Concepedia

A SPRY2 mutation leading to MAPK/ERK pathway inhibition is associated with an autosomal dominant form of IgA nephropathy

Annamaria Milillo, Francesca La Carpia, Stefano Costanzi, Vanessa D’Urbano, Maurizio Martini, Paola Lanuti, Gisella Vischini, Luigi Maria Larocca, Marco Marchisio, Sebastianó Miscia,

European Journal of Human Genetics · 2015 · 21 citations · 21 references

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21

Genome-wide association study identifies susceptibility loci for IgA nephropathy

Ali G. Gharavi, Krzysztof Kiryluk, Murim Choi et al. · Nature Genetics · 2011 · 624 citations · Full text

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IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22–23

Ali G. Gharavi, Yan Yan, Francesco Scolari et al. · Nature Genetics · 2000 · 331 citations · Full text

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A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy

Xue Qing Yu, Ming Li, Hong Zhang et al. · Nature Genetics · 2011 · 311 citations

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IgA1-secreting cell lines from patients with IgA nephropathy produce aberrantly glycosylated IgA1

Hitoshi Suzuki, Zina Moldoveanu, Stacy Hall et al. · Journal of Clinical Investigation · 2008 · 277 citations · Full text

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The Kinase Inhibitor Sorafenib Induces Cell Death through a Process Involving Induction of Endoplasmic Reticulum Stress

Mohamed Rahmani, Eric Maynard Davis, Timothy Ryan Crabtree et al. · Molecular and Cellular Biology · 2007 · 250 citations · Full text

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