المؤلفون: Papazachariou, Louiza, Demosthenous, Panayiota, Pieri, Myrtani, Papagregoriou, Gregory, Savva, Isavella, Stavrou, Christoforos, Zavros, Michael, Athanasiou, Yiannis, Ioannou, Kyriakos, Patsias, Charalambos, Panagides, Alexia, Potamitis, Costas, Demetriou, Kyproula, Prikis, Marios, Hadjigavriel, Michael, Kkolou, Maria, Loukaidou, Panayiota, Pastelli, Androulla, Michael, Aristos, Lazarou, Akis, Arsali, Maria, Damianou, Loukas, Goutziamani, Ioanna, Soloukides, Andreas, Yioukas, Lakis, Elia, Avraam, Zouvani, Ioanna, Polycarpou, Polycarpos, Pierides, Alkis, Voskarides, Konstantinos, Deltas, Constantinos

المساهمون: Duncan, Melinda

المصدر: PLoS ONE ; volume 9, issue 12, page e115015 ; ISSN 1932-6203

الاتاحة: http://dx.doi.org/10.1371/journal.pone.0115015
http://dx.plos.org/10.1371/journal.pone.0115015

المؤلفون: Legendre, Christophe, Cohen, David, Delmas, Yahsou, Feldkamp, Thorsten, Fouque, Denis, Furman, Richard, Gaber, Osama, Greenbaum, Larry, Goodship, Timothy, Haller, Hermann, Herthelius, Maria, Hourmant, Maryvonne, Licht, Christoph, Moulin, Bruno, Sheerin, Neil, Trivelli, Antonella, Bedrosian, Camille L., Loirat, Chantal, Babu, Sunil, Jungraithmayr, Therese, Lebranchu, Yvon, Riedl, Magdalena, Gaber, A. Osama, Bedrosian, Camille, Muus, Petra, Douglas, Kenneth, Remuzzi, Giuseppe, Kourouklaris, Andreas, Ioannou, Kyriakos, Athanasiou, Ioannis, Demetriou, Kyproula, Panagidou, Alexia, Zavros, Michalis, Rodríguez C, Nestor Y., Blasco, Miquel, Arcal, Carola, Quintana, Luis F., Rodríguez de Cordoba, Santiago, Campistol, Josep M., Bachmann, Nadine, Eisenberger, Tobias, Decker, Christian, Bolz, Hanno J., Bergmann, Carsten, Pesce, Francesco, Cox, Sharon N., Serino, Grazia, De Palma, Giuseppe, Sallustio, Fabio P., Schena, Francesco, Falchi, Mario, Pieri, Myrtani, Stefanou, Charalambos, Zaravinos, Apostolos, Erguler, Kamil, Lapathitis, George, Dweep, Harsh, Sticht, Carsten, Anastasiadou, Natassa, Zouvani, Ioanna, Voskarides, Konstantinos, Gretz, Norbert, Deltas, Constantinos C., Ruiz, Anne, Bonny, Olivier, Sallustio, Fabio, Curci, Claudia, Cox, Sharon, Kemter, Elisabeth, Sklenák, Stefanie, Aigner, Bernhard, Wanke, Ruediger, Kitzler, Thomas M., Moskowitz, Jonathan L., Piret, Sian E., Lhotta, Karl, Tashman, Adam, Velez, Erin, Thakker, Rajesh V., Kotanko, Peter, Leierer, Johannes, Rudnicki, Michael, Perco, Paul, Koppelstaetter, Christian, Mayer, Gert, Sá, Maria J.N., Alves, Susana, Storey, Helen, Flinter, Frances, Willems, Patrick