Zobrazeno 1 - 10
of 30
pro vyhledávání: '"dnaH"'
Autor:
Chunchao Zhu, Qin Yang, Jia Xu, Wenyi Zhao, Zizhen Zhang, Danhua Xu, Yeqian Zhang, Enhao Zhao, Gang Zhao
Publikováno v:
Journal of Translational Medicine, Vol 17, Iss 1, Pp 1-11 (2019)
Abstract Background The dynein axonemal heavy chain (DNAH) family of genes encode the dynein axonemal heavy chain, which is involved in cell motility. Genomic variations of DNAH family members have been frequently reported in diverse kinds of maligna
Externí odkaz:
https://doaj.org/article/b6e609632b3f4473b2068133be885ae2
Autor:
Enhao Zhao, Zizhen Zhang, Chunchao Zhu, Yeqian Zhang, Gang Zhao, Qin Yang, Jia Xu, Wenyi Zhao, Danhua Xu
Publikováno v:
Journal of Translational Medicine, Vol 17, Iss 1, Pp 1-11 (2019)
Journal of Translational Medicine
Journal of Translational Medicine
Background The dynein axonemal heavy chain (DNAH) family of genes encode the dynein axonemal heavy chain, which is involved in cell motility. Genomic variations of DNAH family members have been frequently reported in diverse kinds of malignant tumors
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2a86664b64cc0bf0822d2a91d67ce04
http://link.springer.com/article/10.1186/s12967-019-1867-6
http://link.springer.com/article/10.1186/s12967-019-1867-6
Autor:
Hongbin Liu, Fei Gao, Jinlong Ma, Xiuge Wang, Tahir Muhammad, Tao Huang, Xiaochen Yu, Mengjing Li, Haobo Zhang, Chao Liu, Wei Li, Zi-Jiang Chen, Yingying Yin
Publikováno v:
Science Bulletin. 65:854-864
Impaired flagellar development and impaired motility of sperm is a cause of infertility in males. Several genes, including those of the AKAP, CCDC, CFAP, and DNAH families, among others, are involved in the “multiple morphological abnormalities of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::806d64aaf222833c05f54376ea5ef2cb
https://doi.org/10.1016/j.scib.2020.01.023
https://doi.org/10.1016/j.scib.2020.01.023
Publikováno v:
BMC Neurology, Vol 20, Iss 1, Pp 1-5 (2020)
BMC Neurology
BMC Neurology
Background Kartagener syndrome is an autosomal recessive inherited disorder of primary ciliary dyskinesia. Moyamoya syndrome refers to a moyamoya angiopathy associated with other neurological and/or extra-neurological symptoms, or due to a well ident
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb7c7d5f770965111d2555cd55363a18
https://doi.org/10.1186/s12883-020-01895-x
https://doi.org/10.1186/s12883-020-01895-x
Publikováno v:
Basic and clinical andrology
Basic and clinical andrology, BioMed Central, 2019, 29 (1), ⟨10.1186/s12610-019-0083-9⟩
Basic and Clinical Andrology
Basic and Clinical Andrology, Vol 29, Iss 1, Pp 1-8 (2019)
Basic and clinical andrology, BioMed Central, 2019, 29 (1), ⟨10.1186/s12610-019-0083-9⟩
Basic and Clinical Andrology
Basic and Clinical Andrology, Vol 29, Iss 1, Pp 1-8 (2019)
Résumé Les infertilités masculines dues au phénotype de « flagelles courts » ou « Multiple Morphological Abnormalities of the sperm Flagella » (MMAF), sont caractérisées par une asthénozoospermie quasi totale associée à la présence d’
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ca19ef476491488d74432648c9c0068
https://hal.archives-ouvertes.fr/hal-02350815
https://hal.archives-ouvertes.fr/hal-02350815
Autor:
Brandy A. Burgess, D.C. Van Metre, Paul S. Morley, Denise Bolte, Kristy L. Pabilonia, C.B. Weller
Publikováno v:
Journal of Veterinary Internal Medicine
Background Salmonella enterica can significantly impact management of animal facilities. Comprehensive screening is essential for effective control in high-risk populations. Availability of reliable point-of-care diagnostic tests would facilitate the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df6bd08f5a317a72a9f6119cd2c20b5c
http://europepmc.org/articles/PMC4895624
http://europepmc.org/articles/PMC4895624
Akademický článek
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Akademický článek
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Publikováno v:
Journal of AOAC INTERNATIONAL. 92:438-448
A modification to Performance-Tested MethodSM 010403, GeneQuence Listeria Test (DNAH method), is described. The modified method uses a new media formulation, LESS enrichment broth, in single-step enrichment protocols for both foods and environmental
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b1fab1311d01d80934801371257c50e
https://doi.org/10.1093/jaoac/92.2.438
https://doi.org/10.1093/jaoac/92.2.438
Autor:
Silvia Riva, Manila Candusso, Marco Spada, A Bertani, Aurelio Sonzogni, M.G. Alessio, Paola Stroppa, Giuliano Torre, Bruno Gridelli, M. Bravi, Michele Colledan, Maria L. Melzi
Publikováno v:
Liver Transplantation. 12:573-577
Late graft dysfunction (GD) associated with the development of autoantibodies is a common event after pediatric liver transplantation (OLTx) and can present in 2 clinicohistological subsets: de novo autoimmune hepatitis (DNAH) and early chronic rejec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c778d78457cff50d8ee92194aa38c3e7
https://doi.org/10.1002/lt.20673
https://doi.org/10.1002/lt.20673