Rusiniak ME - Search Results

1

Tuberous sclerosis complex exhibits a new renal cystogenic mechanism.

Bissler JJ, Zadjali F, Bridges D, Astrinidis A, Barone S, Yao Y, Redd JR, Siroky BJ, Wang Y, Finley JT, Rusiniak ME, Baumann H, Zahedi K, Gross KW, Soleimani M. Bissler JJ, et al. Among authors: rusiniak me. Physiol Rep. 2019 Jan;7(2):e13983. doi: 10.14814/phy2.13983. Physiol Rep. 2019. PMID: 30675765 Free PMC article.

2

Cells of renin lineage take on a podocyte phenotype in aging nephropathy.

Pippin JW, Glenn ST, Krofft RD, Rusiniak ME, Alpers CE, Hudkins K, Duffield JS, Gross KW, Shankland SJ. Pippin JW, et al. Among authors: rusiniak me. Am J Physiol Renal Physiol. 2014 May 15;306(10):F1198-209. doi: 10.1152/ajprenal.00699.2013. Epub 2014 Mar 19. Am J Physiol Renal Physiol. 2014. PMID: 24647714 Free PMC article.

3

Molecular markers near the mouse brachymorphic (bm) gene, which affects connective tissues and bleeding time.

Rusiniak ME, O'Brien EP, Novak EK, Barone SM, McGarry MP, Reddington M, Swank RT. Rusiniak ME, et al. Mamm Genome. 1996 Feb;7(2):98-102. doi: 10.1007/s003359900027. Mamm Genome. 1996. PMID: 8835524

4

Tracking the stochastic fate of cells of the renin lineage after podocyte depletion using multicolor reporters and intravital imaging.

Kaverina NV, Kadoya H, Eng DG, Rusiniak ME, Sequeira-Lopez ML, Gomez RA, Pippin JW, Gross KW, Peti-Peterdi J, Shankland SJ. Kaverina NV, et al. Among authors: rusiniak me. PLoS One. 2017 Mar 22;12(3):e0173891. doi: 10.1371/journal.pone.0173891. eCollection 2017. PLoS One. 2017. PMID: 28329012 Free PMC article.

5

Targeted destruction of DNA replication protein Cdc6 by cell death pathways in mammals and yeast.

Blanchard F, Rusiniak ME, Sharma K, Sun X, Todorov I, Castellano MM, Gutierrez C, Baumann H, Burhans WC. Blanchard F, et al. Among authors: rusiniak me. Mol Biol Cell. 2002 May;13(5):1536-49. doi: 10.1091/mbc.02-02-0010. Mol Biol Cell. 2002. PMID: 12006651 Free PMC article.

6

Murine Hermansky-Pudlak syndrome genes: regulators of lysosome-related organelles.

Li W, Rusiniak ME, Chintala S, Gautam R, Novak EK, Swank RT. Li W, et al. Among authors: rusiniak me. Bioessays. 2004 Jun;26(6):616-28. doi: 10.1002/bies.20042. Bioessays. 2004. PMID: 15170859 Review.

7

Aberrant lung structure, composition, and function in a murine model of Hermansky-Pudlak syndrome.

Lyerla TA, Rusiniak ME, Borchers M, Jahreis G, Tan J, Ohtake P, Novak EK, Swank RT. Lyerla TA, et al. Among authors: rusiniak me. Am J Physiol Lung Cell Mol Physiol. 2003 Sep;285(3):L643-53. doi: 10.1152/ajplung.00024.2003. Epub 2003 May 30. Am J Physiol Lung Cell Mol Physiol. 2003. PMID: 12777251 Free article.

8

The Slc35d3 gene, encoding an orphan nucleotide sugar transporter, regulates platelet-dense granules.

Chintala S, Tan J, Gautam R, Rusiniak ME, Guo X, Li W, Gahl WA, Huizing M, Spritz RA, Hutton S, Novak EK, Swank RT. Chintala S, et al. Among authors: rusiniak me. Blood. 2007 Feb 15;109(4):1533-40. doi: 10.1182/blood-2006-08-040196. Epub 2006 Oct 24. Blood. 2007. PMID: 17062724 Free PMC article.

9

Mouse models of Hermansky Pudlak syndrome: a review.

Swank RT, Novak EK, McGarry MP, Rusiniak ME, Feng L. Swank RT, et al. Among authors: rusiniak me. Pigment Cell Res. 1998 Apr;11(2):60-80. doi: 10.1111/j.1600-0749.1998.tb00713.x. Pigment Cell Res. 1998. PMID: 9585243 Review.

10

The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindness.

Feng L, Seymour AB, Jiang S, To A, Peden AA, Novak EK, Zhen L, Rusiniak ME, Eicher EM, Robinson MS, Gorin MB, Swank RT. Feng L, et al. Among authors: rusiniak me. Hum Mol Genet. 1999 Feb;8(2):323-30. doi: 10.1093/hmg/8.2.323. Hum Mol Genet. 1999. PMID: 9931340

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