J., Carvalho, Filipa, Oliveira, João, Arsali, Maria, Papazachariou, Louiza, Demosthenous, Panayiota, Lazarou, Akis, Hadjigavriel, Michalis, Stavrou, Christoforos, Yioukkas, Lakis, Deltas, Constantinos, Pierides, Alkis, Kkolou, Maria, Toka, Hakan R., Dibartolo, Salvatore, Lanske, Beate, Brown, Edward M., Pollak, Martin R., Familiari, Alessandra, Zavan, Barbara, Sanna Cherchi, Simone, Fabris, Antonia, Cristofaro, Rosalba, Gambaro, Giovanni, D'Angelo, Angela, Anglani, Franca, Toka, Hakan, Mount, David, Pollak, Martin, Curhan, Gary, Sengöge, Gürkan, Bajari, Tarek, Kupczok, Anna, von Haeseler, Arndt, Schuster, Michael, Pfaller, Walter, Jennings, Paul, Weltermann, Ansgar, Blake, Sophia, Sunder-Plassmann, Gere, Kerti, Andrea, Csohány, Rózsa, Wagner, László, Jávorszky, Eszter, Maka, Erika, Tulassay, Tivadar, Tory, Kálmán, Kingswood, John, Nikolskaya, Natalya, Mbundi, Jana, Kingswood, J., Jozwiak, S., Belousova, E., Frost, M., Kuperman, R., Bebin, M., Korf, B., Flamini, R., Kohrman, M., Sparagana, S., Wu, J., Brechenmacher, T., Stein, K., Bissler, J., Franz, D., Zonnenberg, B., Cheung, W., Wang, J., Lam, D., Budde, K., Ivanitskiy, Lyudvig, Sowershaewa, Evgeniya, Krasnova, Tatyana, Samokhodskaya, Larisa, Safarikova, Marketa, Jana, Reiterova, Jitka, Stekrova, Obeidova, Lena, Kohoutova, Milada, Tesar, Vladimir, Evrengul, Havva, Ertan, Pelin, Serdaroglu, Erkin, Yuksel, Selcuk, Mir, Sevgi, Yang n Ergon, Ezgi, Berdeli, Afig, Zawada, Adam, Rogacev, Kyrill, Rotter, Björn, Winter, Peter, Fliser, Danilo, Heine, Gunnar, Bataille, Stanislas, Moal, Valerie, Berland, Yvon, Daniel, Laurent, Rosado, Consolación, Bueno, Elena, Fraile, Pilar, Lucas, Cristina, Garcóa-Cosmes, Pedro, Tabernero, JoséMatías, González, Rogelio, García-Cosmes, Pedro, Silska-Dittmar, Magdalena, Zaorska, Katarzyna, Malke, Anna, Musielak, Anna, Ostalska-Nowicka, Danuta, Zachwieja, Jacek, K d r, Veysel, Uz, Efkan, Yigit, Ayse, Altuntas, Atila, Yigit, Barbaros, Inal, Salih, Uz, Ebru, Sezer, Mehmet, Yalmaz, Ramazan, Visciano, Bianca, Porto, Caterina, Acampora, Emma, Russo, Roberta, Riccio, Eleonora, Capuano, Ivana, Parenti, Giancarlo, Pisani, Antonio, Conti, Maura, Angioi, Andrea, Floris, Matteo, Melis, Patrizia, Asunis, Anna Maria, Piras, Doloretta, Pani, Antonello, Warnock, David, Guasch, Antonio, Thomas, Christie, Wanner, Christoph, Campbell, Ruth, Vujkovac, Bojan, Okur, Ilyas, Biberoglu, Gürsel, Ezgü, Fatih, Tümer, Leyla, Hasanoglu, Alev, Bicik, Zerrin, Akin, Yasemin, Mumcuoglu, Metin, Ecder, Tevfik, Paliouras, Christos, Mattas, Georgios, Papagiannis, Nikolaos, Ntetskas, Georgios, Lamprianou, Foteini, Karvouniaris, Nikolaos, Alivanis, Polichronis

