Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Han-Zhi Rao"'
Autor:
Shunchuan Zhang, Lauren E Springer, Han-Zhi Rao, Renee G Espinosa Trethewy, Lindsey M Bishop, Meaghan H Hancock, Finn Grey, Christopher M Snyder
Publikováno v:
PLoS Pathogens, Vol 17, Iss 1, p e1009255 (2021)
Cytomegalovirus (CMV) causes clinically important diseases in immune compromised and immune immature individuals. Based largely on work in the mouse model of murine (M)CMV, there is a consensus that myeloid cells are important for disseminating CMV f
Externí odkaz:
https://doaj.org/article/2f6f486f74ff4dc9bae97d0eadfcc6a2
Autor:
Renee G. Espinosa Trethewy, Shunchuan Zhang, Lindsey M. Bishop, Meaghan H. Hancock, Finn Grey, Lauren E. Springer, Han Zhi Rao, Christopher M. Snyder
Publikováno v:
PLoS Pathogens, Vol 17, Iss 1, p e1009255 (2021)
PLoS Pathogens
Zhang, S, Springer, L E, Rao, H-Z, Espinosa Trethewy, R G, Bishop, L M, Hancock, M H, Grey, F & Snyder, C M 2021, ' Hematopoietic cell-mediated dissemination of murine cytomegalovirus is regulated by NK cells and immune evasion ', PLoS Pathogens, vol. 17, no. 1, e1009255 . https://doi.org/10.1371/journal.ppat.1009255
PLoS Pathogens
Zhang, S, Springer, L E, Rao, H-Z, Espinosa Trethewy, R G, Bishop, L M, Hancock, M H, Grey, F & Snyder, C M 2021, ' Hematopoietic cell-mediated dissemination of murine cytomegalovirus is regulated by NK cells and immune evasion ', PLoS Pathogens, vol. 17, no. 1, e1009255 . https://doi.org/10.1371/journal.ppat.1009255
Cytomegalovirus (CMV) causes clinically important diseases in immune compromised and immune immature individuals. Based largely on work in the mouse model of murine (M)CMV, there is a consensus that myeloid cells are important for disseminating CMV f
Publikováno v:
Molecular Therapy. 23:1681-1690
Krabbe disease is an autosomal recessive disorder resulting from defects in the lysosomal enzyme galactocerebrosidase (GALC). GALC deficiency leads to severe neurological features. The only treatment for presymptomatic infantile patients and later-on
Publikováno v:
Molecular Genetics and Metabolism. 114:459-466
Globoid cell leukodystrophy (GLD) or Krabbe disease is an autosomal recessive disorder resulting from the defective lysosomal enzyme galactocerebrosidase (GALC). The lack of GALC enzyme leads to severe neurological symptoms. While most human patients
Publikováno v:
Molecular and Cellular Neuroscience. 30:398-407
Psychosine (galactosylsphingosine) is a toxic metabolite that accumulates in globoid cell leukodystrophy (GLD) due to the deficiency of galactocerebrosidase (GALC) activity. This results in subsequent programmed cell death of oligodendrocytes and dem
Autor:
Paola Luzi, Marie T. Vanier, Han Zhi Rao, Mohammad A. Rafi, Mark T. Curtis, David A. Wenger, Mariam Zaka
Publikováno v:
Molecular Genetics and Metabolism. 86:150-159
Globoid cell leukodystrophy (GLD) is a disorder of the central and peripheral nervous systems caused by the deficiency of the lysosomal enzyme galactocerebrosidase (GALC). The pathological changes associated with the disease include accumulation of g
Publikováno v:
Neurochemical Research. 29:881-889
In order to investigate a role for insulin-like growth factor-1 (IGF-1) in ameliorating the effects of demyelinating events and potentiating remyelination, we have generated transgenic (tg) mice expressing IGF-1 under the control of the myelin basic
Publikováno v:
Gene. 530(2)
Metachromatic leukodystrophy (MLD) is a lysosomal storage disorder caused mainly by mutations in the arylsulfatase A (ARSA) gene. In this manuscript we report sixteen novel mutations identified in the ARSA gene of fifteen unrelated patients affected
Publikováno v:
Molecular therapy : the journal of the American Society of Gene Therapy. 20(11)
Globoid cell leukodystrophy (GLD) or Krabbe disease is a neurodegenerative disorder caused by the deficiency of the lysosomal enzyme galactocerebrosidase (GALC). This deficiency results in accumulation of certain galactolipids including psychosine wh
Publikováno v:
Molecular Therapy. 13
Globoid cell leukodystrophy (GLD) or Krabbe disease is a neurodegenerative disorder that affects both the central and peripheral nervous system (CNS and PNS). The deficiency of the lysosomal enzyme galactocerebrosidase (GALC) leads to the accumulatio