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The role of pyocyanin in Pseudomonas aeruginosa infection

Trends in molecular medicine, 2004-12, Vol.10 (12), p.599-606

2004

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Combination of acid β-glucosidase mutation and Saposin C deficiency in mice reveals Gba1 mutation dependent and tissue-specific disease phenotype

Scientific reports, 2019-04, Vol.9 (1), p.5571-5571, Article 5571

2019

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Neuronopathic Gaucher disease in the mouse: viable combined selective saposin C deficiency and mutant glucocerebrosidase (V394L) mice with glucosylsphingosine and glucosylceramide accumulation and progressive neurological deficits

Human molecular genetics, 2010-03, Vol.19 (6), p.1088-1097

2010

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Pseudomonas aeruginosa Pyocyanin Is Critical for Lung Infection in Mice

Infection and Immunity, 2004-07, Vol.72 (7), p.4275-4278

2004

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Properties of neurons derived from induced pluripotent stem cells of Gaucher disease type 2 patient fibroblasts: potential role in neuropathology

PloS one, 2015-03, Vol.10 (3), p.e0118771-e0118771

2015

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Isofagomine in vivo effects in a neuronopathic Gaucher disease mouse

PloS one, 2011-04, Vol.6 (4), p.e19037-e19037

2011

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Human Targets of Pseudomonas aeruginosa Pyocyanin

Proceedings of the National Academy of Sciences - PNAS, 2003-11, Vol.100 (24), p.14315-14320

2003

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Specific saposin C deficiency: CNS impairment and acid β-glucosidase effects in the mouse

Human molecular genetics, 2010-02, Vol.19 (4), p.634-647

2010

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Combined saposin C and D deficiencies in mice lead to a neuronopathic phenotype, glucosylceramide and α-hydroxy ceramide accumulation, and altered prosaposin trafficking

Human molecular genetics, 2007-04, Vol.16 (8), p.957-971

2007

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In vivo and ex vivo evaluation of L-type calcium channel blockers on acid beta-glucosidase in Gaucher disease mouse models

PloS one, 2009-10, Vol.4 (10), p.e7320-e7320

2009

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Neurological deficits and glycosphingolipid accumulation in saposin B deficient mice

Human molecular genetics, 2008-08, Vol.17 (15), p.2345-2356

2008

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Source Mechanism of the Ms 6.6 Xinyuan-Hejing Earthquake of June 30, 2012

中国地震研究（英文版）, 2015, Vol.29 (2), p.247-257

Ran Huimin Zhang Zhibin Zhao Qing

2015

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Temporal gene expression profiling reveals CEBPD as a candidate regulator of brain disease in prosaposin deficient mice

BMC neuroscience, 2008-08, Vol.9 (1), p.76-76, Article 76

2008

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Pseudomonas aeruginosa pyocyanin inactivates lung epithelial vaculoar ATPase‐dependent cystic fibrosis transmembrane conductance regulator expression and localization

Cellular microbiology, 2006-07, Vol.8 (7), p.1121-1133

2006

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Reversal of advanced disease in lysosomal acid lipase deficient mice: A model for lysosomal acid lipase deficiency disease

Molecular genetics and metabolism, 2014-07, Vol.112 (3), p.229-241

2014

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A Method on a Rapid Generation of Exquisite Textures of Building's Roof Towards Planning

Geomatics and Information Science of Wuhan University, 2015-08, Vol.40 (8), p.1054-1060

2015

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Tissue-specific effects of saposin A and saposin B on glycosphingolipid degradation in mutant mice

Human molecular genetics, 2013-06, Vol.22 (12), p.2435-2450

2013

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In Vivo and Ex Vivo Evaluation of L-Type Calcium Channel Blockers on Acid [beta]-Glucosidase in Gaucher Disease Mouse Models.(Research Article)

PloS one, 2009-10, Vol.4 (10), p.e7320

2009

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Pseudomonas aeruginosa pyocyanin inactivates lung epithelial vacuolar ATPase-dependent cystic fibrosis transmembrane conductance regulator expression and localization

Cellular microbiology, 2006-07, Vol.8 (7), p.1121-1133

2006

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Specific saposin C deficiency: CNS impairment and acid b-glucosidase effects in the mouse