مصطلحات موضوعية: Abstracts

وصف الملف: text/html

Relation: http://ndt.oxfordjournals.org/cgi/content/short/28/suppl_1/i309; http://dx.doi.org/10.1093/ndt/gft126

الاتاحة: http://ndt.oxfordjournals.org/cgi/content/short/28/suppl_1/i309
https://doi.org/10.1093/ndt/gft126

المؤلفون: Liu, Michelle, Shi, Sally, Senthilnathan, Sean, Yu, Julie, Wu, Ellio, Bergmann, Carsten, Zerres, Klaus, Bogdanova, Nadja, COTO, ELIECER, Deltas, Constantinos, Pierides, Alkis, Demetriou, Kyproula, Devuyst, Olivier, Gitomer, Berenice, Laakso, Marku, Lumiaho, Anne, Lamnissou, Klea, Magistroni, Riccardo, Parfrey, Patrick, Breuning, Martijn, Peters, Dorien J.M., Torra, Roser, Winearls, Christopher, Torres, Vicente E., Harris, Peter, Paterson, Andrew D., Pei, York

المصدر: Journal of the American Society of Nephrology, 21(9), 1510-1520, (2010-04-28)

Relation: https://zenodo.org/communities/biobankcy; https://doi.org/10.1681/asn.2010030237; oai:zenodo.org:10025203

الاتاحة: https://doi.org/10.1681/asn.2010030237

المؤلفون: Magistroni, Riccardo, He, Ning, Wang, Kairong, Andrew, Robin, Johnson, Ann, Gabow, Patricia, Dicks, Elizabeth, Parfrey, Patrick, Torra, Roser, San-Millan, Jose L., Coto, Eliecer, van Dijk, Marjan, Breuning, Martijn, Peters, Dorien, Bogdanova, Nadja, Ligabue, Giulia, Albertazzi, Alberto, Hateboer, Nick, Demetriou, Kyproula, Pierides, Alkis, Deltas, Constantinos, St. George-Hyslop, Peter, Ravine, David, Pei, York

المصدر: Journal of the American Society of Nephrology ; volume 14, issue 5, page 1164-1174 ; ISSN 1046-6673

الاتاحة: http://dx.doi.org/10.1097/01.asn.0000061774.90975.25
https://journals.lww.com/00001751-200305000-00007

المؤلفون: Pierides, Alkis M., Athanasiou, Yiannis, Demetriou, Kyproula, Koptides, Michael, Deltas, C. Constantinou

مصطلحات موضوعية: Original Articles

وصف الملف: text/html

Relation: http://ndt.oxfordjournals.org/cgi/content/short/17/6/1014; http://dx.doi.org/10.1093/ndt/17.6.1014

الاتاحة: http://ndt.oxfordjournals.org/cgi/content/short/17/6/1014
https://doi.org/10.1093/ndt/17.6.1014

المؤلفون: Bouba, Ioanna, Koptides, Michael, Mean, Richard, Costi, Constandina-Eleni, Demetriou, Kyproula, Georgiou, Ioannis, Pierides, Alkis, Siamopoulos, Konstantinos, Deltas, C Constantinou

المصدر: European Journal of Human Genetics ; volume 9, issue 9, page 677-684 ; ISSN 1018-4813 1476-5438

الاتاحة: http://dx.doi.org/10.1038/sj.ejhg.5200696
http://www.nature.com/articles/5200696.pdf
http://www.nature.com/articles/5200696

المؤلفون: Dados, Angelos, Omirou, Michalis, Demetriou, Kyproula, Papastephanou, Chara, Ioannides, Ioannis M.

المصدر: Annals of Microbiology ; volume 65, issue 1, page 241-251 ; ISSN 1590-4261 1869-2044

الاتاحة: http://dx.doi.org/10.1007/s13213-014-0856-5
http://link.springer.com/content/pdf/10.1007/s13213-014-0856-5.pdf
http://link.springer.com/article/10.1007/s13213-014-0856-5/fulltext.html
http://link.springer.com/content/pdf/10.1007/s13213-014-0856-5

المؤلفون: Demetriou, Kyproula, Kapazoglou, Aliki, Tondelli, Alessandro, Francia, Enrico, Stanca, Michele A., Bladenopoulos, Konstantinos, Tsaftaris, Athanasios S.

المصدر: Physiologia Plantarum ; volume 136, issue 3, page 358-368 ; ISSN 0031-9317 1399-3054

الاتاحة: http://dx.doi.org/10.1111/j.1399-3054.2009.01236.x
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1399-3054.2009.01236.x
https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1399-3054.2009.01236.x

المؤلفون: Demetriou, Kyproula, Kapazoglou, Aliki, Bladenopoulos, Konstantinos, Tsaftaris, Athanasios S.

المصدر: Plant Molecular Biology Reporter ; volume 28, issue 1, page 9-21 ; ISSN 0735-9640 1572-9818

الاتاحة: http://dx.doi.org/10.1007/s11105-009-0121-4
http://link.springer.com/content/pdf/10.1007/s11105-009-0121-4.pdf
http://link.springer.com/article/10.1007/s11105-009-0121-4/fulltext.html
http://link.springer.com/content/pdf/10.1007/s11105-009-0121-4

المؤلفون: Liu, M., Shi, S., Senthilnathan, S., Yu, J., Wu, E., Bergmann, C., Zerres, K., Bogdanova, N., Coto, E., Constantinou-Deltas, Constantinos D., Pierides, Alkis M., Demetriou, Kyproula, Devuyst, O., Gitomer, B., Laakso, M., Lumiaho, A., Lamnissou, Klea, Magistroni, R., Parfrey, P., Breuning, M., Peters, D. J. M., Torra, R., Winearls, C. G., Torres, V. E., Harris, Peter C., Paterson, A. D., Pei, Y.

