Therapeutic targets in focal and segmental glomerulosclerosis

por Lavin, Peter J., Gbadegesin, Rasheed, Damodaran, Tirupapuliyur V., Winn, Michelle P.
Publicado 2008

EXCLUSION OF HOMOZYGOUS PLCE1 (NPHS3) MUTATIONS IN 69 FAMILIES WITH IDIOPATHIC AND HEREDITARY FSGS

por Gbadegesin, Rasheed, Bartkowiak, Bartlomiej, Lavin, Peter J, Mukerji, Nirvan, Wu, Guanghong, Bowling, Brandy, Eckel, Jason, Damodaran, Tirupapuliyur, Winn, Michelle P
Publicado 2008

Hepatorenal Correction in Murine Glycogen Storage Disease Type I With a Double-stranded Adeno-associated Virus Vector

por Luo, Xiaoyan, Hall, Gentzon, Li, Songtao, Bird, Andrew, Lavin, Peter J, Winn, Michelle P, Kemper, Alex R, Brown, Talmage T, Koeberl, Dwight D
Publicado 2011

Gq signaling causes glomerular injury by activating TRPC6

por Wang, Liming, Jirka, Grant, Rosenberg, Paul B., Buckley, Anne F., Gomez, Jose A., Fields, Timothy A., Winn, Michelle P., Spurney, Robert F.
Publicado en J Clin Invest (2015)

Variability in phenotype induced by the podocin variant R229Q plus a single pathogenic mutation

por Phelan, Paul J., Hall, Gentzon, Wigfall, Delbert, Foreman, John, Nagaraj, Shashi, Malone, Andrew F., Winn, Michelle P., Howell, David N., Gbadegesin, Rasheed
Publicado en Clin Kidney J (2015)

Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis

por Akilesh, Shreeram, Suleiman, Hani, Yu, Haiyang, Stander, M. Christine, Lavin, Peter, Gbadegesin, Rasheed, Antignac, Corinne, Pollak, Martin, Kopp, Jeffrey B., Winn, Michelle P., Shaw, Andrey S.
Publicado 2011

A New Locus for Familial FSGS on Chromosome 2P

por Gbadegesin, Rasheed, Lavin, Peter, Janssens, Louis, Bartkowiak, Bartlomiej, Homstad, Alison, Wu, Guanghong, Bowling, Brandy, Eckel, Jason, Potocky, Chris, Abbott, Diana, Conlon, Peter, Scott, William K., Howell, David, Hauser, Elizabeth, Winn, Michelle P.
Publicado 2010

Modulation of the BP Response to Diet by Genes in the Renin–Angiotensin System and the Adrenergic Nervous System

por Svetkey, Laura P., Harris, Emily L., Martin, Eden, Vollmer, William M., Meltesen, Gayle T., Ricchiuti, Vincent, Williams, Gordon, Appel, Lawrence J., Bray, George A., Moore, Thomas J., Winn, Michelle P., Conlin, Paul R.
Publicado 2010

INVERTED FORMIN 2 MUTATIONS WITH VARIABLE EXPRESION IN PATIENTS WITH SPORADIC AND HEREDITARY FOCAL AND SEGMENTAL GLOMERULOSCLEROSIS

por Gbadegesin, Rasheed, Lavin, Peter J., Hall, Gentzon, Bartkowiak, B, Homstad, A, Jiang, R, Wu, G, Byrd, A, Lynn, Kelvin, Wolfish, Norman, Ottati, Carolina, Stevens, Paul, Howell, David, Conlon, Peter, Winn, Michelle P.
Publicado 2011

Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity

por Hall, Gentzon, Rowell, Janelle, Farinelli, Federica, Gbadegesin, Rasheed A., Lavin, Peter, Wu, Guanghong, Homstad, Alison, Malone, Andrew, Lindsey, Thomas, Jiang, Ruiji, Spurney, Robert, Tomaselli, Gordon F., Kass, David A., Winn, Michelle P.
Publicado 2014

A Hybrid CFHR3-1 Gene Causes Familial C3 Glomerulopathy

por Malik, Talat H., Lavin, Peter J., Goicoechea de Jorge, Elena, Vernon, Katherine A., Rose, Kirsten L., Patel, Mitali P., de Leeuw, Marcel, Neary, John J., Conlon, Peter J., Winn, Michelle P., Pickering, Matthew C.
Publicado 2012

TRPC6 Enhances Angiotensin II-induced Albuminuria

por Eckel, Jason, Lavin, Peter J., Finch, Elizabeth A., Mukerji, Nirvan, Burch, Jarrett, Gbadegesin, Rasheed, Wu, Guanghong, Bowling, Brandy, Byrd, Alison, Hall, Gentzon, Sparks, Matthew, Zhang, Zhu Shan, Homstad, Alison, Barisoni, Laura, Birbaumer, Lutz, Rosenberg, Paul, Winn, Michelle P.
Publicado 2011

