(Q48056738)

8 February 2018

title

The molecular basis of focal cyst formation in human autosomal dominant polycystic kidney disease type I. (English)

1 reference

8 February 2018

autosomal dominant polycystic kidney disease

main subject

0 references

autosomal dominant polycystic kidney

1 reference

Qian F

1

1 reference

8 February 2018

Watnick TJ

series ordinal

2

1 reference

8 February 2018

Onuchic LF

series ordinal

3

1 reference

8 February 2018

Germino GG

series ordinal

4

1 reference

8 February 2018

language of work or name

English

0 references

publication date

1 December 1996

1 reference

8 February 2018

published in

Cell

1 reference

8 February 2018

volume

87

1 reference

8 February 2018

issue

6

1 reference

8 February 2018

page(s)

979-987

1 reference

8 February 2018

Analysis of the genomic sequence for the autosomal dominant polycystic kidney disease (PKD1) gene predicts the presence of a leucine-rich repeat. The American PKD1 Consortium (APKD1 Consortium)

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Polycystic disease of kidney and liver presenting in childhood

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Genetic heterogeneity of polycystic kidney disease in Bulgaria.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Evidence for a third genetic locus for autosomal dominant polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Autosomal dominant polycystic kidney disease: evidence for the existence of a third locus in a Portuguese family

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

The polycystic kidney disease 1 gene encodes a 14 kb transcript and lies within a duplicated region on chromosome 16. The European Polycystic Kidney Disease Consortium

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Clonal analysis of human colorectal tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Somatic mutations of the von Hippel-Lindau disease tumour suppressor gene in non-familial clear cell renal carcinoma

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Autosomal dominant polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Clonality in myeloproliferative disorders: analysis by means of the polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Toad urinary bladder epithelial cells in culture: maintenance of epithelial structure, sodium transport, and response to hormones

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domains

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Localization of a murine recessive polycystic kidney disease mutation and modifying loci that affect disease severity

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Polycystic kidney disease: The complete structure of the PKD1 gene and its protein

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Autosomal dominant polycystic kidney disease: localization of the second gene to chromosome 4q13-q23

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Counselling under genetic heterogeneity: a practical approach.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Splicing mutations of the polycystic kidney disease 1 (PKD1) gene induced by intronic deletion

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Genetic Heterogeneity of Polycystic Kidney Disease in Europe1

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Pausing in simian virus 40 DNA replication by a sequence containing (dG-dA)27.(dT-dC)27

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Characterization of the Han:SPRD rat model for hereditary polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Characterization and expression of a cDNA encoding the human androgen receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Langerhans'-cell histiocytosis (histiocytosis X)--a clonal proliferative disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

Triple helix formation inhibits transcription elongation in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2981793-6

7 January 2021

10.1016/S0092-8674(00)81793-6

Identifiers

DOI

1 reference

8 February 2018

1 reference

8 February 2018