| Year |
Citation |
Score |
| 2023 |
Bullock G, Johnson GS, Pattridge SG, Mhlanga-Mutangadura T, Guo J, Cook J, Campbell RS, Vite CH, Katz ML. A Homozygous Missense Mutation in a Doberman Pinscher Dog with Neurodegeneration, Cytoplasmic Vacuoles, Autofluorescent Storage Granules, and an α-Mannosidase Deficiency. Genes. 14. PMID 37761886 DOI: 10.3390/genes14091746 |
0.307 |
|
| 2022 |
Kick GR, Whiting REH, Ota-Kuroki J, Castaner LJ, Morgan-Jack B, Sabol JC, Meiman EJ, Ortiz F, Katz ML. Intravitreal gene therapy preserves retinal function in a canine model of CLN2 neuronal ceroid lipofuscinosis. Experimental Eye Research. 226: 109344. PMID 36509165 DOI: 10.1016/j.exer.2022.109344 |
0.326 |
|
| 2022 |
Bullock G, Johnson GS, Mhlanga-Mutangadura T, Petesch SC, Thompson S, Goebbels S, Katz ML. Lysosomal Storage Disease Associated with a CNP Sequence Variant in Dalmatian Dogs. Gene. 146513. PMID 35447247 DOI: 10.1016/j.gene.2022.146513 |
0.357 |
|
| 2022 |
Meiman EJ, Kick GR, Jensen CA, Coates JR, Katz ML. Characterization of neurological disease progression in a canine model of CLN5 neuronal ceroid lipofuscinosis. Developmental Neurobiology. 82: 326-344. PMID 35427439 DOI: 10.1002/dneu.22878 |
0.329 |
|
| 2021 |
Kick GR, Meiman EJ, Sabol JC, Whiting REH, Ota-Kuroki J, Castaner LJ, Jensen CA, Katz ML. Visual system pathology in a canine model of CLN5 neuronal ceroid lipofuscinosis. Experimental Eye Research. 108686. PMID 34216614 DOI: 10.1016/j.exer.2021.108686 |
0.326 |
|
| 2020 |
Whiting REH, Robinson GO, Ota-Kuroki J, Lim S, Castaner LJ, Jensen CA, Kowal J, Nguyen A, Corado C, O'Neill CA, Katz ML. Intravitreal enzyme replacement inhibits progression of retinal degeneration in canine CLN2 neuronal ceroid lipofuscinosis. Experimental Eye Research. 108135. PMID 32634395 DOI: 10.1016/J.Exer.2020.108135 |
0.417 |
|
| 2020 |
Whiting REH, Pearce JW, Vansteenkiste DP, Bibi K, Lim S, Robinson GO, Castaner LJ, Sinclair J, Chandra S, Nguyen A, O'Neill CA, Katz ML. Intravitreal enzyme replacement preserves retinal structure and function in canine CLN2 neuronal ceroid lipofuscinosis. Experimental Eye Research. 108130. PMID 32622066 DOI: 10.1016/J.Exer.2020.108130 |
0.436 |
|
| 2020 |
Katz ML, Buckley RM, Biegen V, O'Brien DP, Johnson GC, Warren WC, Lyons LA. Neuronal Ceroid Lipofuscinosis in a Domestic Cat Associated with a DNA Sequence Variant That Creates a Premature Stop Codon in . G3 (Bethesda, Md.). PMID 32518081 DOI: 10.1534/G3.120.401407 |
0.393 |
|
| 2019 |
Ru Y, Corado C, Soon RK, Melton AC, Harris A, Yu GK, Pryer N, Sinclair JR, Katz ML, Ajayi T, Jacoby D, Russell CB, Chandriani S. Neurofilament light is a treatment-responsive biomarker in CLN2 disease. Annals of Clinical and Translational Neurology. PMID 31814335 DOI: 10.1002/Acn3.50942 |
0.408 |
|
| 2019 |
Guo J, Johnson GS, Cook J, Harris OK, Mhlanga-Mutangadura T, Schnabel RD, Jensen CA, Katz ML. Neuronal ceroid lipofuscinosis in a German Shorthaired Pointer associated with a previously reported nonsense variant. Molecular Genetics and Metabolism Reports. 21: 100521. PMID 31687336 DOI: 10.1016/J.Ymgmr.2019.100521 |
0.441 |
|
| 2019 |
Villani NA, Bullock G, Michaels JR, Yamato O, O'Brien DP, Mhlanga-Mutangadura T, Johnson GS, Katz ML. A mixed breed dog with neuronal ceroid lipofuscinosis is homozygous for a CLN5 nonsense mutation previously identified in Border Collies and Australian Cattle Dogs. Molecular Genetics and Metabolism. PMID 31101435 DOI: 10.1016/J.Ymgme.2019.04.003 |
0.472 |
|
| 2019 |
Schmutz I, Jagannathan V, Bartenschlager F, Stein VM, Gruber AD, Leeb T, Katz ML. ATP13A2 missense variant in Australian Cattle Dogs with late onset neuronal ceroid lipofuscinosis. Molecular Genetics and Metabolism. PMID 30956123 DOI: 10.1016/J.Ymgme.2018.11.015 |
0.43 |
|
| 2018 |
Murgiano L, Becker D, Torjman D, Niggel JK, Milano A, Cullen C, Feng R, Wang F, Jagannathan V, Pearce-Kelling S, Katz ML, Leeb T, Aguirre GD. Complex Structural Variant Associated with Non-syndromic Canine Retinal Degeneration. G3 (Bethesda, Md.). PMID 30541930 DOI: 10.1534/G3.118.200859 |
