-
1
-
-
0019507223
-
A differentiation antigen of human NK and K cells identified by a monoclonal antibody (HNK-1)
-
Abo T., Bach C.M. A differentiation antigen of human NK and K cells identified by a monoclonal antibody (HNK-1). J. Immunol. 127:1981;1024-1029.
-
(1981)
J. Immunol.
, vol.127
, pp. 1024-1029
-
-
Abo, T.1
Bach, C.M.2
-
2
-
-
0024399194
-
Neuropathies périphériques chroniques díallure hérédodégénérative corticosensibles: Deux cas
-
Antoine J.C., Michel D., Kopp N., Gonnaud P.M., Laurent B. Neuropathies périphériques chroniques díallure hérédodégénérative corticosensibles: deux cas. Rev. Neurol. 145:1989;469-473.
-
(1989)
Rev. Neurol.
, vol.145
, pp. 469-473
-
-
Antoine, J.C.1
Michel, D.2
Kopp, N.3
Gonnaud, P.M.4
Laurent, B.5
-
3
-
-
0027772413
-
Connexin mutations in X-linked Charcot-Marie-Tooth disease
-
Bergoffen J., Scherer S.S., Wang S., Scott M.O., Bonbe I.J., Paul D.L., Chen K., Lensch M.W., Chance P.F., Fischbeck K.H. Connexin mutations in X-linked Charcot-Marie-Tooth disease. Science. 262:1993;2039-2042.
-
(1993)
Science
, vol.262
, pp. 2039-2042
-
-
Bergoffen, J.1
Scherer, S.S.2
Wang, S.3
Scott, M.O.4
Bonbe, I.J.5
Paul, D.L.6
Chen, K.7
Lensch, M.W.8
Chance, P.F.9
Fischbeck, K.H.10
-
4
-
-
0030919339
-
Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases
-
Birouk N., Gouider R., Le Guern E., Gugenheim M., Tardieu S., Maisonobe T., Le Forestier N., Agid Y., Brice A., Bouche P. Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases. Brain. 120:1997;813-823.
-
(1997)
Brain
, vol.120
, pp. 813-823
-
-
Birouk, N.1
Gouider, R.2
Le Guern, E.3
Gugenheim, M.4
Tardieu, S.5
Maisonobe, T.6
Le Forestier, N.7
Agid, Y.8
Brice, A.9
Bouche, P.10
-
5
-
-
0027340669
-
Serum anti-GQ1b IgG antibody is associated with ophtalmoplegia in Miller Fisher syndrome and Guillain-Barré syndrome
-
Chiba A., Kusunoki S., Obata H., Machinami R., Kanazawa I. Serum anti-GQ1b IgG antibody is associated with ophtalmoplegia in Miller Fisher syndrome and Guillain-Barré syndrome. Neurology. 43:1993;1911-1917.
-
(1993)
Neurology
, vol.43
, pp. 1911-1917
-
-
Chiba, A.1
Kusunoki, S.2
Obata, H.3
MacHinami, R.4
Kanazawa, I.5
-
6
-
-
0027205220
-
Diagnostic criteria for autosomal dominant hereditary motor and sensory neuropathy type 1a
-
De Visser M. Diagnostic criteria for autosomal dominant hereditary motor and sensory neuropathy type 1a. Neuromusc. Disord. 3:1993;77-79.
-
(1993)
Neuromusc. Disord.
, vol.3
, pp. 77-79
-
-
De Visser, M.1
-
7
-
-
0020322459
-
Prednison-responsive hereditary motor and sensory neuropathy
-
Dyck P.J., Swanson C.J., Low P.A., Bartelson J.D., Lambert E.H. Prednison-responsive hereditary motor and sensory neuropathy. Mayo Clin. Proc. 57:1982;239-246.
-
(1982)
Mayo Clin. Proc.
, vol.57
, pp. 239-246
-
-
Dyck, P.J.1
Swanson, C.J.2
Low, P.A.3
Bartelson, J.D.4
Lambert, E.H.5
-
8
-
-
0027270106
-
Hereditary demyelinating motor and sensory neuropathy
-
Gabreels-Festen A.A., Gabreels F.J. Hereditary demyelinating motor and sensory neuropathy. Brain Pathol. 3:1993;135-146.
-
(1993)
Brain Pathol.
