Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Zhaochang Jiang"'
Autor:
Jiabin Lai, Weike Kong, Qiangchang Fu, Zhaochang Jiang, Bohao Sun, Xin Ye, Jing Kong, Shumei Wei, Lifeng Jiang
Publikováno v:
Diagnostic Pathology, Vol 19, Iss 1, Pp 1-8 (2024)
Abstract Background Osteosarcoma is a bone tumor that is characterized by high malignancy and a high mortality rate, and that originates from primitive osteoblastic mesenchymal cells and is most common in rapidly growing long bones. PSMD14, also know
Externí odkaz:
https://doaj.org/article/c4fb8cb7986f48c4a32446bd69a0398b
Publikováno v:
Computer Systems Science and Engineering. 46:521-536
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::811848a81c2ae99d7fe70d7dc5434490
https://doi.org/10.32604/csse.2022.028606
https://doi.org/10.32604/csse.2022.028606
Publikováno v:
Irish Journal of Medical Science (1971 -). 191:2625-2633
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07618841692e3f2a8f00b6d35631f2b0
https://doi.org/10.1007/s11845-021-02911-w
https://doi.org/10.1007/s11845-021-02911-w
Publikováno v:
Mitochondrial DNA Part A. 32:59-65
Mutations in mitochondrial DNA (mtDNA) are important causes for type 2 diabetes mellitus (T2DM). To investigate the association between mtDNA mutations/variants and diabetes, we reported here clini...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95d3dae1298ff67dd9aad9f1bd7690ea
https://doi.org/10.1080/24701394.2020.1856101
https://doi.org/10.1080/24701394.2020.1856101
Publikováno v:
Lecture Notes in Computer Science ISBN: 9783031067938
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4f146a7b75873c4f2d54d7d52e1894b
https://doi.org/10.1007/978-3-031-06794-5_11
https://doi.org/10.1007/978-3-031-06794-5_11
Publikováno v:
Irish journal of medical science. 191(6)
Mutations/variants in mitochondrial genomes are found to be associated with type 2 diabetes mellitus (T2DM), but the pathophysiology of this disease remains largely unknown.The aim of this study is to investigate the relationship between mitochondria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::593b307ec66890f60761e87b6fafac88
https://pubmed.ncbi.nlm.nih.gov/34993838
https://pubmed.ncbi.nlm.nih.gov/34993838
Publikováno v:
Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis. 32(2)
Mutations in mitochondrial DNA (mtDNA) are important causes for type 2 diabetes mellitus (T2DM). To investigate the association between mtDNA mutations/variants and diabetes, we reported here clinical, genetic and biochemical characterization of a Ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b14795338d8c4f28cdd481c327940dd0
https://pubmed.ncbi.nlm.nih.gov/33284036
https://pubmed.ncbi.nlm.nih.gov/33284036
Publikováno v:
International Journal of Molecular Medicine
Polycystic ovary syndrome (PCOS) is a common endocrine disorder with unknown etiology and unsatisfactory clinical treatment. Considering the ethical limitations of studies involving humans, animal models that reflect features of PCOS and insulin resi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2aea70b5ad3422740fde00f8dc54dc51
http://europepmc.org/articles/PMC6257859
http://europepmc.org/articles/PMC6257859
Publikováno v:
Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis. 27(2)
Mutations in mitochondrial DNA (mtDNA) were the most important causes of Leber's hereditary optic neuropathy (LHON). To date, approximately 25 LHON-associated mtDNA mutations have been identified in various ethnic populations. Three primary mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50e82c9a9c1efafa87addadc47c9ba4e
https://pubmed.ncbi.nlm.nih.gov/25186221
https://pubmed.ncbi.nlm.nih.gov/25186221