322 related articles for article (PubMed ID: 11779494)
1. DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiency.
O'Driscoll M; Cerosaletti KM; Girard PM; Dai Y; Stumm M; Kysela B; Hirsch B; Gennery A; Palmer SE; Seidel J; Gatti RA; Varon R; Oettinger MA; Neitzel H; Jeggo PA; Concannon P
Mol Cell; 2001 Dec; 8(6):1175-85. PubMed ID: 11779494
[TBL] [Abstract][Full Text] [Related]
2. XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency.
Guo C; Nakazawa Y; Woodbine L; Björkman A; Shimada M; Fawcett H; Jia N; Ohyama K; Li TS; Nagayama Y; Mitsutake N; Pan-Hammarström Q; Gennery AR; Lehmann AR; Jeggo PA; Ogi T
J Allergy Clin Immunol; 2015 Oct; 136(4):1007-17. PubMed ID: 26255102
[TBL] [Abstract][Full Text] [Related]
3. Analysis of DNA ligase IV mutations found in LIG4 syndrome patients: the impact of two linked polymorphisms.
Girard PM; Kysela B; Härer CJ; Doherty AJ; Jeggo PA
Hum Mol Genet; 2004 Oct; 13(20):2369-76. PubMed ID: 15333585
[TBL] [Abstract][Full Text] [Related]
4. Ligase IV syndrome.
Chistiakov DA
Adv Exp Med Biol; 2010; 685():175-85. PubMed ID: 20687505
[TBL] [Abstract][Full Text] [Related]
5. DNA ligase IV is essential for V(D)J recombination and DNA double-strand break repair in human precursor lymphocytes.
Grawunder U; Zimmer D; Fugmann S; Schwarz K; Lieber MR
Mol Cell; 1998 Oct; 2(4):477-84. PubMed ID: 9809069
[TBL] [Abstract][Full Text] [Related]
6. A patient with mutations in DNA Ligase IV: clinical features and overlap with Nijmegen breakage syndrome.
Ben-Omran TI; Cerosaletti K; Concannon P; Weitzman S; Nezarati MM
Am J Med Genet A; 2005 Sep; 137A(3):283-7. PubMed ID: 16088910
[TBL] [Abstract][Full Text] [Related]
7. Nonhomologous end joining and V(D)J recombination require an additional factor.
Dai Y; Kysela B; Hanakahi LA; Manolis K; Riballo E; Stumm M; Harville TO; West SC; Oettinger MA; Jeggo PA
Proc Natl Acad Sci U S A; 2003 Mar; 100(5):2462-7. PubMed ID: 12604777
[TBL] [Abstract][Full Text] [Related]
8. Different types of V(D)J recombination and end-joining defects in DNA double-strand break repair mutant mammalian cells.
Verkaik NS; Esveldt-van Lange RE; van Heemst D; Brüggenwirth HT; Hoeijmakers JH; Zdzienicka MZ; van Gent DC
Eur J Immunol; 2002 Mar; 32(3):701-9. PubMed ID: 11870614
[TBL] [Abstract][Full Text] [Related]
9. Genetic heterogeneity for a Nijmegen breakage-like syndrome.
Maraschio P; Spadoni E; Tanzarella C; Antoccia A; Di Masi A; Maghnie M; Varon R; Demuth I; Tiepolo L; Danesino C
Clin Genet; 2003 Apr; 63(4):283-90. PubMed ID: 12702161
[TBL] [Abstract][Full Text] [Related]
10. Normal V(D)J coding junction formation in DNA ligase I deficiency syndromes.
Petrini JH; Donovan JW; Dimare C; Weaver DT
J Immunol; 1994 Jan; 152(1):176-83. PubMed ID: 8254190
[TBL] [Abstract][Full Text] [Related]
11. V(D)J recombination in ataxia telangiectasia, Bloom's syndrome, and a DNA ligase I-associated immunodeficiency disorder.
Hsieh CL; Arlett CF; Lieber MR
J Biol Chem; 1993 Sep; 268(27):20105-9. PubMed ID: 8397200
[TBL] [Abstract][Full Text] [Related]
12. Ku80- and DNA ligase IV-deficient plants are sensitive to ionizing radiation and defective in T-DNA integration.
Friesner J; Britt AB
Plant J; 2003 May; 34(4):427-40. PubMed ID: 12753583
[TBL] [Abstract][Full Text] [Related]
13. Impact of DNA ligase IV on the fidelity of end joining in human cells.
Smith J; Riballo E; Kysela B; Baldeyron C; Manolis K; Masson C; Lieber MR; Papadopoulo D; Jeggo P
Nucleic Acids Res; 2003 Apr; 31(8):2157-67. PubMed ID: 12682366
[TBL] [Abstract][Full Text] [Related]
14. Normal V(D)J recombination in cells from patients with Nijmegen breakage syndrome.
Harfst E; Cooper S; Neubauer S; Distel L; Grawunder U
Mol Immunol; 2000 Oct; 37(15):915-29. PubMed ID: 11282395
[TBL] [Abstract][Full Text] [Related]
15. Identification of a defect in DNA ligase IV in a radiosensitive leukaemia patient.
Riballo E; Critchlow SE; Teo SH; Doherty AJ; Priestley A; Broughton B; Kysela B; Beamish H; Plowman N; Arlett CF; Lehmann AR; Jackson SP; Jeggo PA
Curr Biol; 1999 Jul; 9(13):699-702. PubMed ID: 10395545
[TBL] [Abstract][Full Text] [Related]
16. Ligase IV syndrome.
Chistiakov DA; Voronova NV; Chistiakov AP
Eur J Med Genet; 2009; 52(6):373-8. PubMed ID: 19467349
[TBL] [Abstract][Full Text] [Related]
17. Homozygous DNA ligase IV R278H mutation in mice leads to leaky SCID and represents a model for human LIG4 syndrome.
Rucci F; Notarangelo LD; Fazeli A; Patrizi L; Hickernell T; Paganini T; Coakley KM; Detre C; Keszei M; Walter JE; Feldman L; Cheng HL; Poliani PL; Wang JH; Balter BB; Recher M; Andersson EM; Zha S; Giliani S; Terhorst C; Alt FW; Yan CT
Proc Natl Acad Sci U S A; 2010 Feb; 107(7):3024-9. PubMed ID: 20133615
[TBL] [Abstract][Full Text] [Related]
18. V(D)J rearrangement in Nijmegen breakage syndrome.
Yeo TC; Xia D; Hassouneh S; Yang XO; Sabath DE; Sperling K; Gatti RA; Concannon P; Willerford DM
Mol Immunol; 2000 Dec; 37(18):1131-9. PubMed ID: 11451418
[TBL] [Abstract][Full Text] [Related]
19. Mechanism of nonhomologous end-joining in mycobacteria: a low-fidelity repair system driven by Ku, ligase D and ligase C.
Gong C; Bongiorno P; Martins A; Stephanou NC; Zhu H; Shuman S; Glickman MS
Nat Struct Mol Biol; 2005 Apr; 12(4):304-12. PubMed ID: 15778718
[TBL] [Abstract][Full Text] [Related]
20. Severe combined immunodeficiency and microcephaly in siblings with hypomorphic mutations in DNA ligase IV.
Buck D; Moshous D; de Chasseval R; Ma Y; le Deist F; Cavazzana-Calvo M; Fischer A; Casanova JL; Lieber MR; de Villartay JP
Eur J Immunol; 2006 Jan; 36(1):224-35. PubMed ID: 16358361
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]