Jill M. Weimer, Ph.D. - Publications

2006 University of Rochester, Rochester, NY 
Neuroscience Biology

36 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
2019 Johnson TB, Langin LM, Zhao J, Weimer JM, Pearce DA, Kovács AD. Changes in motor behavior, neuropathology, and gut microbiota of a Batten disease mouse model following administration of acidified drinking water. Scientific Reports. 9: 14962. PMID 31628420 DOI: 10.1038/s41598-019-51488-z  0.6
2019 Cain JT, Likhite S, White KA, Timm DJ, Davis SS, Johnson TB, Dennys-Rivers CN, Rinaldi F, Motti D, Corcoran S, Morales P, Pierson C, Hughes SM, Lee SY, Kaspar BK, ... ... Weimer JM, et al. Gene Therapy Corrects Brain and Behavioral Pathologies in CLN6-Batten Disease. Molecular Therapy : the Journal of the American Society of Gene Therapy. PMID 31331814 DOI: 10.1016/j.ymthe.2019.06.015  0.6
2019 Khanna R, Moutal A, White KA, Chefdeville A, Negrao de Assis P, Cai S, Swier VJ, Bellampalli SS, Giunta MD, Darbro BW, Quelle DE, Sieren JC, Wallace MR, Rogers CS, Meyerholz DK, ... Weimer JM, et al. Assessment of nociception and related quality of life measures in a porcine model of Neurofibromatosis type 1. Pain. PMID 31246731 DOI: 10.1097/j.pain.0000000000001648  0.6
2019 Moutal A, White KA, Chefdeville A, Laufmann RN, Vitiello PF, Feinstein D, Weimer JM, Khanna R. Dysregulation of CRMP2 Post-Translational Modifications Drive Its Pathological Functions. Molecular Neurobiology. PMID 30915713 DOI: 10.1007/s12035-019-1568-4  0.6
2019 Johnson TB, Cain JT, White KA, Ramirez-Montealegre D, Pearce DA, Weimer JM. Therapeutic landscape for Batten disease: current treatments and future prospects. Nature Reviews. Neurology. PMID 30783219 DOI: 10.1038/s41582-019-0138-8  0.6
2019 Poppens MJ, Cain JT, Johnson TB, White KA, Davis SS, Laufmann R, Kloth AD, Weimer JM. Tracking sex-dependent differences in a mouse model of CLN6-Batten disease. Orphanet Journal of Rare Diseases. 14: 19. PMID 30665444 DOI: 10.1186/s13023-019-0994-8  0.6
2018 Johnson TB, Mechels K, Anderson RE, Cain JT, Sturdevant DA, Braddock S, Pinz H, Wilson MA, Landsverk M, Roux KJ, Weimer JM. Characterization of a recurrent missense mutation in the forkhead DNA-binding domain of FOXP1. Scientific Reports. 8: 16161. PMID 30385778 DOI: 10.1038/s41598-018-34437-0  0.6
2018 Madeo M, Colbert PL, Vermeer DW, Lucido CT, Cain JT, Vichaya EG, Grossberg AJ, Muirhead D, Rickel AP, Hong Z, Zhao J, Weimer JM, Spanos WC, Lee JH, Dantzer R, et al. Cancer exosomes induce tumor innervation. Nature Communications. 9: 4284. PMID 30327461 DOI: 10.1038/s41467-018-06640-0  0.6
2018 Timm D, Cain JT, Geraets RD, White KA, Koh SY, Kielian T, Pearce DA, Hastings ML, Weimer JM. Searching for novel biomarkers using a mouse model of CLN3-Batten disease. Plos One. 13: e0201470. PMID 30086172 DOI: 10.1371/journal.pone.0201470  0.6
2018 White KA, Swier VJ, Cain JT, Kohlmeyer JL, Meyerholz DK, Tanas MR, Uthoff J, Hammond E, Li H, Rohret FA, Goeken A, Chan CH, Leidinger MR, Umesalma S, Wallace MR, ... ... Weimer JM, et al. A porcine model of neurofibromatosis type 1 that mimics the human disease. Jci Insight. 3. PMID 29925695 DOI: 10.1172/jci.insight.120402  0.6
2017 Beraldi R, Meyerholz DK, Savinov A, Kovács AD, Weimer JM, Dykstra JA, Geraets RD, Pearce DA. Genetic Ataxia Telangiectasia porcine model phenocopies the multisystemic features of the human disease. Biochimica Et Biophysica Acta. PMID 28746835 DOI: 10.1016/j.bbadis.2017.07.020  0.44
