TRPC6 in glomerular health and disease: what we know and what we believe.

Por Schlöndorff, Johannes S., Pollak, Martin R.
Publicado em 2006

GLCCI1 single nucleotide polymorphisms in pediatric nephrotic syndrome

Por Cheong, Hae Il, Kang, Hee Gyung, Schlondorff, Johannes
Publicado em 2012

Gain-of-function Mutations in Transient Receptor Potential C6 (TRPC6) Activate Extracellular Signal-regulated Kinases 1/2 (ERK1/2)

Por Chiluiza, David, Krishna, Sneha, Schumacher, Valérie A., Schlöndorff, Johannes
Publicado em 2013

Inverted Formin 2 Regulates Actin Dynamics by Antagonizing Rho/Diaphanous-related Formin Signaling

Por Sun, Hua, Schlondorff, Johannes, Higgs, Henry N., Pollak, Martin R.
Publicado em 2013

TRPC6 mutations associated with focal segmental glomerulosclerosis cause constitutive activation of NFAT-dependent transcription

Por Schlöndorff, Johannes, del Camino, Donato, Carrasquillo, Robert, Lacey, Vanessa, Pollak, Martin R.
Publicado em 2009

Rho activation of mDia formins is modulated by an interaction with inverted formin 2 (INF2)

Por Sun, Hua, Schlondorff, Johannes S., Brown, Elizabeth J., Higgs, Henry N., Pollak, Martin R.
Publicado em 2011

SNF8, a member of the ESCRT-II complex, interacts with TRPC6 and enhances its channel activity

Por Carrasquillo, Robert, Tian, Dequan, Krishna, Sneha, Pollak, Martin R, Greka, Anna, Schlöndorff, Johannes
Publicado em 2012

Exome sequencing and in vitro studies identified podocalyxin as a candidate gene for focal and segmental glomerulosclerosis

Por Barua, Moumita, Shieh, Eric, Schlondorff, Johannes, Genovese, Giulio, Kaplan, Bernard S, Pollak, Martin R
Publicado em 2013

Disease-associated mutant α-actinin-4 reveals a mechanism for regulating its F-actin-binding affinity

Por Weins, Astrid, Schlondorff, Johannes S., Nakamura, Fumihiko, Denker, Bradley M., Hartwig, John H., Stossel, Thomas P., Pollak, Martin R.
Publicado em 2007

Functional genetic variation in aminopeptidase A (ENPEP): lack of clear association with focal and segmental glomerulosclerosis (FSGS)

Por Tonna, Stephen, Dandapani, Savita V., Uscinski, Andrea, Appel, Gerald B., Schlöndorff, Johannes S., Zhang, Kang, Denker, Bradley M., Pollak, Martin R.
Publicado em 2007

Mutations in the formin protein INF2 cause focal segmental glomerulosclerosis

Por Brown, Elizabeth J., Schlöndorff, Johannes S., Becker, Daniel J., Tsukaguchi, Hiroyasu, Uscinski, Andrea L., Higgs, Henry N., Henderson, Joel M., Pollak, Martin R.
Publicado em 2009

Antagonistic Regulation of Actin Dynamics and Cell Motility by TRPC5 and TRPC6 Channels

Por Tian, Dequan, Jacobo, Sarah M. P., Billing, David, Rozkalne, Anete, Gage, Steven D., Anagnostou, Theodora, Pavenstädt, Hermann, Hsu, Hsiang-Hao, Schlondorff, Johannes, Ramos, Arnolt, Greka, Anna
Publicado em 2010

Mice with mutant Inf2 show impaired podocyte and slit diaphragm integrity in response to protamine induced kidney injury

Por Subramanian, Balajikarthick, Sun, Hua, Yan, Paul, Charoonratana, Victoria T., Higgs, Henry N., Wang, Fang, Lai, Ka-Man V., Valenzuela, David M., Brown, Elizabeth J., Schlöndorff, Johannes S., Pollak, Martin R.
Publicado no Kidney Int (2016)

APOL1 kidney disease risk variants cause cytotoxicity by depleting cellular potassium and inducing stress-activated protein kinases

Por Olabisi, Opeyemi A., Zhang, Jia-Yue, VerPlank, Lynn, Zahler, Nathan, DiBartolo, Salvatore, Heneghan, John F., Schlöndorff, Johannes S., Suh, Jung Hee, Yan, Paul, Alper, Seth L., Friedman, David J., Pollak, Martin R.
Publicado no Proc Natl Acad Sci U S A (2016)