0.435 |
|
| 2017 |
Katz ML, Rustad E, Robinson GO, Whiting REH, Student JT, Coates JR, Narfstrom K. Canine neuronal ceroid lipofuscinoses: Promising models for preclinical testing of therapeutic interventions. Neurobiology of Disease. PMID 28860089 DOI: 10.1016/J.Nbd.2017.08.017 |
0.449 |
|
| 2017 |
Kolicheski A, Johnson GS, Villani NA, O'Brien DP, Mhlanga-Mutangadura T, Wenger DA, Mikoloski K, Eagleson JS, Taylor JF, Schnabel RD, Katz ML. GM2 Gangliosidosis in Shiba Inu Dogs with an In-Frame Deletion in HEXB. Journal of Veterinary Internal Medicine. PMID 28833537 DOI: 10.1111/Jvim.14794 |
0.433 |
|
| 2017 |
Katz ML, Jensen CA, Student JT, Johnson GC, Coates JR. Cervical spinal cord and motor unit pathology in a canine model of SOD1-associated amyotrophic lateral sclerosis. Journal of the Neurological Sciences. 378: 193-203. PMID 28566164 DOI: 10.1016/J.Jns.2017.05.009 |
0.337 |
|
| 2017 |
Katz ML, Johnson GC, Leach SB, Williamson BG, Coates JR, Whiting RE, Vansteenkiste DP, Whitney MS. Extra-neuronal pathology in a canine model of CLN2 neuronal ceroid lipofuscinosis after intracerebroventricular gene therapy that delays neurological disease progression. Gene Therapy. PMID 28079862 DOI: 10.1038/Gt.2017.4 |
0.425 |
|
| 2016 |
Kolicheski A, Barnes Heller HL, Arnold S, Schnabel RD, Taylor JF, Knox CA, Mhlanga-Mutangadura T, O'Brien DP, Johnson GS, Dreyfus J, Katz ML. Homozygous PPT1 Splice Donor Mutation in a Cane Corso Dog With Neuronal Ceroid Lipofuscinosis. Journal of Veterinary Internal Medicine. PMID 28008682 DOI: 10.1111/Jvim.14632 |
0.451 |
|
| 2016 |
Tracy CJ, Whiting RE, Pearce JW, Williamson BG, Vansteenkiste DP, Gillespie LE, Castaner LJ, Bryan JN, Coates JR, Jensen CA, Katz ML. Intravitreal implantation of TPP1-transduced stem cells delays retinal degeneration in canine CLN2 neuronal ceroid lipofuscinosis. Experimental Eye Research. PMID 27637672 DOI: 10.1016/J.Exer.2016.09.003 |
0.472 |
|
| 2016 |
Stroud C, Dmitriev I, Kashentseva E, Bryan JN, Curiel DT, Rindt H, Reinero C, Henry CJ, Bergman PJ, Mason NJ, Gnanandarajah JS, Engiles JB, Gray F, Laughlin D, Gaurnier-Hausser A, ... ... Katz ML, et al. A One Health overview, facilitating advances in comparative medicine and translational research. Clinical and Translational Medicine. 5: 26. PMID 27558513 DOI: 10.1186/S40169-016-0107-4 |
0.325 |
|
| 2016 |
Ashwini A, D'Angelo A, Yamato O, Giordano C, Cagnotti G, Harcourt-Brown T, Mhlanga-Mutangadura T, Guo J, Johnson GS, Katz ML. Neuronal ceroid lipofuscinosis associated with an MFSD8 mutation in Chihuahuas. Molecular Genetics and Metabolism. PMID 27211611 DOI: 10.1016/J.Ymgme.2016.05.008 |
0.505 |
|
| 2016 |
Kolicheski A, Johnson GS, O'Brien DP, Mhlanga-Mutangadura T, Gilliam D, Guo J, Anderson-Sieg TD, Schnabel RD, Taylor JF, Lebowitz A, Swanson B, Hicks D, Niman ZE, Wininger FA, Carpentier MC, ... Katz ML, et al. Australian Cattle Dogs with Neuronal Ceroid Lipofuscinosis are Homozygous for a CLN5 Nonsense Mutation Previously Identified in Border Collies. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. PMID 27203721 DOI: 10.1111/Jvim.13971 |
0.42 |
|
| 2016 |
Ivansson EL, Megquier K, Kozyrev SV, Murén E, Körberg IB, Swofford R, Koltookian M, Tonomura N, Zeng R, Kolicheski AL, Hansen L, Katz ML, Johnson GC, Johnson GS, Coates JR, et al. Variants within the SP110 nuclear body protein modify risk of canine degenerative myelopathy. Proceedings of the National Academy of Sciences of the United States of America. PMID 27185954 DOI: 10.1073/Pnas.1600084113 |
0.426 |
|
| 2016 |
Whiting RE, Jensen CA, Pearce JW, Gillespie LE, Bristow DE, Katz ML. Intracerebroventricular gene therapy that delays neurological disease progression is associated with selective preservation of retinal ganglion cells in a canine model of CLN2 disease. Experimental Eye Research. PMID 27039708 DOI: 10.1016/J.Exer.2016.03.023 |
0.472 |
|
| 2016 |
Tracy CJ, Sanders DN, Bryan JN, Jensen CA, Castaner LJ, Kirk MD, Katz ML. Intravitreal Implantation of Genetically Modified Autologous Bone Marrow-Derived Stem Cells for Treating Retinal Disorders. Advances in Experimental Medicine and Biology. 854: 571-7. PMID 26427461 DOI: 10.1007/978-3-319-17121-0_76 |
