Zobrazeno 1 - 10
of 4 298
pro vyhledávání: '"Chung Lee"'
Publikováno v:
Fulbright Review of Economics and Policy, Vol 4, Iss 2, Pp 180-203 (2024)
Purpose – This study employs advanced modelling to assess the effectiveness of Malaysia’s current energy policies in achieving a low-carbon future. By optimising a 100% renewable energy mix, including energy storage, the research identifies pathw
Externí odkaz:
https://doaj.org/article/90e6be7b34b045f0b22ff1af4bbb75c1
Autor:
Paulina G. Karim, Kuang-Chung Lee
Publikováno v:
Parks, Vol 30, Iss 2, Pp 78-84 (2024)
Landscape approaches have been recognised as an effective solution for reconciling conservation and developmental demands at local scales. Though suitable in various contexts of human-nature interactions, their application is increasingly considered
Externí odkaz:
https://doaj.org/article/39c8ec7bfafb419e96854fd95accff8e
Autor:
Brooke K. Hayes, Marina Harper, Hariprasad Venugopal, Jessica M. Lewis, Amy Wright, Han-Chung Lee, Joel R. Steele, David L. Steer, Ralf B. Schittenhelm, John D. Boyce, Sheena McGowan
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-15 (2024)
Abstract The type VI secretion system (T6SS) is a molecular machine utilised by many Gram-negative bacteria to deliver antibacterial toxins into adjacent cells. Here we present the structure of Tse15, a T6SS Rhs effector from the nosocomial pathogen
Externí odkaz:
https://doaj.org/article/8ac7eabc625b428f98ca3d2616a6f181
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 63, Iss 5, Pp 771-776 (2024)
Objective: To present the ultrasound imaging and genetic diagnosis of a fetus with prenatal lethal form of Gaucher disease. Case report: A 37-year-old primiparous woman was pregnant at her 23 weeks of gestation and the prenatal fetal ultrasound revea
Externí odkaz:
https://doaj.org/article/843b99fd417a415daf64d3afa2e76e0f
Publikováno v:
Kaohsiung Journal of Medical Sciences, Vol 40, Iss 9, Pp 780-788 (2024)
Abstract The gut microbiota undergoes substantial development from birth, and its development in the initial years of life has a potentially lifelong effect on the health of the individual. However, various factors can disrupt the development of the
Externí odkaz:
https://doaj.org/article/58d2304524a64def992b06dceb75ce2f
Autor:
Kon-Ping Lin, Chih-Chao Yang, Yi-Chung Lee, Ming-Jen Lee, John Vest, Marianne T. Sweetser, Matthew T. White, Prajakta Badri, Sung-Tsang Hsieh, Chi-Chao Chao
Publikováno v:
Journal of the Formosan Medical Association, Vol 123, Iss 9, Pp 975-984 (2024)
Background: To examine the efficacy and safety of patisiran, an RNA interference therapeutic, in patients from Taiwan with hereditary transthyretin-mediated (hATTR) amyloidosis with polyneuropathy. Methods: The APOLLO phase 3 trial included patients
Externí odkaz:
https://doaj.org/article/dab5699cac1045209b1a2938728fe680
Autor:
Hsiang-Ting Hsu, Hui-Chen Cheng, Tsung-Wei Hou, Yi-Shiang Tzeng, Jong-Ling Fuh, Shih-Pin Chen, Wei-Ta Chen, Wei-Ju Lee, Yen-Wei Pai, Yi-Chung Lee, Jiing-Feng Lirng, Shuu-Jiun Wang, Yen-Feng Wang
Publikováno v:
The Journal of Headache and Pain, Vol 25, Iss 1, Pp 1-11 (2024)
Abstract Background There have been limited data on idiopathic intracranial hypertension (IIH) in Asians and there remain uncertainties whether a cerebrospinal fluid (CSF) pressure of 250 mm CSF is an optimum diagnostic cutoff. The aims of the presen
Externí odkaz:
https://doaj.org/article/0c0ab929731e4aa7b85e2dc389dc86dd
Autor:
Cheng‐Tsung Hsiao, Tzu‐Yun Tsai, Ting‐Yi Shen, Yu‐Shuen Tsai, Yi‐Chu Liao, Yi‐Chung Lee, Pei‐Chien Tsai
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 7, Pp 1909-1920 (2024)
Abstract Objective TFG mutations have previously been implicated in autosomal recessive hereditary spastic paraplegia (HSP), also known as SPG57. This study aimed to investigate the clinical and molecular features of TFG mutations in a Taiwanese HSP
Externí odkaz:
https://doaj.org/article/283eded396fc435b9379fe01b6dea680
Publikováno v:
Journal of Dental Sciences, Vol 19, Iss 3, Pp 1868-1871 (2024)
Externí odkaz:
https://doaj.org/article/4e9a6befef20414b85393354828706e1
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 41, Iss , Pp 101137- (2024)
D-bifunctional protein (DBP) deficiency, a fatal peroxisomal enzyme disorder, typically manifests with life-threatening symptoms in the first two years of childhood. We present the case of an infant with elevated lysophosphatidylcholine C26:0 (C26:0-
Externí odkaz:
https://doaj.org/article/2da7e6b5faca47eaa114a5d2837c79cb