Sita Reddy, PhD

Associate Professor of Cancer Biology

Co-Director of the Molecular Medicine PhD Program

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Publications

  • Mbnl1 and Mbnl2 regulate brain structural integrity in mice. Commun Biol. 2021 11 30; 4(1):1342.. View in PubMed
  • Transcriptome-wide regulation of pre-mRNA splicing and mRNA localization by muscleblind proteins. Cell. 2012 Aug 17; 150(4):710-24.. View in PubMed
  • A filtering strategy identifies FOXQ1 as a potential effector of lamin A dysfunction. Aging (Albany NY). 2012 Aug; 4(8):567-77.. View in PubMed
  • Lamin A, farnesylation and aging. Exp Cell Res. 2012 Jan 01; 318(1):1-7.. View in PubMed
  • RNA splicing is responsive to MBNL1 dose. PLoS One. 2012; 7(11):e48825.. View in PubMed
  • Expanded CUG repeats Dysregulate RNA splicing by altering the stoichiometry of the muscleblind 1 complex. J Biol Chem. 2011 Nov 04; 286(44):38427-38438.. View in PubMed
  • RNA steady-state defects in myotonic dystrophy are linked to nuclear exclusion of SHARP. EMBO Rep. 2011 Jul 01; 12(7):735-42.. View in PubMed
  • Cell cycle-regulated association between the Werner syndrome protein and its molecular partners. Cell Cycle. 2011 Jun 15; 10(12):2038-40.. View in PubMed
  • Depletion of Ku70/80 reduces the levels of extrachromosomal telomeric circles and inhibits proliferation of ALT cells. Aging (Albany NY). 2011 Apr; 3(4):395-406.. View in PubMed
  • Accumulation of distinct prelamin A variants in human diploid fibroblasts differentially affects cell homeostasis. Exp Cell Res. 2011 Feb 01; 317(3):319-29.. View in PubMed
  • Processing of human telomeres by the Werner syndrome protein. Cell Cycle. 2010 Aug 15; 9(16):3137-8.. View in PubMed
  • Muscleblind-like 1 (Mbnl1) promotes insulin receptor exon 11 inclusion via binding to a downstream evolutionarily conserved intronic enhancer. J Biol Chem. 2010 Aug 13; 285(33):25426-37.. View in PubMed
  • Muscleblind1, but not Dmpk or Six5, contributes to a complex phenotype of muscular and motivational deficits in mouse models of myotonic dystrophy. PLoS One. 2010 Mar 25; 5(3):e9857.. View in PubMed
  • Altered nuclear functions in progeroid syndromes: a paradigm for aging research. ScientificWorldJournal. 2009 Dec 16; 9:1449-62.. View in PubMed
  • Sequence-specific processing of telomeric 3′ overhangs by the Werner syndrome protein exonuclease activity. Aging (Albany NY). 2009 Mar 17; 1(3):289-302.. View in PubMed
  • Perturbation of wild-type lamin A metabolism results in a progeroid phenotype. Aging Cell. 2008 Jun; 7(3):355-67.. View in PubMed
  • WRN controls formation of extrachromosomal telomeric circles and is required for TRF2DeltaB-mediated telomere shortening. Mol Cell Biol. 2008 Mar; 28(6):1892-904.. View in PubMed
  • Cytoplasmic CUG RNA foci are insufficient to elicit key DM1 features. PLoS One. 2008; 3(12):e3968.. View in PubMed
  • Role of myotonic dystrophy protein kinase (DMPK) in glucose homeostasis and muscle insulin action. PLoS One. 2007 Nov 07; 2(11):e1134.. View in PubMed
  • Interaction of muscleblind, CUG-BP1 and hnRNP H proteins in DM1-associated aberrant IR splicing. EMBO J. 2006 Sep 20; 25(18):4271-83.. View in PubMed
  • CK2-mediated stimulation of Pol I transcription by stabilization of UBF-SL1 interaction. Nucleic Acids Res. 2006; 34(17):4752-66.. View in PubMed
  • Decreased expression of DMPK: correlation with CTG repeat expansion and fibre type composition in myotonic dystrophy type 1. Neurol Sci. 2005 Oct; 26(4):235-42.. View in PubMed
  • Myotonia and muscle contractile properties in mice with SIX5 deficiency. Muscle Nerve. 2005 Apr; 31(4):503-5.. View in PubMed
  • Myotonic dystrophy protein kinase phosphorylates phospholamban and regulates calcium uptake in cardiomyocyte sarcoplasmic reticulum. J Biol Chem. 2005 Mar 04; 280(9):8016-21.. View in PubMed
  • MBNL1 is the primary determinant of focus formation and aberrant insulin receptor splicing in DM1. J Biol Chem. 2005 Feb 18; 280(7):5773-80.. View in PubMed
  • In situ hybridization analysis of Dmpk mRNA in adult mouse tissues. Neuromuscul Disord. 2004 Sep; 14(8-9):497-506.. View in PubMed
  • Six5 is required for spermatogenic cell survival and spermiogenesis. Hum Mol Genet. 2004 Jul 15; 13(14):1421-31.. View in PubMed
  • Abnormal Na channel gating in murine cardiac myocytes deficient in myotonic dystrophy protein kinase. Physiol Genomics. 2003 Jan 15; 12(2):147-57.. View in PubMed
  • Characterization of cardiac conduction system abnormalities in mice with targeted disruption of Six5 gene. J Interv Card Electrophysiol. 2002 Oct; 7(2):127-35.. View in PubMed
  • Effects of age and gene dose on skeletal muscle sodium channel gating in mice deficient in myotonic dystrophy protein kinase. Muscle Nerve. 2002 Jun; 25(6):850-7.. View in PubMed
  • Skeletal muscle Na currents in mice heterozygous for Six5 deficiency. Physiol Genomics. 2001 Aug 28; 6(3):153-8.. View in PubMed
  • RNA CUG repeats sequester CUGBP1 and alter protein levels and activity of CUGBP1. J Biol Chem. 2001 Mar 16; 276(11):7820-6.. View in PubMed
  • Skeletal muscle sodium channel gating in mice deficient in myotonic dystrophy protein kinase. Hum Mol Genet. 2000 Sep 22; 9(15):2313-20.. View in PubMed
  • Progressive atrioventricular conduction block in a mouse myotonic dystrophy model. J Interv Card Electrophysiol. 2000 Jun; 4(2):351-8.. View in PubMed
  • Heterozygous loss of Six5 in mice is sufficient to cause ocular cataracts. Nat Genet. 2000 May; 25(1):110-4.. View in PubMed
  • Localization of the sites of conduction abnormalities in a mouse model of myotonic dystrophy. J Cardiovasc Electrophysiol. 1999 Sep; 10(9):1214-20.. View in PubMed
  • DMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy model. J Clin Invest. 1999 Feb; 103(4):R1-7.. View in PubMed
  • CTG repeats show bimodal amplification in E. coli. Cell. 1998 Nov 13; 95(4):531-40.. View in PubMed
  • Altered phosphorylation and intracellular distribution of a (CUG)n triplet repeat RNA-binding protein in patients with myotonic dystrophy and in myotonin protein kinase knockout mice. Proc Natl Acad Sci U S A. 1997 Nov 25; 94(24):13221-6.. View in PubMed
  • Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathy. Nat Genet. 1996 Jul; 13(3):325-35.. View in PubMed

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