0.761 |
|
| 2015 |
Mhlanga-Mutangadura T, Johnson GS, Schnabel RD, Taylor JF, Johnson GC, Katz ML, Diane Shelton G, Lever TE, Giuliano E, Granger N, Shomper J, O'Brien DP. A mutation in the Warburg syndrome gene, RAB3GAP1, causes a similar syndrome with polyneuropathy and neuronal vacuolation in Black Russian Terrier dogs. Neurobiology of Disease. PMID 26607784 DOI: 10.1016/J.Nbd.2015.11.016 |
0.423 |
|
| 2015 |
Katz ML, Tecedor L, Chen Y, Williamson BG, Lysenko E, Wininger FA, Young WM, Johnson GC, Whiting RE, Coates JR, Davidson BL. AAV gene transfer delays disease onset in a TPP1-deficient canine model of the late infantile form of Batten disease. Science Translational Medicine. 7: 313ra180. PMID 26560358 DOI: 10.1126/Scitranslmed.Aac6191 |
0.429 |
|
| 2015 |
Gilliam D, Kolicheski A, Johnson GS, Mhlanga-Mutangadura T, Taylor JF, Schnabel RD, Katz ML. Golden Retriever dogs with neuronal ceroid lipofuscinosis have a two-base-pair deletion and frameshift in CLN5. Molecular Genetics and Metabolism. 115: 101-9. PMID 25934231 DOI: 10.1016/J.Ymgme.2015.04.001 |
0.434 |
|
| 2015 |
Whiting RE, Pearce JW, Castaner LJ, Jensen CA, Katz RJ, Gilliam DH, Katz ML. Multifocal retinopathy in Dachshunds with CLN2 neuronal ceroid lipofuscinosis. Experimental Eye Research. 134: 123-32. PMID 25697710 DOI: 10.1016/J.Exer.2015.02.012 |
0.512 |
|
| 2015 |
Vuillemenot BR, Kennedy D, Cooper JD, Wong AM, Sri S, Doeleman T, Katz ML, Coates JR, Johnson GC, Reed RP, Adams EL, Butt MT, Musson DG, Henshaw J, Keve S, et al. Nonclinical evaluation of CNS-administered TPP1 enzyme replacement in canine CLN2 neuronal ceroid lipofuscinosis. Molecular Genetics and Metabolism. 114: 281-93. PMID 25257657 DOI: 10.1016/J.Ymgme.2014.09.004 |
0.41 |
|
| 2014 |
Guo J, O'Brien DP, Mhlanga-Mutangadura T, Olby NJ, Taylor JF, Schnabel RD, Katz ML, Johnson GS. A rare homozygous MFSD8 single-base-pair deletion and frameshift in the whole genome sequence of a Chinese Crested dog with neuronal ceroid lipofuscinosis. Bmc Veterinary Research. 10: 960. PMID 25551667 DOI: 10.1186/S12917-014-0181-Z |
0.452 |
|
| 2014 |
Whiting RE, Narfström K, Yao G, Pearce JW, Coates JR, Castaner LJ, Jensen CA, Dougherty BN, Vuillemenot BR, Kennedy D, O'Neill CA, Katz ML. Enzyme replacement therapy delays pupillary light reflex deficits in a canine model of late infantile neuronal ceroid lipofuscinosis. Experimental Eye Research. 125: 164-72. PMID 24954537 DOI: 10.1016/J.Exer.2014.06.008 |
0.466 |
|
| 2014 |
Guo J, Johnson GS, Brown HA, Provencher ML, da Costa RC, Mhlanga-Mutangadura T, Taylor JF, Schnabel RD, O'Brien DP, Katz ML. A CLN8 nonsense mutation in the whole genome sequence of a mixed breed dog with neuronal ceroid lipofuscinosis and Australian Shepherd ancestry. Molecular Genetics and Metabolism. 112: 302-9. PMID 24953404 DOI: 10.1016/J.Ymgme.2014.05.014 |
0.494 |
|
| 2014 |
Katz ML, Coates JR, Sibigtroth CM, Taylor JD, Carpentier M, Young WM, Wininger FA, Kennedy D, Vuillemenot BR, O'Neill CA. Enzyme replacement therapy attenuates disease progression in a canine model of late-infantile neuronal ceroid lipofuscinosis (CLN2 disease). Journal of Neuroscience Research. 92: 1591-8. PMID 24938720 DOI: 10.1002/Jnr.23423 |
0.465 |
|
| 2014 |
Morgan BR, Coates JR, Johnson GC, Shelton GD, Katz ML. Characterization of thoracic motor and sensory neurons and spinal nerve roots in canine degenerative myelopathy, a potential disease model of amyotrophic lateral sclerosis. Journal of Neuroscience Research. 92: 531-41. PMID 24375814 DOI: 10.1002/Jnr.23332 |
0.33 |
|
| 2014 |
Chalkley MD, Armien AG, Gilliam DH, Johnson GS, Zeng R, Wünschmann A, Kovi RC, Katz ML. Characterization of neuronal ceroid-lipofuscinosis in 3 cats. Veterinary Pathology. 51: 796-804. PMID 24026940 DOI: 10.1177/0300985813502818 |
0.438 |
|
| 2013 |
Whiting RE, Narfström K, Yao G, Pearce JW, Coates JR, Castaner LJ, Katz ML. Pupillary light reflex deficits in a canine model of late infantile neuronal ceroid lipofuscinosis. Experimental Eye Research. 116: 402-10. PMID 24135299 DOI: 10.1016/J.Exer.2013.10.006 |
