-
1
-
-
79957661916
-
The MADS box transcription factor MEF2C regulates melanocyte development and is a direct transcriptional target and partner of SOX10
-
Agarwal P., Verzi M.P., Nguyen T., Hu J., Ehlers M.L., McCulley D.J., Xu S.M., Dodou E., Anderson J.P., Wei M.L., Black B.L. The MADS box transcription factor MEF2C regulates melanocyte development and is a direct transcriptional target and partner of SOX10. Development 2011, 138:2555-2565.
-
(2011)
Development
, vol.138
, pp. 2555-2565
-
-
Agarwal, P.1
Verzi, M.P.2
Nguyen, T.3
Hu, J.4
Ehlers, M.L.5
McCulley, D.J.6
Xu, S.M.7
Dodou, E.8
Anderson, J.P.9
Wei, M.L.10
Black, B.L.11
-
2
-
-
80052431167
-
Unraveling the transcriptional regulatory machinery in chondrogenesis
-
Akiyama H., Lefebvre V. Unraveling the transcriptional regulatory machinery in chondrogenesis. J. Bone Miner. Metab. 2011, 29:390-395.
-
(2011)
J. Bone Miner. Metab.
, vol.29
, pp. 390-395
-
-
Akiyama, H.1
Lefebvre, V.2
-
3
-
-
38349112858
-
Hirschsprung disease, associated syndromes and genetics: a review
-
Amiel J., Sproat-Emison E., Garcia-Barcelo M., Lantieri F., Burzynski G., Borrego S., Pelet A., Arnold S., Miao X., Griseri P., Brooks A.S., Antinolo G., de Pontual L., Clement-Ziza M., Munnich A., Kashuk C., West K., Wong K.K., Lyonnet S., Chakravarti A., Tam P.K., Ceccherini I., Hofstra R.M., Fernandez R. Hirschsprung disease, associated syndromes and genetics: a review. J. Med. Genet. 2008, 45:1-14.
-
(2008)
J. Med. Genet.
, vol.45
, pp. 1-14
-
-
Amiel, J.1
Sproat-Emison, E.2
Garcia-Barcelo, M.3
Lantieri, F.4
Burzynski, G.5
Borrego, S.6
Pelet, A.7
Arnold, S.8
Miao, X.9
Griseri, P.10
Brooks, A.S.11
Antinolo, G.12
de Pontual, L.13
Clement-Ziza, M.14
Munnich, A.15
Kashuk, C.16
West, K.17
Wong, K.K.18
Lyonnet, S.19
Chakravarti, A.20
Tam, P.K.21
Ceccherini, I.22
Hofstra, R.M.23
Fernandez, R.24
more..
-
4
-
-
31144459828
-
Deletion of long-range sequences at Sox10 compromises developmental expression in a mouse model of Waardenburg-Shah (WS4) syndrome
-
Antonellis A., Bennett W.R., Menheniott T.R., Prasad A.B., Lee-Lin S.Q., Green E.D., Paisley D., Kelsh R.N., Pavan W.J., Ward A. Deletion of long-range sequences at Sox10 compromises developmental expression in a mouse model of Waardenburg-Shah (WS4) syndrome. Hum. Mol. Genet. 2006, 15:259-271.
-
(2006)
Hum. Mol. Genet.
, vol.15
, pp. 259-271
-
-
Antonellis, A.1
Bennett, W.R.2
Menheniott, T.R.3
Prasad, A.B.4
Lee-Lin, S.Q.5
Green, E.D.6
Paisley, D.7
Kelsh, R.N.8
Pavan, W.J.9
Ward, A.10
-
5
-
-
52949123269
-
Identification of neural crest and glial enhancers at the mouse Sox10 locus through transgenesis in zebrafish
-
Antonellis A., Huynh J.L., Lee-Lin S.Q., Vinton R.M., Renaud G., Loftus S.K., Elliot G., Wolfsberg T.G., Green E.D., McCallion A.S., Pavan W.J. Identification of neural crest and glial enhancers at the mouse Sox10 locus through transgenesis in zebrafish. PLoS Genet. 2008, 4:e1000174.
-
(2008)
PLoS Genet.
, vol.4
-
-
Antonellis, A.1
Huynh, J.L.2
Lee-Lin, S.Q.3
Vinton, R.M.4
Renaud, G.5
Loftus, S.K.6
Elliot, G.7
Wolfsberg, T.G.8
Green, E.D.9
McCallion, A.S.10
Pavan, W.J.11
-
6
-
-
0038046074
-
Sox10 regulates the development of neural crest-derived melanocytes in Xenopus
-
Aoki Y., Saint-Germain N., Gyda M., Magner-Fink E., Lee Y.H., Credidio C., Saint-Jeannet J.P. Sox10 regulates the development of neural crest-derived melanocytes in Xenopus. Dev. Biol. 2003, 259:19-33.
-
(2003)
Dev. Biol.
, vol.259
, pp. 19-33
-
-
Aoki, Y.1
Saint-Germain, N.2
Gyda, M.3
Magner-Fink, E.4
Lee, Y.H.5
Credidio, C.6
Saint-Jeannet, J.P.7
-
7
-
-
84864600759
-
Screening of MITF and SOX10 regulatory regions in Waardenburg syndrome type 2
-
Baral V., Chaoui A., Watanabe Y., Goossens M., Attie-Bitach T., Marlin S., Pingault V., Bondurand N. Screening of MITF and SOX10 regulatory regions in Waardenburg syndrome type 2. PLoS One 2012, 7:e41927.
-
(2012)
PLoS One
, vol.7
-
-
Baral, V.1
Chaoui, A.2
Watanabe, Y.3
Goossens, M.4
Attie-Bitach, T.5
Marlin, S.6
Pingault, V.7
Bondurand, N.8
-
8
-
-
61749098571
-
Aplasia of cochlear nerves and olfactory bulbs in association with SOX10 mutation
-
Barnett C.P., Mendoza-Londono R., Blaser S., Gillis J., Dupuis L., Levin A.V., Chiang P.W., Spector E., Reardon W. Aplasia of cochlear nerves and olfactory bulbs in association with SOX10 mutation. Am. J. Med. Genet. A 2009, 149A:431-436.
-
(2009)
Am. J. Med. Genet. A
, vol.149 A
, pp. 431-436
-
-
Barnett, C.P.1
Mendoza-Londono, R.2
Blaser, S.3
Gillis, J.4
Dupuis, L.5
Levin, A.V.6
Chiang, P.W.7
Spector, E.8
Reardon, W.9
-
9
-
-
76549106275
-
SOX E genes: SOX9 and SOX8 in mammalian testis development
-
Barrionuevo F., Scherer G. SOX E genes: SOX9 and SOX8 in mammalian testis development. Int. J. Biochem. Cell Biol. 2009, 42:433-436.
-
(2009)
Int. J. Biochem. Cell Biol.
, vol.42
, pp. 433-436
-
-
Barrionuevo, F.1
Scherer, G.2
-
11
-
-
61349104285
-
Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence
-
Benko S., Fantes J.A., Amiel J., Kleinjan D.J., Thomas S., Ramsay J., Jamshidi N., Essafi A., Heaney S., Gordon C.T., McBride D., Golzio C., Fisher M., Perry P., Abadie V., Ayuso C., Holder-Espinasse M., Kilpatrick N., Lees M.M., Picard A., Temple I.K., Thomas P., Vazquez M.P., Vekemans M., Roest Crollius H., Hastie N.D., Munnich A., Etchevers H.C., Pelet A., Farlie P.G., Fitzpatrick D.R., Lyonnet S. Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence. Nat. Genet. 2009, 41:359-364.
-
(2009)
Nat. Genet.
, vol.41
, pp. 359-364
-
-
Benko, S.1
Fantes, J.A.2
Amiel, J.3
Kleinjan, D.J.4
Thomas, S.5
Ramsay, J.6
Jamshidi, N.7
Essafi, A.8
Heaney, S.9
Gordon, C.T.10
McBride, D.11
Golzio, C.12
Fisher, M.13
Perry, P.14
Abadie, V.15
Ayuso, C.16
Holder-Espinasse, M.17
Kilpatrick, N.18
Lees, M.M.19
Picard, A.20
Temple, I.K.21
Thomas, P.22
Vazquez, M.P.23
Vekemans, M.24
Roest Crollius, H.25
Hastie, N.D.26
Munnich, A.27
Etchevers, H.C.28
Pelet, A.29
Farlie, P.G.30
Fitzpatrick, D.R.31
Lyonnet, S.32
more..
-
12
-
-
84856009018
-
Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex development
-
Benko S., Gordon C.T., Mallet D., Sreenivasan R., Thauvin-Robinet C., Brendehaug A., Thomas S., Bruland O., David M., Nicolino M., Labalme A., Sanlaville D., Callier P., Malan V., Huet F., Molven A., Dijoud F., Munnich A., Faivre L., Amiel J., Harley V., Houge G., Morel Y., Lyonnet S. Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex development. J. Med. Genet. 2011, 48:825-830.
-
(2011)
J. Med. Genet.
, vol.48
, pp. 825-830
-
-
Benko, S.1
Gordon, C.T.2
Mallet, D.3
Sreenivasan, R.4
Thauvin-Robinet, C.5
Brendehaug, A.6
Thomas, S.7
Bruland, O.8
David, M.9
Nicolino, M.10
Labalme, A.11
Sanlaville, D.12
Callier, P.13
Malan, V.14
Huet, F.15
Molven, A.16
Dijoud, F.17
Munnich, A.18
Faivre, L.19
Amiel, J.20
Harley, V.21
Houge, G.22
Morel, Y.23
Lyonnet, S.24
more..
-
13
-
-
77649268343
-
Genomic code for Sox10 activation reveals a key regulatory enhancer for cranial neural crest
-
Betancur P., Bronner-Fraser M., Sauka-Spengler T. Genomic code for Sox10 activation reveals a key regulatory enhancer for cranial neural crest. Proc. Natl. Acad. Sci. USA 2010, 107:3570-3575.
-
(2010)
Proc. Natl. Acad. Sci. USA
, vol.107
, pp. 3570-3575
-
-
Betancur, P.1
Bronner-Fraser, M.2
Sauka-Spengler, T.3
-
14
-
-
80051504942
-
A Sox10 enhancer element common to the otic placode and neural crest is activated by tissue-specific paralogs
-
Betancur P., Sauka-Spengler T., Bronner M. A Sox10 enhancer element common to the otic placode and neural crest is activated by tissue-specific paralogs. Development 2011, 138:3689-3698.
-
(2011)
Development
, vol.138
, pp. 3689-3698
-
-
Betancur, P.1
Sauka-Spengler, T.2
Bronner, M.3
-
15
-
-
0037104626
-
Cell-intrinsic differences between stem cells from different regions of the peripheral nervous system regulate the generation of neural diversity
-
Bixby S., Kruger G.M., Mosher J.T., Joseph N.M., Morrison S.J. Cell-intrinsic differences between stem cells from different regions of the peripheral nervous system regulate the generation of neural diversity. Neuron 2002, 35:643-656.
-
(2002)
Neuron
, vol.35
, pp. 643-656
-
-
Bixby, S.1
Kruger, G.M.2
Mosher, J.T.3
Joseph, N.M.4
Morrison, S.J.5
-
16
-
-
36749094055
-
Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4
-
Bondurand N., Dastot-Le Moal F., Stanchina L., Collot N., Baral V., Marlin S., Attie-Bitach T., Giurgea I., Skopinski L., Reardon W., Toutain A., Sarda P., Echaieb A., Lackmy-Port-Lis M., Touraine R., Amiel J., Goossens M., Pingault V. Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4. Am. J. Hum. Genet. 2007, 81:1169-1185.
-
(2007)
Am. J. Hum. Genet.
, vol.81
, pp. 1169-1185
-
-
Bondurand, N.1
Dastot-Le Moal, F.2
Stanchina, L.3
Collot, N.4
Baral, V.5
Marlin, S.6
Attie-Bitach, T.7
Giurgea, I.8
Skopinski, L.9
Reardon, W.10
Toutain, A.11
Sarda, P.12
Echaieb, A.13
Lackmy-Port-Lis, M.14
Touraine, R.15
Amiel, J.16
Goossens, M.17
Pingault, V.18
-
17
-
-
84865276331
-
Alu-mediated deletion of SOX10 regulatory elements in Waardenburg syndrome type 4
-
Bondurand N., Fouquet V., Baral V., Lecerf L., Loundon N., Goossens M., Duriez B., Labrune P., Pingault V. Alu-mediated deletion of SOX10 regulatory elements in Waardenburg syndrome type 4. Eur. J. Hum. Genet. 2012, 20:990-994.
-
(2012)
Eur. J. Hum. Genet.
