A polycystin‐2 (TRPP2) dimerization domain essential for the function of heteromeric polycystin complexes

A Giamarchi, S Feng, L Rodat‐Despoix, Y Xu… - The EMBO …, 2010 - embopress.org
Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutations in two
genes, PKD1 and PKD2, which encode polycystin‐1 (PC1) and polycystin‐2 (PC2) …

A polycystin-2 (TRPP2) dimerization domain essential for the function of heteromeric polycystin complexes

A Giamarchi, S Feng, L Rodat-Despoix… - The EMBO …, 2010 - eprints.whiterose.ac.uk
Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutations in two
genes, PKD1 and PKD2, which encode polycystin‐1 (PC1) and polycystin‐2 (PC2) …

A polycystin-2 (TRPP2) dimerization domain essential for the function of heteromeric polycystin complexes.

A Giamarchi, S Feng, L Rodat-Despoix, Y Xu… - EMBO Journal, 2010 - hal.science
Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutations in two
genes, PKD1 and PKD2, which encode polycystin-1 (PC1) and polycystin-2 (PC2) …

[HTML][HTML] A polycystin-2 (TRPP2) dimerization domain essential for the function of heteromeric polycystin complexes

A Giamarchi, S Feng, L Rodat-Despoix, Y Xu… - The EMBO …, 2010 - ncbi.nlm.nih.gov
Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutations in two
genes, PKD1 and PKD2, which encode polycystin-1 (PC1) and polycystin-2 (PC2) …

A polycystin-2 (TRPP2) dimerization domain essential for the function of heteromeric polycystin complexes

A Giamarchi, S Feng, L Rodat-Despoix, Y Xu… - EMBO Journal, 2010 - pure.mpg.de
Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutations in two
genes, PKD1 and PKD2, which encode polycystin-1 (PC1) and polycystin-2 (PC2) …

A polycystin-2 (TRPP2) dimerization domain essential for the function of heteromeric polycystin complexes.

A Giamarchi, S Feng, L Rodat-Despoix, Y Xu… - The EMBO …, 2010 - europepmc.org
Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutations in two
genes, PKD1 and PKD2, which encode polycystin-1 (PC1) and polycystin-2 (PC2) …

A polycystin-2 (TRPP2) dimerization domain essential for the function of heteromeric polycystin complexes

A Giamarchi, S Feng, L Rodat-Despoix, Y Xu… - EMBO Journal, 2010 - hero.epa.gov
Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutations in two
genes, PKD1 and PKD2, which encode polycystin-1 (PC1) and polycystin-2 (PC2) …

A polycystin-2 (TRPP2) dimerization domain essential for the function of heteromeric polycystin complexes

A Giamarchi, S Feng, L Rodat-Despoix… - The EMBO …, 2010 - pubmed.ncbi.nlm.nih.gov
Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutations in two
genes, PKD1 and PKD2, which encode polycystin-1 (PC1) and polycystin-2 (PC2) …

[HTML][HTML] A polycystin‐2 (TRPP2) dimerization domain essential for the function of heteromeric polycystin complexes

A Giamarchi, S Feng, L Rodat‐Despoix, Y Xu… - The EMBO …, 2010 - embopress.org
Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutations in two
genes, PKD1 and PKD2, which encode polycystin‐1 (PC1) and polycystin‐2 (PC2) …

A polycystin-2 (TRPP2) dimerization domain essential for the function of heteromeric polycystin complexes.

A Giamarchi, S Feng, L Rodat-Despoix, Y Xu… - The EMBO …, 2010 - europepmc.org
Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutations in two
genes, PKD1 and PKD2, which encode polycystin-1 (PC1) and polycystin-2 (PC2) …