0.426 |
|
| 2013 |
Morgan BR, Coates JR, Johnson GC, Bujnak AC, Katz ML. Characterization of intercostal muscle pathology in canine degenerative myelopathy: a disease model for amyotrophic lateral sclerosis. Journal of Neuroscience Research. 91: 1639-50. PMID 24043596 DOI: 10.1002/Jnr.23287 |
0.327 |
|
| 2013 |
Sanders DN, Zeng R, Wenger DA, Johnson GS, Johnson GC, Decker JE, Katz ML, Platt SR, O'Brien DP. GM2 gangliosidosis associated with a HEXA missense mutation in Japanese Chin dogs: a potential model for Tay Sachs disease. Molecular Genetics and Metabolism. 108: 70-5. PMID 23266199 DOI: 10.1016/J.Ymgme.2012.11.008 |
0.783 |
|
| 2012 |
Shelton GD, Johnson GC, O'Brien DP, Katz ML, Pesayco JP, Chang BJ, Mizisin AP, Coates JR. Degenerative myelopathy associated with a missense mutation in the superoxide dismutase 1 (SOD1) gene progresses to peripheral neuropathy in Pembroke Welsh corgis and boxers. Journal of the Neurological Sciences. 318: 55-64. PMID 22542607 DOI: 10.1016/J.Jns.2012.04.003 |
0.435 |
|
| 2011 |
Wininger FA, Zeng R, Johnson GS, Katz ML, Johnson GC, Bush WW, Jarboe JM, Coates JR. Degenerative myelopathy in a Bernese Mountain Dog with a novel SOD1 missense mutation. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 25: 1166-70. PMID 21848967 DOI: 10.1111/J.1939-1676.2011.0760.X |
0.392 |
|
| 2011 |
Vuillemenot BR, Katz ML, Coates JR, Kennedy D, Tiger P, Kanazono S, Lobel P, Sohar I, Xu S, Cahayag R, Keve S, Koren E, Bunting S, Tsuruda LS, O'Neill CA. Intrathecal tripeptidyl-peptidase 1 reduces lysosomal storage in a canine model of late infantile neuronal ceroid lipofuscinosis. Molecular Genetics and Metabolism. 104: 325-37. PMID 21784683 DOI: 10.1016/J.Ymgme.2011.06.018 |
0.425 |
|
| 2011 |
Sanders DN, Kanazono S, Wininger FA, Whiting RE, Flournoy CA, Coates JR, Castaner LJ, O'Brien DP, Katz ML. A reversal learning task detects cognitive deficits in a Dachshund model of late-infantile neuronal ceroid lipofuscinosis. Genes, Brain, and Behavior. 10: 798-804. PMID 21745338 DOI: 10.1111/J.1601-183X.2011.00718.X |
0.782 |
|
| 2011 |
Farias FH, Zeng R, Johnson GS, Wininger FA, Taylor JF, Schnabel RD, McKay SD, Sanders DN, Lohi H, Seppälä EH, Wade CM, Lindblad-Toh K, O'Brien DP, Katz ML. A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers. Neurobiology of Disease. 42: 468-74. PMID 21362476 DOI: 10.1016/J.Nbd.2011.02.009 |
0.793 |
|
| 2011 |
Zeng R, Farias FH, Johnson GS, McKay SD, Schnabel RD, Decker JE, Taylor JF, Mann CS, Katz ML, Johnson GC, Coates JR, O'Brien DP. A truncated retrotransposon disrupts the GRM1 coding sequence in Coton de Tulear dogs with Bandera's neonatal ataxia. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 25: 267-72. PMID 21281350 DOI: 10.1111/J.1939-1676.2010.0666.X |
0.347 |
|
| 2011 |
Katz ML, Farias FH, Sanders DN, Zeng R, Khan S, Johnson GS, O'Brien DP. A missense mutation in canine CLN6 in an Australian shepherd with neuronal ceroid lipofuscinosis. Journal of Biomedicine & Biotechnology. 2011: 198042. PMID 21234413 DOI: 10.1155/2011/198042 |
0.784 |
|
| 2010 |
Sanders DN, Kanazono S, Coates JR, Johnson GS, Johnson GC, Narfstrom K, O'Brien DP, Katz ML. COGNITIVE DECLINE IN A DOG MODEL FOR AN INHERITED NEURODEGENERATIVE DISEASE USING T-MAZE PERFORMANCE. Journal of Veterinary Behavior : Clinical Applications and Research : Official Journal of : Australian Veterinary Behaviour Interest Group, International Working Dog Breeding Association. 5: 154. PMID 20672015 DOI: 10.1016/J.Jveb.2009.12.020 |
0.779 |
|
| 2010 |
Sanders DN, Farias FH, Johnson GS, Chiang V, Cook JR, O'Brien DP, Hofmann SL, Lu JY, Katz ML. A mutation in canine PPT1 causes early onset neuronal ceroid lipofuscinosis in a Dachshund. Molecular Genetics and Metabolism. 100: 349-56. PMID 20494602 DOI: 10.1016/J.Ymgme.2010.04.009 |
0.799 |
|
| 2010 |
