Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Thanh Dat Ta"'
Autor:
Hung Manh Pham, Duy Phuong Dang, Thanh Dat Ta, Thi Phuong Le, Dinh Phong Phan, Hoai An Trinh, Tuan Viet Tran, Thi Lan Anh Luong, Ha Minh Nguyen, The‐Hung Bui, Thinh Huy Tran, Thanh Van Ta, Van‐Khanh Tran
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 12, Pp n/a-n/a (2023)
Abstract Background Brugada syndrome (BrS) is a rare genetic disease that causes sudden cardiac death (SCD) and arrhythmia. SCN5A pathogenic variants (about 30% of diagnosed patients) are responsible for BrS. Aims Lack of knowledge regarding molecula
Externí odkaz:
https://doaj.org/article/0f0b031ef8d4428c9c6d5ec81044eadf
Autor:
Dao Nguyen Ha Linh, Nguyen Van Huy, Phuoc‐Dung Nguyen, Phuong Le Thi, Hoang Anh Tuan, Trong Van Nguyen, Thu Ha Tran, Hai Anh Tran, Thanh Dat Ta, Tuan L. A. Pham, The‐Hung Bui, Thinh Huy Tran, Thanh Van Ta, Van‐Khanh Tran
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 11, Pp n/a-n/a (2023)
Abstract Background Retinoblastoma (RB), an intraocular malignancy commonly diagnosed in children, is mostly caused by inactivating mutations of both alleles of the RB1 gene. Early genetic screening for RB1 gene mutations would greatly improve treatm
Externí odkaz:
https://doaj.org/article/6aa8a8dd1de147cc936ffd732b2f07dd
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
Autor:
Nam‐Chung Tran, Tuan Anh Nguyen, Thanh Dat Ta, Thinh Huy Tran, Phuoc‐Dung Nguyen, Chi Dung Vu, Van‐Hung Nguyen, The‐Hung Bui, Thanh Van Ta, Van Khanh Tran
Publikováno v:
Clinical Case Reports, Vol 11, Iss 3, Pp n/a-n/a (2023)
Abstract Limb‐girdle muscular dystrophy‐type 2C (LGMD2C) is caused by mutations in the SGCG gene. Here, we report a case of a 26‐year‐old male who had inactive walking due to proximal muscle weakness. Targeted next‐generation sequencing fou
Externí odkaz:
https://doaj.org/article/a0cf2653b0764123ace118f3fbae2f31
Autor:
Thanh Dat Ta, Khanh Tran Van, Thanh Binh Nguyen, Manh Thuong Le, Long Ha Le Hai, Hoang Viet Nguyen
Publikováno v:
Vietnam Journal of Science, Technology and Engineering, Vol 65, Iss 1 (2023)
Major histocompatibility complex class I chain-related A (MICA) is a tumour antigen that is greatly expressed on the surfaces of human malignancies and infection cells, which trigger attachment to immune cells. Although many studies have investigated
Externí odkaz:
https://doaj.org/article/2af335f13f93447b93dad2973e3be6f6
Autor:
Thi Thao Ngo, Thinh Huy Tran, Thanh Dat Ta, Thi Phuong Le, Phuoc Dung Nguyen, Mai Anh Tran, The-Hung Bui, Thanh Van Ta, Van Khanh Tran
Publikováno v:
Anemia, Vol 2022 (2022)
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzyme disorder and is caused by G6PD gene mutations. To date, more than 400 variants in the G6PD gene have been discovered, and about 160 identified variants are associated with
Externí odkaz:
https://doaj.org/article/c8ef4384eb1547e5bc9d346e51db2b40
Autor:
Nam‐Chung Tran, Tuan Anh Nguyen, Thanh Dat Ta, Thinh Huy Tran, Phuoc‐Dung Nguyen, Chi Dung Vu, Van‐Hung Nguyen, The‐Hung Bui, Thanh Van Ta, Van Khanh Tran
Publikováno v:
Clinical Case Reports. 11
Comparative triple-color FISH mapping in eleven Senna species using rDNA and telomeric repeat probes
Autor:
Remnyl Joyce Pellerin, Nicole Bon Campomayor, Do Sin Lee, Thi Hong Nguyen, Hyun Hee Kim, Byung Yong Kang, Thanh Dat Ta, Nomar Espinosa Waminal
Publikováno v:
Horticulture, Environment, and Biotechnology. 62:927-935
Senna is a diverse and paraphyletic genus in the subfamily Caesalpinioideae (Fabaceae Lindl.) comprising various species of industrial and medicinal value. To date, the genome-based taxonomic relationship among several Senna species remains enigmatic
Autor:
Van Khanh Tran, Thinh Huy Tran, Thanh Van Ta, Duc Hinh Nguyen, Dung Chi Vu, Thanh Dat Ta, My Ha Cao, The-Hung Bui, Phuong Thi Le, Long Hoang Luong
Publikováno v:
American Journal of Medical Genetics Part A.
Acromesomelic dysplasias are rare skeletal disorders leading to severe short stature and abnormal skeletal morphology. Acromesomelic dysplasia Maroteaux-type is caused by homozygous or compound heterozygous pathogenic variants in NPR2 that encodes fo
Autor:
Thanh Van Ta, Hoai Quy Nguyen, Thanh Dat Ta, The-Hung Bui, Ha Thu Tran, Thi Mai Anh Dao, Thanh Thi Vu, Tung Son Nguyen, Long Hoang Luong, Van Khanh Tran, Huy Thinh Tran
Primary congenital glaucoma in Vietnam: analysis and identification of novel CYP1B1 variants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::169da47ab98d9feeb7f40fab49349542