, vol.20
, pp. 990-994
-
-
Bondurand, N.1
Fouquet, V.2
Baral, V.3
Lecerf, L.4
Loundon, N.5
Goossens, M.6
Duriez, B.7
Labrune, P.8
Pingault, V.9
-
18
-
-
0035891831
-
Human Connexin 32, a gap junction protein altered in the X-linked form of Charcot-Marie-Tooth disease, is directly regulated by the transcription factor SOX10
-
Bondurand N., Girard M., Pingault V., Lemort N., Dubourg O., Goossens M. Human Connexin 32, a gap junction protein altered in the X-linked form of Charcot-Marie-Tooth disease, is directly regulated by the transcription factor SOX10. Hum. Mol. Genet. 2001, 10:2783-2795.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 2783-2795
-
-
Bondurand, N.1
Girard, M.2
Pingault, V.3
Lemort, N.4
Dubourg, O.5
Goossens, M.6
-
19
-
-
0031663679
-
Expression of the SOX10 gene during human development
-
Bondurand N., Kobetz A., Pingault V., Lemort N., Encha-Razavi F., Couly G., Goerich D.E., Wegner M., Abitbol M., Goossens M. Expression of the SOX10 gene during human development. FEBS Lett. 1998, 432:168-172.
-
(1998)
FEBS Lett.
, vol.432
, pp. 168-172
-
-
Bondurand, N.1
Kobetz, A.2
Pingault, V.3
Lemort, N.4
Encha-Razavi, F.5
Couly, G.6
Goerich, D.E.7
Wegner, M.8
Abitbol, M.9
Goossens, M.10
-
20
-
-
0032848746
-
A molecular analysis of the yemenite deaf-blind hypopigmentation syndrome: SOX10 dysfunction causes different neurocristopathies
-
Bondurand N., Kuhlbrodt K., Pingault V., Enderich J., Sajus M., Tommerup N., Warburg M., Hennekam R.C., Read A.P., Wegner M., Goossens M. A molecular analysis of the yemenite deaf-blind hypopigmentation syndrome: SOX10 dysfunction causes different neurocristopathies. Hum. Mol. Genet. 1999, 8:1785-1789.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1785-1789
-
-
Bondurand, N.1
Kuhlbrodt, K.2
Pingault, V.3
Enderich, J.4
Sajus, M.5
Tommerup, N.6
Warburg, M.7
Hennekam, R.C.8
Read, A.P.9
Wegner, M.10
Goossens, M.11
-
21
-
-
33745079945
-
Maintenance of mammalian enteric nervous system progenitors by SOX10 and endothelin 3 signalling
-
Bondurand N., Natarajan D., Barlow A., Thapar N., Pachnis V. Maintenance of mammalian enteric nervous system progenitors by SOX10 and endothelin 3 signalling. Development 2006, 133:2075-2086.
-
(2006)
Development
, vol.133
, pp. 2075-2086
-
-
Bondurand, N.1
Natarajan, D.2
Barlow, A.3
Thapar, N.4
Pachnis, V.5
-
22
-
-
0346252649
-
Neuron and glia generating progenitors of the mammalian enteric nervous system isolated from foetal and postnatal gut cultures
-
Bondurand N., Natarajan D., Thapar N., Atkins C., Pachnis V. Neuron and glia generating progenitors of the mammalian enteric nervous system isolated from foetal and postnatal gut cultures. Development 2003, 130:6387-6400.
-
(2003)
Development
, vol.130
, pp. 6387-6400
-
-
Bondurand, N.1
Natarajan, D.2
Thapar, N.3
Atkins, C.4
Pachnis, V.5
-
23
-
-
0034641596
-
Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome
-
Bondurand N., Pingault V., Goerich D.E., Lemort N., Sock E., Le Caignec C., Wegner M., Goossens M. Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome. Hum. Mol. Genet. 2000, 9:1907-1917.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1907-1917
-
-
Bondurand, N.1
Pingault, V.2
Goerich, D.E.3
Lemort, N.4
Sock, E.5
Le Caignec, C.6
Wegner, M.7
Goossens, M.8
-
24
-
-
0034669139
-
Phylogeny of the SOX family of developmental transcription factors based on sequence and structural indicators
-
Bowles J., Schepers G., Koopman P. Phylogeny of the SOX family of developmental transcription factors based on sequence and structural indicators. Dev. Biol. 2000, 227:239-255.
-
(2000)
Dev. Biol.
, vol.227
, pp. 239-255
-
-
Bowles, J.1
Schepers, G.2
Koopman, P.3
-
25
-
-
79955855085
-
Sox10 is required for Schwann-cell homeostasis and myelin maintenance in the adult peripheral nerve
-
Bremer M., Frob F., Kichko T., Reeh P., Tamm E.R., Suter U., Wegner M. Sox10 is required for Schwann-cell homeostasis and myelin maintenance in the adult peripheral nerve. Glia 2011, 59:1022-1032.
-
(2011)
Glia
, vol.59
, pp. 1022-1032
-
-
Bremer, M.1
Frob, F.2
Kichko, T.3
Reeh, P.4
Tamm, E.R.5
Suter, U.6
Wegner, M.7
-
26
-
-
70350247357
-
Sox10 promotes the survival of cochlear progenitors during the establishment of the organ of Corti
-
Breuskin I., Bodson M., Thelen N., Thiry M., Borgs L., Nguyen L., Lefebvre P.P., Malgrange B. Sox10 promotes the survival of cochlear progenitors during the establishment of the organ of Corti. Dev. Biol. 2009, 335:327-339.
-
(2009)
Dev. Biol.
, vol.335
, pp. 327-339
-
-
Breuskin, I.1
Bodson, M.2
Thelen, N.3
Thiry, M.4
Borgs, L.5
Nguyen, L.6
Lefebvre, P.P.7
Malgrange, B.8
-
27
-
-
77956329426
-
Glial but not neuronal development in the cochleo-vestibular ganglion requires Sox10
-
Breuskin I., Bodson M., Thelen N., Thiry M., Borgs L., Nguyen L., Stolt C., Wegner M., Lefebvre P.P., Malgrange B. Glial but not neuronal development in the cochleo-vestibular ganglion requires Sox10. J. Neurochem. 2010, 114:1827-1839.
-
(2010)
J. Neurochem.
, vol.114
, pp. 1827-1839
-
-
Breuskin, I.1
Bodson, M.2
Thelen, N.3
Thiry, M.4
Borgs, L.5
Nguyen, L.6
Stolt, C.7
Wegner, M.8
Lefebvre, P.P.9
Malgrange, B.10
-
28
-
-
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., Wegner M. The transcription factor Sox10 is a key regulator of peripheral glial development. Genes Dev. 2001, 15:66-78.
-
(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
-
29
-
-
84860838205
-
Development and evolution of the neural crest: an overview
-
Bronner M.E., LeDouarin N.M. Development and evolution of the neural crest: an overview. Dev. Biol. 2012, 366:2-9.
-
(2012)
Dev. Biol.
, vol.366
, pp. 2-9
-
-
Bronner, M.E.1
LeDouarin, N.M.2
-
30
-
-
52949144953
-
A Sox10 expression screen identifies an amino acid essential for Erbb3 function
-
Buac K., Watkins-Chow D.E., Loftus S.K., Larson D.M., Incao A., Gibney G., Pavan W.J. A Sox10 expression screen identifies an amino acid essential for Erbb3 function. PLoS Genet. 2008, 4:e1000177.
-
(2008)
PLoS Genet.
, vol.4
-
-
Buac, K.1
Watkins-Chow, D.E.2
Loftus, S.K.3
Larson, D.M.4
Incao, A.5
Gibney, G.6
Pavan, W.J.7
-
31
-
-
0035394107
-
Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease
-
Cacheux V., Dastot-Le Moal F., Kaariainen H., Bondurand N., Rintala R., Boissier B., Wilson M., Mowat D., Goossens M. Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease. Hum. Mol. Genet. 2001, 10:1503-1510.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 1503-1510
-
-
Cacheux, V.1
Dastot-Le Moal, F.2
Kaariainen, H.3
Bondurand, N.4
Rintala, R.5
Boissier, B.6
Wilson, M.7
Mowat, D.8
Goossens, M.9
-
32
-
-
5544326532
-
Interactions between Sox10 and EdnrB modulate penetrance and severity of aganglionosis in the Sox10Dom mouse model of Hirschsprung disease
-
Cantrell V.A., Owens S.E., Chandler R.L., Airey D.C., Bradley K.M., Smith J.R., Southard-Smith E.M. Interactions between Sox10 and EdnrB modulate penetrance and severity of aganglionosis in the Sox10Dom mouse model of Hirschsprung disease. Hum. Mol. Genet. 2004, 13:2289-2301.
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 2289-2301
-
-
Cantrell, V.A.1
Owens, S.E.2
Chandler, R.L.3
Airey, D.C.4
Bradley, K.M.5
Smith, J.R.6
Southard-Smith, E.M.7
-
33
-
-
33846041093
-
A direct role for Sox10 in specification of neural crest-derived sensory neurons
-
Carney T.J., Dutton K.A., Greenhill E., Delfino-Machin M., Dufourcq P., Blader P., Kelsh R.N. A direct role for Sox10 in specification of neural crest-derived sensory neurons. Development 2006, 133:4619-4630.
-
(2006)
Development
, vol.133
, pp. 4619-4630
-
-
Carney, T.J.1
Dutton, K.A.2
Greenhill, E.3
Delfino-Machin, M.4
Dufourcq, P.5
Blader, P.6
Kelsh, R.N.7
-
34
-
-
78651259608
-
Bone morphogenetic proteins regulate enteric gliogenesis by modulating ErbB3 signaling
-
Chalazonitis A., D'Autreaux F., Pham T.D., Kessler J.A., Gershon M.D. Bone morphogenetic proteins regulate enteric gliogenesis by modulating ErbB3 signaling. Dev. Biol. 2011, 350:64-79.
-
(2011)
Dev. Biol.
, vol.350
, pp. 64-79
-
-
Chalazonitis, A.1
D'Autreaux, F.2
Pham, T.D.3
Kessler, J.A.4
Gershon, M.D.5
-
35
-
-
81255171487
-
Identification and functional analysis of SOX10 missense mutations in different subtypes of Waardenburg syndrome
-
Chaoui A., Watanabe Y., Touraine R., Baral V., Goossens M., Pingault V., Bondurand N. Identification and functional analysis of SOX10 missense mutations in different subtypes of Waardenburg syndrome. Hum. Mutat. 2011, 32:1436-1449.
-
(2011)
Hum. Mutat.
, vol.32
, pp. 1436-1449
-
-
Chaoui, A.1
Watanabe, Y.2
Touraine, R.3
Baral, V.4
Goossens, M.5
Pingault, V.6
Bondurand, N.7
-
36
-
-
0034733795
-
Chick sox10, a transcription factor expressed in both early neural crest cells and central nervous system
-
Cheng Y., Cheung M., Abu-Elmagd M.M., Orme A., Scotting P.J. Chick sox10, a transcription factor expressed in both early neural crest cells and central nervous system. Brain Res. Dev. Brain Res. 2000, 121:233-241.
-
(2000)
Brain Res. Dev. Brain Res.
, vol.121
, pp. 233-241
-
-
Cheng, Y.1
Cheung, M.2
Abu-Elmagd, M.M.3
Orme, A.4
Scotting, P.J.5
-
37
-
-
0346121540
-
Neural crest development is regulated by the transcription factor Sox9
-
Cheung M., Briscoe J. Neural crest development is regulated by the transcription factor Sox9. Development 2003, 130:5681-5693.
-
(2003)
Development
, vol.130
, pp. 5681-5693
-
-
Cheung, M.1
Briscoe, J.2
-
38
-
-
0035281835
-
Two sox9 genes on duplicated zebrafish chromosomes: expression of similar transcription activators in distinct sites
-
Chiang E.F., Pai C.I., Wyatt M., Yan Y.L., Postlethwait J., Chung B. Two sox9 genes on duplicated zebrafish chromosomes: expression of similar transcription activators in distinct sites. Dev. Biol. 2001, 231:149-163.
-
(2001)
Dev. Biol.
, vol.231
, pp. 149-163
-
-
Chiang, E.F.1
Pai, C.I.2
Wyatt, M.3
Yan, Y.L.4
Postlethwait, J.5
Chung, B.6
-
39
-
-
79960130256
-
Isolation and live imaging of enteric progenitors based on Sox10-Histone2BVenus transgene expression
-
Corpening J.C., Deal K.K., Cantrell V.A., Skelton S.B., Buehler D.P., Southard-Smith E.M. Isolation and live imaging of enteric progenitors based on Sox10-Histone2BVenus transgene expression. Genesis 2011, 49:599-618.
-
(2011)
Genesis
, vol.49
, pp. 599-618
-
-
Corpening, J.C.1
Deal, K.K.2
Cantrell, V.A.3
Skelton, S.B.4
Buehler, D.P.5
Southard-Smith, E.M.6
-
40
-
-
77955284526
-
SOX10 structure-function analysis in the chicken neural tube reveals important insights into its role in human neurocristopathies
-
Cossais F., Wahlbuhl M., Kriesch J., Wegner M. SOX10 structure-function analysis in the chicken neural tube reveals important insights into its role in human neurocristopathies. Hum. Mol. Genet. 2010, 19:2409-2420.
