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Literature DB >> 6519667

Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines.

Abstract

We have investigated the potential for using cyclosporin A to increase the efficiency with which Epstein-Barr virus-transformed human lymphoblast lines can be prepared. Use of this immunosuppressive drug has permitted the development of a procedure with success rates exceeding 95% despite the processing of very large numbers of samples.

Entities: Chemical Species

Mesh：

Substances：
Cyclosporins

Year: 1984 PMID： 6519667 DOI： 10.1007/bf02619631

Source DB: PubMed Journal: In Vitro ISSN： 0073-5655

5 in total

1. A polymorphic DNA marker genetically linked to Huntington's disease.

Authors: J F Gusella; N S Wexler; P M Conneally; S L Naylor; M A Anderson; R E Tanzi; P C Watkins; K Ottina; M R Wallace; A Y Sakaguchi
Journal: Nature Date: 1983 Nov 17-23 Impact factor: 49.962

2. Differential effects of cyclosporin-A on lymphocyte subpopulations.

Authors: S B Leapman; R S Filo; E J Smith; P G Smith
Journal: Transplant Proc Date: 1981-03 Impact factor: 1.066

3. Long-term T-cell-mediated immunity to Epstein-Barr virus in man. III. Activation of cytotoxic T cells in virus-infected leukocyte cultures.

Authors: D J Moss; A B Rickinson; J H Pope
Journal: Int J Cancer Date: 1979-05-15 Impact factor: 7.396

4. Release of infectious Epstein-Barr virus by transformed marmoset leukocytes.

Authors: G Miller; M Lipman
Journal: Proc Natl Acad Sci U S A Date: 1973-01 Impact factor: 11.205

5. Cyclosporin A promotes spontaneous outgrowth in vitro of Epstein-Barr virus-induced B-cell lines.

Authors: A G Bird; S M McLachlan; S Britton
Journal: Nature Date: 1981-01-22 Impact factor: 49.962

5 in total

135 in total

1. A genomic screen of autism: evidence for a multilocus etiology.

Authors: N Risch; D Spiker; L Lotspeich; N Nouri; D Hinds; J Hallmayer; L Kalaydjieva; P McCague; S Dimiceli; T Pitts; L Nguyen; J Yang; C Harper; D Thorpe; S Vermeer; H Young; J Hebert; A Lin; J Ferguson; C Chiotti; S Wiese-Slater; T Rogers; B Salmon; P Nicholas; P B Petersen; C Pingree; W McMahon; D L Wong; L L Cavalli-Sforza; H C Kraemer; R M Myers
Journal: Am J Hum Genet Date: 1999-08 Impact factor: 11.025

2. The gene for May-Hegglin anomaly localizes to a <1-Mb region on chromosome 22q12.3-13.1.

Authors: J A Martignetti; K E Heath; J Harris; N Bizzaro; A Savoia; C L Balduini; R J Desnick
Journal: Am J Hum Genet Date: 2000-03-17 Impact factor: 11.025

3. Linkage disequilibrium at the ADH2 and ADH3 loci and risk of alcoholism.

Authors: M Osier; A J Pakstis; J R Kidd; J F Lee; S J Yin; H C Ko; H J Edenberg; R B Lu; K K Kidd
Journal: Am J Hum Genet Date: 1999-04 Impact factor: 11.025

4. A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q.

Authors: Collette K Hand; Jawad Khoris; François Salachas; François Gros-Louis; Ana Amélia Simões Lopes; Veronique Mayeux-Portas; Carl G Brewer; Robert H Brown; Vincent Meininger; William Camu; Guy A Rouleau
Journal: Am J Hum Genet Date: 2001-11-09 Impact factor: 11.025

9. Biosynthesis, processing, and extracellular release of alpha-L-fucosidase in lymphoid cell lines of different genetic origins.

Authors: R A DiCioccio; K S Brown
Journal: Biochem Genet Date: 1988-06 Impact factor: 1.890

10. Acute intermittent porphyria: identification and expression of exonic mutations in the hydroxymethylbilane synthase gene. An initiation codon missense mutation in the housekeeping transcript causes "variant acute intermittent porphyria" with normal expression of the erythroid-specific enzyme.

Authors: C H Chen; K H Astrin; G Lee; K E Anderson; R J Desnick
Journal: J Clin Invest Date: 1994-11 Impact factor: 14.808