Faculty

Sita Reddy

Sita Reddy

Associate Professor of Cancer Biology;Co-Director of the Molecular Medicine PhD Program
Medicine
HMR 702A, HRM 704, 2011 Zonal Avenue Health Sciences Campus Los Angeles

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

RNA splicing is responsive to MBNL1 dose PLoS One. 2012; 7(11):e48825. . View in PubMed

Lamin A, farnesylation and aging Exp Cell Res. 2012 Jan 01; 318(1):1-7. . 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 Ecoli. 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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