156 related articles for article (PubMed ID: 11737070)
41. Early defects in human T-cell development severely affect distribution and maturation of thymic stromal cells: possible implications for the pathophysiology of Omenn syndrome.
Poliani PL; Facchetti F; Ravanini M; Gennery AR; Villa A; Roifman CM; Notarangelo LD
Blood; 2009 Jul; 114(1):105-8. PubMed ID: 19414857
[TBL] [Abstract][Full Text] [Related]
42. The XPB subunit of repair/transcription factor TFIIH directly interacts with SUG1, a subunit of the 26S proteasome and putative transcription factor.
Weeda G; Rossignol M; Fraser RA; Winkler GS; Vermeulen W; van 't Veer LJ; Ma L; Hoeijmakers JH; Egly JM
Nucleic Acids Res; 1997 Jun; 25(12):2274-83. PubMed ID: 9173976
[TBL] [Abstract][Full Text] [Related]
43. Mechanism of open complex and dual incision formation by human nucleotide excision repair factors.
Evans E; Moggs JG; Hwang JR; Egly JM; Wood RD
EMBO J; 1997 Nov; 16(21):6559-73. PubMed ID: 9351836
[TBL] [Abstract][Full Text] [Related]
44. Different dynamics in nuclear entry of subunits of the repair/transcription factor TFIIH.
Santagati F; Botta E; Stefanini M; Pedrini AM
Nucleic Acids Res; 2001 Apr; 29(7):1574-81. PubMed ID: 11266560
[TBL] [Abstract][Full Text] [Related]
45. TTDA: big impact of a small protein.
Theil AF; Hoeijmakers JH; Vermeulen W
Exp Cell Res; 2014 Nov; 329(1):61-8. PubMed ID: 25016283
[TBL] [Abstract][Full Text] [Related]
46. Genotype-phenotype relationships in trichothiodystrophy patients with novel splicing mutations in the XPD gene.
Botta E; Nardo T; Orioli D; Guglielmino R; Ricotti R; Bondanza S; Benedicenti F; Zambruno G; Stefanini M
Hum Mutat; 2009 Mar; 30(3):438-45. PubMed ID: 19085937
[TBL] [Abstract][Full Text] [Related]
47. Mutations in the XPD gene leading to xeroderma pigmentosum symptoms.
Kobayashi T; Kuraoka I; Saijo M; Nakatsu Y; Tanaka A; Someda Y; Fukuro S; Tanaka K
Hum Mutat; 1997; 9(4):322-31. PubMed ID: 9101292
[TBL] [Abstract][Full Text] [Related]
48. Increased UV light sensitivity in transgenic Drosophila expressing the antisense XPD homolog.
Sandoval MT; Zurita M
Antisense Nucleic Acid Drug Dev; 2001 Apr; 11(2):125-8. PubMed ID: 11334141
[TBL] [Abstract][Full Text] [Related]
49. Xpd, a structural bridge and a functional link.
Chen J; Suter B
Cell Cycle; 2003; 2(6):503-6. PubMed ID: 14504460
[TBL] [Abstract][Full Text] [Related]
50. Human nucleotide excision repair syndromes: molecular clues to unexpected intricacies.
Hoeijmakers JH
Eur J Cancer; 1994; 30A(13):1912-21. PubMed ID: 7734202
[No Abstract] [Full Text] [Related]
51. The relative expression of mutated XPB genes results in xeroderma pigmentosum/Cockayne's syndrome or trichothiodystrophy cellular phenotypes.
Riou L; Zeng L; Chevallier-Lagente O; Stary A; Nikaido O; Taïeb A; Weeda G; Mezzina M; Sarasin A
Hum Mol Genet; 1999 Jun; 8(6):1125-33. PubMed ID: 10332046
[TBL] [Abstract][Full Text] [Related]
52. Transcription factor b (TFIIH) is required during nucleotide-excision repair in yeast.
Wang Z; Svejstrup JQ; Feaver WJ; Wu X; Kornberg RD; Friedberg EC
Nature; 1994 Mar; 368(6466):74-6. PubMed ID: 8107888
[TBL] [Abstract][Full Text] [Related]
53. Structural and mutational analysis of the xeroderma pigmentosum group D (XPD) gene.
Frederick GD; Amirkhan RH; Schultz RA; Friedberg EC
Hum Mol Genet; 1994 Oct; 3(10):1783-8. PubMed ID: 7849702
[TBL] [Abstract][Full Text] [Related]
54. p53 modulation of TFIIH-associated nucleotide excision repair activity.
Wang XW; Yeh H; Schaeffer L; Roy R; Moncollin V; Egly JM; Wang Z; Freidberg EC; Evans MK; Taffe BG
Nat Genet; 1995 Jun; 10(2):188-95. PubMed ID: 7663514
[TBL] [Abstract][Full Text] [Related]
55. The Drosophila melanogaster homologue of the Xeroderma pigmentosum D gene product is located in euchromatic regions and has a dynamic response to UV light-induced lesions in polytene chromosomes.
Reynaud E; Lomelí H; Vázquez M; Zurita M
Mol Biol Cell; 1999 Apr; 10(4):1191-203. PubMed ID: 10198066
[TBL] [Abstract][Full Text] [Related]
56. PIBIDS syndrome in two Brazilian siblings.
Abagge KT; Haupenthal F; Felber GY; Raskin S
BMJ Case Rep; 2018 Dec; 11(1):. PubMed ID: 30580289
[TBL] [Abstract][Full Text] [Related]
57. Rough skin, brittle hair, and photosensitivity: a mild phenotypic variant of trichothiodystrophy.
Savarirayan R; Gardner RJ; Sinclair RD; McDowell M; Cleaver JE
J Med Genet; 2000 Apr; 37(4):312-4. PubMed ID: 10819642
[No Abstract] [Full Text] [Related]
58. A new twist to the tale? Apoptosis.
Warbrick E
Curr Biol; 1996 Sep; 6(9):1057-9. PubMed ID: 8805363
[TBL] [Abstract][Full Text] [Related]
59. Consequences of a mutation in the UNC119 gene for T cell function in idiopathic CD4 lymphopenia.
Gorska MM; Alam R
Curr Allergy Asthma Rep; 2012 Oct; 12(5):396-401. PubMed ID: 22729960
[TBL] [Abstract][Full Text] [Related]
60. PIBI(D)S: clinical and molecular characterization of a new case.
Fortina AB; Alaibac M; Piaserico S; Peserico A
J Eur Acad Dermatol Venereol; 2001 Jan; 15(1):65-9. PubMed ID: 11451329
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]