Identification and functional characterization of protein domains in the transcription factor TWIST

Saethre-Chotzen syndrome is an autosomal dominant inherited disorder with premature fusion of cranial sutures. It is caused by nucleotide sequence changes within or in proximity of the TWIST1 gene. This gene encodes for a bHLH transcription factor, which inhibits osteogenic differentiation by transc...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile nagusia: Singh, Shalini
Beste egile batzuk: Kunz, Jürgen (Dr.) (Tesi aholkularia)
Formatua: Dissertation
Hizkuntza:ingelesa
Argitaratua: Philipps-Universität Marburg 2006
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