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 2409-2420
-
-
Cossais, F.1
Wahlbuhl, M.2
Kriesch, J.3
Wegner, M.4
-
41
-
-
34047235515
-
ZFHX1B mutations in patients with Mowat-Wilson syndrome
-
Dastot-Le Moal F., Wilson M., Mowat D., Collot N., Niel F., Goossens M. ZFHX1B mutations in patients with Mowat-Wilson syndrome. Hum. Mutat. 2007, 28:313-321.
-
(2007)
Hum. Mutat.
, vol.28
, pp. 313-321
-
-
Dastot-Le Moal, F.1
Wilson, M.2
Mowat, D.3
Collot, N.4
Niel, F.5
Goossens, M.6
-
42
-
-
34548044473
-
Epistatic interactions with a common hypomorphic RET allele in syndromic Hirschsprung disease
-
de Pontual L., Pelet A., Clement-Ziza M., Trochet D., Antonarakis S.E., Attie-Bitach T., Beales P.L., Blouin J.L., Dastot-Le Moal F., Dollfus H., Goossens M., Katsanis N., Touraine R., Feingold J., Munnich A., Lyonnet S., Amiel J. Epistatic interactions with a common hypomorphic RET allele in syndromic Hirschsprung disease. Hum. Mutat. 2007, 28:790-796.
-
(2007)
Hum. Mutat.
, vol.28
, pp. 790-796
-
-
de Pontual, L.1
Pelet, A.2
Clement-Ziza, M.3
Trochet, D.4
Antonarakis, S.E.5
Attie-Bitach, T.6
Beales, P.L.7
Blouin, J.L.8
Dastot-Le Moal, F.9
Dollfus, H.10
Goossens, M.11
Katsanis, N.12
Touraine, R.13
Feingold, J.14
Munnich, A.15
Lyonnet, S.16
Amiel, J.17
-
43
-
-
33744922373
-
Distant regulatory elements in a Sox10-beta GEO BAC transgene are required for expression of Sox10 in the enteric nervous system and other neural crest-derived tissues
-
Deal K.K., Cantrell V.A., Chandler R.L., Saunders T.L., Mortlock D.P., Southard-Smith E.M. Distant regulatory elements in a Sox10-beta GEO BAC transgene are required for expression of Sox10 in the enteric nervous system and other neural crest-derived tissues. Dev. Dyn. 2006, 235:1413-1432.
-
(2006)
Dev. Dyn.
, vol.235
, pp. 1413-1432
-
-
Deal, K.K.1
Cantrell, V.A.2
Chandler, R.L.3
Saunders, T.L.4
Mortlock, D.P.5
Southard-Smith, E.M.6
-
44
-
-
57649114691
-
An evolutionarily conserved intronic region controls the spatiotemporal expression of the transcription factor Sox10
-
Dutton J.R., Antonellis A., Carney T.J., Rodrigues F.S., Pavan W.J., Ward A., Kelsh R.N. An evolutionarily conserved intronic region controls the spatiotemporal expression of the transcription factor Sox10. BMC Dev. Biol. 2008, 8:105.
-
(2008)
BMC Dev. Biol.
, vol.8
, pp. 105
-
-
Dutton, J.R.1
Antonellis, A.2
Carney, T.J.3
Rodrigues, F.S.4
Pavan, W.J.5
Ward, A.6
Kelsh, R.N.7
-
45
-
-
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., Kelsh R.N. Zebrafish colourless encodes sox10 and specifies non-ectomesenchymal neural crest fates. Development 2001, 128:4113-4125.
-
(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
-
46
-
-
16244370056
-
Phox2b function in the enteric nervous system is conserved in zebrafish and is sox10-dependent
-
Elworthy S., Pinto J.P., Pettifer A., Cancela M.L., Kelsh R.N. Phox2b function in the enteric nervous system is conserved in zebrafish and is sox10-dependent. Mech. Dev. 2005, 122:659-669.
-
(2005)
Mech. Dev.
, vol.122
, pp. 659-669
-
-
Elworthy, S.1
Pinto, J.P.2
Pettifer, A.3
Cancela, M.L.4
Kelsh, R.N.5
-
47
-
-
77955081986
-
Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability
-
Emison E.S., Garcia-Barcelo M., Grice E.A., Lantieri F., Amiel J., Burzynski G., Fernandez R.M., Hao L., Kashuk C., West K., Miao X., Tam P.K., Griseri P., Ceccherini I., Pelet A., Jannot A.S., de Pontual L., Henrion-Caude A., Lyonnet S., Verheij J.B., Hofstra R.M., Antinolo G., Borrego S., McCallion A.S., Chakravarti A. Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability. Am. J. Hum. Genet. 2010, 87:60-74.
-
(2010)
Am. J. Hum. Genet.
, vol.87
, pp. 60-74
-
-
Emison, E.S.1
Garcia-Barcelo, M.2
Grice, E.A.3
Lantieri, F.4
Amiel, J.5
Burzynski, G.6
Fernandez, R.M.7
Hao, L.8
Kashuk, C.9
West, K.10
Miao, X.11
Tam, P.K.12
Griseri, P.13
Ceccherini, I.14
Pelet, A.15
Jannot, A.S.16
de Pontual, L.17
Henrion-Caude, A.18
Lyonnet, S.19
Verheij, J.B.20
Hofstra, R.M.21
Antinolo, G.22
Borrego, S.23
McCallion, A.S.24
Chakravarti, A.25
more..
-
48
-
-
17244383525
-
A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk
-
Emison E.S., McCallion A.S., Kashuk C.S., Bush R.T., Grice E., Lin S., Portnoy M.E., Cutler D.J., Green E.D., Chakravarti A. A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk. Nature 2005, 434:857-863.
-
(2005)
Nature
, vol.434
, pp. 857-863
-
-
Emison, E.S.1
McCallion, A.S.2
Kashuk, C.S.3
Bush, R.T.4
Grice, E.5
Lin, S.6
Portnoy, M.E.7
Cutler, D.J.8
Green, E.D.9
Chakravarti, A.10
-
49
-
-
77952392377
-
Sox10 is required for Schwann cell identity and progression beyond the immature Schwann cell stage
-
Finzsch M., Schreiner S., Kichko T., Reeh P., Tamm E.R., Bosl M.R., Meijer D., Wegner M. Sox10 is required for Schwann cell identity and progression beyond the immature Schwann cell stage. J. Cell Biol. 2010, 189:701-712.
-
(2010)
J. Cell Biol.
, vol.189
, pp. 701-712
-
-
Finzsch, M.1
Schreiner, S.2
Kichko, T.3
Reeh, P.4
Tamm, E.R.5
Bosl, M.R.6
Meijer, D.7
Wegner, M.8
-
50
-
-
4444312892
-
Sonic hedgehog regulates the proliferation, differentiation, and migration of enteric neural crest cells in gut
-
Fu M., Lui V.C., Sham M.H., Pachnis V., Tam P.K. Sonic hedgehog regulates the proliferation, differentiation, and migration of enteric neural crest cells in gut. J. Cell Biol. 2004, 166:673-684.
-
(2004)
J. Cell Biol.
, vol.166
, pp. 673-684
-
-
Fu, M.1
Lui, V.C.2
Sham, M.H.3
Pachnis, V.4
Tam, P.K.5
-
51
-
-
18544365991
-
Segregation at three loci explains familial and population risk in Hirschsprung disease
-
Gabriel S.B., Salomon R., Pelet A., Angrist M., Amiel J., Fornage M., Attie-Bitach T., Olson J.M., Hofstra R., Buys C., Steffann J., Munnich A., Lyonnet S., Chakravarti A. Segregation at three loci explains familial and population risk in Hirschsprung disease. Nat. Genet. 2002, 31:89-93.
-
(2002)
Nat. Genet.
, vol.31
, pp. 89-93
-
-
Gabriel, S.B.1
Salomon, R.2
Pelet, A.3
Angrist, M.4
Amiel, J.5
Fornage, M.6
Attie-Bitach, T.7
Olson, J.M.8
Hofstra, R.9
Buys, C.10
Steffann, J.11
Munnich, A.12
Lyonnet, S.13
Chakravarti, A.14
-
52
-
-
33646142709
-
Control of myelination in Schwann cells: a Krox20 cis-regulatory element integrates Oct6, Brn2 and Sox10 activities
-
Ghislain J., Charnay P. Control of myelination in Schwann cells: a Krox20 cis-regulatory element integrates Oct6, Brn2 and Sox10 activities. EMBO Rep. 2006, 7:52-58.
-
(2006)
EMBO Rep.
, vol.7
, pp. 52-58
-
-
Ghislain, J.1
Charnay, P.2
-
53
-
-
33344472777
-
Sumoylation of the SOX10 transcription factor regulates its transcriptional activity
-
Girard M., Goossens M. Sumoylation of the SOX10 transcription factor regulates its transcriptional activity. FEBS Lett. 2006, 580:1635-1641.
-
(2006)
FEBS Lett.
, vol.580
, pp. 1635-1641
-
-
Girard, M.1
Goossens, M.2
-
54
-
-
84874987381
-
Building a brain in the gut: development of the enteric nervous system
-
Goldstein A., Hofstra R., Burns A. Building a brain in the gut: development of the enteric nervous system. Clin. Genet. 2013, 83:307-316.
-
(2013)
Clin. Genet.
, vol.83
, pp. 307-316
-
-
Goldstein, A.1
Hofstra, R.2
Burns, A.3
-
55
-
-
70349705754
-
Long-range regulation at the SOX9 locus in development and disease
-
Gordon C.T., Tan T.Y., Benko S., Fitzpatrick D., Lyonnet S., Farlie P.G. Long-range regulation at the SOX9 locus in development and disease. J. Med. Genet. 2009, 46:649-656.
-
(2009)
J. Med. Genet.
, vol.46
, pp. 649-656
-
-
Gordon, C.T.1
Tan, T.Y.2
Benko, S.3
Fitzpatrick, D.4
Lyonnet, S.5
Farlie, P.G.6
-
56
-
-
29644434290
-
Evaluation of the RET regulatory landscape reveals the biological relevance of a HSCR-implicated enhancer
-
Grice E.A., Rochelle E.S., Green E.D., Chakravarti A., McCallion A.S. Evaluation of the RET regulatory landscape reveals the biological relevance of a HSCR-implicated enhancer. Hum. Mol. Genet. 2005, 14:3837-3845.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 3837-3845
-
-
Grice, E.A.1
Rochelle, E.S.2
Green, E.D.3
Chakravarti, A.4
McCallion, A.S.5
-
57
-
-
79952628807
-
The dark brown plumage color in chickens is caused by an 8.3-kb deletion upstream of SOX10
-
Gunnarsson U., Kerje S., Bed'hom B., Sahlqvist A.S., Ekwall O., Tixier-Boichard M., Kampe O., Andersson L. The dark brown plumage color in chickens is caused by an 8.3-kb deletion upstream of SOX10. Pigment Cell Melanoma Res. 2011, 24:268-274.
-
(2011)
Pigment Cell Melanoma Res.
, vol.24
, pp. 268-274
-
-
Gunnarsson, U.1
Kerje, S.2
Bed'hom, B.3
Sahlqvist, A.S.4
Ekwall, O.5
Tixier-Boichard, M.6
Kampe, O.7
Andersson, L.8
-
58
-
-
53049088719
-
Having it both ways: Sox protein function between conservation and innovation
-
Guth S.I., Wegner M. Having it both ways: Sox protein function between conservation and innovation. Cell Mol. Life Sci. 2008, 65:3000-3018.
-
(2008)
Cell Mol. Life Sci.
, vol.65
, pp. 3000-3018
-
-
Guth, S.I.1
Wegner, M.2
-
59
-
-
76549094979
-
SoxE factors as multifunctional neural crest regulatory factors
-
Haldin C.E., LaBonne C. SoxE factors as multifunctional neural crest regulatory factors. Int. J. Biochem. Cell Biol. 2010, 42:441-444.
-
(2010)
Int. J. Biochem. Cell Biol.
, vol.42
, pp. 441-444
-
-
Haldin, C.E.1
LaBonne, C.2
-
60
-
-
33646489010
-
Expression profiling the developing mammalian enteric nervous system identifies marker and candidate Hirschsprung disease genes
-
Heanue T.A., Pachnis V. Expression profiling the developing mammalian enteric nervous system identifies marker and candidate Hirschsprung disease genes. Proc. Natl. Acad. Sci. USA 2006, 103:6919-6924.
-
(2006)
Proc. Natl. Acad. Sci. USA
, vol.103
, pp. 6919-6924
-
-
Heanue, T.A.1
Pachnis, V.2
-
61
-
-
34249007508
-
Enteric nervous system development and Hirschsprung's disease: advances in genetic and stem cell studies
-
Heanue T.A., Pachnis V. Enteric nervous system development and Hirschsprung's disease: advances in genetic and stem cell studies. Nat. Rev. Neurosci. 2007, 8:466-479.
-
(2007)
Nat. Rev. Neurosci.