, vol.3
, pp. 135-146
-
-
Gabreels-Festen, A.A.1
Gabreels, F.J.2
-
9
-
-
0031471867
-
Gene dosage effects in hereditary peripheral neuropathy
-
Gabriel J.M., Erne B., Pareyson D., Sghirlanzoni A., Taroni F., Steck A.J. Gene dosage effects in hereditary peripheral neuropathy. Neurology. 49:1997;1635-1640.
-
(1997)
Neurology
, vol.49
, pp. 1635-1640
-
-
Gabriel, J.M.1
Erne, B.2
Pareyson, D.3
Sghirlanzoni, A.4
Taroni, F.5
Steck, A.J.6
-
10
-
-
0031665679
-
Induction of experimental autoimmune neuritis with peripheral myelin protein-22
-
Gabriel C.M., Hughes R.A.C., Moore S.E., Smith K.J., Walsh F.S. Induction of experimental autoimmune neuritis with peripheral myelin protein-22. Brain. 121:1998;1895-1902.
-
(1998)
Brain
, vol.121
, pp. 1895-1902
-
-
Gabriel, C.M.1
Hughes, R.A.C.2
Moore, S.E.3
Smith, K.J.4
Walsh, F.S.5
-
11
-
-
0015847039
-
A new technique for the assay of infectivity of human adenovirus 5 DNA
-
Graham F.L., Van der Eb A.J. A new technique for the assay of infectivity of human adenovirus 5 DNA. Virology. 52:1973;456.
-
(1973)
Virology
, vol.52
, pp. 456
-
-
Graham, F.L.1
Van Der Eb, A.J.2
-
12
-
-
0032477311
-
Third workshop of the European CMT Consortium: 54th ENMC International Workshop on genotype/phenotype correlations in Charcot-Marie-Tooth type 1 and hereditary neuropathy with liability to pressure palsies
-
Haites N.E., Nelis E., Van Broekhoven C. Third workshop of the European CMT Consortium: 54th ENMC International Workshop on genotype/phenotype correlations in Charcot-Marie-Tooth type 1 and hereditary neuropathy with liability to pressure palsies. Neuromusc. Disord. 8:1998;591-601.
-
(1998)
Neuromusc. Disord.
, vol.8
, pp. 591-601
-
-
Haites, N.E.1
Nelis, E.2
Van Broekhoven, C.3
-
13
-
-
0027209630
-
Immunoreactivity of PMP22, P0, and other 19 to 28 kDa glycoproteins in peripheral nerve myelin of mammals and fish with HNK1 and related antibodies
-
Hammer J.A., O'Shannessy D.J., De Leon M., Gould R., Zand D., Daune G., Quarles R.H. Immunoreactivity of PMP22, P0, and other 19 to 28 kDa glycoproteins in peripheral nerve myelin of mammals and fish with HNK1 and related antibodies. J. Neurosci. Res. 35:1993;546-558.
-
(1993)
J. Neurosci. Res.
, vol.35
, pp. 546-558
-
-
Hammer, J.A.1
O'Shannessy, D.J.2
De Leon, M.3
Gould, R.4
Zand, D.5
Daune, G.6
Quarles, R.H.7
-
14
-
-
0027221141
-
Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the P0 gene
-
Hayasaka K., Himoro M., Sato W., Takada G., Uyemura K., Shimizu N., Bird T.D., Conneally P.M., Chance P.F. Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the P0 gene. Nat. Genet. 5:1993;31-34.
-
(1993)
Nat. Genet.
, vol.5
, pp. 31-34
-
-
Hayasaka, K.1
Himoro, M.2
Sato, W.3
Takada, G.4
Uyemura, K.5
Shimizu, N.6
Bird, T.D.7
Conneally, P.M.8
Chance, P.F.9
-
15
-
-
6844255894
-
Correlation between varying levels of PMP22 expression and the degree of demyelination and reduction in nerve conduction velocity in transgenic mice
-
Huxley C., Passage E., Robertson A.M., Youl B., Huston S., Manson A., Saberan-Djoniedi D., Figarella-Branger D., Pellisier J.F., Thomas P.K., Fontes M. Correlation between varying levels of PMP22 expression and the degree of demyelination and reduction in nerve conduction velocity in transgenic mice. Hum. Mol. Genet. 7:1998;449-458.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 449-458
-
-
Huxley, C.1
Passage, E.2
Robertson, A.M.3
Youl, B.4
Huston, S.5
Manson, A.6
Saberan-Djoniedi, D.7
Figarella-Branger, D.8
Pellisier, J.F.9
Thomas, P.K.10
Fontes, M.11
-
16
-
-
0030561023
-
The antibody repertoire in experimental allergic neuritis: Evidence for PMP22 as a novel neuritogen
-
Koehler N.K., Martin R., Wiethotter H. The antibody repertoire in experimental allergic neuritis: evidence for PMP22 as a novel neuritogen. J. Neuroimmunol. 71:1996;179-189.
