Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesions (Q35881966)

10 August 2017

Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesions (English)

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10 August 2017

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E P Henske

1

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10 August 2017

B W Scheithauer

2

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10 August 2017

M P Short

3

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10 August 2017

R Wollmann

4

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10 August 2017

J Nahmias

5

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10 August 2017

N Hornigold

6

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10 August 2017

M van Slegtenhorst

7

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10 August 2017

C T Welsh

8

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10 August 2017

D J Kwiatkowski

9

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10 August 2017

language of work or name

English

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publication date

1 August 1996

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American Journal of Human Genetics

10 August 2017

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10 August 2017

59

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10 August 2017

2

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10 August 2017

400-406

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Linkage disequilibrium in the region of the autosomal dominant polycystic kidney disease gene (PKD1).

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914733

Report and abstracts of the Third International Workshop on Chromosome 9. Cambridge, United Kingdom, 9-11 April, 1994.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914733

Identification of tuberin, the tuberous sclerosis-2 product. Tuberin possesses specific Rap1GAP activity

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914733

A 5.4-Mb Continuous Pulsed-Field Gel Electrophoresis Map of Human 9q34.1 between ABL and D9S114, Including the Tuberous Sclerosis (TSC1) Region

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914733

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914733

Loss of heterozygosity in the tuberous sclerosis (TSC2) region of chromosome band 16p13 occurs in sporadic as well as TSC-associated renal angiomyolipomas

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914733

Genetic aspects of tuberous sclerosis in the west of Scotland

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914733

Phenotypes of the tuberous sclerosis complex with a revision of diagnostic criteria

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914733

A second-generation linkage map of the human genome

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914733

Evidence for genetic heterogeneity in tuberous sclerosis: one locus on chromosome 9 and at least one locus elsewhere

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914733

Construction of a GT polymorphism map of human 9q

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914733

5′ CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancers

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914733

Loss of heterozygosity on chromosome 16p13.3 in hamartomas from tuberous sclerosis patients.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914733

Two loci for tuberous sclerosis: one on 9q34 and one on 16p13.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914733

Apparent preferential loss of heterozygosity at TSC2 over TSC1 chromosomal region in tuberous sclerosis hamartomas

24 September 2018

1 reference

12 December 2020

Report and abstracts of the Fourth International Workshop on Human Chromosome 3 Mapping

1 reference

12 December 2020

A high-resolution linkage map of human 9q34.1.

1 reference

12 December 2020

1 reference

12 December 2020

A PCR-Based Genetic Linkage Map of Human Chromosome 16

1 reference

12 December 2020

9q34 loss of heterozygosity in a tuberous sclerosis astrocytoma suggests a growth suppressor-like activity also for the TSC1 gene

1 reference

12 December 2020

The tuberous sclerosis gene on chromosome 9q34 acts as a growth suppressor

1 reference

12 December 2020

A 500-kilobase region containing the tuberous sclerosis locus (TSC1) in a 1.7-megabase YAC and cosmid contig

1 reference

12 December 2020

Tuber and subependymal giant cell astrocytoma associated with tuberous sclerosis: an immunohistochemical, ultrastructural, and immunoelectron and microscopic study

1 reference

12 December 2020

Identifiers

1 reference

10 August 2017

PubMed publication ID

8755927

1 reference