Literature DB >> 18265367

Isolation and immortalization of lymphocytes.

Paul D Ling1, Helen M Huls.   

Abstract

Recent advances in Genomics and Proteomics have necessitated a constant supply of DNA derived from specific genotypes. Lymphoblastoid cell lines (LCLs) are of great practical value as an unlimited source of stable genomic DNA and viable cells, which can be used to perform a variety of biochemical and molecular studies. LCLs are typically generated by infection of primary lymphocytes with Epstein-Barr virus (EBV). In this unit, we describe simple procedures for production of EBV, isolation of lymphocytes, EBV infection of lymphocytes, and isolation of the resulting LCLs.

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Year:  2005        PMID: 18265367     DOI: 10.1002/0471142727.mb2802s70

Source DB:  PubMed          Journal:  Curr Protoc Mol Biol        ISSN: 1934-3647


  8 in total

1.  Dysregulation of cotranscriptional alternative splicing underlies CHARGE syndrome.

Authors:  Catherine Bélanger; Félix-Antoine Bérubé-Simard; Elizabeth Leduc; Guillaume Bernas; Philippe M Campeau; Seema R Lalani; Donna M Martin; Stephanie Bielas; Amanda Moccia; Anshika Srivastava; David W Silversides; Nicolas Pilon
Journal:  Proc Natl Acad Sci U S A       Date:  2018-01-08       Impact factor: 11.205

Review 2.  Pharmacogenomic discovery using cell-based models.

Authors:  Marleen Welsh; Lara Mangravite; Marisa Wong Medina; Kelan Tantisira; Wei Zhang; R Stephanie Huang; Howard McLeod; M Eileen Dolan
Journal:  Pharmacol Rev       Date:  2009-12       Impact factor: 25.468

3.  Continued lessons from the INS gene: an intronic mutation causing diabetes through a novel mechanism.

Authors:  David Carmody; Soo-Young Park; Honggang Ye; Marie E Perrone; G Alkorta-Aranburu; Heather M Highland; Craig L Hanis; Louis H Philipson; Graeme I Bell; Siri Atma W Greeley
Journal:  J Med Genet       Date:  2015-06-22       Impact factor: 6.318

4.  Mutations in the Chromatin Regulator Gene BRPF1 Cause Syndromic Intellectual Disability and Deficient Histone Acetylation.

Authors:  Kezhi Yan; Justine Rousseau; Rebecca Okashah Littlejohn; Courtney Kiss; Anna Lehman; Jill A Rosenfeld; Constance T R Stumpel; Alexander P A Stegmann; Laurie Robak; Fernando Scaglia; Thi Tuyet Mai Nguyen; He Fu; Norbert F Ajeawung; Maria Vittoria Camurri; Lin Li; Alice Gardham; Bianca Panis; Mohammed Almannai; Maria J Guillen Sacoto; Berivan Baskin; Claudia Ruivenkamp; Fan Xia; Weimin Bi; Megan T Cho; Thomas P Potjer; Gijs W E Santen; Michael J Parker; Natalie Canham; Margaret McKinnon; Lorraine Potocki; Jennifer J MacKenzie; Elizabeth R Roeder; Philippe M Campeau; Xiang-Jiao Yang
Journal:  Am J Hum Genet       Date:  2016-12-08       Impact factor: 11.025

5.  In depth comparison of an individual's DNA and its lymphoblastoid cell line using whole genome sequencing.

Authors:  Dorothee Nickles; Lohith Madireddy; Shan Yang; Pouya Khankhanian; Steve Lincoln; Stephen L Hauser; Jorge R Oksenberg; Sergio E Baranzini
Journal:  BMC Genomics       Date:  2012-09-14       Impact factor: 3.969

6.  Quantification of small non-coding RNAs allows an accurate comparison of miRNA expression profiles.

Authors:  Andrea Masotti; Viviana Caputo; Letizia Da Sacco; Antonio Pizzuti; Bruno Dallapiccola; Gian Franco Bottazzo
Journal:  J Biomed Biotechnol       Date:  2009-09-01

7.  Genome sequencing uncovers phenocopies in primary progressive multiple sclerosis.

Authors:  Xiaoming Jia; Lohith Madireddy; Stacy Caillier; Adam Santaniello; Federica Esposito; Giancarlo Comi; Olaf Stuve; Yuan Zhou; Bruce Taylor; Trevor Kilpatrick; Filippo Martinelli-Boneschi; Bruce A C Cree; Jorge R Oksenberg; Stephen L Hauser; Sergio E Baranzini
Journal:  Ann Neurol       Date:  2018-07-03       Impact factor: 10.422

8.  Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation.

Authors:  Amy E O'Connell; Maxim V Gerashchenko; Marie-Francoise O'Donohue; Samantha M Rosen; Eric Huntzinger; Diane Gleeson; Antonella Galli; Edward Ryder; Siqi Cao; Quinn Murphy; Shideh Kazerounian; Sarah U Morton; Klaus Schmitz-Abe; Vadim N Gladyshev; Pierre-Emmanuel Gleizes; Bertrand Séraphin; Pankaj B Agrawal
Journal:  PLoS Genet       Date:  2019-02-01       Impact factor: 5.917

  8 in total

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