iPSC reprogramming of fibroblasts from a patient with a Rothmund-Thomson syndrome RTS

Copyright © 2020. Published by Elsevier B.V..

Rothmund-Thomson Syndrome (RTS) is a rare autosomal recessive disease that manifests several clinical features of accelerated aging. These findings include atrophic skin and pigment changes, alopecia, osteopenia, cataracts, and an increased incidence of cancer for patients. Mutations in RECQL4 gene are responsible for cases of RTS. RECQL4 belongs to the RECQ DNA helicase family which has been shown to participate in many aspects of DNA metabolism. To be able to study the cellular defects related to the pathology, we derived an induced pluripotent cell line from RTS patient fibroblasts, with the ability to re-differentiate into the three embryonic germ layers.

Medienart:

E-Artikel

Erscheinungsjahr:

2020

Erschienen:

2020

Enthalten in:

Zur Gesamtaufnahme - volume:45

Enthalten in:

Stem cell research - 45(2020) vom: 30. Mai, Seite 101807

Sprache:

Englisch

Beteiligte Personen:

Gatinois, Vincent [VerfasserIn]
Desprat, Romain [VerfasserIn]
Pichard, Lydiane [VerfasserIn]
Becker, Fabienne [VerfasserIn]
Goldenberg, Alice [VerfasserIn]
Balguerie, Xavier [VerfasserIn]
Pellestor, Franck [VerfasserIn]
Lemaitre, Jean-Marc [VerfasserIn]

Links:

Volltext

Themen:

Journal Article
Research Support, Non-U.S. Gov't

Anmerkungen:

Date Completed 21.06.2021

Date Revised 21.06.2021

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1016/j.scr.2020.101807

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM309992303