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Role of primary cilia in the pathogenesis of polycystic kidney disease

Journal of the American Society of Nephrology, 2007-05, Vol.18 (5), p.1381-1388

Yoder, Bradley K

2007

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High-throughput genome editing and phenotyping facilitated by high resolution melting curve analysis

PloS one, 2014-12, Vol.9 (12), p.e114632

2014

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The Primary Cilium as a Complex Signaling Center

Current biology, 2009-07, Vol.19 (13), p.R526-R535

2009

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Single-Cell RNA Sequencing Identifies Candidate Renal Resident Macrophage Gene Expression Signatures across Species

Journal of the American Society of Nephrology, 2019-05, Vol.30 (5), p.767-781

2019

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MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis

The Journal of cell biology, 2011-03, Vol.192 (6), p.1023-1041

2011

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The Tumor-Associated Glycosyltransferase ST6Gal-I Regulates Stem Cell Transcription Factors and Confers a Cancer Stem Cell Phenotype

Cancer research (Chicago, Ill.), 2016-07, Vol.76 (13), p.3978-3988

2016

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Soluble levels of cytosolic tubulin regulate ciliary length control

Molecular biology of the cell, 2011-03, Vol.22 (6), p.806-816

2011

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Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function

PLoS genetics, 2005-10, Vol.1 (4), p.e53-e53

2005

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An incredible decade for the primary cilium: a look at a once-forgotten organelle

American journal of physiology. Renal physiology, 2005-12, Vol.289 (6), p.F1159-F1169

2005

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The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia

Journal of the American Society of Nephrology, 2002-10, Vol.13 (10), p.2508-2516

2002

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Disruption of Intraflagellar Transport in Adult Mice Leads to Obesity and Slow-Onset Cystic Kidney Disease

Current biology, 2007-09, Vol.17 (18), p.1586-1594

2007

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The primary cilium in cell signaling and cancer

Cancer research (Chicago, Ill.), 2006-07, Vol.66 (13), p.6463-6467

2006

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Ciliary proteins link basal body polarization to planar cell polarity regulation

Nature genetics, 2008-01, Vol.40 (1), p.69-77

2008

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Primary cilia disruption differentially affects the infiltrating and resident macrophage compartment in the liver

American journal of physiology: Gastrointestinal and liver physiology, 2018-06, Vol.314 (6), p.G677-G689

2018

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Inflammation and Fibrosis in Polycystic Kidney Disease

Kidney Development and Disease, 2017, Vol.60, p.323-344

2017

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Intraflagellar transport is essential for endochondral bone formation

Development (Cambridge), 2007-01, Vol.134 (2), p.307-316

2007

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Cilia-driven fluid flow in the zebrafish pronephros, brain and Kupffer's vesicle is required for normal organogenesis

Development (Cambridge), 2005-04, Vol.132 (8), p.1907-1921

2005

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Lack of Primary Cilia Primes Shear-Induced Endothelial-to-Mesenchymal Transition

Circulation research, 2011-04, Vol.108 (9), p.1093-1101

2011

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Role for intraflagellar transport in building a functional transition zone

EMBO reports, 2018-12, Vol.19 (12)

2018

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Hippocampal and cortical primary cilia are required for aversive memory in mice

PloS one, 2014-09, Vol.9 (9), p.e106576-e106576

2014

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Primary cilia enhance kisspeptin receptor signaling on gonadotropin-releasing hormone neurons

Proceedings of the National Academy of Sciences - PNAS, 2014-07, Vol.111 (28), p.10335-10340

2014

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Prioritized polycystic kidney disease drug targets and repurposing candidates from pre-cystic and cystic mouse Pkd2 model gene expression reversion

Molecular medicine (Cambridge, Mass.), 2023-05, Vol.29 (1), p.67-67, Article 67

2023

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Primary Cilia and Signaling Pathways in Mammalian Development, Health and Disease

Nephron. Physiology, 2009-01, Vol.111 (3), p.p39-p53

2009

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Leptin resistance is a secondary consequence of the obesity in ciliopathy mutant mice

Proceedings of the National Academy of Sciences - PNAS, 2013-05, Vol.110 (19), p.7796-7801

2013

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Dysfunctional cilia lead to altered ependyma and choroid plexus function, and result in the formation of hydrocephalus

Development (Cambridge), 2005-12, Vol.132 (23), p.5329-5339

2005

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Role of primary cilia in the pathogenesis of polycystic kidney disease

High-throughput genome editing and phenotyping facilitated by high resolution melting curve analysis

The Primary Cilium as a Complex Signaling Center

Single-Cell RNA Sequencing Identifies Candidate Renal Resident Macrophage Gene Expression Signatures across Species

MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis

The Tumor-Associated Glycosyltransferase ST6Gal-I Regulates Stem Cell Transcription Factors and Confers a Cancer Stem Cell Phenotype

Soluble levels of cytosolic tubulin regulate ciliary length control

Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function

An incredible decade for the primary cilium: a look at a once-forgotten organelle

The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia

Disruption of Intraflagellar Transport in Adult Mice Leads to Obesity and Slow-Onset Cystic Kidney Disease

The primary cilium in cell signaling and cancer

Ciliary proteins link basal body polarization to planar cell polarity regulation

Primary cilia disruption differentially affects the infiltrating and resident macrophage compartment in the liver

Inflammation and Fibrosis in Polycystic Kidney Disease

Intraflagellar transport is essential for endochondral bone formation

Cilia-driven fluid flow in the zebrafish pronephros, brain and Kupffer's vesicle is required for normal organogenesis

Lack of Primary Cilia Primes Shear-Induced Endothelial-to-Mesenchymal Transition

Role for intraflagellar transport in building a functional transition zone

Hippocampal and cortical primary cilia are required for aversive memory in mice

Primary cilia enhance kisspeptin receptor signaling on gonadotropin-releasing hormone neurons

Prioritized polycystic kidney disease drug targets and repurposing candidates from pre-cystic and cystic mouse Pkd2 model gene expression reversion

Primary Cilia and Signaling Pathways in Mammalian Development, Health and Disease

Leptin resistance is a secondary consequence of the obesity in ciliopathy mutant mice

Dysfunctional cilia lead to altered ependyma and choroid plexus function, and result in the formation of hydrocephalus

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