-
1
-
-
0036524611
-
Molecular cell biology of Charcot-Marie-Tooth disease
-
Berger P., Young P., and Suter U. Molecular cell biology of Charcot-Marie-Tooth disease. Neurogenetics 4 (2002) 1-15
-
(2002)
Neurogenetics
, vol.4
, pp. 1-15
-
-
Berger, P.1
Young, P.2
Suter, U.3
-
2
-
-
0035182190
-
The transcription factor Sox10 is a key regulator of peripheral glial development
-
Britsch S., Goerich D.E., Riethmacher D., Peirano R.I., Rossner M., Nave K.A., Birchmeier C., and Wegner M. The transcription factor Sox10 is a key regulator of peripheral glial development. Genes Dev. 15 (2001) 66-78
-
(2001)
Genes Dev.
, vol.15
, pp. 66-78
-
-
Britsch, S.1
Goerich, D.E.2
Riethmacher, D.3
Peirano, R.I.4
Rossner, M.5
Nave, K.A.6
Birchmeier, C.7
Wegner, M.8
-
3
-
-
0036628504
-
Characterization of myelination in the developing zebrafish
-
Brosamle C., and Halpern M.E. Characterization of myelination in the developing zebrafish. Glia 39 (2002) 47-57
-
(2002)
Glia
, vol.39
, pp. 47-57
-
-
Brosamle, C.1
Halpern, M.E.2
-
4
-
-
0037029424
-
Multiple sclerosis
-
Compston A., and Coles A. Multiple sclerosis. Lancet 359 (2002) 1221-1231
-
(2002)
Lancet
, vol.359
, pp. 1221-1231
-
-
Compston, A.1
Coles, A.2
-
5
-
-
12644268233
-
A genetic screen for mutations affecting embryogenesis in zebrafish
-
Driever W., Solnica-Krezel L., Schier A.F., Neuhauss S.C., Malicki J., Stemple D.L., Stainier D.Y., Zwartkruis F., Abdelilah S., Rangini Z., Belak J., and Boggs C. A genetic screen for mutations affecting embryogenesis in zebrafish. Development 123 (1996) 37-46
-
(1996)
Development
, vol.123
, pp. 37-46
-
-
Driever, W.1
Solnica-Krezel, L.2
Schier, A.F.3
Neuhauss, S.C.4
Malicki, J.5
Stemple, D.L.6
Stainier, D.Y.7
Zwartkruis, F.8
Abdelilah, S.9
Rangini, Z.10
Belak, J.11
Boggs, C.12
-
6
-
-
0035173002
-
Zebrafish colourless encodes sox10 and specifies non-ectomesenchymal neural crest fates
-
Dutton K.A., Pauliny A., Lopes S.S., Elworthy S., Carney T.J., Rauch J., Geisler R., Haffter P., and Kelsh R.N. Zebrafish colourless encodes sox10 and specifies non-ectomesenchymal neural crest fates. Development 128 (2001) 4113-4125
-
(2001)
Development
, vol.128
, pp. 4113-4125
-
-
Dutton, K.A.1
Pauliny, A.2
Lopes, S.S.3
Elworthy, S.4
Carney, T.J.5
Rauch, J.6
Geisler, R.7
Haffter, P.8
Kelsh, R.N.9
-
7
-
-
0033777762
-
Neuregulin, a factor with many functions in the life of a Schwann cell
-
Garratt A.N., Britsch S., and Birchmeier C. Neuregulin, a factor with many functions in the life of a Schwann cell. BioEssays 22 (2000) 987-996
-
(2000)
BioEssays
, vol.22
, pp. 987-996
-
-
Garratt, A.N.1
Britsch, S.2
Birchmeier, C.3
-
8
-
-
0034610999
-
A dual role of erbB2 in myelination and in expansion of the Schwann cell precursor pool
-
Garratt A.N., Voiculescu O., Topilko P., Charnay P., and Birchmeier C. A dual role of erbB2 in myelination and in expansion of the Schwann cell precursor pool. J. Cell Biol. 148 (2000) 1035-1046
-
(2000)
J. Cell Biol.
, vol.148
, pp. 1035-1046
-
-
Garratt, A.N.1
Voiculescu, O.2
Topilko, P.3
Charnay, P.4
Birchmeier, C.5
-
9
-
-
0035865035
-
Charcot-Marie-Tooth disease (CMT): distinctive phenotypic and genotypic features in CMT type 2
-
Gemignani F., and Marbini A. Charcot-Marie-Tooth disease (CMT): distinctive phenotypic and genotypic features in CMT type 2. J. Neurol. Sci. 184 (2001) 1-9
-
(2001)