, vol.8
, pp. 466-479
-
-
Heanue, T.A.1
Pachnis, V.2
-
62
-
-
79951820551
-
Prospective identification and isolation of enteric nervous system progenitors using Sox2
-
Heanue T.A., Pachnis V. Prospective identification and isolation of enteric nervous system progenitors using Sox2. Stem Cells 2011, 29:128-140.
-
(2011)
Stem Cells
, vol.29
, pp. 128-140
-
-
Heanue, T.A.1
Pachnis, V.2
-
63
-
-
0032574721
-
Mutation of the Sry-related Sox10 gene in dominant megacolon, a mouse model for human Hirschsprung disease
-
Herbarth B., Pingault V., Bondurand N., Kuhlbrodt K., Hermans-Borgmeyer I., Puliti A., Lemort N., Goossens M., Wegner M. Mutation of the Sry-related Sox10 gene in dominant megacolon, a mouse model for human Hirschsprung disease. Proc. Natl. Acad. Sci. USA 1998, 95:5161-5165.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 5161-5165
-
-
Herbarth, B.1
Pingault, V.2
Bondurand, N.3
Kuhlbrodt, K.4
Hermans-Borgmeyer, I.5
Puliti, A.6
Lemort, N.7
Goossens, M.8
Wegner, M.9
-
64
-
-
83755229011
-
SOX10 regulates expression of the SH3-domain kinase binding protein 1 (Sh3kbp1) locus in Schwann cells via an alternative promoter
-
Hodonsky C.J., Kleinbrink E.L., Charney K.N., Prasad M., Bessling S.L., Jones E.A., Srinivasan R., Svaren J., McCallion A.S., Antonellis A. SOX10 regulates expression of the SH3-domain kinase binding protein 1 (Sh3kbp1) locus in Schwann cells via an alternative promoter. Mol. Cell Neurosci. 2012, 49:85-96.
-
(2012)
Mol. Cell Neurosci.
, vol.49
, pp. 85-96
-
-
Hodonsky, C.J.1
Kleinbrink, E.L.2
Charney, K.N.3
Prasad, M.4
Bessling, S.L.5
Jones, E.A.6
Srinivasan, R.7
Svaren, J.8
McCallion, A.S.9
Antonellis, A.10
-
66
-
-
0041343108
-
Sox10 is required for the early development of the prospective neural crest in Xenopus embryos
-
Honore S.M., Aybar M.J., Mayor R. Sox10 is required for the early development of the prospective neural crest in Xenopus embryos. Dev. Biol. 2003, 260:79-96.
-
(2003)
Dev. Biol.
, vol.260
, pp. 79-96
-
-
Honore, S.M.1
Aybar, M.J.2
Mayor, R.3
-
67
-
-
82255183073
-
Stem cells for GI motility disorders
-
Hotta R., Natarajan D., Burns A.J., Thapar N. Stem cells for GI motility disorders. Curr. Opinions Pharmacol. 2011, 11:617-623.
-
(2011)
Curr. Opinions Pharmacol.
, vol.11
, pp. 617-623
-
-
Hotta, R.1
Natarajan, D.2
Burns, A.J.3
Thapar, N.4
-
68
-
-
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., Lupski J.R. Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations. Nat. Genet. 2004, 36:361-369.
-
(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
-
69
-
-
0036894042
-
Congenital hypomyelinating neuropathy, central dysmyelination, and Waardenburg-Hirschsprung disease: phenotypes linked by SOX10 mutation
-
Inoue K., Shilo K., Boerkoel C.F., Crowe C., Sawady J., Lupski J.R., Agamanolis D.P. Congenital hypomyelinating neuropathy, central dysmyelination, and Waardenburg-Hirschsprung disease: phenotypes linked by SOX10 mutation. Ann. Neurol. 2002, 52:836-842.
-
(2002)
Ann. Neurol.
, vol.52
, pp. 836-842
-
-
Inoue, K.1
Shilo, K.2
Boerkoel, C.F.3
Crowe, C.4
Sawady, J.5
Lupski, J.R.6
Agamanolis, D.P.7
-
70
-
-
33646721953
-
Sox10 regulates ciliary neurotrophic factor gene expression in Schwann cells
-
Ito Y., Wiese S., Funk N., Chittka A., Rossoll W., Bommel H., Watabe K., Wegner M., Sendtner M. Sox10 regulates ciliary neurotrophic factor gene expression in Schwann cells. Proc. Natl. Acad. Sci. USA 2006, 103:7871-7876.
-
(2006)
Proc. Natl. Acad. Sci. USA
, vol.103
, pp. 7871-7876
-
-
Ito, Y.1
Wiese, S.2
Funk, N.3
Chittka, A.4
Rossoll, W.5
Bommel, H.6
Watabe, K.7
Wegner, M.8
Sendtner, M.9
-
71
-
-
79958270504
-
Functional dissection of the Oct6 Schwann cell enhancer reveals an essential role for dimeric Sox10 binding
-
Jagalur N.B., Ghazvini M., Mandemakers W., Driegen S., Maas A., Jones E.A., Jaegle M., Grosveld F., Svaren J., Meijer D. Functional dissection of the Oct6 Schwann cell enhancer reveals an essential role for dimeric Sox10 binding. J. Neurosci. 2011, 31:8585-8594.
-
(2011)
J. Neurosci.
, vol.31
, pp. 8585-8594
-
-
Jagalur, N.B.1
Ghazvini, M.2
Mandemakers, W.3
Driegen, S.4
Maas, A.5
Jones, E.A.6
Jaegle, M.7
Grosveld, F.8
Svaren, J.9
Meijer, D.10
-
72
-
-
79952857195
-
Sex determination and the control of Sox9 expression in mammals
-
Jakob S., Lovell-Badge R. Sex determination and the control of Sox9 expression in mammals. FEBS J. 2011, 278:1002-1009.
-
(2011)
FEBS J.
, vol.278
, pp. 1002-1009
-
-
Jakob, S.1
Lovell-Badge, R.2
-
73
-
-
67749145639
-
Induction of myelin protein zero by early growth response 2 through upstream and intragenic elements
-
Jang S.W., Svaren J. Induction of myelin protein zero by early growth response 2 through upstream and intragenic elements. J. Biol. Chem. 2009, 284:20111-20120.
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 20111-20120
-
-
Jang, S.W.1
Svaren, J.2
-
74
-
-
79953776015
-
Transforming growth factor beta-mediated Sox10 suppression controls mesenchymal progenitor generation in neural crest stem cells
-
John N., Cinelli P., Wegner M., Sommer L. Transforming growth factor beta-mediated Sox10 suppression controls mesenchymal progenitor generation in neural crest stem cells. Stem Cells 2011, 29:689-699.
-
(2011)
Stem Cells
, vol.29
, pp. 689-699
-
-
John, N.1
Cinelli, P.2
Wegner, M.3
Sommer, L.4
-
75
-
-
46749149254
-
Interactions of Sox10 and Egr2 in myelin gene regulation
-
Jones E.A., Jang S.W., Mager G.M., Chang L.W., Srinivasan R., Gokey N.G., Ward R.M., Nagarajan R., Svaren J. Interactions of Sox10 and Egr2 in myelin gene regulation. Neuron Glia Biol. 2007, 3:377-387.
-
(2007)
Neuron Glia Biol.
, vol.3
, pp. 377-387
-
-
Jones, E.A.1
Jang, S.W.2
Mager, G.M.3
Chang, L.W.4
Srinivasan, R.5
Gokey, N.G.6
Ward, R.M.7
Nagarajan, R.8
Svaren, J.9
-
76
-
-
0034175998
-
Pairing SOX off: with partners in the regulation of embryonic development
-
Kamachi Y., Uchikawa M., Kondoh H. Pairing SOX off: with partners in the regulation of embryonic development. Trends Genet. 2000, 16:182-187.
-
(2000)
Trends Genet.
, vol.16
, pp. 182-187
-
-
Kamachi, Y.1
Uchikawa, M.2
Kondoh, H.3
-
77
-
-
0032727413
-
Early death of neural crest cells is responsible for total enteric aganglionosis in Sox10(Dom)/Sox10(Dom) mouse embryos
-
Kapur R.P. Early death of neural crest cells is responsible for total enteric aganglionosis in Sox10(Dom)/Sox10(Dom) mouse embryos. Pediatr. Dev. Pathol. 1999, 2:559-569.
-
(1999)
Pediatr. Dev. Pathol.
, vol.2
, pp. 559-569
-
-
Kapur, R.P.1
-
78
-
-
0029879543
-
Abnormal microenvironmental signals underlie intestinal aganglionosis in dominant megacolon mutant mice
-
Kapur R.P., Livingston R., Doggett B., Sweetser D.A., Siebert J.R., Palmiter R.D. Abnormal microenvironmental signals underlie intestinal aganglionosis in dominant megacolon mutant mice. Dev. Biol. 1996, 174:360-369.
-
(1996)
Dev. Biol.
, vol.174
, pp. 360-369
-
-
Kapur, R.P.1
Livingston, R.2
Doggett, B.3
Sweetser, D.A.4
Siebert, J.R.5
Palmiter, R.D.6
-
79
-
-
78649823499
-
Sry: the master switch in mammalian sex determination
-
Kashimada K., Koopman P. Sry: the master switch in mammalian sex determination. Development 2010, 137:3921-3930.
-
(2010)
Development
, vol.137
, pp. 3921-3930
-
-
Kashimada, K.1
Koopman, P.2
-
80
-
-
33748202079
-
Replacement of the Sox10 transcription factor by Sox8 reveals incomplete functional equivalence
-
Kellerer S., Schreiner S., Stolt C.C., Scholz S., Bosl M.R., Wegner M. Replacement of the Sox10 transcription factor by Sox8 reveals incomplete functional equivalence. Development 2006, 133:2875-2886.
-
(2006)
Development
, vol.133
, pp. 2875-2886
-
-
Kellerer, S.1
Schreiner, S.2
Stolt, C.C.3
Scholz, S.4
Bosl, M.R.5
Wegner, M.6
-
81
-
-
33748944201
-
Sorting out Sox10 functions in neural crest development
-
Kelsh R.N. Sorting out Sox10 functions in neural crest development. Bioessays 2006, 28:788-798.
-
(2006)
Bioessays
, vol.28
, pp. 788-798
-
-
Kelsh, R.N.1
-
82
-
-
12644282543
-
Zebrafish pigmentation mutations and the processes of neural crest development
-
Kelsh R.N., Brand M., Jiang Y.J., Heisenberg C.P., Lin S., Haffter P., Odenthal J., Mullins M.C., van Eeden F.J., Furutani-Seiki M., Granato M., Hammerschmidt M., Kane D.A., Warga R.M., Beuchle D., Vogelsang L., Nusslein-Volhard C. Zebrafish pigmentation mutations and the processes of neural crest development. Development 1996, 123:369-389.
-
(1996)
Development
, vol.123
, pp. 369-389
-
-
Kelsh, R.N.1
Brand, M.2
Jiang, Y.J.3
Heisenberg, C.P.4
Lin, S.5
Haffter, P.6
Odenthal, J.7
Mullins, M.C.8
van Eeden, F.J.9
Furutani-Seiki, M.10
Granato, M.11
Hammerschmidt, M.12
Kane, D.A.13
Warga, R.M.14
Beuchle, D.15
Vogelsang, L.16
Nusslein-Volhard, C.17
-
83
-
-
0033952819
-
The zebrafish colourless gene regulates development of non-ectomesenchymal neural crest derivatives
-
Kelsh R.N., Eisen J.S. The zebrafish colourless gene regulates development of non-ectomesenchymal neural crest derivatives. Development 2000, 127:515-525.
-
(2000)
Development
, vol.127
, pp. 515-525
-
-
Kelsh, R.N.1
Eisen, J.S.2
-
84
-
-
0037431083
-
SOX10 maintains multipotency and inhibits neuronal differentiation of neural crest stem cells
-
Kim J., Lo L., Dormand E., Anderson D.J. SOX10 maintains multipotency and inhibits neuronal differentiation of neural crest stem cells. Neuron 2003, 38:17-31.
-
(2003)
Neuron
, vol.38
, pp. 17-31
-
-
Kim, J.1
Lo, L.2
Dormand, E.3
Anderson, D.J.4
-
85
-
-
0031973873
-
Sox10, a novel transcriptional modulator in glial cells
-
Kuhlbrodt K., Herbarth B., Sock E., Hermans-Borgmeyer I., Wegner M. Sox10, a novel transcriptional modulator in glial cells. J. Neurosci. 1998, 18:237-250.
-
(1998)
J. Neurosci.
, vol.18
, pp. 237-250
-
-
Kuhlbrodt, K.1
Herbarth, B.2
Sock, E.3
Hermans-Borgmeyer, I.4
Wegner, M.5
-
86
-
-
79952332765
-
Olig2 regulates Sox10 expression in oligodendrocyte precursors through an evolutionary conserved distal enhancer
-
Kuspert M., Hammer A., Bosl M.R., Wegner M. Olig2 regulates Sox10 expression in oligodendrocyte precursors through an evolutionary conserved distal enhancer. Nucleic Acids Res. 2011, 39:1280-1293.
