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Items: 49

1.

Immunopanning purification and culture of retinal ganglion cells from mouse.

Fang L, Huang T, Tsilfidis C.

J Neurosci Methods. 2018 Jun 1;303:81-85. doi: 10.1016/j.jneumeth.2018.02.010. Epub 2018 Feb 21. No abstract available.

PMID:
29474821
2.

Overexpression of the X-Linked Inhibitor of Apoptosis Protects Against Retinal Degeneration in a Feline Model of Retinal Detachment.

Wassmer SJ, Leonard BC, Coupland SG, Baker AN, Hamilton J, Hauswirth WW, Tsilfidis C.

Hum Gene Ther. 2017 Jun;28(6):482-492. doi: 10.1089/hum.2016.161. Epub 2017 Mar 23.

3.

Retinal interneuron survival requires non-cell-autonomous Atrx activity.

Lagali PS, Medina CF, Zhao BY, Yan K, Baker AN, Coupland SG, Tsilfidis C, Wallace VA, Picketts DJ.

Hum Mol Genet. 2016 Nov 1;25(21):4787-4803. doi: 10.1093/hmg/ddw306.

PMID:
28173139
4.

Corrigendum: Establishment of a cone photoreceptor transplantation platform based on a novel cone-GFP reporter mouse line.

Smiley S, Nickerson PE, Comanita L, Daftarian N, El-Sehemy A, Tsai EL, Matan-Lithwick S, Yan K, Thurig S, Touahri Y, Dixit R, Aavani T, De Repentigny Y, Baker A, Tsilfidis C, Biernaskie J, Sauvé Y, Schuurmans C, Kothary R, Mears AJ, Wallace VA.

Sci Rep. 2016 Apr 22;6:24012. doi: 10.1038/srep24012. No abstract available.

5.

Establishment of a cone photoreceptor transplantation platform based on a novel cone-GFP reporter mouse line.

Smiley S, Nickerson PE, Comanita L, Daftarian N, El-Sehemy A, Tsai EL, Matan-Lithwick S, Yan K, Thurig S, Touahri Y, Dixit R, Aavani T, De Repentingy Y, Baker A, Tsilfidis C, Biernaskie J, Sauvé Y, Schuurmans C, Kothary R, Mears AJ, Wallace VA.

Sci Rep. 2016 Mar 11;6:22867. doi: 10.1038/srep22867. Erratum in: Sci Rep. 2016 Apr 22;6:24012. De Repentigny, Yves [corrected to De Repentingy, Yves].

6.

The Development of a Cat Model of Retinal Detachment and Re-attachment.

Wassmer S, Leonard BC, Coupland SG, Baker A, Hamilton J, Torlone R, Zacks DN, Tsilfidis C.

Adv Exp Med Biol. 2016;854:315-21. doi: 10.1007/978-3-319-17121-0_42.

PMID:
26427427
7.

A differential response to newt regeneration extract by C2C12 and primary mammalian muscle cells.

Kawesa S, Vanstone J, Tsilfidis C.

Skelet Muscle. 2015 Jun 11;5:19. doi: 10.1186/s13395-015-0044-8. eCollection 2015.

8.

A focus on the optical properties of the regenerated newt lens.

Wassmer S, Beddaoui M, Rajai P, Munger R, Tsilfidis C.

PLoS One. 2013 Aug 22;8(8):e70845. doi: 10.1371/journal.pone.0070845. eCollection 2013.

9.

Distinct roles for Ste20-like kinase SLK in muscle function and regeneration.

Storbeck CJ, Al-Zahrani KN, Sriram R, Kawesa S, O'Reilly P, Daniel K, McKay M, Kothary R, Tsilfidis C, Sabourin LA.

Skelet Muscle. 2013 Jul 1;3(1):16. doi: 10.1186/2044-5040-3-16.

10.

Chitosan microparticles for delivery of proteins to the retina.

Wassmer S, Rafat M, Fong WG, Baker AN, Tsilfidis C.

Acta Biomater. 2013 Aug;9(8):7855-64. doi: 10.1016/j.actbio.2013.04.025. Epub 2013 Apr 23.

PMID:
23623991
11.

Recovery of function following regeneration of the damaged retina in the adult newt, Notophthalmus viridescens.

Beddaoui M, Coupland SG, Tsilfidis C.

Doc Ophthalmol. 2012 Oct;125(2):91-100. doi: 10.1007/s10633-012-9338-x. Epub 2012 Jun 23.

PMID:
22729667
12.

Retinal degeneration and cellular suicide.

Fong WG, Tsilfidis C.

Adv Exp Med Biol. 2012;723:207-14. doi: 10.1007/978-1-4614-0631-0_28. Review. No abstract available.

PMID:
22183335
13.

XIAP therapy increases survival of transplanted rod precursors in a degenerating host retina.

Yao J, Feathers KL, Khanna H, Thompson D, Tsilfidis C, Hauswirth WW, Heckenlively JR, Swaroop A, Zacks DN.

Invest Ophthalmol Vis Sci. 2011 Mar 1;52(3):1567-72. doi: 10.1167/iovs.10-5998. Print 2011 Mar.

