(Q49044766)

18 February 2018

title

Quantification of NF1 transcripts reveals novel highly expressed splice variants (English)

1 reference

18 February 2018

author

Jo Vandesompele

2

1 reference

18 February 2018

Ludwine Messiaen

4

object named as

Ludwine Messiaen

1 reference

18 February 2018

author name string

Ina Vandenbroucke

1

1 reference

18 February 2018

Anne De Paepe

3

1 reference

18 February 2018

language of work or name

English

0 references

publication date

1 July 2002

1 reference

18 February 2018

published in

FEBS Letters

1 reference

18 February 2018

volume

522

1 reference

18 February 2018

issue

1-3

1 reference

18 February 2018

page(s)

71-76

1 reference

18 February 2018

Identification and characterization of transcripts from the neurofibromatosis 1 region: the sequence and genomic structure of EVI2 and mapping of other transcripts

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Expression of two new protein isoforms of the neurofibromatosis type 1 gene product, neurofibromin, in muscle tissues.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Developmental regulation of a neuron-specific neurofibromatosis 1 isoform.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Alternative splicing of exons 29 and 30 in the neurofibromatosis type 1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Molecular cloning of a cDNA coding for neurofibromatosis type 1 protein isoform lacking the domain related to ras GTPase-activating protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Quantification of splice variants using real-time PCR

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Exon 10b of the NF1 gene represents a mutational hotspot and harbors a recurrent missense mutation Y489C associated with aberrant splicing.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Cold shock induces the insertion of a cryptic exon in the neurofibromatosis type 1 (NF1) mRNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Quantitative mRNA analysis of five C-terminal splice variants of the human 5-HT4 receptor in the central nervous system by TaqMan real time RT-PCR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Identification and tissue distribution of two differentially spliced variants of the rat carnitine transporter OCTN2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

The protein product of the neurofibromatosis type 1 gene is expressed at highest abundance in neurons, Schwann cells, and oligodendrocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

The neurofibromatosis type 1 gene encodes a protein related to GAP

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

An alternatively-spliced mRNA in the carboxy terminus of the neurofibromatosis type 1 (NF1) gene is expressed in muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Mutations affecting mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Exhaustive mutation analysis of the NF1 gene allows identification of 95% of mutations and reveals a high frequency of unusual splicing defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Minor lesion mutational spectrum of the entire NF1 gene does not explain its high mutability but points to a functional domain upstream of the GAP-related domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Differential localization of the neurofibromatosis 1 (NF1) gene product, neurofibromin, with the F-actin or microtubule cytoskeleton during differentiation of telencephalic neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Splicing regulation as a potential genetic modifier

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Gene structure prediction and alternative splicing analysis using genomically aligned ESTs

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Isoforms of Jun kinase are differentially expressed and activated in human monocyte/macrophage (THP-1) cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Neurofibromin is enriched in the endoplasmic reticulum of CNS neurons

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

New function for NF1 tumor suppressor

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Illegitimate splicing of the NF1 gene in healthy individuals mimics mutation-induced splicing alterations in NF1 patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

RT-PCR splicing analysis of the NF1 open reading frame

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

The molecular basis of disease variability among cystic fibrosis patients carrying the 3849+10 kb C-->T mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

Variable levels of normal RNA in different fetal organs carrying a cystic fibrosis transmembrane conductance regulator splicing mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

A novel isoform of the neurofibromatosis type-1 mRNA and a switch of isoforms during murine cell differentiation and proliferation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2802%2902887-9

10.1016/S0014-5793(02)02887-9

7 January 2021

Identifiers

DOI

1 reference

18 February 2018

1 reference

18 February 2018