Literature DB >> 2660259

Progress toward human gene therapy.

T Friedmann1.   

Abstract

Current therapies for most human genetic diseases are inadequate. In response to the need for effective treatments, modern molecular genetics is providing tools for an unprecedented new approach to disease treatment through an attack directly on mutant genes. Recent results with several target organs and gene transfer techniques have led to broad medical and scientific acceptance of the feasibility of this "gene therapy" concept for disorders of the bone marrow, liver, and central nervous system; some kinds of cancer; and deficiencies of circulating enzymes, hormones, and coagulation factors. The most well-developed models involve alteration of mutant target genes by gene transfer with recombinant pathogenic viruses in order to express new genetic information and to correct disease phenotypes--the conversion of the swords of pathology into the plowshares of therapy.

Entities:  

Keywords:  Genetics and Reproduction; National Institutes of Health; Recombinant DNA Advisory Committee

Mesh:

Year:  1989        PMID: 2660259     DOI: 10.1126/science.2660259

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  71 in total

Review 1.  Multiple meningiomas of the central nervous system without the stigmata of neurofibromatosis. Clinical and therapeutic study.

Authors:  M Turgut; S Palaoğlu; O E Ozcan; O Gürçay; M Eryilmaz
Journal:  Neurosurg Rev       Date:  1997       Impact factor: 3.042

2.  In vivo retroviral gene transfer into human bronchial epithelia of xenografts.

Authors:  J F Engelhardt; J R Yankaskas; J M Wilson
Journal:  J Clin Invest       Date:  1992-12       Impact factor: 14.808

Review 3.  Future prospects for treatment of hemoglobinopathies.

Authors:  J A Stamatoyannopoulos
Journal:  West J Med       Date:  1992-12

Review 4.  Sequence-specific modification of genomic DNA by small DNA fragments.

Authors:  Dieter C Gruenert; Emanuela Bruscia; Giuseppe Novelli; Alessia Colosimo; Bruno Dallapiccola; Federica Sangiuolo; Kaarin K Goncz
Journal:  J Clin Invest       Date:  2003-09       Impact factor: 14.808

5.  Aerosol gene delivery in vivo.

Authors:  R Stribling; E Brunette; D Liggitt; K Gaensler; R Debs
Journal:  Proc Natl Acad Sci U S A       Date:  1992-12-01       Impact factor: 11.205

6.  Unusually high frequency of reconstitution of long terminal repeats in U3-minus retrovirus vectors by DNA recombination or gene conversion.

Authors:  P Olson; H M Temin; R Dornburg
Journal:  J Virol       Date:  1992-03       Impact factor: 5.103

Review 7.  Cellular transplantation and gene therapy.

Authors:  C Ricordi; S T Ildstad; T E Starzl
Journal:  Clin Transplant       Date:  1993-02       Impact factor: 2.863

8.  Hormonal modulation of a gene injected into rat heart in vivo.

Authors:  R N Kitsis; P M Buttrick; E M McNally; M L Kaplan; L A Leinwand
Journal:  Proc Natl Acad Sci U S A       Date:  1991-05-15       Impact factor: 11.205

9.  E- vectors: development of novel self-inactivating and self-activating retroviral vectors for safer gene therapy.

Authors:  J G Julias; D Hash; V K Pathak
Journal:  J Virol       Date:  1995-11       Impact factor: 5.103

10.  Polymer-Lipid Nanoparticles for Systemic Delivery of mRNA to the Lungs.

Authors:  James C Kaczmarek; Asha K Patel; Kevin J Kauffman; Owen S Fenton; Matthew J Webber; Michael W Heartlein; Frank DeRosa; Daniel G Anderson
Journal:  Angew Chem Int Ed Engl       Date:  2016-09-30       Impact factor: 15.336

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