Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Naphatsamon Uthailak"'
Autor:
Pattaneeya Prangthip, Jumreang Tummatorn, Poom Adisakwattana, Naphatsamon Uthailak, Usa Boonyuen, Phornpimon Tipthara, Joel Tarning, Pavitra Laohapaisan, Charnsak Thongsornkleeb, Somsak Ruchirawat, Onrapak Reamtong
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-13 (2023)
Abstract Parasitic roundworms cause significant sickness and mortality in animals and humans. In livestock, these nematodes have severe economic impact and result in losses in food production on a global scale. None of the currently available drugs i
Externí odkaz:
https://doaj.org/article/6ea568cb3850463eb5bc441b59553465
Autor:
Naphatsamon Uthailak, Poom Adisakwattana, Peerut Chienwichai, Phornpimon Tipthara, Joel Tarning, Charin Thawornkuno, Tipparat Thiangtrongjit, Onrapak Reamtong
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 13 (2023)
Human trichinellosis is a parasitic infection caused by roundworms belonging to the genus Trichinella, especially Trichinella spiralis. Early and accurate clinical diagnoses of trichinellosis are required for efficacious prognosis and treatment. Curr
Externí odkaz:
https://doaj.org/article/d0a6e6d36f6b4ef4b429d69987c28646
Autor:
Naphatsamon Uthailak, Poom Adisakwattana, Tipparat Thiangtrongjit, Yanin Limpanont, Phiraphol Chusongsang, Yupa Chusongsang, Kanthi Tanasarnprasert, Onrapak Reamtong
Publikováno v:
PLoS ONE, Vol 17, Iss 10, p e0275992 (2022)
Schistosomiasis is a neglected tropical disease caused by an infection of the parasitic flatworms schistosomes. Schistosoma mekongi is a restricted Schistosoma species found near the Mekong River, mainly in southern Laos and northern Cambodia. Becaus
Externí odkaz:
https://doaj.org/article/b59558befa754a27ae3d657d6fe505ed
Publikováno v:
Frontiers in Plant Science, Vol 12 (2021)
Gaucher disease is an inherited lysosomal storage disorder caused by a deficiency of functional enzyme β-glucocerebrosidase (GCase). Recombinant GCase has been used in enzyme replacement therapy to treat Gaucher disease. Importantly, the terminal ma
Externí odkaz:
https://doaj.org/article/e7ab9fd5b00e428fa6a5ba8d630eb677
Publikováno v:
Journal of bioscience and bioengineering. 133(5)
Gaucher disease is an inherited lysosomal storage disorder caused by an insufficiency of active β-glucocerebrosidase (GCase). Exogenous recombinant GCase via enzyme replacement therapy is considered the most practical treatment for Gaucher disease.
Autor:
Pornpimol Mahamad, Naphatsamon Uthailak, Watanalai Panbangred, Somchai Yanarojana, Wassana Wijagkanalan, Jean Petre, Pamorn Chittavanich
Publikováno v:
Molecular biotechnology. 59(4-5)
CRM197 is a diphtheria toxin (DT) mutant (G52E) which has been used as a carrier protein for conjugate vaccines. However, it still possesses cytotoxicity toward mammalian cells. The goal of this project was to produce a non-toxic and soluble CRM197EK
Akademický článek
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Publikováno v:
International Journal of Molecular Sciences; Jul2018, Vol. 19 Issue 7, p1972, 1p, 1 Color Photograph, 1 Chart, 4 Graphs