Characterization of FMR1 promoter elements by in vivo-footprinting analysis. (Q35250383)

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4 November 2019

title

Characterization of FMR1 promoter elements by in vivo-footprinting analysis (English)

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4 November 2019

3

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4 November 2019

author name string

S Schwemmle

1

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4 November 2019

E de Graaff

2

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4 November 2019

D Gläser

4

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4 November 2019

D Wöhrle

5

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4 November 2019

I Kennerknecht

6

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4 November 2019

W Just

7

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4 November 2019

B A Oostra

8

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4 November 2019

W Döerfler

9

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4 November 2019

W Vogel

10

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4 November 2019

P Steinbach

11

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4 November 2019

language of work or name

English

0 references

publication date

1 June 1997

1 reference

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American Journal of Human Genetics

4 November 2019

published in

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4 November 2019

volume

60

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4 November 2019

issue

6

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4 November 2019

page(s)

1354-1362

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Characterization and localization of the FMR-1 gene product associated with fragile X syndrome

4 November 2019

cites work

1 reference

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High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndrome

12 July 2018

1 reference

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Cloning of Nrf1, an NF-E2-related transcription factor, by genetic selection in yeast

12 July 2018

1 reference

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Fragile X syndrome unstable element, p(CCG)n, and other simple tandem repeat sequences are binding sites for specific nuclear proteins

12 July 2018

1 reference

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12 July 2018

1 reference

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Instability of the CGG repeat and expression of the FMR1 protein in a male fragile X patient with a lung tumor.

12 July 2018

1 reference

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A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

12 July 2018

1 reference

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Cytosine methylation does not affect binding of transcription factor Sp1

12 July 2018

1 reference

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Enhancers and transcription factors in the control of gene expression.

12 July 2018

1 reference

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Genomic sequencing and methylation analysis by ligation mediated PCR.

12 July 2018

1 reference

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DNA replication origin and transcriptional enhancer in c-myc gene share the c-myc protein binding sequences

12 July 2018

1 reference

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Identification and characterization of a novel transcription factor participating in the expression of eukaryotic initiation factor 2 alpha

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716109

Sequence-specific DNA binding by the c-Myc protein

12 July 2018

1 reference

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Max: a helix-loop-helix zipper protein that forms a sequence-specific DNA-binding complex with Myc

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716109

Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome

12 July 2018

1 reference

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Intracellular leucine zipper interactions suggest c-Myc hetero-oligomerization

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716109

Molecular heterogeneity of the fragile X syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716109

Absence of expression of the FMR-1 gene in fragile X syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716109

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716109

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716109

Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716109

DNA methylation represses FMR-1 transcription in fragile X syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716109

Methylation analysis of CGG sites in the CpG island of the human FMR1 gene

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716109

Normal phenotype in two brothers with a full FMR1 mutation.

12 July 2018

1 reference

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In vitro DNA methylation inhibits FMR-1 promoter.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716109

Molecular analysis of mutations in the gene FMR-1 segregating in fragile X families.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716109

Tissue-specific expression of a FMR1/beta-galactosidase fusion gene in transgenic mice.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716109

Sp1 transcription factor binds DNA and activates transcription even when the binding site is CpG methylated

26 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9199556

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/515456

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9199556%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9199556%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

PubMed publication ID

9199556

1 reference