Literature DB >> 30312873

Generation of induced pluripotent stem cells, KCi002-A derived from a patient with Bardet-Biedl syndrome homozygous for the BBS10 variant c.271insT.

Caroline Amalie Brunbjerg Hey1, Katarina Beata Saltõkowa1, Lasse Jonsgaard Larsen1, Zeynep Tümer1, Karen Brøndum-Nielsen1, Karen Grønskov1, Tina Duelund Hjortshøj1, Lisbeth Birk Møller2.   

Abstract

Bardet-Biedl syndrome (BBS) is genetically heterogeneous with at least 21 genes involved, and BBS10 encodes, together with BBS6 and BBS12, chaperonin-like proteins which are important for the assembly of the multiprotein complex, the BBSome encoded by other BBS genes. Here we describe the successful generation of an induced pluripotent stem cell (iPSC) line KCi002-A from a male with BBS, homozygous for the disease causing variant c.271insT, p.(Cys91fsX95) in BBS10. Resource table.
Copyright © 2018 The Authors. Published by Elsevier B.V. All rights reserved.

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Year:  2018        PMID: 30312873     DOI: 10.1016/j.scr.2018.09.013

Source DB:  PubMed          Journal:  Stem Cell Res        ISSN: 1873-5061            Impact factor:   2.020


  1 in total

1.  BBS Proteins Affect Ciliogenesis and Are Essential for Hedgehog Signaling, but Not for Formation of iPSC-Derived RPE-65 Expressing RPE-Like Cells.

Authors:  Caroline Amalie Brunbjerg Hey; Lasse Jonsgaard Larsen; Zeynep Tümer; Karen Brøndum-Nielsen; Karen Grønskov; Tina Duelund Hjortshøj; Lisbeth Birk Møller
Journal:  Int J Mol Sci       Date:  2021-01-29       Impact factor: 5.923

  1 in total

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