Human molecular genetics, 2010-02, Vol.19 (4), p.634-647

2010

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137. In vivo evaluation of small molecule therapy on Gaucher disease mouse models

Molecular genetics and metabolism, 2009-02, Vol.96 (2), p.S42-S42

2009

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Properties of Neurons Derived from Induced Pluripotent Stem Cells of Gaucher Disease Type 2 Patient Fibroblasts: Potential Role in Neuropathology: e0118771

PloS one, 2015-03, Vol.10 (3)

2015

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Combined saposin C and D deficiencies in mice lead to a neuronopathic phenotype, glucosylceramide and [alpha]-hydroxy ceramide accumulation, and altered prosaposin trafficking

Human molecular genetics, 2007-04, Vol.16 (8), p.957

2007

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Specific saposin C deficiency: CNS impairment and acid -glucosidase effects in the mouse

Human molecular genetics, 2010-02, Vol.19 (4), p.634-647

2010

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Building biological foundries for next-generation synthetic biology

Science China. Life sciences, 2015-07, Vol.58 (7), p.658-665

2015

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The role of pyocyanin in Pseudomonas aeruginosa infection

Combination of acid β-glucosidase mutation and Saposin C deficiency in mice reveals Gba1 mutation dependent and tissue-specific disease phenotype

Neuronopathic Gaucher disease in the mouse: viable combined selective saposin C deficiency and mutant glucocerebrosidase (V394L) mice with glucosylsphingosine and glucosylceramide accumulation and progressive neurological deficits

Pseudomonas aeruginosa Pyocyanin Is Critical for Lung Infection in Mice

Properties of neurons derived from induced pluripotent stem cells of Gaucher disease type 2 patient fibroblasts: potential role in neuropathology

Isofagomine in vivo effects in a neuronopathic Gaucher disease mouse

Human Targets of Pseudomonas aeruginosa Pyocyanin

Specific saposin C deficiency: CNS impairment and acid β-glucosidase effects in the mouse

Combined saposin C and D deficiencies in mice lead to a neuronopathic phenotype, glucosylceramide and α-hydroxy ceramide accumulation, and altered prosaposin trafficking

In vivo and ex vivo evaluation of L-type calcium channel blockers on acid beta-glucosidase in Gaucher disease mouse models

Neurological deficits and glycosphingolipid accumulation in saposin B deficient mice

Source Mechanism of the Ms 6.6 Xinyuan-Hejing Earthquake of June 30, 2012

Temporal gene expression profiling reveals CEBPD as a candidate regulator of brain disease in prosaposin deficient mice

Pseudomonas aeruginosa pyocyanin inactivates lung epithelial vaculoar ATPase‐dependent cystic fibrosis transmembrane conductance regulator expression and localization

Reversal of advanced disease in lysosomal acid lipase deficient mice: A model for lysosomal acid lipase deficiency disease

A Method on a Rapid Generation of Exquisite Textures of Building's Roof Towards Planning

Tissue-specific effects of saposin A and saposin B on glycosphingolipid degradation in mutant mice

In Vivo and Ex Vivo Evaluation of L-Type Calcium Channel Blockers on Acid [beta]-Glucosidase in Gaucher Disease Mouse Models.(Research Article)

Pseudomonas aeruginosa pyocyanin inactivates lung epithelial vacuolar ATPase-dependent cystic fibrosis transmembrane conductance regulator expression and localization

Specific saposin C deficiency: CNS impairment and acid b-glucosidase effects in the mouse

137. In vivo evaluation of small molecule therapy on Gaucher disease mouse models

Properties of Neurons Derived from Induced Pluripotent Stem Cells of Gaucher Disease Type 2 Patient Fibroblasts: Potential Role in Neuropathology: e0118771

Combined saposin C and D deficiencies in mice lead to a neuronopathic phenotype, glucosylceramide and [alpha]-hydroxy ceramide accumulation, and altered prosaposin trafficking

Specific saposin C deficiency: CNS impairment and acid -glucosidase effects in the mouse

Building biological foundries for next-generation synthetic biology

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