Complement Factor I Variants in Complement-Mediated Renal Diseases by Zhang, Yuzhou, Goodfellow, Renee X, Ghiringhelli Borsa, Nicolo, Dunlop, Hannah C, Presti, Stephen A, Meyer, Nicole C, Shao, Dingwu, Roberts, Sarah M, Jones, Michael B, Pitcher, Gabriella R, Taylor, Amanda O, Nester, Carla M, Smith, Richard J H

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Genetic Deficiency of Mtdh Gene in Mice Causes Male Infertility via Impaired Spermatogenesis and Alterations in the Expression of Small Non-coding RNAs by Meng, Xiangbing, Yang, Shujie, Zhang, Yuping, Wang, Xinjun, Goodfellow, Renee X., Jia, Yichen, Thiel, Kristina W., Reyes, Henry D., Yang, Baoli, Leslie, Kimberly K.

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The transcriptional regulator GON4L is required for viability and hematopoiesis in mice by Colgan, Diana F., Goodfellow, Renee X., Colgan, John D.

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Early B Cell Progenitors Deficient for GON4L Fail To Differentiate Due to a Block in Mitotic Cell Division by Barr, Jennifer Y, Goodfellow, Renee X, Colgan, Diana F, Colgan, John D

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A Mutation in Complement Factor B Causing Massive Fluid-Phase Dysregulation of the Alternative Complement Pathway Can Result in Atypical Hemolytic Uremic Syndrome: PO2238 by Zhang, Yuzhou, Kremsdorf, Robin A., Sperati, John, Henriksen, Kammi J., Mori, Mari, Goodfellow, Renee X., Pitcher, Gabriella R., Borsa, Nicolo Ghiringhelli, Taylor, Ronald P., Nester, Carla M., Smith, Richard J.

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Ultra-rare C3 mutation leading to a dominant familial C3 glomerulopathy phenotype by Leonhardt, Alexandria, Hauer, Jill, Ghiringhelli, Nicolo, Zhang, Yuzhou, Meyer, Nicole, Goodfellow, Renee X., Martin, Bertha, Nester, Carla, Smith, Richard

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