-
(2011)
Nucleic Acids Res.
, vol.39
, pp. 1280-1293
-
-
Kuspert, M.1
Hammer, A.2
Bosl, M.R.3
Wegner, M.4
-
87
-
-
84859736483
-
Desert hedgehog links transcription factor Sox10 to perineurial development
-
Kuspert M., Weider M., Muller J., Hermans-Borgmeyer I., Meijer D., Wegner M. Desert hedgehog links transcription factor Sox10 to perineurial development. J. Neurosci. 2012, 32:5472-5480.
-
(2012)
J. Neurosci.
, vol.32
, pp. 5472-5480
-
-
Kuspert, M.1
Weider, M.2
Muller, J.3
Hermans-Borgmeyer, I.4
Meijer, D.5
Wegner, M.6
-
88
-
-
0021747818
-
Association of megacolon with a new dominant spotting gene (Dom) in the mouse
-
Lane P.W., Liu H.M. Association of megacolon with a new dominant spotting gene (Dom) in the mouse. J. Hered. 1984, 75:435-439.
-
(1984)
J. Hered.
, vol.75
, pp. 435-439
-
-
Lane, P.W.1
Liu, H.M.2
-
89
-
-
0033791525
-
Pax3 is required for enteric ganglia formation and functions with Sox10 to modulate expression of c-ret
-
Lang D., Chen F., Milewski R., Li J., Lu M.M., Epstein J.A. Pax3 is required for enteric ganglia formation and functions with Sox10 to modulate expression of c-ret. J. Clin. Invest. 2000, 106:963-971.
-
(2000)
J. Clin. Invest.
, vol.106
, pp. 963-971
-
-
Lang, D.1
Chen, F.2
Milewski, R.3
Li, J.4
Lu, M.M.5
Epstein, J.A.6
-
90
-
-
0037447462
-
Sox10 and Pax3 physically interact to mediate activation of a conserved c-RET enhancer
-
Lang D., Epstein J.A. Sox10 and Pax3 physically interact to mediate activation of a conserved c-RET enhancer. Hum. Mol. Genet. 2003, 12:937-945.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 937-945
-
-
Lang, D.1
Epstein, J.A.2
-
92
-
-
52949104819
-
Identification of direct regulatory targets of the transcription factor Sox10 based on function and conservation
-
Lee K.E., Nam S., Cho E.A., Seong I., Limb J.K., Lee S., Kim J. Identification of direct regulatory targets of the transcription factor Sox10 based on function and conservation. BMC Genomics 2008, 9:408.
-
(2008)
BMC Genomics
, vol.9
, pp. 408
-
-
Lee, K.E.1
Nam, S.2
Cho, E.A.3
Seong, I.4
Limb, J.K.5
Lee, S.6
Kim, J.7
-
93
-
-
0034536338
-
Direct regulation of the Microphthalmia promoter by Sox10 links Waardenburg-Shah syndrome (WS4)-associated hypopigmentation and deafness to WS2
-
Lee M., Goodall J., Verastegui C., Ballotti R., Goding C.R. Direct regulation of the Microphthalmia promoter by Sox10 links Waardenburg-Shah syndrome (WS4)-associated hypopigmentation and deafness to WS2. J. Biol. Chem. 2000, 275:37978-37983.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 37978-37983
-
-
Lee, M.1
Goodall, J.2
Verastegui, C.3
Ballotti, R.4
Goding, C.R.5
-
94
-
-
84866417864
-
SUMOylated SoxE factors recruit Grg4 and function as transcriptional repressors in the neural crest
-
Lee P.C., Taylor-Jaffe K.M., Nordin K.M., Prasad M.S., Lander R.M., Labonne C. SUMOylated SoxE factors recruit Grg4 and function as transcriptional repressors in the neural crest. J. Cell Biol. 2012, 198:799-813.
-
(2012)
J. Cell Biol.
, vol.198
, pp. 799-813
-
-
Lee, P.C.1
Taylor-Jaffe, K.M.2
Nordin, K.M.3
Prasad, M.S.4
Lander, R.M.5
Labonne, C.6
-
95
-
-
34748830336
-
Control of cell fate and differentiation by Sry-related high-mobility-group box (Sox) transcription factors
-
Lefebvre V., Dumitriu B., Penzo-Mendez A., Han Y., Pallavi B. Control of cell fate and differentiation by Sry-related high-mobility-group box (Sox) transcription factors. Int. J. Biochem. Cell Biol. 2007, 39:2195-2214.
-
(2007)
Int. J. Biochem. Cell Biol.
, vol.39
, pp. 2195-2214
-
-
Lefebvre, V.1
Dumitriu, B.2
Penzo-Mendez, A.3
Han, Y.4
Pallavi, B.5
-
96
-
-
70350070157
-
Transcriptional regulation of RET by Nkx2-1, Phox2b, Sox10, and Pax3
-
Leon T.Y., Ngan E.S., Poon H.C., So M.T., Lui V.C., Tam P.K., Garcia-Barcelo M.M. Transcriptional regulation of RET by Nkx2-1, Phox2b, Sox10, and Pax3. J. Pediatr. Surg. 2009, 44:1904-1912.
-
(2009)
J. Pediatr. Surg.
, vol.44
, pp. 1904-1912
-
-
Leon, T.Y.1
Ngan, E.S.2
Poon, H.C.3
So, M.T.4
Lui, V.C.5
Tam, P.K.6
Garcia-Barcelo, M.M.7
-
97
-
-
0033571937
-
Cell type-specific activation of neuronal nicotinic acetylcholine receptor subunit genes by Sox10
-
Liu Q., Melnikova I.N., Hu M., Gardner P.D. Cell type-specific activation of neuronal nicotinic acetylcholine receptor subunit genes by Sox10. J. Neurosci. 1999, 19:9747-9755.
-
(1999)
J. Neurosci.
, vol.19
, pp. 9747-9755
-
-
Liu, Q.1
Melnikova, I.N.2
Hu, M.3
Gardner, P.D.4
-
98
-
-
0346725015
-
Melanocyte-specific expression of dopachrome tautomerase is dependent on synergistic gene activation by the Sox10 and Mitf transcription factors
-
Ludwig A., Rehberg S., Wegner M. Melanocyte-specific expression of dopachrome tautomerase is dependent on synergistic gene activation by the Sox10 and Mitf transcription factors. FEBS Lett. 2004, 556:236-244.
-
(2004)
FEBS Lett.
, vol.556
, pp. 236-244
-
-
Ludwig, A.1
Rehberg, S.2
Wegner, M.3
-
99
-
-
9644277156
-
Identification of Sox8 as a modifier gene in a mouse model of Hirschsprung disease reveals underlying molecular defect
-
Maka M., Stolt C.C., Wegner M. Identification of Sox8 as a modifier gene in a mouse model of Hirschsprung disease reveals underlying molecular defect. Dev. Biol. 2005, 277:155-169.
-
(2005)
Dev. Biol.
, vol.277
, pp. 155-169
-
-
Maka, M.1
Stolt, C.C.2
Wegner, M.3
-
100
-
-
12644264315
-
Mutations affecting development of the zebrafish ear
-
Malicki J., Schier A.F., Solnica-Krezel L., Stemple D.L., Neuhauss S.C., Stainier D.Y., Abdelilah S., Rangini Z., Zwartkruis F., Driever W. Mutations affecting development of the zebrafish ear. Development 1996, 123:275-283.
-
(1996)
Development
, vol.123
, pp. 275-283
-
-
Malicki, J.1
Schier, A.F.2
Solnica-Krezel, L.3
Stemple, D.L.4
Neuhauss, S.C.5
Stainier, D.Y.6
Abdelilah, S.7
Rangini, Z.8
Zwartkruis, F.9
Driever, W.10
-
102
-
-
46249117044
-
A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy
-
Matera I., Watkins-Chow D.E., Loftus S.K., Hou L., Incao A., Silver D.L., Rivas C., Elliott E.C., Baxter L.L., Pavan W.J. A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy. Hum. Mol. Genet. 2008, 17:2118-2131.
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 2118-2131
-
-
Matera, I.1
Watkins-Chow, D.E.2
Loftus, S.K.3
Hou, L.4
Incao, A.5
Silver, D.L.6
Rivas, C.7
Elliott, E.C.8
Baxter, L.L.9
Pavan, W.J.10
-
103
-
-
3242736438
-
Genomic variation in multigenic traits: Hirschsprung disease
-
McCallion A.S., Emison E.S., Kashuk C.S., Bush R.T., Kenton M., Carrasquillo M.M., Jones K.W., Kennedy G.C., Portnoy M.E., Green E.D., Chakravarti A. Genomic variation in multigenic traits: Hirschsprung disease. Cold Spring Harbor Symp. Quant. Biol. 2003, 68:373-381.
-
(2003)
Cold Spring Harbor Symp. Quant. Biol.
, vol.68
, pp. 373-381
-
-
McCallion, A.S.1
Emison, E.S.2
Kashuk, C.S.3
Bush, R.T.4
Kenton, M.5
Carrasquillo, M.M.6
Jones, K.W.7
Kennedy, G.C.8
Portnoy, M.E.9
Green, E.D.10
Chakravarti, A.11
-
104
-
-
19544371371
-
Sox10 overexpression induces neural crest-like cells from all dorsoventral levels of the neural tube but inhibits differentiation
-
McKeown S.J., Lee V.M., Bronner-Fraser M., Newgreen D.F., Farlie P.G. Sox10 overexpression induces neural crest-like cells from all dorsoventral levels of the neural tube but inhibits differentiation. Dev. Dyn. 2005, 233:430-444.
-
(2005)
Dev. Dyn.
, vol.233
, pp. 430-444
-
-
McKeown, S.J.1
Lee, V.M.2
Bronner-Fraser, M.3
Newgreen, D.F.4
Farlie, P.G.5
-
105
-
-
0033809831
-
Synergistic transcriptional activation by Sox10 and Sp1 family members
-
Melnikova I.N., Lin H.R., Blanchette A.R., Gardner P.D. Synergistic transcriptional activation by Sox10 and Sp1 family members. Neuropharmacology 2000, 39:2615-2623.
-
(2000)
Neuropharmacology
, vol.39
, pp. 2615-2623
-
-
Melnikova, I.N.1
Lin, H.R.2
Blanchette, A.R.3
Gardner, P.D.4
-
106
-
-
0037780632
-
The importance of having your SOX on: role of SOX10 in the development of neural crest-derived melanocytes and glia
-
Mollaaghababa R., Pavan W.J. The importance of having your SOX on: role of SOX10 in the development of neural crest-derived melanocytes and glia. Oncogene 2003, 22:3024-3034.
-
(2003)
Oncogene
, vol.22
, pp. 3024-3034
-
-
Mollaaghababa, R.1
Pavan, W.J.2
-
107
-
-
42949088550
-
A de novo missense mutation in the gene encoding the SOX10 transcription factor in a Spanish sporadic case of Waardenburg syndrome type IV
-
Morin M., Vinuela A., Rivera T., Villamar M., Moreno-Pelayo M.A., Moreno F., del Castillo I. A de novo missense mutation in the gene encoding the SOX10 transcription factor in a Spanish sporadic case of Waardenburg syndrome type IV. Am. J. Med. Genet. A 2008, 146A:1032-1037.
-
(2008)
Am. J. Med. Genet. A
, vol.146 A
, pp. 1032-1037
-
-
Morin, M.1
Vinuela, A.2
Rivera, T.3
Villamar, M.4
Moreno-Pelayo, M.A.5
Moreno, F.6
del Castillo, I.7
-
108
-
-
33846906709
-
Intrinsic differences among spatially distinct neural crest stem cells in terms of migratory properties, fate determination, and ability to colonize the enteric nervous system
-
Mosher J.T., Yeager K.J., Kruger G.M., Joseph N.M., Hutchin M.E., Dlugosz A.A., Morrison S.J. Intrinsic differences among spatially distinct neural crest stem cells in terms of migratory properties, fate determination, and ability to colonize the enteric nervous system. Dev. Biol. 2007, 303:1-15.
-
(2007)
Dev. Biol.
, vol.303
, pp. 1-15
-
-
Mosher, J.T.1
Yeager, K.J.2
Kruger, G.M.3
Joseph, N.M.4
Hutchin, M.E.5
Dlugosz, A.A.6
Morrison, S.J.7
-
109
-
-
34248643438
-
The tyrosinase enhancer is activated by Sox10 and Mitf in mouse melanocytes
-
Murisier F., Guichard S., Beermann F. The tyrosinase enhancer is activated by Sox10 and Mitf in mouse melanocytes. Pigment Cell Res. 2007, 20:173-184.
-
(2007)
Pigment Cell Res.
, vol.20
, pp. 173-184
-
-
Murisier, F.1
Guichard, S.2
Beermann, F.3
-
110
-
-
84865960448
-
Autonomic neurocristopathy-associated mutations in PHOX2B dysregulate Sox10 expression
-
Nagashimada M., Ohta H., Li C., Nakao K., Uesaka T., Brunet J.F., Amiel J., Trochet D., Wakayama T., Enomoto H. Autonomic neurocristopathy-associated mutations in PHOX2B dysregulate Sox10 expression. J. Clin. Invest. 2012, 122:3145-3158.