Screening for NPHS2 Mutations May Help Predict FSGS Recurrence after Transplantation

por Jungraithmayr, Therese C., Hofer, Katrin, Cochat, Pierre, Chernin, Gil, Cortina, Gerard, Fargue, Sonja, Grimm, Paul, Knueppel, Tanja, Kowarsch, Andreas, Neuhaus, Thomas, Pagel, Philipp, Pfeiffer, Karl P., Schäfer, Franz, Schönermarck, Ulf, Seeman, Tomas, Toenshoff, Burkhard, Weber, Stefanie, Winn, Michelle P., Zschocke, Johannes, Zimmerhackl, Lothar B.
Publicado 2011

A Novel Missense Mutation of Wilms’ Tumor 1 Causes Autosomal Dominant FSGS

por Hall, Gentzon, Gbadegesin, Rasheed A., Lavin, Peter, Wu, Guanghong, Liu, Yangfan, Oh, Edwin C., Wang, Liming, Spurney, Robert F., Eckel, Jason, Lindsey, Thomas, Homstad, Alison, Malone, Andrew F., Phelan, Paul J., Shaw, Andrey, Howell, David N., Conlon, Peter J., Katsanis, Nicholas, Winn, Michelle P.
Publicado en J Am Soc Nephrol (2015)

TNXB Mutations Can Cause Vesicoureteral Reflux

por Gbadegesin, Rasheed A., Brophy, Patrick D., Adeyemo, Adebowale, Hall, Gentzon, Gupta, Indra R., Hains, David, Bartkowiak, Bartlomeij, Rabinovich, C. Egla, Chandrasekharappa, Settara, Homstad, Alison, Westreich, Katherine, Wu, Guanghong, Liu, Yutao, Holanda, Danniele, Clarke, Jason, Lavin, Peter, Selim, Angelica, Miller, Sara, Wiener, John S., Ross, Sherry S., Foreman, John, Rotimi, Charles, Winn, Michelle P.
Publicado 2013

Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis

por Malone, Andrew F, Phelan, Paul J, Hall, Gentzon, Cetincelik, Umran, Homstad, Alison, Alonso, Andrea, Jiang, Ruiji, Lindsey, Thomas, Wu, Guanghong, Sparks, Matthew A, Smith, Stephen R, Webb, Nicholas J A, Kalra, Philip, Adeyemo, Adebowale, Shaw, Andrey S, Conlon, Peter J, Jennette, J Charles, Howell, David N, Winn, Michelle P, Gbadegesin, Rasheed A
Publicado en Kidney Int (2014)

Mutations in the Gene That Encodes the F-Actin Binding Protein Anillin Cause FSGS

por Gbadegesin, Rasheed A., Hall, Gentzon, Adeyemo, Adebowale, Hanke, Nils, Tossidou, Irini, Burchette, James, Wu, Guanghong, Homstad, Alison, Sparks, Matthew A., Gomez, Jose, Jiang, Ruiji, Alonso, Andrea, Lavin, Peter, Conlon, Peter, Korstanje, Ron, Stander, M. Christine, Shamsan, Ghaidan, Barua, Moumita, Spurney, Robert, Singhal, Pravin C., Kopp, Jeffrey B., Haller, Hermann, Howell, David, Pollak, Martin R., Shaw, Andrey S., Schiffer, Mario, Winn, Michelle P.
Publicado 2014

HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome

por Gbadegesin, Rasheed A., Adeyemo, Adebowale, Webb, Nicholas J.A., Greenbaum, Larry A., Abeyagunawardena, Asiri, Thalgahagoda, Shenal, Kale, Arundhati, Gipson, Debbie, Srivastava, Tarak, Lin, Jen-Jar, Chand, Deepa, Hunley, Tracy E., Brophy, Patrick D., Bagga, Arvind, Sinha, Aditi, Rheault, Michelle N., Ghali, Joanna, Nicholls, Kathy, Abraham, Elizabeth, Janjua, Halima S., Omoloja, Abiodun, Barletta, Gina-Marie, Cai, Yi, Milford, David D., O'Brien, Catherine, Awan, Atif, Belostotsky, Vladimir, Smoyer, William E., Homstad, Alison, Hall, Gentzon, Wu, Guanghong, Nagaraj, Shashi, Wigfall, Delbert, Foreman, John, Winn, Michelle P.
Publicado en J Am Soc Nephrol (2015)