133 related articles for article (PubMed ID: 17952069)
21. p8/TTDA overexpression enhances UV-irradiation resistance and suppresses TFIIH mutations in a Drosophila trichothiodystrophy model.
Aguilar-Fuentes J; Fregoso M; Herrera M; Reynaud E; Braun C; Egly JM; Zurita M
PLoS Genet; 2008 Nov; 4(11):e1000253. PubMed ID: 19008953
[TBL] [Abstract][Full Text] [Related]
22. TFIIH mutations can impact on translational fidelity of the ribosome.
Khalid F; Phan T; Qiang M; Maity P; Lasser T; Wiese S; Penzo M; Alupei M; Orioli D; Scharffetter-Kochanek K; Iben S
Hum Mol Genet; 2023 Mar; 32(7):1102-1113. PubMed ID: 36308430
[TBL] [Abstract][Full Text] [Related]
23. Structural basis for group A trichothiodystrophy.
Kainov DE; Vitorino M; Cavarelli J; Poterszman A; Egly JM
Nat Struct Mol Biol; 2008 Sep; 15(9):980-4. PubMed ID: 19172752
[TBL] [Abstract][Full Text] [Related]
24. Dysregulation of LXR responsive genes contribute to ichthyosis in trichothiodystrophy.
Hashimoto S; Takanari H; Compe E; Egly JM
J Dermatol Sci; 2020 Mar; 97(3):201-207. PubMed ID: 32037099
[TBL] [Abstract][Full Text] [Related]
25. New clinico-genetic classification of trichothiodystrophy.
Morice-Picard F; Cario-André M; Rezvani H; Lacombe D; Sarasin A; Taïeb A
Am J Med Genet A; 2009 Sep; 149A(9):2020-30. PubMed ID: 19681155
[TBL] [Abstract][Full Text] [Related]
26. Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype.
Theil AF; Botta E; Raams A; Smith DEC; Mendes MI; Caligiuri G; Giachetti S; Bione S; Carriero R; Liberi G; Zardoni L; Swagemakers SMA; Salomons GS; Sarasin A; Lehmann A; van der Spek PJ; Ogi T; Hoeijmakers JHJ; Vermeulen W; Orioli D
Am J Hum Genet; 2019 Aug; 105(2):434-440. PubMed ID: 31374204
[TBL] [Abstract][Full Text] [Related]
27. Mutations in the C7orf11 (TTDN1) gene in six nonphotosensitive trichothiodystrophy patients: no obvious genotype-phenotype relationships.
Botta E; Offman J; Nardo T; Ricotti R; Zambruno G; Sansone D; Balestri P; Raams A; Kleijer WJ; Jaspers NG; Sarasin A; Lehmann AR; Stefanini M
Hum Mutat; 2007 Jan; 28(1):92-6. PubMed ID: 16977596
[TBL] [Abstract][Full Text] [Related]
28. Nucleotide Excision Repair and Transcriptional Regulation: TFIIH and Beyond.
Compe E; Egly JM
Annu Rev Biochem; 2016 Jun; 85():265-90. PubMed ID: 27294439
[TBL] [Abstract][Full Text] [Related]
29. Bone fragility and decline in stem cells in prematurely aging DNA repair deficient trichothiodystrophy mice.
Diderich KE; Nicolaije C; Priemel M; Waarsing JH; Day JS; Brandt RM; Schilling AF; Botter SM; Weinans H; van der Horst GT; Hoeijmakers JH; van Leeuwen JP
Age (Dordr); 2012 Aug; 34(4):845-61. PubMed ID: 21814739
[TBL] [Abstract][Full Text] [Related]
30. Trichothiodystrophy causative TFIIEβ mutation affects transcription in highly differentiated tissue.
Theil AF; Mandemaker IK; van den Akker E; Swagemakers SMA; Raams A; Wüst T; Marteijn JA; Giltay JC; Colombijn RM; Moog U; Kotzaeridou U; Ghazvini M; von Lindern M; Hoeijmakers JHJ; Jaspers NGJ; van der Spek PJ; Vermeulen W
Hum Mol Genet; 2017 Dec; 26(23):4689-4698. PubMed ID: 28973399
[TBL] [Abstract][Full Text] [Related]
