SEDLIN forms homodimers: Characterisation of SEDLIN mutations and their interactions with transcription factors MBP1, PITX1 and SF1

Benzer Materyaller

• SEDLIN forms homodimers: characterisation of SEDLIN mutations and their interactions with transcription factors MBP1, PITX1 and SF1.
  Yazar:: Jeyabalan, J, ve diğerleri
  Baskı/Yayın Bilgisi: (2010)
• Spondyloepiphyseal dysplasia tarda (SEDT)-associated sedlin mutations disrupt interactions with C-MYC promoter-binding protein 1 (MBP-1), pituitary homeobox 1 (PITX1) and stercidogenic factor 1 (SF1)
  Yazar:: Nesbit, M, ve diğerleri
  Baskı/Yayın Bilgisi: (2007)
• A 5-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a 6-generation Arkansas kindred.
  Yazar:: Mumm, S, ve diğerleri
  Baskı/Yayın Bilgisi: (2000)
• A five-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a six-generation Arkansas kindred.
  Yazar:: Mumm, S, ve diğerleri
  Baskı/Yayın Bilgisi: (2000)
• Clinical Diagnosis of X-Linked Spondyloepiphyseal Dysplasia Tarda and a Novel Missense Mutation in the Sedlin Gene (SEDL)
  Yazar:: Lei Kong, ve diğerleri
  Baskı/Yayın Bilgisi: (2018-01-01)