14.

Smn deficiency causes neuritogenesis and neurogenesis defects in the retinal neurons of a mouse model of spinal muscular atrophy.

Liu H, Beauvais A, Baker AN, Tsilfidis C, Kothary R.

Dev Neurobiol. 2011 Feb;71(2):153-69. doi: 10.1002/dneu.20840.

15.

PEG-PLA microparticles for encapsulation and delivery of Tat-EGFP to retinal cells.

Rafat M, Cléroux CA, Fong WG, Baker AN, Leonard BC, O'Connor MD, Tsilfidis C.

Biomaterials. 2010 Apr;31(12):3414-21. doi: 10.1016/j.biomaterials.2010.01.031. Epub 2010 Feb 9.

PMID:
20149443
16.

XIAP effects on retinal detachment-induced photoreceptor apoptosis [corrected].

Zadro-Lamoureux LA, Zacks DN, Baker AN, Zheng QD, Hauswirth WW, Tsilfidis C.

Invest Ophthalmol Vis Sci. 2009 Mar;50(3):1448-53. doi: 10.1167/iovs.08-2855. Epub 2008 Dec 5. Erratum in: Invest Ophthalmol Vis Sci. 2009 Apr;50(4):1530.

17.

XIAP protection of photoreceptors in animal models of retinitis pigmentosa.

Leonard KC, Petrin D, Coupland SG, Baker AN, Leonard BC, LaCasse EC, Hauswirth WW, Korneluk RG, Tsilfidis C.

PLoS One. 2007 Mar 21;2(3):e314.

18.

Newt opportunities for understanding the dedifferentiation process.

Chaar ZY, Tsilfidis C.

ScientificWorldJournal. 2006 Jul 7;6 Suppl 1:55-64. Review.

20.
21.

XIAP-mediated neuroprotection in retinal ischemia.

Renwick J, Narang MA, Coupland SG, Xuan JY, Baker AN, Brousseau J, Petrin D, Munger R, Leonard BC, Hauswirth WW, Korneluk RG, Tsilfidis C.

Gene Ther. 2006 Feb;13(4):339-47.

PMID:
16307001
23.

Identification of cDNAs associated with late dedifferentiation in adult newt forelimb regeneration.

Vascotto SG, Beug S, Liversage RA, Tsilfidis C.

Dev Dyn. 2005 Jun;233(2):347-55.

24.

Growth and apoptosis during larval forelimb development and adult forelimb regeneration in the newt ( Notophthalmus viridescens).

Vlaskalin T, Wong CJ, Tsilfidis C.

Dev Genes Evol. 2004 Sep;214(9):423-31. Epub 2004 Aug 21.

PMID:
15322877
25.

XIAP protects photoreceptors from n-methyl-n-nitrosourea-induced retinal degeneration.

Petrin D, Baker A, Brousseau J, Coupland S, Liston P, Hauswirth WW, Komeluk RG, Tsilfidis C.

Adv Exp Med Biol. 2003;533:385-93. No abstract available.

PMID:
15180289
26.

Linkage study between congenital cataracts and five crystallin loci.

Barr CL, Levin AV, Kovacs R, Muller W, Barsoum-Homsy M, Zachary D, Clark RA, Tsilfidis C.

Am J Med Genet A. 2003 Aug 15;121A(1):15-9.

PMID:
12900895
27.

Structural and functional protection of photoreceptors from MNU-induced retinal degeneration by the X-linked inhibitor of apoptosis.

Petrin D, Baker A, Coupland SG, Liston P, Narang M, Damji K, Leonard B, Chiodo VA, Timmers A, Hauswirth W, Korneluk RG, Tsilfidis C.

Invest Ophthalmol Vis Sci. 2003 Jun;44(6):2757-63.

PMID:
12766084
28.

Hox C6 expression during development and regeneration of forelimbs in larval Notophthalmus viridescens.

Khan PA, Tsilfidis C, Liversage RA.

Dev Genes Evol. 1999 Jun;209(6):323-9.

PMID:
10370113
30.

Gene localization for aculeiform cataract, on chromosome 2q33-35.

Héon E, Liu S, Billingsley G, Bernasconi O, Tsilfidis C, Schorderet DF, Munier FL.

Am J Hum Genet. 1998 Sep;63(3):921-6. No abstract available. Erratum in: Am J Hum Genet 1999 Jan;64(1):334. Tsifildis C [corrected to Tsilfidis C].

31.

A novel family of T-box genes in urodele amphibian limb development and regeneration: candidate genes involved in vertebrate forelimb/hindlimb patterning.

Simon HG, Kittappa R, Khan PA, Tsilfidis C, Liversage RA, Oppenheimer S.

Development. 1997 Apr;124(7):1355-66.

32.

Isolation of a novel G protein-coupled receptor (GPR4) localized to chromosome 19q13.3.

Mahadevan MS, Baird S, Bailly JE, Shutler GG, Sabourin LA, Tsilfidis C, Neville CE, Narang M, Korneluk RG.

Genomics. 1995 Nov 1;30(1):84-8.

PMID:
8595909
33.

