-
1
-
-
56249127149
-
The making of a melanocyte: the specification of melanoblasts from the neural crest
-
Thomas AJ, Erickson CA, (2008) The making of a melanocyte: the specification of melanoblasts from the neural crest. Pigment Cell Melanoma Res 21: 598-610.
-
(2008)
Pigment Cell Melanoma Res
, vol.21
, pp. 598-610
-
-
Thomas, A.J.1
Erickson, C.A.2
-
2
-
-
0024280901
-
The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene
-
Geissler EN, Ryan MA, Housman DE, (1988) The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene. Cell 55: 185-192.
-
(1988)
Cell
, vol.55
, pp. 185-192
-
-
Geissler, E.N.1
Ryan, M.A.2
Housman, D.E.3
-
3
-
-
0027204149
-
Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein
-
Hodgkinson CA, Moore KJ, Nakayama A, Steingrímsson E, Copeland NG, et al. (1993) Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein. Cell 74: 395-404.
-
(1993)
Cell
, vol.74
, pp. 395-404
-
-
Hodgkinson, C.A.1
Moore, K.J.2
Nakayama, A.3
Steingrímsson, E.4
Copeland, N.G.5
-
4
-
-
40149083619
-
The secreted metalloprotease ADAMTS20 is required for melanoblast survival
-
doi:10.1371/journal.pgen.1000003
-
Silver DL, Hou L, Somerville R, Young ME, Apte SS, et al. (2008) The secreted metalloprotease ADAMTS20 is required for melanoblast survival. PLoS Genet 4: e1000003 doi:10.1371/journal.pgen.1000003.
-
(2008)
PLoS Genet
, vol.4
-
-
Silver, D.L.1
Hou, L.2
Somerville, R.3
Young, M.E.4
Apte, S.S.5
-
5
-
-
67650992296
-
FOXD3 regulates the lineage switch between neural crest-derived glial cells and pigment cells by repressing MITF through a non-canonical mechanism
-
Thomas AJ, Erickson CA, (2009) FOXD3 regulates the lineage switch between neural crest-derived glial cells and pigment cells by repressing MITF through a non-canonical mechanism. Development 136: 1849-1858.
-
(2009)
Development
, vol.136
, pp. 1849-1858
-
-
Thomas, A.J.1
Erickson, C.A.2
-
6
-
-
0035117420
-
PAX3 is expressed in human melanomas and contributes to tumor cell survival
-
Scholl FA, Kamarashev J, Murmann OV, Geertsen R, Dummer R, et al. (2001) PAX3 is expressed in human melanomas and contributes to tumor cell survival. Cancer Res 61: 823-826.
-
(2001)
Cancer Res
, vol.61
, pp. 823-826
-
-
Scholl, F.A.1
Kamarashev, J.2
Murmann, O.V.3
Geertsen, R.4
Dummer, R.5
-
7
-
-
2642532618
-
Spotlight on spotted mice: a review of white spotting mouse mutants and associated human pigmentation disorders
-
Baxter LL, Hou L, Loftus SK, Pavan WJ, (2004) Spotlight on spotted mice: a review of white spotting mouse mutants and associated human pigmentation disorders. Pigment Cell Res 17: 215-224.
-
(2004)
Pigment Cell Res
, vol.17
, pp. 215-224
-
-
Baxter, L.L.1
Hou, L.2
Loftus, S.K.3
Pavan, W.J.4
-
8
-
-
41149125422
-
Genetic analysis of white facial and leg markings in the Swiss Franches-Montagnes Horse breed
-
Rieder S, Hagger C, Obexer-Ruff G, Leeb T, Poncet PA, (2008) Genetic analysis of white facial and leg markings in the Swiss Franches-Montagnes Horse breed. J Hered 99: 130-136.
-
(2008)
J Hered
, vol.99
, pp. 130-136
-
-
Rieder, S.1
Hagger, C.2
Obexer-Ruff, G.3
Leeb, T.4
Poncet, P.A.5
-
10
-
-
27744434902
-
Exon skipping in the KIT gene causes a Sabino spotting pattern in horses
-
Brooks SA, Bailey E, (2005) Exon skipping in the KIT gene causes a Sabino spotting pattern in horses. Mamm Genome 16: 893-902.
-
(2005)
Mamm Genome
, vol.16
, pp. 893-902
-
-
Brooks, S.A.1
Bailey, E.2
-
11
-
-
39049123708
-
A chromosome inversion near the KIT gene and the Tobiano spotting pattern in horses
-
Brooks SA, Lear TL, Adelson DL, Bailey E, (2007) A chromosome inversion near the KIT gene and the Tobiano spotting pattern in horses. Cytogenet Genome Res 119: 225-230.
