(Q34740084)

4 August 2017

title

Variation in age at ESRD in autosomal dominant polycystic kidney disease (English)

1 reference

autosomal dominant polycystic kidney disease

4 August 2017

main subject

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autosomal dominant polycystic kidney

1 reference

inferred from title

author

Robert William Schrier

9

object named as

Robert W Schrier

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4 August 2017

Berenice Y Reed

1

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4 August 2017

Kim McFann

2

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4 August 2017

Mir R Bekheirnia

3

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4 August 2017

Niloofar Nobakhthaghighi

4

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4 August 2017

Amirali Masoumi

5

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4 August 2017

Ann M Johnson

6

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4 August 2017

Alireza A Shamshirsaz

7

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4 August 2017

Catherine L Kelleher

8

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4 August 2017

publication date

1 February 2008

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American Journal of Kidney Diseases

4 August 2017

published in

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4 August 2017

volume

51

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4 August 2017

issue

2

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4 August 2017

page(s)

173-183

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Modifier genes play a significant role in the phenotypic expression of PKD1.

4 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747334

Progressive loss of renal function is an age-dependent heritable trait in type 1 autosomal dominant polycystic kidney disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747334

Bilateral polycystic disease of the kidneys; a follow-up of two hundred and eighty-four patients and their families

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747334

A 2.5 kb polypyrimidine tract in the PKD1 gene contains at least 23 H-DNA-forming sequences.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747334

A stable, nonsense mutation associated with a case of infantile onset polycystic kidney disease 1 (PKD1).

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747334

Mutagenesis in mammalian cells induced by triple helix formation and transcription-coupled repair

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747334

Anticipation of age at renal death in autosomal dominant polycystic kidney disease (ADPKD)?

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747334

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747334

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747334

Anticipation in Huntington's disease is inherited through the male line but may originate in the female

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747334

Anticipation in myotonic dystrophy: fact or fiction?

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747334

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747334

Factors affecting the progression of renal disease in autosomal-dominant polycystic kidney disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747334

Anticipation in myotonic dystrophy: new light on an old problem

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747334

Role of keratinocyte growth factor in the pathogenesis of autosomal dominant polycystic kidney disease.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747334

Cardiac and renal effects of standard versus rigorous blood pressure control in autosomal-dominant polycystic kidney disease: results of a seven-year prospective randomized study

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747334

Anticipation of end stage renal disease in patients with autosomal dominant polycystic kidney disease in successive generations

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2747334

A complete mutation screen of the ADPKD genes by DHPLC

26 October 2018

1 reference

12 December 2020

Autosomal dominant polycystic kidney disease in childhood: a longitudinal study

1 reference

12 December 2020

Inheritance of a stable mutation in a family with early-onset disease

1 reference

12 December 2020

On new hypotheses about autosomal dominant polycystic kidney disease type 1

1 reference

12 December 2020

Is there evidence for anticipation in autosomal-dominant polycystic kidney disease?

1 reference

12 December 2020

Anticipation of end-stage renal disease in autosomal dominant polycystic kidney disease

1 reference

12 December 2020

Autosomal dominant polycystic kidney disease with anticipation and Caroli's disease associated with a PKD1 mutation Rapid Communication

1 reference

12 December 2020

10.1053/J.AJKD.2007.10.037

Identifiers

DOI

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4 August 2017

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4 August 2017

1 reference