Hammel M - Search Results

1

SFTA2--a novel secretory peptide highly expressed in the lung--is modulated by lipopolysaccharide but not hyperoxia.

Mittal RA, Hammel M, Schwarz J, Heschl KM, Bretschneider N, Flemmer AW, Herber-Jonat S, Königshoff M, Eickelberg O, Holzinger A. Mittal RA, et al. Among authors: hammel m. PLoS One. 2012;7(6):e40011. doi: 10.1371/journal.pone.0040011. Epub 2012 Jun 29. PLoS One. 2012. PMID: 22768197 Free PMC article.

2

Abca3 haploinsufficiency is a risk factor for lung injury induced by hyperoxia or mechanical ventilation in a murine model.

Herber-Jonat S, Mittal R, Huppmann M, Hammel M, Liebisch G, Yildirim AÖ, Eickelberg O, Schmitz G, Hrabé de Angelis M, Flemmer AW, Holzinger A. Herber-Jonat S, et al. Among authors: hammel m. Pediatr Res. 2013 Oct;74(4):384-92. doi: 10.1038/pr.2013.127. Epub 2013 Jul 23. Pediatr Res. 2013. PMID: 23881110

3

Heterozygous SOX9 mutations allowing for residual DNA-binding and transcriptional activation lead to the acampomelic variant of campomelic dysplasia.

Staffler A, Hammel M, Wahlbuhl M, Bidlingmaier C, Flemmer AW, Pagel P, Nicolai T, Wegner M, Holzinger A. Staffler A, et al. Among authors: hammel m. Hum Mutat. 2010 Jun;31(6):E1436-44. doi: 10.1002/humu.21238. Hum Mutat. 2010. PMID: 20513132

4

Targeted inactivation of the murine Abca3 gene leads to respiratory failure in newborns with defective lamellar bodies.

Hammel M, Michel G, Hoefer C, Klaften M, Müller-Höcker J, de Angelis MH, Holzinger A. Hammel M, et al. Biochem Biophys Res Commun. 2007 Aug 10;359(4):947-51. doi: 10.1016/j.bbrc.2007.05.219. Epub 2007 Jun 11. Biochem Biophys Res Commun. 2007. PMID: 17577581

5

Congenital Central Hypoventilation Syndrome due to PHOX2b gene defects: inheritance from asymptomatic parents.

Hammel M, Klein M, Trips T, Priessmann H, Ankermann T, Holzinger A. Hammel M, et al. Klin Padiatr. 2009 Sep;221(5):286-9. doi: 10.1055/s-0029-1220941. Epub 2009 Aug 25. Klin Padiatr. 2009. PMID: 19707990

6

A novel 17 bp deletion in the PHOX2B gene causes congenital central hypoventilation syndrome with total aganglionosis of the small and large intestine.

Holzinger A, Mittal RA, Kachel W, Priessmann H, Hammel M, Ihrler S, Till H, Münch HG. Holzinger A, et al. Among authors: hammel m. Am J Med Genet A. 2005 Nov 15;139(1):50-1. doi: 10.1002/ajmg.a.30975. Am J Med Genet A. 2005. PMID: 16222683 No abstract available.

7

S. aureus Eap is a polyvalent inhibitor of neutrophil serine proteases.

Mishra N, Gido CD, Herdendorf TJ, Hammel M, Hura GL, Fu ZQ, Geisbrecht BV. Mishra N, et al. Among authors: hammel m. J Biol Chem. 2024 Sep;300(9):107627. doi: 10.1016/j.jbc.2024.107627. Epub 2024 Aug 3. J Biol Chem. 2024. PMID: 39098536 Free PMC article.

8

Structural and biochemical basis for regiospecificity of the flavonoid glycosyltransferase UGT95A1.

Sirirungruang S, Blay V, Scott YF, Pereira JH, Hammel M, Barnum CR, Adams PD, Shih PM. Sirirungruang S, et al. Among authors: hammel m. J Biol Chem. 2024 Sep;300(9):107602. doi: 10.1016/j.jbc.2024.107602. Epub 2024 Jul 24. J Biol Chem. 2024. PMID: 39059496 Free PMC article.

9

ASCC1 structures and bioinformatics reveal a novel helix-clasp-helix RNA-binding motif linked to a two-histidine phosphodiesterase.

Chinnam NB, Thapar R, Arvai AS, Sarker AH, Soll JM, Paul T, Syed A, Rosenberg DJ, Hammel M, Bacolla A, Katsonis P, Asthana A, Tsai MS, Ivanov I, Lichtarge O, Silverman RH, Mosammaparast N, Tsutakawa SE, Tainer JA. Chinnam NB, et al. Among authors: hammel m. J Biol Chem. 2024 Jun;300(6):107368. doi: 10.1016/j.jbc.2024.107368. Epub 2024 May 14. J Biol Chem. 2024. PMID: 38750793 Free PMC article.

10

Effects of N-glycans on the structure of human IgA2.

Ruocco V, Grünwald-Gruber C, Rad B, Tscheliessnig R, Hammel M, Strasser R. Ruocco V, et al. Among authors: hammel m. Front Mol Biosci. 2024 Apr 5;11:1390659. doi: 10.3389/fmolb.2024.1390659. eCollection 2024. Front Mol Biosci. 2024. PMID: 38645274 Free PMC article.

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