Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ma, Thi Huyen Thuong"'
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:
Ma, Thi Huyen Thuong1,2 (AUTHOR), Luong, Thi Lan Anh3 (AUTHOR), Hoang, Thu Lan3 (AUTHOR), Nguyen, Thi Thanh Hoa1 (AUTHOR), Vu, Thi Ha3 (AUTHOR), Tran, Van Khoa4 (AUTHOR), Nguyen, Duy Bac4 (AUTHOR), Trieu, Tien Sang4 (AUTHOR), Nguyen, Hai Ha1,2 (AUTHOR), Nong, Van Hai1,2 (AUTHOR), Nguyen, Dang Ton1,2 (AUTHOR) dtnguyen@igr.ac.vn
Publikováno v:
Molecular Genetics & Genomic Medicine. Aug2021, Vol. 9 Issue 8, p1-11. 11p.
Akademický článek
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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; Volume 13; Issue 10; Pages: 1884
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c3da127e112d1285b3a402514c2aa05
https://pubmed.ncbi.nlm.nih.gov/36292769
https://pubmed.ncbi.nlm.nih.gov/36292769
Publikováno v:
Vietnam Journal of Biotechnology. 19:223-228
Epidermolysis bullosa simplex (EBS) is a group of epidermolysis bullosa (EB) and accounts for 75-85% EB cases. Most EBS patients are caused by mutations in KRT5 or KRT14, encoding for keratin 5 and keratin 14, respectively, which impair the structura
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f59134afbb03ea74d95bf2366906c361
https://doi.org/10.15625/1811-4989/16111
https://doi.org/10.15625/1811-4989/16111
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45c9ea77e7fbf2ef6098c72954b9243c
https://pubmed.ncbi.nlm.nih.gov/35870188
https://pubmed.ncbi.nlm.nih.gov/35870188
Autor:
Nong Van Hai, Ma Thi Huyen Thuong, Vu Phuong Nhung, Tran Thi Bich Ngoc, Nguyen Thi Hoa, Nguyen Thuy Duong, Nguyen Hai Ha, Nguyen Dang Ton
Publikováno v:
Vietnam Journal of Biotechnology. 15:625-631
Retinoblastoma (Rb) is a malignant retinal tumor on young children which is often founded before the age of 5. This cancer disease appears when both of RB1 alleles on 13q14.2 chromosome are mutated. The aim of this research is to evaluate the ability
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6d47d799661fbed1c9400413d95e39f
https://doi.org/10.15625/1811-4989/15/4/13402
https://doi.org/10.15625/1811-4989/15/4/13402
Autor:
Duong Thu Trang, Nguyen Minh Phu, Do Manh Hung, Vu Phuong Nhung, Nguyen Ngan Ha, Ma Thi Huyen Thuong, Tran Thi Bich Ngoc, Nguyen Xuan Hiep, Nguyen Dang Ton, Nong Van Hai, Nguyen Hai Ha
Publikováno v:
Molecular Vision; 2022, Vol. 28, p480-491, 12p