Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome

Lignende værker

• In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?
  af: Motahari, Zahra, et al.
  Udgivet: (2019)
• Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation
  af: Paronett, Elizabeth M., et al.
  Udgivet: (2015)
• Disrupted Coordination of Hypoglossal Motor Control in a Mouse Model of Pediatric Dysphagia in DiGeorge/22q11.2 Deletion Syndrome
  af: Wang, Xin, et al.
  Udgivet: (2020)
• Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome
  af: Meechan, Daniel W., et al.
  Udgivet: (2009)
• Transcriptional dysregulation in developing trigeminal sensory neurons in the LgDel mouse model of DiGeorge 22q11.2 deletion syndrome
  af: Maynard, Thomas M, et al.
  Udgivet: (2020)