(Q48059267)

8 February 2018

title

Three novel mutations of the NF1 gene detected by temperature gradient gel electrophoresis of exons 5 and 8. (English)

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8 February 2018

author

Peter Robinson

2

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8 February 2018

author name string

Horn D

1

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8 February 2018

Böddrich A

3

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8 February 2018

Buske A

4

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8 February 2018

Tinschert S

5

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8 February 2018

Nürnberg P

6

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8 February 2018

publication date

1 October 1996

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8 February 2018

published in

Electrophoresis

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8 February 2018

volume

17

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8 February 2018

page(s)

1559-1563

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8 February 2018

issue

10

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8 February 2018

Identification and characterization of the gene for neurofibromatosis type 1.

cites work

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Genomic organization of the neurofibromatosis 1 gene (NF1).

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Neurofibromatosis 1 (NF1) mRNAs expressed in the central nervous system are differentially spliced in the 5' part of the gene.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

cDNA cloning of the type 1 neurofibromatosis gene: complete sequence of the NF1 gene product

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

The neurofibromatosis type 1 gene encodes a protein related to GAP

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Benign neurofibromas in type 1 neurofibromatosis (NF1) show somatic deletions of the NF1 gene

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Molecular genetics of neurofibromatosis type 1 (NF1)

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Identification of neurofibromatosis 1 (NF1) homologous loci by direct sequencing, fluorescence in situ hybridization, and PCR amplification of somatic cell hybrids.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

[31] Detection and localization of single base changes by denaturing gradient gel electrophoresis

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Mutation detection by denaturing gradient gel electrophoresis (DGGE).

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Molecular analysis of phenylketonuria in Denmark: 99% of the mutations detected by denaturing gradient gel electrophoresis.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Characterization of four mutations in the neurofibromatosis type 1 gene by denaturing gradient gel electrophoresis (DGGE)

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Temperature-gradient gel electrophoresis of nucleic acids: analysis of conformational transitions, sequence variations, and protein-nucleic acid interactions.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Detecting base pair substitutions in DNA fragments by temperature-gradient gel electrophoresis

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Two recurrent nonsense mutations and a 4 bp deletion in a quasi-symmetric element in exon 37 of the NF1 gene

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Recurrent 2-bp deletion in exon 10c of the NF1 gene in two cases of von Recklinghausen neurofibromatosis

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Reduced neurofibromin content but normal GAP activity in a patient with neurofibromatosis type 1 caused by a five base pair duplication in exon 12b of the NF1 gene

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Computational simulation of DNA melting and its application to denaturing gradient gel electrophoresis

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Psoralen-modified oligonucleotide primers improve detection of mutations by denaturing gradient gel electrophoresis and provide an alternative to GC-clamping

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Characterization of six mutations in exon 37 of neurofibromatosis type 1 gene

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

An RsaI polymorphism in the transcribed region of the neurofibromatosis (NF1)-gene.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

The skipping of constitutive exons in vivo induced by nonsense mutations

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Characterisation of inherited and sporadic mutations in neurofibromatosis type-1

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Characterisation of a novel splice donor mutation affecting position +1 in intron 18 of the NF-1 gene

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Characterization of an intron 31 splice junction mutation in the neurofibromatosis type 1 (NF1) gene.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Exon skipping associated with A-->G transition at +4 of the IVS33 splice donor site of the neurofibromatosis type 1 (NF1) gene.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

The rapid detection of unknown mutations in nucleic acids.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Detection of 81 of 81 known mouse beta-globin promoter mutations with T4 endonuclease VII--the EMC method

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Bi-directional dideoxy fingerprinting (Bi-ddF): a rapid method for quantitative detection of mutations in genomic regions of 300-600 bp

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150171011

7 January 2021

Identifiers

DOI

10.1002/ELPS.1150171011

1 reference

8 February 2018

PubMed ID

8957181

1 reference

8 February 2018