P. Goodyer

T. Feest, R. Thakker, O. Wrong, 1999, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

PAX2 Activates WNT4 Expression during Mammalian Kidney Development*

J. Pelletier, M. Eccles, M. Little, 2006, Journal of Biological Chemistry.

Ureteric bud apoptosis and renal hypoplasia in transgenic PAX2-Bax fetal mice mimics the renal-coloboma syndrome.

J. Julien, C. Stayner, M. Eccles, 2003, Journal of the American Society of Nephrology : JASN.

Disorders of tubular transport

P. Goodyer, 2006 .

Wilms Tumor Suppressor, WT1, Suppresses Epigenetic Silencing of the β-Catenin Gene*

Murielle M. Akpa, D. Iglesias, Leelee Chu, 2014, The Journal of Biological Chemistry.

CLCN5 chloride-channel mutations in six new North American families with X-linked nephrolithiasis.

J. Midgley, P. Goodyer, S. Scheinman, 1998, Kidney international.

Priming the renal progenitor cell

Murielle M. Akpa, D. Iglesias, P. Goodyer, 2014, Pediatric Nephrology.

Defective intramitochondrial NADH oxidation in skin fibroblasts from an infant with fatal neonatal lacticacidemia.

B. Robinson, P. Goodyer, N. McKay, 1985, American journal of human genetics.

The relationship of 4-aminobutyric acid metabolism to ammoniagenesis in renal cortex.

P. Goodyer, C. Scriver, G. Lancaster, 1980, Biochimica et biophysica acta.

Analysis of the Heymann nephritogenic glycoprotein in rat, mouse, and human kidney.

P. Goodyer, B. Kaplan, M. Mills, 1986, Biochemistry and cell biology = Biochimie et biologie cellulaire.

GABA and Taurine What Are Metabolites Like This Doing in Places Like That

R. Rozen, P. Goodyer, C. Scriver, 1982 .

Respiratory chain defects in the mitochondria of cultured skin fibroblasts from three patients with lacticacidemia.

B. Robinson, P. Goodyer, A. Baudet, 1986, The Journal of clinical investigation.

The molecular basis for the two different clinical presentations of classical pyruvate carboxylase deficiency.

B. Robinson, P. Goodyer, J. Oei, 1984, American journal of human genetics.

T-Cell Factor/ β -Catenin Activity is Suppressed Normally in Two Independent Models of Autosomal Dominant Polycystic Kidney Disease

G. Germino, S. Somlo, D. Iglesias, 2014 .

A no-nonsense approach to hereditary kidney disease

Murielle M. Akpa, P. Goodyer, Emma Brasell, 2019, Pediatric Nephrology.

A common molecular basis for three inherited kidney stone diseases

M. Devoto, B. Harding, S. Fisher, 1996, Nature.

LGL1, a novel branching morphogen in developing kidney, is induced by retinoic acid.

P. Goodyer, N. Sweezey, F. Kaplan, 2007, American journal of physiology. Renal physiology.

Nephropathic cystinosis: an international consensus document.

D. Trauner, W. Gahl, C. Antignac, 2014, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

First NIH/Office of Rare Diseases Conference on Cystinosis: past, present, and future

M. Sarwal, D. Trauner, W. Gahl, 2005, Pediatric Nephrology.

Full Review Nephropathic cystinosis: an international consensus document

D. Trauner, W. Gahl, C. Antignac, 2014 .

The novel aminoglycoside, ELX-02, permits CTNSW138X translational read-through and restores lysosomal cystine efflux in cystinosis

Y. Yamanaka, Murielle M. Akpa, Leelee Chu, 2019, PloS one.

Paired-Box genes are frequently expressed in cancer and often required for cancer cell survival

M. Eccles, Chaoming Zhou, P. Goodyer, 2003, Oncogene.

The aminoglycoside geneticin permits translational readthrough of the CTNS W138X nonsense mutation in fibroblasts from patients with nephropathic cystinosis

D. Iglesias, Leelee Chu, P. Goodyer, 2018, Pediatric Nephrology.

WT1 is a modifier of the Pax2 mutant phenotype: cooperation and interaction between WT1 and Pax2

J. Pelletier, M. Eccles, T. Lee, 2003, Oncogene.

Hypophosphatemic Rickets.

P. Goodyer, M. Bitzan, 2019, Pediatric clinics of North America.

Insulin-like growth factor-1 enhances epidermal growth factor receptor activation and renal tubular cell regeneration in postischemic acute renal failure.

