Basement membranes: cell scaffoldings and signaling platforms von Yurchenco, Peter D

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Laminins in basement membrane assembly von Hohenester, Erhard, Yurchenco, Peter D.

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Polymerizing laminins in development, health, and disease von Yurchenco, Peter D., Kulczyk, Arkadiusz W.

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Dual transgene amelioration of Lama2-null muscular dystrophy von McKee, Karen K., Yurchenco, Peter D.

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Linker Protein Repair of LAMA2 Dystrophic Neuromuscular Basement Membranes von Yurchenco, Peter D, McKee, Karen K

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The nature and biology of basement membranes von Pozzi, Ambra, Yurchenco, Peter D., Iozzo, Renato V.

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Amelioration of muscle and nerve pathology of Lama2-related dystrophy by AAV9-laminin-αLN-linker protein von McKee, Karen K, Yurchenco, Peter D

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Laminin functions in tissue morphogenesis von Miner, Jeffrey H, Yurchenco, Peter D

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A laminin 511 matrix is regulated by TAZ and functions as the ligand for the α6Bβ1 integrin to sustain breast cancer stem cells von Chang, Cheng, Goel, Hira Lal, Gao, Huijie, Pursell, Bryan, Shultz, Leonard D, Greiner, Dale L, Ingerpuu, Sulev, Patarroyo, Manuel, Cao, Shiliang, Lim, Elgene, Mao, Junhao, McKee, Karen Kulju, Yurchenco, Peter D, Mercurio, Arthur M

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Laminin assembles into separate basement membrane and fibrillar matrices in Schwann cells von Tsiper, Maria V, Yurchenco, Peter D

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Integrin and dystroglycan compensate each other to mediate laminin-dependent basement membrane assembly and epiblast polarization von Li, Shaohua, Qi, Yanmei, McKee, Karen, Liu, Jie, Hsu, June, Yurchenco, Peter D.

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Pathogenicity of a Human Laminin β2 Mutation Revealed in Models of Alport Syndrome von Funk, Steven D., Bayer, Raymond H., Malone, Andrew F., McKee, Karen K., Yurchenco, Peter D., Miner, Jeffrey H.

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A mutation affecting laminin alpha 5 polymerisation gives rise to a syndromic developmental disorder von Jones, Lynelle K, Lam, Rachel, McKee, Karen K, Aleksandrova, Maya, Dowling, John, Alexander, Stephen I, Mallawaarachchi, Amali, Cottle, Denny L, Short, Kieran M, Pais, Lynn, Miner, Jeffery H, Mallett, Andrew J, Simons, Cas, McCarthy, Hugh, Yurchenco, Peter D, Smyth, Ian M

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Chimeric protein identification of dystrophic, Pierson and other laminin polymerization residues von McKee, Karen K., Aleksandrova, Maya, Yurchenco, Peter D.

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Role of Laminin Terminal Globular Domains in Basement Membrane Assembly von McKee, Karen K., Harrison, David, Capizzi, Stephanie, Yurchenco, Peter D.

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Structural decoding of netrin-4 reveals a regulatory function towards mature basement membranes von Reuten, Raphael, Patel, Trushar R., McDougall, Matthew, Rama, Nicolas, Nikodemus, Denise, Gibert, Benjamin, Delcros, Jean-Guy, Prein, Carina, Meier, Markus, Metzger, Stéphanie, Zhou, Zhigang, Kaltenberg, Jennifer, McKee, Karen K., Bald, Tobias, Tüting, Thomas, Zigrino, Paola, Djonov, Valentin, Bloch, Wilhelm, Clausen-Schaumann, Hauke, Poschl, Ernst, Yurchenco, Peter D., Ehrbar, Martin, Mehlen, Patrick, Stetefeld, Jörg, Koch, Manuel

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A deletion in the N-terminal polymerizing domain of laminin β2 is a new mouse model of chronic nephrotic syndrome von Funk, Steven D., Bayer, Raymond H., McKee, Karen K., Okada, Kazushi, Nishimune, Hiroshi, Yurchenco, Peter D., Miner, Jeffrey H.

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Exogenous laminin exhibits a unique vascular pattern in the brain via binding to dystroglycan and integrins von Ruan, Jingsong, McKee, Karen K, Yurchenco, Peter D, Yao, Yao

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Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype von McKee, Karen K, Crosson, Stephanie C, Meinen, Sarina, Reinhard, Judith R, Rüegg, Markus A, Yurchenco, Peter D

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Perlecan is recruited by dystroglycan to nodes of Ranvier and binds the clustering molecule gliomedin von Colombelli, Cristina, Palmisano, Marilena, Eshed-Eisenbach, Yael, Zambroni, Desirée, Pavoni, Ernesto, Ferri, Cinzia, Saccucci, Stefania, Nicole, Sophie, Soininen, Raija, McKee, Karen K, Yurchenco, Peter D, Peles, Elior, Wrabetz, Lawrence, Feltri, M Laura

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