(Q51741625)

11 April 2018

editorial

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review article

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title

The diversity of PKD1 alleles: implications for disease pathogenesis and genetic counseling. (English)

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11 April 2018

author name string

Richard N Sandford

series ordinal

1

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11 April 2018

language of work or name

English

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publication date

1 April 2009

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11 April 2018

published in

Kidney International

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11 April 2018

volume

75

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11 April 2018

issue

8

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11 April 2018

page(s)

765-767

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11 April 2018

https://scigraph.springernature.com/pub.10.1038/ki.2009.17

exact match

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cites work

Approaches to testing new treatments in autosomal dominant polycystic kidney disease: insights from the CRISP and HALT-PKD studies

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.17

7 January 2021

Comprehensive molecular diagnostics in autosomal dominant polycystic kidney disease

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https://api.crossref.org/works/10.1038%2FKI.2009.17

7 January 2021

Role of primary cilia in the pathogenesis of polycystic kidney disease

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https://api.crossref.org/works/10.1038%2FKI.2009.17

7 January 2021

Genotype-phenotype correlations in autosomal dominant and autosomal recessive polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.17

7 January 2021

Cyst number but not the rate of cystic growth is associated with the mutated gene in autosomal dominant polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.17

7 January 2021

Bilineal disease and trans-heterozygotes in autosomal dominant polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.17

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.17

7 January 2021

Evaluating the clinical utility of a molecular genetic test for polycystic kidney disease.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.17

7 January 2021

The Position of the Polycystic Kidney Disease 1 (PKD1) Gene Mutation Correlates with the Severity of Renal Disease

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.17

7 January 2021

Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.17

7 January 2021

Lowering of Pkd1 expression is sufficient to cause polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.17

7 January 2021

Incompletely penetrant PKD1 alleles suggest a role for gene dosage in cyst initiation in polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.17

7 January 2021

Prenatal diagnosis of autosomal dominant polycystic kidney disease (PKD1) presenting in utero and prognosis for very early onset disease

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.17

7 January 2021

Perinatal deaths in a family with autosomal dominant polycystic kidney disease and a PKD2 mutation

1 reference

https://api.crossref.org/works/10.1038%2FKI.2009.17

7 January 2021

Identifiers

DOI

10.1038/KI.2009.17

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11 April 2018

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11 April 2018