Tafel, Oliver, Latzin, Philipp, Paul, Karl, Winter, Tobias, Woischnik, Markus, Griese, Matthias
Abstract Background The surfactant proteins B (SP-B) and C (SP-C) are important for the stability and function of the alveolar surfactant film. Their involvement and down-regulation in inflammatory...
Galetskiy, Dmitry, Woischnik, Markus, Ripper, Jan, Griese, Matthias, Przybylski, Michael
The mutation (g.1286T>C) of the pulmonary surfactant-associated protein C gene (SFTPC) leads to the I73T substitution in the precursor protein (pro-SP-C) and results in interstitial lung disease with...
Müller, Hanna, End, Caroline, Renner, Marcus, Helmke, Burkhard M, Gassler, Nikolaus, Weiss, Christel, ...
Abstract Background Deleted in Malignant Brain Tumors 1 (DMBT1) is a secreted scavenger receptor cysteine-rich protein that binds various bacteria and is thought to participate in innate pulmonary...
Bai, Yu, Galetskiy, Dmitry, Damoc, Eugen, Ripper, Jan, Woischnik, Markus, Griese, Matthias, ...
High-resolution Fourier transform ion cyclotron resonance (FTICR) mass spectrometry was developed and applied to the proteome analysis of bronchoalveolar lavage fluid (BALF) from a patient with...
Hornef, Nada, Olbrich, Heike, Horvath, Judit, Zariwala, Maimoona A., Fliegauf, Manfred, Loges, Niki Tomas, ...
Rationale: Primary ciliary dyskinesia (PCD) is characterized by recurrent airway infections and randomization of left–right body asymmetry. To date, autosomal recessive mutations have only been...
Hornef, Nada, Olbrich, Heike, Horvath, Judit, Zariwala, Maimoona A., Fliegauf, Manfred, Loges, Niki Tomas, ...
Rationale: Primary ciliary dyskinesia (PCD) is characterized by recurrent airway infections and randomization of left–right body asymmetry. To date, autosomal recessive mutations have only been...
Therapeutic lung lavages in children and adults (2005)
Paschen, Christian, Reiter, Karl, Stanzel, Franz, Teschler, Helmut, Griese, Matthias
Abstract Background Pulmonary alveolar proteinosis (PAP) is a rare disease, characterized by excessive intra-alveolar accumulation of surfactant lipids and proteins. Therapeutic whole lung lavages...
Sequential analysis of surfactant, lung function and inflammation in cystic fibrosis patients (2005)
Griese, Matthias, Essl, Robert, Schmidt, Reinhold, Ballmann, Manfred, Paul, Karl, Rietschel, Ernst, ...
Abstract Background In a cross-sectional analysis of cystic fibrosis (CF) patients with mild lung disease, reduced surfactant activity was correlated to increased neutrophilic airway inflammation,...
A role for MCP-1/CCR2 in interstitial lung disease in children (2005)
Hartl, Dominik, Griese, Matthias, Nicolai, Thomas, Zissel, Gernot, Prell, Christine, Reinhardt, Dietrich, ...
Abstract Background Interstitial lung diseases (ILD) are chronic inflammatory disorders leading to pulmonary fibrosis. Monocyte chemotactic protein 1 (MCP-1) promotes collagen synthesis and deletion...
Griese, Matthias, Schumacher, Silja, Tredano, Mohammed, Steinecker, Manuela, Braun, Annika, Guttentag, Susan, ...
Abstract Background Abnormalities of the intracellular metabolism of the hydrophobic surfactant proteins SP-B and SP-C and their precursors may be causally linked to chronic childhood diffuse lung...
Interstitial lung disease in children – genetic background and associated phenotypes (2005)
Hartl, Dominik, Griese, Matthias
Abstract Interstitial lung disease in children represents a group of rare chronic respiratory disorders. There is growing evidence that mutations in the surfactant protein C gene play a role in the...
Thesis (doctoral)--Rheinisch-Westfälische Technische Hochschule Aachen, 1985.
Interstitial lung disease in children – genetic background and associated phenotypes
Hartl, Dominik, Griese, Matthias
Interstitial lung disease in children represents a group of rare chronic respiratory disorders. There is growing evidence that mutations in the surfactant protein C gene play a role in the...
A role for MCP-1/CCR2 in interstitial lung disease in children
Hartl, Dominik, Griese, Matthias, Nicolai, Thomas, Zissel, Gernot, Prell, Christine, Reinhardt, Dietrich, ...
Expression profiles of hydrophobic surfactant proteins in children with diffuse chronic lung disease
Griese, Matthias, Schumacher, Silja, Tredano, Mohammed, Steinecker, Manuela, Braun, Annika, Guttentag, Susan, ...
Sequential analysis of surfactant, lung function and inflammation in cystic fibrosis patients
Griese, Matthias, Essl, Robert, Schmidt, Reinhold, Ballmann, Manfred, Paul, Karl, Rietschel, Ernst, ...
Therapeutic lung lavages in children and adults
Paschen, Christian, Reiter, Karl, Stanzel, Franz, Teschler, Helmut, Griese, Matthias
Interstitial lung disease in children – genetic background and associated phenotypes
Hartl, Dominik, Griese, Matthias
Interstitial lung disease in children represents a group of rare chronic respiratory disorders. There is growing evidence that mutations in the surfactant protein C gene play a role in the...
A role for MCP-1/CCR2 in interstitial lung disease in children
Hartl, Dominik, Griese, Matthias, Nicolai, Thomas, Zissel, Gernot, Prell, Christine, Reinhardt, Dietrich, ...
Expression profiles of hydrophobic surfactant proteins in children with diffuse chronic lung disease
Griese, Matthias, Schumacher, Silja, Tredano, Mohammed, Steinecker, Manuela, Braun, Annika, Guttentag, Susan, ...
Sequential analysis of surfactant, lung function and inflammation in cystic fibrosis patients
Griese, Matthias, Essl, Robert, Schmidt, Reinhold, Ballmann, Manfred, Paul, Karl, Rietschel, Ernst, ...
Therapeutic lung lavages in children and adults
Paschen, Christian, Reiter, Karl, Stanzel, Franz, Teschler, Helmut, Griese, Matthias
Müller, Hanna, End, Caroline, Renner, Marcus, Helmke, Burkhard M, Gassler, Nikolaus, Weiss, Christel, ...
DNAH5 Mutations Are a Common Cause of Primary Ciliary Dyskinesia with Outer Dynein Arm Defects
Hornef, Nada, Olbrich, Heike, Horvath, Judit, Zariwala, Maimoona A., Fliegauf, Manfred, Loges, Niki Tomas, ...
Rationale: Primary ciliary dyskinesia (PCD) is characterized by recurrent airway infections and randomization of left–right body asymmetry. To date, autosomal recessive mutations have only been...