Search Results - Ranjzad, Parisa

Congenital Disorders of the Human Urinary Tract: Recent Insights From Genetic and Molecular Studies by Woolf, Adrian S., Lopes, Filipa M., Ranjzad, Parisa, Roberts, Neil A.

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Development of Viral Vectors for Use in Cardiovascular Gene Therapy by Williams, Paul D., Ranjzad, Parisa, Kakar, Salik J., Kingston, Paul A.

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Ex Vivo Modeling of Chemical Synergy in Prenatal Kidney Cystogenesis by Anders, Corina, Ashton, Nick, Ranjzad, Parisa, Dilworth, Mark R., Woolf, Adrian S.

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Comparative Proteomics Study of Streptozotocin-induced Diabetic Nephropathy in Rats Kidneys Transfected with Adenovirus-mediated Fibromodulin Gene by Maleki, Akram, Ramazani, Ali, Foroutan, Maryam, Biglari, Alireza, Ranjzad, Parisa, Mellati, Ali Awsat

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Cytokeratin 15 Marks Basal Epithelia in Developing Ureters and Is Upregulated in a Subset of Urothelial Cell Carcinomas by Tai, Guangping, Ranjzad, Parisa, Marriage, Fiona, Rehman, Samrina, Denley, Helen, Dixon, Jill, Mitchell, Karen, Day, Philip J. R., Woolf, Adrian S.

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Aberrant Differentiation of Human Pluripotent Stem Cell-Derived Kidney Precursor Cells inside Mouse Vascularized Bioreactors by Ranjzad, Parisa, Jinks, Jessica, Salahi, Amir P., Bantounas, Ioannis, Derby, Brian, Kimber, Susan J., Woolf, Adrian S., Wong, Jason K.F.

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Generation of Functioning Nephrons by Implanting Human Pluripotent Stem Cell-Derived Kidney Progenitors by Bantounas, Ioannis, Ranjzad, Parisa, Tengku, Faris, Silajdžić, Edina, Forster, Duncan, Asselin, Marie-Claude, Lewis, Philip, Lennon, Rachel, Plagge, Antonius, Wang, Qi, Woolf, Adrian S., Kimber, Susan J.

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Measures of kidney function by minimally invasive techniques correlate with histological glomerular damage in SCID mice with adriamycin-induced nephropathy by Scarfe, Lauren, Rak-Raszewska, Aleksandra, Geraci, Stefania, Darssan, Darsy, Sharkey, Jack, Huang, Jiaguo, Burton, Neal C., Mason, David, Ranjzad, Parisa, Kenny, Simon, Gretz, Norbert, Lévy, Raphaël, Kevin Park, B., García-Fiñana, Marta, Woolf, Adrian S., Murray, Patricia, Wilm, Bettina

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Uncovering genetic mechanisms of kidney aging through transcriptomics, genomics, and epigenomics by Rowland, Joshua, Akbarov, Artur, Eales, James, Xu, Xiaoguang, Dormer, John P., Guo, Hui, Denniff, Matthew, Jiang, Xiao, Ranjzad, Parisa, Nazgiewicz, Alicja, Prestes, Priscilla Ribeiro, Antczak, Andrzej, Szulinska, Monika, Wise, Ingrid A., Zukowska-Szczechowska, Ewa, Bogdanski, Pawel, Woolf, Adrian S., Samani, Nilesh J., Charchar, Fadi J., Tomaszewski, Maciej

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Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like Syndrome by Weber, Stefanie, Thiele, Holger, Mir, Sevgi, Toliat, Mohammad Reza, Sozeri, Betül, Reutter, Heiko, Draaken, Markus, Ludwig, Michael, Altmüller, Janine, Frommolt, Peter, Stuart, Helen M., Ranjzad, Parisa, Hanley, Neil A., Jennings, Rachel, Newman, William G., Wilcox, Duncan T., Thiel, Uwe, Schlingmann, Karl Peter, Beetz, Rolf, Hoyer, Peter F., Konrad, Martin, Schaefer, Franz, Nürnberg, Peter, Woolf, Adrian S.

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