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 em 2010

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 em 2014

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 em 2011

RARE VARIANTS IN TENASCIN GENES IN A COHORT OF CHILDREN WITH PRIMARY VESICOURETERIC REFLUX

Por Elahi, Shan, Homstad, Alison, Vaidya, Himani, Stout, Jennifer, Hall, Gentzon, Wu, Guanghong, Conlon, Peter, Routh, Jonathan C., Wiener, John S., Ross, Sherry S., Nagaraj, Shashi, Wigfall, Delbert, Foreman, John, Adeyemo, Adebowale, Gupta, Indra R., Brophy, Patrick D., Rabinovich, C. Egla, Gbadegesin, Rasheed A.
Publicado no Pediatr Nephrol (2015)

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 no 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 em 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 no 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 em 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 no J Am Soc Nephrol (2015)