| Year |
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| 2018 |
Xie K, Ryan DP, Pearson BL, Henzel KS, Neff F, Vidal RO, Hennion M, Lehmann I, Schleif M, Schröder S, Adler T, Rathkolb B, Rozman J, Schütz AL, Prehn C, ... ... Matynia A, et al. Epigenetic alterations in longevity regulators, reduced life span, and exacerbated aging-related pathology in old father offspring mice. Proceedings of the National Academy of Sciences of the United States of America. PMID 29467291 DOI: 10.1073/pnas.1707337115 |
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| 2016 |
Condro MC, Matynia A, Foster NN, Ago Y, Rajbhandari AK, Jayaram B, Parikh S, Diep AL, Nguyen E, May V, Dong HW, Waschek JA. High-resolution characterization of a PACAP-EGFP transgenic mouse model for mapping PACAP-expressing neurons. The Journal of Comparative Neurology. PMID 27197019 DOI: 10.1002/cne.24035 |
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| 2016 |
Loewendorf AI, Matynia A, Saribekyan H, Gross N, Csete M, Harrington M. Roads Less Traveled: Sexual Dimorphism and Mast Cell Contributions to Migraine Pathology. Frontiers in Immunology. 7: 140. PMID 27148260 DOI: 10.3389/fimmu.2016.00140 |
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| 2016 |
Strom SP, Clark MJ, Martinez A, Garcia S, Abelazeem AA, Matynia A, Parikh S, Sullivan LS, Bowne SJ, Daiger SP, Gorin MB. De Novo Occurrence of a Variant in ARL3 and Apparent Autosomal Dominant Transmission of Retinitis Pigmentosa. Plos One. 11: e0150944. PMID 26964041 DOI: 10.1371/journal.pone.0150944 |
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| 2015 |
Matynia A, Parikh S, Deot N, Wong A, Kim P, Nusinowitz S, Gorin MB. Light aversion and corneal mechanical sensitivity are altered by intrinscally photosensitive retinal ganglion cells in a mouse model of corneal surface damage. Experimental Eye Research. 137: 57-62. PMID 26070985 DOI: 10.1016/j.exer.2015.05.025 |
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| 2013 |
Matynia A, Gorin MB. Unanswered questions in headache: so what is photophobia, anyway? Headache. 53: 1681-2. PMID 24111756 DOI: 10.1111/head.12229 |
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| 2012 |
Matynia A, Parikh S, Chen B, Kim P, McNeill DS, Nusinowitz S, Evans C, Gorin MB. Intrinsically photosensitive retinal ganglion cells are the primary but not exclusive circuit for light aversion. Experimental Eye Research. 105: 60-9. PMID 23078956 DOI: 10.1016/j.exer.2012.09.012 |
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| 2011 |
Schmidt TM, Do MT, Dacey D, Lucas R, Hattar S, Matynia A. Melanopsin-positive intrinsically photosensitive retinal ganglion cells: from form to function. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 16094-101. PMID 22072661 DOI: 10.1523/JNEUROSCI.4132-11.2011 |
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| 2010 |
Matynia A, Ng CH, Dansithong W, Chiang A, Silva AJ, Reddy S. Muscleblind1, but not Dmpk or Six5, contributes to a complex phenotype of muscular and motivational deficits in mouse models of myotonic dystrophy. Plos One. 5: e9857. PMID 20360842 DOI: 10.1371/journal.pone.0009857 |
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| 2009 |
Hutnick LK, Golshani P, Namihira M, Xue Z, Matynia A, Yang XW, Silva AJ, Schweizer FE, Fan G. DNA hypomethylation restricted to the murine forebrain induces cortical degeneration and impairs postnatal neuronal maturation. Human Molecular Genetics. 18: 2875-88. PMID 19433415 DOI: 10.1093/hmg/ddp222 |
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| 2008 |
Matynia A, Anagnostaras SG, Wiltgen BJ, Lacuesta M, Fanselow MS, Silva AJ. A high through-put reverse genetic screen identifies two genes involved in remote memory in mice. Plos One. 3: e2121. PMID 18464936 DOI: 10.1371/journal.pone.0002121 |
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| 2007 |
