Found: 15
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Loss of supervillin causes myopathy with myofibrillar disorganization and autophagic vacuoles.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Glycogenin is Dispensable for Glycogen Synthesis in Human Muscle, and Glycogenin Deficiency Causes Polyglucosan Storage.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Potential Natural Products Regulation of Molecular Signaling Pathway in Dermal Papilla Stem Cells.
- Published in:
- Molecules, 2023, v. 28, n. 14, p. 5517, doi. 10.3390/molecules28145517
- By:
- Publication type:
- Article
Proteomic profiling of polyglucosan bodies associated with glycogenin‐1 deficiency in skeletal muscle.
- Published in:
- Neuropathology & Applied Neurobiology, 2024, v. 50, n. 3, p. 1, doi. 10.1111/nan.12995
- By:
- Publication type:
- Article
Respiratory chain dysfunction in perifascicular muscle fibres in patients with dermatomyositis is associated with mitochondrial DNA depletion.
- Published in:
- Neuropathology & Applied Neurobiology, 2022, v. 48, n. 7, p. 1, doi. 10.1111/nan.12841
- By:
- Publication type:
- Article
Analysis of an independent tumor suppressor locus telomeric to Tp53 suggested Inpp5k and Myo1c as novel tumor suppressor gene candidates in this region.
- Published in:
- BMC Genetics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12863-015-0238-4
- By:
- Publication type:
- Article
Analysis of an independent tumor suppressor locus telomeric to Tp53 suggested Inpp5k and Myo1c as novel tumor suppressor gene candidates in this region
- Published in:
- BMC Genetics, 2015, v. 16, n. 1, p. 80, doi. 10.1186/s12863-015-0238-4
- By:
- Publication type:
- Article
Abnormal expression of myosin heavy chains in early postnatal stages of spinal muscular atrophy type I at single fibre level.
- Published in:
- Acta Myologica, 2024, v. 43, n. 3, p. 89, doi. 10.36185/2532-1900-398
- By:
- Publication type:
- Article
Expression pattern of mitochondrial respiratory chain enzymes in skeletal muscle of patients with mitochondrial myopathy associated with the homoplasmic m.14674T>C variant.
- Published in:
- Brain Pathology, 2022, v. 32, n. 4, p. 1, doi. 10.1111/bpa.13038
- By:
- Publication type:
- Article
Mitochondrial DNA variants in inclusion body myositis characterized by deep sequencing.
- Published in:
- Brain Pathology, 2021, v. 31, n. 3, p. 1, doi. 10.1111/bpa.12931
- By:
- Publication type:
- Article
Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 11, p. 1919, doi. 10.1093/hmg/ddz032
- By:
- Publication type:
- Article
Progressive external ophthalmoplegia associated with novel MT‐TN mutations.
- Published in:
- Acta Neurologica Scandinavica, 2021, v. 143, n. 1, p. 103, doi. 10.1111/ane.13339
- By:
- Publication type:
- Article
Lowered Expression of Tumor Suppressor Candidate MYO1C Stimulates Cell Proliferation, Suppresses Cell Adhesion and Activates AKT.
- Published in:
- PLoS ONE, 2016, v. 11, n. 10, p. 1, doi. 10.1371/journal.pone.0164063
- By:
- Publication type:
- Article
Structural modification of resveratrol analogue exhibits anticancer activity against lung cancer stem cells via suppression of Akt signaling pathway.
- Published in:
- BMC Complementary Medicine & Therapies, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12906-023-04016-6
- By:
- Publication type:
- Article
Shrimp Lipid Prevents Endoplasmic Reticulum-Mediated Endothelial Cell Damage.
- Published in:
- Foods, 2022, v. 11, n. 19, p. 3076, doi. 10.3390/foods11193076
- By:
- Publication type:
- Article