J. Neurol. Sci.
, vol.184
, pp. 1-9
-
-
Gemignani, F.1
Marbini, A.2
-
10
-
-
0037118261
-
Migration and function of a glial subtype in the vertebrate peripheral nervous system
-
Gilmour D.T., Maischein H.M., and Nusslein-Volhard C. Migration and function of a glial subtype in the vertebrate peripheral nervous system. Neuron 34 (2002) 577-588
-
(2002)
Neuron
, vol.34
, pp. 577-588
-
-
Gilmour, D.T.1
Maischein, H.M.2
Nusslein-Volhard, C.3
-
11
-
-
11344262287
-
Regulation of latent sensory hair cell precursors by glia in the zebrafish lateral line
-
Grant K.A., Raible D.W., and Piotrowski T. Regulation of latent sensory hair cell precursors by glia in the zebrafish lateral line. Neuron 45 (2005) 69-80
-
(2005)
Neuron
, vol.45
, pp. 69-80
-
-
Grant, K.A.1
Raible, D.W.2
Piotrowski, T.3
-
12
-
-
12644303221
-
The identification of genes with unique and essential functions in the development of the zebrafish, Danio rerio
-
Haffter P., Granato M., Brand M., Mullins M.C., Hammerschmidt M., Kane D.A., Odenthal J., van Eeden F.J., Jiang Y.J., Heisenberg C.P., Kelsh R.N., Furutani-Seiki M., Vogelsang E., Beuchle D., Schach U., Fabian C., and Nusslein-Volhard C. The identification of genes with unique and essential functions in the development of the zebrafish, Danio rerio. Development 123 (1996) 1-36
-
(1996)
Development
, vol.123
, pp. 1-36
-
-
Haffter, P.1
Granato, M.2
Brand, M.3
Mullins, M.C.4
Hammerschmidt, M.5
Kane, D.A.6
Odenthal, J.7
van Eeden, F.J.8
Jiang, Y.J.9
Heisenberg, C.P.10
Kelsh, R.N.11
Furutani-Seiki, M.12
Vogelsang, E.13
Beuchle, D.14
Schach, U.15
Fabian, C.16
Nusslein-Volhard, C.17
-
13
-
-
0037224513
-
Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients
-
Hattori N., Yamamoto M., Yoshihara T., Koike H., Nakagawa M., Yoshikawa H., Ohnishi A., Hayasaka K., Onodera O., Baba M., Yasuda H., Saito T., Nakashima K., Kira J., Kaji R., Oka N., and Sobue G. Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients. Brain 126 (2003) 134-151
-
(2003)
Brain
, vol.126
, pp. 134-151
-
-
Hattori, N.1
Yamamoto, M.2
Yoshihara, T.3
Koike, H.4
Nakagawa, M.5
Yoshikawa, H.6
Ohnishi, A.7
Hayasaka, K.8
Onodera, O.9
Baba, M.10
Yasuda, H.11
Saito, T.12
Nakashima, K.13
Kira, J.14
Kaji, R.15
Oka, N.16
Sobue, G.17
-
14
-
-
0027221141
-
Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene
-
Hayasaka K., Himoro M., Sato W., Takada G., Uyemura K., Shimizu N., Bird T.D., Conneally P.M., and Chance P.F. Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin 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
-
-
12144285746
-
Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations
-
Inoue K., Khajavi M., Ohyama T., Hirabayashi S., Wilson J., Reggin J.D., Mancias P., Butler I.J., Wilkinson M.F., Wegner M., and Lupski J.R. Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations. Nat. Genet. 36 (2004) 361-369
-
(2004)
Nat. Genet.
, vol.36
, pp. 361-369
-
-
Inoue, K.1
Khajavi, M.2
Ohyama, T.3
Hirabayashi, S.4
Wilson, J.5
Reggin, J.D.6
Mancias, P.7
Butler, I.J.8
Wilkinson, M.F.9
Wegner, M.10
Lupski, J.R.11
-
16
-
-
0029795302
-
The POU factor Oct-6 and Schwann cell differentiation
-
Jaegle M., Mandemakers W., Broos L., Zwart R., Karis A., Visser P., Grosveld F., and Meijer D. The POU factor Oct-6 and Schwann cell differentiation. Science 273 (1996) 507-510
-
(1996)
Science
, vol.273
, pp. 507-510
-
-
Jaegle, M.1
Mandemakers, W.2
Broos, L.3
Zwart, R.4
Karis, A.5
Visser, P.6
Grosveld, F.7
Meijer, D.8
-
17
-
-
0038623319
-
The POU proteins Brn-2 and Oct-6 share important functions in Schwann cell development
-
Jaegle M., Ghazvini M., Mandemakers W., Piirsoo M., Driegen S., Levavasseur F., Raghoenath S., Grosveld F., and Meijer D. The POU proteins Brn-2 and Oct-6 share important functions in Schwann cell development. Genes Dev. 17 (2003) 1380-1391
-
(2003)
Genes Dev.
