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Frontiers in Endocrinology
|
July 17, 2023
Investigating the role of ASCC1 in the causation of bone fragility
Barbara Voraberger, Johannes A Mayr, Nadja Fratzl-Zelman, et al.
Journal of Hepatology
|
May 7, 2016
Severe respiratory complex III defect prevents liver adaptation to prolonged fasting
Laura S Kremer, Caroline L'hermitte-Stead, Pierre Lesimple, et al.
Nature Communications
|
December 18, 2025
Single cell spatial transcriptomics integration deciphers the morphological heterogeneity of atherosclerotic carotid arteries
Jessica Pauli, Daniel Garger, Fatemeh Peymani, et al.
Annals of Clinical and Translational Neurology
|
October 1, 2025
The Diverse Neuromuscular Spectrum of VPS13A Disease
Anne Buchberger, Evamaria Riedel, Marie Hackenberg, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
September 26, 2022
Mitochondrial diseases mimicking autoimmune diseases of the CNS and good response to steroids initially
Adela Della Marina, Annikki Bertolini, Andreas Wegener-Panzer, et al.
Plos One
|
September 7, 2012
Extensive natural variation for cellular hydrogen peroxide release is genetically controlled
Homa Attar, Karen Bedard, Eugenia Migliavacca, et al.
European Journal of Neurology
|
March 10, 2025
Genetic Etiology Influences the Low-Frequency Components of Globus Pallidus Internus Electrophysiology in Dystonia
Ahmet Kaymak, Luigi M Romito, Fabiana Colucci, et al.
Clinical Epigenetics
|
October 23, 2020
Smoking-related changes in DNA methylation and gene expression are associated with cardio-metabolic traits
Silvana C E Maas, Michelle M J Mens, Brigitte Kühnel, et al.
Neuron
|
January 24, 2024
Direct neuronal reprogramming of NDUFS4 patient cells identifies the unfolded protein response as a novel general reprogramming hurdle
Giovanna Sonsalla, Ana Belen Malpartida, Therese Riedemann, et al.
Journal of Inherited Metabolic Disease
|
December 7, 2021
Identification and characterization of novel MPC1 gene variants causing mitochondrial pyruvate carrier deficiency
Huafang Jiang, Ahmad Alahmad, Song Fu, et al.
Page
of 40
Search research articles
Search
Showing results (171-180 of 395) with videos related to
Sort By:
Page
of 40
Frontiers in Endocrinology
|
July 17, 2023
Investigating the role of ASCC1 in the causation of bone fragility
Barbara Voraberger, Johannes A Mayr, Nadja Fratzl-Zelman, et al.
Journal of Hepatology
|
May 7, 2016
Severe respiratory complex III defect prevents liver adaptation to prolonged fasting
Laura S Kremer, Caroline L'hermitte-Stead, Pierre Lesimple, et al.
Nature Communications
|
December 18, 2025
Single cell spatial transcriptomics integration deciphers the morphological heterogeneity of atherosclerotic carotid arteries
Jessica Pauli, Daniel Garger, Fatemeh Peymani, et al.
Annals of Clinical and Translational Neurology
|
October 1, 2025
The Diverse Neuromuscular Spectrum of VPS13A Disease
Anne Buchberger, Evamaria Riedel, Marie Hackenberg, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
September 26, 2022
Mitochondrial diseases mimicking autoimmune diseases of the CNS and good response to steroids initially
Adela Della Marina, Annikki Bertolini, Andreas Wegener-Panzer, et al.
Plos One
|
September 7, 2012
Extensive natural variation for cellular hydrogen peroxide release is genetically controlled
Homa Attar, Karen Bedard, Eugenia Migliavacca, et al.
European Journal of Neurology
|
March 10, 2025
Genetic Etiology Influences the Low-Frequency Components of Globus Pallidus Internus Electrophysiology in Dystonia
Ahmet Kaymak, Luigi M Romito, Fabiana Colucci, et al.
Clinical Epigenetics
|
October 23, 2020
Smoking-related changes in DNA methylation and gene expression are associated with cardio-metabolic traits
Silvana C E Maas, Michelle M J Mens, Brigitte Kühnel, et al.
Neuron
|
January 24, 2024
Direct neuronal reprogramming of NDUFS4 patient cells identifies the unfolded protein response as a novel general reprogramming hurdle
Giovanna Sonsalla, Ana Belen Malpartida, Therese Riedemann, et al.
Journal of Inherited Metabolic Disease
|
December 7, 2021
Identification and characterization of novel MPC1 gene variants causing mitochondrial pyruvate carrier deficiency
Huafang Jiang, Ahmad Alahmad, Song Fu, et al.
Page
of 40