-
(2012)
J. Clin. Invest.
, vol.122
, pp. 3145-3158
-
-
Nagashimada, M.1
Ohta, H.2
Li, C.3
Nakao, K.4
Uesaka, T.5
Brunet, J.F.6
Amiel, J.7
Trochet, D.8
Wakayama, T.9
Enomoto, H.10
-
111
-
-
43449136765
-
Hirschsprung's disease, acrocallosal syndrome, and congenital hydrocephalus: report of 2 patients and literature review
-
Nakakimura S., Sasaki F., Okada T., Arisue A., Cho K., Yoshino M., Kanemura Y., Yamasaki M., Todo S. Hirschsprung's disease, acrocallosal syndrome, and congenital hydrocephalus: report of 2 patients and literature review. J. Pediatr. Surg. 2008, 43:E13-17.
-
(2008)
J. Pediatr. Surg.
, vol.43
-
-
Nakakimura, S.1
Sasaki, F.2
Okada, T.3
Arisue, A.4
Cho, K.5
Yoshino, M.6
Kanemura, Y.7
Yamasaki, M.8
Todo, S.9
-
112
-
-
84871963175
-
Development and developmental disorders of the enteric nervous system
-
Obermayr F., Hotta R., Enomoto H., Young H.M. Development and developmental disorders of the enteric nervous system. Nat. Rev. Gastroenterol. Hepatol. 2012, 10:43-57.
-
(2012)
Nat. Rev. Gastroenterol. Hepatol.
, vol.10
, pp. 43-57
-
-
Obermayr, F.1
Hotta, R.2
Enomoto, H.3
Young, H.M.4
-
113
-
-
0030738352
-
Hydrocephalus and Hirschsprung's disease in a patient with a mutation of L1CAM
-
Okamoto N., Wada Y., Goto M. Hydrocephalus and Hirschsprung's disease in a patient with a mutation of L1CAM. J. Med. Genet. 1997, 34:670-671.
-
(1997)
J. Med. Genet.
, vol.34
, pp. 670-671
-
-
Okamoto, N.1
Wada, Y.2
Goto, M.3
-
114
-
-
20644436686
-
Genome-wide linkage identifies novel modifier loci of aganglionosis in the Sox10Dom model of Hirschsprung disease
-
Owens S.E., Broman K.W., Wiltshire T., Elmore J.B., Bradley K.M., Smith J.R., Southard-Smith E.M. Genome-wide linkage identifies novel modifier loci of aganglionosis in the Sox10Dom model of Hirschsprung disease. Hum. Mol. Genet. 2005, 14:1549-1558.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 1549-1558
-
-
Owens, S.E.1
Broman, K.W.2
Wiltshire, T.3
Elmore, J.B.4
Bradley, K.M.5
Smith, J.R.6
Southard-Smith, E.M.7
-
115
-
-
0037112741
-
Sox10 haploinsufficiency affects maintenance of progenitor cells in a mouse model of Hirschsprung disease
-
Paratore C., Eichenberger C., Suter U., Sommer L. Sox10 haploinsufficiency affects maintenance of progenitor cells in a mouse model of Hirschsprung disease. Hum. Mol. Genet. 2002, 11:3075-3085.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 3075-3085
-
-
Paratore, C.1
Eichenberger, C.2
Suter, U.3
Sommer, L.4
-
116
-
-
0034756577
-
Survival and glial fate acquisition of neural crest cells are regulated by an interplay between the transcription factor Sox10 and extrinsic combinatorial signaling
-
Paratore C., Goerich D.E., Suter U., Wegner M., Sommer L. Survival and glial fate acquisition of neural crest cells are regulated by an interplay between the transcription factor Sox10 and extrinsic combinatorial signaling. Development 2001, 128:3949-3961.
-
(2001)
Development
, vol.128
, pp. 3949-3961
-
-
Paratore, C.1
Goerich, D.E.2
Suter, U.3
Wegner, M.4
Sommer, L.5
-
117
-
-
0034004661
-
Protein zero gene expression is regulated by the glial transcription factor Sox10
-
Peirano R.I., Goerich D.E., Riethmacher D., Wegner M. Protein zero gene expression is regulated by the glial transcription factor Sox10. Mol. Cell Biol. 2000, 20:3198-3209.
-
(2000)
Mol. Cell Biol.
, vol.20
, pp. 3198-3209
-
-
Peirano, R.I.1
Goerich, D.E.2
Riethmacher, D.3
Wegner, M.4
-
118
-
-
0034663531
-
The glial transcription factor Sox10 binds to DNA both as monomer and dimer with different functional consequences
-
Peirano R.I., Wegner M. The glial transcription factor Sox10 binds to DNA both as monomer and dimer with different functional consequences. Nucleic Acids Res. 2000, 28:3047-3055.
-
(2000)
Nucleic Acids Res.
, vol.28
, pp. 3047-3055
-
-
Peirano, R.I.1
Wegner, M.2
-
119
-
-
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., Goossens M. SOX10 mutations in patients with Waardenburg-Hirschsprung disease. Nat. Genet. 1998, 18:171-173.
-
(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
-
120
-
-
77950389859
-
Review and update of mutations causing Waardenburg syndrome
-
Pingault V., Ente D., Dastot-Le Moal F., Goossens M., Marlin S., Bondurand N. Review and update of mutations causing Waardenburg syndrome. Hum. Mutat. 2010, 31:391-406.
-
(2010)
Hum. Mutat.
, vol.31
, pp. 391-406
-
-
Pingault, V.1
Ente, D.2
Dastot-Le Moal, F.3
Goossens, M.4
Marlin, S.5
Bondurand, N.6
-
121
-
-
0036705658
-
SOX10 mutations in chronic intestinal pseudo-obstruction suggest a complex physiopathological mechanism
-
Pingault V., Girard M., Bondurand N., Dorkins H., Van Maldergem L., Mowat D., Shimotake T., Verma I., Baumann C., Goossens M. SOX10 mutations in chronic intestinal pseudo-obstruction suggest a complex physiopathological mechanism. Hum. Genet. 2002, 111:198-206.
-
(2002)
Hum. Genet.
, vol.111
, pp. 198-206
-
-
Pingault, V.1
Girard, M.2
Bondurand, N.3
Dorkins, H.4
Van Maldergem, L.5
Mowat, D.6
Shimotake, T.7
Verma, I.8
Baumann, C.9
Goossens, M.10
-
122
-
-
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., Landrieu P. Peripheral neuropathy with hypomyelination, chronic intestinal pseudo-obstruction and deafness: a developmental "neural crest syndrome" related to a SOX10 mutation. Ann. Neurol. 2000, 48:671-676.
-
(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
-
123
-
-
0031017089
-
Human homology and candidate genes for the dominant megacolon locus, a mouse model of Hirschsprung disease
-
Pingault V., Puliti A., Prehu M.O., Samadi A., Bondurand N., Goossens M. Human homology and candidate genes for the dominant megacolon locus, a mouse model of Hirschsprung disease. Genomics 1997, 39:86-89.
-
(1997)
Genomics
, vol.39
, pp. 86-89
-
-
Pingault, V.1
Puliti, A.2
Prehu, M.O.3
Samadi, A.4
Bondurand, N.5
Goossens, M.6
-
124
-
-
0033906468
-
Transcription factor hierarchy in Waardenburg syndrome: regulation of MITF expression by SOX10 and PAX3
-
Potterf S.B., Furumura M., Dunn K.J., Arnheiter H., Pavan W.J. Transcription factor hierarchy in Waardenburg syndrome: regulation of MITF expression by SOX10 and PAX3. Hum. Genet. 2000, 107:1-6.
-
(2000)
Hum. Genet.
, vol.107
, pp. 1-6
-
-
Potterf, S.B.1
Furumura, M.2
Dunn, K.J.3
Arnheiter, H.4
Pavan, W.J.5
-
125
-
-
0035884056
-
Analysis of SOX10 function in neural crest-derived melanocyte development: SOX10-dependent transcriptional control of dopachrome tautomerase
-
Potterf S.B., Mollaaghababa R., Hou L., Southard-Smith E.M., Hornyak T.J., Arnheiter H., Pavan W.J. Analysis of SOX10 function in neural crest-derived melanocyte development: SOX10-dependent transcriptional control of dopachrome tautomerase. Dev. Biol. 2001, 237:245-257.
-
(2001)
Dev. Biol.
, vol.237
, pp. 245-257
-
-
Potterf, S.B.1
Mollaaghababa, R.2
Hou, L.3
Southard-Smith, E.M.4
Hornyak, T.J.5
Arnheiter, H.6
Pavan, W.J.7
-
126
-
-
79958279111
-
SOX10 directly modulates ERBB3 transcription via an intronic neural crest enhancer
-
Prasad M.K., Reed X., Gorkin D.U., Cronin J.C., McAdow A.R., Chain K., Hodonsky C.J., Jones E.A., Svaren J., Antonellis A., Johnson S.L., Loftus S.K., Pavan W.J., McCallion A.S. SOX10 directly modulates ERBB3 transcription via an intronic neural crest enhancer. BMC Dev. Biol. 2011, 11:40.
-
(2011)
BMC Dev. Biol.
, vol.11
, pp. 40
-
-
Prasad, M.K.1
Reed, X.2
Gorkin, D.U.3
Cronin, J.C.4
McAdow, A.R.5
Chain, K.6
Hodonsky, C.J.7
Jones, E.A.8
Svaren, J.9
Antonellis, A.10
Johnson, S.L.11
Loftus, S.K.12
Pavan, W.J.13
McCallion, A.S.14
-
127
-
-
0029401522
-
A high-resolution genetic map of mouse chromosome 15 encompassing the Dominant megacolon (Dom) locus
-
Puliti A., Prehu M.O., Simon-Chazottes D., Ferkdadji L., Peuchmaur M., Goossens M., Guenet J.L. A high-resolution genetic map of mouse chromosome 15 encompassing the Dominant megacolon (Dom) locus. Mamm. Genome 1995, 6:763-768.
-
(1995)
Mamm. Genome
, vol.6
, pp. 763-768
-
-
Puliti, A.1
Prehu, M.O.2
Simon-Chazottes, D.3
Ferkdadji, L.4
Peuchmaur, M.5
Goossens, M.6
Guenet, J.L.7
-
128
-
-
0031660707
-
The SOX10/Sox10 gene from human and mouse: sequence, expression, and transactivation by the encoded HMG domain transcription factor
-
Pusch C., Hustert E., Pfeifer D., Sudbeck P., Kist R., Roe B., Wang Z., Balling R., Blin N., Scherer G. The SOX10/Sox10 gene from human and mouse: sequence, expression, and transactivation by the encoded HMG domain transcription factor. Hum. Genet. 1998, 103:115-123.
-
(1998)
Hum. Genet.
, vol.103
, pp. 115-123
-
-
Pusch, C.1
Hustert, E.2
Pfeifer, D.3
Sudbeck, P.4
Kist, R.5
Roe, B.6
Wang, Z.7
Balling, R.8
Blin, N.9
Scherer, G.10
-
129
-
-
0036312041
-
Sox10 is an active nucleocytoplasmic shuttle protein, and shuttling is crucial for Sox10-mediated transactivation
-
Rehberg S., Lischka P., Glaser G., Stamminger T., Wegner M., Rosorius O. Sox10 is an active nucleocytoplasmic shuttle protein, and shuttling is crucial for Sox10-mediated transactivation. Mol. Cell Biol. 2002, 22:5826-5834.
-
(2002)
Mol. Cell Biol.
, vol.22
, pp. 5826-5834
-
-
Rehberg, S.1
Lischka, P.2
Glaser, G.3
Stamminger, T.4
Wegner, M.5
Rosorius, O.6
-
130
-
-
77954564977
-
Involvement of SOX10 in the pathogenesis of Hirschsprung disease: report of a truncating mutation in an isolated patient
-
Sanchez-Mejias A., Watanabe Y., R M.F., Lopez-Alonso M., Antinolo G., Bondurand N., Borrego S. Involvement of SOX10 in the pathogenesis of Hirschsprung disease: report of a truncating mutation in an isolated patient. J. Mol. Med. 2010, 88:507-514.
-
(2010)
J. Mol. Med.
, vol.88
, pp. 507-514
-
-
Sanchez-Mejias, A.1
Watanabe, Y.R.M.F.2
Lopez-Alonso, M.3
Antinolo, G.4
Bondurand, N.5
Borrego, S.6
-
131
-
-
0034654222
-
Cloning and characterisation of the Sry-related transcription factor gene Sox8
-
Schepers G.E., Bullejos M., Hosking B.M., Koopman P. Cloning and characterisation of the Sry-related transcription factor gene Sox8. Nucleic Acids Res. 2000, 28:1473-1480.
-
(2000)
Nucleic Acids Res.
