Parisa Ranjzad
Manchester, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 10 publications
Haploinsufficiency of the mouse Tshz3 gene leads to kidney defects.
Journal: Human molecular genetics
Published: August 24, 2021
Congenital Disorders of the Human Urinary Tract: Recent Insights From Genetic and Molecular Studies.
Congenital Disorders of the Human Urinary Tract: Recent Insights From Genetic and Molecular Studies.
Journal: Frontiers in pediatrics
Published: December 02, 2018
Uncovering genetic mechanisms of kidney aging through transcriptomics, genomics, and epigenomics.
Journal: Kidney international
Published: April 02, 2018
Generation of Functioning Nephrons by Implanting Human Pluripotent Stem Cell-Derived Kidney Progenitors.
Journal: Stem cell reports
Published: August 24, 2017
Measures of kidney function by minimally invasive techniques correlate with histological glomerular damage in SCID mice with adriamycin-induced nephropathy.
Journal: Scientific reports
Published: February 03, 2015
Periluminal expression of a secreted transforming growth factor-β type II receptor inhibits in-stent neointima formation following adenovirus-mediated stent-based intracoronary gene transfer.
Journal: Human gene therapy
Published: February 04, 2014
Comparative Proteomics Study of Streptozotocin-induced Diabetic Nephropathy in Rats Kidneys Transfected with Adenovirus-mediated Fibromodulin Gene.
Journal: Avicenna journal of medical biotechnology
Published: October 28, 2013
Ex vivo modeling of chemical synergy in prenatal kidney cystogenesis.
Journal: PloS one
Published: August 21, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026