Generation of a human iPSC line, INMi002-A, carrying the most prevalent USH2A variant associated with Usher syndrome type 2

Những quyển sách tương tự

• Generation of an iPSC line, INMi001-A, carrying the two most common USH2A mutations from a compound heterozygote with non-syndromic retinitis pigmentosa
  Bằng: Carla Sanjurjo-Soriano, et al.
  Được phát hành: (2018-12-01)
• Generation of a human iPSC line, INMi005-A, from a patient with non-syndromic USH2A-associated retinitis pigmentosa
  Bằng: Carla Sanjurjo-Soriano, et al.
  Được phát hành: (2022-04-01)
• Generation of a human iPSC line, INMi004-A, with a point mutation in CRX associated with autosomal dominant Leber congenital amaurosis
  Bằng: Nejla Erkilic, et al.
  Được phát hành: (2019-07-01)
• Genome Editing in Patient iPSCs Corrects the Most Prevalent USH2A Mutations and Reveals Intriguing Mutant mRNA Expression Profiles
  Bằng: Carla Sanjurjo-Soriano, et al.
  Được phát hành: (2020-06-01)
• USH2A variants causing retinitis pigmentosa or Usher syndrome provoke differential retinal phenotypes in disease-specific organoids
  Bằng: Carla Sanjurjo-Soriano, et al.
  Được phát hành: (2023-10-01)