المساهمون: Constantinou-Deltas, Constantinos D. [0000-0001-5549-9169], UCL - SSS/IREC/NEFR - Pôle de Néphrologie, UCL - (SLuc) Service de néphrologie

المصدر: JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Journal of the American Society of Nephrology, 21(9), 1510-20
Università degli studi di Modena e Reggio Emilia-IRIS
Journal of the American Society of Nephrology
J.Am.Soc.Nephrol.
Journal of the American Society of Nephrology, Vol. 21, no.9, p. 1510-1520 (2010)

مصطلحات موضوعية: Oncology, Nephrology, Candidate gene, glomerulus filtration rate, genotype, kidney disease, urologic and male genital diseases, Cohort Studies, single nucleotide polymorphism, middle aged, genetic variability, kidney cyst, genetics, gene mutation, Genetics, adult, article, General Medicine, Middle Aged, cohort analysis, Polycystic Kidney, Autosomal Dominant, female genital diseases and pregnancy complications, Phenotype, priority journal, beta catenin, polycystin, Intercellular Signaling Peptides and Proteins, Chemokines, Adult, medicine.medical_specialty, TRPP Cation Channels, gene locus, Genotype, phenotype, Autosomal dominant polycystic kidney disease, Single-nucleotide polymorphism, Biology, DKK3 protein, human, Polymorphism, Single Nucleotide, Internal medicine, Genetic variation, medicine, Humans, signal peptide, Genetic variability, human, DKK3 gene, gene, Adaptor Proteins, Signal Transducing, ADPKD, PKD1, medicine.disease, major clinical study, Wnt protein, kidney failure, kidney polycystic disease, polycystic kidney disease 1 protein, Basic Research, adolescent, Mutation, mutation, Kidney disease

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c319706fa64dc401a77cd77ea5caeb7
https://hdl.handle.net/1887/119239

المؤلفون: Demetriou, Kyproula, Δημητρίου, Κυπρούλα

Relation: http://elocus.lib.uoc.gr:443/dlib/a/b/7/metadata-dlib-2005demetriou.tkl; 297414

الاتاحة: http://elocus.lib.uoc.gr:443/dlib/a/b/7/metadata-dlib-2005demetriou.tkl

المؤلفون: Lamnissou, Klea, Zirogiannis, P., Trygonis, S., Demetriou, Kyproula, Pierides, Alkis M., Koptides, Michael, Constantinou-Deltas, Constantinos D.

المساهمون: Constantinou-Deltas, Constantinos D. 0000-0001-5549-9169

المصدر: Genetic testing ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-9744227212&partnerID=40&md5=a4a84c8bc68f25b6d9eb42c7b2ddf9dc ; Genet.Test.

مصطلحات موضوعية: Cyprus, Greece, article, human, Humans, adult, aged, controlled study, female, major clinical study, Middle Aged, kidney polycystic disease, disease course, male, allele, genetic association, Caucasian, data analysis, diabetes mellitus, gene frequency, genotype, statistical analysis, genetic polymorphism, Genetic Predisposition to Disease, Fisher exact test, population research, disease association, cohort analysis, Alleles, Introns

Relation: http://gnosis.library.ucy.ac.cy/handle/7/53221

الاتاحة: http://gnosis.library.ucy.ac.cy/handle/7/53221

المؤلفون: Koptides, Michael, Mean, Richard, Stavrou, Christoforos, Pierides, Alkis, Demetriou, Kyproula, Nakayama, Tomohiro, Hildebrandt, Friedhelm, Fuchshuber, Arno, Constantinou-Deltas, Constantinos D.

المصدر: Molecular and Cellular Probes. - 15, 6 (2001) , 357-361, ISSN: 0890-8508

Relation: https://freidok.uni-freiburg.de/data/42289

الاتاحة: https://freidok.uni-freiburg.de/data/42289
https://doi.org/10.1006/mcpr.2001.0381

المؤلفون: Demetriou, Kyproula, H’Maltezou, Eleni, Pierides, Alkis M.

