Steiner, Bernhard

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Journal Article

Steiner, Bernhard; Rosendahl, Jonas; Witt, Heiko; Teich, Niels; Keim, Volker; Schulz, Hans-Ulrich; Pfützer, Roland; Löhr, Matthias; Lühr, Matthias; Gress, Thomas M; Nickel, Renate; Landt, Olfert; Koudova, Monika; Macek, Milan; Farre, Antoni; Casals, Teresa; Desax, Marie-Claire; Gallati, Sabina; Gomez-Lira, Macarena; Audrezet, Marie Pierre; ... (2011). Common CFTR haplotypes and susceptibility to chronic pancreatitis and congenital bilateral absence of the vas deferens. Human mutation, 32(8), pp. 912-20. Hoboken, N.J.: Wiley-Blackwell 10.1002/humu.21511

Sanz, Javier; von Känel, Thomas; Schneider, Mircea; Steiner, Bernhard; Schaller, André; Gallati, Sabina (2010). The CFTR frameshift mutation 3905insT and its effect at transcript and protein level. European journal of human genetics, 18(2), pp. 212-7. Houndmills, UK: Nature Publishing Group 10.1038/ejhg.2009.140

Meienberg, Janine; Rohrbach, Marianne; Neuenschwander, Stefan; Spanaus, Katharina; Giunta, Cecilia; Alonso, Sira; Arnold, Eliane; Henggeler, Caroline; Regenass, Stephan; Patrignani, Andrea; Azzarello-Burri, Silvia; Steiner, Bernhard; Nygren, Anders O H; Carrel, Thierry; Steinmann, Beat; Mátyás, Gábor (2010). Hemizygous deletion of COL3A1, COL5A2, and MSTN causes a complex phenotype with aortic dissection: a lesson for and from true haploinsufficiency. European journal of human genetics, 18(12), pp. 1315-21. Houndmills, UK: Nature Publishing Group 10.1038/ejhg.2010.105

Pavlovic, Mladen; Schaller, André; Steiner, Bernhard; Berdat, Pascal; Carrel, Thierry; Pfammatter, Jean-Pierre; Ammann, Roland A; Gallati, Sabina (2005). Gender modulates the expression of calcium-regulating proteins in pediatric atrial myocardium. Experimental biology and medicine, 230(11), pp. 853-9. Maywood, N.J.: Society for Experimental Biology & Medicine

Steiner, Bernhard; Truninger, Kaspar; Sanz, Javier; Schaller, André; Gallati, Sabina (2004). The role of common single-nucleotide polymorphisms on exon 9 and exon 12 skipping in nonmutated CFTR alleles. Human mutation, 24(2), pp. 120-9. Hoboken, N.J.: Wiley-Blackwell 10.1002/humu.20064

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