Zobrazeno 1 - 10
of 85
pro vyhledávání: '"molecular genetic test"'
Autor:
Ataf H. Sabir, Elizabeth Morley, Jameela Sheikh, Alistair D. Calder, Ana Beleza-Meireles, Moira S. Cheung, Alessandra Cocca, Mattias Jansson, Suzanne Lillis, Yogen Patel, Shu Yau, Christine M. Hall, Amaka C. Offiah, Melita Irving
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-14 (2021)
Abstract Background Skeletal dysplasia (SD) conditions are rare genetic diseases of the skeleton, encompassing a heterogeneous group of over 400 disorders, and represent approximately 5% of all congenital anomalies. Developments in genetic and treatm
Externí odkaz:
https://doaj.org/article/2ba7db3ffb1d4355907a9d8ece8ef189
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Su Jin Kim, Sae-Mi Lee, Jong-Moon Choi, Ja-Hyun Jang, Hyun Gi Kim, Jung-Taek Kim, Jae Ho Cho, Young Bae Sohn
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Skeletal dysplasia (SD), a heterogeneous disease group with rare incidence and various clinical manifestations, is associated with multiple causative genes. For clinicians, accurate diagnosis of SD is clinically and genetically difficult. The develop
Externí odkaz:
https://doaj.org/article/ef986d9ce7e0492c92393eaf13c5f113
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Кубанский научный медицинский вестник, Vol 25, Iss 3, Pp 139-148 (2018)
Aim. To analyze modern literature dealing with the issues of finding highly informative modern methods of early diagnostics of malignant tumors of thyroid.Materials and methods. The study of recent Russian and foreign literature in the databases RSCI
Externí odkaz:
https://doaj.org/article/45d040f03e774e8ead0001d1134143ce
Publikováno v:
Applied Sciences, Vol 11, Iss 2, p 684 (2021)
MTConnect standard technology provides simplicity, flexibility, and scalability in integrating various equipment and operating systems and enabling accurate and consistent data collection from any MTConnect-compatible system. Using MTConnect technolo
Externí odkaz:
https://doaj.org/article/9bb871f938274e1abd3a71e249279421
Publikováno v:
Russian Journal of Genetics. 57:936-941
The goal of this work was to develop a molecular genetic test system for determining the BLAD mutation using real-time PCR and to test pedigree cattle on breeding farms of Kostroma oblast. The materials for the study were samples of biological materi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5dea19f9f8412c7325d534865b3619c9
https://doi.org/10.1134/s1022795421080135
https://doi.org/10.1134/s1022795421080135
Autor:
L. V. Petrova, E. V. Sevastyanova, A. M. Vasilieva, E. A. Kuklina, Yu. A. Soloviev, L. N. Chernousova
Publikováno v:
Tuberkulez i Bolezni Lëgkih, Vol 97, Iss 9, Pp 40-44 (2019)
The objective of the study: to investigate the effect of the molecular genetic test of PCR-RT within the procedure of microbiological diagnosis of tuberculosis on the efficacy of chemotherapy in patients with multiple drug resistant tuberculosis in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::f5094b340a22884b55bad2608d1990ff
https://www.tibl-journal.com/jour/article/view/1335
https://www.tibl-journal.com/jour/article/view/1335
Publikováno v:
Clinical Chemistry and Laboratory Medicine (CCLM). 57:1136-1141
Background The process of technology validation and transfer of new molecular diagnostic tests towards the clinic faces challenges and needs to be improved. There is no empirical measure of the chronology and pace of technology transfer of molecular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb88c98b40c4c3f1ebf9cce2e7c0712c
https://doi.org/10.1515/cclm-2018-1126
https://doi.org/10.1515/cclm-2018-1126
Autor:
Melita Irving, Moira Cheung, Ana Beleza-Meireles, Christine Hall, Yogen Patel, S. Lillis, Alessandra Cocca, Shu Yau, Jameela Sheikh, Alistair Calder, Elizabeth Morley, Ataf H. Sabir, Mattias Jansson, Amaka C. Offiah
Publikováno v:
BMC Medical Genomics
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-14 (2021)
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-14 (2021)
Background Skeletal dysplasia (SD) conditions are rare genetic diseases of the skeleton, encompassing a heterogeneous group of over 400 disorders, and represent approximately 5% of all congenital anomalies. Developments in genetic and treatment techn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15a884fa2654269375be8b4d58be6ff4
https://eprints.whiterose.ac.uk/176215/6/s12920-021-00993-0.pdf
https://eprints.whiterose.ac.uk/176215/6/s12920-021-00993-0.pdf
