C Tsilfidis
Overview
Explore the profile of C Tsilfidis including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
23
Citations
1043
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0
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Recent Articles
1.
Renwick J, Narang M, Coupland S, Xuan J, Baker A, Brousseau J, et al.
Gene Ther
. 2005 Nov;
13(4):339-47.
PMID: 16307001
Retinal ischemia results in the loss of vision in a number of ocular diseases including acute glaucoma, diabetic retinopathy, hypertensive retinopathy and retinal vascular occlusion. Recent studies have shown that...
2.
Khan P, Tsilfidis C, LIVERSAGE R
Dev Genes Evol
. 1999 Jun;
209(6):323-9.
PMID: 10370113
A central theme concerning the epimorphic regenerative potential of urodele amphibian appendages is that limb regeneration in the adult parallels larval limb development. Results of previous research have led to...
3.
Cadinouche M, LIVERSAGE R, Muller W, Tsilfidis C
Dev Dyn
. 1999 Mar;
214(3):259-68.
PMID: 10090152
Larval and adult newts provide important experimental models to study limb development and regeneration. These animals have exceptional ability to regenerate their appendages, as well as other vital structures. Our...
4.
Heon E, Liu S, Billingsley G, Bernasconi O, Tsilfidis C, Schorderet D, et al.
Am J Hum Genet
. 1998 Aug;
63(3):921-6.
PMID: 9718335
No abstract available.
5.
Simon H, Kittappa R, Khan P, Tsilfidis C, LIVERSAGE R, Oppenheimer S
Development
. 1997 Apr;
124(7):1355-66.
PMID: 9118806
In certain urodeles, a lost appendage, including hand and foot, can be completely replaced through epimorphic regeneration. The regeneration process involves cellular activities similar to those described for embryogenesis. Working...
6.
Mahadevan M, Baird S, Bailly J, Shutler G, Sabourin L, Tsilfidis C, et al.
Genomics
. 1995 Nov;
30(1):84-8.
PMID: 8595909
We present the cloning and sequencing of the human gene for a novel G-protein coupled receptor (GPR4), from the critical myotonic dystrophy (DM) region on chromosome 19q13.3. The homologous porcine...
7.
Whiting E, Tsilfidis C, Surh L, Mackenzie A, Korneluk R
Eur J Hum Genet
. 1995 Jan;
3(3):195-202.
PMID: 7583045
Myotonic dystrophy (DM) is an autosomal dominant neuromuscular disease which has been shown to be caused by an unstable trinucleotide repeat located on chromosome 19q. We have conducted extensive haplotype...
8.
Barcelo J, Pluscauskas M, Mackenzie A, Tsilfidis C, Narang M, Korneluk R
Am J Hum Genet
. 1994 Jun;
54(6):1124-5.
PMID: 8198135
No abstract available.
9.
Barcelo J, Mahadevan M, Tsilfidis C, Mackenzie A, Korneluk R
Hum Mol Genet
. 1993 Jun;
2(6):705-9.
PMID: 8353489
The amplification of the CTG trinucleotide repeat in myotonic dystrophy (DM) correlates with increasingly severe phenotypes. We designate its minimal amplification the 'protomutation' since it is the mutation itself at...
10.
OHoy K, Tsilfidis C, Mahadevan M, Neville C, Barcelo J, Hunter A, et al.
Science
. 1993 Feb;
259(5096):809-12.
PMID: 8094260
Myotonic dystrophy (DM) is an autosomal-dominant disorder that affects 1 in 8000 individuals. Amplification of an unstable trinucleotide CTG repeat, located within the 3' untranslated region of a gene, correlates...