A frequent HincII polymorphism identified by the human chromosome 19q13.3 probe pKEX0.8 (D19S118) von TSILFIDIS, C. T, SHUTLER, G, MAHADEVAN, M, KORNELUK, R. G

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Neonatal hyperoxia in mice triggers long-term cognitive deficits via impairments in cerebrovascular function and neurogenesis von Lithopoulos, Marissa A., Toussay, Xavier, Zhong, Shumei, Xu, Liqun, Mustafa, Shamimunisa B., Ouellette, Julie, Freitas-Andrade, Moises, Comin, Cesar H., Bassam, Hayam A., Baker, Adam N., Sun, Yiren, Wakem, Michael, Moreira, Alvaro G., Blanco, Cynthia L., Vadivel, Arul, Tsilfidis, Catherine, Seidner, Steven R., Slack, Ruth S., Lagace, Diane C., Wang, Jing, Lacoste, Baptiste, Thébaud, Bernard

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Neonatal hyperoxia in mice triggers long-term cognitive deficits via impairments in cerebrovascular function and neurogenesis von Lithopoulos, Marissa A, Toussay, Xavier, Zhong, Shumei, Xu, Liqun, Mustafa, Shamimunisa B, Ouellette, Julie, Freitas-Andrade, Moises, Comin, Cesar H, Bassam, Hayam A, Baker, Adam N, Sun, Yiren, Wakem, Michael, Moreira, Alvaro G, Blanco, Cynthia L, Vadivel, Arul, Tsilfidis, Catherine, Seidner, Steven R, Slack, Ruth S, Lagace, Diane C, Wang, Jing, Lacoste, Baptiste, Thébaud, Bernard

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XIAP protection of photoreceptors in animal models of retinitis pigmentosa von Leonard, Kevin C, Petrin, Dino, Coupland, Stuart G, Baker, Adam N, Leonard, Brian C, LaCasse, Eric C, Hauswirth, William W, Korneluk, Robert G, Tsilfidis, Catherine

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Myotonic Dystrophy Mutation: An Unstable CTG Repeat in the 3′ Untranslated Region of the Gene von Mahadevan, Mani, Tsilfidis, Catherine, Sabourin, Luc, Shutler, Gary, Amemiya, Chris, Jansen, Gert, Neville, Catherine, Narang, Monica, Barceló, Juana, O'Hoy, Kim, Leblond, Suzanne, Earle-Macdonald, Jane, De Jong, Pieter J., Wieringa, Bé, Korneluk, Robert G.

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Overexpression of the X-Linked Inhibitor of Apoptosis Protects Against Retinal Degeneration in a Feline Model of Retinal Detachment von Wassmer, Sarah J, Leonard, Brian C, Coupland, Stuart G, Baker, Adam N, Hamilton, John, Hauswirth, William W, Tsilfidis, Catherine

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Safety and Efficacy of Adeno-Associated Viral Gene Therapy in Patients With Retinal Degeneration: A Systematic Review and Meta-Analysis von Sobh, Mohamad, Lagali, Pamela S, Ghiasi, Maryam, Montroy, Joshua, Dollin, Michael, Hurley, Bernard, Leonard, Brian C, Dimopoulos, Ioannis, Lafreniere, Mackenzie, Fergusson, Dean A, Lalu, Manoj M, Tsilfidis, Catherine

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Growth and apoptosis during larval forelimb development and adult forelimb regeneration in the newt ( Notophthalmus viridescens) von Vlaskalin, Tatjana, Wong, Christine J, Tsilfidis, Catherine

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PEG–PLA microparticles for encapsulation and delivery of Tat-EGFP to retinal cells von Rafat, Mehrdad, Cléroux, Carolyne A, Fong, Wai Gin, Baker, Adam N, Leonard, Brian C, O'Connor, Michael D, Tsilfidis, Catherine

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Structural and Functional Protection of Photoreceptors from MNU-Induced Retinal Degeneration by the X-Linked Inhibitor of Apoptosis von Petrin, Dino, Baker, Adam, Coupland, Stuart G, Liston, Peter, Narang, Monica, Damji, Karim, Leonard, Brian, Chiodo, Vince A, Timmers, Adrian, Hauswirth, William, Korneluk, Robert G, Tsilfidis, Catherine

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Newt opportunities for understanding the dedifferentiation process von Chaar, Ziad Y, Tsilfidis, Catherine

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Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy von Mettler, Gabrielle, Barceló, Juana, Tsilfidis, Catherine, Korneluk, Robert G, MacKenzie, Alex E

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Cloning of the essential myotonic dystrophy region and mapping of the putative defect von Aslanidis, Charalampos, Jansen, Gert, Amemiya, Chris, Shutler, Gary, Mahadevan, Mani, Tsilfidis, Catherine, Chen, Chira, Alleman, Jennifer, Wormskamp, Nicole G. M, Vooijs, Mark, Buxton, Jessica, Johnson, Keith, Smeets, Hubertus J. M, Lennon, Gregory G, Carrano, Anthony V, Korneluk, Robert G, Wieringa, Bé, de Jong, Pieter J

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XIAP-mediated neuroprotection in retinal ischemia von RENWICK, J, NARANG, M. A, KORNELUK, R. G, TSILFIDIS, C, COUPLAND, S. G, XUAN, J. Y, BAKER, A. N, BROUSSEAU, J, PETRIN, D, MUNGER, R, LEONARD, B. C, HAUSWIRTH, W. W

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A novel family of T-box genes in urodele amphibian limb development and regeneration: candidate genes involved in vertebrate forelimb/hindlimb patterning von Simon, H G, Kittappa, R, Khan, P A, Tsilfidis, C, Liversage, R A, Oppenheimer, S

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PEG-PLAmicroparticles for encapsulation and delivery of Tat-EGFP to retinal cells von Rafat, Mehrdad, Cléroux, Carolyne A., Fong, Wai Gin, Baker, Adam N., Leonard, Brian C., O'Connor, Michael D., Tsilfidis, Catherine

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Newt orthologue of Growth arrest‐specific 6 (NvGas6) is implicated in stress response during newt forelimb regeneration von Beug, Shawn, Vascotto, Sandy G., Tsilfidis, Catherine

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The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy von Hunter, A, Tsilfidis, C, Mettler, G, Jacob, P, Mahadevan, M, Surh, L, Korneluk, R

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Identification of cDNAs associated with late dedifferentiation in adult newt forelimb regeneration von Vascotto, Sandy G., Beug, Shawn, Liversage, Richard A., Tsilfidis, Catherine

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Nv beta -actin and NvGAPDH as normalization factors for gene expression analysis in limb regenerates and cultured blastema cells of the adult newt, Notophthalmus viridescens von Vascotto, S G, Beug, S, Liversage, R A, Tsilfidis, C

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