Related references
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Sry associates with the heterochromatin protein I complex by interacting with a KRAB domain protein
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A microdeletion in the ligand binding domain of human steroidogenic factor 1 causes XY sex reversal without adrenal insufficiency
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SOX9 is up-regulated by the transient expression of SRY specifically in Sertoli cell precursors
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A mutated form of steroidogenic factor 1 (SF-1 G35E) that causes sex reversal in humans fails to synergize with transcription factor GATA-4
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Novel mutations affecting SRY DNA-binding activity:: the HMG box N65H associated with 46,XY pure gonadal dysgenesis and the familial non-HMG box R30I associated with variable phenotypes
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Active genes are tri-methylated at K4 of histone H3
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A nuclear export signal within the high mobility group domain regulates the nucleocytoplasmic translocation of SOX9 during sexual determination
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A direct role of SRY and SOX proteins in pre-mRNA splicing
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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)
Compound effects of point mutations causing campomelic dysplasia/autosomal sex reversal upon SOX9 structure, nuclear transport, DNA binding, and transcriptional activation
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