Related references
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AMERICAN JOURNAL OF HUMAN GENETICS (2007)
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A tissue-restricted cAMP transcriptional response -: SOX10 modulates α-melanocyte-stimulating hormone-triggered expression of microphthalmia-associated transcription factor in melanocytes
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SOX10 mutations in chronic intestinal pseudo-obstruction suggest a complex physiopathological mechanism
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EK Nishimura et al.
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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
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The transcription factors SOX9 and SOX10 are vitiligo autoantigens in autoimmune polyendocrine syndrome type I
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JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
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DEVELOPMENTAL BIOLOGY (2001)
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MOLECULAR ENDOCRINOLOGY (2001)
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S Britsch et al.
GENES & DEVELOPMENT (2001)
Mice null for Sox18 are viable and display a mild coat defect
D Pennisi et al.
MOLECULAR AND CELLULAR BIOLOGY (2000)
Direct regulation of the Microphthalmia promoter by Sox10 links Waardenburg-Shah syndrome (WS4)-associated hypopigmentation and deafness to WS2
M Lee et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Phylogeny of the SOX family of developmental transcription factors based on sequence and structural indicators
J Bowles et al.
DEVELOPMENTAL BIOLOGY (2000)
Domains of Brn-2 that mediate homodimerization and interaction with general and melanocytic transcription factors
DJ Smit et al.
EUROPEAN JOURNAL OF BIOCHEMISTRY (2000)
Regulation of the microphthalmia-associated transcription factor gene by the Waardenburg syndrome type 4 gene, SOX10
C Verastegui et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
The glial transcription factor Sox10 binds to DNA both as monomer and dimer with different functional consequences
RI Peirano et al.
NUCLEIC ACIDS RESEARCH (2000)
Interaction among SOX10 PAX3 and MITF, three genes altered in Waardenburg syndrome
N Bondurand et al.
HUMAN MOLECULAR GENETICS (2000)
Transcription factor hierarchy in Waardenburg syndrome: regulation of MITF expression by SOX10 and PAX3
SB Potterf et al.
HUMAN GENETICS (2000)
Neurological phenotype in Waardenburg syndrome type 4 correlates with novel SOX10 truncating mutations and expression in developing brain
RL Touraine et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)
Pairing SOX off with partners in the regulation of embryonic development
Y Kamachi et al.
TRENDS IN GENETICS (2000)