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Emil Ylikallio

Showing results (21-30 of 43) with videos related to

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Plos One|July 11, 2013
The overexpression of Twinkle helicase ameliorates the progression of cardiac fibrosis and heart failure in pressure overload model in miceAtsushi Tanaka, Tomomi Ide, Takeo Fujino, et al.
Journal of Community Genetics|April 6, 2020
Attitudes towards genetic testing and information: does parenthood shape the views?Antti Saastamoinen, Virva Hyttinen, Mika Kortelainen, et al.
Neurology. Genetics|April 12, 2016
PFKM gene defect and glycogen storage disease GSDVII with misleading enzyme histochemistryMari Auranen, Johanna Palmio, Emil Ylikallio, et al.
FEBS Open Bio|May 5, 2022
Structural insights into Charcot-Marie-Tooth disease-linked mutations in human GDAP1Aleksi Sutinen, Giang Thi Tuyet Nguyen, Arne Raasakka, et al.
Frontiers in Neurology|June 16, 2016
Unique Exercise Lactate Profile in Muscle Phosphofructokinase Deficiency (Tarui Disease); Difference Compared with McArdle DiseasePäivi Piirilä, Minna E Similä, Johanna Palmio, et al.
Frontiers in Neurology|March 7, 2022
Serum Creatine, Not Neurofilament Light, Is Elevated in CHCHD10-Linked Spinal Muscular AtrophyJulius Järvilehto, Sandra Harjuhaahto, Edouard Palu, et al.
Plos Genetics|January 13, 2025
IP3 receptor depletion in a spontaneous canine model of Charcot-Marie-Tooth disease 1J with amelogenesis imperfectaMarjo K Hytönen, Julius Rönkkö, Sruthi Hundi, et al.
Cell Calcium|July 23, 2023
Human IP<sub>3</sub> receptor triple knockout stem cells remain pluripotent despite altered mitochondrial metabolismJulius Rönkkö, Yago Rodriguez, Tiina Rasila, et al.
Journal of Neuromuscular Diseases|December 3, 2016
Decreased Aerobic Capacity in ANO5-Muscular DystrophyEmil Ylikallio, Mari Auranen, Ibrahim Mahjneh, et al.
Neurobiology of Disease|May 22, 2020
ALS and Parkinson's disease genes CHCHD10 and CHCHD2 modify synaptic transcriptomes in human iPSC-derived motor neuronsSandra Harjuhaahto, Tiina S Rasila, Svetlana M Molchanova, et al.
Pageof 5

Showing results (21-30 of 43) with videos related to

Sort By:
Pageof 5
Plos One|July 11, 2013
The overexpression of Twinkle helicase ameliorates the progression of cardiac fibrosis and heart failure in pressure overload model in miceAtsushi Tanaka, Tomomi Ide, Takeo Fujino, et al.
Journal of Community Genetics|April 6, 2020
Attitudes towards genetic testing and information: does parenthood shape the views?Antti Saastamoinen, Virva Hyttinen, Mika Kortelainen, et al.
Neurology. Genetics|April 12, 2016
PFKM gene defect and glycogen storage disease GSDVII with misleading enzyme histochemistryMari Auranen, Johanna Palmio, Emil Ylikallio, et al.
FEBS Open Bio|May 5, 2022
Structural insights into Charcot-Marie-Tooth disease-linked mutations in human GDAP1Aleksi Sutinen, Giang Thi Tuyet Nguyen, Arne Raasakka, et al.
Frontiers in Neurology|June 16, 2016
Unique Exercise Lactate Profile in Muscle Phosphofructokinase Deficiency (Tarui Disease); Difference Compared with McArdle DiseasePäivi Piirilä, Minna E Similä, Johanna Palmio, et al.
Frontiers in Neurology|March 7, 2022
Serum Creatine, Not Neurofilament Light, Is Elevated in CHCHD10-Linked Spinal Muscular AtrophyJulius Järvilehto, Sandra Harjuhaahto, Edouard Palu, et al.
Plos Genetics|January 13, 2025
IP3 receptor depletion in a spontaneous canine model of Charcot-Marie-Tooth disease 1J with amelogenesis imperfectaMarjo K Hytönen, Julius Rönkkö, Sruthi Hundi, et al.
Cell Calcium|July 23, 2023
Human IP<sub>3</sub> receptor triple knockout stem cells remain pluripotent despite altered mitochondrial metabolismJulius Rönkkö, Yago Rodriguez, Tiina Rasila, et al.
Journal of Neuromuscular Diseases|December 3, 2016
Decreased Aerobic Capacity in ANO5-Muscular DystrophyEmil Ylikallio, Mari Auranen, Ibrahim Mahjneh, et al.
Neurobiology of Disease|May 22, 2020
ALS and Parkinson's disease genes CHCHD10 and CHCHD2 modify synaptic transcriptomes in human iPSC-derived motor neuronsSandra Harjuhaahto, Tiina S Rasila, Svetlana M Molchanova, et al.
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