Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Vu Phuong Nhung"'
Autor:
Nguyen Duc Thuan, Vu Phuong Nhung, Hoang Thi Dung, Nhu Dinh Son, Nguyen Hai Ha, Nguyen Dang Ton
Publikováno v:
Journal of Movement Disorders, Vol 15, Iss 2, Pp 193-195 (2022)
Externí odkaz:
https://doaj.org/article/857532963d3f4183a472f5a1329c436a
Autor:
Vu Phuong Nhung, Nguyen Dang Ton, Tran Thi Bich Ngoc, Ma Thi Huyen Thuong, Nguyen Thi Thanh Hai, Kim Thi Phuong Oanh, Le Thi Thu Hien, Pham Ngoc Thach, Nong Van Hai, Nguyen Hai Ha
Publikováno v:
Genes, Vol 13, Iss 10, p 1884 (2022)
Since the emergence and rapid transmission of SARS-CoV-2, numerous scientific reports have searched for the association of host genetic variants with COVID-19, but the data are mostly acquired from Europe. In the current work, we explored the link be
Externí odkaz:
https://doaj.org/article/2462b608bf134847a02e810786042376
Autor:
Nguyen Dang Ton, Nguyen Duc Thuan, Ma Thi Huyen Thuong, Tran Thi Bich Ngoc, Vu Phuong Nhung, Nguyen Thi Thanh Hoa, Nguyen Hoai Nam, Hoang Thi Dung, Nhu Dinh Son, Nguyen Van Ba, Nguyen Duy Bac, Tran Ngoc Tai, Le Thi Kim Dung, Nguyen Trong Hung, Nguyen Thuy Duong, Nguyen Hai Ha, Nong Van Hai
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 10, Pp n/a-n/a (2020)
Abstract Background Early‐onset Parkinson's disease (EOPD) refers to that of patients who have been diagnosed or had onset of motor symptoms before age 50, accounting for 4% of Parkinson's disease patients. The PRKN and PINK1 genes, both involved i
Externí odkaz:
https://doaj.org/article/585ba16254974becac38f7c99b75ec93
Autor:
Vu Phuong Nhung1, Nguyen Huong Giang2, Nguyen Thi Hong Nhung1, Nguyen Dang Ton1,3, Nguyen Hai Ha1,3 nguyenhaiha@igr.ac.vn
Publikováno v:
Journal of Biology / TẠp chí Sinh HỌc. Dec2022, Vol. 44 Issue 4, p111-122. 12p.
Publikováno v:
Academia Journal of Biology. 44:112-122
Filaggrin is a key protein that facilitates terminal differentiation of the epidermis and maintains skin barrier function. Mutations in the gene encoding filaggrin (FLG) have been identified to cause ichthyosis vulgaris, increase the risk of atopic d
Akademický článek
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Autor:
Nguyen Dang Ton1,2, Vu Phuong Nhung1, Duong Thu Trang1, Nguyen Thi Thanh Hoa1, Nguyen Hoai Nam1, Hoang Thi Thuan2, Ho Anh Son3, Nguyen Thi Thanh Hai4,5, Pham Ngoc Thach4, Nong Van Hai1,2, Nguyen Hai Ha1,2 nguyenhaiha@igr.ac.vn
Publikováno v:
Journal of Biology / TẠp chí Sinh HỌc. 2021, Vol. 43 Issue 1, p119-128. 10p.
Autor:
Ma Thi Huyen Thuong, Luong Thi Lan Anh, Vu Phuong Nhung, Tran Thi Bich Ngoc, Hoang Thu Lan, Doan Kim Phuong, Nguyen Hai Ha, Nong Van Hai, Nguyen Dang Ton
Publikováno v:
Journal of clinical laboratory analysis. 36(9)
Oculocutaneous albinism (OCA) is an autosomal recessive disease with hypopigmentation in skin, hair, and eyes, causing by the complete absence or reduction of melanin in melanocytes. Many types of OCA were observed based on the mutation in different
Autor:
Vu Binh Giang, Nguyen Dang Ton, Bach Thi Nhu Quynh, Vu Phuong Nhung, Nguyen Thi Hoa, Hoang Thi Thu Yen, Nguyen Hai Ha
Publikováno v:
Vietnam Journal of Biotechnology. 18:425-435
Irinotecan is a medicine commonly used to treat cancer. Carboxylesterase converts irinotecan into SN-38, a substance with 100 times more cytotoxicity than the original compound. SN-38 is inactivated by glucuronidation in the liver to the inactive for
Autor:
Nguyen Thi Hoa, Vu Phuong Nhung, Nguyen Dang Ton, Nguyen Phan Anh, Nguyen Hai Ha, Le Thi Bich Thao
Publikováno v:
Vietnam Journal of Biotechnology. 17:589-594
Warfarin is a well-known anticoagulant that capable of reducing the activity of vitamin K-dependent clotting factors. It has been widely used for cardiovascular patients. However, patient’s genotype of CYP2C9 and VKORC1 remarkably affects the metab