, vol.17
, pp. 1380-1391
-
-
Jaegle, M.1
Ghazvini, M.2
Mandemakers, W.3
Piirsoo, M.4
Driegen, S.5
Levavasseur, F.6
Raghoenath, S.7
Grosveld, F.8
Meijer, D.9
-
18
-
-
0036799650
-
Multiple sclerosis: re-expression of a developmental pathway that restricts oligodendrocyte maturation
-
John G.R., Shankar S.L., Shafit-Zagardo B., Massimi A., Lee S.C., Raine C.S., and Brosnan C.F. Multiple sclerosis: re-expression of a developmental pathway that restricts oligodendrocyte maturation. Nat. Med. 8 (2002) 1115-1121
-
(2002)
Nat. Med.
, vol.8
, pp. 1115-1121
-
-
John, G.R.1
Shankar, S.L.2
Shafit-Zagardo, B.3
Massimi, A.4
Lee, S.C.5
Raine, C.S.6
Brosnan, C.F.7
-
19
-
-
20444457446
-
Multiple sclerosis-Novel insights and new therapeutic strategies
-
Kieseier B.C., Hemmer B., and Hartung H.P. Multiple sclerosis-Novel insights and new therapeutic strategies. Curr. Opin. Neurol. 18 (2005) 211-220
-
(2005)
Curr. Opin. Neurol.
, vol.18
, pp. 211-220
-
-
Kieseier, B.C.1
Hemmer, B.2
Hartung, H.P.3
-
20
-
-
0027749249
-
A functionally conserved homolog of the Drosophila segment polarity gene hh is expressed in tissues with polarizing activity in zebrafish embryos
-
Krauss S., Concordet J.P., and Ingham P.W. A functionally conserved homolog of the Drosophila segment polarity gene hh is expressed in tissues with polarizing activity in zebrafish embryos. Cell 75 (1993) 1431-1444
-
(1993)
Cell
, vol.75
, pp. 1431-1444
-
-
Krauss, S.1
Concordet, J.P.2
Ingham, P.W.3
-
21
-
-
0032103773
-
Comparison of sequence and function of the Oct-6 genes in zebrafish, chicken and mouse
-
Levavasseur F., Mandemakers W., Visser P., Broos L., Grosveld F., Zivkovic D., and Meijer D. Comparison of sequence and function of the Oct-6 genes in zebrafish, chicken and mouse. Mech. Dev. 74 (1998) 89-98
-
(1998)
Mech. Dev.
, vol.74
, pp. 89-98
-
-
Levavasseur, F.1
Mandemakers, W.2
Visser, P.3
Broos, L.4
Grosveld, F.5
Zivkovic, D.6
Meijer, D.7
-
22
-
-
0033153156
-
Laser ablations reveal functional relationships of segmental hindbrain neurons in zebrafish
-
Liu K.S., and Fetcho J.R. Laser ablations reveal functional relationships of segmental hindbrain neurons in zebrafish. Neuron 23 (1999) 325-335
-
(1999)
Neuron
, vol.23
, pp. 325-335
-
-
Liu, K.S.1
Fetcho, J.R.2
-
23
-
-
12444347847
-
Supernumerary neuromasts in the posterior lateral line of zebrafish lacking peripheral glia
-
Lopez-Schier H., and Hudspeth A.J. Supernumerary neuromasts in the posterior lateral line of zebrafish lacking peripheral glia. Proc. Natl. Acad. Sci. U. S. A. 102 (2005) 1496-1501
-
(2005)
Proc. Natl. Acad. Sci. U. S. A.
