Monica M. Jablonski - Publications

Affiliations: 
University of Tennessee Health Science Center, Memphis, TN, United States 
Area:
Neuroscience Biology

58 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Chintalapudi SR, Djenderedjian L, Stiemke AB, Steinle JJ, Jablonski MM, Morales-Tirado VM. Isolation and Molecular Profiling of Primary Mouse Retinal Ganglion Cells: Comparison of Phenotypes from Healthy and Glaucomatous Retinas. Frontiers in Aging Neuroscience. 8: 93. PMID 27242509 DOI: 10.3389/fnagi.2016.00093  0.52
2016 Li H, Palamoor M, Jablonski MM. Poly(ortho ester) nanoparticles targeted for chronic intraocular diseases: ocular safety and localization after intravitreal injection. Nanotoxicology. 1-27. PMID 27108911 DOI: 10.1080/17435390.2016.1181808  0.52
2016 Lu H, Lu L, Williams RW, Jablonski MM. Iris transillumination defect and its gene modulators do not correlate with intraocular pressure in the BXD family of mice Molecular Vision. 22: 224-233.  0.52
2015 Chintalapudi SR, Morales-Tirado VM, Williams RW, Jablonski MM. Multipronged Approach to Identify and Validate a Novel Upstream Regulator of Sncg in Mouse Retinal Ganglion Cells. The Febs Journal. PMID 26663874 DOI: 10.1111/febs.13620  0.52
2015 Sahu B, Chavali VR, Alapati A, Suk J, Bartsch DU, Jablonski MM, Ayyagari R. Presence of rd8 mutation does not alter the ocular phenotype of late-onset retinal degeneration mouse model. Molecular Vision. 21: 273-84. PMID 25814825  0.52
2014 Mary-Sinclair MN, Wang X, Swanson DJ, Sung CY, Mendonca EA, Wroblewski K, Baumer SH, Goldowitz D, Jablonski MM, Skapek SX. Varied manifestations of persistent hyperplastic primary vitreous with graded somatic mosaic deletion of a single gene. Molecular Vision. 20: 215-30. PMID 24623965  0.52
2014 Swaminathan S, Li H, Palamoor M, de Obarrio WT, Madhura D, Meibohm B, Jablonski MM. Novel endogenous glycan therapy for retinal diseases: safety, in vitro stability, ocular pharmacokinetic modeling, and biodistribution. The Aaps Journal. 16: 311-23. PMID 24470212 DOI: 10.1208/s12248-014-9563-1  0.52
2014 Palamoor M, Jablonski MM. Comparative study on diffusion and evaporation emulsion methods used to load hydrophilic drugs in poly(ortho ester) nanoparticle emulsions Powder Technology. 253: 53-62. DOI: 10.1016/j.powtec.2013.11.014  0.52
2013 Palamoor M, Jablonski MM. Synthesis, characterization and in vitro studies of celecoxib-loaded poly(ortho ester) nanoparticles targeted for intraocular drug delivery. Colloids and Surfaces. B, Biointerfaces. 112: 474-82. PMID 24103464 DOI: 10.1016/j.colsurfb.2013.07.039  0.52
2013 Ibrahim MM, Abd-Elgawad AE, Soliman OA, Jablonski MM. Novel topical ophthalmic formulations for management of glaucoma. Pharmaceutical Research. 30: 2818-31. PMID 23771565 DOI: 10.1007/s11095-013-1109-1  0.52
2013 Swaminathan S, Lu H, Williams RW, Lu L, Jablonski MM. Genetic modulation of the iris transillumination defect: a systems genetics analysis using the expanded family of BXD glaucoma strains. Pigment Cell & Melanoma Research. 26: 487-98. PMID 23582180 DOI: 10.1111/pcmr.12106  0.52
