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Transcription Factor 21 Is Required for Branching Morphogenesis and Regulates the Gdnf-Axis in Kidney Development

Journal of the American Society of Nephrology, 2018-12, Vol.29 (12), p.2795-2808

2018

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Maternally Inherited Birk Barel Mental Retardation Dysmorphism Syndrome Caused by a Mutation in the Genomically Imprinted Potassium Channel KCNK9

American journal of human genetics, 2008-08, Vol.83 (2), p.193-199

2008

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Hyperphosphatemic familial tumoral calcinosis: Response to acetazolamide and postulated mechanisms

American journal of medical genetics. Part A, 2014-06, Vol.164A (6), p.1545-1549

2014

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Does History of Prematurity Prompt Blood Pressure Evaluations at Primary Care Visits?

Global pediatric health, 2019, Vol.6, p.2333794X19828314-2333794X19828314

2019

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Transcription Factor 21 Is Required for Normal Vascular Development of the Kidney: FR-PO363

Journal of the American Society of Nephrology, 2022-11, Vol.33 (11S), p.423-423

2022

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Non-endothelial expression of Endomucin in the mouse and human choroid

Experimental eye research, 2024-08, p.110054

2024

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Stromal Transcription Factor 21 Is Critical for Development of the Interstitium and Nephron Progenitor Cells via Interaction with Wnt/β-Catenin Signaling: PO0610

Journal of the American Society of Nephrology, 2021-10, Vol.32 (10S), p.227-228

2021

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Transcription Factor 21 Regulates Nephron Progenitor Cells Self-Renewal/Induction and Podocyte Development: PO0876

Journal of the American Society of Nephrology, 2020-10, Vol.31 (10S), p.308-308

2020

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Renin Cell Development: Insights From Chromatin Accessibility and Single-Cell Transcriptomics

Circulation research, 2023-08, Vol.133 (4), p.369-371

2023

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Applicability of estimating glomerular filtration rate equations in pediatric patients: comparison with a measured glomerular filtration rate by iohexol clearance

Translational research : the journal of laboratory and clinical medicine, 2015-03, Vol.165 (3), p.437-445

2015

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Race, obesity, and the renin-angiotensin-aldosterone system: treatment response in children with primary hypertension

Pediatric nephrology (Berlin, West), 2017-09, Vol.32 (9), p.1585-1594

2017

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Pathogenesis of urinary tract infections with normal female anatomy

The Lancet infectious diseases, 2004-10, Vol.4 (10), p.631-635

2004

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Mitochondrial Complex III Deficiency Associated with a Homozygous Mutation in UQCRQ

American journal of human genetics, 2008-05, Vol.82 (5), p.1211-1216

2008

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Clinical Approach to Proximal Renal Tubular Acidosis in Children

Advances in chronic kidney disease, 2018-07, Vol.25 (4), p.351-357

2018

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Divergent roles of Smad3 and PI3-kinase in murine adriamycin nephropathy indicate distinct mechanisms of proteinuria and fibrogenesis

Kidney international, 2012-09, Vol.82 (5), p.525-536

2012

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Stromal Transcription Factor 21 Regulates Development of the Renal Stroma via Interaction with Wnt/ β -Catenin Signaling

Kidney360, 2022-07, Vol.3 (7), p.1228

2022

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Applicability of Estimating GFR Equations in Pediatric Patients: Comparison to a Measured GFR by Iohexol Clearance

Translational research : the journal of laboratory and clinical medicine, 2014-10, Vol.165 (3), p.437-445

2014

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Fluid Management: Pharmacologic and Renal Replacement Therapies

Pediatric critical care medicine, 2016-08, Vol.17 (8 Suppl 1), p.S257-S265

2016

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Seborrhea-like dermatitis with psoriasiform elements caused by a mutation in ZNF750 , encoding a putative C2H2 zinc finger protein

Nature genetics, 2006-07, Vol.38 (7), p.749-751

2006

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Transient neonatal hyperkalemia in the antenatal (ROMK defective) Bartter syndrome

The Journal of pediatrics, 2003-03, Vol.142 (3), p.318-323

2003

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Genetic kidney diseases in the pediatric population of southern Israel

Pediatric nephrology (Berlin, West), 2006-07, Vol.21 (7), p.910-916

2006

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Familial hemolytic uremic syndrome associated with complement factor H deficiency

The Journal of pediatrics, 2001-03, Vol.138 (3), p.412-417

2001

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A conceptual framework for the molecular pathogenesis of progressive kidney disease

Pediatric nephrology (Berlin, West), 2010-11, Vol.25 (11), p.2223-2230

2010

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Maternally Inherited Birk Bard Mental Retardation Dysmorphism Syndrome Caused by a Mutation in the Genomically Imprinted Potassium Channel KCNK9

American journal of human genetics, 2008-08, Vol.83 (2), p.193

2008

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Genetic and phenotypic aspects of autosomal recessive polycystic kidney disease in southern Israel

הרפואה, 2004-07, Vol.143 (7), p.466

2004

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Transcription Factor 21 Is Required for Branching Morphogenesis and Regulates the Gdnf-Axis in Kidney Development

Maternally Inherited Birk Barel Mental Retardation Dysmorphism Syndrome Caused by a Mutation in the Genomically Imprinted Potassium Channel KCNK9

Hyperphosphatemic familial tumoral calcinosis: Response to acetazolamide and postulated mechanisms

Does History of Prematurity Prompt Blood Pressure Evaluations at Primary Care Visits?

Transcription Factor 21 Is Required for Normal Vascular Development of the Kidney: FR-PO363

Non-endothelial expression of Endomucin in the mouse and human choroid

Stromal Transcription Factor 21 Is Critical for Development of the Interstitium and Nephron Progenitor Cells via Interaction with Wnt/β-Catenin Signaling: PO0610

Transcription Factor 21 Regulates Nephron Progenitor Cells Self-Renewal/Induction and Podocyte Development: PO0876

Renin Cell Development: Insights From Chromatin Accessibility and Single-Cell Transcriptomics

Applicability of estimating glomerular filtration rate equations in pediatric patients: comparison with a measured glomerular filtration rate by iohexol clearance

Race, obesity, and the renin-angiotensin-aldosterone system: treatment response in children with primary hypertension

Pathogenesis of urinary tract infections with normal female anatomy

Mitochondrial Complex III Deficiency Associated with a Homozygous Mutation in UQCRQ

Clinical Approach to Proximal Renal Tubular Acidosis in Children

Divergent roles of Smad3 and PI3-kinase in murine adriamycin nephropathy indicate distinct mechanisms of proteinuria and fibrogenesis

Stromal Transcription Factor 21 Regulates Development of the Renal Stroma via Interaction with Wnt/ β -Catenin Signaling

Applicability of Estimating GFR Equations in Pediatric Patients: Comparison to a Measured GFR by Iohexol Clearance

Fluid Management: Pharmacologic and Renal Replacement Therapies

Seborrhea-like dermatitis with psoriasiform elements caused by a mutation in ZNF750 , encoding a putative C2H2 zinc finger protein

Transient neonatal hyperkalemia in the antenatal (ROMK defective) Bartter syndrome

Genetic kidney diseases in the pediatric population of southern Israel

Familial hemolytic uremic syndrome associated with complement factor H deficiency

A conceptual framework for the molecular pathogenesis of progressive kidney disease

Maternally Inherited Birk Bard Mental Retardation Dysmorphism Syndrome Caused by a Mutation in the Genomically Imprinted Potassium Channel KCNK9

Genetic and phenotypic aspects of autosomal recessive polycystic kidney disease in southern Israel

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