94 results on '"Pansarasa, Orietta"'
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52. 3D Printed Conductive Nanocellulose Scaffolds for the Differentiation of Human Neuroblastoma Cells
53. Brain Oxidative Damage Following Acute Immobilization and Mild Emotional Stress
54. ACTIN SLIDING VELOCITY ON PURE MYOSIN ISOFORMS FROM DYSTROPHIC MOUSE MUSCLES
55. Structural and functional alterations of muscle fibres in the novel mouse model of facioscapulohumeral muscular dystrophy
56. Oxidative Damage after Severe Head Injury and Its Relationship to Neurological Outcome
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
59. Altered immune system in frailty: Genetics and diet may influence inflammation
60. Bioink Composition and Printing Parameters for 3D Modeling Neural Tissue
61. HuR interacts with lincBRN1a and lincBRN1b during neuronal stem cells differentiation
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
65. From Neuronal Differentiation of iPSCs to 3D Neuro-Organoids: Modelling and Therapy of Neurodegenerative Diseases
66. Curcumin and Novel Synthetic Analogs in Cell-Based Studies of Alzheimer’s Disease
67. Long non coding RNAs and ALS: Still much to do
68. Antioxidant pathways in human aged skeletal muscle: relationship with the distribution of type II fibers
69. HSC70 expression is reduced in lymphomonocytes of sporadic ALS patients and contributes to TDP-43 accumulation.
70. A pilot study assessing T1-weighted muscle MRI in amyotrophic lateral sclerosis (ALS)
71. A motor neuron strategy to save time and energy in neurodegeneration: adaptive protein stoichiometry
72. Pathological Proteins Are Transported by Extracellular Vesicles of Sporadic Amyotrophic Lateral Sclerosis Patients
73. SOD1 in Amyotrophic Lateral Sclerosis: “Ambivalent” Behavior Connected to the Disease
74. Long non-coding and coding RNAs characterization in Peripheral Blood Mononuclear Cells and Spinal Cord from Amyotrophic Lateral Sclerosis patients
75. SOD1, from Bench to Bed: New Role for the Oldest Protein Implicated in ALS
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
84. Amyotrophic lateral sclerosis and environmental factors.
85. Corrigendum: Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs
86. Resistance training of long duration modulates force and unloaded shortening velocity of single muscle fibres of young women
87. Structural and functional alterations of muscle fibres in the novel mouse model of facioscapulohumeral muscular dystrophy
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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