Schlöndorff JS - Search Results

1

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

Schlöndorff JS, Pollak MR. Schlöndorff JS, et al. Semin Cell Dev Biol. 2006 Dec;17(6):667-74. doi: 10.1016/j.semcdb.2006.11.003. Epub 2006 Nov 20. Semin Cell Dev Biol. 2006. PMID: 17116414 Free PMC article. Review.

2

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

Schlöndorff J, Del Camino D, Carrasquillo R, Lacey V, Pollak MR. Schlöndorff J, et al. Am J Physiol Cell Physiol. 2009 Mar;296(3):C558-69. doi: 10.1152/ajpcell.00077.2008. Epub 2009 Jan 7. Am J Physiol Cell Physiol. 2009. PMID: 19129465 Free PMC article.

3

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

Carrasquillo R, Tian D, Krishna S, Pollak MR, Greka A, Schlöndorff J. Carrasquillo R, et al. BMC Cell Biol. 2012 Nov 21;13:33. doi: 10.1186/1471-2121-13-33. BMC Cell Biol. 2012. PMID: 23171048 Free PMC article.

4

Inverted formin 2 regulates actin dynamics by antagonizing Rho/diaphanous-related formin signaling.

Sun H, Schlondorff J, Higgs HN, Pollak MR. Sun H, et al. J Am Soc Nephrol. 2013 May;24(6):917-29. doi: 10.1681/ASN.2012080834. Epub 2013 Apr 25. J Am Soc Nephrol. 2013. PMID: 23620398 Free PMC article.

5

The Glomerular Disease Study and Trial Consortium: A Grassroots Initiative to Foster Collaboration and Innovation.

Poyan Mehr A, Sadeghi-Najafabadi M, Chau K, Messmer J, Pai R, Roy N, Friedman D, Pollak MR, Schlondorff J, Naljayan M, Singh T, Lecker SH, Rodby R, Germain M, Rennke H, Stillman IE. Poyan Mehr A, et al. Kidney Int Rep. 2018 Sep 21;4(1):20-29. doi: 10.1016/j.ekir.2018.09.012. eCollection 2019 Jan. Kidney Int Rep. 2018. PMID: 30596165 Free PMC article. Review.

6

Phosphorylation of ACTN4 Leads to Podocyte Vulnerability and Proteinuric Glomerulosclerosis.

Feng D, Kumar M, Muntel J, Gurley SB, Birrane G, Stillman IE, Ding L, Wang M, Ahmed S, Schlondorff J, Alper SL, Ferrante T, Marquez SL, Ng CF, Novak R, Ingber DE, Steen H, Pollak MR. Feng D, et al. J Am Soc Nephrol. 2020 Jul;31(7):1479-1495. doi: 10.1681/ASN.2019101032. Epub 2020 Jun 15. J Am Soc Nephrol. 2020. PMID: 32540856 Free PMC article.

7

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

Weins A, Schlondorff JS, Nakamura F, Denker BM, Hartwig JH, Stossel TP, Pollak MR. Weins A, et al. Among authors: schlondorff js. Proc Natl Acad Sci U S A. 2007 Oct 9;104(41):16080-5. doi: 10.1073/pnas.0702451104. Epub 2007 Sep 27. Proc Natl Acad Sci U S A. 2007. PMID: 17901210 Free PMC article.

8

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

Tonna S, Dandapani SV, Uscinski A, Appel GB, Schlöndorff JS, Zhang K, Denker BM, Pollak MR. Tonna S, et al. Among authors: schlondorff js. Gene. 2008 Feb 29;410(1):44-52. doi: 10.1016/j.gene.2007.11.014. Epub 2007 Dec 3. Gene. 2008. PMID: 18206321 Free PMC article.

9

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis.

Brown EJ, Schlöndorff JS, Becker DJ, Tsukaguchi H, Tonna SJ, Uscinski AL, Higgs HN, Henderson JM, Pollak MR. Brown EJ, et al. Among authors: schlondorff js. Nat Genet. 2010 Jan;42(1):72-6. doi: 10.1038/ng.505. Epub 2009 Dec 20. Nat Genet. 2010. PMID: 20023659 Free PMC article.

10

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

Barua M, Shieh E, Schlondorff J, Genovese G, Kaplan BS, Pollak MR. Barua M, et al. Kidney Int. 2014 Jan;85(1):124-33. doi: 10.1038/ki.2013.354. Epub 2013 Sep 18. Kidney Int. 2014. PMID: 24048372 Free PMC article.

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