2013 Templeton JP, Freeman NE, Nickerson JM, Jablonski MM, Rex TS, Williams RW, Geisert EE. Innate immune network in the retina activated by optic nerve crush. Investigative Ophthalmology & Visual Science. 54: 2599-606. PMID 23493296 DOI: 10.1167/iovs.12-11175  0.52
2013 Ibrahim MM, Abd-Elgawad AE, Soliman OA, Jablonski MM. Nanoparticle-based topical ophthalmic formulations for sustained celecoxib release. Journal of Pharmaceutical Sciences. 102: 1036-53. PMID 23293035 DOI: 10.1002/jps.23417  0.52
2013 Palamoor M, Jablonski MM. Poly(ortho ester) nanoparticle-based targeted intraocular therapy for controlled release of hydrophilic molecules. Molecular Pharmaceutics. 10: 701-8. PMID 23256649 DOI: 10.1021/mp300488s  0.52
2011 Lu H, Li L, Watson ER, Williams RW, Geisert EE, Jablonski MM, Lu L. Complex interactions of Tyrp1 in the eye. Molecular Vision. 17: 2455-68. PMID 21976956  0.52
2011 Lu H, Wang X, Pullen M, Guan H, Chen H, Sahu S, Zhang B, Chen H, Williams RW, Geisert EE, Lu L, Jablonski MM. Genetic dissection of the Gpnmb network in the eye. Investigative Ophthalmology & Visual Science. 52: 4132-42. PMID 21398278 DOI: 10.1167/iovs.10-6493  0.52
2011 Chavali VR, Khan NW, Cukras CA, Bartsch DU, Jablonski MM, Ayyagari R. A CTRP5 gene S163R mutation knock-in mouse model for late-onset retinal degeneration. Human Molecular Genetics. 20: 2000-14. PMID 21349921 DOI: 10.1093/hmg/ddr080  0.52
2011 Jablonski MM, Freeman NE, Orr WE, Templeton JP, Lu L, Williams RW, Geisert EE. Genetic pathways regulating glutamate levels in retinal Müller cells. Neurochemical Research. 36: 594-603. PMID 20882406 DOI: 10.1007/s11064-010-0277-1  0.52
2010 Wang X, Tong Y, Giorgianni F, Beranova-Giorgianni S, Penn JS, Jablonski MM. Cellular retinol binding protein 1 modulates photoreceptor outer segment folding in the isolated eye. Developmental Neurobiology. 70: 623-35. PMID 20506167 DOI: 10.1002/dneu.20798  0.52
2010 Nookala S, Gandrakota R, Wohabrebbi A, Wang X, Howell D, Giorgianni F, Beranova-Giorgianni S, Desiderio DM, Jablonski MM. In search of the identity of the XAP-1 antigen: a protein localized to cone outer segments. Investigative Ophthalmology & Visual Science. 51: 2736-43. PMID 20042652 DOI: 10.1167/iovs.09-4286  0.52
2009 Vasireddy V, Jablonski MM, Khan NW, Wang XF, Sahu P, Sparrow JR, Ayyagari R. Elovl4 5-bp deletion knock-in mouse model for Stargardt-like macular degeneration demonstrates accumulation of ELOVL4 and lipofuscin. Experimental Eye Research. 89: 905-12. PMID 19682985 DOI: 10.1016/j.exer.2009.07.021  0.52
2009 Reddy GB, Vasireddy V, Mandal MN, Tiruvalluru M, Wang XF, Jablonski MM, Nappanveettil G, Ayyagari R. A novel rat model with obesity-associated retinal degeneration. Investigative Ophthalmology & Visual Science. 50: 3456-63. PMID 19369235 DOI: 10.1167/iovs.08-2498  0.52
2009 Wang X, Nookala S, Narayanan C, Giorgianni F, Beranova-Giorgianni S, McCollum G, Gerling I, Penn JS, Jablonski MM. Proteomic analysis of the retina: removal of RPE alters outer segment assembly and retinal protein expression. Glia. 57: 380-92. PMID 18803304 DOI: 10.1002/glia.20765  0.52