المصدر: Blood Purification ; volume 19, issue 3, page 308-313 ; ISSN 0253-5068 1421-9735

الاتاحة: http://dx.doi.org/10.1159/000046959
https://www.karger.com/Article/Pdf/46959

المؤلفون: Koptides, Michael, Mean, R., Demetriou, Kyproula, Constantinides, Rolandos, Pierides, Alkis M., Harris, Peter C., Constantinou-Deltas, Constantinos D.

المساهمون: Constantinou-Deltas, Constantinos D. 0000-0001-5549-9169

المصدر: Human mutation ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-0034243483&partnerID=40&md5=1c444722cc499aae3f2d5d5ee315eff9 ; Hum.Mutat.

مصطلحات موضوعية: article, human, Humans, aged, kidney polycystic disease, single nucleotide polymorphism, amino acid sequence, middle aged, molecular genetics, protein, Animals, Mice, animal, mouse, genetics, Molecular Sequence Data, sequence homology, Amino Acid, Proteins, pedigree, Polycystic Kidney, Autosomal Dominant, gene duplication, missense mutation, Mutation, Missense, polycystin, TRPP Cation Channels, polycystic kidney disease 1 protein, Polymorphism

Relation: http://gnosis.library.ucy.ac.cy/handle/7/53191

الاتاحة: http://gnosis.library.ucy.ac.cy/handle/7/53191

المؤلفون: Koptides, Michael, Mean, R., Demetriou, Kyproula, Pierides, Alkis M., Constantinou-Deltas, Constantinos D.

المساهمون: Constantinou-Deltas, Constantinos D. 0000-0001-5549-9169

المصدر: Human molecular genetics ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-0034639655&partnerID=40&md5=8b9944fef8d2b2c6be4604cd30600a7b ; Hum.Mol.Genet.

مصطلحات موضوعية: article, human, Humans, female, priority journal, clinical article, kidney polycystic disease, disease course, male, pathogenesis, Loss of Heterozygosity, phenotype, gene expression, Base Sequence, gene mutation, Molecular Sequence Data, Polymerase Chain Reaction, Membrane Proteins, DNA Mutational Analysis, Heterozygote, Proteins, Pedigree, Amino Acid Sequence, Polycystic Kidney, Autosomal Dominant, autosomal dominant inheritance, polycystin, Polymorphism, Single-Stranded Conformational, TRPP Cation Channels

Relation: http://gnosis.library.ucy.ac.cy/handle/7/53192

الاتاحة: http://gnosis.library.ucy.ac.cy/handle/7/53192

المؤلفون: Demetriou, Kyproula, Tziakouri, Chrysa H., Anninou, Kristiana, Eleftheriou, Andri, Koptides, Michael, Nicolaou, Alexia, Constantinou-Deltas, Constantinos D., Pierides, Alkis M.

المساهمون: Constantinou-Deltas, Constantinos D. 0000-0001-5549-9169

المصدر: Nephrology Dialysis Transplantation ; https://www.scopus.com/inward/record.uri?eid=2-s2.0-0033978150&partnerID=40&md5=19f52d380a22bf8dcd09e796a93b0b8b ; Nephrol.Dial.Transplant.

مصطلحات موضوعية: age, article, human, Humans, adult, female, major clinical study, Middle Aged, priority journal, Aging, pain, adolescent, kidney polycystic disease, male, hypertension, Child, ultrasound, False Positive Reactions, hematuria, cause of death, hemodialysis, DNA, gene mutation, preschool child, genetic analysis, urinary tract infection, school child, Ultrasonography, nephrolithiasis, DNA Mutational Analysis

Relation: http://gnosis.library.ucy.ac.cy/handle/7/53043

الاتاحة: http://gnosis.library.ucy.ac.cy/handle/7/53043

المؤلفون: Koptides, Michael, Mean, R., Stavrou, Christoforos V., Pierides, Alkis M., Demetriou, Kyproula, Nakayama, T., Hildebrandt, F., Fuchshuber, A., Constantinou-Deltas, Constantinos D.

