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Results: 1 to 20 of 25

1.

A second dose of a CFTR cDNA-liposome complex is as effective as the first dose in restoring cAMP-dependent chloride secretion to null CF mice trachea.

Goddard CA, Ratcliff R, Anderson JR, Glenn E, Brown S, Gill DR, Hyde SC, MacVinish LJ, Huang L, Higgins CF, Cuthbert AW, Evans MJ, Colledge WH.

Gene Ther. 1997 Nov;4(11):1231-6.

PMID:
9425447
[PubMed - indexed for MEDLINE]
Free Article
2.

Gene therapy for renal diseases.

Lien YH, Lai LW.

Kidney Int Suppl. 1997 Oct;61:S85-8. Review.

PMID:
9328975
[PubMed - indexed for MEDLINE]
3.

Characterization of cationic liposome-mediated gene transfer in vivo by intravenous administration.

Song YK, Liu F, Chu S, Liu D.

Hum Gene Ther. 1997 Sep 1;8(13):1585-94.

PMID:
9322091
[PubMed - indexed for MEDLINE]
4.

Kidney-targeted liposome-mediated gene transfer in mice.

Lai LW, Moeckel GW, Lien YH.

Gene Ther. 1997 May;4(5):426-31.

PMID:
9274719
[PubMed - indexed for MEDLINE]
Free Article
5.

Liposome-mediated gene transfer into the tubules.

Lien YH, Lai LW.

Exp Nephrol. 1997 Mar-Apr;5(2):132-6. Review. No abstract available.

PMID:
9108995
[PubMed - indexed for MEDLINE]
6.

A novel cationic lipid greatly enhances plasmid DNA delivery and expression in mouse lung.

Wheeler CJ, Felgner PL, Tsai YJ, Marshall J, Sukhu L, Doh SG, Hartikka J, Nietupski J, Manthorpe M, Nichols M, Plewe M, Liang X, Norman J, Smith A, Cheng SH.

Proc Natl Acad Sci U S A. 1996 Oct 15;93(21):11454-9.

PMID:
8876156
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK.

Simon DB, Karet FE, Rodriguez-Soriano J, Hamdan JH, DiPietro A, Trachtman H, Sanjad SA, Lifton RP.

Nat Genet. 1996 Oct;14(2):152-6.

PMID:
8841184
[PubMed - indexed for MEDLINE]
8.

Human alpha 1-antitrypsin gene transfer to in vivo mouse hepatocytes.

Aliño SF, Bobadilla M, Crespo J, Lejarreta M.

Hum Gene Ther. 1996 Mar 1;7(4):531-6.

PMID:
8800748
[PubMed - indexed for MEDLINE]
9.

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.

Simon DB, Nelson-Williams C, Bia MJ, Ellison D, Karet FE, Molina AM, Vaara I, Iwata F, Cushner HM, Koolen M, Gainza FJ, Gitleman HJ, Lifton RP.

Nat Genet. 1996 Jan;12(1):24-30.

PMID:
8528245
[PubMed - indexed for MEDLINE]
10.

Nonviral gene therapy: the promise of genes as pharmaceutical products.

Ledley FD.

Hum Gene Ther. 1995 Sep;6(9):1129-44. Review.

PMID:
8527471
[PubMed - indexed for MEDLINE]
11.

Direct gene transfer with DNA-liposome complexes in melanoma: expression, biologic activity, and lack of toxicity in humans.

Nabel GJ, Nabel EG, Yang ZY, Fox BA, Plautz GE, Gao X, Huang L, Shu S, Gordon D, Chang AE.

Proc Natl Acad Sci U S A. 1993 Dec 1;90(23):11307-11.

PMID:
8248244
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Systemic gene expression after intravenous DNA delivery into adult mice.

Zhu N, Liggitt D, Liu Y, Debs R.

Science. 1993 Jul 9;261(5118):209-11.

PMID:
7687073
[PubMed - indexed for MEDLINE]
13.

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

Caplen NJ, Alton EW, Middleton PG, Dorin JR, Stevenson BJ, Gao X, Durham SR, Jeffery PK, Hodson ME, Coutelle C, et al.

Nat Med. 1995 Jan;1(1):39-46. Erratum in: Nat Med 1995 Mar;1(3):272.

PMID:
7584951
[PubMed - indexed for MEDLINE]
14.

Systemic gene therapy: biodistribution and long-term expression of a transgene in mice.

Thierry AR, Lunardi-Iskandar Y, Bryant JL, Rabinovich P, Gallo RC, Mahan LC.

Proc Natl Acad Sci U S A. 1995 Oct 10;92(21):9742-6.

PMID:
7568209
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel gene.

van Lieburg AF, Verdijk MA, Knoers VV, van Essen AJ, Proesmans W, Mallmann R, Monnens LA, van Oost BA, van Os CH, Deen PM.

Am J Hum Genet. 1994 Oct;55(4):648-52.

PMID:
7524315
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Intracellular distribution of carbonic anhydrase in the rat kidney.

Lönnerholm G, Ridderstråle Y.

Kidney Int. 1980 Feb;17(2):162-74.

PMID:
6770166
[PubMed - indexed for MEDLINE]
17.

Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.

Sly WS, Hewett-Emmett D, Whyte MP, Yu YS, Tashian RE.

Proc Natl Acad Sci U S A. 1983 May;80(9):2752-6.

PMID:
6405388
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Cloning of mouse carbonic anhydrase mRNA and its induction in mouse erythroleukemic cells.

Curtis PJ.

J Biol Chem. 1983 Apr 10;258(7):4459-63.

PMID:
6187736
[PubMed - indexed for MEDLINE]
Free Article
19.

N-ethyl-N-nitrosourea-induced null mutation at the mouse Car-2 locus: an animal model for human carbonic anhydrase II deficiency syndrome.

Lewis SE, Erickson RP, Barnett LB, Venta PJ, Tashian RE.

Proc Natl Acad Sci U S A. 1988 Mar;85(6):1962-6.

PMID:
3126501
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Lipofection: a highly efficient, lipid-mediated DNA-transfection procedure.

Felgner PL, Gadek TR, Holm M, Roman R, Chan HW, Wenz M, Northrop JP, Ringold GM, Danielsen M.

Proc Natl Acad Sci U S A. 1987 Nov;84(21):7413-7.

PMID:
2823261
[PubMed - indexed for MEDLINE]
Free PMC Article

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