2017 Geraets RD, Langin LM, Cain JT, Parker CM, Beraldi R, Kovacs AD, Weimer JM, Pearce DA. A tailored mouse model of CLN2 disease: A nonsense mutant for testing personalized therapies. Plos One. 12: e0176526. PMID 28464005 DOI: 10.1371/journal.pone.0176526  0.6
2017 Cain JT, Kim DI, Quast M, Shivega WG, Patrick RJ, Moser C, Reuter S, Perez M, Myers A, Weimer JM, Roux KJ, Landsverk M. Nonsense pathogenic variants in exon 1 of PHOX2B lead to translational reinitiation in congenital central hypoventilation syndrome. American Journal of Medical Genetics. Part A. PMID 28371199 DOI: 10.1002/ajmg.a.38162  0.6
2016 White KA, Hutton SR, Weimer JM, Sheridan PA. Diet-induced obesity prolongs neuroinflammation and recruits CCR2(+) monocytes to the brain following herpes simplex virus (HSV)-1 latency in mice. Brain, Behavior, and Immunity. PMID 27311830 DOI: 10.1016/j.bbi.2016.06.007  1
2016 Geraets RD, Koh SY, Hastings ML, Kielian T, Pearce DA, Weimer JM. Moving towards effective therapeutic strategies for Neuronal Ceroid Lipofuscinosis. Orphanet Journal of Rare Diseases. 11: 40. PMID 27083890 DOI: 10.1186/s13023-016-0414-2  1
2015 Brudvig JJ, Weimer JM. X MARCKS the spot: myristoylated alanine-rich C kinase substrate in neuronal function and disease. Frontiers in Cellular Neuroscience. 9: 407. PMID 26528135 DOI: 10.3389/fncel.2015.00407  1
2015 Beraldi R, Chan CH, Rogers CS, Kovács AD, Meyerholz DK, Trantzas C, Lambertz AM, Darbro BW, Weber KL, White KA, Rheeden RV, Kruer MC, Dacken BA, Wang XJ, Davis BT, ... ... Weimer JM, et al. A novel porcine model of ataxia telangiectasia reproduces neurological features and motor deficits of human disease. Human Molecular Genetics. PMID 26374845 DOI: 10.1093/hmg/ddv356  1
2015 Watzlawik JO, Kahoud RJ, O'Toole RJ, White KA, Ogden AR, Painter MM, Wootla B, Papke LM, Denic A, Weimer JM, Carey WA, Rodriguez M. Abbreviated exposure to hypoxia is sufficient to induce CNS dysmyelination, modulate spinal motor neuron composition, and impair motor development in neonatal mice. Plos One. 10: e0128007. PMID 26020269 DOI: 10.1371/journal.pone.0128007  1
2015 Muthusamy N, Sommerville LJ, Moeser AJ, Stumpo DJ, Sannes P, Adler K, Blackshear PJ, Weimer JM, Ghashghaei HT. MARCKS-dependent mucin clearance and lipid metabolism in ependymal cells are required for maintenance of forebrain homeostasis during aging. Aging Cell. PMID 26010231 DOI: 10.1111/acel.12354  1
2014 Zhang X, Ling J, Barcia G, Jing L, Wu J, Barry BJ, Mochida GH, Hill RS, Weimer JM, Stein Q, Poduri A, Partlow JN, Ville D, Dulac O, Yu TW, et al. Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizures. American Journal of Human Genetics. 94: 547-58. PMID 24656866 DOI: 10.1016/j.ajhg.2014.03.003  1
2013 Morgan JP, Magee H, Wong A, Nelson T, Koch B, Cooper JD, Weimer JM. A murine model of variant late infantile ceroid lipofuscinosis recapitulates behavioral and pathological phenotypes of human disease. Plos One. 8: e78694. PMID 24223841 DOI: 10.1371/journal.pone.0078694  1
2009 Moy SS, Ghashghaei HT, Nonneman RJ, Weimer JM, Yokota Y, Lee D, Lai C, Threadgill DW, Anton ES. Deficient NRG1-ERBB signaling alters social approach: relevance to genetic mouse models of schizophrenia. Journal of Neurodevelopmental Disorders. 1: 302-12. PMID 21547722 DOI: 10.1007/s11689-009-9017-8  1
2009 Weimer JM, Yokota Y, Stanco A, Stumpo DJ, Blackshear PJ, Anton ES. MARCKS modulates radial progenitor placement, proliferation and organization in the developing cerebral cortex. Development (Cambridge, England). 136: 2965-75. PMID 19666823 DOI: 10.1242/dev.036616  1
