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Brain research. Molecular brain research, v.84 no.1/2, 2000년, pp.141 - 145
Watanabe, Ken-ichi (Department of Molecular Biology and Applied Physiology, Tohoku University School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8575, Japan) , Takeda, Kazuhisa (Department of Molecular Biology and Applied Physiology, Tohoku University School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8575, Japan) , Katori, Yukio (Department of Otorhinolaryngology, Tohoku University School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8574, Japan) , Ikeda, Katsuhisa (Department of Otorhinolaryngology, Tohoku University School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8574, Japan) , Oshima, Takeshi (Department of Otorhinolaryngology, Tohoku University School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8574, Japan) , Yasumoto, Ken-ichi (Department of Molecular Biology and Applied Physiology, Tohoku University School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8575, Japan) , Saito, Hideo (Department of Molecular Biology and Applied Physiology, Tohoku University School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980) , Takasaka, Tomonori , Shibahara, Shigeki
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AbstractMutations in the SOX10 gene, encoding a cell-lineage specific transcription factor, are associated with congenital deafness. We analyzed the expression of Sox10 mRNA in developing mouse inner ear by in situ hybridization. Sox10 mRNA is expressed in the entire epithelia of the otic vesicle at...
FEBS Lett. Bondurand 432 168 1998 10.1016/S0014-5793(98)00843-6 Expression of the SOX10 gene during human development
Hum. Mol. Genet. Bondurand 8 1785 1999 10.1093/hmg/8.9.1785 A molecular analysis of the yemenite deaf-blind hypopigmentation syndrome: SOX10 dysfunction causes different neurocristopathies
Proc. Natl. Acad. Sci. USA Herbarth 95 5161 1998 10.1073/pnas.95.9.5161 Mutation of the Sry-related Sox10 gene in Dominant megacolon, a mouse model for human Hirschsprung disease
Cell Hodgkinson 74 395 1993 10.1016/0092-8674(93)90429-T Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein
J. Neurosci. Kuhlbrodt 18 237 1998 10.1523/JNEUROSCI.18-01-00237.1998 Sox10, a novel transcriptional modulator in glial cells
J. Biol. Chem. Kuhlbrodt 273 23033 1998 10.1074/jbc.273.36.23033 Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients
Mech. Dev. Nakayama 70 155 1998 10.1016/S0925-4773(97)00188-3 Mutations in microphthalmia, the mouse homolog of the human deafness gene MITF, affect neuroepithelial and neural crest-derived melanocytes differently
Nat. Genet. Pingault 18 171 1998 10.1038/ng0298-171 SOX10 mutations in patients with Waardenburg-Hirschsprung disease
Hum. Genet. Pusch 103 115 1998 10.1007/s004390050793 The SOX10/Sox10 gene from human and mouse: sequence, expression, and transactivation by the encoded HMG domain transcription factor
Histochemistry Schaeren-Wiemers 100 431 1993 10.1007/BF00267823 A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: in situ hybridization using digoxigenin-labelled cRNA probes
Genome Res. Southard-Smith 9 215 1999 10.1101/gr.9.3.215 The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome
Nat. Genet. Southard-Smith 18 60 1998 10.1038/ng0198-60 Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model
Hear. Res. Spicer 79 161 1994 10.1016/0378-5955(94)90137-6 Differences along the place-frequency map in the structure of supporting cells in the gerbil cochlea
J. Biol. Chem. Takeda 275 14013 2000 10.1074/jbc.C000113200 Induction of melanocyte-specific microphthalmia-associated transcription factor by Wnt-3a
Nat. Genet. Tassabehji 8 251 1994 10.1038/ng1194-251 Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene
Mech. Dev. Torres 71 5 1998 10.1016/S0925-4773(97)00155-X The development of the vertebrate inner ear
Nucleic Acids Res. Wegner 27 1409 1999 10.1093/nar/27.6.1409 From head to toes: the multiple facets of Sox proteins
Nucleic Acids Res. Wright 21 744 1993 10.1093/nar/21.3.744 Seven new members of the Sox gene family expressed during mouse development
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