-
(1996)
J. Neuroimmunol.
, vol.71
, pp. 179-189
-
-
Koehler, N.K.1
Martin, R.2
Wiethotter, H.3
-
19
-
-
0025868571
-
DNA duplication associated with Charcot-Marie-Tooth disease type 1A
-
Lupski J.R., Montes de Oca-Luna R., Slaugenhaupt S.I., Pentoa L., Guzzerra V., Trask B.J., Saucedo-Cardenas O., Barker D.F., Killian J.M., Garcia C.A., Chakravarti A., Patel P. DNA duplication associated with Charcot-Marie-Tooth disease type 1A. Cell. 66:1991;219-232.
-
(1991)
Cell
, vol.66
, pp. 219-232
-
-
Lupski, J.R.1
Montes De Oca-Luna, R.2
Slaugenhaupt, S.I.3
Pentoa, L.4
Guzzerra, V.5
Trask, B.J.6
Saucedo-Cardenas, O.7
Barker, D.F.8
Killian, J.M.9
Garcia, C.A.10
Chakravarti, A.11
Patel, P.12
-
20
-
-
0026849499
-
Gene dosage effect is a mechanism for Charcot-Marie-Tooth disease type 1A
-
Lupski J.R., Wise C.A., Kuwano A., Pentao L., Parke J.T., Glaze D.G., Ledbetter D.H., Greenberg F., Patel P.I. Gene dosage effect is a mechanism for Charcot-Marie-Tooth disease type 1A. Nat. Genet. 1:1992;29-33.
-
(1992)
Nat. Genet.
, vol.1
, pp. 29-33
-
-
Lupski, J.R.1
Wise, C.A.2
Kuwano, A.3
Pentao, L.4
Parke, J.T.5
Glaze, D.G.6
Ledbetter, D.H.7
Greenberg, F.8
Patel, P.I.9
-
21
-
-
0029843863
-
Impaired differentiation of Schwann cells in transgenic mice with increased PMP22 gene dosage
-
Magyar J.P., Martini R., Ruelicke T., Aguzzi A., Adlkofer K., Dembic Z., Zielasek J., Toyka K.V., Suter U. Impaired differentiation of Schwann cells in transgenic mice with increased PMP22 gene dosage. J. Neurosci. 16:1996;5351-5360.
-
(1996)
J. Neurosci.
, vol.16
, pp. 5351-5360
-
-
Magyar, J.P.1
Martini, R.2
Ruelicke, T.3
Aguzzi, A.4
Adlkofer, K.5
Dembic, Z.6
Zielasek, J.7
Toyka, K.V.8
Suter, U.9
-
22
-
-
0025328309
-
A growth-arrest specific (gas) gene codes for a membrane protein
-
Manfioletti G., Ruaro M.E., Del Sal G., Philipson L., Schneider C. A growth-arrest specific (gas) gene codes for a membrane protein. Mol. Cell. Biol. 10:1990;2924-2930.
-
(1990)
Mol. Cell. Biol.
, vol.10
, pp. 2924-2930
-
-
Manfioletti, G.1
Ruaro, M.E.2
Del Sal, G.3
Philipson, L.4
Schneider, C.5
-
23
-
-
0026879838
-
Peripheral myelin protein 22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A
-
Matsunami N., Smith B., Ballard L., Lensch M.W., Robertson M., Albertson H., Hanemann C.O., Müller H.W., Bird T.D., White R., Chance P.F. Peripheral myelin protein 22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A. Nat. Genet. 1:1992;176-179.
-
(1992)
Nat. Genet.