, vol.102
, pp. 1496-1501
-
-
Lopez-Schier, H.1
Hudspeth, A.J.2
-
24
-
-
0033767315
-
Sonic hedgehog-regulated oligodendrocyte lineage genes encoding bHLH proteins in the mammalian central nervous system
-
Lu Q.R., Yuk D., Alberta J.A., Zhu Z., Pawlitzky I., Chan J., McMahon A.P., Stiles C.D., and Rowitch D.H. Sonic hedgehog-regulated oligodendrocyte lineage genes encoding bHLH proteins in the mammalian central nervous system. Neuron 25 (2000) 317-329
-
(2000)
Neuron
, vol.25
, pp. 317-329
-
-
Lu, Q.R.1
Yuk, D.2
Alberta, J.A.3
Zhu, Z.4
Pawlitzky, I.5
Chan, J.6
McMahon, A.P.7
Stiles, C.D.8
Rowitch, D.H.9
-
25
-
-
0037023529
-
Common developmental requirement for Olig function indicates a motor neuron/oligodendrocyte connection
-
Lu Q.R., Sun T., Zhu Z., Ma N., Garcia M., Stiles C.D., and Rowitch D.H. Common developmental requirement for Olig function indicates a motor neuron/oligodendrocyte connection. Cell 109 (2002) 75-86
-
(2002)
Cell
, vol.109
, pp. 75-86
-
-
Lu, Q.R.1
Sun, T.2
Zhu, Z.3
Ma, N.4
Garcia, M.5
Stiles, C.D.6
Rowitch, D.H.7
-
26
-
-
15744394897
-
erbb3 and erbb2 are essential for Schwann cell migration and myelination in zebrafish
-
Lyons D.A., Pogoda H.M., Voas M.G., Woods I.G., Diamond B., Nix R., Arana N., Jacobs J., and Talbot W.S. erbb3 and erbb2 are essential for Schwann cell migration and myelination in zebrafish. Curr. Biol. 15 (2005) 513-524
-
(2005)
Curr. Biol.
, vol.15
, pp. 513-524
-
-
Lyons, D.A.1
Pogoda, H.M.2
Voas, M.G.3
Woods, I.G.4
Diamond, B.5
Nix, R.6
Arana, N.7
Jacobs, J.8
Talbot, W.S.9
-
27
-
-
0029896428
-
Glial growth factor 2, a soluble neuregulin, directly increases Schwann cell motility and indirectly promotes neurite outgrowth
-
Mahanthappa N.K., Anton E.S., and Matthew W.D. Glial growth factor 2, a soluble neuregulin, directly increases Schwann cell motility and indirectly promotes neurite outgrowth. J. Neurosci. 16 (1996) 4673-4683
-
(1996)
J. Neurosci.
, vol.16
, pp. 4673-4683
-
-
Mahanthappa, N.K.1
Anton, E.S.2
Matthew, W.D.3
-
28
-
-
0035048547
-
The neuron-glia signal beta-neuregulin promotes Schwann cell motility via the MAPK pathway
-
Meintanis S., Thomaidou D., Jessen K.R., Mirsky R., and Matsas R. The neuron-glia signal beta-neuregulin promotes Schwann cell motility via the MAPK pathway. Glia 34 (2001) 39-51
-
(2001)
Glia
, vol.34
, pp. 39-51
-
-
Meintanis, S.1
Thomaidou, D.2
Jessen, K.R.3
Mirsky, R.4
Matsas, R.5
-
29
-
-
2142707240
-
Rho kinase regulates Schwann cell myelination and formation of associated axonal domains
-
Melendez-Vasquez C.V., Einheber S., and Salzer J.L. Rho kinase regulates Schwann cell myelination and formation of associated axonal domains. J. Neurosci. 24 (2004) 3953-3963
-
(2004)