Farias FH, Johnson GS, Taylor JF, Giuliano E, Katz ML, Sanders DN, Schnabel RD, McKay SD, Khan S, Gharahkhani P, O'Leary CA, Pettitt L, Forman OP, Boursnell M, McLaughlin B, et al. An ADAMTS17 splice donor site mutation in dogs with primary lens luxation. Investigative Ophthalmology & Visual Science. 51: 4716-21. PMID 20375329 DOI: 10.1167/Iovs.09-5142 |
0.78 |
|
| 2009 |
Hainsworth DP, Liu GT, Hamm CW, Katz ML. Funduscopic and angiographic appearance in the neuronal ceroid lipofuscinoses. Retina (Philadelphia, Pa.). 29: 657-68. PMID 19289983 DOI: 10.1097/Iae.0B013E31819B0542 |
0.41 |
|
| 2009 |
Awano T, Johnson GS, Wade CM, Katz ML, Johnson GC, Taylor JF, Perloski M, Biagi T, Baranowska I, Long S, March PA, Olby NJ, Shelton GD, Khan S, O'Brien DP, et al. Genome-wide association analysis reveals a SOD1 mutation in canine degenerative myelopathy that resembles amyotrophic lateral sclerosis. Proceedings of the National Academy of Sciences of the United States of America. 106: 2794-9. PMID 19188595 DOI: 10.1073/Pnas.0812297106 |
0.43 |
|
| 2008 |
Katz ML, Coates JR, Cooper JJ, O'Brien DP, Jeong M, Narfström K. Retinal pathology in a canine model of late infantile neuronal ceroid lipofuscinosis. Investigative Ophthalmology & Visual Science. 49: 2686-95. PMID 18344450 DOI: 10.1167/Iovs.08-1712 |
0.491 |
|
| 2008 |
Chen X, Johnson GS, Schnabel RD, Taylor JF, Johnson GC, Parker HG, Patterson EE, Katz ML, Awano T, Khan S, O'Brien DP. A neonatal encephalopathy with seizures in standard poodle dogs with a missense mutation in the canine ortholog of ATF2. Neurogenetics. 9: 41-9. PMID 18074159 DOI: 10.1007/S10048-007-0112-2 |
0.4 |
|
| 2008 |
Katz ML, Johnson GS, Tullis GE, Lei B. Phenotypic characterization of a mouse model of juvenile neuronal ceroid lipofuscinosis. Neurobiology of Disease. 29: 242-53. PMID 17962032 DOI: 10.1016/J.Nbd.2007.08.017 |
0.464 |
|
| 2007 |
Katz ML, Sanders DN, Mooney BP, Johnson GS. Accumulation of glial fibrillary acidic protein and histone H4 in brain storage bodies of Tibetan terriers with hereditary neuronal ceroid lipofuscinosis. Journal of Inherited Metabolic Disease. 30: 952-63. PMID 18004671 DOI: 10.1007/S10545-007-0683-Y |
0.758 |
|
| 2006 |
Lei B, Tullis GE, Kirk MD, Zhang K, Katz ML. Ocular phenotype in a mouse gene knockout model for infantile neuronal ceroid lipofuscinosis. Journal of Neuroscience Research. 84: 1139-49. PMID 16881055 DOI: 10.1002/Jnr.21008 |
0.466 |
|
| 2006 |
Awano T, Katz ML, O'Brien DP, Sohar I, Lobel P, Coates JR, Khan S, Johnson GC, Giger U, Johnson GS. A frame shift mutation in canine TPP1 (the ortholog of human CLN2) in a juvenile Dachshund with neuronal ceroid lipofuscinosis. Molecular Genetics and Metabolism. 89: 254-60. PMID 16621647 DOI: 10.1016/J.Ymgme.2006.02.016 |
0.495 |
|
| 2006 |
Awano T, Katz ML, O'Brien DP, Taylor JF, Evans J, Khan S, Sohar I, Lobel P, Johnson GS. A mutation in the cathepsin D gene (CTSD) in American Bulldogs with neuronal ceroid lipofuscinosis. Molecular Genetics and Metabolism. 87: 341-8. PMID 16386934 DOI: 10.1016/J.Ymgme.2005.11.005 |
0.419 |
|
| 2006 |
Meyer JS, Katz ML, Maruniak JA, Kirk MD. Embryonic stem cell-derived neural progenitors incorporate into degenerating retina and enhance survival of host photoreceptors. Stem Cells (Dayton, Ohio). 24: 274-83. PMID 16123383 DOI: 10.1634/Stemcells.2005-0059 |
0.364 |
|
| 2005 |
Meyer JS, Katz ML, Kirk MD. Stem cells for retinal degenerative disorders. Annals of the New York Academy of Sciences. 1049: 135-45. PMID 15965113 DOI: 10.1196/Annals.1334.013 |
0.374 |
|
| 2005 |
Wendt KD, Lei B, Schachtman TR, Tullis GE, Ibe ME, Katz ML. Behavioral assessment in mouse models of neuronal ceroid lipofuscinosis using a light-cued T-maze. Behavioural Brain Research. 161: 175-82. PMID 15885820 DOI: 10.1016/J.Bbr.2005.02.024 |
0.38 |
|
| 2005 |
Katz ML, Wendt KD, Sanders DN. RPE65 gene mutation prevents development of autofluorescence in retinal pigment epithelial phagosomes. Mechanisms of Ageing and Development. 126: 513-21. PMID 15722110 DOI: 10.1016/J.Mad.2004.11.004 |
0.768 |
|
| 2005 |