31. Nucleolar TFIIE plays a role in ribosomal biogenesis and performance.
Phan T; Maity P; Ludwig C; Streit L; Michaelis J; Tsesmelis M; Scharffetter-Kochanek K; Iben S
Nucleic Acids Res; 2021 Nov; 49(19):11197-11210. PubMed ID: 34581812
[TBL] [Abstract][Full Text] [Related]
32. Disruption of TTDA results in complete nucleotide excision repair deficiency and embryonic lethality.
Theil AF; Nonnekens J; Steurer B; Mari PO; de Wit J; Lemaitre C; Marteijn JA; Raams A; Maas A; Vermeij M; Essers J; Hoeijmakers JH; Giglia-Mari G; Vermeulen W
PLoS Genet; 2013 Apr; 9(4):e1003431. PubMed ID: 23637614
[TBL] [Abstract][Full Text] [Related]
33. Small molecule-based targeting of TTD-A dimerization to control TFIIH transcriptional activity represents a potential strategy for anticancer therapy.
Gervais V; Muller I; Mari PO; Mourcet A; Movellan KT; Ramos P; Marcoux J; Guillet V; Javaid S; Burlet-Schiltz O; Czaplicki G; Milon A; Giglia-Mari G
J Biol Chem; 2018 Sep; 293(39):14974-14988. PubMed ID: 30068551
[TBL] [Abstract][Full Text] [Related]
34. Analysis of Drosophila p8 and p52 mutants reveals distinct roles for the maintenance of TFIIH stability and male germ cell differentiation.
Cruz-Becerra G; Juárez M; Valadez-Graham V; Zurita M
Open Biol; 2016 Oct; 6(10):. PubMed ID: 27805905
[TBL] [Abstract][Full Text] [Related]
35. Effects of postnatal dietary choline supplementation on motor regional brain volume and growth factor expression in a mouse model of Rett syndrome.
Nag N; Mellott TJ; Berger-Sweeney JE
Brain Res; 2008 Oct; 1237():101-9. PubMed ID: 18778693
[TBL] [Abstract][Full Text] [Related]
36. Ribosomal Dysfunction Is a Common Pathomechanism in Different Forms of Trichothiodystrophy.
Zhu G; Khalid F; Zhang D; Cao Z; Maity P; Kestler HA; Orioli D; Scharffetter-Kochanek K; Iben S
Cells; 2023 Jul; 12(14):. PubMed ID: 37508541
[TBL] [Abstract][Full Text] [Related]
37. Do all of the neurologic diseases in patients with DNA repair gene mutations result from the accumulation of DNA damage?
Brooks PJ; Cheng TF; Cooper L
DNA Repair (Amst); 2008 Jun; 7(6):834-48. PubMed ID: 18339586
[TBL] [Abstract][Full Text] [Related]
38. Atrophy and degeneration in sciatic nerve of presymptomatic mice carrying the Huntington's disease mutation.
Wade A; Jacobs P; Morton AJ
Brain Res; 2008 Jan; 1188():61-8. PubMed ID: 18062944
[TBL] [Abstract][Full Text] [Related]
39. The functional relationship between co-repressor N-CoR and SMRT in mediating transcriptional repression by thyroid hormone receptor alpha.
Choi KC; Oh SY; Kang HB; Lee YH; Haam S; Kim HI; Kim K; Ahn YH; Kim KS; Yoon HG
Biochem J; 2008 Apr; 411(1):19-26. PubMed ID: 18052923
[TBL] [Abstract][Full Text] [Related]
40. IRS-2 branch of IGF-1 receptor signaling is essential for appropriate timing of myelination.
Freude S; Leeser U; Müller M; Hettich MM; Udelhoven M; Schilbach K; Tobe K; Kadowaki T; Köhler C; Schröder H; Krone W; Brüning JC; Schubert M
J Neurochem; 2008 Nov; 107(4):907-17. PubMed ID: 18717815
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
