27 July 2018

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Heterochromatin on the inactive X chromosome delays replication timing without affecting origin usage

27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine

27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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27 July 2018

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25 September 2018

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Coordination of replication and transcription along a Drosophila chromosome.

25 September 2018

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Occupancy and synergistic activation of the FMR1 promoter by Nrf-1 and Sp1 in vivo

25 September 2018

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25 September 2018

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25 September 2018

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Same origins of DNA replication function on the active and inactive human X chromosomes

25 September 2018

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Multiple functional elements comprise a Mammalian chromosomal replicator

25 September 2018

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CpG methylation modifies the genetic stability of cloned repeat sequences

25 September 2018

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A decade of molecular studies of fragile X syndrome

25 September 2018

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Identification of a binding region for human origin recognition complex proteins 1 and 2 that coincides with an origin of DNA replication

25 September 2018

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Methylation mosaicism of 5'-(CGG)(n)-3' repeats in fragile X, premutation and normal individuals

25 September 2018

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CGG/CCG repeats exhibit orientation-dependent instability and orientation-independent fragility in Saccharomyces cerevisiae

25 September 2018

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FISH-detected delay in replication timing of mutated FMR1 alleles on both active and inactive X-chromosomes.

25 September 2018

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25 September 2018

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Triplet repeats form secondary structures that escape DNA repair in yeast

25 September 2018

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Initiation of DNA replication at CpG islands in mammalian chromosomes

25 September 2018

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Characterization of the full fragile X syndrome mutation in fetal gametes

25 September 2018

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Normal phenotype in two brothers with a full FMR1 mutation.

25 September 2018

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Greater susceptibility to mutations in lagging strand of DNA replication in Escherichia coli than in leading strand.

25 September 2018

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Mapping of an origin of DNA replication near the transcriptional promoter of the human HPRT gene

25 September 2018

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12 December 2020

Association of fragile X syndrome with delayed replication of the FMR1 gene

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12 December 2020

Trinucleotide repeats affect DNA replication in vivo

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12 December 2020

Major DNA replication initiation sites in the c-myc locus in human cells

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12 December 2020

The origin recognition complex marks a replication origin in the human TOP1 gene promoter

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12 December 2020

At physiological pH, d(CCG)15 forms a hairpin containing protonated cytosines and a distorted helix

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12 December 2020

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12 December 2020

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12 December 2020

Transition in specification of embryonic metazoan DNA replication origins

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12 December 2020

Expansions of CAG repeat tracts are frequent in a yeast mutant defective in Okazaki fragment maturation

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12 December 2020

Transition from premutation to full mutation in fragile X syndrome is likely to be prezygotic

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12 December 2020

Identifiers

DOI

10.1128/MCB.01382-06

1 reference

9 August 2017

1 reference

9 August 2017

1 reference