J. Neurosci.
, vol.24
, pp. 3953-3963
-
-
Melendez-Vasquez, C.V.1
Einheber, S.2
Salzer, J.L.3
-
30
-
-
2342444048
-
Axonal neuregulin-1 regulates myelin sheath thickness
-
Michailov G.V., Sereda M.W., Brinkmann B.G., Fischer T.M., Haug B., Birchmeier C., Role L., Lai C., Schwab M.H., and Nave K.A. Axonal neuregulin-1 regulates myelin sheath thickness. Science 304 (2004) 700-703
-
(2004)
Science
, vol.304
, pp. 700-703
-
-
Michailov, G.V.1
Sereda, M.W.2
Brinkmann, B.G.3
Fischer, T.M.4
Haug, B.5
Birchmeier, C.6
Role, L.7
Lai, C.8
Schwab, M.H.9
Nave, K.A.10
-
31
-
-
0033152451
-
Rescue of the cardiac defect in ErbB2 mutant mice reveals essential roles of ErbB2 in peripheral nervous system development
-
Morris J.K., Lin W., Hauser C., Marchuk Y., Getman D., and Lee K.F. Rescue of the cardiac defect in ErbB2 mutant mice reveals essential roles of ErbB2 in peripheral nervous system development. Neuron 23 (1999) 273-283
-
(1999)
Neuron
, vol.23
, pp. 273-283
-
-
Morris, J.K.1
Lin, W.2
Hauser, C.3
Marchuk, Y.4
Getman, D.5
Lee, K.F.6
-
32
-
-
20144367738
-
Monorail/Foxa2 regulates floorplate differentiation and specification of oligodendrocytes, serotonergic raphe neurones and cranial motoneurones
-
Norton W.H., Mangoli M., Lele Z., Pogoda H.M., Diamond B., Mercurio S., Russell C., Teraoka H., Stickney H.L., Rauch G.J., Heisenberg C.P., Houart C., Schilling T.F., Frohnhoefer H.G., Rastegar S., Neumann C.J., Gardiner R.M., Strahle U., Geisler R., Rees M., Talbot W.S., and Wilson S.W. Monorail/Foxa2 regulates floorplate differentiation and specification of oligodendrocytes, serotonergic raphe neurones and cranial motoneurones. Development 132 (2005) 645-658
-
(2005)
Development
, vol.132
, pp. 645-658
-
-
Norton, W.H.1
Mangoli, M.2
Lele, Z.3
Pogoda, H.M.4
Diamond, B.5
Mercurio, S.6
Russell, C.7
Teraoka, H.8
Stickney, H.L.9
Rauch, G.J.10
Heisenberg, C.P.11
Houart, C.12
Schilling, T.F.13
Frohnhoefer, H.G.14
Rastegar, S.15
Neumann, C.J.16
Gardiner, R.M.17
Strahle, U.18
Geisler, R.19
Rees, M.20
Talbot, W.S.21
Wilson, S.W.22
more..
-
33
-
-
0027172623
-
Cloning of the zebrafish krox-20 gene (krx-20) and its expression during hindbrain development
-
Oxtoby E., and Jowett T. Cloning of the zebrafish krox-20 gene (krx-20) and its expression during hindbrain development. Nucleic Acids Res. 21 (1993) 1087-1095
-
(1993)
Nucleic Acids Res.
, vol.21
, pp. 1087-1095
-
-
Oxtoby, E.1
Jowett, T.2
-
34
-
-
0036036430
-
olig2 is required for zebrafish primary motor neuron and oligodendrocyte development
-
Park H.C., Mehta A., Richardson J.S., and Appel B. olig2 is required for zebrafish primary motor neuron and oligodendrocyte development. Dev. Biol. 248 (2002) 356-368
-
(2002)
Dev. Biol.
, vol.248
, pp. 356-368
-
-
Park, H.C.1
Mehta, A.2
Richardson, J.S.3
Appel, B.4
-
35
-
-
12144284478
-
Spatial and temporal regulation of ventral spinal cord precursor specification by Hedgehog signaling
-
Park H.C., Shin J., and Appel B. Spatial and temporal regulation of ventral spinal cord precursor specification by Hedgehog signaling. Development 131 (2004) 5959-5969
-
(2004)
Development
, vol.131
, pp. 5959-5969
-
-
Park, H.C.1
Shin, J.2
Appel, B.3
-
36
-
-
0026879614
-
The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A
-
Patel P.I., Roa B.B., Welcher A.A., Schoener-Scott R., Trask B.J., Pentao L., Snipes G.J., Garcia C.A., Francke U., Shooter E.M., Lupski J.R., and Suter U. The gene for the peripheral myelin protein PMP-22 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
Trask, 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
-
37
-
-
17344366171
-
SOX10 mutations in patients with Waardenburg-Hirschsprung disease
-
Pingault V., Bondurand N., Kuhlbrodt K., Goerich D.E., Prehu M.O., Puliti A., Herbarth B., Hermans-Borgmeyer I., Legius E., Matthijs G., Amiel J., Lyonnet S., Ceccherini I., Romeo G., Smith J.C., Read A.P., Wegner M., and Goossens M. SOX10 mutations in patients with Waardenburg-Hirschsprung disease. Nat. Genet. 18 (1998) 171-173
-
(1998)
Nat. Genet.
