Kurenai Tanji
Affiliations: | Pathology | Columbia University, New York, NY |
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"Kurenai Tanji"Bio:
Columbia University College of Physicians & Surgeons
Pathology Department
680 West 168th Street PH15 Stem-124
New York, NY 10032
United States
Mean distance: 106866
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Publications
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| Hidalgo-Gutierrez A, Shintaku J, Ramon J, et al. (2024) Guanylate Kinase 1 Deficiency: A Novel and Potentially Treatable Mitochondrial DNA Depletion/Deletions Disease. Annals of Neurology |
| Carberry N, Yu S, Fayerman RN, et al. (2022) Leptomeningeal Disease Secondary to Thr60Ala Transthyretin Amyloidosis: Case Report and Review of the Literature. The Neurohospitalist. 13: 90-95 |
| Shintaku J, Pernice WM, Eyaid W, et al. (2022) RRM1 variants cause a mitochondrial DNA maintenance disorder via impaired de novo nucleotide synthesis. The Journal of Clinical Investigation |
| Thakur KT, Miller EH, Glendinning MD, et al. (2021) COVID-19 neuropathology at Columbia University Irving Medical Center/New York Presbyterian Hospital. Brain : a Journal of Neurology |
| Kripps KA, Friederich MW, Chen T, et al. (2020) A novel acceptor stem variant in mitochondrial tRNA impairs mitochondrial translation and is associated with a severe phenotype. Molecular Genetics and Metabolism |
| Franco-Iborra S, Tanji K. (2020) Histochemical and immunohistochemical staining methods to visualize mitochondrial proteins and activity. Methods in Cell Biology. 155: 247-270 |
| Shakri AR, Zhong TJ, Ma W, et al. (2019) Upregulation of ZIP14 and Altered Zinc Homeostasis in Muscles in Pancreatic Cancer Cachexia. Cancers. 12 |
| Berardo A, Emmanuele V, Vargas W, et al. (2019) Leber hereditary optic neuropathy plus dystonia, and transverse myelitis due to double mutations in MT-ND4 and MT-ND6. Journal of Neurology |
| Lopez-Gomez C, Hewan H, Sierra C, et al. (2019) Bioavailability and cytosolic kinases modulate response to deoxynucleoside therapy in TK2 deficiency. Ebiomedicine |
| Wang Y, Shin JY, Nakanishi K, et al. (2019) Postnatal Development of Mice with Combined Genetic Depletions of Lamin A/C, Emerin and Lamina-associated Polypeptide 1. Human Molecular Genetics |