A. Cybulsky, P. Goodyer, R. Fine, 1995, The Journal of laboratory and clinical medicine.

Acute poststreptococcal glomerulonephritis mimicking Henoch-Schönlein purpura.

P. Goodyer, B. Kaplan, J. de Chadarévian, 1978, The Journal of pediatrics.

Primary renal hypoplasia in humans and mice with PAX2 mutations: evidence of increased apoptosis in fetal kidneys of Pax2(1Neu) +/- mutant mice.

H. Cunliffe, M. Eccles, N. Cho, 2000, Human molecular genetics.

Suppression of ureteric bud apoptosis rescues nephron endowment and adult renal function in Pax2 mutant mice.

M. Eccles, P. Goodyer, A. Dziarmaga, 2006, Journal of the American Society of Nephrology : JASN.

Clinical features of X-linked nephrolithiasis in childhood

R. Thakker, P. Goodyer, S. Scheinman, 1998, Pediatric Nephrology.

Effects of PAX2 expression in a human fetal kidney (HEK293) cell line.

E. Torban, P. Goodyer, 1998, Biochimica et biophysica acta.

Amelioration of murine lupus nephritis by dimethylsulfoxide.

P. Goodyer, B. Kaplan, J. de Chadarévian, 1987, Clinical immunology and immunopathology.

Interactions of dimethyl sulfoxide and nonsteroidal anti-inflammatory agents in passive Heymann's nephritis.

P. Goodyer, J. S. Fong, B. Kaplan, 1986, The Journal of laboratory and clinical medicine.

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

C. Cremers, C. Morton, R. Lifton, 1999, Nature Genetics.

Effects of maternal vitamin A status on kidney development: a pilot study

P. Goodyer, A. Kurpad, A. Iyengar, 2007, Pediatric Nephrology.

Common variants of the glial cell-derived neurotrophic factor gene do not influence kidney size of the healthy newborn

M. Bouchard, M. Lemire, P. Goodyer, 2009, Pediatric Nephrology.

A common variant of the PAX2 gene is associated with reduced newborn kidney size.

M. Lemire, P. Goodyer, C. Raju, 2007, Journal of the American Society of Nephrology : JASN.

Expression of growth-related genes in human fetal kidney.

P. Goodyer, C. Goodyer, L. Mulligan, 1991, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Newborn Serum Retinoic Acid Level Is Associated With Variants of Genes in the Retinol Metabolism Pathway

A. Montpetit, P. Goodyer, L. Lakhal-Chaieb, 2010, Pediatric Research.

Molecular determinants of WNT9b responsiveness in nephron progenitor cells

Courtney M. Karner, Leah Hammond, P. Goodyer, 2018, bioRxiv.

WNT/β-Catenin Signaling Is Required for Integration of CD24+ Renal Progenitor Cells into Glycerol-Damaged Adult Renal Tubules

D. Iglesias, Leelee Chu, P. Goodyer, 2015, Stem cells international.

Canonical WNT signaling during kidney development.

D. Dufort, D. Iglesias, Leelee Chu, 2007, American journal of physiology. Renal physiology.

PAX 2 is reactivated in urinary tract obstruction and partially protects collecting duct cells from programmed cell death

P. Goodyer, J. Capolicchio, R. Jednak, 2007 .

PAX2 is reactivated in urinary tract obstruction and partially protects collecting duct cells from programmed cell death.

P. Goodyer, J. Capolicchio, R. Jednak, 2007, American journal of physiology. Renal physiology.

T-cell factor/β-catenin activity is suppressed in two different models of autosomal dominant polycystic kidney disease.

G. Germino, S. Somlo, D. Iglesias, 2011, Kidney international.

Acute glomerulonephritis and hemolytic uremic syndrome.

P. Goodyer, B. Kaplan, J. de Chadarévian, 1980, Canadian Medical Association journal.

Epidermal growth factor receptor activation in developing rat kidney.

A. Cybulsky, P. Goodyer, A. McTavish, 1994, The American journal of physiology.

Repression of the retinoic acid receptor-alpha gene by the Wilms' tumor suppressor gene product, wt1.

J. Pelletier, W. Bruening, E. Torban, 1995, Oncogene.

Observations on the evolution and treatment of idiopathic infantile hypercalcemia.

