-
1
-
-
0028268350
-
Differential expression of two mRNA species indicates a dual function of peripheral myelin protein PMP22 in cell growth and myelination
-
Bosse F, Zoidl G, Wilms S, Gillen CP, Kuhn HG, Müller HW. 1994. Differential expression of two mRNA species indicates a dual function of peripheral myelin protein PMP22 in cell growth and myelination. J Neurosci Res 37:529-537.
-
(1994)
J Neurosci Res
, vol.37
, pp. 529-537
-
-
Bosse, F.1
Zoidl, G.2
Wilms, S.3
Gillen, C.P.4
Kuhn, H.G.5
Müller, H.W.6
-
2
-
-
0033555901
-
Post-transcriptional regulation of the peripheral myelin protein gene PMP22/Gas3
-
Bosse F, Brodbeck J, Müller HW. 1999. Post-transcriptional regulation of the peripheral myelin protein gene PMP22/Gas3. J Neurosci Res 55:164-177.
-
(1999)
J Neurosci Res
, vol.55
, pp. 164-177
-
-
Bosse, F.1
Brodbeck, J.2
Müller, H.W.3
-
3
-
-
0032836436
-
Rho-dependent regulation of cell spreading by the tetraspan membrane protein Gas3/PMP22
-
Brancolini C, Marcinotto S, Edomi P, Agostini E, Fiorentini C, Müller HW, Schneider C. 1999. Rho-dependent regulation of cell spreading by the tetraspan membrane protein Gas3/PMP22. Mol Biol Cell 10:2441-2459.
-
(1999)
Mol Biol Cell
, vol.10
, pp. 2441-2459
-
-
Brancolini, C.1
Marcinotto, S.2
Edomi, P.3
Agostini, E.4
Fiorentini, C.5
Müller, H.W.6
Schneider, C.7
-
4
-
-
0027981751
-
Molecular genetics of Charcot-Marie-Tooth disease and related neuropathies
-
Chance PF, Fischbeck KH. 1994. Molecular genetics of Charcot-Marie-Tooth disease and related neuropathies. Hum Mol Genet 3:1503-1507.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1503-1507
-
-
Chance, P.F.1
Fischbeck, K.H.2
-
5
-
-
0031290336
-
Charcot-Marie-Tooth disease and related peripheral neuropathies
-
De Jonghe P, Timmerman V, Nelis E, Martin J-J, Van Broeckhoven C. 1997. Charcot-Marie-Tooth disease and related peripheral neuropathies. J Peripher Nerv Syst 2:370-387.
-
(1997)
J Peripher Nerv Syst
, vol.2
, pp. 370-387
-
-
De Jonghe, P.1
Timmerman, V.2
Nelis, E.3
Martin, J.-J.4
Van Broeckhoven, C.5
-
6
-
-
0031972929
-
Overloaded endoplasmic reticulum-Golgi compartments, a possible pathomechanism of peripheral neuropathies caused by mutations of the peripheral myelin protein PMP22
-
D'Urso D, Prior R, Greiner-Petter R, Gabreëls-Festen AAWM, Müller HW. 1998. Overloaded endoplasmic reticulum-Golgi compartments, a possible pathomechanism of peripheral neuropathies caused by mutations of the peripheral myelin protein PMP22. J Neurosci 18:731-740.
-
(1998)
J Neurosci
, vol.18
, pp. 731-740
-
-
D'Urso, D.1
Prior, R.2
Greiner-Petter, R.3
Gabreëls-Festen, A.4
Müller, H.W.5
-
7
-
-
0033134949
-
Peripheral myelin protein 22 and protein zero: A novel association in peripheral nervous system myelin
-
D'Urso D, Ehrhardt P, Müller HW. 1999. Peripheral myelin protein 22 and protein zero: a novel association in peripheral nervous system myelin. J Neurosci 19:3396-3403.
-
(1999)
J Neurosci
, vol.19
, pp. 3396-3403
-
-
D'Urso, D.1
Ehrhardt, P.2
Müller, H.W.3
-
8
-
-
0031781215
-
Fate of Schwann cells in CMT1A and HNPP: Evidence for apoptosis
-
Erdem S, Mendell JR, Sahenk Z. 1998. Fate of Schwann cells in CMT1A and HNPP: evidence for apoptosis. J Neuropathol Exp Neurol 57:635-642.
