(Q51996297)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9488501%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

title

Assessment of FMR1 expression by reverse transcriptase-polymerase chain reaction of KH domains (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9488501%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

1

1 reference

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9 November 2019

author name string

Y De Diego

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9488501%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

E Pintado

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9488501%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

publication date

1 February 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9488501%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

published in

Translational Research

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9488501%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

volume

131

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9488501%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9488501%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

page(s)

170-173

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9488501%20AND%20SRC:MED&resulttype=core&format=json

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

9 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3

Fragile X genotype characterized by an unstable region of DNA.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3

FMR1 protein: conserved RNP family domains and selective RNA binding

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3

The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3

Localized Bicaudal-C RNA encodes a protein containing a KH domain, the RNA binding motif of FMR1.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3

7 January 2021

RNA-protein complexes

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3

Essential role for KH domains in RNA binding: impaired RNA binding by a mutation in the KH domain of FMR1 that causes fragile X syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3

Three-dimensional structure and stability of the KH domain: molecular insights into the fragile X syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3

The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3

A heterogeneous set of FMR1 proteins is widely distributed in mouse tissues and is modulated in cell culture

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3

Characterization of FMR1 proteins isolated from different tissues

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3

Alternative splicing in the fragile X gene FMR1.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3

Instability of the CGG repeat at the FRAXA locus and variable phenotypic expression in a large fragile X pedigree.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3

Translational suppression by trinucleotide repeat expansion at FMR1.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-2143%2898%2990160-3