, vol.18
, pp. 171-173
-
-
Pingault, V.1
Bondurand, N.2
Kuhlbrodt, K.3
Goerich, D.E.4
Prehu, M.O.5
Puliti, A.6
Herbarth, B.7
Hermans-Borgmeyer, I.8
Legius, E.9
Matthijs, G.10
Amiel, J.11
Lyonnet, S.12
Ceccherini, I.13
Romeo, G.14
Smith, J.C.15
Read, A.P.16
Wegner, M.17
Goossens, M.18
-
38
-
-
0034295096
-
Peripheral neuropathy with hypomyelination, chronic intestinal pseudo-obstruction and deafness: a developmental "neural crest syndrome" related to a SOX10 mutation
-
Pingault V., Guiochon-Mantel A., Bondurand N., Faure C., Lacroix C., Lyonnet S., Goossens M., and Landrieu P. Peripheral neuropathy with hypomyelination, chronic intestinal pseudo-obstruction and deafness: a developmental "neural crest syndrome" related to a SOX10 mutation. Ann. Neurol. 48 (2000) 671-676
-
(2000)
Ann. Neurol.
, vol.48
, pp. 671-676
-
-
Pingault, V.1
Guiochon-Mantel, A.2
Bondurand, N.3
Faure, C.4
Lacroix, C.5
Lyonnet, S.6
Goossens, M.7
Landrieu, P.8
-
39
-
-
0141987863
-
Polarized domains of myelinated axons
-
Salzer J.L. Polarized domains of myelinated axons. Neuron 40 (2003) 297-318
-
(2003)
Neuron
, vol.40
, pp. 297-318
-
-
Salzer, J.L.1
-
40
-
-
0014384476
-
A modified method for lead staining of thin sections
-
Sato T. A modified method for lead staining of thin sections. J. Electron. Microsc. (Tokyo) 17 (1968) 158-159
-
(1968)
J. Electron. Microsc. (Tokyo)
, vol.17
, pp. 158-159
-
-
Sato, T.1
-
41
-
-
0036130074
-
Recent progress on the molecular organization of myelinated axons
-
Scherer S.S., and Arroyo E.J. Recent progress on the molecular organization of myelinated axons. J. Peripher. Nerv. Syst. 7 (2002) 1-12
-
(2002)
J. Peripher. Nerv. Syst.
, vol.7
, pp. 1-12
-
-
Scherer, S.S.1
Arroyo, E.J.2
-
42
-
-
25144469422
-
Mechanisms of axon ensheathment and myelin growth
-
Sherman D.L., and Brophy P.J. Mechanisms of axon ensheathment and myelin growth. Nat. Rev., Neurosci. 6 (2005) 683-690
-
(2005)
Nat. Rev., Neurosci.
, vol.6
, pp. 683-690
-
-
Sherman, D.L.1
Brophy, P.J.2
-
43
-
-
0037080877
-
Terminal differentiation of myelin-forming oligodendrocytes depends on the transcription factor Sox10
-
Stolt C.C., Rehberg S., Ader M., Lommes P., Riethmacher D., Schachner M., Bartsch U., and Wegner M. Terminal differentiation of myelin-forming oligodendrocytes depends on the transcription factor Sox10. Genes Dev. 16 (2002) 165-170
-
(2002)
Genes Dev.
, vol.16
, pp. 165-170
-
-
Stolt, C.C.1
Rehberg, S.2
Ader, M.3
Lommes, P.4
Riethmacher, D.5
Schachner, M.6
Bartsch, U.7
Wegner, M.8
-
44
-
-
0141833983
-
Disease mechanisms in inherited neuropathies
-
Suter U., and Scherer S.S. Disease mechanisms in inherited neuropathies. Nat. Rev., Neurosci. 4 (2003) 714-726
-
(2003)
Nat. Rev., Neurosci.
, vol.4
, pp. 714-726
-
-
Suter, U.1
Scherer, S.S.2
-
45
-
-
0029808996
-
Cell death in the Schwann cell lineage and its regulation by neuregulin
-
Syroid D.E., Maycox P.R., Burrola P.G., Liu N., Wen D., Lee K.F., Lemke G., and Kilpatrick T.J. Cell death in the Schwann cell lineage and its regulation by neuregulin. Proc. Natl. Acad. Sci. U. S. A. 93 (1996) 9229-9234
-
(1996)
Proc. Natl. Acad. Sci. U. S. A.
, vol.93
, pp. 9229-9234
-
-
Syroid, D.E.1
Maycox, P.R.2
Burrola, P.G.3
Liu, N.4
Wen, D.5
Lee, K.F.6
Lemke, G.7
Kilpatrick, T.J.8
-
46
-
-
0037046813
-
The basic helix-loop-helix factor olig2 is essential for the development of motoneuron and oligodendrocyte lineages
-
Takebayashi H., Nabeshima Y., Yoshida S., Chisaka O., and Ikenaka K. The basic helix-loop-helix factor olig2 is essential for the development of motoneuron and oligodendrocyte lineages. Curr. Biol. 12 (2002) 1157-1163
-
(2002)
Curr. Biol.