-
(1998)
J Neuropathol Exp Neurol
, vol.57
, pp. 635-642
-
-
Erdem, S.1
Mendell, J.R.2
Sahenk, Z.3
-
9
-
-
0029159803
-
Apoptotic phenotype induced by overexpression of wild-type gas3/PMP22: Its relation to the demyelinating peripheral neuropathy CMT1A
-
Fabretti E, Edomi P, Brancolini C, Schneider C. 1995. Apoptotic phenotype induced by overexpression of wild-type gas3/PMP22: its relation to the demyelinating peripheral neuropathy CMT1A. Genes Dev 9:1846-1856.
-
(1995)
Genes Dev
, vol.9
, pp. 1846-1856
-
-
Fabretti, E.1
Edomi, P.2
Brancolini, C.3
Schneider, C.4
-
10
-
-
0028800889
-
Charcot-Marie-Tooth disease type 1A: Morphological phenotype of the 17p duplication versus PMP22 point mutations
-
Gabreëls-Festen AAWM, Bolhuis P, Hoogendijk JE, Valentijn LJ, Eshuis EJHM, Gabriels FJM. 1995. Charcot-Marie-Tooth disease type 1A: morphological phenotype of the 17p duplication versus PMP22 point mutations. Acta Neuropathol 90:645-649.
-
(1995)
Acta Neuropathol
, vol.90
, pp. 645-649
-
-
Gabreëls-Festen, A.A.W.M.1
Bolhuis, P.2
Hoogendijk, J.E.3
Valentijn, L.J.4
Eshuis, E.J.H.M.5
Gabriels, F.J.M.6
-
11
-
-
0029955993
-
Low affinity NGF receptor expression in CMT1A nerve biopsies of different disease stages
-
Hanemann CO, Gabreëls-Festen AAWM, Müller HW, Stoll G. 1996. Low affinity NGF receptor expression in CMT1A nerve biopsies of different disease stages. Brain 119:1461-1469.
-
(1996)
Brain
, vol.119
, pp. 1461-1469
-
-
Hanemann, C.O.1
Gabreëls-Festen, A.A.W.M.2
Müller, H.W.3
Stoll, G.4
-
12
-
-
1842412458
-
Schwann cell differentiation in Charcot-Marie-Tooth disease type 1A (CMT1A): Normal number of myelinating Schwann cells in young CMT1A patients and neural cell adhesion molecule expression in onion bulbs
-
Hanemann CO, Gabreëls-Festen AAWM, Stoll G, Müller HW. 1997. Schwann cell differentiation in Charcot-Marie-Tooth disease type 1A (CMT1A): normal number of myelinating Schwann cells in young CMT1A patients and neural cell adhesion molecule expression in onion bulbs. Acta Neuropathol 94:310-315.
-
(1997)
Acta Neuropathol
, vol.94
, pp. 310-315
-
-
Hanemann, C.O.1
Gabreëls-Festen, A.A.W.M.2
Stoll, G.3
Müller, H.W.4
-
13
-
-
0032125441
-
Pathogenesis of Charcot-Marie-Tooth 1A (CMT1A) neuropathy
-
Hanemann CO, Müller HW. 1998. Pathogenesis of Charcot-Marie-Tooth 1A (CMT1A) neuropathy. Trends Neurosci 21:282-286.
-
(1998)
Trends Neurosci
, vol.21
, pp. 282-286
-
-
Hanemann, C.O.1
Müller, H.W.2
-
14
-
-
0032104866
-
Improved culture methods to expand Schwann cells with altered growth behaviour from CMT1A patients
-
Hanemann CO, Rosenbaum C, Kupfer S, Wosch S, Stoegbauer F, Müller HW. 1998. Improved culture methods to expand Schwann cells with altered growth behaviour from CMT1A patients. Glia 23:89-98.
-
(1998)
Glia
, vol.23
, pp. 89-98
-
-
Hanemann, C.O.1
Rosenbaum, C.2
Kupfer, S.3
Wosch, S.4
Stoegbauer, F.5
Müller, H.W.6
-
15
-
-
0028839225
-
Transgenic systems in studying myelin gene expression
-
Ikenaka K, Kagawa T. 1995. Transgenic systems in studying myelin gene expression. Dev Neurosci 17:127-136.
-
(1995)
Dev Neurosci
, vol.17
, pp. 127-136
-
-
Ikenaka, K.1
Kagawa, T.2
-
16
-
-
0025328309
-
A growth arrest-specific gene codes for a membrane protein
-
Manfioletti G, Ruaro E, Del Sal G, Phillpson L, Schneider C. 1990. A growth arrest-specific gene codes for a membrane protein. Mol Cell Biol 10:2924-2930.
