David Groneberg

Prof. David Groneberg

Institute of Occupational Medicine, Social Medicine and Environmental Medicine, Goethe University Frankfurt, 60590 Frankfurt, Germany

Research Focus & Metrics

Academic Career Length

27Years (2000-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 September 2006 in Journal of Occupational Medicine and Toxicology
Verified
Journal Article
Open access
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JGJohannes Godt
Johannes Godt
FSFranziska Scheidig
Franziska Scheidig
CGChristian Große-Siestrup
Christian Große-Siestrup
VEVera Esche
Vera Esche
PBPaul Brandenburg
Paul Brandenburg
David GronebergDavid Groneberg
David Groneberg
Cadmium (Cd) has been in industrial use for a long period of time. Its serious toxicity moved into scientific focus during the middle of the last century. In this review, we discuss historic and recent developments of toxicological and epidemiological questions, including exposition sources, resorption pathways and organ damage processes.

2 December 2007 in Nature Genetics
Verified
Journal Article
Closed access
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JRJonas Rosendahl
Jonas Rosendahl
HWHeiko Witt
Heiko Witt
RSRichárd Szmola
Richárd Szmola
EBEesh Bhatia
Eesh Bhatia
BÓBéla Ózsvári
Béla Ózsvári
MSMiklos Sahin-Toth
Miklos Sahin-Toth

15 December 2004 in American Journal of Respiratory and Critical Care Medicine
Verified
Journal Article
Closed access
David GronebergDavid Groneberg
David Groneberg
ANAkio Niimi
Akio Niimi
QDQ. Thai Dinh
Q. Thai Dinh
Borja G CosíoBorja G Cosío
Borja G Cosío
MHMark Hew
Mark Hew
KCKian Chung
Kian Chung
Transient receptor potential vanniloid-1 (TRPV-1) mediates the cough response induced by the pepper extract capsaicin and is expressed in sensory nerves that innervate the airway wall. We determined the expression of TRPV-1 in the airways of patients with chronic persistent cough of diverse causes and with an enhanced capsaicin cough response. We obtained airway mucosal biopsies by fiberoptic bronchoscopy in 29 patients with chronic cough and 16 healthy volunteers without a cough. Immunostaining for nerve profiles with anti–protein gene product (PGP)-9.5 antibody showed no increase in nerve profiles in the airway epithelium of patients with chronic cough; however, with an anti–TRPV-1 antibody, there was a fivefold increase of TRPV-1 staining nerve profiles (p < 0.001). There was a significant correlation between capsaicin tussive response and the number of TRPV-1–positive nerves within the patients with cough. Our findings indicate that TRPV-1 receptors may contribute to an enhanced cough reflex and the cough response in chronic persistent cough of diverse causes.

18 August 2013 in Nature Genetics
Verified
Journal Article
Closed access
PDF file
HWHeiko Witt
Heiko Witt
SBSebastian Beer
Sebastian Beer
JRJonas Rosendahl
Jonas Rosendahl
Jian-Min ChenJian-Min Chen
Jian-Min Chen
GCGiriraj Ratan Chandak
Giriraj Ratan Chandak
MSMiklos Sahin-Toth
Miklos Sahin-Toth

20 December 2006 in Clinical & Experimental Allergy
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Journal Article
Closed access
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Wojciech FeleszkoWojciech Feleszko
Wojciech Feleszko
Joanna JaworskaJoanna Jaworska
Joanna Jaworska
RRR‐D. Rha
R‐D. Rha
SSS. Steinhausen
S. Steinhausen
AAA. Avagyan
A. Avagyan
EHE. Hamelmann
E. Hamelmann

14 May 2006 in Nature Genetics
Verified
Journal Article
Open access
PDF file
HWHeiko Witt
Heiko Witt
MSMiklos Sahin-Toth
Miklos Sahin-Toth
OLOlfert Landt
Olfert Landt
Jian-Min ChenJian-Min Chen
Jian-Min Chen
TKThilo Kähne
Thilo Kähne
Claude FérecClaude Férec
Claude Férec
Chronic pancreatitis is a common inflammatory disease of the pancreas. Mutations in the genes encoding cationic trypsinogen (PRSS1)1 and the pancreatic secretory trypsin inhibitor (SPINK1)2 are associated with chronic pancreatitis. Because increased proteolytic activity owing to mutated PRSS1 enhances the risk for chronic pancreatitis, mutations in the gene encoding anionic trypsinogen (PRSS2) may also predispose to disease. Here we analyzed PRSS2 in individuals with chronic pancreatitis and controls and found, to our surprise, that a variant of codon 191 (G191R) is overrepresented in control subjects: G191R was present in 220/6,459 (3.4%) controls but in only 32/2,466 (1.3%) affected individuals (odds ratio 0.37; P = 1.1 × 10−8). Upon activation by enterokinase or trypsin, purified recombinant G191R protein showed a complete loss of trypsin activity owing to the introduction of a new tryptic cleavage site that renders the enzyme hypersensitive to autocatalytic proteolysis. In conclusion, the G191R variant of PRSS2 mitigates intrapancreatic trypsin activity and thereby protects against chronic pancreatitis.