Response to COL4A3/COL4A4 heterozygous mutations with TBMN presenting as focal segmental glomerulosclerosis

Por Gbadegesin, Rasheed A
Publicado no Kidney Int (2015)

Translating genetic findings in hereditary nephrotic syndrome: the missing loops

Por Hall, Gentzon, Gbadegesin, Rasheed A.
Publicado no Am J Physiol Renal Physiol (2015)

The Genetics of Nephrotic Syndrome

Por Rheault, Michelle N., Gbadegesin, Rasheed A.
Publicado no J Pediatr Genet (2015)

GENETICS OF CHILDHOOD STEROID SENSITIVE NEPHROTIC SYNDROME (SSNS)

Por Karp, Alana M., Gbadegesin, Rasheed A.
Publicado no Pediatr Nephrol (2016)

GENETIC TESTING IN NEPHROTIC SYNDROME: CHALLENGES AND OPPORTUNITIES

Por Gbadegesin, Rasheed, Winn, Michelle, Smoyer, William E.
Publicado em 2013

PATHOGENESIS AND THERAPY OF FOCAL SEGMENTAL GLOMERULOSCLEROSIS: AN UPDATE

Por Gbadegesin, Rasheed, Lavin, Peter, Foreman, John, Winn, Michelle
Publicado em 2010

Therapeutic targets in focal and segmental glomerulosclerosis

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

Vesicoureteral reflux and the extracellular matrix connection

Por Tokhmafshan, Fatima, Brophy, Patrick D., Gbadegesin, Rasheed A., Gupta, Indra R.
Publicado no Pediatr Nephrol (2016)

Specific Podocin Mutations Correlate with Age of Onset in Steroid-Resistant Nephrotic Syndrome

Por Hinkes, Bernward, Vlangos, Christopher, Heeringa, Saskia, Mucha, Bettina, Gbadegesin, Rasheed, Liu, Jinhong, Hasselbacher, Katrin, Ozaltin, Fatih, Hildebrandt, Friedhelm
Publicado em 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 em 2008

Efficacy of Antibiotic Prophylaxis in Children with Vesicoureteral Reflux: Systematic Review and Meta-Analysis

Por Wang, Hsin-Hsiao S., Gbadegesin, Rasheed A., Foreman, John W., Nagaraj, Shashi K., Wigfall, Delbert R., Wiener, John S., Routh, Jonathan C.
Publicado no J Urol (2014)

Dysregulation of WTI (−KTS) is Associated with the Kidney-Specific Effects of the LMX1B R246Q Mutation

Por Hall, Gentzon, Lane, Brandon, Chryst-Ladd, Megan, Wu, Guanghong, Lin, Jen-Jar, Qin, XueJun, Hauser, Elizabeth R., Gbadegesin, Rasheed
Publicado no Sci Rep (2017)

Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome

Por Chernin, Gil, Heeringa, Saskia F., Gbadegesin, Rasheed, Liu, Jinhong, Hinkes, Bernward G., Vlangos, Christopher N., Vega-Warner, Virginia, Hildebrandt, Friedhelm
Publicado no Pediatr Nephrol (2008)

Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome

Por Heeringa, Saskia F., Vlangos, Christopher N., Chernin, Gil, Hinkes, Bernward, Gbadegesin, Rasheed, Liu, Jinhong, Hoskins, Bethan E., Ozaltin, Fatih, Hildebrandt, Friedhelm
Publicado em 2008

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 no 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 em 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 em 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 em 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 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