(Q40649650)

22 September 2017

Immortalized epithelial cells from human autosomal dominant polycystic kidney cysts (English)

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autosomal dominant polycystic kidney

22 September 2017

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1 reference

1 reference

https://api.crossref.org/works/10.1152/AJPRENAL.00310.2002

31 December 2023

author name string

Mahmoud Loghman-Adham

1

1 reference

22 September 2017

Barbara Kariuki

4

1 reference

22 September 2017

Jing Zhou

5

1 reference

22 September 2017

Surya M. Nauli

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12734101

31 December 2023

Carlos E. Soto

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12734101

31 December 2023

language of work or name

1 reference

6 May 2003

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full work available at URL

22 September 2017

https://digitalcommons.chapman.edu/cgi/viewcontent.cgi?article=1008&context=pharmacy_articles

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12734101

http://intl-ajprenal.physiology.org/cgi/content/abstract/285/3/F397

31 December 2023

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12734101

https://www.physiology.org/doi/pdf/10.1152/ajprenal.00310.2002

31 December 2023

1 reference

https://api.crossref.org/works/10.1152/AJPRENAL.00310.2002

American Journal of Physiology - Renal Physiology

31 December 2023

published in

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22 September 2017

285

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22 September 2017

F397-412

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22 September 2017

3

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describes a project that uses

22 September 2017

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Molecular genetics and pathogenesis of autosomal dominant polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Hereditary polycystic kidney disease (adult form): a microdissection study of two cases at an early stage of the disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

The genetics and physiology of polycystic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Transport function of the naturally occurring pathogenic polycystin-2 mutant, R742X.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Differentiated mammalian cell lines immortalized by temperature-sensitive tumor viruses

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Tissue culture of human kidney epithelial cells of proximal tubule origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Identification and localization of polycystin, the PKD1 gene product

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Polycystin-2, the protein mutated in autosomal dominant polycystic kidney disease (ADPKD), is a Ca2+-permeable nonselective cation channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Polycystic kidney disease: a predominance of giant nephrons

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Creation of human tumour cells with defined genetic elements

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Autosomal dominant polycystic kidney disease: clues to pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Anion secretion by the inner medullary collecting duct. Evidence for involvement of the cystic fibrosis transmembrane conductance regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

The T/t common exon of simian virus 40, JC, and BK polyomavirus T antigens can functionally replace the J-domain of the Escherichia coli DnaJ molecular chaperone

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Autosomal dominant polycystic kidney disease: molecular genetics and molecular pathogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

A conditionally immortalized cell line from murine proximal tubule

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Anion secretion drives fluid secretion by monolayers of cultured human polycystic cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Coordinate expression of the autosomal dominant polycystic kidney disease proteins, polycystin-2 and polycystin-1, in normal and cystic tissue.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Enhanced transformation of human fibroblasts by origin-defective simian virus 40.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Growth of Madin-Darby canine kidney epithelial cell (MDCK) line in hormone-supplemented, serum-free medium

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

A loss-of-function model for cystogenesis in human autosomal dominant polycystic kidney disease type 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Polycystin-2 is a novel cation channel implicated in defective intracellular Ca(2+) homeostasis in polycystic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Polycystin, the polycystic kidney disease 1 protein, is expressed by epithelial cells in fetal, adult, and polycystic kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Epithelial cell polarity and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Identification of renal podocytes in multiple species: higher vertebrates are vimentin positive/lower vertebrates are desmin positive

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00310.2002

Angiogenesis in autosomal-dominant polycystic kidney disease

21 January 2018

4

1 reference

https://api.crossref.org/works/10.1152/AJPRENAL.00310.2002

Monoclonal antibodies for high-resolution localization of NHE3 in adult and neonatal rat kidney

31 December 2023

5

1 reference

https://api.crossref.org/works/10.1152/AJPRENAL.00310.2002

Expression of aquaporins-1 and -2 during nephrogenesis and in autosomal dominant polycystic kidney disease

31 December 2023

11

1 reference

https://api.crossref.org/works/10.1152/AJPRENAL.00310.2002

Immortalization of virus-free human placental cells that express tissue-specific functions

31 December 2023

25

1 reference

https://api.crossref.org/works/10.1152/AJPRENAL.00310.2002

A new method for studying human polycystic kidney disease epithelia in culture

31 December 2023

42

1 reference

https://api.crossref.org/works/10.1152/AJPRENAL.00310.2002

31 December 2023

Identifiers

1 reference

22 September 2017

1 reference