نتائج البحث - Katriina Aalto‐Setälä
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Finnish type of low density lipoprotein receptor gene mutation (FH-Helsinki) deletes exons encoding the carboxy-terminal part of the receptor and creates an internalization-defecti... حسب Katriina Aalto‐Setälä, Eero Helve, Petri T. Kovanen, Kimmo Kontula
منشور في 1989Artigo -
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Apolipoprotein E polymorphism determined by restriction enzyme analysis of DNA amplified by polymerase chain reaction: convenient alternative to phenotyping by isoelectric focusing حسب Kimmo Kontula, Katriina Aalto‐Setälä, T Kuusi, Lasse Hämäläinen, A C Syvänen
منشور في 1990Artigo -
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Video image-based analysis of single human induced pluripotent stem cell derived cardiomyocyte beating dynamics using digital image correlation حسب Antti Ahola, Anna Kiviaho, Kim Larsson, Markus Honkanen, Katriina Aalto‐Setälä, Jari Hyttinen
منشور في 2014Artigo -
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Primary structure of human insulin‐like growth factor‐binding protein/placental protein 12 and tissue‐specific expression of its mRNA حسب Mervi Julkunen, Riitta Koistinen, Katriina Aalto‐Setälä, Markku Seppälä, Olli A. Jänne, Kimmo Kontula
منشور في 1988Artigo -
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Antiarrhythmic Effects of Dantrolene in Patients with Catecholaminergic Polymorphic Ventricular Tachycardia and Replication of the Responses Using iPSC Models حسب Kirsi Penttinen, Heikki Swan, Sari Vanninen, Jere Paavola, Annukka M. Lahtinen, Kimmo Kontula, Katriina Aalto‐Setälä
منشور في 2015Artigo -
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Automatic Optimization of an in Silico Model of Human iPSC Derived Cardiomyocytes Recapitulating Calcium Handling Abnormalities حسب Michelangelo Paci, Risto-Pekka Pölönen, Dario Cori, Kirsi Penttinen, Katriina Aalto‐Setälä, Stefano Severi, Jari Hyttinen
منشور في 2018Artigo -
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Mutation‐Specific Phenotypes in hiPSC‐Derived Cardiomyocytes Carrying Either Myosin‐Binding Protein C Or <i>α</i>‐Tropomyosin Mutation for Hypertrophic Cardiomyopathy حسب Marisa Ojala, Chandra Prajapati, Risto-Pekka Pölönen, Kristiina Rajala, Mari Pekkanen-Mattila, Jyrki Rasku, Kim Larsson, Katriina Aalto‐Setälä
منشور في 2015Artigo -
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The familial hypercholesterolemia (FH)-North Karelia mutation of the low density lipoprotein receptor gene deletes seven nucleotides of exon 6 and is a common cause of FH in Finlan... حسب Ulla‐Maija Koivisto, Hannu Turtola, Katriina Aalto‐Setälä, Bert Top, Rune R. Frants, Petri T. Kovanen, A C Syvänen, Kimmo Kontula
منشور في 1992Artigo -
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Compromised Barrier Function in Human Induced Pluripotent Stem-Cell-Derived Retinal Pigment Epithelial Cells from Type 2 Diabetic Patients حسب Mostafa Kiamehr, Alexa Klettner, Elisabeth Richert, Ali Koskela, Arto Koistinen, Heli Skottman, Kai Kaarniranta, Katriina Aalto‐Setälä, Kati Juuti‐Uusitalo
منشور في 2019Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Gene
Medicine
Genetics
Internal medicine
Embryonic stem cell
Induced pluripotent stem cell
Biochemistry
Endocrinology
Cell biology
Chemistry
Cholesterol
Computer science
Cardiology
Molecular biology
Neuroscience
Artificial intelligence
Calcium
Electrophysiology
Lipoprotein
Myocyte
Apolipoprotein B
Disease
Genotype
Receptor
Regenerative medicine
Repolarization
Stem cell
Triglyceride
Afterdepolarization