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Items: 13

1.

Chemically modified hCFTR mRNAs recuperate lung function in a mouse model of cystic fibrosis.

Haque AKMA, Dewerth A, Antony JS, Riethmüller J, Schweizer GR, Weinmann P, Latifi N, Yasar H, Pedemonte N, Sondo E, Weidensee B, Ralhan A, Laval J, Schlegel P, Seitz C, Loretz B, Lehr CM, Handgretinger R, Kormann MSD.

Sci Rep. 2018 Nov 13;8(1):16776. doi: 10.1038/s41598-018-34960-0.

2.

Human T cells modulate myeloid-derived suppressor cells through a TNF-α-mediated mechanism.

Bauswein M, Singh A, Ralhan A, Neri D, Fuchs K, Blanz KD, Schäfer I, Hector A, Handgretinger R, Hartl D, Rieber N.

Immunol Lett. 2018 Oct;202:31-37. doi: 10.1016/j.imlet.2018.07.010. Epub 2018 Aug 1.

PMID:
30076856
3.

Fungal Pathogens in CF Airways: Leave or Treat?

Singh A, Ralhan A, Schwarz C, Hartl D, Hector A.

Mycopathologia. 2018 Feb;183(1):119-137. doi: 10.1007/s11046-017-0184-y. Epub 2017 Aug 2. Review.

PMID:
28770417
4.

Current Concepts and Controversies in Innate Immunity of Cystic Fibrosis Lung Disease.

Ralhan A, Laval J, Lelis F, Ballbach M, Grund C, Hector A, Hartl D.

J Innate Immun. 2016;8(6):531-540. Epub 2016 Jul 1. Review.

5.

High rates of glucose utilization in the gas gland of Atlantic cod (Gadus morhua) are supported by GLUT1 and HK1b.

Clow KA, Short CE, Hall JR, Gendron RL, Paradis H, Ralhan A, Driedzic WR.

J Exp Biol. 2016 Sep 1;219(Pt 17):2763-73. doi: 10.1242/jeb.141721. Epub 2016 Jul 8.

6.

Chitinase activation in patients with fungus-associated cystic fibrosis lung disease.

Hector A, Chotirmall SH, Lavelle GM, Mirković B, Horan D, Eichler L, Mezger M, Singh A, Ralhan A, Berenbrinker S, Mack I, Ensenauer R, Riethmüller J, Graepler-Mainka U, Murray MA, Griese M, McElvaney NG, Hartl D.

J Allergy Clin Immunol. 2016 Oct;138(4):1183-1189.e4. doi: 10.1016/j.jaci.2016.01.031. Epub 2016 Apr 4.

PMID:
27056270
7.

Microbial colonization and lung function in adolescents with cystic fibrosis.

Hector A, Kirn T, Ralhan A, Graepler-Mainka U, Berenbrinker S, Riethmueller J, Hogardt M, Wagner M, Pfleger A, Autenrieth I, Kappler M, Griese M, Eber E, Martus P, Hartl D.

J Cyst Fibros. 2016 May;15(3):340-9. doi: 10.1016/j.jcf.2016.01.004. Epub 2016 Feb 5.

8.

Neutrophils in cystic fibrosis.

Laval J, Ralhan A, Hartl D.

Biol Chem. 2016 Jun 1;397(6):485-96. doi: 10.1515/hsz-2015-0271. Review.

PMID:
26854289
9.

Fatty Acids Secreted by Anaerobes. Fueling Inflammation in Cystic Fibrosis Lungs.

Ralhan A, Hartl D.

Am J Respir Crit Care Med. 2015 Dec 1;192(11):1270-1. doi: 10.1164/rccm.201508-1556ED. No abstract available.

PMID:
26623683
10.

Regulatory T-cell impairment in cystic fibrosis patients with chronic pseudomonas infection.

Hector A, Schäfer H, Pöschel S, Fischer A, Fritzsching B, Ralhan A, Carevic M, Öz H, Zundel S, Hogardt M, Bakele M, Rieber N, Riethmueller J, Graepler-Mainka U, Stahl M, Bender A, Frick JS, Mall M, Hartl D.

Am J Respir Crit Care Med. 2015 Apr 15;191(8):914-23. doi: 10.1164/rccm.201407-1381OC.

PMID:
25632992
12.

The vascular pathogen Verticillium longisporum requires a jasmonic acid-independent COI1 function in roots to elicit disease symptoms in Arabidopsis shoots.

Ralhan A, Schöttle S, Thurow C, Iven T, Feussner I, Polle A, Gatz C.

Plant Physiol. 2012 Jul;159(3):1192-203. doi: 10.1104/pp.112.198598. Epub 2012 May 25.

13.

A fall and near-fall assessment and evaluation system.

Dinh A, Shi Y, Teng D, Ralhan A, Chen L, Dal Bello-Haas V, Basran J, Ko SB, McCrowsky C.

Open Biomed Eng J. 2009 Jan 21;3:1-7. doi: 10.2174/1874120700903010001.

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