(Q35881966)

10 August 2017

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

1 reference

10 August 2017

1 reference

E P Henske

1

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10 August 2017

B W Scheithauer

2

1 reference

10 August 2017

M P Short

3

1 reference

10 August 2017

R Wollmann

4

1 reference

10 August 2017

J Nahmias

5

1 reference

10 August 2017

N Hornigold

6

1 reference

10 August 2017

M van Slegtenhorst

7

1 reference

10 August 2017

C T Welsh

8

1 reference

10 August 2017

D J Kwiatkowski

9

1 reference

10 August 2017

language of work or name

English

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publication date

1 August 1996

1 reference

American Journal of Human Genetics

10 August 2017

1 reference

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