Structural basis for the Trembler-J phenotype of Charcot-Marie-Tooth disease.
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Molecular mechanisms of disease-causing missense mutationsMyelin-specific proteins: a structurally diverse group of membrane-interacting molecules.The homology model of PMP22 suggests mutations resulting in peripheral neuropathy disrupt transmembrane helix packing.The PMP22 gene and its related diseases.Long-term analyses of innervation and neuromuscular integrity in the Trembler-J mouse model of Charcot-Marie-Tooth diseaseThe safety dance: biophysics of membrane protein folding and misfolding in a cellular contextReversible folding of human peripheral myelin protein 22, a tetraspan membrane protein.Peripheral myelin protein 22 alters membrane architecture.Conformational Stability and Pathogenic Misfolding of the Integral Membrane Protein PMP22.Dodecyl-β-melibioside Detergent Micelles as a Medium for Membrane Proteins.
P2860
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P2860
Structural basis for the Trembler-J phenotype of Charcot-Marie-Tooth disease.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Structural basis for the Trembler-J phenotype of Charcot-Marie-Tooth disease.
@en
type
label
Structural basis for the Trembler-J phenotype of Charcot-Marie-Tooth disease.
@en
prefLabel
Structural basis for the Trembler-J phenotype of Charcot-Marie-Tooth disease.
@en
P2093
P2860
P1433
P1476
Structural basis for the Trembler-J phenotype of Charcot-Marie-Tooth disease.
@en
P2093
Arina Hadziselimovic
Charles R Sanders
Kevin L Schey
Masayoshi Sakakura
P2860
P304
P356
10.1016/J.STR.2011.05.009
P577
2011-08-01T00:00:00Z