-
(1990)
Mol Cell Biol
, vol.10
, pp. 2924-2930
-
-
Manfioletti, G.1
Ruaro, E.2
Del Sal, G.3
Phillpson, L.4
Schneider, C.5
-
17
-
-
0030696172
-
Animal models for inherited peripheral neuropathies
-
Martini R. 1997. Animal models for inherited peripheral neuropathies. J Anat 191:321-336.
-
(1997)
J Anat
, vol.191
, pp. 321-336
-
-
Martini, R.1
-
18
-
-
0030668164
-
Advances in Charcot-Marie-Tooth disease research: Cellular function of CMT-related proteins, transgenic animal models, and pathomechanism
-
Müller HW, Suter U, Van Broeckhoven C, Hanemann O, Nelis E, Timmerman V, Sancho S, Barrio L, Bolhuis P, Dermietzel R, Frank M, Gabreëls-Festen A, Gillen C, Haites N, Levi G, Mariman E, Martini R, Nave K, Rautenstrauss B, Schachner M, Schenone A, Schneider C, Schröder M, Willecke K. 1997. Advances in Charcot-Marie-Tooth disease research: cellular function of CMT-related proteins, transgenic animal models, and pathomechanism. Neurobiol Disease 4:215-220.
-
(1997)
Neurobiol Disease
, vol.4
, pp. 215-220
-
-
Müller, H.W.1
Suter, U.2
Van Broeckhoven, C.3
Hanemann, O.4
Nelis, E.5
Timmerman, V.6
Sancho, S.7
Barrio, L.8
Bolhuis, P.9
Dermietzel, R.10
Frank, M.11
Gabreëls-Festen, A.12
Gillen, C.13
Haites, N.14
Levi, G.15
Mariman, E.16
Martini, R.17
Nave, K.18
Rautenstrauss, B.19
Schachner, M.20
Schenone, A.21
Schneider, C.22
Schröder, M.23
Willecke, K.24
more..
-
19
-
-
0030900850
-
Aberrant protein trafficking in Trembler suggests a disease mechanism for hereditary human peripheral neuropathies
-
Naef R, Adlkofer K, Lescher B, Suter U. 1997. Aberrant protein trafficking in Trembler suggests a disease mechanism for hereditary human peripheral neuropathies. Mol Cell Neurosci 9:13-25.
-
(1997)
Mol Cell Neurosci
, vol.9
, pp. 13-25
-
-
Naef, R.1
Adlkofer, K.2
Lescher, B.3
Suter, U.4
-
20
-
-
0028122616
-
Neurological mouse mutants and the genes of myelin
-
Nave K. 1994. Neurological mouse mutants and the genes of myelin. J Neurosci Res 38:607-612.
-
(1994)
J Neurosci Res
, vol.38
, pp. 607-612
-
-
Nave, K.1
-
21
-
-
0002768920
-
X-linked developmental defects of myelination, from mouse mutants to human genetic diseases
-
Nave K, Boespflug-Tanguy O. 1996. X-linked developmental defects of myelination, from mouse mutants to human genetic diseases. Neuroscientist 2:33-43.
-
(1996)
Neuroscientist
, vol.2
, pp. 33-43
-
-
Nave, K.1
Boespflug-Tanguy, O.2
-
22
-
-
0031081340
-
The ER-overload response: Activation of NF-κB
-
Pahl HL, Bäuerle PA. 1997. The ER-overload response: activation of NF-κB. Trends Biochem 22:63-67.
-
(1997)
Trends Biochem
, vol.22
, pp. 63-67
-
-
Pahl, H.L.1
Bäuerle, P.A.2
-
23
-
-
0028231331
-
Charcot-Marie-Tooth disease: A new paradigm for the mechanism of inherited disease
-
Patel PI, Lupski JR. 1994. Charcot-Marie-Tooth disease: a new paradigm for the mechanism of inherited disease. Trends Genet 10:128-133.
-
(1994)
Trends Genet
, vol.10
, pp. 128-133
-
-
Patel, P.I.1
Lupski, J.R.2
-
24
-
-
0030246987
-
Crystal structure of the extracellular domain from P0, the major structural protein of peripheral nerve myelin
-
Shapiro L, Doyle JP, Hensley P, Colman DR, Hendrickson WA. 1996. Crystal structure of the extracellular domain from P0, the major structural protein of peripheral nerve myelin. Neuron 17:435-449.
