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Literature DB >> 26872601

DUX4 Is Derepressed in Late-Differentiating Keratinocytes in Conjunction with Loss of H3K9me3 Epigenetic Repression.

Orla M Gannon¹, Lilia Merida de Long¹, Nicholas A Saunders².

Abstract

Entities: Gene

Mesh：

Substances：

Year: 2016 PMID： 26872601 DOI： 10.1016/j.jid.2016.01.027

Source DB: PubMed Journal: J Invest Dermatol ISSN： 0022-202X Impact factor: 8.551

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8 in total

1. Smchd1 haploinsufficiency exacerbates the phenotype of a transgenic FSHD1 mouse model.

Authors: Jessica C de Greef; Yvonne D Krom; Bianca den Hamer; Lauren Snider; Yosuke Hiramuki; Rob F P van den Akker; Kelsey Breslin; Miha Pakusch; Daniela C F Salvatori; Bram Slütter; Rabi Tawil; Marnie E Blewitt; Stephen J Tapscott; Silvère M van der Maarel
Journal: Hum Mol Genet Date: 2018-02-15 Impact factor: 6.150

2. Monosomy 18p is a risk factor for facioscapulohumeral dystrophy.

Authors: Judit Balog; Remko Goossens; Richard J L F Lemmers; Kirsten R Straasheijm; Patrick J van der Vliet; Anita van den Heuvel; Chiara Cambieri; Nicolas Capet; Léonard Feasson; Veronique Manel; Julian Contet; Marjolein Kriek; Colleen M Donlin-Smith; Claudia A L Ruivenkamp; Patricia Heard; Stephen J Tapscott; Jannine D Cody; Rabi Tawil; Sabrina Sacconi; Silvère M van der Maarel
Journal: J Med Genet Date: 2018-03-21 Impact factor: 6.318

Review 3. Facioscapulohumeral Muscular Dystrophy: Update on Pathogenesis and Future Treatments.

Authors: Johanna Hamel; Rabi Tawil
Journal: Neurotherapeutics Date: 2018-10 Impact factor: 7.620

4. Effect of SUV39H1 Histone Methyltransferase Knockout on Expression of Differentiation-Associated Genes in HaCaT Keratinocytes.

Authors: Barbara Sobiak; Wiesława Leśniak
Journal: Cells Date: 2020-12-07 Impact factor: 6.600

DUX4 Is Derepressed in Late-Differentiating Keratinocytes in Conjunction with Loss of H3K9me3 Epigenetic Repression.

1. Smchd1 haploinsufficiency exacerbates the phenotype of a transgenic FSHD1 mouse model.

2. Monosomy 18p is a risk factor for facioscapulohumeral dystrophy.

Review 3. Facioscapulohumeral Muscular Dystrophy: Update on Pathogenesis and Future Treatments.

4. Effect of SUV39H1 Histone Methyltransferase Knockout on Expression of Differentiation-Associated Genes in HaCaT Keratinocytes.

5. Gene Editing Targeting the DUX4 Polyadenylation Signal: A Therapy for FSHD?

Review 6. Homeostasis, regeneration and tumour formation in the mammalian epidermis.

Review 7. The prospects of targeting DUX4 in facioscapulohumeral muscular dystrophy.

8. Dnmt3b regulates DUX4 expression in a tissue-dependent manner in transgenic D4Z4 mice.