Evans J, Katz ML, Levesque D, Shelton GD, de Lahunta A, O'Brien D. A variant form of neuronal ceroid lipofuscinosis in American bulldogs. Journal of Veterinary Internal Medicine / American College of Veterinary Internal Medicine. 19: 44-51. PMID 15715047 DOI: 10.1111/J.1939-1676.2005.Tb02657.X |
0.415 |
|
| 2005 |
Katz ML, Narfström K, Johnson GS, O'Brien DP. Assessment of retinal function and characterization of lysosomal storage body accumulation in the retinas and brains of Tibetan Terriers with ceroid-lipofuscinosis. American Journal of Veterinary Research. 66: 67-76. PMID 15691038 DOI: 10.2460/Ajvr.2005.66.67 |
0.444 |
|
| 2005 |
Katz ML, Khan S, Awano T, Shahid SA, Siakotos AN, Johnson GS. A mutation in the CLN8 gene in English Setter dogs with neuronal ceroid-lipofuscinosis. Biochemical and Biophysical Research Communications. 327: 541-7. PMID 15629147 DOI: 10.1016/J.Bbrc.2004.12.038 |
0.396 |
|
| 2005 |
Narfstrom K, Tullis G, Bragadottir R, Seeliger M, Rakoczy EP, Katz ML. 434. Long-Term Effects on Retinal Function and Structure Using AAV-Mediated Gene Therapy in Blind RPE65 Null Mutation Dogs Molecular Therapy. 11. DOI: 10.1016/J.Ymthe.2005.06.436 |
0.384 |
|
| 2004 |
Meyer JS, Katz ML, Maruniak JA, Kirk MD. Neural differentiation of mouse embryonic stem cells in vitro and after transplantation into eyes of mutant mice with rapid retinal degeneration. Brain Research. 1014: 131-44. PMID 15212999 DOI: 10.1016/J.Brainres.2004.04.019 |
0.347 |
|
| 2004 |
Wendt KD, Jensen CA, Tindall R, Katz ML. Comparison of conventional and microwave-assisted processing of mouse retinas for transmission electron microscopy Journal of Microscopy. 214: 80-88. PMID 15049872 DOI: 10.1111/J.0022-2720.2004.01310.X |
0.308 |
|
| 2003 |
Narfström K, Katz ML, Ford M, Redmond TM, Rakoczy E, Bragadóttir R. In vivo gene therapy in young and adult RPE65-/- dogs produces long-term visual improvement. The Journal of Heredity. 94: 31-7. PMID 12692160 DOI: 10.1093/Jhered/Esg015 |
0.374 |
|
| 2003 |
Narfström K, Katz ML, Bragadottir R, Seeliger M, Boulanger A, Redmond TM, Caro L, Lai CM, Rakoczy PE. Functional and structural recovery of the retina after gene therapy in the RPE65 null mutation dog. Investigative Ophthalmology & Visual Science. 44: 1663-72. PMID 12657607 DOI: 10.1167/Iovs.02-0595 |
0.348 |
|
| 2002 |
Katz ML. Potential role of retinal pigment epithelial lipofuscin accumulation in age-related macular degeneration. Archives of Gerontology and Geriatrics. 34: 359-70. PMID 14764336 DOI: 10.1016/S0167-4943(02)00012-2 |
0.414 |
|
| 2002 |
Katz ML. Potential reversibility of lipofuscin accumulation. Archives of Gerontology and Geriatrics. 34: 311-7. PMID 14764332 DOI: 10.1016/S0167-4943(02)00008-0 |
0.358 |
|
| 2002 |
Katz ML, Robison WG. What is lipofuscin? Defining characteristics and differentiation from other autofluorescent lysosomal storage bodies. Archives of Gerontology and Geriatrics. 34: 169-84. PMID 14764321 DOI: 10.1016/S0167-4943(02)00005-5 |
0.34 |
|
| 2002 |
Hainsworth DP, Katz ML, Sanders DA, Sanders DN, Wright EJ, Sturek M. Retinal capillary basement membrane thickening in a porcine model of diabetes mellitus. Comparative Medicine. 52: 523-9. PMID 12540165 |
0.719 |
|
| 2002 |
Katz ML, Sanders DA, Sanders DN, Hansen EA, Johnson GS. Assessment of plasma carnitine concentrations in relation to ceroid lipofuscinosis in Tibetan Terriers. American Journal of Veterinary Research. 63: 890-5. PMID 12061538 DOI: 10.2460/Ajvr.2002.63.890 |
0.731 |
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| 2001 |
Siakotos AN, Hutchins GD, Farlow MR, Katz ML. Assessment of dietary therapies in a canine model of Batten disease. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 5: 151-6. PMID 11588988 DOI: 10.1053/Ejpn.2000.0453 |
0.351 |
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| 2001 |
Katz ML, Johnson GS. Mouse gene knockout models for the CLN2 and CLN3 forms of ceroid lipofuscinosis European Journal of Paediatric Neurology. 5: 109-114. PMID 11588979 DOI: 10.1053/Ejpn.2000.0445 |
0.428 |
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| 2001 |
Katz ML, Shibuya H, Johnson GS. 10 Animal models for the ceroid lipofuscinoses Advances in Genetics. 45: 183-203. PMID 11332773 DOI: 10.1016/S0065-2660(01)45011-5 |