2008 Berry RB, Werner DF, Wang X, Jablonski MM, Homanics GE, Mittleman G, Matthews DB. Mice with targeted genetic reduction of GABA(A) receptor alpha1 subunits display performance differences in Morris water maze tasks. Neurobiology of Learning and Memory. 90: 580-3. PMID 18625330 DOI: 10.1016/j.nlm.2008.06.004  0.52
2007 Mura M, Sereda C, Jablonski MM, MacDonald IM, Iannaccone A. Clinical and functional findings in choroideremia due to complete deletion of the CHM gene. Archives of Ophthalmology (Chicago, Ill. : 1960). 125: 1107-13. PMID 17698759 DOI: 10.1001/archopht.125.8.1107  0.52
2007 Jablonski MM, Iannaccone A, Reynolds DH, Gallaher P, Allen S, Wang X, Reiner A. Age-related decline in VIP-positive parasympathetic nerve fibers in the human submacular choroid. Investigative Ophthalmology & Visual Science. 48: 479-85. PMID 17251439 DOI: 10.1167/iovs.06-0972  0.52
2006 Mandal MN, Vasireddy V, Jablonski MM, Wang X, Heckenlively JR, Hughes BA, Reddy GB, Ayyagari R. Spatial and temporal expression of MFRP and its interaction with CTRP5. Investigative Ophthalmology & Visual Science. 47: 5514-21. PMID 17122143 DOI: 10.1167/iovs.06-0449  0.52
2006 Mandal MN, Vasireddy V, Reddy GB, Wang X, Moroi SE, Pattnaik BR, Hughes BA, Heckenlively JR, Hitchcock PF, Jablonski MM, Ayyagari R. CTRP5 is a membrane-associated and secretory protein in the RPE and ciliary body and the S163R mutation of CTRP5 impairs its secretion. Investigative Ophthalmology & Visual Science. 47: 5505-13. PMID 17122142 DOI: 10.1167/iovs.06-0312  0.52
2006 Vasireddy V, Jablonski MM, Mandal MN, Raz-Prag D, Wang XF, Nizol L, Iannaccone A, Musch DC, Bush RA, Salem N, Sieving PA, Ayyagari R. Elovl4 5-bp-deletion knock-in mice develop progressive photoreceptor degeneration. Investigative Ophthalmology & Visual Science. 47: 4558-68. PMID 17003453 DOI: 10.1167/iovs.06-0353  0.52
2006 Iannaccone A, Mura M, Dyka FM, Ciccarelli ML, Yashar BM, Ayyagari R, Jablonski MM, Molday RS. An unusual X-linked retinoschisis phenotype and biochemical characterization of the W112C RS1 mutation. Vision Research. 46: 3845-52. PMID 16884758 DOI: 10.1016/j.visres.2006.06.011  0.52
2006 Talamas E, Jackson L, Koeberl M, Jackson T, McElwee JL, Hawes NL, Chang B, Jablonski MM, Sidjanin DJ. Early transposable element insertion in intron 9 of the Hsf4 gene results in autosomal recessive cataracts in lop11 and ldis1 mice. Genomics. 88: 44-51. PMID 16595169 DOI: 10.1016/j.ygeno.2006.02.012  0.52
2005 Johnson DK, Rinchik EM, Moustaid-Moussa N, Miller DR, Williams RW, Michaud EJ, Jablonski MM, Elberger A, Hamre K, Smeyne R, Chesler E, Goldowitz D. Phenotype screening for genetically determined age-onset disorders and increased longevity in ENU-mutagenized mice. Age (Dordrecht, Netherlands). 27: 75-90. PMID 23598606 DOI: 10.1007/s11357-005-4131-3  0.52
2005 Wang X, Iannaccone A, Jablonski MM. Contribution of Müller cells toward the regulation of photoreceptor outer segment assembly. Neuron Glia Biology. 1: 1-6. PMID 16528406 DOI: 10.1017/s1740925x05000049  0.32
2005 Jablonski MM, Wang X, Lu L, Miller DR, Rinchik EM, Williams RW, Goldowitz D. The Tennessee Mouse Genome Consortium: identification of ocular mutants. Visual Neuroscience. 22: 595-604. PMID 16332270 DOI: 10.1017/S0952523805225087  0.52
