| scholarly article | Q13442814 |
| P2093 | author name string | Christoph D Schmid | |
| Mathias Mäurer | |||
| Igor Kobsar | |||
| Rudolf Martini | |||
| Martin Berghoff | |||
| Stefano Carenini | |||
| P2860 | cites work | Bone resorption by osteoclasts | Q28145169 |
| Late-onset neurodegeneration in mice with increased dosage of the proteolipid protein gene | Q28509913 | ||
| Absence of monocyte chemoattractant protein 1 in mice leads to decreased local macrophage recruitment and antigen-specific T helper cell type 1 immune response in experimental autoimmune encephalomyelitis | Q28755978 | ||
| Overview of Charcot-Marie-Tooth disease type 1A. | Q33787272 | ||
| Tetraspan myelin protein PMP22 and demyelinating peripheral neuropathies: new facts and hypotheses | Q33811088 | ||
| Classification of the hereditary motor and sensory neuropathies | Q33924887 | ||
| Animal models for inherited peripheral neuropathies: chances to find treatment strategies? | Q33971773 | ||
| The effect of myelinating Schwann cells on axons. | Q34194525 | ||
| Leukodystrophies: recent developments in genetics, molecular biology, pathogenesis and treatment | Q34260331 | ||
| Electron microscope observations on demyelination and remyelination in experimental allergic neuritis. I. Demyelination | Q36574232 | ||
| The role of macrophages in demyelinating peripheral nervous system of mice heterozygously deficient in p0. | Q40717477 | ||
| Human autoimmune neuropathies | Q40864286 | ||
| Molecular bases of myelin formation as revealed by investigations on mice deficient in glial cell surface molecules | Q41426004 | ||
| Animal models for inherited peripheral neuropathies. | Q41674427 | ||
| Bone marrow transfer from wild-type mice reverts the beneficial effect of genetically mediated immune deficiency in myelin mutants. | Q42652577 | ||
| Tolerance induction in double specific T-cell receptor transgenic mice varies with antigen | Q43554100 | ||
| Connexin32-null mice develop demyelinating peripheral neuropathy | Q47700279 | ||
| Monocyte chemoattractant protein 1 is responsible for macrophage recruitment following injury to sciatic nerve | Q47810586 | ||
| Axonal Swellings and Degeneration in Mice Lacking the Major Proteolipid of Myelin | Q48004959 | ||
| Mouse Models of Myelin Diseases | Q48357457 | ||
| Reactive microglia in dysmyelination and demyelination | Q48912211 | ||
| Macrophage-related demyelination in peripheral nerves of mice deficient in the gap junction protein connexin 32. | Q52123737 | ||
| Phagocytosis of myelin in demyelinative disease: a review | Q52533835 | ||
| Occurrence of active demyelinating lesions in children with hereditary motor and sensory neuropathy (HMSN) type I | Q67585880 | ||
| Corticosteroid-responsive dominantly inherited neuropathy in childhood | Q67914373 | ||
| Early morphological features in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I) | Q68096428 | ||
| Prednisone-responsive hereditary motor and sensory neuropathy | Q70316076 | ||
| Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies | Q71794009 | ||
| Absence of MHC class II molecules reduces CNS demyelination, microglial/macrophage infiltration, and twitching in murine globoid cell leukodystrophy | Q72149254 | ||
| Mechanism of demyelination in experimental allergic neuritis. Electron microscopic studies | Q72338060 | ||
| The chemokine receptor CCR2 is involved in macrophage recruitment to the injured peripheral nervous system | Q73056519 | ||
| Immune deficiency in mouse models for inherited peripheral neuropathies leads to improved myelin maintenance | Q73348017 | ||
| Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32 | Q73382747 | ||
| Influence of injury and cytokines on synthesis of monocyte chemoattractant protein-1 mRNA in peripheral nervous tissue | Q73418903 | ||
| Heterozygous P0 knockout mice develop a peripheral neuropathy that resembles chronic inflammatory demyelinating polyneuropathy (CIDP) | Q73483984 | ||
| Connexin channels in Schwann cells and the development of the X-linked form of Charcot-Marie-Tooth disease | Q73635193 | ||
| Mutations in connexin 32: the molecular and biophysical bases for the X-linked form of Charcot-Marie-Tooth disease | Q73635198 | ||
| Increased expression of chemokines (MCP-1, MIP-1alpha, RANTES) after peripheral nerve transection | Q74034002 | ||
| MIP-1alpha, MCP-1, GM-CSF, and TNF-alpha control the immune cell response that mediates rapid phagocytosis of myelin from the adult mouse spinal cord | Q74096662 | ||
| Chronic inflammatory demyelinating polyneuropathy caused by HIV infection in a patient with asymptomatic CMT 1A | Q74151190 | ||
| P0 protein is a target antigen in chronic inflammatory demyelinating polyradiculoneuropathy | Q74517987 | ||
| Acute inflammatory neuropathy in Charcot-Marie-Tooth disease | Q74608113 | ||
| Disease mechanisms and potential therapeutic strategies in Charcot–Marie–Tooth disease | Q77110246 | ||
| Impaired sensory function in heterozygous P0 knockout mice is associated with nodal changes in sensory nerves | Q77466487 | ||
| P433 | issue | 4 | |
| P1104 | number of pages | 10 | |
| P304 | page(s) | 405-414 | |
| P577 | publication date | 2002-04-01 | |
| P13046 | publication type of scholarly work | review article | Q7318358 |
| P1433 | published in | Journal of Anatomy | Q2108124 |
| P1476 | title | Role of immune cells in animal models for inherited neuropathies: facts and visions | |
| P478 | volume | 200 |
| Q59876149 | A novel GJB1 frameshift mutation produces a transient CNS symptom of X-linked Charcot–Marie–Tooth disease |
| Q53662944 | Aging of myelinating glial cells predominantly affects lipid metabolism and immune response pathways |
| Q51237153 | Altered ion channels in an animal model of Charcot-Marie-Tooth disease type IA. |
| Q34205721 | Connexin 47 (Cx47)-deficient mice with enhanced green fluorescent protein reporter gene reveal predominant oligodendrocytic expression of Cx47 and display vacuolized myelin in the CNS. |
| Q35209953 | Disease mechanisms in inherited neuropathies |
| Q38265030 | GJB1-associated X-linked Charcot-Marie-Tooth disease, a disorder affecting the central and peripheral nervous systems |
| Q37574396 | Innate immunity in the nervous system |
| Q36900083 | Mechanisms of disease: inherited demyelinating neuropathies--from basic to clinical research |
| Q30483471 | Models of autoimmune demyelination in the central nervous system: on the way to translational medicine |
| Q38205157 | Molecules involved in the crosstalk between immune- and peripheral nerve Schwann cells. |
| Q28205102 | Muscle inflammation and MHC class I up-regulation in muscular dystrophy with lack of dysferlin: an immunopathological study |
| Q83100173 | On the longevity of resident endoneurial macrophages in the peripheral nervous system: a study of physiological macrophage turnover in bone marrow chimeric mice |
| Q43156136 | Remodeling of motor nerve terminals in demyelinating axons of periaxin-null mice. |
| Q36507170 | Role of immune cells in animal models for inherited peripheral neuropathies |
| Q24242777 | Treatment for Charcot-Marie-Tooth disease |
| Q24244335 | Treatment for Charcot-Marie-Tooth disease |
| Q81098161 | [The role of the immune system in hereditary demyelinating neuropathies] |
Search more.