P. Goodyer, B. Kaplan, A. Frank, 1984, The Journal of pediatrics.

PHEX expression in parathyroid gland and parathyroid hormone dysregulation in X-linked hypophosphatemia

P. Goodyer, T. Blydt-Hansen, H. Tenenhouse, 1999, Pediatric Nephrology.

Lymphocyte subsets during and after rabbit anti-thymocyte globulin induction in pediatric renal transplantation: sustained T cell depletion.

P. Goodyer, B. Mazer, L. Bell, 1997, Transplantation proceedings.

Recurrent Focal Segmental Glomerulosclerosis: A Discrete Clinical Entity

E. Torban, P. Goodyer, M. Bitzan, 2012, International journal of nephrology.

Use of genomic and functional analysis to characterize patients with steroid-resistant nephrotic syndrome

Thomas M. Kitzler, E. Torban, P. Goodyer, 2018, Pediatric Nephrology.

Erratum: Pediatr Nephrol (2000) 15:7–10

P. Goodyer, L. Murray, S. Champoux, 2001, Pediatric nephrology (Berlin, West).

Polyuria and proteinuria in cystinosis have no impact on renal transplantation

D. Geary, D. Hébert, P. Goodyer, 2000, Pediatric Nephrology.

Novel unbiased assay for circulating podocyte-toxic factors associated with recurrent focal segmental glomerulosclerosis.

Thomas M. Kitzler, A. Cybulsky, E. Torban, 2016, American journal of physiology. Renal physiology.

Intrinsic tumor necrosis factor-α pathway is activated in a subset of patients with focal segmental glomerulosclerosis

Thomas M. Kitzler, A. Cybulsky, E. Torban, 2019, PloS one.

The pathogenesis of multicystic dysplastic kidney disease: insights from the study of fetal kidneys.

V. Han, P. Goodyer, C. Goodyer, 1996, Laboratory investigation; a journal of technical methods and pathology.

MICROENCAPSULATED XANTHINE OXIDASE AS EXPERIMENTAL THERAPY IN LESCH-NYHAN DISEASE

R. Palmour, P. Goodyer, T. Reade, 1989, The Lancet.

Turner's syndrome, 46X, del (X) (p 11), persistent complement activation and membranoproliferative glomerulonephritis.

P. Goodyer, J. S. Fong, B. Kaplan, 1982, American journal of nephrology.

Pax2 gene dosage influences cystogenesis in autosomal dominant polycystic kidney disease.

G. Germino, Jing Zhou, C. Stayner, 2006, Human molecular genetics.

Pax 2 gene dosage influences cystogenesis in autosomal dominant polycystic kidney disease

G. Germino, Jing Zhou, C. Stayner, 2006 .

A common RET variant is associated with reduced newborn kidney size and function.

M. Hughson, M. Lemire, W. Hoy, 2008, Journal of the American Society of Nephrology : JASN.

The Hemolytic-Uremic Syndromes: The Most Important Cause of Acute Renal Failure in Infants and Children

P. Goodyer, J. S. Fong, B. Kaplan, 1984 .

Properties of γ-aminobutyric acid synthesis by rat renal cortex

P. Goodyer, C. Scriver, M. Mills, 1982 .

Effect of nitisinone (NTBC) treatment on the clinical course of hepatorenal tyrosinemia in Québec.

John J. Mitchell, S. Lindstedt, E. Holme, 2012, Molecular genetics and metabolism.

PAX3 is Expressed in the Stromal Compartment of the Developing Kidney and in Wilms Tumors with Myogenic Phenotype

M. Eccles, A. Reeve, N. Jabado, 2009, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Two novel 1α-hydroxylase mutations in French-Canadians with vitamin D dependency rickets type I

T. Saruta, S. Wakino, T. Monkawa, 1998 .

Expression of the epidermal growth factor receptor in fetal kidney

A. Cybulsky, P. Goodyer, C. Goodyer, 1993, Pediatric Nephrology.

Unraveling the natural history of presymptomatic cystinuria

P. Goodyer, Fatima Tokhmafshan, 2023, Current opinion in nephrology and hypertension.

A gamma-aminobutyric acid-specific transport mechanism in mammalian kidney.

R. Rozen, P. Goodyer, C. Scriver, 1985, Biochimica et biophysica acta.

A human ALDH1A2 gene variant is associated with increased newborn kidney size and serum retinoic acid.

A. Montpetit, P. Goodyer, L. Lakhal-Chaieb, 2010, Kidney international.

Wilms tumor arising in a child with X-linked nephrogenic diabetes insipidus

N. Jabado, D. Bichet, D. Iglesias, 2009, Pediatric Nephrology.