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Nur77 protects the bladder urothelium from intracellular bacterial infection

Nature communications, 2024-09, Vol.15 (1), p.8308-14, Article 8308

2024

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Distinct and sequential tissue-specific activities of the LIM-class homeobox gene Lim1 for tubular morphogenesis during kidney development

Development (Cambridge), 2005-06, Vol.132 (12), p.2809-2823

2005

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Foxd1-dependent signals control cellularity in the renal capsule, a structure required for normal renal development

Development (Cambridge), 2005-02, Vol.132 (3), p.529-539

2005

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Development, regeneration and tumorigenesis of the urothelium

Development (Cambridge), 2022-05, Vol.149 (9)

2022

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c-kit delineates a distinct domain of progenitors in the developing kidney

Developmental biology, 2006-11, Vol.299 (1), p.238-249

2006

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A mucosal imprint left by prior Escherichia coli bladder infection sensitizes to recurrent disease

Nature microbiology, 2016-10, Vol.2 (1), p.16196, Article 16196

2016

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FGFR3b Extracellular Loop Mutation Lacks Tumorigenicity In Vivo but Collaborates with p53/pRB Deficiency to Induce High-grade Papillary Urothelial Carcinoma

Scientific reports, 2016-05, Vol.6 (1), p.25596-25596, Article 25596

2016

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novel pleckstrin homology-related gene family defined by Ipl/Tssc3, TDAG51, and Tih1: tissue-specific expression, chromosomal location, and parental imprinting

Mammalian genome, 1999-12, Vol.10 (12), p.1150-1159

1999

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Pathways of Vitamin A Delivery to the Embryo: Insights from a New Tunable Model of Embryonic Vitamin A Deficiency

Endocrinology (Philadelphia), 2005-10, Vol.146 (10), p.4479-4490

2005

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Distal ureter morphogenesis depends on epithelial cell remodeling mediated by vitamin A and Ret

Nature genetics, 2002-09, Vol.32 (1), p.109-115

2002

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A high-resolution anatomical ontology of the developing murine genitourinary tract

Gene Expression Patterns, 2007-06, Vol.7 (6), p.680-699

2007

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Characterization of a New Member of the Fatty Acid-binding Protein Family That Binds All-trans-retinol

The Journal of biological chemistry, 2001-01, Vol.276 (2), p.1353-1360

2001

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Retinoid Inactivation: Survival Factor for Male Germ Cells

Endocrinology (Philadelphia), 2007-10, Vol.148 (10), p.4557-4559

2007

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Pleiotropy of Congenital Anomalies of Kidney and Urinary Tract (CAKUT) Phenotypes in Human 16p11.2 Microdeletion Syndrome Is Recapitulated in Mouse Models of Tbx6 Deletion: PO1346

Journal of the American Society of Nephrology, 2021-10, Vol.32 (10S), p.429-429

2021

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The copy number variation landscape of congenital anomalies of the kidney and urinary tract

Nature genetics, 2019-01, Vol.51 (1), p.117-127

2019

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Organotypic culture of the urogenital tract

Methods in molecular biology (Clifton, N.J.), 2012, Vol.886, p.45

2012

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Large-Scale Exome Sequencing Analysis Implicates FOXQ1, FOXI2, EXOSC2, and MMP15 as Candidate Genes for Human Congenital Obstructive Uropathy: SA-PO813

Journal of the American Society of Nephrology, 2023-11, Vol.34 (11S), p.955-955

2023

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The Multimodal Role of TBX6 in Kidney and Urinary Tract Development and Disease: FR-OR15

Journal of the American Society of Nephrology, 2023-11, Vol.34 (11S), p.33-33

2023

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Abstract A027: The role of nuclear receptors as promoters of luminal tumors and suppressors of basal/squamous tumors

Clinical cancer research, 2024-05, Vol.30 (10_Supplement), p.A027-A027

2024

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Development of Kidney Resident and Recruited Macrophages: PO1443

