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Issue DateTitleAuthor(s)
Feb-2021The postmedieval Latvian oral microbiome in the context of modern dental calculus and modern dental plaque microbial profilesKazarina, Alisa; Petersone‐Gordina, Elina; Kimsis, Janis; Kuzmicka, Jevgenija; Zayakin, Pawel; Griškjans, Žans; Gerhards, Guntis; Ranka, Renate; Rīga Stradiņš University
24-Feb-2022Monogenic Versus Multifactorial Inheritance in the Development of Isolated Cleft Palate : A Whole Genome Sequencing StudyLace, Baiba; Pajusalu, Sander; Livcane, Diana; Grīnfelde, Ieva; Akota, Ilze; Mauliņa, Ieva; Barkāne, Biruta; Stavusis, Janis; Inashkina, Inna; Rīga Stradiņš University
Oct-2002Germline MSH2 and MLH1 mutational spectrum in HNPCC families from Poland and the Baltic States.Kurzawski, G.; Suchy, J.; Kladny, J.; Safranow, K.; Jakubowska, A.; Elsakov, P.; Kucinskas, V.; Gardovskis, Jānis; Irmejs, A.; Sibul, H.; Huzarski, T.; Byrski, T.; Debniak, T.; Cybulski, C.; Gronwald, J.; Oszurek, O.; Clark, J.; Goźdź, S.; Niepsuj, S.; Slomski, R.; Plawski, A.; Lacka-Wojciechowska, A.; Rozmiarek, A.; Fiszer-Maliszewska, L.; Bebenek, M.; Sorokin, D.; Stawicka, M.; Godlewski, D.; Richter, P.; Brozek, I.; Wysocka, B.; Jawień, A.; Banaszkiewicz, Z.; Kowalczyk, J.; Czudowska, D.; Goretzki, P. E.; Moeslein, G.; Lubinski, J.; Department of Surgery
1-Jan-2019The cancer aneuploidy paradox : In the light of evolutionSalmina, Kristine; Huna, Anda; Kalejs, Martins; Pjanova, Dace; Scherthan, Harry; Cragg, Mark S.; Erenpreisa, Jekaterina; Scientific Laboratory of Biomechanics
21-Dec-2019Association of variants in the CP, ATOX1 and COMMD1 genes with Wilson disease symptoms in LatviaZarina, A.; Tolmane, I.; Krumina, Z.; Tutane, A. I.; Gailite, L.; Scientific Laboratory of Molecular Genetics; Department of Biology and Microbiology
Jul-2017Genetic variation spectrum in ATP7B gene identified in Latvian patients with Wilson diseaseZarina, Agnese; Tolmane, Ieva; Kreile, Madara; Chernushenko, Aleksandrs; Cernevska, Gunta; Pukite, Ieva; Micule, Ieva; Krumina, Zita; Krumina, Astrida; Rozentale, Baiba; Piekuse, Linda; Scientific Laboratory of Molecular Genetics
27-Oct-2011Genotype-phenotype correlations among BRCA1 4153delA and 5382insC mutation carriers from LatviaPlakhins, Grigorijs; Irmejs, Arvids; Gardovskis, Andris; Subatniece, Signe; Rozite, Santa; Bitina, Marianna; Keire, Guntars; Purkalne, Gunta; Teibe, Uldis; Trofimovics, Genadijs; Miklasevics, Edvins; Gardovskis, Janis; Hereditary Cancer Research Department
14-Jun-2013BRCA1/2 mutation screening in high-risk breast/ovarian cancer families and sporadic cancer patient surveilling for hidden high-risk familiesBerzina, Dace; Nakazawa-Miklasevica, Miki; Zestkova, Jekaterina; Aksenoka, Karina; Irmejs, Arvids; Gardovskis, Andris; Kalniete, Dagnija; Gardovskis, Janis; Miklasevics, Edvins; RSU Institute of Oncology
13-Aug-2019Meta-analysis of cancer triploidy : Rearrangements of genome complements in male human tumors are characterized by XXY karyotypesVainshelbaum, Ninel M.; Zayakin, Pawel; Kleina, Regina; Giuliani, Alessandro; Erenpreisa, Jekaterina; Department of Pathology
Apr-2004The Western and Eastern Roots of the Saami - The Story of Genetic "Outliers" Told by Mitochondrial DNA and Y ChromosomesTambets, Kristiina; Rootsi, Siiri; Kivisild, Toomas; Help, Hela; Serk, Piia; Loogväli, Eva Liis; Tolk, Helle Viivi; Reidla, Maere; Metspalu, Ene; Pliss, Liana; Balanovsky, Oleg; Pshenichnov, Andrey; Balanovska, Elena; Gubina, Marina; Zhadanov, Sergey; Osipova, Ludmila; Damba, Larisa; Voevoda, Mikhail; Kutuev, Ildus; Bermisheva, Marina; Khusnutdinova, Elza; Gusar, Vladislava; Grechanina, Elena; Parik, Jüri; Pennarun, Erwan; Richard, Christelle; Chaventre, Andre; Moisan, Jean Paul; Barać, Lovorka; Peričić, Marijana; Rudan, Pavao; Terzić, Rifat; Mikerezi, Ilia; Krumina, Astrida; Baumanis, Viesturs; Koziel, Slawomir; Rickards, Olga; De Stefano, Gian Franco; Anagnou, Nicholas; Pappa, Kalliopi I.; Michalodimitrakis, Emmanuel; Ferák, Vladimir; Füredi, Sandor; Komel, Radovan; Beckman, Lars; Villems, Richard

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