[HTML][HTML] Ciliary exclusion of Polycystin-2 promotes kidney cystogenesis in an autosomal dominant polycystic kidney disease model

RV Walker, JL Keynton, DT Grimes… - Nature …, 2019 - nature.com
The human PKD2 locus encodes Polycystin-2 (PC2), a TRPP channel that localises to
several distinct cellular compartments, including the cilium. PKD2 mutations cause …

Ciliary exclusion of Polycystin-2 promotes kidney cystogenesis in an autosomal dominant polycystic kidney disease model.

RV Walker, JL Keynton, DT Grimes… - Nature …, 2019 - search.ebscohost.com
The human PKD2 locus encodes Polycystin-2 (PC2), a TRPP channel that localises to
several distinct cellular compartments, including the cilium. PKD2 mutations cause …

Ciliary exclusion of Polycystin-2 promotes kidney cystogenesis in an autosomal dominant polycystic kidney disease model.

RV Walker, JL Keynton, DT Grimes… - Nature …, 2019 - europepmc.org
The human PKD2 locus encodes Polycystin-2 (PC2), a TRPP channel that localises to
several distinct cellular compartments, including the cilium. PKD2 mutations cause …

Ciliary exclusion of Polycystin-2 promotes kidney cystogenesis in an autosomal dominant polycystic kidney disease model

RV Walker, JL Keynton, DT Grimes… - Nature …, 2019 - ideas.repec.org
The human PKD2 locus encodes Polycystin-2 (PC2), a TRPP channel that localises to
several distinct cellular compartments, including the cilium. PKD2 mutations cause …

[HTML][HTML] Ciliary exclusion of Polycystin-2 promotes kidney cystogenesis in an autosomal dominant polycystic kidney disease model

RV Walker, JL Keynton, DT Grimes… - Nature …, 2019 - ncbi.nlm.nih.gov
The human PKD2 locus encodes Polycystin-2 (PC2), a TRPP channel that localises to
several distinct cellular compartments, including the cilium. PKD2 mutations cause …

Ciliary exclusion of Polycystin-2 promotes kidney cystogenesis in an autosomal dominant polycystic kidney disease model

RV Walker, JL Keynton, DT Grimes… - Nature …, 2019 - cir.nii.ac.jp
抄録< jats: title> Abstract</jats: title>< jats: p> The human< jats: italic> PKD2</jats: italic>
locus encodes Polycystin-2 (PC2), a TRPP channel that localises to several distinct cellular …

[引用][C] Ciliary exclusion of Polycystin-2 promotes kidney cystogenesis in an autosomal dominant polycystic kidney disease model

RV Walker, JL Keynton, DT Grimes… - NATURE …, 2019 - qmro.qmul.ac.uk
Ciliary exclusion of Polycystin-2 promotes kidney cystogenesis in an autosomal dominant
polycystic kidney disease model Toggle navigation Login Toggle navigation Ciliary …

[PDF][PDF] Ciliary exclusion of Polycystin-2 promotes kidney cystogenesis in an autosomal dominant polycystic kidney disease model

RV Walker, JL Keynton, DT Grimes, V Sreekumar… - grimes-lab.com
The Pkd2lrm4 (E442G) point mutation was identified in an ENU-driven forward genetic
screen looking for left–right (LR) patterning mutants 37. During the establishment of LR …

Ciliary exclusion of Polycystin-2 promotes kidney cystogenesis in an autosomal dominant polycystic kidney disease model

RV Walker, JL Keynton, DT Grimes… - Nature …, 2019 - pubmed.ncbi.nlm.nih.gov
The human PKD2 locus encodes Polycystin-2 (PC2), a TRPP channel that localises to
several distinct cellular compartments, including the cilium. PKD2 mutations cause …

Ciliary exclusion of Polycystin-2 promotes kidney cystogenesis in an autosomal dominant polycystic kidney disease model

RV Walker, JL Keynton, DT Grimes… - Nature …, 2019 - econpapers.repec.org
The human PKD2 locus encodes Polycystin-2 (PC2), a TRPP channel that localises to
several distinct cellular compartments, including the cilium. PKD2 mutations cause …