, vol.1
, pp. 176-179
-
-
Matsunami, N.1
Smith, B.2
Ballard, L.3
Lensch, M.W.4
Robertson, M.5
Albertson, H.6
Hanemann, C.O.7
Müller, H.W.8
Bird, T.D.9
White, R.10
Chance, P.F.11
-
24
-
-
0032103882
-
Many facets of the peripheral myelin protein PMP22 in myelination and disease
-
Naef R., Suter U. Many facets of the peripheral myelin protein PMP22 in myelination and disease. Micros. Res. Tech. 41:1998;359-371.
-
(1998)
Micros. Res. Tech.
, vol.41
, pp. 359-371
-
-
Naef, R.1
Suter, U.2
-
25
-
-
0030012076
-
A new point mutation affecting the fourth transmembrane domain of PMP22 results in severe de novo Charcot-Marie-Tooth disease
-
Navon R., Seifried B., Gal-On N.S., Sadeh M. A new point mutation affecting the fourth transmembrane domain of PMP22 results in severe de novo Charcot-Marie-Tooth disease. Hum. Genet. 97:1996;685-687.
-
(1996)
Hum. Genet.
, vol.97
, pp. 685-687
-
-
Navon, R.1
Seifried, B.2
Gal-On, N.S.3
Sadeh, M.4
-
26
-
-
0027196844
-
Detection and processing of peripheral myelin protein PMP22 in cultured Schwann cells
-
Nelis E., Timmerman V., De Jonghe P., Pareek S., Suter U., Snipes G.J., Welcher A.A., Shooter E.M., Murphy R.A. Detection and processing of peripheral myelin protein PMP22 in cultured Schwann cells. J. Biol. Chem. 268:1993;10372-10379.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 10372-10379
-
-
Nelis, E.1
Timmerman, V.2
De Jonghe, P.3
Pareek, S.4
Suter, U.5
Snipes, G.J.6
Welcher, A.A.7
Shooter, E.M.8
Murphy, R.A.9
-
27
-
-
0031867488
-
Mutation analysis of the nerve specific promoter of the peripheral myelin protein 22 gene in CMT1A disease and HNPP
-
Nelis E., De Jonghe P., De Vriendt E., Patel P.I., Martin J.J., Van Broeckhoven C. Mutation analysis of the nerve specific promoter of the peripheral myelin protein 22 gene in CMT1A disease and HNPP. J. Med. Genet. 35:1998;590-593.
-
(1998)
J. Med. Genet.
, vol.35
, pp. 590-593
-
-
Nelis, E.1
De Jonghe, P.2
De Vriendt, E.3
Patel, P.I.4
Martin, J.J.5
Van Broeckhoven, C.6
-
28
-
-
0026879614
-
The gene for the peripheral myelin protein PMP22 is a candidate for Charcot-Marie-Tooth disease type 1A
-
Patel P.I., Roa B.B., Welcher A.A., Schoener-Scott R., Trash B.J., Pentao L., Snipes G.J., Garcia C.A., Francke U., Shooter E.M., Lupski J.R., Suter U. The gene for the peripheral myelin protein PMP22 is a candidate for Charcot-Marie-Tooth disease type 1A. Nat. Genet. 1:1992;159-165.
-
(1992)
Nat. Genet.
, vol.1
, pp. 159-165
-
-
Patel, P.I.1
Roa, B.B.2
Welcher, A.A.3
Schoener-Scott, R.4
Trash, B.J.5
Pentao, L.6
Snipes, G.J.7
Garcia, C.A.8
Francke, U.9
Shooter, E.M.10
Lupski, J.R.11
Suter, U.12
-
29
-
-
0025997898
-
Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)
-
Raeymaekers P., Timmerman V., Nelis E., De Jinghe P., Hoogendijk J.E., Baas F., Barker D.F. Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). Neuromuscul. Disord. 1:1991;93-97.
-
(1991)
Neuromuscul. Disord.
, vol.1
, pp. 93-97
-
-
Raeymaekers, P.1
Timmerman, V.2
Nelis, E.3
De Jinghe, P.4
Hoogendijk, J.E.5
Baas, F.6
Barker, D.F.7
-
30
-
-
0027314668
-
Charcot-Marie-Tooth type 1A: Association with a spontaneous point mutation in the PMP22 gene
-
Roa B.B., Garcia C.A., Suter U., Kulpa D.A., Wise C.A., Mueller J., Welcher A.A., Snipes G.J., Shooter E.M., Patel P.I., Lupski J.R. Charcot-Marie-Tooth type 1A: association with a spontaneous point mutation in the PMP22 gene. N. Engl. J. Med. 329:1993;96-101.