-
(2007)
Cytogenet Genome Res
, vol.119
, pp. 225-230
-
-
Brooks, S.A.1
Lear, T.L.2
Adelson, D.L.3
Bailey, E.4
-
12
-
-
37349023135
-
Allelic heterogeneity at the equine KIT locus in dominant white (W) horses
-
doi:10.1371/journal.pgen.0030195
-
Haase B, Brooks SA, Schlumbaum A, Azor PJ, Bailey E, et al. (2007) Allelic heterogeneity at the equine KIT locus in dominant white (W) horses. PLoS Genet 3: e195 doi:10.1371/journal.pgen.0030195.
-
(2007)
PLoS Genet
, vol.3
-
-
Haase, B.1
Brooks, S.A.2
Schlumbaum, A.3
Azor, P.J.4
Bailey, E.5
-
13
-
-
69949166667
-
Seven novel KIT mutations in horses with white coat colour phenotypes
-
Haase B, Brooks SA, Tozaki T, Burger D, Poncet PA, et al. (2009) Seven novel KIT mutations in horses with white coat colour phenotypes. Anim Genet 40: 623-629.
-
(2009)
Anim Genet
, vol.40
, pp. 623-629
-
-
Haase, B.1
Brooks, S.A.2
Tozaki, T.3
Burger, D.4
Poncet, P.A.5
-
14
-
-
79955903837
-
Five novel KIT mutations in horses with white coat colour phenotypes
-
Haase B, Rieder S, Tozaki T, Hasegawa T, Penedo MC, et al. (2011) Five novel KIT mutations in horses with white coat colour phenotypes. Anim Genet 42: 337-339.
-
(2011)
Anim Genet
, vol.42
, pp. 337-339
-
-
Haase, B.1
Rieder, S.2
Tozaki, T.3
Hasegawa, T.4
Penedo, M.C.5
-
15
-
-
0031828292
-
A missense mutation in the endothelin-B receptor gene is associated with Lethal White Foal Syndrome: an equine version of Hirschsprung disease
-
Metallinos DL, Bowling AT, Rine J, (1998) A missense mutation in the endothelin-B receptor gene is associated with Lethal White Foal Syndrome: an equine version of Hirschsprung disease. Mamm Genome 9: 426-431.
-
(1998)
Mamm Genome
, vol.9
, pp. 426-431
-
-
Metallinos, D.L.1
Bowling, A.T.2
Rine, J.3
-
16
-
-
0032053530
-
Endothelin receptor B polymorphism associated with lethal white foal syndrome in horses
-
Santschi EM, Purdy AK, Valberg SJ, Vrotsos PD, Kaese H, et al. (1998) Endothelin receptor B polymorphism associated with lethal white foal syndrome in horses. Mamm Genome 9: 306-309.
-
(1998)
Mamm Genome
, vol.9
, pp. 306-309
-
-
Santschi, E.M.1
Purdy, A.K.2
Valberg, S.J.3
Vrotsos, P.D.4
Kaese, H.5
-
17
-
-
0031831546
-
A dinucleotide mutation in the endothelin-B receptor gene is associated with lethal white foal syndrome (LWFS); a horse variant of Hirschsprung disease
-
Yang GC, Croaker D, Zhang AL, Manglick P, Cartmill T, et al. (1998) A dinucleotide mutation in the endothelin-B receptor gene is associated with lethal white foal syndrome (LWFS); a horse variant of Hirschsprung disease. Hum Mol Genet 7: 1047-1052.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 1047-1052
-
-
Yang, G.C.1
Croaker, D.2
Zhang, A.L.3
Manglick, P.4
Cartmill, T.5
-
18
-
-
77950389859
-
Review and update of mutations causing Waardenburg syndrome
-
Pingault V, Ente D, Dastot-Le Moal F, Goossens M, Marlin S, et al. (2010) Review and update of mutations causing Waardenburg syndrome. Hum Mutat 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
-
20
-
-
0344731080
-
Crystal structure of the human Pax6 paired domain-DNA complex reveals specific roles for the linker region and carboxy-terminal subdomain in DNA binding
-
Xu HE, Rould MA, Xu W, Epstein JA, Maas RL, et al. (1999) Crystal structure of the human Pax6 paired domain-DNA complex reveals specific roles for the linker region and carboxy-terminal subdomain in DNA binding. Genes Dev 13: 1263-1275.
-
(1999)
Genes Dev
, vol.13
, pp. 1263-1275
-
-
Xu, H.E.1
Rould, M.A.2
Xu, W.3
Epstein, J.A.4
Maas, R.L.5
-
21
-
-
0029917487
-
Identification of a melanocyte-type promoter of the microphthalmia-associated transcription factor gene
-
Fuse N, Yasumoto K, Suzuki H, Takahashi K, Shibahara S, (1996) Identification of a melanocyte-type promoter of the microphthalmia-associated transcription factor gene. Biochem Biophys Res Commun 219: 702-707.