, vol.28
, pp. 1473-1480
-
-
Schepers, G.E.1
Bullejos, M.2
Hosking, B.M.3
Koopman, P.4
-
132
-
-
0036696817
-
Twenty pairs of sox: extent, homology, and nomenclature of the mouse and human sox transcription factor gene families
-
Schepers G.E., Teasdale R.D., Koopman P. Twenty pairs of sox: extent, homology, and nomenclature of the mouse and human sox transcription factor gene families. Dev. Cell 2002, 3:167-170.
-
(2002)
Dev. Cell
, vol.3
, pp. 167-170
-
-
Schepers, G.E.1
Teasdale, R.D.2
Koopman, P.3
-
133
-
-
27144478022
-
The high-mobility group transcription factor Sox10 interacts with the N-myc-interacting protein Nmi
-
Schlierf B., Lang S., Kosian T., Werner T., Wegner M. The high-mobility group transcription factor Sox10 interacts with the N-myc-interacting protein Nmi. J. Mol. Biol. 2005, 353:1033-1042.
-
(2005)
J. Mol. Biol.
, vol.353
, pp. 1033-1042
-
-
Schlierf, B.1
Lang, S.2
Kosian, T.3
Werner, T.4
Wegner, M.5
-
134
-
-
33745900532
-
Expression of connexin47 in oligodendrocytes is regulated by the Sox10 transcription factor
-
Schlierf B., Werner T., Glaser G., Wegner M. Expression of connexin47 in oligodendrocytes is regulated by the Sox10 transcription factor. J. Mol. Biol. 2006, 361:11-21.
-
(2006)
J. Mol. Biol.
, vol.361
, pp. 11-21
-
-
Schlierf, B.1
Werner, T.2
Glaser, G.3
Wegner, M.4
-
135
-
-
35548972867
-
Hypomorphic Sox10 alleles reveal novel protein functions and unravel developmental differences in glial lineages
-
Schreiner S., Cossais F., Fischer K., Scholz S., Bosl M.R., Holtmann B., Sendtner M., Wegner M. Hypomorphic Sox10 alleles reveal novel protein functions and unravel developmental differences in glial lineages. Development 2007, 134:3271-3281.
-
(2007)
Development
, vol.134
, pp. 3271-3281
-
-
Schreiner, S.1
Cossais, F.2
Fischer, K.3
Scholz, S.4
Bosl, M.R.5
Holtmann, B.6
Sendtner, M.7
Wegner, M.8
-
136
-
-
41749086707
-
Transcription factor assembly on the nicotinic receptor beta4 subunit gene promoter
-
Scofield M.D., Bruschweiler-Li L., Mou Z., Gardner P.D. Transcription factor assembly on the nicotinic receptor beta4 subunit gene promoter. NeuroReport 2008, 19:687-690.
-
(2008)
NeuroReport
, vol.19
, pp. 687-690
-
-
Scofield, M.D.1
Bruschweiler-Li, L.2
Mou, Z.3
Gardner, P.D.4
-
137
-
-
19244374248
-
Novel mutations of SOX10 suggest a dominant negative role in Waardenburg-Shah syndrome
-
Sham M.H., Lui V.C., Chen B.L., Fu M., Tam P.K. Novel mutations of SOX10 suggest a dominant negative role in Waardenburg-Shah syndrome. J. Med. Genet. 2001, 38:E30.
-
(2001)
J. Med. Genet.
, vol.38
-
-
Sham, M.H.1
Lui, V.C.2
Chen, B.L.3
Fu, M.4
Tam, P.K.5
-
138
-
-
0346157329
-
The ins and outs of transcriptional control: nucleocytoplasmic shuttling in development and disease
-
Smith J.M., Koopman P.A. The ins and outs of transcriptional control: nucleocytoplasmic shuttling in development and disease. Trends Genet. 2004, 20:4-8.
-
(2004)
Trends Genet.
, vol.20
, pp. 4-8
-
-
Smith, J.M.1
Koopman, P.A.2
-
139
-
-
0034807930
-
Idiopathic weight reduction in mice deficient in the high-mobility-group transcription factor Sox8
-
Sock E., Schmidt K., Hermanns-Borgmeyer I., Bosl M.R., Wegner M. Idiopathic weight reduction in mice deficient in the high-mobility-group transcription factor Sox8. Mol. Cell Biol. 2001, 21:6951-6959.
-
(2001)
Mol. Cell Biol.
, vol.21
, pp. 6951-6959
-
-
Sock, E.1
Schmidt, K.2
Hermanns-Borgmeyer, I.3
Bosl, M.R.4
Wegner, M.5
-
140
-
-
0035204526
-
Development and degeneration of dorsal root ganglia in the absence of the HMG-domain transcription factor Sox10
-
Sonnenberg-Riethmacher E., Miehe M., Stolt C.C., Goerich D.E., Wegner M., Riethmacher D. Development and degeneration of dorsal root ganglia in the absence of the HMG-domain transcription factor Sox10. Mech. Dev. 2001, 109:253-265.
-
(2001)
Mech. Dev.
, vol.109
, pp. 253-265
-
-
Sonnenberg-Riethmacher, E.1
Miehe, M.2
Stolt, C.C.3
Goerich, D.E.4
Wegner, M.5
Riethmacher, D.6
-
141
-
-
0032898565
-
The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome
-
Southard-Smith E.M., Angrist M., Ellison J.S., Agarwala R., Baxevanis A.D., Chakravarti A., Pavan W.J. The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome. Genome Res. 1999, 9:215-225.
-
(1999)
Genome Res.
, vol.9
, pp. 215-225
-
-
Southard-Smith, E.M.1
Angrist, M.2
Ellison, J.S.3
Agarwala, R.4
Baxevanis, A.D.5
Chakravarti, A.6
Pavan, W.J.7
-
142
-
-
0032864687
-
Comparative analyses of the Dominant megacolon-SOX10 genomic interval in mouse and human
-
Southard-Smith E.M., Collins J.E., Ellison J.S., Smith K.J., Baxevanis A.D., Touchman J.W., Green E.D., Dunham I., Pavan W.J. Comparative analyses of the Dominant megacolon-SOX10 genomic interval in mouse and human. Mamm. Genome 1999, 10:744-749.
-
(1999)
Mamm. Genome
, vol.10
, pp. 744-749
-
-
Southard-Smith, E.M.1
Collins, J.E.2
Ellison, J.S.3
Smith, K.J.4
Baxevanis, A.D.5
Touchman, J.W.6
Green, E.D.7
Dunham, I.8
Pavan, W.J.9
-
143
-
-
0031984825
-
Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model
-
Southard-Smith E.M., Kos L., Pavan W.J. Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model. Nat. Genet. 1998, 18:60-64.
-
(1998)
Nat. Genet.
, vol.18
, pp. 60-64
-
-
Southard-Smith, E.M.1
Kos, L.2
Pavan, W.J.3
-
144
-
-
84864910444
-
Genome-wide analysis of EGR2/SOX10 binding in myelinating peripheral nerve
-
Srinivasan R., Sun G., Keles S., Jones E.A., Jang S.W., Krueger C., Moran J.J., Svaren J. Genome-wide analysis of EGR2/SOX10 binding in myelinating peripheral nerve. Nucleic Acids Res. 2012, 40:6449-6460.
-
(2012)
Nucleic Acids Res.
, vol.40
, pp. 6449-6460
-
-
Srinivasan, R.1
Sun, G.2
Keles, S.3
Jones, E.A.4
Jang, S.W.5
Krueger, C.6
Moran, J.J.7
Svaren, J.8
-
145
-
-
33746027408
-
Interactions between Sox10, Edn3 and Ednrb during enteric nervous system and melanocyte development
-
Stanchina L., Baral V., Robert F., Pingault V., Lemort N., Pachnis V., Goossens M., Bondurand N. Interactions between Sox10, Edn3 and Ednrb during enteric nervous system and melanocyte development. Dev. Biol. 2006, 295:232-249.
-
(2006)
Dev. Biol.
, vol.295
, pp. 232-249
-
-
Stanchina, L.1
Baral, V.2
Robert, F.3
Pingault, V.4
Lemort, N.5
Pachnis, V.6
Goossens, M.7
Bondurand, N.8
-
146
-
-
77952304708
-
Genetic interaction between Sox10 and Zfhx1b during enteric nervous system development
-
Stanchina L., Van de Putte T., Goossens M., Huylebroeck D., Bondurand N. Genetic interaction between Sox10 and Zfhx1b during enteric nervous system development. Dev. Biol. 2010, 341:416-428.
-
(2010)
Dev. Biol.
, vol.341
, pp. 416-428
-
-
Stanchina, L.1
Van de Putte, T.2
Goossens, M.3
Huylebroeck, D.4
Bondurand, N.5
-
147
-
-
3042705838
-
Transcription factors Sox8 and Sox10 perform non-equivalent roles during oligodendrocyte development despite functional redundancy
-
Stolt C.C., Lommes P., Friedrich R.P., Wegner M. Transcription factors Sox8 and Sox10 perform non-equivalent roles during oligodendrocyte development despite functional redundancy. Development 2004, 131:2349-2358.
-
(2004)
Development
, vol.131
, pp. 2349-2358
-
-
Stolt, C.C.1
Lommes, P.2
Friedrich, R.P.3
Wegner, M.4
-
148
-
-
55249094611
-
The transcription factor Sox5 modulates Sox10 function during melanocyte development
-
Stolt C.C., Lommes P., Hillgartner S., Wegner M. The transcription factor Sox5 modulates Sox10 function during melanocyte development. Nucleic Acids Res. 2008, 36:5427-5440.
-
(2008)
Nucleic Acids Res.
, vol.36
, pp. 5427-5440
-
-
Stolt, C.C.1
Lommes, P.2
Hillgartner, S.3
Wegner, M.4
-
149
-
-
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., Wegner M. Terminal differentiation of myelin-forming oligodendrocytes depends on the transcription factor Sox10. Genes Dev. 2002, 16:165-170.
-
(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
-
150
-
-
76549123335
-
SoxE function in vertebrate nervous system development
-
Stolt C.C., Wegner M. SoxE function in vertebrate nervous system development. Int. J. Biochem. Cell Biol. 2009, 42:437-440.
-
(2009)
Int. J. Biochem. Cell Biol.
, vol.42
, pp. 437-440
-
-
Stolt, C.C.1
Wegner, M.2
-
152
-
-
27644490228
-
SoxE factors function equivalently during neural crest and inner ear development and their activity is regulated by SUMOylation
-
Taylor K.M., Labonne C. SoxE factors function equivalently during neural crest and inner ear development and their activity is regulated by SUMOylation. Dev. Cell 2005, 9:593-603.
-
(2005)
Dev. Cell
, vol.9
, pp. 593-603
-
-
Taylor, K.M.1
Labonne, C.2
-
153
-
-
80051672849
-
B1 and B2 Sox gene expression during neural plate development in chicken and mouse embryos: universal versus species-dependent features
-
Uchikawa M., Yoshida M., Iwafuchi-Doi M., Matsuda K., Ishida Y., Takemoto T., Kondoh H. B1 and B2 Sox gene expression during neural plate development in chicken and mouse embryos: universal versus species-dependent features. Dev. Growth Differ. 2011, 53:761-771.
-
(2011)
Dev. Growth Differ.
, vol.53
, pp. 761-771
-
-
Uchikawa, M.1
Yoshida, M.2
Iwafuchi-Doi, M.3
Matsuda, K.4
Ishida, Y.5
Takemoto, T.6
Kondoh, H.7
-
154
-
-
0141733234
-
Transcriptional regulation by activation and repression elements located at the 5'-noncoding region of the human alpha9 nicotinic receptor subunit gene
-
Valor L.M., Castillo M., Ortiz J.A., Criado M. Transcriptional regulation by activation and repression elements located at the 5'-noncoding region of the human alpha9 nicotinic receptor subunit gene. J. Biol. Chem. 2003, 278:37249-37255.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 37249-37255
-
-
Valor, L.M.1
Castillo, M.2
Ortiz, J.A.3
Criado, M.4
-
155
-
-
0034613374
-
Regulation of the microphthalmia-associated transcription factor gene by the Waardenburg syndrome type 4 gene, SOX10
-
Verastegui C., Bille K., Ortonne J.P., Ballotti R. Regulation of the microphthalmia-associated transcription factor gene by the Waardenburg syndrome type 4 gene, SOX10. J. Biol. Chem. 2000, 275:30757-30760.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 30757-30760
-
-
Verastegui, C.1
Bille, K.2
Ortonne, J.P.3
Ballotti, R.4
-
156
-
-
84855283288
-
Transcription factor Sox10 orchestrates activity of a neural crest-specific enhancer in the vicinity of its gene
-
Wahlbuhl M., Reiprich S., Vogl M.R., Bosl M.R., Wegner M. Transcription factor Sox10 orchestrates activity of a neural crest-specific enhancer in the vicinity of its gene. Nucleic Acids Res. 2011, 40:88-101.
-
(2011)
Nucleic Acids Res.
