top of page

[New paper] The mechanism in which AKT3 pathway causes cortical malformation

  • Writer: sak042
    sak042
  • Nov 2, 2015
  • 1 min read

A new paper published in Nature Medicine

In this study, Sangwoo Kim joined to identify how abnormal AKT3 pathway activation causes malformation of cortical development.

An AKT3-FOXG1-reelin network underlies defective migration in human focal malformations of cortical development http://www.nature.com/nm/journal/v21/n12/full/nm.3982.html Collaboration with Joseph G. Gleeson (UCSD)

Comments


Featured Posts
Recent Posts
Search By Tags
Follow Us
  • Facebook Basic Square
  • Twitter Basic Square
  • Google+ Basic Square

서울특별시 서대문구 연세로 50-1, 연세대학교 의과대학 신관 616호

#616 Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun-gu, Seoul 03722, South Korea  

+82-2-2228-2589

02-2228-2589 (inside Korea)

  • w-facebook
  • Twitter Clean
  • w-googleplus
  • W-Pinterest

© Since 2014 Translational Genome Informatics Laboratory,

Yonsei University College of Medicine.

Proudly created with Wix.com

bottom of page