Результати пошуку - Rots, Dmitrijs
- Показ 1 - 10 результатів із 10
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Analysis of possible genetic risk factors contributing to development of childhood acute lymphoblastic leukaemia in the Latvian population за авторством Kreile, Madara, Piekuse, Linda, Rots, Dmitrijs, Dobele, Zane, Kovalova, Zhanna, Lace, Baiba
Опубліковано 2016Текст -
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Genetic landscape of preterm birth due to cervical insufficiency: Comprehensive gene analysis and patient next-generation sequencing data interpretation за авторством Volozonoka, Ludmila, Rots, Dmitrijs, Kempa, Inga, Kornete, Anna, Rezeberga, Dace, Gailite, Linda, Miskova, Anna
Опубліковано 2020Текст -
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A Higher Polygenic Risk Score Is Associated with a Higher Recurrence Rate of Atrial Fibrillation in Direct Current Cardioversion-Treated Patients за авторством Vogel, Simon, Rudaka, Irina, Rots, Dmitrijs, Isakova, Jekaterīna, Kalējs, Oskars, Vīksne, Kristīne, Gailīte, Linda
Опубліковано 2021Текст -
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Association of ARID5B Genetic Variants with Risk of Childhood B Cell Precursor Acute Lymphoblastic Leukaemia in Latvia за авторством Kreile, Madara, Rots, Dmitrijs, Zarina, Agnese, Rautiainen, Linda, Visnevska-Preciniece, Zelma, Kovalova, Zhanna, Gailite, Linda
Опубліковано 2018Текст -
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UGT1A1 Variants c.864+5G>T and c.996+2_996+5del of a Crigler-Najjar Patient Induce Aberrant Splicing in Minigene Assays за авторством Gailite, Linda, Valenzuela-Palomo, Alberto, Sanoguera-Miralles, Lara, Rots, Dmitrijs, Kreile, Madara, Velasco, Eladio A.
Опубліковано 2020Текст -
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Novel Variant of the Androgen Receptor Gene in a Patient With Complete Androgen Insensitivity Syndrome and Polyorchidism за авторством Konrade, Ilze, Zavorikina, Julija, Fridvalde, Aija, Rots, Dmitrijs, Kalere, Ieva, Strumfa, Ilze, Dambrova, Maija, Gailite, Linda
Опубліковано 2019Текст -
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Clinical Phenotyping and Biomarkers in Spinal and Bulbar Muscular Atrophy за авторством Millere, Elina, Rots, Dmitrijs, Glazere, Ieva, Taurina, Gita, Kurjane, Natalja, Priedite, Viktorija, Gailite, Linda, Blennow, Kaj, Zetterberg, Henrik, Kenina, Viktorija
Опубліковано 2021Текст -
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Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature за авторством Rots, Dmitrijs, Chater-Diehl, Eric, Dingemans, Alexander J.M., Goodman, Sarah J., Siu, Michelle T., Cytrynbaum, Cheryl, Choufani, Sanaa, Hoang, Ny, Walker, Susan, Awamleh, Zain, Charkow, Joshua, Meyn, Stephen, Pfundt, Rolph, Rinne, Tuula, Gardeitchik, Thatjana, de Vries, Bert B.A., Deden, A. Chantal, Leenders, Erika, Kwint, Michael, Stumpel, Constance T.R.M., Stevens, Servi J.C., Vermeulen, Jeroen R., van Harssel, Jeske V.T., Bosch, Danielle G.M., van Gassen, Koen L.I., van Binsbergen, Ellen, de Geus, Christa M., Brackel, Hein, Hempel, Maja, Lessel, Davor, Denecke, Jonas, Slavotinek, Anne, Strober, Jonathan, Crunk, Amy, Folk, Leandra, Wentzensen, Ingrid M., Yang, Hui, Zou, Fanggeng, Millan, Francisca, Person, Richard, Xie, Yili, Liu, Shuxi, Ousager, Lilian B., Larsen, Martin, Schultz-Rogers, Laura, Morava, Eva, Klee, Eric W., Berry, Ian R., Campbell, Jennifer, Lindstrom, Kristin, Pruniski, Brianna, Neumeyer, Ann M., Radley, Jessica A., Phornphutkul, Chanika, Schmidt, Berkley, Wilson, William G., Õunap, Katrin, Reinson, Karit, Pajusalu, Sander, van Haeringen, Arie, Ruivenkamp, Claudia, Cuperus, Roos, Santos-Simarro, Fernando, Palomares-Bralo, María, Pacio-Míguez, Marta, Ritter, Alyssa, Bhoj, Elizabeth, Tønne, Elin, Tveten, Kristian, Cappuccio, Gerarda, Brunetti-Pierri, Nicola, Rowe, Leah, Bunn, Jason, Saenz, Margarita, Platzer, Konrad, Mertens, Mareike, Caluseriu, Oana, Nowaczyk, Małgorzata J.M., Cohn, Ronald D., Kannu, Peter, Alkhunaizi, Ebba, Chitayat, David, Scherer, Stephen W., Brunner, Han G., Vissers, Lisenka E.L.M., Kleefstra, Tjitske, Koolen, David A., Weksberg, Rosanna
Опубліковано 2021Текст