SFTA2--a novel secretory peptide highly expressed in the lung--is modulated by lipopolysaccharide but not hyperoxia
Mittal, Rashmi A, Hammel, Markus, Schwarz, Johannes, Heschl, Katharina M, Bretschneider, Nancy, Flemmer, Andreas W, Herber-Jonat, Susanne, Königshoff, Melanie, Eickelberg, Oliver, Holzinger, Andreas
Published in PloS one (29.06.2012)
Published in PloS one (29.06.2012)
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Journal Article
Heterozygous SOX9 mutations allowing for residual DNA-binding and transcriptional activation lead to the acampomelic variant of campomelic dysplasia
Staffler, Alex, Hammel, Markus, Wahlbuhl, Mandy, Bidlingmaier, Christoph, Flemmer, Andreas W, Pagel, Philipp, Nicolai, Thomas, Wegner, Michael, Holzinger, Andreas
Published in Human mutation (01.06.2010)
Published in Human mutation (01.06.2010)
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Journal Article
Abca3 haploinsufficiency is a risk factor for lung injury induced by hyperoxia or mechanical ventilation in a murine model
Herber-Jonat, Susanne, Mittal, Rashmi, Huppmann, Marceline, Hammel, Markus, Liebisch, Gerhard, Yildirim, Ali Önder, Eickelberg, Oliver, Schmitz, Gerd, Hrabé de Angelis, Martin, Flemmer, Andreas W., Holzinger, Andreas
Published in Pediatric research (01.10.2013)
Published in Pediatric research (01.10.2013)
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Targeted inactivation of the murine Abca3 gene leads to respiratory failure in newborns with defective lamellar bodies
Hammel, Markus, Michel, Geert, Hoefer, Christina, Klaften, Matthias, Müller-Höcker, Josef, de Angelis, Martin Hrabé, Holzinger, Andreas
Published in Biochemical and biophysical research communications (10.08.2007)
Published in Biochemical and biophysical research communications (10.08.2007)
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Journal Article
A novel 17 bp deletion in the PHOX2B gene causes congenital central hypoventilation syndrome with total aganglionosis of the small and large intestine
Holzinger, Andreas, Mittal, Rashmi A., Kachel, Walter, Priessmann, Helga, Hammel, Markus, Ihrler, Stephan, Till, Holger, Münch, Hans-Georg
Published in American journal of medical genetics. Part A (15.11.2005)
Published in American journal of medical genetics. Part A (15.11.2005)
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Journal Article
Inhibitors of APOL1 and uses thereof
HAMMEL MARKUS, TAY CHRISTOPHER E, NICOLAS, OLIVIER, DENIS, FR, KRUEGER ERIC B, COME, JON, H, MALTAIS FRANCOIS, LEFORT BENJAMIN, DAKIN LES A, RIC, DORSCH WILLIAM A, NANTHAKUMAR, SHANKAR, SHANKAR, D, CAO JIAN, FORTIER, ARNAUD
Year of Publication 28.03.2023
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Year of Publication 28.03.2023
Patent
A novel 17 bp deletion in the PHOX2B gene causes congenital central hypoventilation syndrome with total aganglionosis of the small and large intestine
Holzinger, Andreas, Mittal, Rashmi A, Kachel, Walter, Priessmann, Helga, Hammel, Markus, Ihrler, Stephan, Till, Holger, Münch, Hans-Georg
Published in American journal of medical genetics. Part A (15.11.2005)
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Published in American journal of medical genetics. Part A (15.11.2005)
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