2005 Vasireddy V, Vijayasarathy C, Huang J, Wang XF, Jablonski MM, Petty HR, Sieving PA, Ayyagari R. Stargardt-like macular dystrophy protein ELOVL4 exerts a dominant negative effect by recruiting wild-type protein into aggresomes. Molecular Vision. 11: 665-76. PMID 16163264  0.52
2005 Jablonski MM, Dalke C, Wang X, Lu L, Manly KF, Pretsch W, Favor J, Pardue MT, Rinchik EM, Williams RW, Goldowitz D, Graw J. An ENU-induced mutation in Rs1h causes disruption of retinal structure and function. Molecular Vision. 11: 569-81. PMID 16088326  0.52
2005 Iannaccone A, Mykytyn K, Persico AM, Searby CC, Baldi A, Jablonski MM, Sheffield VC. Clinical evidence of decreased olfaction in Bardet-Biedl syndrome caused by a deletion in the BBS4 gene. American Journal of Medical Genetics. Part A. 132: 343-6. PMID 15654695 DOI: 10.1002/ajmg.a.30512  0.52
2004 Wang X, Iannaccone A, Jablonski MM. Contribution of Müller cells toward the regulation of photoreceptor outer segment assembly. Neuron Glia Biology. 1: 291-6. PMID 18634602 DOI: doi:10.1017/S1740925X05000049  0.32
2004 Martin AC, Thornton JD, Liu J, Wang X, Zuo J, Jablonski MM, Chaum E, Zindy F, Skapek SX. Pathogenesis of persistent hyperplastic primary vitreous in mice lacking the Arf tumor suppressor gene Investigative Ophthalmology and Visual Science. 45: 3387-3396. PMID 15452040 DOI: 10.1167/iovs.04-0349  0.52
2004 Jablonski MM, Lu L, Wang X, Chesler EJ, Carps E, Qi S, Gu J, Williams RW. The ldis1 lens mutation in RIIIS/J mice maps to chromosome 8 near cadherin 1. Molecular Vision. 10: 577-87. PMID 15343150  0.52
2004 Iannaccone A, Wang X, Jablonski MM, Kuo SF, Baldi A, Cosgrove D, Morton CC, Swaroop A. Increasing evidence for syndromic phenotypes associated with RPGR mutations. American Journal of Ophthalmology. 137: 785-6; author reply . PMID 15059739 DOI: 10.1016/j.ajo.2003.11.050  0.52
2004 Ambasudhan R, Wang X, Jablonski MM, Thompson DA, Lagali PS, Wong PW, Sieving PA, Ayyagari R. Atrophic macular degeneration mutations in ELOVL4 result in the intracellular misrouting of the protein. Genomics. 83: 615-25. PMID 15028284 DOI: 10.1016/j.ygeno.2003.10.004  0.52
2003 Jablonski MM. The intact Xenopus laevis eye rudiment: a quasi-in vivo system for the study of retinal development and degenerations. Advances in Experimental Medicine and Biology. 533: 189-96. PMID 15180264  0.52
2003 Wang X, Iannaccone A, Jablonski MM. Permissive glycan support of photoreceptor outer segment assembly occurs via a non-metabolic mechanism. Molecular Vision. 9: 701-9. PMID 14685143  0.52
2003 Iannaccone A, Breuer DK, Wang XF, Kuo SF, Normando EM, Filippova E, Baldi A, Hiriyanna S, MacDonald CB, Baldi F, Cosgrove D, Morton CC, Swaroop A, Jablonski MM. Clinical and immunohistochemical evidence for an X linked retinitis pigmentosa syndrome with recurrent infections and hearing loss in association with an RPGR mutation. Journal of Medical Genetics. 40: e118. PMID 14627685  0.52
2003 Semenova E, Wang X, Jablonski MM, Levorse J, Tilghman SM. An engineered 800 kilobase deletion of Uchl3 and Lmo7 on mouse chromosome 14 causes defects in viability, postnatal growth and degeneration of muscle and retina. Human Molecular Genetics. 12: 1301-12. PMID 12761045 DOI: 10.1093/hmg/ddg140  0.52
