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1 th disease type 1B is caused by mutations in myelin protein zero.
2 response to neuregulin1 and did not express myelin protein zero.
3 ells and are autoreactive against peripheral myelin protein zero.
4 changes, we found increased transcripts for myelin protein zero, a gene that, when mutated, can caus
5 mice, but not in the mice with deficiency of myelin protein zero, a major structural protein of compa
6 heral nerves in both mice and humans targets myelin protein zero, an Ag for which expression is Aire-
7 We characterized the mpz gene, which encodes myelin protein zero and is up-regulated in oligodendrogl
8 chwann cell markers, including Pou3f1, Egr2, myelin protein zero and myelin basic protein, is reduced
9 tant alleles: two for connexin 32, three for myelin protein zero, and two for peripheral myelin prote
10 eral proteins: peripheral myelin protein 22, myelin protein zero, connexin 32, early growth response
12 t cause severe disease, such as those in the myelin protein zero gene (MPZ) and the peripheral myelin
15 defective Aire-mediated central tolerance to myelin protein zero initiates an autoimmune Th1 effector
16 ropathy in part because the misfolded mutant myelin protein zero is retained in the endoplasmic retic
17 mpz gene, encoding the ortholog of mammalian myelin protein zero, is expressed in oligodendrocytes of
18 st homology to myelin protein zero (MPZ) and myelin protein zero-like 2 (MPZL2, also called epithelia
21 , transcription factor AP-1, dystroglycan 1, myelin protein zero, mitogen-activated protein kinase 3,
22 e promoters of specific myelin genes such as myelin protein zero (MPZ) and myelin basic protein (MBP)
23 hesion molecule with the highest homology to myelin protein zero (MPZ) and myelin protein zero-like 2
24 dy light chain variable domain (V(L))(1) and myelin protein zero (MPZ) are representatives of the fun
26 nation of the peripheral nervous system, the myelin protein zero (Mpz) gene is induced to produce the
27 have identified five novel mutations in the myelin protein zero (MPZ) gene, encoding the major struc
31 lar genetic testing showed a complex de novo myelin protein zero (MPZ) mutation consisting of a 3bp d
32 he GJB1 gene under the Schwann cell-specific myelin protein zero (Mpz) promoter was generated and del
33 was expressed in transgenic mice using a rat myelin protein zero (Mpz) promoter, which is exclusively
34 ipheral nervous system (PNS) myelin protein, myelin protein zero (MPZ), cause Charcot-Marie-Tooth Dis
35 ability of these cells to induce KROX20 and myelin protein zero (MPZ), localizes NFATC4 to the nucle
38 ssion of myelination-associated genes (e.g., myelin protein zero; Mpz), and failed to myelinate axons
39 duplication), 11 a connexin 32 mutation, 5 a myelin protein zero mutation, 5 a peripheral myelin prot
41 y studies on the cytoplasmic domain of human myelin protein zero (P0) (hP0-cyt) suggest that H-bondin
42 ress the early determinants of their lineage myelin protein zero (P0) and/or fatty acid binding prote
43 r example, deletion of serine 63 (S63del) in myelin protein zero (P0) induces P0 accumulation in the
46 Point mutations in the cytoplasmic domain of myelin protein zero (P0; the major myelin protein in the
47 on in MPZ causing a gain of glycosylation in myelin protein zero, the main protein of peripheral nerv
48 such as periaxin, myelin basic protein, and myelin protein zero, was decreased, genes associated wit
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