未登录 HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome 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. 分享 收藏
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A Novel Missense Mutation of Wilms' Tumor 1 Causes Autosomal Dominant FSGS 威尔姆斯肿瘤1的新型错义突变导致常染色体显性FSGS 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. 分享 收藏
Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis 罕见的遗传性COL4A3/COL4A4变异可能被误认为是家族性局灶节段性肾小球硬化 Malone, Andrew F.; Phelan, Paul J.; Hall, Gentzon; Cetincelik, Umran; Homstad, Alison; Alonso, Andrea S.; Jiang, Ruiji; Lindsey, Thomas B.; Wu, Guanghong; Sparks, Matthew A.; Smith, Stephen R.; Webb, Nicholas J. A.; Kalra, Philip A.; Adeyemo, Adebowale A.; Shaw, Andrey S.; Conlon, Peter J.; Jennette, J. Charles; Howell, David N.; Winn, Michelle P.; Gbadegesin, Rasheed A. 分享 收藏
Mutations in the Gene That Encodes the F-Actin Binding Protein Anillin Cause FSGS 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. 分享 收藏
Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity 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. 分享 收藏
TNXB Mutations Can Cause Vesicoureteral Reflux 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. 分享 收藏
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A Hybrid CFHR3-1 Gene Causes Familial C3 Glomerulopathy Malik, Talat H.; Lavin, Peter J.; de Jorge, Elena Goicoechea; Vernon, Katherine A.; Rose, Kirsten L.; Patel, Mitali P.; de Leeuw, Marcel; Neary, John J.; Conlon, Peter J.; Winn, Michelle P.; Pickering, Matthew C. 分享 收藏
Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis 在散发性和遗传性局灶性和节段性肾小球硬化症患者中具有可变表达的反向formin 2突变 Gbadegesin, Rasheed A.; Lavin, Peter J.; Hall, Gentzon; Bartkowiak, Bartlomiej; Homstad, Alison; Jiang, Ruiji; Wu, Guanghong; Byrd, Alison; Lynn, Kelvin; Wolfish, Norman; Ottati, Carolina; Stevens, Paul; Howell, David; Conlon, Peter; Winn, Michelle P. 分享 收藏
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Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis 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. 分享 收藏
TRPC6 Enhances Angiotensin II-induced Albuminuria 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. 分享 收藏
Screening for NPHS2 Mutations May Help Predict FSGS Recurrence after Transplantation 筛查NPHS2突变可能有助于预测移植后FSGS复发 Jungraithmayr, Therese C.; Hofer, Katrin; Cochatt, Pierre; Chemin, Gil; Cortina, Gerard; Fargue, Sonja; Grimm, Paul; Knueppel, Tanja; Kowarsch, Andreas; Neuhaus, Thomas; Pagel, Philipp; Pfeiffer, Karl P.; Schaefer, Franz; Schoenermarck, Ulf; Seeman, Tomas; Toenshoff, Burkhard; Weber, Stefanie; Winn, Michelle P.; Zschocke, Johannes; Zimmerhackl, Lothar B. 分享 收藏
Modulation of the BP Response to Diet by Genes in the Renin-Angiotensin System and the Adrenergic Nervous System 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. 分享 收藏
A New Locus for Familial FSGS on Chromosome 2P 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. 分享 收藏
TRPC1 Channels Are Critical for Hypertrophic Signaling in the Heart Seth, Malini; Zhang, Zhu-Shan; Mao, Lan; Graham, Victoria; Burch, Jarrett; Stiber, Jonathan; Tsiokas, Leonidas; Winn, Michelle; Abramowitz, Joel; Rockman, Howard A.; Birnbaumer, Lutz; Rosenberg, Paul 分享 收藏
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Association of genetic polymorphisms with risk of renal injury after coronary bypass graft surgery Stafford-Smith, M; Podgoreanu, M; Swaminathan, M; Phillips-Bute, B; Mathew, JP; Hauser, EH; Winn, MP; Milano, C; Nielsen, DM; Smith, M; Morris, R; Newman, MF; Schwinn, DA 分享 收藏
Parkin mutations and susceptibility alleles in late-onset Parkinson's disease Oliveira, SA; Scott, WK; Martin, ER; Nance, MA; Watts, RL; Hubble, JP; Koller, WC; Pahwa, R; Stern, MB; Hiner, BC; Ondo, WG; Allen, FH; Scott, BL; Goetz, CG; Small, GW; Mastaglia, F; Stajich, JM; Zhang, FY; Booze, MW; Winn, MP; Middleton, LT; Haines, JL; Pericak-Vance, MA; Vance, JM 分享 收藏
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