-
(1993)
N. Engl. J. Med.
, vol.329
, pp. 96-101
-
-
Roa, B.B.1
Garcia, C.A.2
Suter, U.3
Kulpa, D.A.4
Wise, C.A.5
Mueller, J.6
Welcher, A.A.7
Snipes, G.J.8
Shooter, E.M.9
Patel, P.I.10
Lupski, J.R.11
-
31
-
-
13344249760
-
Duplication of the PMP22 gene in 17p partial trisomy patients with Charcot-Marie-Tooth type 1A neuropathy
-
Roa B.B., Greenberg F., Gunaratne P., Sauer C.M., Lubinksy M.S., Kozma C., Meck J.M., Magenis R.E., Shaffer L.G., Lupski J.R. Duplication of the PMP22 gene in 17p partial trisomy patients with Charcot-Marie-Tooth type 1A neuropathy. Hum. Genet. 97:1996;642-649.
-
(1996)
Hum. Genet.
, vol.97
, pp. 642-649
-
-
Roa, B.B.1
Greenberg, F.2
Gunaratne, P.3
Sauer, C.M.4
Lubinksy, M.S.5
Kozma, C.6
Meck, J.M.7
Magenis, R.E.8
Shaffer, L.G.9
Lupski, J.R.10
-
32
-
-
15844393894
-
A transgenic rat model of Charcot-Marie-Tooth disease
-
Sereda M., Griffiths I., Pulhofer A., Stewart H., Rossner M.J., Zimmermann F., Magyar J.P., Schneider A., Hund E., Meink H.M., Suter U., Nave K.A. A transgenic rat model of Charcot-Marie-Tooth disease. Neuron. 16:1996;1049-1060.
-
(1996)
Neuron
, vol.16
, pp. 1049-1060
-
-
Sereda, M.1
Griffiths, I.2
Pulhofer, A.3
Stewart, H.4
Rossner, M.J.5
Zimmermann, F.6
Magyar, J.P.7
Schneider, A.8
Hund, E.9
Meink, H.M.10
Suter, U.11
Nave, K.A.12
-
33
-
-
0023765743
-
Genes specifically expressed at growth arrest of mammalian cells
-
Schneider C., King R.M., Philipson L. Genes specifically expressed at growth arrest of mammalian cells. Cell. 54:1988;787-793.
-
(1988)
Cell
, vol.54
, pp. 787-793
-
-
Schneider, C.1
King, R.M.2
Philipson, L.3
-
34
-
-
0029014126
-
Molecular anatomy and genetics of myelin proteins in peripheral nervous system
-
Snipes G.J., Suter U. Molecular anatomy and genetics of myelin proteins in peripheral nervous system. J. Anat. 186:1995;483-494.
-
(1995)
J. Anat.
, vol.186
, pp. 483-494
-
-
Snipes, G.J.1
Suter, U.2
-
35
-
-
0027425265
-
Human peripheral myelin protein 22 carries the L2/HNK1 carbohydrate adhesion epitope
-
Snipes G.J., Suter U., Shooter E.M. Human peripheral myelin protein 22 carries the L2/HNK1 carbohydrate adhesion epitope. J. Neurochem. 61:1993;1961-1964.
-
(1993)
J. Neurochem.
, vol.61
, pp. 1961-1964
-
-
Snipes, G.J.1
Suter, U.2
Shooter, E.M.3
-
36
-
-
0026879615
-
The peripheral myelin protein gene PMP22 is contained within the Charcot-Marie-Tooth disease type 1A duplication
-
Timmermann V., Nelis E., Van Hul W., Nieuwenhuijsen B.W., Chen K.L., Ben Othman K., Cullen B., Leachz R.J., Hanemann C.O., De Jonghe P., Raeymaekers P., van Ommen G.-J.B., Martin J.J., Müller H.W., Vance J.M., Fishbeck K.H., Van Broeckhoven C. The peripheral myelin protein gene PMP22 is contained within the Charcot-Marie-Tooth disease type 1A duplication. Nat. Genet. 1:1992;171-175.