Han JH, Kushner SA, Yiu AP, Cole CJ, Matynia A, Brown RA, Neve RL, Guzowski JF, Silva AJ, Josselyn SA. Neuronal competition and selection during memory formation. Science (New York, N.Y.). 316: 457-60. PMID 17446403 DOI: 10.1126/science.1139438 |
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| 2006 |
Nagy V, Bozdagi O, Matynia A, Balcerzyk M, Okulski P, Dzwonek J, Costa RM, Silva AJ, Kaczmarek L, Huntley GW. Matrix metalloproteinase-9 is required for hippocampal late-phase long-term potentiation and memory. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 1923-34. PMID 16481424 DOI: 10.1523/JNEUROSCI.4359-05.2006 |
1 |
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| 2005 |
Ehninger D, Matynia A, Silva AJ. Trafficking in emotions. Nature Neuroscience. 8: 548-50. PMID 15856058 DOI: 10.1038/nn0505-548 |
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| 2003 |
Rudzki Z, Matynia A, Przybylik-Mazurek E, Darczuk A, Szybiński Z, Piatkowska-Jakubas B, Wójcik M, Skotnicki AB. [Hypopituitarism and hematological abnormalities mimicking myelodysplastic syndrome. Report of four cases]. Polskie Archiwum Medycyny WewnęTrznej. 110: 1003-11. PMID 14699694 |
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| 2002 |
Matynia A, Kushner SA, Silva AJ. Genetic approaches to molecular and cellular cognition: a focus on LTP and learning and memory. Annual Review of Genetics. 36: 687-720. PMID 12429705 DOI: 10.1146/annurev.genet.36.062802.091007 |
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| 2002 |
Matynia A, Salus SS, Sazer S. Three proteins required for early steps in the protein secretory pathway also affect nuclear envelope structure and cell cycle progression in fission yeast. Journal of Cell Science. 115: 421-31. PMID 11839792 |
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| 2001 |
Matynia A, Anagnostaras SG, Silva AJ. Weaving the molecular and cognitive strands of memory. Neuron. 32: 557-9. PMID 11719197 DOI: 10.1016/S0896-6273(01)00510-4 |
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| 1998 |
Matynia A, Mueller U, Ong N, Demeter J, Granger AL, Hinata K, Sazer S. Isolation and characterization of fission yeast sns mutants defective at the mitosis-to-interphase transition. Genetics. 148: 1799-811. PMID 9560394 |
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| 1996 |
Matynia A, Dimitrov K, Mueller U, He X, Sazer S. Perturbations in the spi1p GTPase cycle of Schizosaccharomyces pombe through its GTPase-activating protein and guanine nucleotide exchange factor components result in similar phenotypic consequences. Molecular and Cellular Biology. 16: 6352-62. PMID 8887664 |
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| 1995 |
Ouspenski II, Mueller UW, Matynia A, Sazer S, Elledge SJ, Brinkley BR. Ran-binding protein-1 is an essential component of the Ran/RCC1 molecular switch system in budding yeast. The Journal of Biological Chemistry. 270: 1975-8. PMID 7836422 DOI: 10.1074/jbc.270.5.1975 |
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| 1995 |
Tieu PT, Bach G, Matynia A, Hwang M, Neufeld EF. Four novel mutations underlying mild or intermediate forms of alpha-L-iduronidase deficiency (MPS IS and MPS IH/S). Human Mutation. 6: 55-9. PMID 7550232 DOI: 10.1002/humu.1380060111 |
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| 1994 |
Kakkis ED, Matynia A, Jonas AJ, Neufeld EF. Overexpression of the human lysosomal enzyme alpha-L-iduronidase in Chinese hamster ovary cells. Protein Expression and Purification. 5: 225-32. PMID 7950365 DOI: 10.1006/prep.1994.1035 |
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| 1993 |
Bach G, Moskowitz SM, Tieu PT, Matynia A, Neufeld EF. Molecular analysis of Hurler syndrome in Druze and Muslim Arab patients in Israel: multiple allelic mutations of the IDUA gene in a small geographic area. American Journal of Human Genetics. 53: 330-8. PMID 8328452 |
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