Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Hui-Zhi Zhao"'
Publikováno v:
Journal of International Medical Research, Vol 48 (2020)
The sudden outbreak of severe acute respiratory syndrome coronavirus 2 pneumonia posed a significant challenge to medical professionals because treatment of critically ill patients requires the efforts of a multidisciplinary team. To highlight this p
Externí odkaz:
https://doaj.org/article/427bad9ed3db417eb3ed610f7b8287fa
Publikováno v:
PLoS ONE, Vol 7, Iss 1 (2012)
Externí odkaz:
https://doaj.org/article/ac0b6fffdf2c42ffa6cf1d9fe1edd99d
Publikováno v:
PLoS ONE, Vol 6, Iss 11, p e27461 (2011)
Sanfilippo syndrome type B (MPS IIIB) is characterized by profound mental retardation in childhood, dementia and death in late adolescence; it is caused by deficiency of α-N-acetylglucosaminidase and resulting lysosomal storage of heparan sulfate. A
Externí odkaz:
https://doaj.org/article/ca1182ff83834bcdbb3bb7ef938c24e2
Publikováno v:
Nephrology. 24:1009-1016
Aim Pulmonary infection (PI) is the leading cause of death in patients with primary membranous nephropathy on immunosuppressive therapy. A rating score was thus developed to foresee the risk of PI in such patients. Methods We reviewed the charts of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31a9b2e97dd69831f3db6e3413bd0913
https://doi.org/10.1111/nep.13544
https://doi.org/10.1111/nep.13544
Publikováno v:
Applied Mechanics and Materials. :2638-2642
Acoustic wave can cause particle vibration in the process of transmission and the energy consumption gradually, and the acoustic wave amplitude will attenuation. Through analysising the propagation path of acoustic wave in the layer media in the proc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75dda6cff2aafc1055a5793413956d48
https://doi.org/10.4028/www.scientific.net/amm.229-231.2638
https://doi.org/10.4028/www.scientific.net/amm.229-231.2638
Publikováno v:
Journal of Neuroscience Research. 69:30-38
Sanfilippo syndrome type B (MPS III B) is a neurodegenerative disorder characterized by profound mental retardation and early death. It is caused by deficiency of a lysosomal enzyme involved in heparan sulfate (HS) degradation. Because HS accumulatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b50a00ae4ac434934bd31e6dd74ea1c7
https://doi.org/10.1002/jnr.10278
https://doi.org/10.1002/jnr.10278
Autor:
Kunihiko Suzuki, Elizabeth F. Neufeld, Wei-Hong Yu, Stephan G. Anagnostaras, Karen M. Lyons, Hui-Zhi Zhao, Marie T. Vanier, Nora Rozengurt, Michael S. Fanselow, Hong Hua Li
Publikováno v:
Proceedings of the National Academy of Sciences. 96:14505-14510
The Sanfilippo syndrome type B is an autosomal recessive disorder caused by mutation in the gene ( NAGLU ) encoding α- N -acetylglucosaminidase, a lysosomal enzyme required for the stepwise degradation of heparan sulfate. The most serious manifestat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f43b90439b76186023df77280f42737
https://doi.org/10.1073/pnas.96.25.14505
https://doi.org/10.1073/pnas.96.25.14505
Autor:
Phuong T. Tieu, Zhaoyang Zhao, Hong G. Zhao, David A. Greenberg, Hui Zhi Zhao, Artur Schmidtchen, Paola Di Natale, Elizabeth F. Neufeld, Yan Huang, Hong Hua Li, Samson Cheng, Chester B. Whitley
Publikováno v:
The American Journal of Human Genetics. 62:64-69
Sanfilippo syndrome type B (mucopolysaccharidosis III B) is a rare autosomal recessive disease caused by deficiency of alpha-N-acetylglucosaminidase, one of the enzymes required for the lysosomal degradation of heparan sulfate. The gene for this enzy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae62f1ec2cff83a73ff6d4d60ecb0916
https://doi.org/10.1086/301685
https://doi.org/10.1086/301685
Autor:
Kazuhiro Ohmi, Elizabeth F. Neufeld, Stanislav L. Karsten, Lili C. Kudo, Hui-Zhi Zhao, Sergey Ryazantsev
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 106(20)
Sanfilippo syndrome type B (mucopolysaccharidosis III B, MPS III B) is an autosomal recessive, neurodegenerative disease of children, characterized by profound mental retardation and dementia. The primary cause is mutation in the NAGLU gene, resultin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::339986ea4a3a280f790dfa15fa5b586e
https://pubmed.ncbi.nlm.nih.gov/19416848
https://pubmed.ncbi.nlm.nih.gov/19416848
The neurodegenerative disease MPS III B (Sanfilippo syndrome type B) is caused by mutations in the gene encoding the lysosomal enzyme α- N -acetylglucosaminidase, with a resulting block in heparan sulfate degradation. A mouse model with disruption o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6299156add34e6814368c4e486222d62
https://europepmc.org/articles/PMC1892176/
https://europepmc.org/articles/PMC1892176/