, vol.40
, pp. 88-101
-
-
Wahlbuhl, M.1
Reiprich, S.2
Vogl, M.R.3
Bosl, M.R.4
Wegner, M.5
-
157
-
-
84855283288
-
Transcription factor Sox10 orchestrates activity of a neural crest-specific enhancer in the vicinity of its gene
-
Wahlbuhl M., Reiprich S., Vogl M.R., Bosl M.R., Wegner M. Transcription factor Sox10 orchestrates activity of a neural crest-specific enhancer in the vicinity of its gene. Nucleic Acids Res. 2012, 40:88-101.
-
(2012)
Nucleic Acids Res.
, vol.40
, pp. 88-101
-
-
Wahlbuhl, M.1
Reiprich, S.2
Vogl, M.R.3
Bosl, M.R.4
Wegner, M.5
-
158
-
-
0035065576
-
Mutations in SIP1, encoding Smad interacting protein-1, cause a form of Hirschsprung disease
-
Wakamatsu N., Yamada Y., Yamada K., Ono T., Nomura N., Taniguchi H., Kitoh H., Mutoh N., Yamanaka T., Mushiake K., Kato K., Sonta S., Nagaya M. Mutations in SIP1, encoding Smad interacting protein-1, cause a form of Hirschsprung disease. Nat. Genet. 2001, 27:369-370.
-
(2001)
Nat. Genet.
, vol.27
, pp. 369-370
-
-
Wakamatsu, N.1
Yamada, Y.2
Yamada, K.3
Ono, T.4
Nomura, N.5
Taniguchi, H.6
Kitoh, H.7
Mutoh, N.8
Yamanaka, T.9
Mushiake, K.10
Kato, K.11
Sonta, S.12
Nagaya, M.13
-
159
-
-
77957759545
-
L1cam acts as a modifier gene during enteric nervous system development
-
Wallace A.S., Schmidt C., Schachner M., Wegner M., Anderson R.B. L1cam acts as a modifier gene during enteric nervous system development. Neurobiol. Dis. 2010, 40:622-633.
-
(2010)
Neurobiol. Dis.
, vol.40
, pp. 622-633
-
-
Wallace, A.S.1
Schmidt, C.2
Schachner, M.3
Wegner, M.4
Anderson, R.B.5
-
160
-
-
77958470157
-
Genetic background impacts developmental potential of enteric neural crest-derived progenitors in the Sox10Dom model of Hirschsprung disease
-
Walters L.C., Cantrell V.A., Weller K.P., Mosher J.T., Southard-Smith E.M. Genetic background impacts developmental potential of enteric neural crest-derived progenitors in the Sox10Dom model of Hirschsprung disease. Hum. Mol. Genet. 2010, 19:4353-4372.
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 4353-4372
-
-
Walters, L.C.1
Cantrell, V.A.2
Weller, K.P.3
Mosher, J.T.4
Southard-Smith, E.M.5
-
161
-
-
0034624244
-
Expression of the Sox10 gene during mouse inner ear development
-
Watanabe K., Takeda K., Katori Y., Ikeda K., Oshima T., Yasumoto K., Saito H., Takasaka T., Shibahara S. Expression of the Sox10 gene during mouse inner ear development. Brain Res. Mol. Brain Res. 2000, 84:141-145.
-
(2000)
Brain Res. Mol. Brain Res.
, vol.84
, pp. 141-145
-
-
Watanabe, K.1
Takeda, K.2
Katori, Y.3
Ikeda, K.4
Oshima, T.5
Yasumoto, K.6
Saito, H.7
Takasaka, T.8
Shibahara, S.9
-
162
-
-
0036016309
-
Identification of a distal enhancer for the melanocyte-specific promoter of the MITF gene
-
Watanabe K., Takeda K., Yasumoto K., Udono T., Saito H., Ikeda K., Takasaka T., Takahashi K., Kobayashi T., Tachibana M., Shibahara S. Identification of a distal enhancer for the melanocyte-specific promoter of the MITF gene. Pigment Cell Res. 2002, 15:201-211.
-
(2002)
Pigment Cell Res.
, vol.15
, pp. 201-211
-
-
Watanabe, K.1
Takeda, K.2
Yasumoto, K.3
Udono, T.4
Saito, H.5
Ikeda, K.6
Takasaka, T.7
Takahashi, K.8
Kobayashi, T.9
Tachibana, M.10
Shibahara, S.11
-
163
-
-
84878375858
-
-
Sox10 and Itgb1 interaction in enteric neural crest cell migration, Dev Biol. 2013, ppi: S0012-1606 00193-0
-
Watanabe Y., Broders-Bondon F., Baral V., Paul-Gilloteaux P., Pingault V., Dufour S., Bondurand N., Sox10 and Itgb1 interaction in enteric neural crest cell migration, Dev Biol. 2013, ppi: S0012-1606 (13)00193-0.
-
, Issue.13
-
-
Watanabe, Y.1
Broders-Bondon, F.2
Baral, V.3
Paul-Gilloteaux, P.4
Pingault, V.5
Dufour, S.6
Bondurand, N.7
-
164
-
-
0033559518
-
-
From head to toes: the multiple facets of Sox proteins, Nucleic Acids Res.
-
Wegner M., From head to toes: the multiple facets of Sox proteins, Nucleic Acids Res. 27, 1999, 1409-1420.
-
(1999)
, vol.27
, pp. 1409-1420
-
-
Wegner, M.1
-
165
-
-
15944396539
-
Secrets to a healthy Sox life: lessons for melanocytes
-
Wegner M. Secrets to a healthy Sox life: lessons for melanocytes. Pigment Cell Res. 2005, 18:74-85.
-
(2005)
Pigment Cell Res.
, vol.18
, pp. 74-85
-
-
Wegner, M.1
-
166
-
-
76549090706
-
All purpose Sox: the many roles of Sox proteins in gene expression
-
Wegner M. All purpose Sox: the many roles of Sox proteins in gene expression. Int. J. Biochem. Cell Biol. 2009, 42:381-390.
-
(2009)
Int. J. Biochem. Cell Biol.
, vol.42
, pp. 381-390
-
-
Wegner, M.1
-
167
-
-
26944436250
-
From stem cells to neurons and glia: a Soxist's view of neural development
-
Wegner M., Stolt C.C. From stem cells to neurons and glia: a Soxist's view of neural development. Trends Neurosci. 2005, 28:583-588.
-
(2005)
Trends Neurosci.
, vol.28
, pp. 583-588
-
-
Wegner, M.1
Stolt, C.C.2
-
168
-
-
10644289340
-
Sox10 acts as a tissue-specific transcription factor enhancing activation of the myelin basic protein gene promoter by p27Kip1 and Sp1
-
Wei Q., Miskimins W.K., Miskimins R. Sox10 acts as a tissue-specific transcription factor enhancing activation of the myelin basic protein gene promoter by p27Kip1 and Sp1. J. Neurosci. Res. 2004, 78:796-802.
-
(2004)
J. Neurosci. Res.
, vol.78
, pp. 796-802
-
-
Wei, Q.1
Miskimins, W.K.2
Miskimins, R.3
-
169
-
-
84864011150
-
Chromatin-remodeling factor brg1 is required for schwann cell differentiation and myelination
-
Weider M., Kuspert M., Bischof M., Vogl M.R., Hornig J., Loy K., Kosian T., Muller J., Hillgartner S., Tamm E.R., Metzger D., Wegner M. Chromatin-remodeling factor brg1 is required for schwann cell differentiation and myelination. Dev. Cell 2012, 23:193-201.
-
(2012)
Dev. Cell
, vol.23
, pp. 193-201
-
-
Weider, M.1
Kuspert, M.2
Bischof, M.3
Vogl, M.R.4
Hornig, J.5
Loy, K.6
Kosian, T.7
Muller, J.8
Hillgartner, S.9
Tamm, E.R.10
Metzger, D.11
Wegner, M.12
-
170
-
-
36148967738
-
Multiple conserved regulatory elements with overlapping functions determine Sox10 expression in mouse embryogenesis
-
Werner T., Hammer A., Wahlbuhl M., Bosl M.R., Wegner M. Multiple conserved regulatory elements with overlapping functions determine Sox10 expression in mouse embryogenesis. Nucleic Acids Res. 2007, 35:6526-6538.
-
(2007)
Nucleic Acids Res.
, vol.35
, pp. 6526-6538
-
-
Werner, T.1
Hammer, A.2
Wahlbuhl, M.3
Bosl, M.R.4
Wegner, M.5
-
171
-
-
0036668285
-
Matching SOX: partner proteins and co-factors of the SOX family of transcriptional regulators
-
Wilson M., Koopman P. Matching SOX: partner proteins and co-factors of the SOX family of transcriptional regulators. Curr. Opinions Genet. Dev. 2002, 12:441-446.
-
(2002)
Curr. Opinions Genet. Dev.
, vol.12
, pp. 441-446
-
-
Wilson, M.1
Koopman, P.2
-
172
-
-
33645802974
-
The high-mobility-group domain of Sox proteins interacts with DNA-binding domains of many transcription factors
-
Wissmuller S., Kosian T., Wolf M., Finzsch M., Wegner M. The high-mobility-group domain of Sox proteins interacts with DNA-binding domains of many transcription factors. Nucleic Acids Res. 2006, 34:1735-1744.
-
(2006)
Nucleic Acids Res.
, vol.34
, pp. 1735-1744
-
-
Wissmuller, S.1
Kosian, T.2
Wolf, M.3
Finzsch, M.4
Wegner, M.5
-
173
-
-
79955031482
-
Genomically integrated transgenes are stably and conditionally expressed in neural crest cell-specific lineages
-
Yokota Y., Saito D., Tadokoro R., Takahashi Y. Genomically integrated transgenes are stably and conditionally expressed in neural crest cell-specific lineages. Dev. Biol. 2011, 353:382-395.
-
(2011)
Dev. Biol.
, vol.353
, pp. 382-395
-
-
Yokota, Y.1
Saito, D.2
Tadokoro, R.3
Takahashi, Y.4
-
174
-
-
33845304972
-
Functional difference of the SOX10 mutant proteins responsible for the phenotypic variability in auditory-pigmentary disorders
-
Yokoyama S., Takeda K., Shibahara S. Functional difference of the SOX10 mutant proteins responsible for the phenotypic variability in auditory-pigmentary disorders. J. Biochem. 2006, 140:491-499.
-
(2006)
J. Biochem.
, vol.140
, pp. 491-499
-
-
Yokoyama, S.1
Takeda, K.2
Shibahara, S.3
-
175
-
-
2942625882
-
Dynamics of neural crest-derived cell migration in the embryonic mouse gut
-
Young H.M., Bergner A.J., Anderson R.B., Enomoto H., Milbrandt J., Newgreen D.F., Whitington P.M. Dynamics of neural crest-derived cell migration in the embryonic mouse gut. Dev. Biol. 2004, 270:455-473.
-
(2004)
Dev. Biol.
, vol.270
, pp. 455-473
-
-
Young, H.M.1
Bergner, A.J.2
Anderson, R.B.3
Enomoto, H.4
Milbrandt, J.5
Newgreen, D.F.6
Whitington, P.M.7
-
176
-
-
0037467620
-
Acquisition of neuronal and glial markers by neural crest-derived cells in the mouse intestine
-
Young H.M., Bergner A.J., Muller T. Acquisition of neuronal and glial markers by neural crest-derived cells in the mouse intestine. J. Comp. Neurol. 2003, 456:1-11.
-
(2003)
J. Comp. Neurol.
, vol.456
, pp. 1-11
-
-
Young, H.M.1
Bergner, A.J.2
Muller, T.3
-
177
-
-
84872509787
-
Olig2 targets chromatin remodelers to enhancers to initiate oligodendrocyte differentiation
-
Yu Y., Chen Y., Kim B., Wang H., Zhao C., He X., Liu L., Liu W., Wu L.M., Mao M., Chan J.R., Wu J., Lu Q.R. Olig2 targets chromatin remodelers to enhancers to initiate oligodendrocyte differentiation. Cell 2013, 152:248-261.
-
(2013)
Cell
, vol.152
, pp. 248-261
-
-
Yu, Y.1
Chen, Y.2
Kim, B.3
Wang, H.4
Zhao, C.5
He, X.6
Liu, L.7
Liu, W.8
Wu, L.M.9
Mao, M.10
Chan, J.R.11
Wu, J.12
Lu, Q.R.13
-
178
-
-
3042766528
-
Spatiotemporal regulation of endothelin receptor-B by SOX10 in neural crest-derived enteric neuron precursors
-
Zhu L., Lee H.O., Jordan C.S., Cantrell V.A., Southard-Smith E.M., Shin M.K. Spatiotemporal regulation of endothelin receptor-B by SOX10 in neural crest-derived enteric neuron precursors. Nat. Genet. 2004, 36:732-737.
-
(2004)
Nat. Genet.
, vol.36
, pp. 732-737
-
-
Zhu, L.1
Lee, H.O.2
Jordan, C.S.3
Cantrell, V.A.4
Southard-Smith, E.M.5
Shin, M.K.6
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