Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Constantinides, Rolandos"'
Autor:
Xenophontos, Stavroulla L., Constantinides, Rolandos, Hayashi, Tomohito, Mochizuki, Toshio, Somlo, Stefan, Pierides, Alkis M., Constantinou-Deltas, Constantinos D.
Publikováno v:
Human molecular genetics
Hum.Mol.Genet.
Hum.Mol.Genet.
Mutations in the PKD2 gene on the long arm of chromosome 4 are responsible for ~ 15% of cases of polycystic kidney disease. Perhaps the only difference from the more common ADPKD1 cases is the rate of progression of cystic changes, and the age of ons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d47d003f608bf65512e80a244f9e397f
https://doi.org/10.1093/hmg/6.6.949
https://doi.org/10.1093/hmg/6.6.949
Autor:
Koptides, Michael, Constantinides, Rolandos, Kyriakides, George K., Hadjigavriel, Michalis, Patsalis, Philippos C., Pierides, Alkis M., Constantinou-Deltas, Constantinos D.
Publikováno v:
Human genetics
Hum.Genet.
Hum.Genet.
Loss of heterozygosity (LOH) is a molecular phenomenon that denotes the loss of one of the two alleles at a specific locus. It is frequently associated with tumour suppressor genes in various cancers and also with hyper-proliferative disorders, altho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e977c6c1e36634997c80b7fb04104bdc
https://pubmed.ncbi.nlm.nih.gov/9921908
https://pubmed.ncbi.nlm.nih.gov/9921908
Autor:
Constantinides, Rolandos, Xenophontos, Stavroulla L., Neophytou, Pavlos, Nomura, Shinsuke, Pierides, Alkis M., Constantinou-Deltas, Constantinos D.
Publikováno v:
Human genetics
Hum.Genet.
Hum.Genet.
The PKD1 gene, which is responsible for the most common form of autosomal dominant polycystic kidney disease, has recently been cloned and sequenced. Many disease-causing mutations have been characterized in this gene, most of them resulting in prema
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cedeb5469e6057ca531c82646c5935c
https://pubmed.ncbi.nlm.nih.gov/9150733
https://pubmed.ncbi.nlm.nih.gov/9150733
Autor:
Neophytou, Pavlos, Constantinides, Rolandos, Lazarou, Akis, Pierides, Alkis M., Constantinou-Deltas, Constantinos D.
Publikováno v:
Human genetics
Hum.Genet.
Hum.Genet.
Mutations in the PKD1 gene on the short arm of chromosome 16 account for 85%-90% of polycystic kidney disease patients in the Caucasian population. After the recent characterization of the gene, we started a search for mutations in its 3'-end unique
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0357447ad3d3af57e5c20bb9d42d111a
https://pubmed.ncbi.nlm.nih.gov/8792818
https://pubmed.ncbi.nlm.nih.gov/8792818
Autor:
Koptides, Michael, Constantinides, Rolandos, Kyriakides, George, Hadjigavriel, Michael, Patsalis, Philippos C., Pierides, Alkis, Constantinou Deltas, C.
Publikováno v:
Human Genetics; Dec1998, Vol. 103 Issue 6, p709-717, 9p
Autor:
Koptides, Michael, Mean, Richard, Demetriou, Kyproula, Constantinides, Rolandos, Pierides, Alkis, Harris, Peter C., Deltas, C. Constantinou
Publikováno v:
Human Mutation; Aug2000, Vol. 16 Issue 2, p176-176, 1p