Heterogeneity and overlaps in nucleotide excision repair disorders-Reference-Cited by-同舟云学术

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Heterogeneity and overlaps in nucleotide excision repair disorders

Published:2019-04-22 Issue:1 Volume:97 Page:12-24
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Ferri Debora¹,Orioli Donata¹,Botta Elena¹^ORCID

Affiliation:

1. Istituto di Genetica Molecolare (IGM)Consiglio Nazionale delle Ricerche Pavia Italy

Funder

Associazione Italiana per la Ricerca sul Cancro

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cge.13545

Reference77 articles.

1. Understanding nucleotide excision repair and its roles in cancer and ageing

2. Nucleotide excision repair in humans

3. Xeroderma pigmentosum

4. Xeroderma pigmentosum complementation group F: A rare cause of cerebellar ataxia with chorea

5. Xeroderma pigmentosum is a definite cause of Huntington's disease-like syndrome

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1. STK19 is a transcription-coupled repair factor that participates in UVSSA ubiquitination and TFIIH loading;2024-07-18

2. Deep learning with a small dataset predicts chromatin remodelling contribution to winter dormancy of apple axillary buds;Tree Physiology;2024-06-21

3. Persistent TFIIH binding to non-excised DNA damage causes cell and developmental failure;Nature Communications;2024-04-25

4. DNA repair-related heritable photosensitivity syndromes: Mutation landscape in a multiethnic cohort of 17 multigenerational families with high degree of consanguinity;DNA Repair;2024-04

5. TFIIH central activity in nucleotide excision repair to prevent disease;DNA Repair;2023-12

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