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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
11  Id2 was found to augment activation of Mpz (myelin protein zero) expression.
12 t cause severe disease, such as those in the myelin protein zero gene (MPZ) and the peripheral myelin
13               More than 120 mutations in the Myelin Protein Zero gene (MPZ, P0) cause various forms o
14                                     The Mpz (myelin protein zero) gene codes for the principal compon
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
19 issense mutation in the predicted Ig protein Myelin Protein Zero-Like 3 (Mpzl3).
20          We therefore named this gene Mpzl3 (myelin protein zero-like 3).
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
25                                 Mutations in myelin protein zero (MPZ) cause Charcot-Marie-Tooth dise
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
28 eral neuropathies caused by mutations in the myelin protein zero (MPZ) gene.
29                                              Myelin protein zero (MPZ) is a member of the immunoglobu
30                                              Myelin protein zero (MPZ) is the major integral membrane
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
36          Mutations in MPZ, the gene encoding myelin protein zero (MPZ), the major protein constituent
37 the most abundant peripheral myelin protein, Myelin protein zero (Mpz).
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
40 ent with a CMT2 clinical phenotype had three myelin protein zero mutations (I89N+V92M+I162M).
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
44 utase active mutant SOD1(G93A) driven by the myelin protein zero (P0) promoter.
45 at neuregulin-1 (NRG1) induces expression of myelin protein zero (P0).
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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