Journal of the American Society of Nephrology, 2021-10, Vol.32 (10S), p.456-456

2021

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Mouse and Human Studies Support DSTYK Loss of Function as a Low Penetrance and Variable Expressivity Risk Factor for Urinary Tract Anomalies and Movement Disorders: TH-PO486

Journal of the American Society of Nephrology, 2023-11, Vol.34 (11S), p.224-224

2023

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Deletion of Crkl Splice Isoforms in the Mouse Kidney Disrupts Intercompartmental Signaling Required for Progenitor Renewal and Branched Morphogenesis: SA-PO326

Journal of the American Society of Nephrology, 2023-11, Vol.34 (11S), p.813-813

2023

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Urine Microbiota Analysis and mGWAS in Children With Urinary Tract Infections and Vesicoureteral Reflux: SA-PO606

Journal of the American Society of Nephrology, 2022-11, Vol.33 (11S), p.771-771

2022

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MP42-04 CHARACTERIZING DEVELOPMENT OF THE HUMAN LOWER URINARY TRACT: ANATOMIC FEATURES AND MOLECULAR EXPRESSION OF THE URETERIC BUD AND CLOACA

The Journal of urology, 2017-04, Vol.197 (4), p.e545-e545

2017

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Nur77 protects the bladder urothelium from intracellular bacterial infection

Distinct and sequential tissue-specific activities of the LIM-class homeobox gene Lim1 for tubular morphogenesis during kidney development

Foxd1-dependent signals control cellularity in the renal capsule, a structure required for normal renal development

Development, regeneration and tumorigenesis of the urothelium

c-kit delineates a distinct domain of progenitors in the developing kidney

Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies

A mucosal imprint left by prior Escherichia coli bladder infection sensitizes to recurrent disease

FGFR3b Extracellular Loop Mutation Lacks Tumorigenicity In Vivo but Collaborates with p53/pRB Deficiency to Induce High-grade Papillary Urothelial Carcinoma

novel pleckstrin homology-related gene family defined by Ipl/Tssc3, TDAG51, and Tih1: tissue-specific expression, chromosomal location, and parental imprinting

Pathways of Vitamin A Delivery to the Embryo: Insights from a New Tunable Model of Embryonic Vitamin A Deficiency

Distal ureter morphogenesis depends on epithelial cell remodeling mediated by vitamin A and Ret

A high-resolution anatomical ontology of the developing murine genitourinary tract

Characterization of a New Member of the Fatty Acid-binding Protein Family That Binds All-trans-retinol

Retinoid Inactivation: Survival Factor for Male Germ Cells

Pleiotropy of Congenital Anomalies of Kidney and Urinary Tract (CAKUT) Phenotypes in Human 16p11.2 Microdeletion Syndrome Is Recapitulated in Mouse Models of Tbx6 Deletion: PO1346

The copy number variation landscape of congenital anomalies of the kidney and urinary tract

Organotypic culture of the urogenital tract

Large-Scale Exome Sequencing Analysis Implicates FOXQ1, FOXI2, EXOSC2, and MMP15 as Candidate Genes for Human Congenital Obstructive Uropathy: SA-PO813

The Multimodal Role of TBX6 in Kidney and Urinary Tract Development and Disease: FR-OR15

Abstract A027: The role of nuclear receptors as promoters of luminal tumors and suppressors of basal/squamous tumors

Development of Kidney Resident and Recruited Macrophages: PO1443

Mouse and Human Studies Support DSTYK Loss of Function as a Low Penetrance and Variable Expressivity Risk Factor for Urinary Tract Anomalies and Movement Disorders: TH-PO486

Deletion of Crkl Splice Isoforms in the Mouse Kidney Disrupts Intercompartmental Signaling Required for Progenitor Renewal and Branched Morphogenesis: SA-PO326

Urine Microbiota Analysis and mGWAS in Children With Urinary Tract Infections and Vesicoureteral Reflux: SA-PO606

MP42-04 CHARACTERIZING DEVELOPMENT OF THE HUMAN LOWER URINARY TRACT: ANATOMIC FEATURES AND MOLECULAR EXPRESSION OF THE URETERIC BUD AND CLOACA

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