Joseph Boulanger Selected Research

Inborn Genetic Diseases (Disease, Hereditary)

1/2019

Dysregulated Expression of microRNA-21 and Disease-Related Genes in Human Patients and in a Mouse Model of Alport Syndrome.

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Joseph Boulanger Research Topics

Disease

2	Hereditary Nephritis (Alport Syndrome) 01/2022 - 01/2019
2	Fibrosis (Cirrhosis) 01/2022 - 01/2020
2	Proteinuria 01/2022 - 01/2019
2	Chronic Kidney Disease-Mineral and Bone Disorder (Renal Rickets) 10/2012 - 08/2012
1	Renal Insufficiency (Renal Failure) 01/2022
1	Nephrocalcinosis 01/2022
1	Cysts 01/2020
1	Glomerulonephritis 01/2020
1	Polycystic Kidney Diseases (Polycystic Kidney Disease) 01/2020
1	Inborn Genetic Diseases (Disease, Hereditary) 01/2019
1	Kidney Diseases (Kidney Disease) 01/2019
1	Hyperphosphatemia 10/2012
1	Uremia 10/2012
1	Chronic Renal Insufficiency 08/2012

Drug/Important Bio-Agent (IBA)

3	Phosphates (Orthophosphate)IBA 01/2022 - 10/2012
2	MineralsIBA 10/2012 - 08/2012
1	Interleukin-18 (Interleukin 18)IBA 01/2020
1	Collagen Type I (Type I Collagen)IBA 01/2020
1	CollagenIBA 01/2020
1	Lipocalin-2IBA 01/2020
1	OligonucleotidesIBA 01/2019
1	Collagen Type IV (Type IV Collagen)IBA 01/2019
1	Biomarkers (Surrogate Marker)IBA 01/2019
1	ParaffinIBA 01/2019
1	Adenine FDA LinkGeneric 10/2012
1	Sevelamer (RenaGel)FDA Link 10/2012
1	CateninsIBA 08/2012
1	Hormones (Hormone)IBA 08/2012
1	Proteins (Proteins, Gene)FDA Link 08/2012

Therapy/Procedure

1	Nephrectomy 01/2022
1	Therapeutics 01/2022