-
(1996)
Biochem Biophys Res Commun
, vol.219
, pp. 702-707
-
-
Fuse, N.1
Yasumoto, K.2
Suzuki, H.3
Takahashi, K.4
Shibahara, S.5
-
22
-
-
0034641596
-
Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome
-
Bondurand N, Pingault V, Goerich DE, Lemort N, Sock E, et al. (2000) Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome. Hum Mol Genet 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
-
23
-
-
34248656736
-
Evolutionary sequence comparison of the Mitf gene reveals novel conserved domains
-
Hallsson JH, Haflidadóttir BS, Schepsky A, Arnheiter H, Steingrímsson E, (2007) Evolutionary sequence comparison of the Mitf gene reveals novel conserved domains. Pigment Cell Res 20: 185-200.
-
(2007)
Pigment Cell Res
, vol.20
, pp. 185-200
-
-
Hallsson, J.H.1
Haflidadóttir, B.S.2
Schepsky, A.3
Arnheiter, H.4
Steingrímsson, E.5
-
24
-
-
35648953308
-
Efficient mapping of mendelian traits in dogs through genome-wide association
-
Karlsson EK, Baranowska I, Wade CM, Salmon Hillbertz NH, Zody MC, et al. (2007) Efficient mapping of mendelian traits in dogs through genome-wide association. Nat Genet 39: 1321-1328.
-
(2007)
Nat Genet
, vol.39
, pp. 1321-1328
-
-
Karlsson, E.K.1
Baranowska, I.2
Wade, C.M.3
Salmon Hillbertz, N.H.4
Zody, M.C.5
-
25
-
-
0034045615
-
Tietz syndrome (hypopigmentation/deafness) caused by mutation of MITF
-
Smith SD, Kelley PM, Kenyon JB, Hoover D, (2000) Tietz syndrome (hypopigmentation/deafness) caused by mutation of MITF. J Med Genet 37: 446-448.
-
(2000)
J Med Genet
, vol.37
, pp. 446-448
-
-
Smith, S.D.1
Kelley, P.M.2
Kenyon, J.B.3
Hoover, D.4
-
26
-
-
0025925068
-
Splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3
-
Epstein DJ, Vekemans M, Gros P, (1991) Splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3. Cell 67: 767-774.
-
(1991)
Cell
, vol.67
, pp. 767-774
-
-
Epstein, D.J.1
Vekemans, M.2
Gros, P.3
-
27
-
-
0027204149
-
Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein
-
Hodgkinson CA, Moore KJ, Nakayama A, Steingrímsson E, Copeland NG, et al. (1993) Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein. Cell 74: 395-404.
-
(1993)
Cell
, vol.74
, pp. 395-404
-
-
Hodgkinson, C.A.1
Moore, K.J.2
Nakayama, A.3
Steingrímsson, E.4
Copeland, N.G.5
-
28
-
-
0026408851
-
Common white facial markings in bay and chestnut Arabian horses and their hybrids
-
Woolf CM, (1991) Common white facial markings in bay and chestnut Arabian horses and their hybrids. J Hered 82: 167-169.
-
(1991)
J Hered
, vol.82
, pp. 167-169
-
-
Woolf, C.M.1
-
29
-
-
10944234560
-
Melanocytes and the microphthalmia transcription factor network
-
Steingrímsson E, Copeland NG, Jenkins NA, (2004) Melanocytes and the microphthalmia transcription factor network. Annu Rev Genet 38: 365-411.
-
(2004)
Annu Rev Genet
, vol.38
, pp. 365-411
-
-
Steingrímsson, E.1
Copeland, N.G.2
Jenkins, N.A.3
-
30
-
-
34548292504
-
PLINK: a tool set for whole-genome association and population-based linkage analyses
-
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, et al. (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81: 559-575.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.5
-
31
-
-
0036338150
-
Merlin - rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR, (2002) Merlin- rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 30: 97-101.
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
32
-
-
80052284219
-
Structural basis of simultaneous recruitment of the transcriptional regulators LMO2 and FOG1/ZFPM1 by the transcription factor GATA1
-
Wilkinson-White L, Gamsjaeger R, Dastmalchi S, Wienert B, Stokes PH, et al. (2011) Structural basis of simultaneous recruitment of the transcriptional regulators LMO2 and FOG1/ZFPM1 by the transcription factor GATA1. Proc Natl Acad Sci USA 108: 14443-14448.
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, pp. 14443-14448
-
-
Wilkinson-White, L.1
Gamsjaeger, R.2
Dastmalchi, S.3
Wienert, B.4
Stokes, P.H.5
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