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57. Lymphoblastoid cell lines as a model to understand amyotrophic lateral sclerosis disease mechanisms

58. HSC70 expression is reduced in lymphomonocytes of sporadic ALS patients and contributes to TDP-43 accumulation

60. Bioink Composition and Printing Parameters for 3D Modeling Neural Tissue

62. Nuclear Phospho-SOD1 Protects DNA from Oxidative Stress Damage in Amyotrophic Lateral Sclerosis

63. Leukocyte Derived Microvesicles as Disease Progression Biomarkers in Slow Progressing Amyotrophic Lateral Sclerosis Patients

64. RNA-Seq profiling in peripheral blood mononuclear cells of amyotrophic lateral sclerosis patients and controls

69. HSC70 expression is reduced in lymphomonocytes of sporadic ALS patients and contributes to TDP-43 accumulation.

71. A motor neuron strategy to save time and energy in neurodegeneration: adaptive protein stoichiometry

74. Long non-coding and coding RNAs characterization in Peripheral Blood Mononuclear Cells and Spinal Cord from Amyotrophic Lateral Sclerosis patients

76. Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

77. A Surveillance Function of the HSPB8-BAG3-HSP70 Chaperone Complex Ensures Stress Granule Integrity and Dynamism

78. Hydrogen peroxide-mediated induction of SOD1 gene transcription is independent from Nrf2 in a cellular model of neurodegeneration

79. From Transcriptome to Noncoding RNAs: Implications in ALS Mechanism

80. Corrigendum: mesoangioblast stem cells ameliorate muscle function in dystrophic dogs

81. Correction: Corrigendum: Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs

82. Altered Intracellular Localization of SOD1 in Leukocytes from Patients with Sporadic Amyotrophic Lateral Sclerosis

83. Correction: Corrigendum: Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs

85. Corrigendum: Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs

88. Chimeric Adeno-Associated Virus/Antisense U1 Small Nuclear RNA Effectively Rescues Dystrophin Synthesis and Muscle Function by Local Treatment of mdx Mice

89. Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

90. Hsp90‐mediated regulation of DYRK3 couples stress granule disassembly and growth via mTORC1 signaling

91. From Neuronal Differentiation of iPSCs to 3D Neural Organoids : Modeling of Neurodegenerative Diseases

92. Colchicine treatment in amyotrophic lateral sclerosis: safety, biological and clinical effects in a randomized clinical trial.

93. APOE 5'UTR Methylation Pattern Analysis in Blood and Brain Tissue from Alzheimer's Disease Affected Patients.

94. Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.

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