| 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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