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51. Lipocalin 2 is present in the EAE brain and is modulated by natalizumab

52. Transcriptome signature of the adult mouse choroid plexus

53. Human-specific transcriptional regulation of CNS development genes by FOXP2

54. BAC Transgenic Expression of Human TREM2-R47H Remodels Amyloid Plaques but Unable to Reprogram Plaque-associated Microglial Reactivity in 5xFAD Mice

60. Mapping brain gene coexpression in daytime transcriptomes unveils diurnal molecular networks and deciphers perturbation gene signatures

62. Generation of a molecular interactome of the glioblastoma perivascular niche reveals Integrin Binding Sialoprotein as a key mediator of tumor cell migration

63. IAPP-induced beta cell stress recapitulates the islet transcriptome in type 2 diabetes

65. Mitochondria-Targeted Cholesterol Oximes Increase Dopamine-Related Gene Expression and Behavior in Mice Over-Expressing Alpha-Synuclein, a Model of Pre-Manifest Parkinson’s Disease

67. A Molecular Interactome of the Glioblastoma Perivascular Niche Reveals Integrin Binding Sialoprotein as a Key Mediator of Tumor Cell Migration

71. Serotonergic modulation of visual neurons in Drosophila melanogaster

72. AD-linked R47H-TREM2mutation induces disease-enhancing proinflammatory microglial states in mice and humans

73. Type 2 Diabetes is a Beta Cell Protein Misfolding Disease

74. Serotonergic modulation of visual neurons inDrosophila melanogaster

76. AD-Linked TREM2 Mutation Induces Unique Microglial States Associated with Toxic Function in Tauopathy

78. C. elegansgranulins promote an age-associated decline in protein homeostasis via lysosomal protease inhibition

81. A molecular cascade modulates MAP1B and confers resistance to mTOR inhibition in human glioblastoma

83. Robust axonal regeneration occurs in the injured CAST/Ei mouse central nervous system

84. Decoding the Long Noncoding RNA During Cardiac Maturation: A Roadmap for Functional Discovery.

85. Decoding the Long Noncoding RNA During Cardiac Maturation

86. CRISPR-Cas9 targeted deletion of the C9orf72 repeat expansion mutation corrects cellular phenotypes in patient-derived iPS cells

87. Characterization of expression quantitative trait loci in extensively phenotyped pedigrees ascertained for bipolar disorder

88. Mutation of Senataxin Alters Disease-Specific Transcriptional Networks in Patients with Ataxia with Oculomotor Apraxia Type 2 (P2.126)

89. Chronic administration of cholesterol oximes in mice increases transcription of cytoprotective genes and improves transcriptome alterations induced by alpha-synuclein overexpression in nigrostriatal dopaminergic neurons

91. Accelerating axonal growth promotes motor recovery after peripheral nerve injury in mice

95. Multiple sclerosis and iron homeostasis

97. Functional Genomic Analyses Identify Pathways Dysregulated by Progranulin Deficiency, Implicating Wnt Signaling

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