Pierides A - Search Results

1

PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein.

Mochizuki T, Wu G, Hayashi T, Xenophontos SL, Veldhuisen B, Saris JJ, Reynolds DM, Cai Y, Gabow PA, Pierides A, Kimberling WJ, Breuning MH, Deltas CC, Peters DJ, Somlo S. Mochizuki T, et al. Among authors: pierides a. Science. 1996 May 31;272(5266):1339-42. doi: 10.1126/science.272.5266.1339. Science. 1996. PMID: 8650545

2

Presymptomatic molecular diagnosis of autosomal dominant polycystic kidney disease using PKD1- and PKD2-linked markers in Cypriot families.

Deltas CC, Christodoulou K, Tjakouri C, Pierides A. Deltas CC, et al. Among authors: pierides a. Clin Genet. 1996 Jul;50(1):10-8. doi: 10.1111/j.1399-0004.1996.tb02339.x. Clin Genet. 1996. PMID: 8891380

3

New amino acid polymorphism, Ala/Val4058, in exon 45 of the polycystic kidney disease 1 gene: evolution of alleles.

Constantinides R, Xenophontos S, Neophytou P, Nomura S, Pierides A, Deltas CC. Constantinides R, et al. Among authors: pierides a. Hum Genet. 1997 May;99(5):644-7. doi: 10.1007/s004390050421. Hum Genet. 1997. PMID: 9150733

4

A translation frameshift mutation induced by a cytosine insertion in the polycystic kidney disease 2 gene (PDK2).

Xenophontos S, Constantinides R, Hayashi T, Mochizuki T, Somlo S, Pierides A, Deltas CC. Xenophontos S, et al. Among authors: pierides a. Hum Mol Genet. 1997 Jun;6(6):949-52. doi: 10.1093/hmg/6.6.949. Hum Mol Genet. 1997. PMID: 9175744

5

Loss of heterozygosity in polycystic kidney disease with a missense mutation in the repeated region of PKD1.

Koptides M, Constantinides R, Kyriakides G, Hadjigavriel M, Patsalis PC, Pierides A, Deltas CC. Koptides M, et al. Among authors: pierides a. Hum Genet. 1998 Dec;103(6):709-17. doi: 10.1007/s004390050896. Hum Genet. 1998. PMID: 9921908

6

Genetic evidence for a trans-heterozygous model for cystogenesis in autosomal dominant polycystic kidney disease.

Koptides M, Mean R, Demetriou K, Pierides A, Deltas CC. Koptides M, et al. Among authors: pierides a. Hum Mol Genet. 2000 Feb 12;9(3):447-52. doi: 10.1093/hmg/9.3.447. Hum Mol Genet. 2000. PMID: 10655555

7

Screening of the PKD1 duplicated region reveals multiple single nucleotide polymorphisms and a de novo mutation in Hellenic polycystic kidney disease families.

Koptides M, Mean R, Demetriou K, Constantinides R, Pierides A, Harris PC, Deltas CC. Koptides M, et al. Among authors: pierides a. Hum Mutat. 2000 Aug;16(2):176. doi: 10.1002/1098-1004(200008)16:2<176::AID-HUMU11>3.0.CO;2-H. Hum Mutat. 2000. PMID: 10923040

8

Novel PKD1 deletions and missense variants in a cohort of Hellenic polycystic kidney disease families.

Bouba I, Koptides M, Mean R, Costi CE, Demetriou K, Georgiou I, Pierides A, Siamopoulos K, Deltas CC. Bouba I, et al. Among authors: pierides a. Eur J Hum Genet. 2001 Sep;9(9):677-84. doi: 10.1038/sj.ejhg.5200696. Eur J Hum Genet. 2001. PMID: 11571556

9

Genetic heterogeneity in adult dominant polycystic kidney disease in Cypriot families.

Constantinou-Deltas CD, Papageorgiou E, Boteva K, Christodoulou K, Breuning MH, Peter DJ, Pierides A. Constantinou-Deltas CD, et al. Among authors: pierides a. Hum Genet. 1995 Apr;95(4):416-23. doi: 10.1007/BF00208967. Hum Genet. 1995. PMID: 7705838

10

Detection of a novel nonsense mutation and an intragenic polymorphism in the PKD1 gene of a Cypriot family with autosomal dominant polycystic kidney disease.

Neophytou P, Constantinides R, Lazarou A, Pierides A, Deltas CC. Neophytou P, et al. Among authors: pierides a. Hum Genet. 1996 Oct;98(4):437-42. doi: 10.1007/s004390050235. Hum Genet. 1996. PMID: 8792818

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