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Issue Date	Title	Author(s)
Jul-2017	Genetic variation spectrum in ATP7B gene identified in Latvian patients with Wilson disease	Zarina, 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
29-Oct-2010	Population screening for hereditary and familial cancer syndromes in Valka district of Latvia	Vanags, Andrejs; Štrumfa, Ilze; Gardovskis, Andris; Borošenko, Viktors; Aboliņš, Arnis; Teibe, Uldis; Trofimovičs, Genadijs; Miklaševičs, Edvins; Gardovskis, Janis; Hereditary Cancer Research Department
27-Oct-2011	Genotype-phenotype correlations among BRCA1 4153delA and 5382insC mutation carriers from Latvia	Plakhins, 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
15-Mar-2006	Pilot study on low penetrance breast and colorectal cancer predisposition markers in Latvia	Irmejs, Arvids; Miklasevics, Edvins; Boroschenko, Viktors; Gardovskis, Andris; Vanags, Andrejs; Melbarde-Gorkusa, Inga; Bitina, Marianna; Suchy, Janina; Gardovskis, Janis; Hereditary Cancer Research Department
14-Jun-2013	BRCA1/2 mutation screening in high-risk breast/ovarian cancer families and sporadic cancer patient surveilling for hidden high-risk families	Berzina, Dace; Nakazawa-Miklasevica, Miki; Zestkova, Jekaterina; Aksenoka, Karina; Irmejs, Arvids; Gardovskis, Andris; Kalniete, Dagnija; Gardovskis, Janis; Miklasevics, Edvins; RSU Institute of Oncology
15-Jun-2008	Comment on the article Genetic contribution to all cancers : The first demonstration using the model of breast cancers from Poland stratified by age at diagnosis and tumour pathology by Lubinski et al., Breast Cancer Res Treat 2008 Apr 15	Irmejs, Arvids; Miklaševics, Edvins; Štrumfa, Ilze; Gardovskis, Janis; Hereditary Cancer Research Department
Jan-2022	Transient expression of inactive RB in mesenchymal stem cells impairs their adipogenic potential and is associated with hypermethylation of the PPARγ2 promoter	Baryshev, Mikhail; Petrov, Nikolai; Ryabov, Vladimir; Popov, Boris; Institute of Microbiology and Virology
14-Apr-2012	Challenges in the management of a patient with Cowden syndrome : Case report and literature review	Melbarde-Gorkuša, Inga; Irmejs, Arvids; Berziņa, Dace; Štrumfa, Ilze; Aboliņš, Arnis; Gardovskis, Andris; Subatniece, Signe; Trofimovičs, Genadijs; Gardovskis, Janis; Miklaševičs, Edvins; Hereditary Cancer Research Department
13-Aug-2019	Meta-analysis of cancer triploidy : Rearrangements of genome complements in male human tumors are characterized by XXY karyotypes	Vainshelbaum, Ninel M.; Zayakin, Pawel; Kleina, Regina; Giuliani, Alessandro; Erenpreisa, Jekaterina; Department of Pathology
18-Sep-2014	Rare diseases and orphan drugs : Latvian story	Logviss, Konstantins; Krievins, Dainis; Purvina, Santa; Department of Internal Diseases

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