Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Chi‐Bao Bui"'
Autor:
Yen Thi My Nguyen, Bao-Quoc Vu, Duy-Khai Nguyen, Ngoc-Vinh Quach, Liem Thanh Bui, Jeonghan Hong, Chi-Bao Bui
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-13 (2024)
Abstract Neonatal intensive care unit (NICU), particularly in treating developmental and epileptic encephalopathy (DEE) and metabolic epilepsy (ME), requires a deep understanding of their complex etiologies and treatment responses. After excluding tr
Externí odkaz:
https://doaj.org/article/82f123a85d2440b7ba55d63af1b5887e
Altered skin microbiome, inflammation, and JAK/STAT signaling in Southeast Asian ichthyosis patients
Autor:
Minh Ho, Huynh-Nga Nguyen, Minh Van Hoang, Tien Thuy Thi Bui, Bao-Quoc Vu, Truc Huong Thi Dinh, Hoa Thi My Vo, Diana C. Blaydon, Sherif A. Eldirany, Christopher G. Bunick, Chi-Bao Bui
Publikováno v:
Human Genomics, Vol 18, Iss 1, Pp 1-23 (2024)
Abstract Background Congenital ichthyosis (CI) is a collective group of rare hereditary skin disorders. Patients present with epidermal scaling, fissuring, chronic inflammation, and increased susceptibility to infections. Recently, there is increased
Externí odkaz:
https://doaj.org/article/c266ef2f01f948169fd063d60f778cb7
Autor:
Anh Nguyen Lien Phan, Thuy Thi Thanh Pham, Xinh Thi Phan, Nghia Huynh, Tuan Minh Nguyen, Cuc Tran Thu Cao, Duong Thuy Nguyen, Khanh Thi Xuan Luong, Tam Thi Minh Nguyen, Anh Ngoc Kim Tran, Linh Thi Truc Pham, Vy Vuong Thao Nguyen, Sigrid Swagemakers, Chi‐Bao Bui, Petrus Martinus Van Hagen
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 8, Pp n/a-n/a (2021)
Abstract Background X‐linked hyper‐IgM syndrome (XHIGM) is a rare primary immunodeficiency caused by CD40 ligand defects. Methods We identified three patients with XHIGM in Ho Chi Minh City, Vietnam. Whole‐exome sequencing, immunological analys
Externí odkaz:
https://doaj.org/article/0ec76ae80e114e07ab80a8c6c31d35d3
Autor:
Anh N. L. Phan, Thuy T. T. Pham, Nghia Huynh, Tuan M. Nguyen, Cuc T. T. Cao, Duong T. Nguyen, Duc T. Le, Chi‐Bao Bui
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 5, Pp n/a-n/a (2020)
Abstract Background Lipopolysaccharide‐responsive and beige‐like anchor (LRBA) deficiency is a rare autosomal recessive common variable immunodeficiency (CVID), affecting 1:25,000–1:50,000 people worldwide. Biallelic mutations in the gene LRBA
Externí odkaz:
https://doaj.org/article/8bde6b5ce82d483bbbbca531205f69f2
Autor:
Van-Linh Nguyen, Cong-Tri Truong, Binh Cao Quan Nguyen, Thanh-Niem Van Vo, Trong-Thuc Dao, Van-Dan Nguyen, Dieu-Thuong Thi Trinh, Hieu Kim Huynh, Chi-Bao Bui
Publikováno v:
PLoS ONE, Vol 12, Iss 10, p e0185674 (2017)
Due to the high-cost and limitations of current wound healing treatments, the search for alternative approaches or drugs, particularly from medicinal plants, is of key importance. In this study, we report anti-inflammatory and wound healing activitie
Externí odkaz:
https://doaj.org/article/0702f89657914db0a41d09a03135912e
Autor:
Minh Hiep Nguyen, Nguyen Thanh Tung Vu, Manh Cong Nguyen, Vuong Thao Vy Nguyen, Chi Bao Bui, Thi Huynh Nga Nguyen
Publikováno v:
Biomedical Research and Therapy. 9:4822-4831
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::525492b7a7000ba6e111db175db3195a
https://doi.org/10.15419/bmrat.v9i1.719
https://doi.org/10.15419/bmrat.v9i1.719
Publikováno v:
Biomedical Research and Therapy. 8:4809-4817
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::edcd62fd06f7c5b12747bffac2aa3ee6
https://doi.org/10.15419/bmrat.v8i12.717
https://doi.org/10.15419/bmrat.v8i12.717
Altered skin microbiome, inflammation, and JAK/STAT signaling in Southeast Asian ichthyosis patients
Autor:
Minh Ho, Huynh-Nga Nguyen, Minh Van Hoang, Tien Thuy Thi Bui, Bao-Quoc Vu, Truc Huong Thi Dinh, Vo Hoa Thi My, Diana Blaydon, Sherif A. Eldirany, Christopher G. Bunick, Chi-Bao Bui
Cutaneous ichthyosis (CI) is a collective group of monogenetic disorders of cornification demonstrating epidermal scaling, fissuring, chronic skin inflammation, and increased susceptibility to infection. In healthy individuals the skin microbiome lim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5ee536e43f70776a1fe4c812e8e88b2
https://doi.org/10.1101/2022.08.02.22277646
https://doi.org/10.1101/2022.08.02.22277646
Autor:
Chi-Bao Bui, Thao Thi Phuong Duong, Vien The Tran, Thuy Thanh T. Pham, Tung Vu, Gia Cac Chau, Thanh-Niem Van Vo, Vinh Nguyen, Dieu-Thuong Thi Trinh, Minh Van Hoang
Publikováno v:
Human Genome Variation, Vol 7, Iss 1, Pp 1-8 (2020)
Human Genome Variation
Human Genome Variation
Xeroderma pigmentosum (XP) group D, a severe disease often typified by extreme sun sensitivity, can be caused by ERCC2 mutations. ERCC2 encodes an adenosine triphosphate (ATP)-dependent DNA helicase, namely XP group D protein (XPD). The XPD, one of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::695b92bea337e97b144f967af6ea05d7
http://link.springer.com/article/10.1038/s41439-020-0089-z
http://link.springer.com/article/10.1038/s41439-020-0089-z
Publikováno v:
Epilepsy Research. 190:107094
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0881d5c1f9f68a4cbf96f6ad94aa8fe
https://doi.org/10.1016/j.eplepsyres.2023.107094
https://doi.org/10.1016/j.eplepsyres.2023.107094