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BMC Cancer
|
June 27, 2019
Intertumoral heterogeneity in patient-specific drug sensitivities in treatment-naïve glioblastoma
Erlend Skaga, Evgeny Kulesskiy, Artem Fayzullin, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
November 14, 2018
Associations of increased physical performance and change in body composition with molecular pathways of heart disease and diabetes risk
Johannes Kettunen, Anni Joensuu, Maria Hagnäs, et al.
BJOG : an International Journal of Obstetrics and Gynaecology
|
May 8, 2023
Identification of complement factor H variants that predispose to pre-eclampsia: A genetic and functional study
A Inkeri Lokki, Zhen Ren, Michael Triebwasser, et al.
Brain : a Journal of Neurology
|
August 1, 2025
Alzheimer and cardiovascular genetic scores and cognition: the FINGER randomized controlled trial
Gazi Saadmaan, Maria Carolina Dalmasso, Maleeha Maria, et al.
Plos Genetics
|
May 6, 2020
Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucoma
Yosuke Tanigawa, Michael Wainberg, Juha Karjalainen, et al.
Circulation. Cardiovascular Genetics
|
December 8, 2017
Genetic Variants Contributing to Circulating Matrix Metalloproteinase 8 Levels and Their Association With Cardiovascular Diseases: A Genome-Wide Analysis
Aino Salminen, Efthymia Vlachopoulou, Aki S Havulinna, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 13, 2009
Association of variation in the interleukin-1 gene family with diabetes and glucose homeostasis
Kari Luotola, Rauni Pääkkönen, Mervi Alanne, et al.
European Journal of Medical Genetics
|
July 22, 2018
Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant
Valtter B Virtanen, Perttu P Salo, Jia Cao, et al.
Atherosclerosis
|
September 3, 2002
Coronary artery calcification is related to functional polymorphism of matrix metalloproteinase 3: the Helsinki Sudden Death Study
Perttu J Pöllänen, Terho Lehtimäki, Erkki Ilveskoski, et al.
Nature Human Behaviour
|
April 20, 2023
Nationwide health, socio-economic and genetic predictors of COVID-19 vaccination status in Finland
Tuomo Hartonen, Bradley Jermy, Hanna Sõnajalg, et al.
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of 40
Search research articles
Search
Showing results (151-160 of 398) with videos related to
Sort By:
Page
of 40
BMC Cancer
|
June 27, 2019
Intertumoral heterogeneity in patient-specific drug sensitivities in treatment-naïve glioblastoma
Erlend Skaga, Evgeny Kulesskiy, Artem Fayzullin, et al.
American Journal of Physiology. Endocrinology and Metabolism
|
November 14, 2018
Associations of increased physical performance and change in body composition with molecular pathways of heart disease and diabetes risk
Johannes Kettunen, Anni Joensuu, Maria Hagnäs, et al.
BJOG : an International Journal of Obstetrics and Gynaecology
|
May 8, 2023
Identification of complement factor H variants that predispose to pre-eclampsia: A genetic and functional study
A Inkeri Lokki, Zhen Ren, Michael Triebwasser, et al.
Brain : a Journal of Neurology
|
August 1, 2025
Alzheimer and cardiovascular genetic scores and cognition: the FINGER randomized controlled trial
Gazi Saadmaan, Maria Carolina Dalmasso, Maleeha Maria, et al.
Plos Genetics
|
May 6, 2020
Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucoma
Yosuke Tanigawa, Michael Wainberg, Juha Karjalainen, et al.
Circulation. Cardiovascular Genetics
|
December 8, 2017
Genetic Variants Contributing to Circulating Matrix Metalloproteinase 8 Levels and Their Association With Cardiovascular Diseases: A Genome-Wide Analysis
Aino Salminen, Efthymia Vlachopoulou, Aki S Havulinna, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 13, 2009
Association of variation in the interleukin-1 gene family with diabetes and glucose homeostasis
Kari Luotola, Rauni Pääkkönen, Mervi Alanne, et al.
European Journal of Medical Genetics
|
July 22, 2018
Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant
Valtter B Virtanen, Perttu P Salo, Jia Cao, et al.
Atherosclerosis
|
September 3, 2002
Coronary artery calcification is related to functional polymorphism of matrix metalloproteinase 3: the Helsinki Sudden Death Study
Perttu J Pöllänen, Terho Lehtimäki, Erkki Ilveskoski, et al.
Nature Human Behaviour
|
April 20, 2023
Nationwide health, socio-economic and genetic predictors of COVID-19 vaccination status in Finland
Tuomo Hartonen, Bradley Jermy, Hanna Sõnajalg, et al.
Page
of 40