, vol.12
, pp. 1157-1163
-
-
Takebayashi, H.1
Nabeshima, Y.2
Yoshida, S.3
Chisaka, O.4
Ikenaka, K.5
-
47
-
-
0032614994
-
Positional cloning of mutated zebrafish genes
-
Talbot W.S., and Schier A.F. Positional cloning of mutated zebrafish genes. Methods Cell Biol. 60 (1999) 259-286
-
(1999)
Methods Cell Biol.
, vol.60
, pp. 259-286
-
-
Talbot, W.S.1
Schier, A.F.2
-
48
-
-
23944503110
-
Neuregulin-1 type III determines the ensheathment fate of axons
-
Taveggia C., Zanazzi G., Petrylak A., Yano H., Rosenbluth J., Einheber S., Xu X., Esper R.M., Loeb J.A., Shrager P., Chao M.V., Falls D.L., Role L., and Salzer J.L. Neuregulin-1 type III determines the ensheathment fate of axons. Neuron 47 (2005) 681-694
-
(2005)
Neuron
, vol.47
, pp. 681-694
-
-
Taveggia, C.1
Zanazzi, G.2
Petrylak, A.3
Yano, H.4
Rosenbluth, J.5
Einheber, S.6
Xu, X.7
Esper, R.M.8
Loeb, J.A.9
Shrager, P.10
Chao, M.V.11
Falls, D.L.12
Role, L.13
Salzer, J.L.14
-
49
-
-
0028170203
-
Goosecoid expression in neurectoderm and mesendoderm is disrupted in zebrafish cyclops gastrulas
-
Thisse C., Thisse B., Halpern M.E., and Postlethwait J.H. Goosecoid expression in neurectoderm and mesendoderm is disrupted in zebrafish cyclops gastrulas. Dev. Biol. 164 (1994) 420-429
-
(1994)
Dev. Biol.
, vol.164
, pp. 420-429
-
-
Thisse, C.1
Thisse, B.2
Halpern, M.E.3
Postlethwait, J.H.4
-
50
-
-
0027984497
-
Krox-20 controls myelination in the peripheral nervous system
-
Topilko P., Schneider-Maunoury S., Levi G., Baron-Van Evercooren A., Chennoufi A.B., Seitanidou T., Babinet C., and Charnay P. Krox-20 controls myelination in the peripheral nervous system. Nature 371 (1994) 796-799
-
(1994)
Nature
, vol.371
, pp. 796-799
-
-
Topilko, P.1
Schneider-Maunoury, S.2
Levi, G.3
Baron-Van Evercooren, A.4
Chennoufi, A.B.5
Seitanidou, T.6
Babinet, C.7
Charnay, P.8
-
51
-
-
0024392732
-
Pelizaeus-Merzbacher disease: tight linkage to proteolipid protein gene exon variant
-
Trofatter J.A., Dlouhy S.R., DeMyer W., Conneally P.M., and Hodes M.E. Pelizaeus-Merzbacher disease: tight linkage to proteolipid protein gene exon variant. Proc. Natl. Acad. Sci. U. S. A. 86 (1989) 9427-9430
-
(1989)
Proc. Natl. Acad. Sci. U. S. A.
, vol.86
, pp. 9427-9430
-
-
Trofatter, J.A.1
Dlouhy, S.R.2
DeMyer, W.3
Conneally, P.M.4
Hodes, M.E.5
-
53
-
-
0032126751
-
Notch receptor activation inhibits oligodendrocyte differentiation
-
Wang S., Sdrulla A.D., diSibio G., Bush G., Nofziger D., Hicks C., Weinmaster G., and Barres B.A. Notch receptor activation inhibits oligodendrocyte differentiation. Neuron 21 (1998) 63-75
-
(1998)
Neuron
, vol.21
, pp. 63-75
-
-
Wang, S.1
Sdrulla, A.D.2
diSibio, G.3
Bush, G.4
Nofziger, D.5
Hicks, C.6
Weinmaster, G.7
Barres, B.A.8
-
54
-
-
0031943222
-
Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies
-
Warner L.E., Mancias P., Butler I.J., McDonald C.M., Keppen L., Koob K.G., and Lupski J.R. Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies. Nat. Genet. 18 (1998) 382-384
-
(1998)
Nat. Genet.
