140 results on '"Pham-Dinh D"'
Search Results
2. Alexander disease: putative mechanisms of an astrocytic encephalopathy
3. Linkage analysis of candidate myelin genes in familial multiple sclerosis
4. Increased density of oligodendrocytes in childhood ataxia with diffuse central hypomyelination (CACH) syndrome: neuropathological and biochemical study of two cases
5. X-linked dominant Charcot-Marie-Tooth neuropathy (CMTX): new mutations in the connexin32 gene
6. TheE. coli EnvY gene encodes a high affinity opioid binding site
7. TGF-β1 PRODUCTION IN RESPONSE TO MYELIN OLIGODENDROCYTE GLYCOPROTEIN IN MUL TIPLE SCLEROSIS AND HEAL THY CONTROLS
8. STUDIES ON MUTATED PLP IN IMMORTALIZED JIMPY OLIGODENDROCYTE CELL LINES
9. Infantile Alexander Disease: spectrum of GFAP mutations and genotype-phenol-type correlation
10. Pyruvate carboxylase deficiencies: Complementation studies between “French” and “American” phenotypes in cultured fibroblasts
11. Antibodies to native myelin oligodendrocyte glycoprotein are serologic markers of early inflammation in multiple sclerosis
12. Antibodies to native myelin oligodendrocyte glycoprotein are serologic markers of early inflammation in multiple sclerosis
13. The gene encoding the large human neurofilament subunit (NF-H) maps to the q121–q131 region on human chromosome 22
14. The Brown Norway opticospinal model of demyelination: Does it mimic multiple sclerosis or neuromyelitis optica?
15. Genetic homogeneity of Pelizaeus-Merzbacher disease: tight linkage to the proteolipoprotein locus in 16 affected families. PMD Clinical Group
16. The gene encoding for the major brain proteolipid (PLP) maps on the q-22 band of the human X chromosome
17. Identification of a Val I 45 IIe substitution in the human myelin oligodendrocyte glycoprotein: lack of association with multiple sclerosis
18. Trois gènes et quatre neuropathies périphériques myéliniques : premières corrélations génotype/phénotype
19. Recherche du défaut moléculaire dans un cas de dysmyélinisation avee préservation des oligodendrocytes
20. Leucodystrophie avec macrocrânie et prolifération des oligodendrocytes
21. Myelin/oligodendrocyte glycoprotein is a member of a subset of the immunoglobulin superfamily encoded within the major histocompatibility complex.
22. Mutations du gène codant pour les protéolipides de la myéline (PLP et DM20) et démyélinisations liées au chromosome X
23. Developmental regulation of calmodulin gene expression in rat brain and skeletal muscle.
24. Pelizaeus-Merzbacher disease: a valine to phenylalanine point mutation in a putative extracellular loop of myelin proteolipid.
25. In situ Localization of NF-H Neurofilament Subunit mRNAs in Rat Brain
26. The E. coli EnvY gene encodes a high affinity opioid binding site.
27. Major Myelin proteolipid: the 4-alpha-helix topology.
28. Citrulline in amniotic fluid and the prenatal diagnosis of citrullinemia.
29. Myelin proteolipid protein (PLP and DM‐20) transcripts are deleted in jimpy mutant mice.
30. Chronic vomiting in a case of citrullinaemia detected after treatment by total parenteral nutrition.
31. Improved method for the antenatal diagnosis of citrullinemia
32. The structural gene coding for myelin-associated proteolipid protein is mutated in jimpy mice
33. Characterization of enzymatic deficiencies of branched chain amino-acid catabolism in human fibroblasts by genetic complementation
34. Pyruvate carboxylase deficiencies: Complementation studies between “French” and “American” phenotypes in cultured fibroblasts
35. The large neurofilament subunit (NF-H) of the rat: cDNA cloning and in situ detection
36. Estradiol inhibits ongoing autoimmune neuroinflammation and NFkappaB-dependent CCL2 expression in reactive astrocytes.
37. Tumor-like enlargement of the optic chiasm in an infant with Alexander disease.
38. Autoimmunity against myelin oligodendrocyte glycoprotein is dispensable for the initiation although essential for the progression of chronic encephalomyelitis in common marmosets.
39. Dynamics of mutated GFAP aggregates revealed by real-time imaging of an astrocyte model of Alexander disease.
40. [Promoting myelin repair in disorders such as multiple sclerosis and some types of leukodystrophy: current studies].
41. T cell repertoire diversity is required for relapses in myelin oligodendrocyte glycoprotein-induced experimental autoimmune encephalomyelitis.
42. Complex alternative splicing of the myelin oligodendrocyte glycoprotein gene is unique to human and non-human primates.
43. Upregulation of alpha-synuclein in neurons and glia in inflammatory demyelinating disease.
44. Persistence of autoreactive myelin oligodendrocyte glycoprotein (MOG)-specific T cell repertoires in MOG-expressing mice.
45. Antibodies to native myelin oligodendrocyte glycoprotein are serologic markers of early inflammation in multiple sclerosis.
46. Axon loss is responsible for chronic neurological deficit following inflammatory demyelination in the rat.
47. Native myelin oligodendrocyte glycoprotein promotes severe chronic neurological disease and demyelination in Biozzi ABH mice.
48. Myelin oligodendrocyte glycoprotein is expressed in the peripheral nervous system of rodents and primates.
49. Myelin/oligodendrocyte glycoprotein-deficient (MOG-deficient) mice reveal lack of immune tolerance to MOG in wild-type mice.
50. Evidence for cytokine dysregulation in multiple sclerosis: peripheral blood mononuclear cell production of pro-inflammatory and anti-inflammatory cytokines during relapse and remission.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.