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

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...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awdur: Singh, Shalini
Awduron Eraill: Kunz, Jürgen (Dr.) (Cynghorydd traethodau ymchwil)
Fformat: Dissertation
Iaith:Saesneg
Cyhoeddwyd: Philipps-Universität Marburg 2006
Pynciau:
Transcription factor
TWIST
Medizin
Protein domains
Nucleus localization signal
Medical sciences Medicine
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