Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Koptides, Michael"'
Autor:
Stavrou, Christoforos, Koptides, Michael, Tombazos, Christos, Psara, Evlalia, Patsias, Charalambos, Zouvani, Ioanna, Kyriacou, Kyriacos, Hildebrandt, Friedhelm, Christofides, Tasos, Pierides, Alkis, Deltas, C. Constantinou *
Publikováno v:
In Kidney International October 2002 62(4):1385-1394
Autor:
Koptides, Michael, Mean, Richard, Stavrou, Christoforos, Pierides, Alkis, Demetriou, Kyproula, Nakayama, Tomohiro, Hildebrandt, Friedhelm, Fuchshuber, Arno, Deltas, C.Constantinou
Publikováno v:
In Molecular and Cellular Probes December 2001 15(6):357-361
Autor:
Bouba, Ioanna, Koptides, Michael, Mean, Richard, Costi, Constandina-Eleni, Demetriou, Kyproula, Georgiou, Ioannis, Pierides, Alkis, Siamopoulos, Konstantinos, Deltas, C Constantinou
Publikováno v:
European Journal of Human Genetics. Sep2001, Vol. 9 Issue 9, p677. 8p.
Publikováno v:
BioTechniques
36 758 760 Cited By :5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4485::63d2097d0e7efc4a20cd5a1cd3c3f334
http://gnosis.library.ucy.ac.cy/handle/7/53243
http://gnosis.library.ucy.ac.cy/handle/7/53243
Autor:
Lamnissou, Klea, Zirogiannis, P., Trygonis, S., Demetriou, Kyproula, Pierides, Alkis M., Koptides, Michael, Constantinou-Deltas, Constantinos D.
Publikováno v:
Genetic testing
Genet.Test.
Genet.Test.
Nitric oxide (NO) is thought to be an important factor in the deterioration of renal function. A variable-number tandem 27-bp repeat in intron 4 of the endothelial cell nitric oxide synthase (NOS3) gene has been found to be associated with the plasma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4485::19ee23aec16af89cb128e0f6e00c4296
http://gnosis.library.ucy.ac.cy/handle/7/53221
http://gnosis.library.ucy.ac.cy/handle/7/53221
Autor:
Koptides, Michael, Mean, R., Stavrou, Christoforos V., Pierides, Alkis M., Demetriou, Kyproula, Nakayama, T., Hildebrandt, F., Fuchshuber, A., Constantinou-Deltas, Constantinos D.
Publikováno v:
Molecular and cellular probes
Mol.Cell.Probes
Mol.Cell.Probes
Autosomal dominant medullary cystic kidney disease (ADMCKD) is an adult-onset heterogeneous genetic nephropathy characterized by salt wasting and end-stage renal failure. The gene responsible for ADMCKD-1 was mapped on chromosome 1 q21 and it is flan
Autor:
Stavrou, Christoforos V., Koptides, Michael, Tombazos, C., Psara, E., Patsias, Charalambos, Zouvani, Ioanna, Kyriacou, Kyriacos C., Hildebrandt, F., Christofides, Tasos C., Pierides, Alkis M., Constantinou-Deltas, Constantinos D.
Publikováno v:
Kidney international
Kidney Int.
Kidney Int.
Background. Autosomal-dominant medullary cystic kidney disease (ADMCKD), a hereditary chronic interstitial nephropathy, recently attracted attention because of the cloning or mapping of certain gene loci, namely NPHP1, NPHP2 and NPHP3 for familial ju
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4485::ec2d38cc84544fb9bf343ad229351398
http://gnosis.library.ucy.ac.cy/handle/7/57657
http://gnosis.library.ucy.ac.cy/handle/7/57657
Autor:
Constantinou-Deltas, Constantinos D., Mean, R., Rossou, Elena, Costi, Constantina Eleni, Koupepidou, P., Hadjiyanni, I., Koptides, Michael, Hadjiroussos, V., Petrou, P., Pierides, Alkis M., Lamnissou, Klea, Koptides, M.
Publikováno v:
Genetic testing
Genet.Test.
Genet.Test.
Familial Mediterranean Fever (FMF) is an autosomal recessive disease of high prevalence within Mediterranean countries and particularly common in four ethnic populations: Arabs, non-Ashkenazi Jews, Armenians, and Turks. The responsible gene MEFV has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52a12a8ee6a53a386fdd61b15eccb048
http://gnosis.library.ucy.ac.cy/handle/7/53025
http://gnosis.library.ucy.ac.cy/handle/7/53025
Autor:
Bouba, I., Koptides, Michael, Mean, R., Costi, Constantina Eleni, Demetriou, Kyproula, Georgiou, Ioannis A., Pierides, Alkis M., Siamopoulos, K., Constantinou-Deltas, Constantinos D.
Publikováno v:
European Journal of Human Genetics
Eur.J.Hum.Genet.
Eur.J.Hum.Genet.
The autosomal dominant form of polycystic kidney disease is a very frequent genetically heterogeneous inherited condition affecting approximately 1: 1000 individuals of the Caucasian population. The main symptom is the formation of fluid-filled cysts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f8bdc22a0d4b58ec39152bf626c8f39
http://gnosis.library.ucy.ac.cy/handle/7/52957
http://gnosis.library.ucy.ac.cy/handle/7/52957
Autor:
Rüschendorf, F., Fuchshuber, A., Kroiss, S., Karle, S., Berthold, S., Huck, K., Burton, C., Rahman, N., Koptides, Michael, Constantinou-Deltas, Constantinos D., Otto, E., Feest, T., Hildebrandt, F.
Publikováno v:
Genomics
Autosomal dominant medullary cystic kidney disease (MCKD) is an adult onset tubulointerstitial nephropathy that leads to salt wasting and end-stage renal failure. A gene locus (MCKD1) has been mapped on chromosome 1q21. Here we report on a large MCKD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5000f708356d77fb4727ab219a5933d
http://gnosis.library.ucy.ac.cy/handle/7/53077
http://gnosis.library.ucy.ac.cy/handle/7/53077