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Ppia is the most stable housekeeping gene for qRT-PCR normalization in kidneys of three Pkd1-deficient mouse models

Scientific reports, 2021-10, Vol.11 (1), p.19798-19798, Article 19798

2021

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Smoking accelerates renal cystic disease and worsens cardiac phenotype in Pkd1-deficient mice

Scientific reports, 2021-07, Vol.11 (1), p.14443-16, Article 14443

2021

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Schistosoma mansoni infection as a trigger to collapsing glomerulopathy in a patient with high-risk APOL1 genotype

PLoS neglected tropical diseases, 2020-10, Vol.14 (10), p.e0008582-e0008582

2020

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Pkd1 Haploinsufficiency Increases Renal Damage and Induces Microcyst Formation following Ischemia/Reperfusion

Journal of the American Society of Nephrology, 2009-11, Vol.20 (11), p.2389-2402

2009

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Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1

Journal of molecular medicine (Berlin, Germany), 2014-10, Vol.92 (10), p.1045-1056

2014

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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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Caffeine Accelerates Cystic Kidney Disease in a Pkd1-Deficient Mouse Model

Cellular physiology and biochemistry, 2019, Vol.52 (5), p.1061-1074

2019

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Renal cyst growth is the main determinant for hypertension and concentrating deficit in Pkd1-deficient mice

Kidney international, 2014-05, Vol.85 (5), p.1137-1150

2014

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PKHD1, the Polycystic Kidney and Hepatic Disease 1 Gene, Encodes a Novel Large Protein Containing Multiple Immunoglobulin-Like Plexin-Transcription–Factor Domains and Parallel Beta-Helix 1 Repeats

American journal of human genetics, 2002-05, Vol.70 (5), p.1305-1317

2002

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Polyductin undergoes notch-like processing and regulated release from primary cilia

Human molecular genetics, 2007-04, Vol.16 (8), p.942-956

2007

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Genetic interaction studies link autosomal dominant and recessive polycystic kidney disease in a common pathway

Human molecular genetics, 2007-08, Vol.16 (16), p.1940-1950

2007

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Biliary and Pancreatic Dysgenesis in Mice Harboring a Mutation in Pkhd1

The American journal of pathology, 2008-02, Vol.172 (2), p.417-429

2008

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The Molecular Basis of Focal Cyst Formation in Human Autosomal Dominant Polycystic Kidney Disease Type I

Cell, 1996-12, Vol.87 (6), p.979-987

1996

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Macromolecular assembly of polycystin-2 intracytosolic C-terminal domain

Proceedings of the National Academy of Sciences - PNAS, 2011-06, Vol.108 (24), p.9833-9838

2011

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Polyductin, the PKHD1 gene product, comprises isoforms expressed in plasma membrane, primary cilium, and cytoplasm

Kidney international, 2004-10, Vol.66 (4), p.1345-1355

2004

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Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1)

Journal of the American Society of Nephrology, 2003, Vol.14 (1), p.76-89

2003

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Idiopathic collapsing glomerulopathy is associated with APOL1 high-risk genotypes or Mendelian variants in most affected individuals in a highly admixed population

Kidney international, 2024-03, Vol.105 (3), p.593-607

2024

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Milder presentation of recessive polycystic kidney disease requires presence of amino acid substitution mutations

Journal of the American Society of Nephrology, 2003-08, Vol.14 (8), p.2004-2014

2003

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Brazilian Network of Pediatric Nephrotic Syndrome (REBRASNI)

Kidney international reports, 2020-03, Vol.5 (3), p.358-362

2020

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Periostin and polycystic kidney disease: more pieces in the puzzle

American journal of physiology. Renal physiology, 2019-01, Vol.316 (1), p.F159-F161

2019

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Collapsing glomerulopathy following SARS-CoV-2 adenovirus-vector–based vaccine: report of 2 cases

Kidney international, 2022-03, Vol.101 (3), p.637-639

2022

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Somatic Mutation in Individual Liver Cysts Supports a Two-Hit Model of Cystogenesis in Autosomal Dominant Polycystic Kidney Disease

Molecular cell, 1998-08, Vol.2 (2), p.247-251

1998

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Cardiac dysfunction in Pkd1-deficient mice with phenotype rescue by galectin-3 knockout

Kidney international, 2016-09, Vol.90 (3), p.580-597

2016

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Disruption of polycystin-1 cleavage leads to cardiac metabolic rewiring in mice

Biochimica et biophysica acta. Molecular basis of disease, 2022-06, Vol.1868 (6), p.166371-166371, Article 166371

2022

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Giant Renal Angiomyolipoma Following Ovarian Stimulation Therapy

Urology (Ridgewood, N.J.), 2018-02, Vol.112, p.e3-e4

2018

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Ppia is the most stable housekeeping gene for qRT-PCR normalization in kidneys of three Pkd1-deficient mouse models

Smoking accelerates renal cystic disease and worsens cardiac phenotype in Pkd1-deficient mice

Schistosoma mansoni infection as a trigger to collapsing glomerulopathy in a patient with high-risk APOL1 genotype

Pkd1 Haploinsufficiency Increases Renal Damage and Induces Microcyst Formation following Ischemia/Reperfusion

Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1

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

Caffeine Accelerates Cystic Kidney Disease in a Pkd1-Deficient Mouse Model

Renal cyst growth is the main determinant for hypertension and concentrating deficit in Pkd1-deficient mice

PKHD1, the Polycystic Kidney and Hepatic Disease 1 Gene, Encodes a Novel Large Protein Containing Multiple Immunoglobulin-Like Plexin-Transcription–Factor Domains and Parallel Beta-Helix 1 Repeats

Polyductin undergoes notch-like processing and regulated release from primary cilia

Genetic interaction studies link autosomal dominant and recessive polycystic kidney disease in a common pathway

Biliary and Pancreatic Dysgenesis in Mice Harboring a Mutation in Pkhd1

The Molecular Basis of Focal Cyst Formation in Human Autosomal Dominant Polycystic Kidney Disease Type I

Macromolecular assembly of polycystin-2 intracytosolic C-terminal domain

Polyductin, the PKHD1 gene product, comprises isoforms expressed in plasma membrane, primary cilium, and cytoplasm

Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1)

Idiopathic collapsing glomerulopathy is associated with APOL1 high-risk genotypes or Mendelian variants in most affected individuals in a highly admixed population

Milder presentation of recessive polycystic kidney disease requires presence of amino acid substitution mutations

Brazilian Network of Pediatric Nephrotic Syndrome (REBRASNI)

Periostin and polycystic kidney disease: more pieces in the puzzle

Collapsing glomerulopathy following SARS-CoV-2 adenovirus-vector–based vaccine: report of 2 cases

Somatic Mutation in Individual Liver Cysts Supports a Two-Hit Model of Cystogenesis in Autosomal Dominant Polycystic Kidney Disease

Cardiac dysfunction in Pkd1-deficient mice with phenotype rescue by galectin-3 knockout

Disruption of polycystin-1 cleavage leads to cardiac metabolic rewiring in mice

Giant Renal Angiomyolipoma Following Ovarian Stimulation Therapy

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