Generation of TWO iPSC lines (CRICKi009-A; CRICKi010-A) from patients with type 1 von Hippel-Lindau (VHL) and histopathologically confirmed renal cell carcinoma (RCC)

VHL disease is an inherited and autosomal dominant disorder affecting 1 in 36,0000 individuals worldwide. It is caused by von Hippel-Lindau (VHL) gene mutations and can affect both genders and all ethnic backgrounds (Nordstrom-O’Brien et al., 2009; Maher, 2004). Here, we generated and characterised...

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Bibliographic Details
Main Authors: Liani G. Devito, Eugénie S. Lim, Samuel M. O’Toole, Scott T.C. Shepherd, Daqi Deng, Hugang Feng, Taja Barber, William M. Drake, Samra Turajlic, Lyn Healy
Format: Article
Language:English
Published: Elsevier 2024-12-01
Series:Stem Cell Research
Online Access:http://www.sciencedirect.com/science/article/pii/S187350612400309X
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