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Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: Two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A)

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Author(s):
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Kobayashi, Gerson S. ; Vieira-Silva, Gleiciele A. ; Varella-Branco, Elisa ; Moreira, Danielle P. ; Kitajima, Joao Paulo F. W. ; Hemza, Claudia R. M. L. ; Mingroni-Netto, Regina C. ; Lojudice, Fernando H. ; Oiticica, Jeanne ; Bento, Ricardo F. ; Batissoco, Ana C. ; Lezirovitz, Karina
Total Authors: 12
Document type: Journal article
Source: STEM CELL RESEARCH; v. 71, p. 5-pg., 2023-09-01.
Abstract

The DFNA58 locus contains a genomic duplication involving three protein-coding genes (CNRIP1, PLEK, and PPP3R1 & PRIME;s exon 1) and other uncharacterized lncRNA genes (LOC101927723, LOC107985892 and LOC102724389). To clarify the role of these genes in hearing and precisely determine their role in hearing loss, four iPSC lines were generated from two carriers and two noncarriers of the duplication. (AU)

FAPESP's process: 13/08028-1 - CEGH-CEL - Human Genome and Stem Cell Research Center
Grantee:Mayana Zatz
Support Opportunities: Research Grants - Research, Innovation and Dissemination Centers - RIDC
FAPESP's process: 18/03433-9 - 145/5000 Use of IPS cells and animal models to elucidate the pathophysiology of post-lingual sensorineural hearing loss of genetic etiology
Grantee:Karina Lezirovitz Mandelbaum
Support Opportunities: Regular Research Grants
FAPESP's process: 14/13071-6 - Identification of novel genes and functional studies in nonsyndromic deafness
Grantee:Karina Lezirovitz Mandelbaum
Support Opportunities: Regular Research Grants