-
(1996)
Neuron
, vol.17
, pp. 435-449
-
-
Shapiro, L.1
Doyle, J.P.2
Hensley, P.3
Colman, D.R.4
Hendrickson, W.A.5
-
25
-
-
0026554289
-
A leucin-to-prolin mutation in the putative first transmembrane domain of the 22 kD peripheral myelin protein in Trembler-J mouse
-
Suter U, Moskow JJ, Welcher AA, Snipes GJ, Kosaras B, Sidman RL, Buchberg AM, Shooter EM. 1992a. A leucin-to-prolin mutation in the putative first transmembrane domain of the 22 kD peripheral myelin protein in Trembler-J mouse. Proc Natl Acad Sci USA 89:4382-4386.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 4382-4386
-
-
Suter, U.1
Moskow, J.J.2
Welcher, A.A.3
Snipes, G.J.4
Kosaras, B.5
Sidman, R.L.6
Buchberg, A.M.7
Shooter, E.M.8
-
26
-
-
0026605507
-
Trembler mouse carries a point mutation in a myelin gene
-
Suter U, Welcher AA, Ozcelik T, Snipes GJ, Kosaras B, Francke U, Billings-Gagliardi S, Sidman RL, Shooter EM. 1992b. Trembler mouse carries a point mutation in a myelin gene. Nature 356:241-244.
-
(1992)
Nature
, vol.356
, pp. 241-244
-
-
Suter, U.1
Welcher, A.A.2
Ozcelik, T.3
Snipes, G.J.4
Kosaras, B.5
Francke, U.6
Billings-Gagliardi, S.7
Sidman, R.L.8
Shooter, E.M.9
-
27
-
-
0028073907
-
Regulation of tissue-specific expression of alternative peripheral myelin protein-22 (PMP22) gene transcripts by two promoters
-
Suter U, Snipes JG, Schoener-Scott R, Welcher AA, Pareek S, Lupski JR, Murphy RA, Shooter EM, Patel PI. 1994. Regulation of tissue-specific expression of alternative peripheral myelin protein-22 (PMP22) gene transcripts by two promoters. J Biol Chem 269:25795-25808.
-
(1994)
J Biol Chem
, vol.269
, pp. 25795-25808
-
-
Suter, U.1
Snipes, J.G.2
Schoener-Scott, R.3
Welcher, A.A.4
Pareek, S.5
Lupski, J.R.6
Murphy, R.A.7
Shooter, E.M.8
Patel, P.I.9
-
28
-
-
0028902548
-
Biology and genetics of hereditary motor and sensory neuropathies
-
Suter U, Snipes GJ. 1995. Biology and genetics of hereditary motor and sensory neuropathies. Ann Rev Neurosci 18:45-75.
-
(1995)
Ann Rev Neurosci
, vol.18
, pp. 45-75
-
-
Suter, U.1
Snipes, G.J.2
-
29
-
-
0033559844
-
Transport of Trembler-J mutant peripheral myelin protein 22 is blocked in the intermediate compartment and affects the transport of the wild-type protein by direct interaction
-
Tobler AR, Notterpek L, Naef R, Tayler V, Suter U, Shooter EM. 1999. Transport of Trembler-J mutant peripheral myelin protein 22 is blocked in the intermediate compartment and affects the transport of the wild-type protein by direct interaction. J Neurosci 19:2027-2036.
-
(1999)
J Neurosci
, vol.19
, pp. 2027-2036
-
-
Tobler, A.R.1
Notterpek, L.2
Naef, R.3
Tayler, V.4
Suter, U.5
Shooter, E.M.6
-
30
-
-
0028950408
-
Retroviral-mediated gene transfer of the peripheral myelin protein PMP22 in Schwann cells: Modulation of cell growth
-
Zoidl G, Blass-Kampmann S, D'Urso D, Schmalenbach C, Müller HW. 1995. Retroviral-mediated gene transfer of the peripheral myelin protein PMP22 in Schwann cells: modulation of cell growth. EMBO J 14:1122-1128.
-
(1995)
EMBO J
, vol.14
, pp. 1122-1128
-
-
Zoidl, G.1
Blass-Kampmann, S.2
D'Urso, D.3
Schmalenbach, C.4
Müller, H.W.5
|