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Results: 1 to 20 of 79

Similar articles for PubMed (Select 22606534)

1.

Acute Muscle Trauma due to Overexercise in an Otherwise Healthy Patient with Cystic Fibrosis.

Neubauer H, Wirth C, Ruf K, Hebestreit H, Beer M.

Case Rep Pediatr. 2012;2012:527989. doi: 10.1155/2012/527989. Epub 2012 Jan 23.

2.

Cystic fibrosis transmembrane conductance regulator in human muscle: Dysfunction causes abnormal metabolic recovery in exercise.

Lamhonwah AM, Bear CE, Huan LJ, Kim Chiaw P, Ackerley CA, Tein I.

Ann Neurol. 2010 Jun;67(6):802-8. doi: 10.1002/ana.21982.

PMID:
20517942
3.
4.

Sequential targeting of CFTR by BAC vectors generates a novel pig model of cystic fibrosis.

Klymiuk N, Mundhenk L, Kraehe K, Wuensch A, Plog S, Emrich D, Langenmayer MC, Stehr M, Holzinger A, Kröner C, Richter A, Kessler B, Kurome M, Eddicks M, Nagashima H, Heinritzi K, Gruber AD, Wolf E.

J Mol Med (Berl). 2012 May;90(5):597-608. doi: 10.1007/s00109-011-0839-y. Epub 2011 Dec 15.

PMID:
22170306
5.

Down-regulation of the anti-inflammatory protein annexin A1 in cystic fibrosis knock-out mice and patients.

Bensalem N, Ventura AP, Vallée B, Lipecka J, Tondelier D, Davezac N, Dos Santos A, Perretti M, Fajac A, Sermet-Gaudelus I, Renouil M, Lesure JF, Halgand F, Laprévote O, Edelman A.

Mol Cell Proteomics. 2005 Oct;4(10):1591-601. Epub 2005 Jul 12.

6.

Mouse models of chronic lung infection with Pseudomonas aeruginosa: models for the study of cystic fibrosis.

Stotland PK, Radzioch D, Stevenson MM.

Pediatr Pulmonol. 2000 Nov;30(5):413-24. Review.

PMID:
11064433
7.

Cholangiocyte biology and cystic fibrosis liver disease.

Feranchak AP, Sokol RJ.

Semin Liver Dis. 2001 Nov;21(4):471-88. Review.

PMID:
11745036
8.
9.

Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.

Alibakhshi R, Kianishirazi R, Cassiman JJ, Zamani M, Cuppens H.

J Cyst Fibros. 2008 Mar;7(2):102-9. Epub 2007 Jul 27.

10.

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

Gill DR, Southern KW, Mofford KA, Seddon T, Huang L, Sorgi F, Thomson A, MacVinish LJ, Ratcliff R, Bilton D, Lane DJ, Littlewood JM, Webb AK, Middleton PG, Colledge WH, Cuthbert AW, Evans MJ, Higgins CF, Hyde SC.

Gene Ther. 1997 Mar;4(3):199-209.

11.

Pancreatitis among patients with cystic fibrosis: correlation with pancreatic status and genotype.

De Boeck K, Weren M, Proesmans M, Kerem E.

Pediatrics. 2005 Apr;115(4):e463-9. Epub 2005 Mar 16.

PMID:
15772171
12.

Vector-specific complementation profiles of two independent primary defects in cystic fibrosis airways.

Zhang Y, Jiang Q, Dudus L, Yankaskas JR, Engelhardt JF.

Hum Gene Ther. 1998 Mar 20;9(5):635-48.

PMID:
9551612
13.

CFTR Cl- channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis.

Hirtz S, Gonska T, Seydewitz HH, Thomas J, Greiner P, Kuehr J, Brandis M, Eichler I, Rocha H, Lopes AI, Barreto C, Ramalho A, Amaral MD, Kunzelmann K, Mall M.

Gastroenterology. 2004 Oct;127(4):1085-95.

PMID:
15480987
14.

Gene therapy for cystic fibrosis using E1-deleted adenovirus: a phase I trial in the nasal cavity. The University of North Carolina at Chapel Hill.

Boucher RC, Knowles MR, Johnson LG, Olsen JC, Pickles R, Wilson JM, Engelhardt J, Yang Y, Grossman M.

Hum Gene Ther. 1994 May;5(5):615-39.

PMID:
7519885
15.
16.

Genotype and phenotype in cystic fibrosis.

Zielenski J.

Respiration. 2000;67(2):117-33. Review.

17.

Role of the amiloride-sensitive epithelial Na+ channel in the pathogenesis and as a therapeutic target for cystic fibrosis lung disease.

Mall MA.

Exp Physiol. 2009 Feb;94(2):171-4. doi: 10.1113/expphysiol.2008.042994. Epub 2008 Dec 5.

18.

Natural history of pancreatitis associated with cystic fibrosis gene mutations.

Frulloni L, Castellani C, Bovo P, Vaona B, Calore B, Liani C, Mastella G, Cavallini G.

Dig Liver Dis. 2003 Mar;35(3):179-85.

PMID:
12779072
19.

[Cystic fibrosis from the exocrine pancreatic point of view].

Virgilis D.

Harefuah. 2004 Jan;143(1):67-72, 83. Review. Hebrew.

PMID:
14748292
20.

The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitis.

Bishop MD, Freedman SD, Zielenski J, Ahmed N, Dupuis A, Martin S, Ellis L, Shea J, Hopper I, Corey M, Kortan P, Haber G, Ross C, Tzountzouris J, Steele L, Ray PN, Tsui LC, Durie PR.

Hum Genet. 2005 Dec;118(3-4):372-81. Epub 2005 Sep 29.

PMID:
16193325
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