0.402 |
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| 2000 |
Bensaoula T, Shibuya H, Katz ML, Smith JE, Johnson GS, John SK, Milam AH. Histopathologic and immunocytochemical analysis of the retina and ocular tissues in Batten disease. Ophthalmology. 107: 1746-53. PMID 10964839 DOI: 10.1016/S0161-6420(00)00264-5 |
0.468 |
|
| 1999 |
Katz ML, Liu PC, Grob-Nunn SE, Shibuya H, Johnson GS. Characterization and chromosomal mapping of a mouse ortholog of the late-infantile ceroid-lipofuscinosis gene CLN2 Mammalian Genome. 10: 1050-1053. PMID 10556422 DOI: 10.1007/S003359901160 |
0.337 |
|
| 1999 |
Katz ML, Shibuya H, Liu PC, Kaur S, Gao CL, Johnson GS. A mouse gene knockout model for juvenile ceroid-lipofuscinosis (Batten disease). Journal of Neuroscience Research. 57: 551-6. PMID 10440905 DOI: 10.1002/(Sici)1097-4547(19990815)57:4<551::Aid-Jnr15>3.0.Co;2-R |
0.43 |
|
| 1999 |
Katz ML, Gao CL, Rice LM. Long-term variations in cyclic light intensity and dietary vitamin A intake modulate lipofuscin content of the retinal pigment epithelium. Journal of Neuroscience Research. 57: 106-16. PMID 10397640 DOI: 10.1002/(Sici)1097-4547(19990701)57:1<106::Aid-Jnr11>3.0.Co;2-Z |
0.309 |
|
| 1999 |
Riis RC, Jackson C, Rebhun W, Katz ML, Loew E, Summers B, Cummings J, de Lahunta A, Divers T, Mohammed H. Ocular manifestations of equine motor neuron disease. Equine Veterinary Journal. 31: 99-110. PMID 10213421 DOI: 10.1111/J.2042-3306.1999.Tb03801.X |
0.41 |
|
| 1998 |
Siakotos AN, Blair PS, Savill JD, Katz ML. Altered mitochondrial function in canine ceroid-lipofuscinosis Neurochemical Research. 23: 983-989. PMID 9690741 DOI: 10.1023/A:1021036506299 |
0.316 |
|
| 1998 |
Shibuya H, Liu PC, Katz ML, Siakotos AN, Nonneman DJ, Johnson GS. Coding sequence and exon/intron organization of the canine CLN3 (Batten disease) gene and its exclusion as the locus for ceroid-lipofuscinosis in English setter dogs. Journal of Neuroscience Research. 52: 268-75. PMID 9590435 DOI: 10.1002/(Sici)1097-4547(19980501)52:3<268::Aid-Jnr3>3.0.Co;2-B |
0.4 |
|
| 1998 |
Liou GI, Matragoon S, Chen DM, Gao CL, Zhang L, Fei Y, Katz ML, Stark WS. Visual sensitivity and interphotoreceptor retinoid binding protein in the mouse: regulation by vitamin A. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 12: 129-38. PMID 9438418 DOI: 10.1096/Fasebj.12.1.129 |
0.315 |
|
| 1997 |
Katz ML, Rice LM, Gao CL. Dietary carnitine supplements slow disease progression in a putative mouse model for hereditary ceroid-lipofuscinosis. Journal of Neuroscience Research. 50: 123-32. PMID 9379488 DOI: 10.1002/(Sici)1097-4547(19971001)50:1<123::Aid-Jnr13>3.0.Co;2-C |
0.463 |
|
| 1997 |
Katz ML, Siakotos AN, Gao Q, Freiha B, Chin DT. Late-infanfile ceroid-lipofuscinosis : Lysine methylation of mitochondrial ATP synthase subunit c from lysosomal storage bodies Biochimica Et Biophysica Acta - Molecular Basis of Disease. 1361: 66-74. PMID 9247091 DOI: 10.1016/S0925-4439(97)00017-3 |
0.327 |
|
| 1996 |
Katz ML, Gao CL, Rice LM. Formation of lipofuscin-like fluorophores by reaction of retinal with photoreceptor outer segments and liposomes. Mechanisms of Ageing and Development. 92: 159-74. PMID 9080396 DOI: 10.1016/S0047-6374(96)01817-9 |
0.305 |
|
| 1996 |
Katz ML. Decreased plasma carnitine and trimethyl-L-lysine levels associated with lysosomal accumulation of a trimethyl-L-lysine containing protein in Batten disease Biochimica Et Biophysica Acta - Molecular Basis of Disease. 1317: 192-198. PMID 8988235 DOI: 10.1016/S0925-4439(96)00054-3 |
0.372 |
|
| 1995 |
Katz ML, Gao CL. Vitamin A incorporation into lipofuscin-like inclusions in the retinal pigment epithelium Mechanisms of Ageing and Development. 84: 29-38. PMID 8719775 DOI: 10.1016/0047-6374(95)01633-B |
0.337 |
|
| 1995 |
Katz ML, Siakotos AN. Canine hereditary ceroid-lipofuscinosis: Evidence for a defect in the carnitine biosynthetic pathway American Journal of Medical Genetics. 57: 266-271. PMID 7668343 DOI: 10.1002/Ajmg.1320570231 |
0.379 |
|
| 1993 |
Katz ML, Chen DM, Stientjes HJ, Stark WS. Photoreceptor recovery in retinoid-deprived rats after vitamin A replinishment Experimental Eye Research. 56: 671-682. PMID 8595809 DOI: 10.1006/Exer.1993.1084 |
0.324 |
|
| 1993 |
Katz ML, Gao CL, Stientjes HJ. Regulation of the interphotoreceptor retinoid-binding protein content of the retina by vitamin A Experimental Eye Research. 57: 393-401. PMID 8282025 DOI: 10.1006/Exer.1993.1140 |
0.319 |
|
| 1992 |
Katz ML, Norberg M. Influence of dietary vitamin A on autofluorescence of leupeptin-induced inclusions in the retinal pigment epithelium. Experimental Eye Research. 54: 239-46. PMID 1559552 DOI: 10.1016/S0014-4835(05)80213-1 |
0.355 |
|
| 1992 |
Katz ML, Gerhardt KO. Methylated lysine in storage body protein of sheep with hereditary ceroid-lipofuscinosis Bba - Molecular Basis of Disease. 1138: 97-108. PMID 1540666 DOI: 10.1016/0925-4439(92)90048-R |
0.348 |
|
| 1990 |
Katz ML, Gerhardt KO. Storage protein in hereditary ceroid-lipofuscinosis contains S-methylated methionine Mechanisms of Ageing and Development. 53: 277-290. PMID 2376986 DOI: 10.1016/0047-6374(90)90045-H |
0.325 |
|
| 1989 |
Katz ML, Shanker MJ. Development of lipofuscin-like fluorescence in the retinal pigment epithelium in response to protease inhibitor treatment Mechanisms of Ageing and Development. 49: 23-40. PMID 2747298 DOI: 10.1016/0047-6374(89)90065-1 |
0.361 |
|
| 1988 |
Eldred GE, Katz ML. Fluorophores of the human retinal pigment epithelium: Separation and spectral characterization Experimental Eye Research. 47: 71-86. PMID 3409988 DOI: 10.1016/0014-4835(88)90025-5 |
0.318 |
|
| 1988 |
Katz ML, Eldred GE, Siakotos AN, Koppang N. Characterization of disease-specific brain fluorophores in ceroid-lipofuscinosis American Journal of Medical Genetics. Supplement. 5: 253-264. PMID 3146323 DOI: 10.1002/Ajmg.1320310628 |
0.318 |
|
| 1987 |
Katz ML, Drea CM, Robison WG. Age-related alterations in vitamin A metabolism in the rat retina. Experimental Eye Research. 44: 939-49. PMID 3653281 DOI: 10.1016/S0014-4835(87)80055-6 |
0.325 |
|
| 1987 |
Katz ML, Eldred GE, Robison WG. Lipofuscin autofluorescence: Evidence for vitamin A involvement in the retina Mechanisms of Ageing and Development. 39: 81-90. PMID 3613689 DOI: 10.1016/0047-6374(87)90088-1 |
0.34 |
|
| 1986 |
Katz ML, Drea CM, Eldred GE, Hess HH, Robison WG. Influence of early photoreceptor degeneration on lipofuscin in the retinal pigment epithelium. Experimental Eye Research. 43: 561-73. PMID 3792460 DOI: 10.1016/S0014-4835(86)80023-9 |
0.344 |
|
| 1986 |
Katz ML, Robison WG. Evidence of cell loss from the rat retina during senescence Experimental Eye Research. 42: 293-304. PMID 3709700 DOI: 10.1016/0014-4835(86)90022-9 |
0.332 |
|
| 1985 |
Katz ML, Robison WG. Senescence and the retinal pigment epithelium: Alterations in basal plasma membrane morphology Mechanisms of Ageing and Development. 30: 99-105. PMID 3999816 DOI: 10.1016/0047-6374(85)90062-4 |
0.353 |
|
| 1984 |
Katz ML, Robison WG. Age-related changes in the retinal pigment epithelium of pigmented rats Experimental Eye Research. 38: 137-151. PMID 6714331 DOI: 10.1016/0014-4835(84)90098-8 |
0.338 |
|
| 1983 |
Katz ML, Robison WG. Lipofuscin response to the 'aging-reversal' drug centrophenoxine in rat retinal pigment epithelium and frontal cortex Journals of Gerontology. 38: 525-531. PMID 6411800 DOI: 10.1093/Geronj/38.5.525 |
0.312 |
|
| 1982 |
Katz ML, Parker KR, Handelman GJ, Bramel TL, Dratz EA. Effects of antioxidant nutrient deficiency on the retina and retinal pigment epithelium of albino rats: a light and electron microscopic study Experimental Eye Research. 34: 339-369. PMID 7067744 DOI: 10.1016/0014-4835(82)90082-3 |
0.339 |
|
| 1982 |
Katz ML, Parker KR, Handelman GJ, Farnsworth CC, Dratz EA. STRUCTURAL AND BIOCHEMICAL EFFECTS OF ANTIOXIDANT NUTRIENT DEFICIENCY ON THE RAT RETINA AND RETINAL PIGMENT EPITHELIUM Annals of the New York Academy of Sciences. 393: 196-197. DOI: 10.1111/J.1749-6632.1982.Tb31251.X |
0.306 |
|
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