-
(1992)
Nat. Genet.
, vol.1
, pp. 171-175
-
-
Timmermann, V.1
Nelis, E.2
Van Hul, W.3
Nieuwenhuijsen, B.W.4
Chen, K.L.5
Ben Othman, K.6
Cullen, B.7
Leachz, R.J.8
Hanemann, C.O.9
De Jonghe, P.10
Raeymaekers, P.11
Van Ommen, G.-J.B.12
Martin, J.J.13
Müller, H.W.14
Vance, J.M.15
Fishbeck, K.H.16
Van Broeckhoven, C.17
-
37
-
-
0027031611
-
Identical point mutation of PMP22 in TremblerJ mouse and Charcot-Marie-Tooth disease type 1A
-
Valentijn L.J., Baas F., Wolterman R.A., Hoogendijk J.E., van den Bosch N.H.A., Zorn I., Grabreels-Festen A.A., de Visser M., Bolhuis P.A. Identical point mutation of PMP22 in TremblerJ mouse and Charcot-Marie-Tooth disease type 1A. Nat. Genet. 2:1993;288-291.
-
(1993)
Nat. Genet.
, vol.2
, pp. 288-291
-
-
Valentijn, L.J.1
Baas, F.2
Wolterman, R.A.3
Hoogendijk, J.E.4
Van Den Bosch, N.H.A.5
Zorn, I.6
Grabreels-Festen, A.A.7
De Visser, M.8
Bolhuis, P.A.9
-
38
-
-
0029931697
-
Ultrastructural PMP22 expression in inherited demyelinating neuropathies
-
Vallat J.M., Sindou P., Preux P.M., Tabaraud F., Milor A.M., Couratier P., LeGuern E., Brice A. Ultrastructural PMP22 expression in inherited demyelinating neuropathies. Ann. Neurol. 39:1996;813-817.
-
(1996)
Ann. Neurol.
, vol.39
, pp. 813-817
-
-
Vallat, J.M.1
Sindou, P.2
Preux, P.M.3
Tabaraud, F.4
Milor, A.M.5
Couratier, P.6
Leguern, E.7
Brice, A.8
-
40
-
-
0028221758
-
Elevated expression of messenger RNA for peripheral myelin protein 22 in biopsied peripheral nerves of patients with Charcot-Marie-Tooth disease type 1A
-
Yoshikawa H., Nishimura T., Nakatsuji Y., Fujimura H., Himoro M., Hayasaka K., Sakjoda S., Yanagihara T. Elevated expression of messenger RNA for peripheral myelin protein 22 in biopsied peripheral nerves of patients with Charcot-Marie-Tooth disease type 1A. Ann. Neurol. 35:1994;445-450.
-
(1994)
Ann. Neurol.
, vol.35
, pp. 445-450
-
-
Yoshikawa, H.1
Nishimura, T.2
Nakatsuji, Y.3
Fujimura, H.4
Himoro, M.5
Hayasaka, K.6
Sakjoda, S.7
Yanagihara, T.8
-
41
-
-
0030011973
-
Genetic heterogeneity in Charcot-Marie-Tooth neuropathy type2
-
Yoshioka R., Dyck P.J., Chance P.F. Genetic heterogeneity in Charcot-Marie-Tooth neuropathy type2. Neurology. 46:1996;569-571.
-
(1996)
Neurology
, vol.46
, pp. 569-571
-
-
Yoshioka, R.1
Dyck, P.J.2
Chance, P.F.3
-
42
-
-
0031054533
-
Influence of elevated expression of rat wild type PMP22 and its mutant PMP22 (Trembler) on cell growth of NIH3T3 fibroblasts
-
Zoidl G., D'Urso D., Blass-Kampmann S., Schmalenbach C., Kuhn R., Müller H.W. Influence of elevated expression of rat wild type PMP22 and its mutant PMP22 (Trembler) on cell growth of NIH3T3 fibroblasts. Cell Tissue Res. 287:1997;459-470.
-
(1997)
Cell Tissue Res.
, vol.287
, pp. 459-470
-
-
Zoidl, G.1
D'Urso, D.2
Blass-Kampmann, S.3
Schmalenbach, C.4
Kuhn, R.5
Müller, H.W.6
|