Works matching AU Hatakeyama, Hideyuki
Results: 17
Mitochondrial Complex III Deficiency Caused by a Homozygous UQCRC2 Mutation Presenting with Neonatal-Onset Recurrent Metabolic Decompensation.
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- Human Mutation, 2013, v. 34, n. 3, p. 446, doi. 10.1002/humu.22257
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- Article
Advancing Veterinary Oncology: Next-Generation Diagnostics for Early Cancer Detection and Clinical Implementation.
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- Animals (2076-2615), 2025, v. 15, n. 3, p. 389, doi. 10.3390/ani15030389
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- Article
Mitochondrial respiratory dysfunction disturbs neuronal and cardiac lineage commitment of human iPSCs.
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- Cell Death & Disease, 2017, v. 8, n. 1, p. e2551, doi. 10.1038/cddis.2016.484
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- Article
Non-Invasive Detection of Tumors by Volatile Organic Compounds in Urine.
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- Biomedicines, 2025, v. 13, n. 1, p. 109, doi. 10.3390/biomedicines13010109
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- Article
N-NOSE Proves Effective for Early Cancer Detection: Real-World Data from Third-Party Medical Institutions.
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- Biomedicines, 2024, v. 12, n. 11, p. 2546, doi. 10.3390/biomedicines12112546
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- Article
Pancreatic Cancer and Detection Methods.
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- Biomedicines, 2023, v. 11, n. 9, p. 2557, doi. 10.3390/biomedicines11092557
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- Article
Impaired respiratory function in MELAS-induced pluripotent stem cells with high heteroplasmy levels.
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- FEBS Open Bio, 2015, v. 5, p. 219, doi. 10.1016/j.fob.2015.03.008
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- Article
Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagy.
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- Human Molecular Genetics, 2011, v. 20, n. 19, p. 3841, doi. 10.1093/hmg/ddr305
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- Article
Molecular pathomechanisms and cell-type-specific disease phenotypes of MELAS caused by mutant mitochondrial tRNA<sup>Trp</sup>.
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- Acta Neuropathologica Communications, 2015, v. 3, n. 1, p. 1, doi. 10.1186/s40478-015-0227-x
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- Article
Reversible infantile respiratory chain deficiency: A clinical and molecular study.
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- Annals of Neurology, 2010, v. 68, n. 6, p. 845, doi. 10.1002/ana.22111
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- Article
Bridging the gap in cervical cancer screening for underserved communities: MCED and the promise of future technologies.
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- Frontiers in Oncology, 2024, p. 01, doi. 10.3389/fonc.2024.1407008
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- Article
A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy.
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- 2011
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- Publication type:
- Report
Concise Review: Heteroplasmic Mitochondrial DNA Mutations and Mitochondrial Diseases: Toward iPSC-Based Disease Modeling, Drug Discovery, and Regenerative Therapeutics.
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- Stem Cells, 2016, v. 34, n. 4, p. 801, doi. 10.1002/stem.2292
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- Article
Mitochondrial respiratory dysfunction caused by a heteroplasmic mitochondrial DNA mutation blocks cellular reprogramming.
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- Human Molecular Genetics, 2015, v. 24, n. 16, p. 4698, doi. 10.1093/hmg/ddv201
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- Article
Clinical Possibility of Caenorhabditis elegans as a Novel Evaluation Tool for Esophageal Cancer Patients Receiving Chemotherapy: A Prospective Study.
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- Cancers, 2023, v. 15, n. 15, p. 3870, doi. 10.3390/cancers15153870
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- Article
Correction: Evaluation of N-NOSE as a surveillance tool for recurrence in gastric and esophageal cancers: a prospective cohort study.
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- 2025
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- Correction Notice
Evaluation of N-NOSE as a surveillance tool for recurrence in gastric and esophageal cancers: a prospective cohort study.
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- BMC Cancer, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12885-024-13327-x
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- Article