Convergent myotonic dystrophy (DM) haplotypes: potential inconsistencies in human disease gene localization.

Whiting EJ, Tsilfidis C, Surh L, MacKenzie AE, Korneluk RG.

Eur J Hum Genet. 1995;3(3):195-202.

PMID:
7583045
34.

Additive influence of maternal and offspring DM-kinase gene CTG repeat lengths in the genesis of congenital myotonic dystrophy.

Barceló JM, Pluscauskas M, MacKenzie AE, Tsilfidis C, Narang M, Korneluk RG.

Am J Hum Genet. 1994 Jun;54(6):1124-5. No abstract available.

35.

Intergenerational stability of the myotonic dystrophy protomutation.

Barceló JM, Mahadevan MS, Tsilfidis C, MacKenzie AE, Korneluk RG.

Hum Mol Genet. 1993 Jun;2(6):705-9.

PMID:
8353489
36.

Reduction in size of the myotonic dystrophy trinucleotide repeat mutation during transmission.

O'Hoy KL, Tsilfidis C, Mahadevan MS, Neville CE, Barceló J, Hunter AG, Korneluk RG.

Science. 1993 Feb 5;259(5096):809-12.

PMID:
8094260
37.

Decrease in the size of the myotonic dystrophy CTG repeat during transmission from parent to child: implications for genetic counselling and genetic anticipation.

Hunter AG, Jacob P, O'Hoy K, MacDonald I, Mettler G, Tsilfidis C, Korneluk RG.

Am J Med Genet. 1993 Feb 1;45(3):401-7.

PMID:
8434633
38.

The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy.

Hunter A, Tsilfidis C, Mettler G, Jacob P, Mahadevan M, Surh L, Korneluk R.

J Med Genet. 1992 Nov;29(11):774-9.

39.

Physical mapping and cloning of the proximal segment of the myotonic dystrophy gene region.

Shutler G, Korneluk RG, Tsilfidis C, Mahadevan M, Bailly J, Smeets H, Jansen G, Wieringa B, Lohman F, Aslanidis C, et al.

Genomics. 1992 Jul;13(3):518-25.

PMID:
1639380
40.

Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19q.

Jansen G, de Jong PJ, Amemiya C, Aslanidis C, Shaw DJ, Harley HG, Brook JD, Fenwick R, Korneluk RG, Tsilfidis C, et al.

Genomics. 1992 Jul;13(3):509-17.

PMID:
1639379
41.

Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy.

Tsilfidis C, MacKenzie AE, Mettler G, Barceló J, Korneluk RG.

Nat Genet. 1992 Jun;1(3):192-5.

PMID:
1303233
42.

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene.

Mahadevan M, Tsilfidis C, Sabourin L, Shutler G, Amemiya C, Jansen G, Neville C, Narang M, Barceló J, O'Hoy K, et al.

Science. 1992 Mar 6;255(5049):1253-5.

PMID:
1546325
43.

Cloning of the essential myotonic dystrophy region and mapping of the putative defect.

Aslanidis C, Jansen G, Amemiya C, Shutler G, Mahadevan M, Tsilfidis C, Chen C, Alleman J, Wormskamp NG, Vooijs M, et al.

Nature. 1992 Feb 6;355(6360):548-51.

PMID:
1346925
44.

D19S51 is closely linked with and maps distal to the myotonic dystrophy locus on 19q.

Tsilfidis C, MacKenzie AE, Shutler G, Leblond S, Bailly J, Johnson K, Williamson R, Siegel-Bartelt J, Korneluk RG, Shelbourne P.

Am J Hum Genet. 1991 Nov;49(5):961-5. Erratum in: Am J Hum Genet 1992 Mar;50(3):659.

45.

An insertion polymorphism identified by the probe pE0.8 (D19S115) at 19q13.3.

Shutler G, Leblond S, Bailly J, MacKenzie AE, Tsilfidis C, Korneluk RG.

Nucleic Acids Res. 1991 Mar 11;19(5):1159. No abstract available.

46.

RFLP identified by the probe pKE0.6 (D19S117) at human chromosome 19q13.3.

Shutler G, Tsilfidis C, Leblond S, Korneluk RG.

Nucleic Acids Res. 1991 Mar 11;19(5):1158. No abstract available.

47.

An SstI RFLP detected by the probe pKE2.1 (D19S116) localized to human chromosome 19q13.3.

Tsilfidis C, Shutler G, Leblond S, Korneluk RG.

Nucleic Acids Res. 1991 Mar 11;19(5):1158. No abstract available.

48.

A three allele insertion polymorphism is identified by the human chromosome 19q13.3 probe pKBE0.8 (D19S119).

Korneluk RG, Tsilfidis C, Shutler G, Mahadevan M, Bailly J, Surh LC.

Nucleic Acids Res. 1991 Mar 11;19(5):1157. No abstract available.

49.

A frequent HincII polymorphism identified by the human chromosome 19q13.3 probe pKEX0.8 (D19S118).

Tsilfidis C, Shutler G, Mahadevan M, Korneluk RG.

Nucleic Acids Res. 1991 Mar 11;19(5):1157. No abstract available.

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