Functional analysis of natural mutations in two TWIST protein motifs.

समान संसाधन

• Disruption of TWIST1 translation by 5′ UTR variants in Saethre‐Chotzen syndrome
  द्वारा: Zhou, Y, और अन्य
  प्रकाशित: (2018)
• Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome.
  द्वारा: Twigg, SR, और अन्य
  प्रकाशित: (2004)
• Evolution of the Twist Subfamily Vertebrate Proteins: Discovery of a Signature Motif and Origin of the Twist1 Glycine-Rich Motifs in the Amino-Terminus Disordered Domain.
  द्वारा: Yacidzohara Rodriguez, और अन्य
  प्रकाशित: (2016-01-01)
• Expanding the phenotype of craniofrontonasal syndrome: two unrelated boys with EFNB1 mutations and congenital diaphragmatic hernia.
  द्वारा: Vasudevan, P, और अन्य
  प्रकाशित: (2006)
• Correction: Evolution of the Twist Subfamily Vertebrate Proteins: Discovery of a Signature Motif and Origin of the Twist1 Glycine-Rich Motifs in the Amino-Terminus Disordered Domain.
  द्वारा: Yacidzohara Rodriguez, और अन्य
  प्रकाशित: (2016-01-01)