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PRDM16 controls a brown fat/skeletal muscle switch

Nature, 2008-08, Vol.454 (7207), p.961-967

2008

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Estimating the selective effects of heterozygous protein-truncating variants from human exome data

Nature genetics, 2017-05, Vol.49 (5), p.806-810

2017

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Differential requirements of tubulin genes in mammalian forebrain development

PLoS genetics, 2019-08, Vol.15 (8), p.e1008243

2019

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NEK8 Links the ATR-Regulated Replication Stress Response and S Phase CDK Activity to Renal Ciliopathies

Molecular cell, 2013-08, Vol.51 (4), p.423-439

2013

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Amyloid accelerates tau propagation and toxicity in a model of early Alzheimer's disease

Acta neuropathologica communications, 2015-03, Vol.3 (1), p.14, Article 14

2015

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Mutation mapping and identification by whole-genome sequencing

Genome research, 2012-08, Vol.22 (8), p.1541-1548

2012

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Loss of function of Colgalt1 disrupts collagen post-translational modification and causes musculoskeletal defects

Disease models & mechanisms, 2019-06, Vol.12 (6)

2019

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Inv acts as a molecular anchor for Nphp3 and Nek8 in the proximal segment of primary cilia

Cytoskeleton (Hoboken, N.J.), 2010-02, Vol.67 (2), p.112-119

2010

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zebrafish foxj1a transcription factor regulates cilia function in response to injury and epithelial stretch

Proceedings of the National Academy of Sciences - PNAS, 2010-10, Vol.107 (43), p.18499-18504

2010

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TAT-mediated PRDX6 protein transduction protects against eye lens epithelial cell death and delays lens opacity

American Journal of Physiology: Cell Physiology, 2008-03, Vol.294 (3), p.C842-C855

2008

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Optimizing Genomic Methods for Mapping and Identification of Candidate Variants in ENU Mutagenesis Screens Using Inbred Mice

G3 : genes - genomes - genetics, 2018-02, Vol.8 (2), p.401-409

2018

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Nek8 Regulates the Expression and Localization of Polycystin-1 and Polycystin-2

Journal of the American Society of Nephrology, 2008-03, Vol.19 (3), p.469-476

2008

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Loss of the Ciliary Kinase Nek8 Causes Left-Right Asymmetry Defects

Journal of the American Society of Nephrology, 2013-01, Vol.24 (1), p.100-112

2013

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ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterning

Nature communications, 2015-01, Vol.6 (1), p.6023-6023, Article 6023

2015

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Mutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in Mice

G3 : genes - genomes - genetics, 2016-08, Vol.6 (8), p.2479-2487

2016

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Impaired Organic Anion Transport in Kidney and Choroid Plexus of Organic Anion Transporter 3 (Oat3 (Slc22a8)) Knockout Mice

The Journal of biological chemistry, 2002-07, Vol.277 (30), p.26934-26943

2002

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Cholesterol metabolism is required for intracellular hedgehog signal transduction in vivo

PLoS genetics, 2011-09, Vol.7 (9), p.e1002224

2011

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Improvement of ENU Mutagenesis Efficiency Using Serial Injection and Mismatch Repair Deficiency Mice

PloS one, 2016-07, Vol.11 (7), p.e0159377

2016

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Spiny mice activate unique transcriptional programs after severe kidney injury regenerating organ function without fibrosis

iScience, 2021-11, Vol.24 (11), p.103269, Article 103269

2021

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Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease

The Journal of clinical investigation, 2002-02, Vol.109 (4), p.533-540

2002

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A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafish

Development (Cambridge), 2002-12, Vol.129 (24), p.5839-5846

2002

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A spontaneous Fatp4/Scl27a4 splice site mutation in a new murine model for congenital ichthyosis

PloS one, 2012-11, Vol.7 (11), p.e50634-e50634

2012

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Reelin Mediates Hippocampal Cajal-Retzius Cell Positioning and Infrapyramidal Blade Morphogenesis

Journal of developmental biology, 2020-09, Vol.8 (3), p.1

2020

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Dysfunction of intraflagellar transport-A causes hyperphagia-induced obesity and metabolic syndrome

Disease models & mechanisms, 2016-07, Vol.9 (7), p.789-798

2016

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Gata4 Is Necessary for Normal Pulmonary Lobar Development

American journal of respiratory cell and molecular biology, 2007-04, Vol.36 (4), p.391-397

2007

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PRDM16 controls a brown fat/skeletal muscle switch

Estimating the selective effects of heterozygous protein-truncating variants from human exome data

Differential requirements of tubulin genes in mammalian forebrain development

NEK8 Links the ATR-Regulated Replication Stress Response and S Phase CDK Activity to Renal Ciliopathies

Amyloid accelerates tau propagation and toxicity in a model of early Alzheimer's disease

Mutation mapping and identification by whole-genome sequencing

Loss of function of Colgalt1 disrupts collagen post-translational modification and causes musculoskeletal defects

Inv acts as a molecular anchor for Nphp3 and Nek8 in the proximal segment of primary cilia

zebrafish foxj1a transcription factor regulates cilia function in response to injury and epithelial stretch

TAT-mediated PRDX6 protein transduction protects against eye lens epithelial cell death and delays lens opacity

Optimizing Genomic Methods for Mapping and Identification of Candidate Variants in ENU Mutagenesis Screens Using Inbred Mice

Nek8 Regulates the Expression and Localization of Polycystin-1 and Polycystin-2

Loss of the Ciliary Kinase Nek8 Causes Left-Right Asymmetry Defects

ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterning

Mutations in Dnaaf1 and Lrrc48 Cause Hydrocephalus, Laterality Defects, and Sinusitis in Mice

Impaired Organic Anion Transport in Kidney and Choroid Plexus of Organic Anion Transporter 3 (Oat3 (Slc22a8)) Knockout Mice

Cholesterol metabolism is required for intracellular hedgehog signal transduction in vivo

Improvement of ENU Mutagenesis Efficiency Using Serial Injection and Mismatch Repair Deficiency Mice

Spiny mice activate unique transcriptional programs after severe kidney injury regenerating organ function without fibrosis

Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease

A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafish

A spontaneous Fatp4/Scl27a4 splice site mutation in a new murine model for congenital ichthyosis

Reelin Mediates Hippocampal Cajal-Retzius Cell Positioning and Infrapyramidal Blade Morphogenesis

Dysfunction of intraflagellar transport-A causes hyperphagia-induced obesity and metabolic syndrome

Gata4 Is Necessary for Normal Pulmonary Lobar Development

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