Zobrazeno 1 - 10 of 108 pro vyhledávání: '"Nguyen Van Tung"'
1
Akademický článek
Identifying the Pathogenic Variants in Heart Genes in Vietnamese Sudden Unexplained Death Victims by Next-Generation Sequencing
Autor: Tho Nguyen Tat, Nguyen Thi Kim Lien, Hung Luu Sy, To Ta Van, Duc Dang Viet, Hoa Nguyen Thi, Nguyen Van Tung, Le Tat Thanh, Nguyen Thi Xuan, Nguyen Huy Hoang
Publikováno v: Diagnostics, Vol 14, Iss 17, p 1876 (2024)
In forensics, one-third of sudden deaths remain unexplained after a forensic autopsy. A majority of these sudden unexplained deaths (SUDs) are considered to be caused by inherited cardiovascular diseases. In this study, we investigated 40 young SUD c
Externí odkaz: https://doaj.org/article/1507b9bae49342da83ce66964bf21fc5
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2
Akademický článek
The adsorption kinetic and isotherm studies of metal ions (Co2+, Sr2+, Cs+) on Fe3O4 nanoparticle of radioactive importance
Autor: Do Quoc Hung, Luu Xuan Dinh, Nguyen Van Tung, Le Thi Mai Huong, Nguyen Thi Lien, Pham Thanh Minh, Thu-Huong Le
Publikováno v: Results in Chemistry, Vol 6, Iss , Pp 101095- (2023)
The release of radionuclide elements from nuclear, medical, research, and defense fields has become a serious environmental problem. Hence, the investigation of the adsorption kinetic and isotherm of metal ions (Co2+, Sr2+, and Cs+) which are commonl
Externí odkaz: https://doaj.org/article/2f621afb0b3f407bb19d7b9775f04d24
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3
Akademický článek
Genome Characteristics of the Endophytic Fungus Talaromyces sp. DC2 Isolated from Catharanthus roseus (L.) G. Don
Autor: Nguyen Duc Quan, Ngoc-Lan Nguyen, Tran Thi Huong Giang, Nguyen Thi Thanh Ngan, Nguyen Thanh Hien, Nguyen Van Tung, Nguyen Hoang Thanh Trang, Nguyen Thi Kim Lien, Huy Hoang Nguyen
Publikováno v: Journal of Fungi, Vol 10, Iss 5, p 352 (2024)
Talaromyces sp. DC2 is an endophytic fungus that was isolated from the stem of Catharanthus roseus (L.) G. Don in Hanoi, Vietnam and is capable of producing vinca alkaloids. This study utilizes the PacBio Sequel technology to completely sequence the
Externí odkaz: https://doaj.org/article/cc6515705314474f94ed998b32ad7655
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4
Akademický článek
Novel mutations in the SGCA gene in unrelated Vietnamese patients with limb-girdle muscular dystrophies disease
Autor: Nam Chung Tran, Nguyen Thi Kim Lien, Thanh Dat Ta, Van Hung Nguyen, Huy Thinh Tran, Nguyen Van Tung, Nguyen Thi Xuan, Nguyen Huy Hoang, Van Khanh Tran
Publikováno v: Frontiers in Genetics, Vol 14 (2023)
Background: Limb-girdle muscular dystrophy (LGMD) is a group of inherited neuromuscular disorders characterized by atrophy and weakness in the shoulders and hips. Over 30 subtypes have been described in five dominant (LGMD type 1 or LGMDD) and 27 rec
Externí odkaz: https://doaj.org/article/fd6fe81c66bc4b39a302cf13a0717f01
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5
Akademický článek
Case Report: Novel rare mutation c.6353C > G in the ABCA12 gene causing harlequin ichthyosis identified by whole exome sequencing
Autor: Van Khanh Tran, Quang Minh Diep, Qiu Zilong, Le Thi Phuong, Hai Anh Tran, Nguyen Van Tung, Nguyen Thi Kim Lien, Nguyen Thi Xuan, Le Thi Ha, Thanh Van Ta, Thinh Huy Tran, Nguyen Huy Hoang
Publikováno v: Frontiers in Pediatrics, Vol 11 (2023)
BackgroundHarlequin ichthyosis (HI) is a severe rare genetic disease that mainly affects the skin. Neonates with this disease are born with thick skin and large diamond-shaped plates covering most of their bodies. Affected neonates lose the ability t
Externí odkaz: https://doaj.org/article/ca519a899c2e4d529e2a60e94cf7f822
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6
Akademický článek
Synthesis of Colloidal Silicon Quantum Dot from Rice Husk Ash
Autor: Thu-Huong Le, Dang Thi Thanh Le, Nguyen Van Tung
Publikováno v: Journal of Chemistry, Vol 2021 (2021)
This article describes the synthesis procedure of colloidal silicon quantum dot (Si QDs) from rice husk ash. The silicon quantum dots were capped with 1-octadecene by thermal hydrosilylation under argon gas to obtain octadecyl-Si QDs (ODE-Si QDs). Th
Externí odkaz: https://doaj.org/article/43b00f91e8ee4021891e57a1631cc832
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8
Akademický článek
De novo NIPBL Mutations in Vietnamese Patients with Cornelia de Lange Syndrome
Autor: Duong Chi Thanh, Can Thi Bich Ngoc, Ngoc-Lan Nguyen, Chi Dung Vu, Nguyen Van Tung, Huy Hoang Nguyen
Publikováno v: Medicina, Vol 56, Iss 2, p 76 (2020)
Cornelia de Lange Syndrome (CdLS) is a rare congenital genetic disease causing abnormal unique facial phenotypes, several defects in organs and body parts, and mental disorder or intellectual disorder traits. Main causes of CdLS have been reported as
Externí odkaz: https://doaj.org/article/24454f972f43466bbb86927fcfa7e697
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9
Akademický článek
The Role of p.Ser1105Ser (in NPHS1 Gene) and p.Arg548Leu (in PLCE1 Gene) with Disease Status of Vietnamese Patients with Congenital Nephrotic Syndrome: Benign or Pathogenic?
Autor: Nguyen Thi Kim Lien, Pham Van Dem, Nguyen Thu Huong, Tran Minh Dien, Ta Thi Thu Thuy, Nguyen Van Tung, Nguyen Huy Hoang, Nguyen Thi Quynh Huong
Publikováno v: Medicina, Vol 55, Iss 4, p 102 (2019)
Background and Objectives: Congenital nephrotic syndrome (CNS), a genetic disease caused by mutations in genes on autosomes, usually occurs in the first three months after birth. A number of genetic mutations in genes, which encode for the components
Externí odkaz: https://doaj.org/article/5d0268199b084ecf9dc2f66b79092407
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