Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling

פריטים דומים

• Pathological consequences of MICU1 mutations on mitochondrial calcium signalling and bioenergetics()
  מאת: Bhosale, Gauri, et al.
  יצא לאור: (2017)
• Pathological consequences of MICU1 mutations on mitochondrial calcium signalling and bioenergetics
  מאת: Gauri Bhosale, et al.
  יצא לאור: (2017)
• Aberrant Wnt signalling and cellular over-proliferation in a novel mouse model of Meckel–Gruber syndrome
  מאת: Gabrielle Wheway, et al.
  יצא לאור: (2013)
• Variable expressivity of ciliopathy neurological phenotypes that encompass Meckel–Gruber syndrome and Joubert syndrome is caused by complex de-regulated ciliogenesis, Shh and Wnt signalling defects
  מאת: Abdelhamed, Zakia A., et al.
  יצא לאור: (2013)
• Variable expressivity of ciliopathy neurological phenotypes that encompass Meckel–Gruber syndrome and Joubert syndrome is caused by complex de-regulated ciliogenesis, Shh and Wnt signalling defects
  מאת: Zakia A. Abdelhamed, et al.
  יצא לאור: (2013)