Pamela S. Lagali, B.Sc., M.Sc., Ph.D. - Publications

Affiliations: 
Regenerative Medicine Ottawa Hospital Research Institute/University of Ottawa 
Area:
visual system, retinal degeneration

14 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 Ringuette R, Atkins M, Lagali PS, Bassett EA, Campbell C, Mazerolle C, Mears AJ, Picketts DJ, Wallace VA. A notch-Gli2 axis sustains hedgehog responsiveness of neural progenitors and Müller glia. Developmental Biology. PMID 26795056 DOI: 10.1016/j.ydbio.2016.01.006  0.76
2014 Cronin T, Vandenberghe LH, Hantz P, Juttner J, Reimann A, Kacsó AE, Huckfeldt RM, Busskamp V, Kohler H, Lagali PS, Roska B, Bennett J. Efficient transduction and optogenetic stimulation of retinal bipolar cells by a synthetic adeno-associated virus capsid and promoter. Embo Molecular Medicine. 6: 1175-90. PMID 25092770 DOI: 10.15252/emmm.201404077  0.76
2014 Alvarez-Saavedra M, De Repentigny Y, Lagali PS, Raghu Ram EV, Yan K, Hashem E, Ivanochko D, Huh MS, Yang D, Mears AJ, Todd MA, Corcoran CP, Bassett EA, Tokarew NJ, Kokavec J, et al. Snf2h-mediated chromatin organization and histone H1 dynamics govern cerebellar morphogenesis and neural maturation. Nature Communications. 5: 4181. PMID 24946904 DOI: 10.1038/ncomms5181  0.76
2013 McNeill B, Mazerolle C, Bassett EA, Mears AJ, Ringuette R, Lagali P, Picketts DJ, Paes K, Rice D, Wallace VA. Hedgehog regulates Norrie disease protein to drive neural progenitor self-renewal. Human Molecular Genetics. 22: 1005-16. PMID 23201751 DOI: 10.1093/hmg/dds505  0.76
2011 Lagali PS, Picketts DJ. Matters of life and death: the role of chromatin remodeling proteins in retinal neuron survival. Journal of Ocular Biology, Diseases, and Informatics. 4: 111-20. PMID 23289056 DOI: 10.1007/s12177-012-9080-3  0.76
2010 Lagali PS, Corcoran CP, Picketts DJ. Hippocampus development and function: role of epigenetic factors and implications for cognitive disease. Clinical Genetics. 78: 321-33. PMID 20681996 DOI: 10.1111/j.1399-0004.2010.01503.x  0.76
2009 Boldogkoi Z, Balint K, Awatramani GB, Balya D, Busskamp V, Viney TJ, Lagali PS, Duebel J, Pásti E, Tombácz D, Tóth JS, Takács IF, Scherf BG, Roska B. Genetically timed, activity-sensor and rainbow transsynaptic viral tools. Nature Methods. 6: 127-30. PMID 19122667 DOI: 10.1038/nmeth.1292  0.76
2008 Lagali PS, Balya D, Awatramani GB, Münch TA, Kim DS, Busskamp V, Cepko CL, Roska B. Light-activated channels targeted to ON bipolar cells restore visual function in retinal degeneration. Nature Neuroscience. 11: 667-75. PMID 18432197 DOI: 10.1038/nn.2117  0.76
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  0.76
2003 Lagali PS, Ayyagari R, Wong PW. An integrated genetic approach to identify candidate genes for human chromosome 6q-linked retinal disorders. Advances in Experimental Medicine and Biology. 533: 19-28. PMID 15180243  0.76
2003 Lagali PS, Liu J, Ambasudhan R, Kakuk LE, Bernstein SL, Seigel GM, Wong PW, Ayyagari R. Evolutionarily conserved ELOVL4 gene expression in the vertebrate retina. Investigative Ophthalmology & Visual Science. 44: 2841-50. PMID 12824221 DOI: 10.1167/iovs.02-0991  0.76
2002 Lagali PS, Kakuk LE, Griesinger IB, Wong PW, Ayyagari R. Identification and characterization of C6orf37, a novel candidate human retinal disease gene on chromosome 6q14. Biochemical and Biophysical Research Communications. 293: 356-65. PMID 12054608 DOI: 10.1016/S0006-291X(02)00228-0  0.76
2001 Zhang K, Kniazeva M, Han M, Li W, Yu Z, Yang Z, Li Y, Metzker ML, Allikmets R, Zack DJ, Kakuk LE, Lagali PS, Wong PW, MacDonald IM, Sieving PA, et al. A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy. Nature Genetics. 27: 89-93. PMID 11138005 DOI: 10.1038/83817  0.76
2000 Lagali PS, MacDonald IM, Griesinger IB, Chambers ML, Ayyagari R, Wong PW. Autosomal dominant Stargardt-like macular dystrophy segregating in a large Canadian family. Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie. 35: 315-24. PMID 11091913  0.76
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