Luc Dannhoffer
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Explore the profile of Luc Dannhoffer including associated specialties, affiliations and a list of published articles.
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11
Citations
186
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Recent Articles
1.
Canu M, Fourneau J, Coq J, Dannhoffer L, Cieniewski-Bernard C, Stevens L, et al.
Ann Phys Rehabil Med
. 2018 Nov;
62(2):122-127.
PMID: 30394346
Activity-dependent processes addressing the central nervous system (CNS) and musculoskeletal structures are critical for maintaining motor performance. Chronic reduction in activity, whether due to a sedentary lifestyle or extended bed...
2.
Bertrand J, Dannhoffer L, Antigny F, Vachel L, Jayle C, Vandebrouck C, et al.
Eur J Pharmacol
. 2015 Aug;
765:337-45.
PMID: 26265544
TRPC6 plays important human physiological functions, notably in artery and arterioles constriction, in regulation of vascular volume and in bronchial muscle constriction. It is implicated in pulmonary hypertension, cardiovascular disease,...
3.
Blouquit-Laye S, Dannhoffer L, Braun C, Dinh-Xuan A, Sage E, Chinet T
Am J Physiol Lung Cell Mol Physiol
. 2012 Jul;
303(7):L617-25.
PMID: 22773693
The airways of patients with cystic fibrosis (CF) exhibit decreased nitric oxide (NO) concentrations, which might affect airway function. The aim of this study was to determine the effects of...
4.
Dannhoffer L, Billet A, Jollivet M, Melin-Heschel P, Faveau C, Becq F
Front Pharmacol
. 2011 Sep;
2:48.
PMID: 21897819
Cystic fibrosis (CF) is a major inherited disorder involving abnormalities of fluid and electrolyte transport in a number of different organs due to abnormal function of cystic fibrosis transmembrane conductance...
5.
Antigny F, Norez C, Dannhoffer L, Bertrand J, Raveau D, Corbi P, et al.
Am J Respir Cell Mol Biol
. 2010 Mar;
44(1):83-90.
PMID: 20203293
In cystic fibrosis (CF), abnormal control of cellular Ca(2+) homeostasis is observed. We hypothesized that transient receptor potential canonical (TRPC) channels could be a link between the abnormal Ca(2+) concentrations...
6.
Catherinot E, Roux A, Macheras E, Hubert D, Matmar M, Dannhoffer L, et al.
J Clin Microbiol
. 2008 Nov;
47(1):271-4.
PMID: 19020061
We report the case of a cystic fibrosis patient colonized with a smooth-morphotype form of Mycobacterium abscessus who developed acute respiratory failure with the emergence of an isogenic rough (R)...
7.
Dannhoffer L, Blouquit-Laye S, Regnier A, Chinet T
Am J Respir Cell Mol Biol
. 2008 Nov;
40(6):717-23.
PMID: 19011164
Cystic fibrosis (CF) airway epithelia exhibit altered Cl(-) and Na(+) transport properties and increased IL-8 secretion. In the present study, we examined whether a small proportion of cells with a...
8.
Norez C, Vandebrouck C, Antigny F, Dannhoffer L, Blondel M, Becq F
Eur J Pharmacol
. 2008 Jul;
592(1-3):33-40.
PMID: 18640110
In cystic fibrosis respiratory epithelial cells, the absence or dysfunction of the chloride channel CFTR (Cystic Fibrosis Transmembrane conductance Regulator) results in reduced chloride ion transport. In contrast, Ca2+-stimulated Cl-...
9.
Regnier A, Dannhoffer L, Blouquit-Laye S, Bakari M, Naline E, Chinet T
Hum Pathol
. 2007 Nov;
39(3):368-76.
PMID: 18045644
The determination of the expression of cystic fibrosis transmembrane conductance regulator (CFTR) in the lung is essential for a full understanding of the normal lung physiology and the pathogenesis of...
10.
Noel S, Strale P, Dannhoffer L, Wilke M, deJonge H, Rogier C, et al.
J Cyst Fibros
. 2007 Sep;
7(2):128-33.
PMID: 17766192
Background: Physiologically, salivary secretion is controlled by cholinergic and adrenergic pathways but the role of ionic channels in this process is not yet clearly understood. In cystic fibrosis (CF), most...