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Ciliary membrane proteins traffic through the Golgi via a Rabep1/GGA1/Arl3-dependent mechanism

Nature communications, 2014-11, Vol.5 (1), p.5482-5482, Article 5482

2014

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Inhibition of histone deacetylase 6 activity reduces cyst growth in polycystic kidney disease

Kidney international, 2016-07, Vol.90 (1), p.90-99

2016

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Fibrocystin/Polyductin releases a C-terminal fragment that translocates into mitochondria and suppresses cystogenesis

Nature communications, 2023-10, Vol.14 (1), p.6513-6513, Article 6513

2023

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Polycystin‐1 dependent regulation of polycystin‐2 via GRP94, a member of HSP90 family that resides in the endoplasmic reticulum

The FASEB journal, 2021-10, Vol.35 (10), p.e21865-n/a

2021

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A genetic screen in Drosophila reveals an unexpected role for the KIP1 ubiquitination-promoting complex in male fertility

PLoS genetics, 2020-12, Vol.16 (12), p.e1009217-e1009217

2020

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Polycystin Signaling Is Required for Directed Endothelial Cell Migration and Lymphatic Development

Cell reports (Cambridge), 2014-05, Vol.7 (3), p.634-644

2014

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Refining the Developmental Window That Determines Different Kinetics of Cystogenesis After Pkd2 Inactivation in Mice: FR-PO248

Journal of the American Society of Nephrology, 2022-11, Vol.33 (11S), p.394-394

2022

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Pkd1 and Pkd2 are required for normal placental development

PloS one, 2010-09, Vol.5 (9), p.e12821

2010

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NEDD4-family E3 ligase dysfunction due to PKHD1/Pkhd1 defects suggests a mechanistic model for ARPKD pathobiology

Scientific reports, 2017-08, Vol.7 (1), p.7733-16, Article 7733

2017

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Loss of Polycystin Function in Lymphatic Cells Impair CTP1a Expression and Fatty Acid Uptake: PO1242

Journal of the American Society of Nephrology, 2021-10, Vol.32 (10S), p.401-401

2021

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The polycystin complex mediates Wnt/Ca(2+) signalling

Nature cell biology, 2016-07, Vol.18 (7), p.752

2016

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A Novel Pattern of Mutation in Uromodulin Disorders: Autosomal Dominant Medullary Cystic Kidney Disease Type 2, Familial Juvenile Hyperuricemic Nephropathy, and Autosomal Dominant Glomerulocystic Kidney Disease

American journal of kidney diseases, 2005-07, Vol.46 (1), p.52-57

2005

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4181 THE AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE PROTEIN, FPC, RELEASES MITOCHONDRIA LOCALISING FRAGMENTS INVOLVED IN PREVENTING CYSTOGENESIS

Nephrology, dialysis, transplantation, 2023-06, Vol.38 (Supplement_1)

2023

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Cleavage of Pkhd1 Results in a Small Fragment That Localizes and Functions Within Mitochondria: FR-PO281

Journal of the American Society of Nephrology, 2022-11, Vol.33 (11S), p.402-402

2022

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Mice With a Genomic Deletion of Pkhd1 Exons 3-67 Have Minimal Renal Manifestations but Evidence of Transcriptional Network Changes by snRNA Sequencing: FR-PO282

Journal of the American Society of Nephrology, 2022-11, Vol.33 (11S), p.402-402

2022

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Generation of Mice Expressing an N-Terminal SNAP-Tagged Pkd1 Allele: FR-PO257

Journal of the American Society of Nephrology, 2022-11, Vol.33 (11S), p.396-396

2022

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A novel ARPKD mouse model with near-complete deletion of the Polycystic Kidney and Hepatic Disease 1 (Pkhd1) genomic locus presents with multiple phenotypes but not renal cysts

Kidney international, 2023-09, Vol.104 (3), p.611-616

2023

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Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotype

American journal of human genetics, 2022-01, Vol.109 (1), p.136-156

2022

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A novel model of autosomal recessive polycystic kidney questions the role of the fibrocystin C-terminus in disease mechanism

Kidney international, 2017-11, Vol.92 (5), p.1130-1144

2017

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TWEAK Signaling Pathway Blockade Slows Cyst Growth and Disease Progression in Autosomal Dominant Polycystic Kidney Disease