2002 Koenekoop RK, Fishman GA, Iannaccone A, Ezzeldin H, Ciccarelli ML, Baldi A, Sunness JS, Lotery AJ, Jablonski MM, Pittler SJ, Maumenee I. Electroretinographic abnormalities in parents of patients with Leber congenital amaurosis who have heterozygous GUCY2D mutations. Archives of Ophthalmology (Chicago, Ill. : 1960). 120: 1325-30. PMID 12365911  0.52
2002 Wohabrebbi A, Umstot ES, Iannaccone A, Desiderio DM, Jablonski MM. Downregulation of a unique photoreceptor protein correlates with improper outer segment assembly. Journal of Neuroscience Research. 67: 298-308. PMID 11813234 DOI: 10.1002/jnr.10107  0.52
2002 Bhattacharya G, Miller C, Kimberling WJ, Jablonski MM, Cosgrove D. Localization and expression of usherin: a novel basement membrane protein defective in people with Usher's syndrome type IIa. Hearing Research. 163: 1-11. PMID 11788194 DOI: 10.1016/S0378-5955(01)00344-6  0.52
2001 Skapek SX, Lin SCJ, Jablonski MM, Mckeller RN, Tan M, Hu N, Lee EYHP. Persistent expression of cyclin D1 disrupts normal photoreceptor differentiation and retina development Oncogene. 20: 6742-6751. PMID 11709709 DOI: 10.1038/sj.onc.1204876  0.52
2001 Jablonski MM. Investigating the mechanisms of retinal degenerations with antisense oligonucleotides Documenta Ophthalmologica. 102: 179-196. PMID 11556485 DOI: 10.1023/A:1017518717710  0.52
2001 Jablonski MM, Tombran-Tink J, Mrazek DA, Iannaccone A. Pigment epithelium-derived factor supports normal Müller cell development and glutamine synthetase expression after removal of the retinal pigment epithelium Glia. 35: 14-25. PMID 11424188 DOI: 10.1002/glia.1066  0.52
2001 Jablonski MM, Graney MJ, Kritchevsky SB, Iannaccone A. Reliability assessment of a rod photoreceptor outer segment grading system Experimental Eye Research. 72: 573-579. PMID 11311049 DOI: 10.1006/exer.2001.0987  0.52
2001 Jablonski MM, Iannaccone A. Lactose supports Müller cell protein expression patterns in the absence of the retinal pigment epithelium Molecular Vision. 7: 27-35. PMID 11239243  0.52
2000 Jablonski MM, Iannaccone A. Targeted disruption of Muller cell metabolism induces photoreceptor dysmorphogenesis Glia. 32: 192-204. PMID 11008218 DOI: 10.1002/1098-1136(200011)32:2<192::AID-GLIA80>3.0.CO;2-6  0.52
2000 Jablonski MM, Tombran-Tink J, Mrazek DA, Iannaccone A. Pigment epithelium-derived factor supports normal development of photoreceptor neurons and opsin expression after retinal pigment epithelium removal Journal of Neuroscience. 20: 7149-7157. PMID 11007870  0.52
2000 Jablonski MM, Ervin CS. Closer look at lactose-mediated support of retinal morphogenesis Anatomical Record. 259: 205-214. PMID 10820322 DOI: 10.1002/(SICI)1097-0185(20000601)259:2<205::AID-AR10>3.0.CO;2-4  0.52
1999 Jablonski MM, Wohabrebbi A, Ervin CS. Lactose promotes organized photoreceptor outer segment assembly and preserves expression of photoreceptor proteins in retinal degeneration. Molecular Vision. 5: 16. PMID 10449803  0.52
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