Torthaí cuardaigh - Alison Homstad
- 1 - 7 toradh as 7 á dtaispeáint
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1
Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis de réir Rasheed Gbadegesin, Peter Lavin, Gentzon Hall, Bartlomiej Bartkowiak, Alison Homstad, Ruiji Jiang, Guanghong Wu, Alison Byrd, Kelvin L. Lynn, Norman M. Wolfish, Carolina Ottati, Paul E. Stevens, David N. Howell, Peter J. Conlon, Michelle P. Winn
Foilsithe / Cruthaithe 2011Artigo -
2
TRPC6 Enhances Angiotensin II-induced Albuminuria de réir Jason Eckel, Peter Lavin, Elizabeth Finch, Nirvan Mukerji, Jarrett Burch, Rasheed Gbadegesin, Guanghong Wu, Brandy L. Bowling, Alison Byrd, Gentzon Hall, Matthew A. Sparks, Zhu Shan Zhang, Alison Homstad, Laura Barisoni, Lutz Birbaumer, Paul B. Rosenberg, Michelle P. Winn
Foilsithe / Cruthaithe 2011Artigo -
3
A Novel Missense Mutation of Wilms’ Tumor 1 Causes Autosomal Dominant FSGS de réir Gentzon Hall, Rasheed Gbadegesin, Peter Lavin, Guanghong Wu, Yangfan Liu, Edwin C. Oh, Liming Wang, Robert F. Spurney, Jason Eckel, Thomas Lindsey, Alison Homstad, Andrew F. Malone, Paul J. Phelan, Andréy S. Shaw, David N. Howell, Peter J. Conlon, Nicholas Katsanis, Michelle P. Winn
Foilsithe / Cruthaithe 2014Artigo -
4
Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis de réir Andrew F. Malone, Paul J. Phelan, Gentzon Hall, Ümran Çetinçelik, Alison Homstad, Andrea Alonso, Ruiji Jiang, Thomas Lindsey, Guanghong Wu, Matthew A. Sparks, Stephen R. Smith, Nicholas J.A. Webb, Philip A. Kalra, Adebowale Adeyemo, Andréy S. Shaw, Peter J. Conlon, J. Charles Jennette, David N. Howell, Michelle P. Winn, Rasheed Gbadegesin
Foilsithe / Cruthaithe 2014Artigo -
5
TNXB Mutations Can Cause Vesicoureteral Reflux de réir Rasheed Gbadegesin, Patrick D. Brophy, Adebowale Adeyemo, Gentzon Hall, Indra R. Gupta, David S. Hains, Bartlomeij Bartkowiak, C. Egla Rabinovich, Settara C. Chandrasekharappa, Alison Homstad, Katherine D. Westreich, Guanghong Wu, Yutao Liu, Danniele G. Holanda, Jason Clarke, Peter Lavin, Angelica Selim, Sara Miller, John S. Wiener, Sherry S. Ross, John W. Foreman, Charles N. Rotimi, Michelle P. Winn
Foilsithe / Cruthaithe 2013Artigo -
6
Mutations in the Gene That Encodes the F-Actin Binding Protein Anillin Cause FSGS de réir Rasheed Gbadegesin, Gentzon Hall, Adebowale Adeyemo, Nils Hanke, Irini Tossidou, James L. Burchette, Guanghong Wu, Alison Homstad, Matthew A. Sparks, José A. Gómez, Ruiji Jiang, Andrea Alonso, Peter Lavin, Peter J. Conlon, Ron Korstanje, M. Ständer, Ghaidan A. Shamsan, Moumita Barua, Robert F. Spurney, Pravin C. Singhal, Jeffrey B. Kopp, Hermann Haller, David N. Howell, Martin R. Pollak, Andréy S. Shaw, Mario Schiffer, Michelle P. Winn
Foilsithe / Cruthaithe 2014Artigo -
7
HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome de réir Rasheed Gbadegesin, Adebowale Adeyemo, Nicholas J.A. Webb, Larry A. Greenbaum, Asiri Abeyagunawardena, Shenal Thalgahagoda, Arundhati S. Kale, Debbie S. Gipson, Tarak Srivastava, Jen-Jar Lin, Deepa H. Chand, Tracy E. Hunley, Patrick D. Brophy, Arvind Bagga, Aditi Sinha, Michelle N. Rheault, Joanna R. Ghali, Kathy Nicholls, Elizabeth Abraham, Halima S. Janjua, Abiodun Omoloja, Gina-Marie Barletta, Yi Cai, David Milford, Catherine O’Brien, Atif Awan, Vladimir Belostotsky, William E. Smoyer, Alison Homstad, Gentzon Hall, Guanghong Wu, Shashi Nagaraj, Delbert R. Wigfall, John W. Foreman, Michelle P. Winn
Foilsithe / Cruthaithe 2014Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Genetics
Kidney
Medicine
Focal segmental glomerulosclerosis
Gene
Glomerulonephritis
Mutation
Endocrinology
Exome sequencing
Internal medicine
Missense mutation
Pathology
Proteinuria
Cancer research
Disease
Exome
Kidney disease
Nephrotic syndrome
Podocyte
Slit diaphragm
Actin cytoskeleton
Albuminuria
Alport syndrome
Angiotensin II
Antigen
Candidate gene
Cell
Cell biology
Chemistry