(Q28270283)

English

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

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scholarly article

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

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fragile X syndrome

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author name string

C Verheij

1

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C E Bakker

2

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E de Graaff

3

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J Keulemans

4

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R Willemsen

5

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A J Verkerk

6

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H Galjaard

7

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A J Reuser

8

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A T Hoogeveen

9

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B A Oostra

10

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language of work or name

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publication date

24 June 1993

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363

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722-4

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6431

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Prevalence of the fragile-X syndrome in mentally retarded boys in a Swedish county.

1 reference

https://api.crossref.org/works/10.1038%2F363722A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Population incidence and segregation ratios in the Martin-Bell syndrome.

1 reference

https://api.crossref.org/works/10.1038%2F363722A0

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F363722A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2F363722A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Fragile X genotype characterized by an unstable region of DNA.

1 reference

https://api.crossref.org/works/10.1038%2F363722A0

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F363722A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Isolation of sequences that span the fragile X and identification of a fragile X-related CpG island

1 reference

https://api.crossref.org/works/10.1038%2F363722A0

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F363722A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Single-step purification of polypeptides expressed in Escherichia coli as fusions with glutathione S-transferase

1 reference

https://api.crossref.org/works/10.1038%2F363722A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Solid Phase Peptide Synthesis. I. The Synthesis of a Tetrapeptide

1 reference

https://api.crossref.org/works/10.1038%2F363722A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Alternative splicing in the fragile X gene FMR1.

1 reference

https://api.crossref.org/works/10.1038%2F363722A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome.

1 reference

https://api.crossref.org/works/10.1038%2F363722A0

7 January 2021

based on heuristic

inferred from DOI database lookup

A point mutation in the FMR-1 gene associated with fragile X mental retardation

1 reference

https://api.crossref.org/works/10.1038%2F363722A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Immunocytochemistry of lysosomal hydrolases and their precursor forms in normal and mutant human cells

1 reference

https://api.crossref.org/works/10.1038%2F363722A0

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/363722A0

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Consolidated OpenCitations Corpus – April 2017

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OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

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Springer Nature article ID

10.1038/363722a0

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