(Q34327568)

1 August 2017

title

Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein (English)

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1 August 2017

16

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1 August 2017

21

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1 August 2017

Marie Mangelsdorf

4

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Nicholas K Moschonas

object named as

Nicholas K Moschonas

19

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Kerstin Kutsche

18

object named as

Kerstin Kutsche

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1 August 2017

20

Reiner Siebert

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1 August 2017

17

Grant R Sutherland

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1 August 2017

Theologia Sarafidou

1

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1 August 2017

Christina Kahl

2

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1 August 2017

Isabel Martinez-Garay

3

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1 August 2017

Stefan Gesk

5

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1 August 2017

Elizabeth Baker

6

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1 August 2017

Maria Kokkinaki

7

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1 August 2017

Polly Talley

8

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1 August 2017

Edna L Maltby

9

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1 August 2017

Lisa French

10

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1 August 2017

Lana Harder

11

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1 August 2017

Bernd Hinzmann

12

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1 August 2017

Carlo Nobile

13

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1 August 2017

Kathy Richkind

14

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1 August 2017

Merran Finnis

15

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1 August 2017

European Collaborative Consortium for the Study of ADLTE

22

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1 August 2017

publication date

1 July 2004

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1 August 2017

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1 August 2017

volume

84

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1 August 2017

issue

1

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1 August 2017

page(s)

69-81

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FHIT as tumor suppressor: mechanisms and therapeutic opportunities

1 August 2017

cites work

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

7 January 2021

Common fragile sites.

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

FMR1 gene and fragile X syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

The FMR2 gene, FRAXE and non-specific X-linked mental retardation: clinical and molecular aspects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

Physical linkage of the fragile site FRA11B and a Jacobsen syndrome chromosome deletion breakpoint in 11q23.3.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

Population cytogenetics of autosomal fragile sites.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

Autosomal folate sensitive fragile sites in normal and mentally retarded individuals in Greece

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

Microsatellite instability and deletion analysis of chromosome 10 in human prostate cancer.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

Identification of two distinct tumor-suppressor loci on the long arm of chromosome 10 in small cell lung cancer

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

Second stage of a genome scan of schizophrenia: study of five positive regions in an expanded sample

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

A novel gene, LGI1, from 10q24 is rearranged and downregulated in malignant brain tumors

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

A refined physical and EST map spanning 7.4 Mb of 10q24, a region involved in neurological disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

Sequence and structure-based prediction of eukaryotic protein phosphorylation sites

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

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%2FJ.YGENO.2003.12.017

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%2FJ.YGENO.2003.12.017

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

The cloning of FRAXF: trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

Co-localisation of CCG repeats and chromosome deletion breakpoints in Jacobsen syndrome: evidence for a common mechanism of chromosome breakage

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

Molecular basis of p(CCG)n repeat instability at the FRA16A fragile site locus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

A novel gene, FAM11A, associated with the FRAXF CpG island is transcriptionally silent in FRAXF full mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

Expression of the LGI1 gene product in astrocytic gliomas: downregulation with malignant progression

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

An Integrated Physical and Genetic Map Spanning Chromosome Band 10q24

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

A physical map of the human genome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

Initial sequencing and analysis of the human genome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

A new gene family (FAM9) of low-copy repeats in Xp22.3 expressed exclusively in testis: implications for recombinations in this region

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

A new technique for the assay of infectivity of human adenovirus 5 DNA

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

Isolation and characterisation of (AC)n microsatellite genetic markers from human chromosome 16

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.017

10.1016/J.YGENO.2003.12.017

7 January 2021

Identifiers

DOI

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1 August 2017

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