نتائج البحث

A PCR-independent approach for mtDNA enrichment and next-generation sequencing: comprehensive evaluation and clinical application.

• Authors : Liang, Dong; Zhu, Lin; Zhu, Yuqing

Subjects: MITOCHONDRIAL DNA; NUCLEOTIDE sequencing; CLINICAL medicine

• Source: Journal of Translational Medicine; 4/25/2024, Vol. 22 Issue 1, p1-12, 12p

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Mitochondrial heteroplasmic shifts reveal a positive selection of breast cancer.

• Authors : Li, Yanni; Sundquist, Kristina; Vats, Sakshi

Subjects: BREAST cancer; MITOCHONDRIAL DNA; MITOCHONDRIASWEDEN

• Source: Journal of Translational Medicine; 11/21/2023, Vol. 21 Issue 1, p1-14, 14p

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Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in Chinese patients.

• Authors : Zhang AM; Key Laboratory of Animal Models and Human Disease Mechanisms of Chinese Academy of Sciences & Yunnan Province, Kunming Institute of Zoology, Kunming, Yunnan 650223, China.; Jia X

Subjects: Mutation*/Mutation*/Mutation*/physiology; Asian People/Asian People/Asian People/*genetics ; DNA, Mitochondrial/DNA, Mitochondrial/DNA, Mitochondrial/*genetics

• Source: Journal of translational medicine [J Transl Med] 2012 Mar 09; Vol. 10, pp. 43. Date of Electronic Publication: 2012 Mar 09.Publisher: BioMed Central Country of Publication: England NLM ID: 101190741 Publication Model: Electronic Cited Medium: Internet ISSN: 1479-5876

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Wolfram syndrome, a rare neurodegenerative disease: from pathogenesis to future treatment perspectives

• Authors : Maria Teresa Pallotta; Giorgia Tascini; Roberta Crispoldi

Subjects: Deafness; Diabetes insipidus; Optic atrophy

• Source: Journal of Translational Medicine, Vol 17, Iss 1, Pp 1-12 (2019)

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Wolfram syndrome, a rare neurodegenerative disease: from pathogenesis to future treatment perspectives

• Authors : Giorgia Tascini; Roberta Crispoldi; Susanna Esposito

Subjects: 0301 basic medicine; Male; lcsh:Medicine

• Source: Journal of Translational MedicineJournal of Translational Medicine, Vol 17, Iss 1, Pp 1-12 (2019)

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TRPA1 promotes cisplatin-induced acute kidney injury via regulating the endoplasmic reticulum stress-mitochondrial damage.

• Authors : Deng, Fei^1,2,3 (AUTHOR); Zhang, Heping⁴ (AUTHOR); Zhou, Wei³ (AUTHOR)

• Source: Journal of Translational Medicine. 10/5/2023, Vol. 21 Issue 1, p1-17. 17p.

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Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in Chinese patients

• Authors : A-Mei Zhang; Xiangming Guo; Yong-Gang Yao

Subjects: congenital, hereditary, and neonatal diseases and abnormalities; LEBER HEREDITARY OPTIC NEUROPATHY; Mitochondrial DNA

• Source: Journal of Translational Medicine, Vol 10, Iss 1, p 43 (2012)Journal of Translational Medicine

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Wolfram syndrome, a rare neurodegenerative disease: from pathogenesis to future treatment perspectives.

• Authors : Pallotta, Maria Teresa¹ (AUTHOR) ; Tascini, Giorgia² (AUTHOR) ; Crispoldi, Roberta² (AUTHOR)

• Source: Journal of Translational Medicine. 7/23/2019, Vol. 17 Issue 1, pN.PAG-N.PAG. 1p.

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TRPA1 promotes cisplatin-induced acute kidney injury via regulating the endoplasmic reticulum stress-mitochondrial damage

• Authors : Fei Deng; Heping Zhang; Wei Zhou

Subjects: Cisplatin; Acute kidney injury; TRPA1

• Source: Journal of Translational Medicine, Vol 21, Iss 1, Pp 1-17 (2023)

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