Constantinos Deltas
Constantinos Deltas
Professor of Genetics, University of Cyprus
Adresă de e-mail confirmată pe ucy.ac.cy - Pagina de pornire
Citat de
Citat de
PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein
T Mochizuki, G Wu, T Hayashi, SL Xenophontos, B Veldhuisen, JJ Saris, ...
Science 272 (5266), 1339-1342, 1996
microRNAs: a newly described class of encoded molecules that play a role in health and disease
K Felekkis, E Touvana, C Stefanou, C Deltas
Hippokratia 14 (4), 236, 2010
An error in dystrophin mRNA processing in golden retriever muscular dystrophy, an animal homologue of Duchenne muscular dystrophy
NJH Sharp, JN Kornegay, SD Van Camp, MH Herbstreith, SL Secore, ...
Genomics 13 (1), 115-121, 1992
Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis
DP Gale, EG De Jorge, HT Cook, R Martinez-Barricarte, A Hadjisavvas, ...
The Lancet 376 (9743), 794-801, 2010
Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease
DJM Peters, L Spruit, JJ Saris, D Ravine, LA Sandkuijl, R Fossdal, ...
Nature genetics 5 (4), 359-362, 1993
Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management—a KDIGO consensus report
KU Eckardt, SL Alper, C Antignac, AJ Bleyer, D Chauveau, K Dahan, ...
Kidney international 88 (4), 676-683, 2015
COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy
K Voskarides, L Damianou, V Neocleous, I Zouvani, S Christodoulidou, ...
Journal of the American Society of Nephrology 18 (11), 3004-3016, 2007
Familial C3 glomerulopathy associated with CFHR5 mutations: clinical characteristics of 91 patients in 16 pedigrees
Y Athanasiou, K Voskarides, DP Gale, L Damianou, C Patsias, M Zavros, ...
Clinical Journal of the American Society of Nephrology 6 (6), 1436-1446, 2011
Mutation in a gene for type I procollagen (COL1A2) in a woman with postmenopausal osteoporosis: evidence for phenotypic and genotypic overlap with mild osteogenesis imperfecta.
LD Spotila, CD Constantinou, L Sereda, A Ganguly, BL Riggs, ...
Proceedings of the National Academy of Sciences 88 (12), 5423-5427, 1991
Expert consensus guidelines for the genetic diagnosis of Alport syndrome
J Savige, F Ariani, F Mari, M Bruttini, A Renieri, O Gross, C Deltas, ...
Pediatric Nephrology 34, 1175-1189, 2019
Chromosome 1 localization of a gene for autosomal dominant medullary cystic kidney disease (ADMCKD)
K Christodoulou, M Tsingis, C Stavrou, A Eleftheriou, P Papapavlou, ...
Human molecular genetics 7 (5), 905-911, 1998
Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes …
A Pierides, K Voskarides, Y Athanasiou, K Ioannou, L Damianou, M Arsali, ...
Nephrology Dialysis Transplantation 24 (9), 2721-2729, 2009
Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney disease
R Magistroni, N He, K Wang, R Andrew, A Johnson, P Gabow, E Dicks, ...
Journal of the American Society of Nephrology 14 (5), 1164-1174, 2003
Small molecule targets TMED9 and promotes lysosomal degradation to reverse proteinopathy
M Dvela-Levitt, M Kost-Alimova, M Emani, E Kohnert, R Thompson, ...
Cell 178 (3), 521-535. e23, 2019
Germinal and Somatic Mutations in the PKD2 Gene of Renal Cysts in Autosomal Dominant Polycystic Kidney Disease
M Koptides, C Hadjimichael, P Koupepidou, A Pierides, CC Deltas
Human molecular genetics 8 (3), 509-513, 1999
Genetic evidence for a trans-heterozygous model for cystogenesis in autosomal dominant polycystic kidney disease
M Koptides, R Mean, K Demetriou, A Pierides, CC Deltas
Human molecular genetics 9 (3), 447-452, 2000
Mutation analysis of coding sequences for type I procollagen in individuals with low bone density
LD Spotila, A Colige, L Sereda, CD Constantinou‐Deltas, MP Whyte, ...
Journal of Bone and Mineral Research 9 (6), 923-932, 1994
A European spectrum of pharmacogenomic biomarkers: implications for clinical pharmacogenomics
C Mizzi, E Dalabira, J Kumuthini, N Dzimiri, I Balogh, N Bașak, R Böhm, ...
PloS one 11 (9), e0162866, 2016
Type I procollagen: The gene‐protein system that harbors most of the mutations causing osteogenesis imperfecta and probably more common heritable disorders of connective tissue
DJ Prockop, CD Constantinou, KE Dombrowski, Y Hojima, KE Kadler, ...
American journal of medical genetics 34 (1), 60-67, 1989
Molecular genetics of familial hematuric diseases
C Deltas, A Pierides, K Voskarides
Nephrology Dialysis Transplantation 28 (12), 2946-2960, 2013
Sistemul nu poate realiza operația în acest moment. Încercați din nou mai târziu.
Articole 1–20