, vol.18
, pp. 382-384
-
-
Warner, L.E.1
Mancias, P.2
Butler, I.J.3
McDonald, C.M.4
Keppen, L.5
Koob, K.G.6
Lupski, J.R.7
-
55
-
-
0033214223
-
Peripheral nervous system defects in erbB2 mutants following genetic rescue of heart development
-
Woldeyesus M.T., Britsch S., Riethmacher D., Xu L., Sonnenberg-Riethmacher E., Abou-Rebyeh F., Harvey R., Caroni P., and Birchmeier C. Peripheral nervous system defects in erbB2 mutants following genetic rescue of heart development. Genes Dev. 13 (1999) 2538-2548
-
(1999)
Genes Dev.
, vol.13
, pp. 2538-2548
-
-
Woldeyesus, M.T.1
Britsch, S.2
Riethmacher, D.3
Xu, L.4
Sonnenberg-Riethmacher, E.5
Abou-Rebyeh, F.6
Harvey, R.7
Caroni, P.8
Birchmeier, C.9
-
56
-
-
24344440632
-
The zebrafish gene map defines ancestral vertebrate chromosomes
-
Woods I.G., Wilson C., Friedlander B., Chang P., Reyes D.K., Nix R., Kelly P.D., Chu F., Postlethwait J.H., and Talbot W.S. The zebrafish gene map defines ancestral vertebrate chromosomes. Genome Res. 15 (2005) 1307-1314
-
(2005)
Genome Res.
, vol.15
, pp. 1307-1314
-
-
Woods, I.G.1
Wilson, C.2
Friedlander, B.3
Chang, P.4
Reyes, D.K.5
Nix, R.6
Kelly, P.D.7
Chu, F.8
Postlethwait, J.H.9
Talbot, W.S.10
-
57
-
-
33645858252
-
nsf is essential for organization of myelinated axons in zebrafish
-
Woods I.G., Lyons D.A., Voas M.G., Pogoda H.M., and Talbot W.S. nsf is essential for organization of myelinated axons in zebrafish. Curr. Biol. 16 (2006) 636-648
-
(2006)
Curr. Biol.
, vol.16
, pp. 636-648
-
-
Woods, I.G.1
Lyons, D.A.2
Voas, M.G.3
Pogoda, H.M.4
Talbot, W.S.5
-
58
-
-
20144388760
-
A pair of Sox: distinct and overlapping functions of zebrafish sox9 co-orthologs in craniofacial and pectoral fin development
-
Yan Y.L., Willoughby J., Liu D., Crump J.G., Wilson C., Miller C.T., Singer A., Kimmel C., Westerfield M., and Postlethwait J.H. A pair of Sox: distinct and overlapping functions of zebrafish sox9 co-orthologs in craniofacial and pectoral fin development. Development 132 (2005) 1069-1083
-
(2005)
Development
, vol.132
, pp. 1069-1083
-
-
Yan, Y.L.1
Willoughby, J.2
Liu, D.3
Crump, J.G.4
Wilson, C.5
Miller, C.T.6
Singer, A.7
Kimmel, C.8
Westerfield, M.9
Postlethwait, J.H.10
-
59
-
-
0037023492
-
The bHLH transcription factors OLIG2 and OLIG1 couple neuronal and glial subtype specification
-
Zhou Q., and Anderson D.J. The bHLH transcription factors OLIG2 and OLIG1 couple neuronal and glial subtype specification. Cell 109 (2002) 61-73
-
(2002)
Cell
, vol.109
, pp. 61-73
-
-
Zhou, Q.1
Anderson, D.J.2
-
61
-
-
0033764232
-
Identification of a novel family of oligodendrocyte lineage-specific basic helix-loop-helix transcription factors
-
Zhou Q., Wang S., and Anderson D.J. Identification of a novel family of oligodendrocyte lineage-specific basic helix-loop-helix transcription factors. Neuron 25 (2000) 331-343
-
(2000)
Neuron
, vol.25
, pp. 331-343
-
-
Zhou, Q.1
Wang, S.2
Anderson, D.J.3
-
62
-
-
0030221510
-
The transcription factors SCIP and Krox-20 mark distinct stages and cell fates in Schwann cell differentiation
-
Zorick T.S., Syroid D.E., Arroyo E., Scherer S.S., and Lemke G. The transcription factors SCIP and Krox-20 mark distinct stages and cell fates in Schwann cell differentiation. Mol. Cell. Neurosci. 8 (1996) 129-145
-
(1996)
Mol. Cell. Neurosci.
, vol.8
, pp. 129-145
-
-
Zorick, T.S.1
Syroid, D.E.2
Arroyo, E.3
Scherer, S.S.4
Lemke, G.5
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