SALL1, the gene mutated in Townes-Brocks syndrome, encodes a transcriptional repressor which interacts with TRF1/PIN2 and localizes to pericentromeric heterochromatin

Human Molecular Genetics

Volumn 10, Issue 26, 2001, Pages 3017-3024

  Netzer, Christian ^a   Rieger, Leonie ^a   Brero, Alessandro ^b   Zhang, Chang Dong ^a,b   Hinzke, Markus ^a   Kohlhase, Jürgen ^a   Bohlander, Stefan K ^a,b  

^a UNIVERSITY OF GÖTTINGEN   (Germany)

^b UNIVERSITY OF MUNICH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BINDING PROTEIN; GREEN FLUORESCENT PROTEIN; HISTONE DEACETYLASE INHIBITOR; HYBRID PROTEIN; TRANSCRIPTION FACTOR; TRICHOSTATIN A;

AMINO TERMINAL SEQUENCE; ANIMAL CELL; ANUS ATRESIA; ARTICLE; ASSAY; AUTOSOMAL DOMINANT DISORDER; CENTROMERE; CHROMATIN STRUCTURE; CHROMOSOME; CONFOCAL MICROSCOPY; CONTROLLED STUDY; DROSOPHILA; EPIFLUORESCENCE MICROSCOPY; GENE LOCATION; GENE MAPPING; GENE SEQUENCE; GENE SILENCING; GENETIC TRANSCRIPTION; GENETIC TRANSFECTION; HETEROCHROMATIN; IMMUNOFLUORESCENCE; IN VITRO STUDY; MALFORMATION SYNDROME; MAMMAL CELL; MOLECULAR INTERACTION; NONHUMAN; PERCEPTION DEAFNESS; PRIORITY JOURNAL; PROTEIN LOCALIZATION; REPRESSOR GENE; SEQUENCE HOMOLOGY; TELOMERE; THUMB MALFORMATION; TOWNES BROCKS SYNDROME; TWO HYBRID SYSTEM; YEAST;

ANIMALIA; MAMMALIA;

EID: 0035894741     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/10.26.3017     Document Type: Article

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