Zobrazeno 1 - 10
of 149
pro vyhledávání: '"CHUNG-HSING WANG"'
Autor:
Yu-Wen Pan, Tsung-Ying Ou, Yen-Yin Chou, Pao-Lin Kuo, Hui-Pin Hsiao, Pao-Chin Chiu, Ju-Li Lin, Fu-Sung Lo, Chung-Hsing Wang, Peng-Chieh Chen, Meng-Che Tsai
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-11 (2024)
Abstract Background Syndromic ciliopathies are a group of congenital disorders characterized by broad clinical and genetic overlap, including obesity, visual problems, skeletal anomalies, mental retardation, and renal diseases. The hallmark of the pa
Externí odkaz:
https://doaj.org/article/73060ee9b5c9490996048dfd21858c78
Autor:
Chung-Hsing Wang, Yu‐Nan Huang, Wen-Ling Liao, Ai-Ru Hsieh, Wei-De Lin, Kai-Wen Liu, Wen-Li Lu, Chieh‐Chen Huang, Yin-Hsiu Chien, Ni-Chung Lee, Pen-Hua Su, Fuu-Jen Tsai
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-16 (2024)
Abstract Background Osteoporosis and its primary complication, fragility fractures, contribute to substantial global morbidity and mortality. Gaucher disease (GD) is caused by glucocerebrosidase (GBA1) deficiency, leading to skeletal complications. T
Externí odkaz:
https://doaj.org/article/0c1baf8b9b3b4b928fe4f713814a049b
Publikováno v:
Pediatrics and Neonatology, Vol 65, Iss 1, Pp 64-70 (2024)
Background: Recent studies have demonstrated a global decline in the age at menarche. Our study aimed to determine the age at menarche of Taiwanese women born between 1943 and 1989. Methods: Data were obtained from the Taiwan Biobank. To view the tre
Externí odkaz:
https://doaj.org/article/d571665b4d93417a883d538c0ca98f94
Autor:
Wen-Li Lu, Yin-Hsiu Chien, Fuu-Jen Tsai, Wuh-Liang Hwu, Yen-Yin Chou, Shao-Yin Chu, Meng-Ju Li, An-Ju Lee, Chao-Chuan Liao, Chung-Hsing Wang, Ni-Chung Lee
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-11 (2023)
Abstract Background Gaucher disease (GD) is a lysosomal storage disorder characterized by deficient glucocerebrosidase activity that results from biallelic mutations in the GBA1 gene. Its phenotypic variability allows GD to be classified into 3 subty
Externí odkaz:
https://doaj.org/article/5f203ea9af2e4503addb3c547dbeafed
Publikováno v:
Pediatrics and Neonatology, Vol 64, Iss 4, Pp 465-467 (2023)
Externí odkaz:
https://doaj.org/article/945bb443e3024c42bbbc75848dd0a7e4
Autor:
Jian-Shiun Chiou, Chi-Fung Cheng, Wen-Miin Liang, Chen-Hsing Chou, Chung-Hsing Wang, Wei-De Lin, Mu-Lin Chiu, Wei-Chung Cheng, Cheng-Wen Lin, Ting-Hsu Lin, Chiu-Chu Liao, Shao-Mei Huang, Chang-Hai Tsai, Ying-Ju Lin, Fuu-Jen Tsai
Publikováno v:
BMC Medicine, Vol 20, Iss 1, Pp 1-23 (2022)
Abstract Background Height is an important anthropometric measurement and is associated with many health-related outcomes. Genome-wide association studies (GWASs) have identified hundreds of genetic loci associated with height, mainly in individuals
Externí odkaz:
https://doaj.org/article/c0a57999fd1d4fc5b21762c8a676995e
Publikováno v:
Children, Vol 10, Iss 8, p 1351 (2023)
Background: Individuals with Down syndrome are at a higher risk of cardiac, renal, and other health issues due to a complex disease physiology. However, few data exist on long-term disease risks to guide prevention and care. We aimed to determine the
Externí odkaz:
https://doaj.org/article/b4a9722380644b6daded52dee460f164
Autor:
Yen-Hua Huang, Tzu-Chien Su, Chung-Hsing Wang, Siew-Lee Wong, Yin-Hsiu Chien, Yu-Tai Wang, Wuh-Liang Hwu, Ni-Chung Lee
Publikováno v:
Scientific Data, Vol 8, Iss 1, Pp 1-7 (2021)
Measurement(s) RNA-Seq • RNA Technology Type(s) Illumina HiSeq. 2500 • RNA sequencing Sample Characteristic - Organism Homo sapiens Machine-accessible metadata file describing the reported data: https://doi.org/10.6084/m9.figshare.15022521
Externí odkaz:
https://doaj.org/article/dfd184f6e423491a94f604ea86e277d6
Autor:
Ni-Chung Lee, Yin-Hsiu Chien, Chung-Hsing Wang, Siew-Lee Wong, Steven Shinn-Forng Peng, Fuu-Jen Tsai, Wuh-Liang Hwu
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 31, Iss , Pp 100867- (2022)
Patients with Gaucher disease type 3 (GD3), especially those with GBA p.L444P homozygous mutation, often suffer from complications including lymphadenopathy even under regular enzyme replacement therapy (ERT). In order to improve their outcome, we ad
Externí odkaz:
https://doaj.org/article/9efc48fb07074a09b1aa6e13abc647fc
Autor:
Chung-Hsing Wang, Hung-Rong Yen, Wen-Li Lu, Hsieh-Hsun Ho, Wen-Yang Lin, Yi-Wei Kuo, Yen-Yu Huang, Shin-Yu Tsai, Hung-Chih Lin
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
IntroductionType 1 diabetes mellitus (T1DM) is characterized by autoimmune destruction of pancreatic β cells. Previous study has discovered that probiotic strains residing in the gut play essential roles in host immune regulation. However, few clini
Externí odkaz:
https://doaj.org/article/5d8e15e74e6349bf932e977b2d5f24c7