Journal of the American Society of Nephrology, 2021-08, Vol.32 (8), p.1913-1932

2021

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A cleavage product of Polycystin-1 is a mitochondrial matrix protein that affects mitochondria morphology and function when heterologously expressed

Scientific reports, 2018-02, Vol.8 (1), p.2743-19, Article 2743

2018

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Tracking Polycystin2 In Vivo Using a Novel Engineered Pkd2-HALO Allele: FR-PO252

Journal of the American Society of Nephrology, 2022-11, Vol.33 (11S), p.395-395

2022

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Polycystin-2-dependent transcriptome reveals early response of autosomal dominant polycystic kidney disease

Physiological genomics, 2023-11, Vol.55 (11), p.565

2023

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GDNF drives rapid tubule morphogenesis in a novel 3D in vitro model for ADPKD

Journal of cell science, 2020-07, Vol.133 (14)

2020

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GDNF drives rapid tubule morphogenesis in novel 3D in vitro model for ADPKD

Journal of cell science, 2020-01

2020

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Ciliary membrane proteins traffic through the Golgi via a Rabep1/GGA1/Arl3-dependent mechanism

Inhibition of histone deacetylase 6 activity reduces cyst growth in polycystic kidney disease

Fibrocystin/Polyductin releases a C-terminal fragment that translocates into mitochondria and suppresses cystogenesis

Polycystin‐1 dependent regulation of polycystin‐2 via GRP94, a member of HSP90 family that resides in the endoplasmic reticulum

A genetic screen in Drosophila reveals an unexpected role for the KIP1 ubiquitination-promoting complex in male fertility

Polycystin Signaling Is Required for Directed Endothelial Cell Migration and Lymphatic Development

Refining the Developmental Window That Determines Different Kinetics of Cystogenesis After Pkd2 Inactivation in Mice: FR-PO248

Pkd1 and Pkd2 are required for normal placental development

NEDD4-family E3 ligase dysfunction due to PKHD1/Pkhd1 defects suggests a mechanistic model for ARPKD pathobiology

Loss of Polycystin Function in Lymphatic Cells Impair CTP1a Expression and Fatty Acid Uptake: PO1242

The polycystin complex mediates Wnt/Ca(2+) signalling

A Novel Pattern of Mutation in Uromodulin Disorders: Autosomal Dominant Medullary Cystic Kidney Disease Type 2, Familial Juvenile Hyperuricemic Nephropathy, and Autosomal Dominant Glomerulocystic Kidney Disease

4181 THE AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE PROTEIN, FPC, RELEASES MITOCHONDRIA LOCALISING FRAGMENTS INVOLVED IN PREVENTING CYSTOGENESIS

Cleavage of Pkhd1 Results in a Small Fragment That Localizes and Functions Within Mitochondria: FR-PO281

Mice With a Genomic Deletion of Pkhd1 Exons 3-67 Have Minimal Renal Manifestations but Evidence of Transcriptional Network Changes by snRNA Sequencing: FR-PO282

Generation of Mice Expressing an N-Terminal SNAP-Tagged Pkd1 Allele: FR-PO257

A novel ARPKD mouse model with near-complete deletion of the Polycystic Kidney and Hepatic Disease 1 (Pkhd1) genomic locus presents with multiple phenotypes but not renal cysts

Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotype

A novel model of autosomal recessive polycystic kidney questions the role of the fibrocystin C-terminus in disease mechanism

TWEAK Signaling Pathway Blockade Slows Cyst Growth and Disease Progression in Autosomal Dominant Polycystic Kidney Disease

A cleavage product of Polycystin-1 is a mitochondrial matrix protein that affects mitochondria morphology and function when heterologously expressed

Tracking Polycystin2 In Vivo Using a Novel Engineered Pkd2-HALO Allele: FR-PO252

Polycystin-2-dependent transcriptome reveals early response of autosomal dominant polycystic kidney disease

GDNF drives rapid tubule morphogenesis in a novel 3D in vitro model for ADPKD

GDNF drives rapid tubule morphogenesis in novel 3D in vitro model for ADPKD

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