2009 Weimer JM, Benedict JW, Getty AL, Pontikis CC, Lim MJ, Cooper JD, Pearce DA. Cerebellar defects in a mouse model of juvenile neuronal ceroid lipofuscinosis. Brain Research. 1266: 93-107. PMID 19230832 DOI: 10.1016/j.brainres.2009.02.009  1
2008 Weimer JM, Stanco A, Cheng JG, Vargo AC, Voora S, Anton ES. A BAC transgenic mouse model to analyze the function of astroglial SPARCL1 (SC1) in the central nervous system. Glia. 56: 935-41. PMID 18381651 DOI: 10.1002/glia.20666  1
2007 Ghashghaei HT, Weimer JM, Schmid RS, Yokota Y, McCarthy KD, Popko B, Anton ES. Reinduction of ErbB2 in astrocytes promotes radial glial progenitor identity in adult cerebral cortex. Genes & Development. 21: 3258-71. PMID 18079173 DOI: 10.1101/gad.1580407  1
2007 Weimer JM, Benedict JW, Elshatory YM, Short DW, Ramirez-Montealegre D, Ryan DA, Alexander NA, Federoff HJ, Cooper JD, Pearce DA. Alterations in striatal dopamine catabolism precede loss of substantia nigra neurons in a mouse model of juvenile neuronal ceroid lipofuscinosis. Brain Research. 1162: 98-112. PMID 17617387 DOI: 10.1016/j.brainres.2007.05.018  1
2006 Kovács AD, Weimer JM, Pearce DA. Selectively increased sensitivity of cerebellar granule cells to AMPA receptor-mediated excitotoxicity in a mouse model of Batten disease. Neurobiology of Disease. 22: 575-85. PMID 16483786 DOI: 10.1016/j.nbd.2005.12.018  1
2006 Weimer JM, Custer AW, Benedict JW, Alexander NA, Kingsley E, Federoff HJ, Cooper JD, Pearce DA. Visual deficits in a mouse model of Batten disease are the result of optic nerve degeneration and loss of dorsal lateral geniculate thalamic neurons. Neurobiology of Disease. 22: 284-93. PMID 16412658 DOI: 10.1016/j.nbd.2005.11.008  1
2006 Weimer JM, Anton ES. Doubling up on microtubule stabilizers: synergistic functions of doublecortin-like kinase and doublecortin in the developing cerebral cortex. Neuron. 49: 3-4. PMID 16387632 DOI: 10.1016/j.neuron.2005.12.016  1
2005 Kwon JM, Rothberg PG, Leman AR, Weimer JM, Mink JW, Pearce DA. Novel CLN3 mutation predicted to cause complete loss of protein function does not modify the classical JNCL phenotype. Neuroscience Letters. 387: 111-4. PMID 16087292 DOI: 10.1016/j.neulet.2005.07.023  1
2005 Weimer JM, Chattopadhyay S, Custer AW, Pearce DA. Elevation of Hook1 in a disease model of Batten disease does not affect a novel interaction between Ankyrin G and Hook1. Biochemical and Biophysical Research Communications. 330: 1176-81. PMID 15823567 DOI: 10.1016/j.bbrc.2005.03.103  1
2005 Phillips SN, Benedict JW, Weimer JM, Pearce DA. CLN3, the protein associated with batten disease: structure, function and localization. Journal of Neuroscience Research. 79: 573-83. PMID 15657902 DOI: 10.1002/jnr.20367  1
2002 Weimer JM, Kriscenski-Perry E, Elshatory Y, Pearce DA. The neuronal ceroid lipofuscinoses: mutations in different proteins result in similar disease. Neuromolecular Medicine. 1: 111-24. PMID 12025857 DOI: 10.1385/NMM:1:2:111  1
2000 Yao PJ, Weimer JM, O'Herron TM, Coleman PD. Clathrin assembly protein AP-2 is detected in both neurons and glia, and its reduction is prominent in layer II of frontal cortex in Alzheimer's disease. Neurobiology of Aging. 21: 921-9. PMID 11124443 DOI: 10.1016/S0197-4580(00)00228-1  1
1998 Chow N, Cox C, Callahan LM, Weimer JM, Guo L, Coleman PD. Expression profiles of multiple genes in single neurons of Alzheimer's disease. Proceedings of the National Academy of Sciences of the United States of America. 95: 9620-5. PMID 9689130 DOI: 10.1073/pnas.95.16.9620  1
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