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23 in total

1. A placebo-controlled study of liposome-mediated gene transfer to the nasal epithelium of patients with cystic fibrosis.

Authors: D R Gill; K W Southern; K A Mofford; T Seddon; L Huang; F Sorgi; A Thomson; L J MacVinish; R Ratcliff; D Bilton; D J Lane; J M Littlewood; A K Webb; P G Middleton; W H Colledge; A W Cuthbert; M J Evans; C F Higgins; S C Hyde
Journal: Gene Ther Date: 1997-03 Impact factor: 5.250

Review 2. Molecular structure and assembly of the tight junction.

Authors: B M Denker; S K Nigam
Journal: Am J Physiol Date: 1998-01

3. A phase I study of an adeno-associated virus-CFTR gene vector in adult CF patients with mild lung disease.

Authors: T Flotte; B Carter; C Conrad; W Guggino; T Reynolds; B Rosenstein; G Taylor; S Walden; R Wetzel
Journal: Hum Gene Ther Date: 1996-06-10 Impact factor: 5.695

Review 4. Tight junctions and the molecular basis for regulation of paracellular permeability.

Authors: J M Anderson; C M Van Itallie
Journal: Am J Physiol Date: 1995-10

Review 5. Adenoviruses as gene-delivery vehicles.

Authors: J M Wilson
Journal: N Engl J Med Date: 1996-05-02 Impact factor: 91.245

6. Aerosol administration of a recombinant adenovirus expressing CFTR to cystic fibrosis patients: a phase I clinical trial.

Authors: G Bellon; L Michel-Calemard; D Thouvenot; V Jagneaux; F Poitevin; C Malcus; N Accart; M P Layani; M Aymard; H Bernon; J Bienvenu; M Courtney; G Döring; B Gilly; R Gilly; D Lamy; H Levrey; Y Morel; C Paulin; F Perraud; L Rodillon; C Sené; S So; F Touraine-Moulin; A Pavirani
Journal: Hum Gene Ther Date: 1997-01-01 Impact factor: 5.695

Bad for cats, good for humans? Modified feline immunodeficiency virus for gene therapy.

1. A placebo-controlled study of liposome-mediated gene transfer to the nasal epithelium of patients with cystic fibrosis.

Review 2. Molecular structure and assembly of the tight junction.

3. A phase I study of an adeno-associated virus-CFTR gene vector in adult CF patients with mild lung disease.

Review 4. Tight junctions and the molecular basis for regulation of paracellular permeability.

Review 5. Adenoviruses as gene-delivery vehicles.

6. Aerosol administration of a recombinant adenovirus expressing CFTR to cystic fibrosis patients: a phase I clinical trial.

7. Lentiviral vectors for gene therapy of cystic fibrosis.

8. Efficient transduction of nondividing human cells by feline immunodeficiency virus lentiviral vectors.

9. Transient permeabilization of airway epithelium by mucosal water.

10. Liposome-mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis.