Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Susanna H. M. Sluka"'
Autor:
Susanna H. M. Sluka, Simon F. Stämpfli, Alexander Akhmedov, Tanja Klein-Rodewald, Adrián Sanz-Moreno, Marion Horsch, Paula Grest, Andrea S. Rothmeier, Birgit Rathkolb, Anja Schrewe, Johannes Beckers, Frauke Neff, Eckhard Wolf, Giovanni G. Camici, Helmut Fuchs, Valerie Gailus-Durner, Martin Hrabě de Angelis, Thomas F. Lüscher, Wolfram Ruf, Felix C. Tanner
Publikováno v:
Haematologica, Vol 105, Iss 10 (2019)
Tissue factor is highly expressed in sub-endothelial tissue. The extracellular allosteric disulfide bond Cys186-Cys209 of human tissue factor shows high evolutionary conservation and in vitro evidence suggests that it significantly contributes to tis
Externí odkaz:
https://doaj.org/article/9e77045e036d4067992ce4f520c8687c
Autor:
Nina Lenherr, