Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Min-Ju Chan"'
Autor:
Chih-Kuang Chuang, Hsiang-Yu Lin, Tuan-Jen Wang, You-Hsin Huang, Min-Ju Chan, Hsuan-Chieh Liao, Yun-Ting Lo, Li-Yun Wang, Ru-Yi Tu, Yi-Ya Fang, Tzu-Lin Chen, Hui-Chen Ho, Chuan-Chi Chiang, Shuan-Pei Lin
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-14 (2018)
Abstract Background Mucopolysaccharidoses (MPS) are lysosomal storage diseases in which mutations of genes encoding for lysosomal enzymes cause defects in the degradation of glycosaminoglycans (GAGs). The accumulation of GAGs in lysosomes results in
Externí odkaz:
https://doaj.org/article/e244afb1161b4788b8a01e337d90fa30
Autor:
Min-Ju Chan, 詹旻儒
99
When the consumer electronic products will be more lightweight and portable, the conception of system-on-chip (SoC) technology is widely used. Therefore, the network-on-chip (NoC) becomes the key technology for enhancing the overall performan
When the consumer electronic products will be more lightweight and portable, the conception of system-on-chip (SoC) technology is widely used. Therefore, the network-on-chip (NoC) becomes the key technology for enhancing the overall performan
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/04548035294127082441
Autor:
Yi-Ya Fang, Tzu-Lin Chen, Tuan-Jen Wang, Li-Yun Wang, Hsuan-Chieh Liao, You-Hsin Huang, Chuan-Chi Chiang, Ru-Yi Tu, Yun-Ting Lo, Min-Ju Chan, Chih-Kuang Chuang, Shuan-Pei Lin, Hui-Chen Ho, Hsiang-Yu Lin
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-14 (2018)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Mucopolysaccharidoses (MPS) are lysosomal storage diseases in which mutations of genes encoding for lysosomal enzymes cause defects in the degradation of glycosaminoglycans (GAGs). The accumulation of GAGs in lysosomes results in cellular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54c45075cd749336a1d86300c5d121ca
http://link.springer.com/article/10.1186/s13023-018-0816-4
http://link.springer.com/article/10.1186/s13023-018-0816-4
Autor:
Hsuan-Chieh Liao, Chia-Feng Yang, Chun Kai Huang, Dau-Ming Niu, Michael H. Gelb, Min-Ju Chan, Chuan-Chi Chiang
BACKGROUND Deficiency of the lysosomal enzyme acid α-glucosidase (GAA) causes Pompe disease. Newborn screening for Pompe disease is ongoing, and improved methods for distinguishing affected patients from those with pseudodeficiency, especially in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dda452e9d5b6be3432aed4c1d255cac4
https://europepmc.org/articles/PMC5524447/
https://europepmc.org/articles/PMC5524447/
Autor:
Wei De Lin, Hsuan-Chieh Liao, Hao Chuan Liu, Chung Hsing Wang, Fuu Jen Tsai, Chuan Chi Chiang, Min Ju Chan, Yann Jang Chen, He Jin Gao, Shu Min Kao, Chia Feng Yang, Yu Hsiu Huang, Chun Kai Huang, Dau Ming Niu
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 431
Background Interest in lysosomal storage diseases in newborn screening programs has increased in recent years. Two techniques, fluorescence (4-MU) and tandem mass spectrometry (MS/MS) methods are frequently used. We report a pilot study of large scal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7baaa7cd42392f0157239e85a4b9cf0
https://pubmed.ncbi.nlm.nih.gov/24513544
https://pubmed.ncbi.nlm.nih.gov/24513544
Autor:
Hsuan-Chieh Liao, Min-Ju Chan, Chia-Feng Yang, Chuan-Chi Chiang, Dau-Ming Niu, Chun-Kai Huang, Gelb, Michael H.
Publikováno v:
Clinical Chemistry; 2017, Vol. 63 Issue 7, p1271-1277, 7p, 2 Graphs
Autor:
Min-Ju Chan, Chun-Lung Hsu
Publikováno v:
2010 IEEE 25th International Symposium on Defect & Fault Tolerance in VLSI Systems (DFT); 2010, p122-128, 7p
Autor:
Min Ju Chan, 詹閔茹
99
Background：Studies of dysgraphic and normal individuals have led to several hypotheses regarding how neural substrates function when the brain is engaged in writing. Three brain regions compose what has been regarded as the “writing cente
Background：Studies of dysgraphic and normal individuals have led to several hypotheses regarding how neural substrates function when the brain is engaged in writing. Three brain regions compose what has been regarded as the “writing cente
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/40866629041216926166