المساهمون: Constantinou-Deltas, Constantinos D. [0000-0001-5549-9169]

المصدر: Molecular and cellular probes
Mol.Cell.Probes

مصطلحات موضوعية: Candidate gene, Cystic kidneys, arginine, Medullary cystic kidney disease, chromosome 1q, 3' Untranslated Regions, Genes, Dominant, Genetics, article, allele, blood pressure regulation, Polycystic Kidney, Autosomal Dominant, Stop codon, unclassified drug, priority journal, Hypertension, glutamine, 5' untranslated region, Hypotension, gene insertion, amino acid substitution, mutational analysis, marker gene, onset age, Adult, gene locus, Sequence analysis, DNA screening, Locus (genetics), gene sequence, Biology, Nephropathy, autosomal dominant disorder, atrial natriuretic factor receptor, medullary sponge kidney, medicine, stop codon, Humans, human, Allele, NPR1, Molecular Biology, Gene, atrial natriuretic factor receptor 1, Polymorphism, Genetic, gene deletion, human cell, DNA, salt losing nephritis, gene mapping, Cell Biology, Sequence Analysis, DNA, 3' untranslated region, medicine.disease, major clinical study, insertion sequences, kidney failure, gene function, MCKD1, DNA polymorphism, Guanylate Cyclase, Cyprus, sodium excretion, Polymorphisms, Receptors, Atrial Natriuretic Factor

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddf5d249a7a59a0b278f08918b110c14
https://pubmed.ncbi.nlm.nih.gov/11851379

المؤلفون: Bouba, I., Koptides, Michael, Mean, R., Costi, Constantina Eleni, Demetriou, Kyproula, Georgiou, Ioannis A., Pierides, Alkis M., Siamopoulos, K., Constantinou-Deltas, Constantinos D.

المساهمون: Constantinou-Deltas, Constantinos D. [0000-0001-5549-9169]

المصدر: European Journal of Human Genetics
Eur.J.Hum.Genet.

مصطلحات موضوعية: Male, glycoprotein, family, gene amplification, polymerase chain reaction, DNA Mutational Analysis, PKD1, Variation (Genetics), genetic analysis, medicine.disease_cause, genetic heterogeneity, Cohort Studies, Exon, Polycystic kidney disease, Missense mutation, membrane protein, exon, gene mutation, Proteins/*genetics, Genetics (clinical), Polymorphism, Single-Stranded Conformational, Sequence Deletion, Genetics, Mutation, disease course, mother, article, protein domain, cohort analysis, Polycystic Kidney, Autosomal Dominant, symptom, chromosome 16p, Stop codon, Polycystic Kidney, Autosomal Dominant/*genetics, unclassified drug, Pedigree, genetic code, female, priority journal, polycystin, Female, Mutations, mutagenesis, amino acid substitution, TRPP Cation Channels, single strand conformation polymorphism, prevalence, Mutation, Missense, Biology, Caucasian, Renal disease, male, Sequence Homology, Nucleic Acid, medicine, Humans, controlled study, Amino Acid Sequence, human, liquid, Polymorphism, Gene, Family Health, Polymorphism, Genetic, polycystin 1, Base Sequence, Sequence Homology, Amino Acid, End-stage renal failure, Genetic heterogeneity, gene deletion, screening, missense mutation, gene duplication, Genetic Variation, Proteins, DNA, medicine.disease, major clinical study, amino acid sequence, kidney failure, autosomal dominant inheritance, kidney polycystic disease, DNA/chemistry/genetics, age, DNA polymorphism, measurement, codon

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f8bdc22a0d4b58ec39152bf626c8f39
http://gnosis.library.ucy.ac.cy/handle/7/52957

المؤلفون: UCL - SSS/IREC/NEFR - Pôle de Néphrologie, UCL - (SLuc) Service de néphrologie, Liu, Michelle, Shi, Sally, Senthilnathan, Sean, Yu, Julie, Wu, Elliot, Bergmann, Carsten, Zerres, Klaus, Bogdanova, Nadja, Coto, Eliecer, Deltas, Constantinos, Pierides, Alkis, Demetriou, Kyproula, Devuyst, Olivier, Gitomer, Berenice, Laakso, Marku, Lumiaho, Anne, Lamnissou, Klea, Magistroni, Riccardo, Parfrey, Patrick, Breuning, Martijn, Peters, Dorien J M, Torra, Roser, Winearls, Christopher G, Torres, Vicente E, Harris, Peter C, Paterson, Andrew D, Pei, York

المصدر: Journal of the American Society of Nephrology, Vol. 21, no.9, p. 1510-1520 (2010)

مصطلحات الفهرس: Adult, Polymorphism, Single Nucleotide, TRPP Cation Channels, Cohort Studies, Genotype, Humans, Intercellular Signaling Peptides and Proteins, Middle Aged, Mutation, Phenotype, Polycystic Kidney, Autosomal Dominant, info:eu-repo/semantics/article

URL: http://hdl.handle.net/2078.1/123145