These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
159 related articles for article (PubMed ID: 7717401)
1. Characterization of nine novel mutations in the CD40 ligand gene in patients with X-linked hyper IgM syndrome of various ancestry. Macchi P; Villa A; Strina D; Sacco MG; Morali F; Brugnoni D; Giliani S; Mantuano E; Fasth A; Andersson B Am J Hum Genet; 1995 Apr; 56(4):898-906. PubMed ID: 7717401 [TBL] [Abstract][Full Text] [Related]
2. Mutations of the CD40 ligand gene in 13 Japanese patients with X-linked hyper-IgM syndrome. Nonoyama S; Shimadzu M; Toru H; Seyama K; Nunoi H; Neubauer M; Yata J; Och HD Hum Genet; 1997 May; 99(5):624-7. PubMed ID: 9150729 [TBL] [Abstract][Full Text] [Related]
3. Mutations of the CD40 ligand gene and its effect on CD40 ligand expression in patients with X-linked hyper IgM syndrome. Seyama K; Nonoyama S; Gangsaas I; Hollenbaugh D; Pabst HF; Aruffo A; Ochs HD Blood; 1998 Oct; 92(7):2421-34. PubMed ID: 9746782 [TBL] [Abstract][Full Text] [Related]
4. CD40 ligand mutations in x-linked immunodeficiency with hyper-IgM. DiSanto JP; Bonnefoy JY; Gauchat JF; Fischer A; de Saint Basile G Nature; 1993 Feb; 361(6412):541-3. PubMed ID: 8094231 [TBL] [Abstract][Full Text] [Related]
5. Somatic mutations in human Ig variable genes correlate with a partially functional CD40-ligand in the X-linked hyper-IgM syndrome. Razanajaona D; van Kooten C; Lebecque S; Bridon JM; Ho S; Smith S; Callard R; Banchereau J; Brière F J Immunol; 1996 Aug; 157(4):1492-8. PubMed ID: 8759730 [TBL] [Abstract][Full Text] [Related]
6. Defective expression of CD40 ligand on T cells causes "X-linked immunodeficiency with hyper-IgM (HIGM1)". Kroczek RA; Graf D; Brugnoni D; Giliani S; Korthüer U; Ugazio A; Senger G; Mages HW; Villa A; Notarangelo LD Immunol Rev; 1994 Apr; 138():39-59. PubMed ID: 7915248 [TBL] [Abstract][Full Text] [Related]
7. Deletions in the ligand for CD40 in X-linked immunoglobulin deficiency with normal or elevated IgM (HIGMX-1). Ramesh N; Fuleihan R; Ramesh V; Lederman S; Yellin MJ; Sharma S; Chess L; Rosen FS; Geha RS Int Immunol; 1993 Jul; 5(7):769-73. PubMed ID: 8103673 [TBL] [Abstract][Full Text] [Related]
8. CD40 ligand mutants responsible for X-linked hyper-IgM syndrome associate with wild type CD40 ligand. Seyama K; Osborne WR; Ochs HD J Biol Chem; 1999 Apr; 274(16):11310-20. PubMed ID: 10196221 [TBL] [Abstract][Full Text] [Related]
9. CD40lbase: a database of CD40L gene mutations causing X-linked hyper-IgM syndrome. Notarangelo LD; Peitsch MC; Abrahamsen TG; Bachelot C; Bordigoni P; Cant AJ; Chapel H; Clementi M; Deacock S; de Saint Basile G; Duse M; Espanol T; Etzioni A; Fasth A; Fischer A; Giliani S; Gomez L; Hammarstorm L; Jones A; Kanariou M; Kinnon C; Klemola T; Kroczek RA; Levy J; Matamoros N; Monafo V; Paolucci P; Reznick I; Sanal O; Smith CI; Thompson RA; Tovo P; Villa A; Vihinen M; Vossen J; Zegers BJ Immunol Today; 1996 Nov; 17(11):511-6. PubMed ID: 8961627 [TBL] [Abstract][Full Text] [Related]
10. Organization of the human CD40L gene: implications for molecular defects in X chromosome-linked hyper-IgM syndrome and prenatal diagnosis. Villa A; Notarangelo LD; Di Santo JP; Macchi PP; Strina D; Frattini A; Lucchini F; Patrosso CM; Giliani S; Mantuano E Proc Natl Acad Sci U S A; 1994 Mar; 91(6):2110-4. PubMed ID: 7907793 [TBL] [Abstract][Full Text] [Related]
11. A single strand conformation polymorphism study of CD40 ligand. Efficient mutation analysis and carrier detection for X-linked hyper IgM syndrome. Lin Q; Rohrer J; Allen RC; Larché M; Greene JM; Shigeoka AO; Gatti RA; Derauf DC; Belmont JW; Conley ME J Clin Invest; 1996 Jan; 97(1):196-201. PubMed ID: 8550833 [TBL] [Abstract][Full Text] [Related]
12. Structural organization of the gene for CD40 ligand: molecular analysis for diagnosis of X-linked hyper-IgM syndrome. Shimadzu M; Nunoi H; Terasaki H; Ninomiya R; Iwata M; Kanegasaka S; Matsuda I Biochim Biophys Acta; 1995 Jan; 1260(1):67-72. PubMed ID: 7999797 [TBL] [Abstract][Full Text] [Related]
14. Genomic structure and PCR-SSCP analysis of the human CD40 ligand gene: its application to prenatal screening for X-linked hyper-IgM syndrome. Seyama K; Kira S; Ishidoh K; Souma S; Miyakawa T; Kominami E Hum Genet; 1996 Feb; 97(2):180-5. PubMed ID: 8566950 [TBL] [Abstract][Full Text] [Related]
16. Enteroviral meningoencephalitis as a complication of X-linked hyper IgM syndrome. Cunningham CK; Bonville CA; Ochs HD; Seyama K; John PA; Rotbart HA; Weiner LB J Pediatr; 1999 May; 134(5):584-8. PubMed ID: 10228294 [TBL] [Abstract][Full Text] [Related]
17. CD40 ligand expression deficiency in a female carrier of the X-linked hyper-IgM syndrome as a result of X chromosome lyonization. de Saint Basile G; Tabone MD; Durandy A; Phan F; Fischer A; Le Deist F Eur J Immunol; 1999 Jan; 29(1):367-73. PubMed ID: 9933119 [TBL] [Abstract][Full Text] [Related]
18. The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome. Aruffo A; Farrington M; Hollenbaugh D; Li X; Milatovich A; Nonoyama S; Bajorath J; Grosmaire LS; Stenkamp R; Neubauer M Cell; 1993 Jan; 72(2):291-300. PubMed ID: 7678782 [TBL] [Abstract][Full Text] [Related]
19. A novel splice-site mutation in the CD40L gene in a patient with X-linked hyper-IgM syndrome. Dezsö D; Orth U; Heilbronner H; Gal A Hum Mutat; 1996; 7(2):181-2. PubMed ID: 8829642 [No Abstract] [Full Text] [Related]
20. Molecular pathology of the X-linked hyper-immunoglobulin M syndrome: detection of wild-type transcripts in a patient with a complex splicing defect of the CD40 ligand. Ameratunga R; McKee J; French J; Prestidge R; Fanslow W; Marbrook J Clin Diagn Lab Immunol; 1996 Nov; 3(6):722-6. PubMed ID: 8914765 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]