Mall MA - Search Results

1

Ion mobility-tandem mass spectrometry of mucin-type O-glycans.

Bechtella L, Chunsheng J, Fentker K, Ertürk GR, Safferthal M, Polewski Ł, Götze M, Graeber SY, Vos GM, Struwe WB, Mall MA, Mertins P, Karlsson NG, Pagel K. Bechtella L, et al. Among authors: mall ma. Nat Commun. 2024 Mar 23;15(1):2611. doi: 10.1038/s41467-024-46825-4. Nat Commun. 2024. PMID: 38521783 Free PMC article.

2

The ENaC-overexpressing mouse as a model of cystic fibrosis lung disease.

Zhou Z, Duerr J, Johannesson B, Schubert SC, Treis D, Harm M, Graeber SY, Dalpke A, Schultz C, Mall MA. Zhou Z, et al. Among authors: mall ma. J Cyst Fibros. 2011 Jun;10 Suppl 2:S172-82. doi: 10.1016/S1569-1993(11)60021-0. J Cyst Fibros. 2011. PMID: 21658636 Free article. Review.

3

Hypertonic saline is effective in the prevention and treatment of mucus obstruction, but not airway inflammation, in mice with chronic obstructive lung disease.

Graeber SY, Zhou-Suckow Z, Schatterny J, Hirtz S, Boucher RC, Mall MA. Graeber SY, et al. Among authors: mall ma. Am J Respir Cell Mol Biol. 2013 Sep;49(3):410-7. doi: 10.1165/rcmb.2013-0050OC. Am J Respir Cell Mol Biol. 2013. PMID: 23590312 Free PMC article.

4

Early cystic fibrosis lung disease: Role of airway surface dehydration and lessons from preventive rehydration therapies in mice.

Mall MA, Graeber SY, Stahl M, Zhou-Suckow Z. Mall MA, et al. Int J Biochem Cell Biol. 2014 Jul;52:174-9. doi: 10.1016/j.biocel.2014.02.006. Epub 2014 Feb 20. Int J Biochem Cell Biol. 2014. PMID: 24561284 Review.

5

Comparison of microbiomes from different niches of upper and lower airways in children and adolescents with cystic fibrosis.

Boutin S, Graeber SY, Weitnauer M, Panitz J, Stahl M, Clausznitzer D, Kaderali L, Einarsson G, Tunney MM, Elborn JS, Mall MA, Dalpke AH. Boutin S, et al. Among authors: mall ma. PLoS One. 2015 Jan 28;10(1):e0116029. doi: 10.1371/journal.pone.0116029. eCollection 2015. PLoS One. 2015. PMID: 25629612 Free PMC article.

6

Intestinal Current Measurements Detect Activation of Mutant CFTR in Patients with Cystic Fibrosis with the G551D Mutation Treated with Ivacaftor.

Graeber SY, Hug MJ, Sommerburg O, Hirtz S, Hentschel J, Heinzmann A, Dopfer C, Schulz A, Mainz JG, Tümmler B, Mall MA. Graeber SY, et al. Among authors: mall ma. Am J Respir Crit Care Med. 2015 Nov 15;192(10):1252-5. doi: 10.1164/rccm.201507-1271LE. Am J Respir Crit Care Med. 2015. PMID: 26568242 No abstract available.

7

Comparison of Lung Clearance Index and Magnetic Resonance Imaging for Assessment of Lung Disease in Children with Cystic Fibrosis.

Stahl M, Wielpütz MO, Graeber SY, Joachim C, Sommerburg O, Kauczor HU, Puderbach M, Eichinger M, Mall MA. Stahl M, et al. Among authors: mall ma. Am J Respir Crit Care Med. 2017 Feb 1;195(3):349-359. doi: 10.1164/rccm.201604-0893OC. Am J Respir Crit Care Med. 2017. PMID: 27575911 Clinical Trial.

8

Early detection and sensitive monitoring of CF lung disease: Prospects of improved and safer imaging.

Mall MA, Stahl M, Graeber SY, Sommerburg O, Kauczor HU, Wielpütz MO. Mall MA, et al. Pediatr Pulmonol. 2016 Oct;51(S44):S49-S60. doi: 10.1002/ppul.23537. Pediatr Pulmonol. 2016. PMID: 27662104 Review.

9

Three-center feasibility of lung clearance index in infants and preschool children with cystic fibrosis and other lung diseases.

Stahl M, Graeber SY, Joachim C, Barth S, Ricklefs I, Diekmann G, Kopp MV, Naehrlich L, Mall MA. Stahl M, et al. Among authors: mall ma. J Cyst Fibros. 2018 Mar;17(2):249-255. doi: 10.1016/j.jcf.2017.08.001. Epub 2017 Aug 12. J Cyst Fibros. 2018. PMID: 28811149 Free article.

10

Chronic but not intermittent infection with Pseudomonas aeruginosa is associated with global changes of the lung microbiome in cystic fibrosis.

Boutin S, Graeber SY, Stahl M, Dittrich AS, Mall MA, Dalpke AH. Boutin S, et al. Among authors: mall ma. Eur Respir J. 2017 Oct 5;50(4):1701086. doi: 10.1183/13993003.01086-2017. Print 2017 Oct. Eur Respir J. 2017. PMID: 28982777 Free article. No abstract available.

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