Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Nhung Phuong, Vu"'
Autor:
Hai Xuan Tang, Muoi Dang Ho, Nhung Phuong Vu, Hung Vu Cao, Vinh Anh Ngo, Van Thi Nguyen, Thuan Duc Nguyen, Ton Dang Nguyen
Publikováno v:
Medicina, Vol 60, Iss 4, p 637 (2024)
Background and Objectives: Drug resistant epilepsy (DRE) is a major hurdle in epilepsy, which hinders clinical care, patients’ management and treatment outcomes. DRE may partially result from genetic variants that alter proteins responsible for dru
Externí odkaz:
https://doaj.org/article/401f8ff6466740aa86677eabf8d0b673
Autor:
Nhung Phuong Vu, Hoa Thi Thanh Nguyen, Ngoc Thi Bich Tran, Ton Dang Nguyen, Hue Thi Thu Huynh, Xuan Thi Nguyen, Duong Thuy Nguyen, Hai Van Nong, Ha Hai Nguyen
Publikováno v:
Annals of Human Biology, Vol 46, Iss 6, Pp 491-497 (2019)
Background: Genetic polymorphism of CYP2C19 has been shown to affect enzyme activity and thereby contribute to inter-individual variability in drug metabolism and response. The complete genetic variation of CYP2C19 in Vietnam still remains obscure ev
Externí odkaz:
https://doaj.org/article/cb589314e21840cc8b9cfa0cebd569ac
Autor:
Nhung Phuong Vu, Hai Thi Tran, Nga Bich Vu, Thuong Thi Huyen Ma, Ton Dang Nguyen, Hai Van Nong, Ha Hai Nguyen
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 35:1206-1210
Objectives Familial partial lipodystrophy type 2 is the most well-known subtype of lipodystrophy. We describe for the first time the phenotype of a case with lipodystrophy, who carried heterozygous mutation c.G1394A (p.G465D) in the LMNA gene. Case p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6dc40c6da95178f719fe672157d0027e
https://doi.org/10.1515/jpem-2022-0208
https://doi.org/10.1515/jpem-2022-0208
Akademický článek
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Autor:
Hoa Thi Thanh Nguyen, Hai Van Nong, Duong Thuy Nguyen, Ton Dang Nguyen, Ha Hai Nguyen, Hue Thi Thu Huynh, Xuan Thi Nguyen, Nhung Phuong Vu, Ngoc Thi Bich Tran
Publikováno v:
Annals of Human Biology. 46:491-497
Background: Genetic polymorphism of CYP2C19 has been shown to affect enzyme activity and thereby contribute to inter-individual variability in drug metabolism and response. The complete genetic variation of CYP2C19 in Vietnam still remains obscure ev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff5fa7e966384ce1b1c6643d391c316b
https://doi.org/10.1080/03014460.2019.1687750
https://doi.org/10.1080/03014460.2019.1687750
Autor:
Thuong Thi Huyen Ma, Quynh Thi Nhu Bach, Ha Hai Nguyen, Nhung Phuong Vu, Thang Hong Vu, Hai Van Nong, Ton Dang Nguyen
Publikováno v:
Medicine
Supplemental Digital Content is available in the text
CYP2D6 genetic variations could result in alteration of CYP2D6 enzyme activity, leading to dissimilarity among individuals in regard of drug metabolism. This study aims to detect all genetic
CYP2D6 genetic variations could result in alteration of CYP2D6 enzyme activity, leading to dissimilarity among individuals in regard of drug metabolism. This study aims to detect all genetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43b070e513eae43eb3d63c09078009ac
https://pubmed.ncbi.nlm.nih.gov/31145348
https://pubmed.ncbi.nlm.nih.gov/31145348
Autor:
Ming Ta Michael Lee, Thuong Thi Huyen Ma, Nhung Phuong Vu, Hai Van Nong, Hue Thi Thu Huynh, Ngoc Thi Bich Tran, Ha Hai Nguyen, Duong Thuy Nguyen, Ton Dang Nguyen
Publikováno v:
Molecular biology reports. 45(5)
Genetic variations in CYP2C9 are associated to inter-individual variability of drugs metabolism and response. The only report has been done previously mainly focusing on the common variant alleles of CYP2C9 in Vietnamese Kinh subjects. However, littl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58bd735656535f7ce31c914a7d73b4df
https://pubmed.ncbi.nlm.nih.gov/29978384
https://pubmed.ncbi.nlm.nih.gov/29978384
Autor:
Ha Hai, Nguyen, Hoa Thi Thanh, Nguyen, Nhung Phuong, Vu, Quynh Thuy, Le, Chau Minh, Pham, Thuong Thi, Huyen, Hung, Manh, Hang Le Bich, Pham, Ton Dang, Nguyen, Hien Thi Thu, Le, Hai, Van Nong
Publikováno v:
Molecular Vision
Purpose Retinoblastoma (Rb) is a rare and unique eye cancer that usually develops in the retinas of children less than 5 years old due to mutations in the RB1 gene. About 40% of affected individuals have the heritable form making genetics testing of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b651418d2e31fe942100cad2a0a91b19
https://pubmed.ncbi.nlm.nih.gov/29568217
https://pubmed.ncbi.nlm.nih.gov/29568217
Akademický článek
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Akademický článek
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