Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Dagnija Kalniete"'
Autor:
Dagnija Kalniete
Promocijas darbs izstrādāts: RSU, Onkoloģijas institūtā. Aizstāvēsana: 2015. gada 12. oktobrī plkst. 15.00 Rīgas Stradiņa universitātes Medicīnas promocijas padomes atklātā sēdē Rīgā, Dzirciema ielā 16, Hipokrāta auditorijā.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7215123b850741a241a98ab78f8c0909
https://doi.org/10.25143/prom-rsu_2015-16_pdk
https://doi.org/10.25143/prom-rsu_2015-16_pdk
Autor:
Dagnija Kalniete, Miki Nakazawa‑Miklasevica, Gunta Purkalne, Elina Skuja, Edvins Miklasevics, Zanda Daneberga, Arnis Abolins
Publikováno v:
Molecular and Clinical Oncology
Metastatic dissemination of the primary tumor is the major cause of death in colorectal cancer (CRC) patients. Multiple chromosomal breaks and chromothripsis, a phenomenon involving multiple chromosomal fragmentations occurring in a single catastroph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9de77f704208b3e297bde575a61e6cb
https://doi.org/10.3892/mco.2017.1123
https://doi.org/10.3892/mco.2017.1123
Autor:
E. Vjaters, J. Plonis, Dagnija Kalniete, Janis Gardovskis, Edvins Miklasevics, Miki Nakazawa-Miklasevica, Arvids Irmejs
Publikováno v:
Balkan Journal of Medical Genetics, Vol 18, Iss 2, Pp 33-36 (2015)
Our objective was to determine: 1) whether the checkpoint kinase 2 (CHEK2) del5395 (g.27417113-27422508 del, NC_000022.11) is a founder mutation in the Latvian population, 2) if there is an association between CHEK2 del5395 mutation and cancer risk,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::268a8fe5615a98cbf2cdef4cb16340db
https://doi.org/10.1515/bjmg-2015-0083
https://doi.org/10.1515/bjmg-2015-0083
Autor:
Edvins Miklasevics, Mikko Kupila, Dagnija Kalniete, Inese Eglite, Dace Berzina, Monta Ustinova, Gunta Purkalne, Zanda Daneberga
Publikováno v:
Acta Chirurgica Latviensis. 15:8-11
Summary Introduction. Lynch syndrome, previously more commonly known as hereditary nonpolyposis colorectal cancer, is a hereditary cancer syndrome with an autosomal dominant inheritance pattern. Usually it is caused by mutations the MMR genes. In 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0928f4bb2d9d058c7f666a7db5536739
https://doi.org/10.1515/chilat-2016-0002
https://doi.org/10.1515/chilat-2016-0002
Autor:
Zanda Daneberga, Elza Broka, Dagnija Kalniete, Miki Nakazawa-Miklasevica, Monta Ustinova, Elina Skuja, Gunta Purkalne, Edvins Miklasevics
Publikováno v:
Acta Chirurgica Latviensis. 15:3-7
Summary Introduction. Colorectal cancer (CRC) is the third most common cancer worldwide. Evaluation of patient response to the applied therapy regime is still challenging. Routine laboratory tests during follow-up do not provide necessary information
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ba5ba52359b772396b7815652716b49
https://doi.org/10.1515/chilat-2016-0001
https://doi.org/10.1515/chilat-2016-0001
Autor:
Dagnija Kalniete, Elina Skuja, Elza Broka, Gunta Purkalne, Edvins Miklasevics, Miki Nakazawa-Miklasevica, Zanda Daneberga, Monta Ustinova
Publikováno v:
Acta Chirurgica Latviensis. 14:3-7
Summary Introduction. Anaemia is a clinically important and increasingly frequent finding in cardiac surgery. Whether preoperative anaemia is an independent risk factor for adverse outcomes after elective cardiac surgery is still under discussion. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4998f4fcf2e0dc8b11da9d2b05decc52
https://doi.org/10.1515/chilat-2015-0001
https://doi.org/10.1515/chilat-2015-0001
Autor:
Edvins Miklasevics, Miki Nakazawa-Miklasevica, Arvids Irmejs, Arnis Abolins, Ilze Strumfa, Dagnija Kalniete, Janis Gardovskis, Genadijs Trofimovics
Publikováno v:
Acta Chirurgica Latviensis. 13:7-12
Summary Introduction. MicroRNAs are a class of small, non-coding RNA molecules able to regulate gene expression at the post-transcriptional level through binding to the 3’-UTR of the targeted mRNA, thus suppressing translation of the mRNA. In vario
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b76c2abc6939c419cfa91e3d128b6ba
https://doi.org/10.2478/chilat-2013-0002
https://doi.org/10.2478/chilat-2013-0002
Autor:
Zanda Daneberga, Dagnija Kalniete, Miki Nakazawa-Miklasevica, Elīna Skuja, Edvins Miklasevics, Arnis Abolins, Gunta Purkalne
Publikováno v:
European Journal of Cancer. 69:S120-S121
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7942f66390017c697be0b2847a6de888
https://doi.org/10.1016/s0959-8049(16)32959-8
https://doi.org/10.1016/s0959-8049(16)32959-8
Autor:
K. Aksenoka, P. Vaganovs, Miki Nakazawa-Miklasevica, Edvins Miklasevics, J. Plonis, A. Irmejs, Janis Gardovskis, K. Miculis, S. Pildava, Dagnija Kalniete, A. Malevskis, E. Vjaters
Publikováno v:
European Urology Supplements. 14:e1125
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64f7a78ac751c7350e2053bd14bb3ffc
https://doi.org/10.1016/s1569-9056(15)30028-2
https://doi.org/10.1016/s1569-9056(15)30028-2
Autor:
Dagnija Kalniete, Jekaterina Zestkova, Arvids Irmejs, Janis Gardovskis, Karina Aksenoka, Andris Gardovskis, Dace Berzina, Miki Nakazawa-Miklasevica, Edvins Miklasevics
Publikováno v:
BMC Medical Genetics
Background The estimated ratio of hereditary breast/ovarian cancer (HBOC) based on family history is 1.5% in Latvia. This is significantly lower than the European average of 5–10%. Molecular markers like mutations and SNPs can help distinguish HBOC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68b0de2e896a1e1980c707779014db02