Iqbal et al., 2003 - Google Patents
Alzheimer neurofibrillary degeneration: therapeutic targets and high-throughput assaysIqbal et al., 2003
View PDF- Document ID
- 808709672938188109
- Author
- Iqbal K
- Alonso A
- El-Akkad E
- Gong C
- Haque N
- Khatoon S
- Pei J
- Tanimukai H
- Tsujio I
- Wang J
- Inge G
- Publication year
- Publication venue
- Journal of Molecular Neuroscience
External Links
Snippet
Neurofibrillary degeneration has primary and pivotal involvement in the pathogenesis of Alzheimer disease (AD) and other tauopathies. The inhibition of this lesion offers a promising therapeutic approach. The microtubule-associated protein (MAP) tau is …
- 230000001225 therapeutic 0 title abstract description 13
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
- G01N33/6893—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids related to diseases not provided for elsewhere
- G01N33/6896—Neurological disorders, e.g. Alzheimer's disease
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
- G01N33/5008—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
- G01N33/502—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics for testing non-proliferative effects
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2800/00—Detection or diagnosis of diseases
- G01N2800/28—Neurological disorders
- G01N2800/2814—Dementia; Cognitive disorders
- G01N2800/2821—Alzheimer
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2800/00—Detection or diagnosis of diseases
- G01N2800/28—Neurological disorders
- G01N2800/2835—Movement disorders, e.g. Parkinson, Huntington, Tourette
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
- G01N2333/46—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans from vertebrates
- G01N2333/47—Assays involving proteins of known structure or function as defined in the subgroups
- G01N2333/4701—G01N2333/4701
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/90—Enzymes; Proenzymes
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2500/00—Screening for compounds of potential therapeutic value
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Iqbal et al. | Alzheimer neurofibrillary degeneration: therapeutic targets and high-throughput assays | |
| Iqbal et al. | Alzheimer neurofibrillary degeneration: significance, etiopathogenesis, therapeutics and prevention | |
| Pîrşcoveanu et al. | Tau protein in neurodegenerative diseases-a review | |
| Lee et al. | Neurodegenerative tauopathies | |
| Mandelkow et al. | Biochemistry and cell biology of tau protein in neurofibrillary degeneration | |
| Gong et al. | Dysregulation of protein phosphorylation/dephosphorylation in Alzheimer′ s disease: a therapeutic target | |
| Lee | Disruption of the cytoskeleton in Alzheimer's disease | |
| Wang et al. | The expression of calcium/calmodulin-dependent protein kinase II-α in the hippocampus of patients with Alzheimer's disease and its links with AD-related pathology | |
| Iqbal et al. | Significance and mechanism of Alzheimer neurofibrillary degeneration and therapeutic targets to inhibit this lesion | |
| Ho et al. | Altered p59Fyn kinase expression accompanies disease progression in Alzheimer's disease: implications for its functional role | |
| US8367360B2 (en) | Method of screening for inhibitors of tau protein phosphororylation by tyrosine kinase c-Abl | |
| Taymans et al. | Mechanisms in dominant parkinsonism: The toxic triangle of LRRK2, α‐synuclein, and tau | |
| Watanabe et al. | The participation of insulin-like growth factor-binding protein 3 released by astrocytes in the pathology of Alzheimer’s disease | |
| Shanley et al. | LRRK2 facilitates tau phosphorylation through strong interaction with tau and cdk5 | |
| US10016414B2 (en) | Modulation of ubiquitination of synaptic proteins for the treatment of neurodegenerative and psychiatric disorders | |
| Iqbal et al. | Developing pharmacological therapies for Alzheimer disease | |
| Abdi et al. | 14-3-3 proteins—a moonlight protein complex with therapeutic potential in neurological disorder: in-depth review with Alzheimer’s disease | |
| Delobel et al. | Cell-cycle markers in a transgenic mouse model of human tauopathy: increased levels of cyclin-dependent kinase inhibitors p21Cip1 and p27Kip1 | |
| Iqbal et al. | Pharmacological targets to inhibit Alzheimer neurofibrillary degeneration | |
| Khalid et al. | Alzheimer neurofibrillary degeneration | |
| Iqbal et al. | Pivotal role of neurofibrillary degeneration in Alzheimer disease and therapeutic targets | |
| Montalto | Study of a cyclic nucleotide-mediated mechanism that could favor an antiaggregant conformation of tau protein | |
| Hark | Pulse-Chase Proteomics of Alzheimer's Disease Models Reveals Synaptic Dysfunction Originates in Presynaptic Terminals | |
| Kanungo et al. | Deregulation of cytoskeletal protein phosphorylation and neurodegeneration | |
| Fallacara et al. | Inhibitors of tau-phosphorylating kinases |