Lozynska O - Search Results

1

Differential expression of utrophin-A and -B promoters in the central nervous system (CNS) of normal and dystrophic mdx mice.

Baby SM, Bogdanovich S, Willmann G, Basu U, Lozynska O, Khurana TS. Baby SM, et al. Among authors: lozynska o. Brain Pathol. 2010 Mar;20(2):323-42. doi: 10.1111/j.1750-3639.2009.00275.x. Epub 2009 May 22. Brain Pathol. 2010. PMID: 19486009 Free PMC article.

2

Ets-2 repressor factor silences extrasynaptic utrophin by N-box mediated repression in skeletal muscle.

Perkins KJ, Basu U, Budak MT, Ketterer C, Baby SM, Lozynska O, Lunde JA, Jasmin BJ, Rubinstein NA, Khurana TS. Perkins KJ, et al. Among authors: lozynska o. Mol Biol Cell. 2007 Aug;18(8):2864-72. doi: 10.1091/mbc.e06-12-1069. Epub 2007 May 16. Mol Biol Cell. 2007. PMID: 17507653 Free PMC article.

3

Heregulin-induced epigenetic regulation of the utrophin-A promoter.

Basu U, Gyrd-Hansen M, Baby SM, Lozynska O, Krag TO, Jensen CJ, Frödin M, Khurana TS. Basu U, et al. Among authors: lozynska o. FEBS Lett. 2007 Sep 4;581(22):4153-8. doi: 10.1016/j.febslet.2007.07.021. Epub 2007 Jul 23. FEBS Lett. 2007. PMID: 17692845 Free PMC article.

4

Translational regulation of utrophin by miRNAs.

Basu U, Lozynska O, Moorwood C, Patel G, Wilton SD, Khurana TS. Basu U, et al. Among authors: lozynska o. PLoS One. 2011;6(12):e29376. doi: 10.1371/journal.pone.0029376. Epub 2011 Dec 27. PLoS One. 2011. PMID: 22216264 Free PMC article.

5

Layer-specific differences of gene expression in extraocular muscles identified by laser-capture microscopy.

Budak MT, Bogdanovich S, Wiesen MH, Lozynska O, Khurana TS, Rubinstein NA. Budak MT, et al. Among authors: lozynska o. Physiol Genomics. 2004 Dec 15;20(1):55-65. doi: 10.1152/physiolgenomics.00191.2004. Epub 2004 Oct 5. Physiol Genomics. 2004. PMID: 15467012 Free article.

6

C. elegans dysferlin homolog fer-1 is expressed in muscle, and fer-1 mutations initiate altered gene expression of muscle enriched genes.

Krajacic P, Hermanowski J, Lozynska O, Khurana TS, Lamitina T. Krajacic P, et al. Among authors: lozynska o. Physiol Genomics. 2009 Dec 30;40(1):8-14. doi: 10.1152/physiolgenomics.00106.2009. Epub 2009 Sep 15. Physiol Genomics. 2009. PMID: 19755517 Free PMC article.

7

Drug discovery for Duchenne muscular dystrophy via utrophin promoter activation screening.

Moorwood C, Lozynska O, Suri N, Napper AD, Diamond SL, Khurana TS. Moorwood C, et al. Among authors: lozynska o. PLoS One. 2011;6(10):e26169. doi: 10.1371/journal.pone.0026169. Epub 2011 Oct 20. PLoS One. 2011. PMID: 22028826 Free PMC article.

8

QSulf1 remodels the 6-O sulfation states of cell surface heparan sulfate proteoglycans to promote Wnt signaling.

Ai X, Do AT, Lozynska O, Kusche-Gullberg M, Lindahl U, Emerson CP Jr. Ai X, et al. Among authors: lozynska o. J Cell Biol. 2003 Jul 21;162(2):341-51. doi: 10.1083/jcb.200212083. Epub 2003 Jul 14. J Cell Biol. 2003. PMID: 12860968 Free PMC article.

9

Identification of a novel pathogenic missense mutation in PRPF31 using whole exome sequencing: a case report.

Bryant L, Lozynska O, Marsh A, Papp TE, van Gorder L, Serrano LW, Gai X, Maguire AM, Aleman TS, Bennett J. Bryant L, et al. Among authors: lozynska o. Br J Ophthalmol. 2019 Jun;103(6):761-767. doi: 10.1136/bjophthalmol-2017-311405. Epub 2018 Jul 20. Br J Ophthalmol. 2019. PMID: 30030392 Free PMC article.

10

On variants and disease-causing mutations: Case studies of a SEMA4A variant identified in inherited blindness.

Bryant L, Lozynska O, Han G, Morgan JIW, Gai X, Maguire AM, Aleman T, Bennett J. Bryant L, et al. Among authors: lozynska o. Ophthalmic Genet. 2018 Jan-Feb;39(1):144-146. doi: 10.1080/13816810.2017.1354384. Epub 2017 Aug 14. Ophthalmic Genet. 2018. PMID: 28805479 Free PMC article.

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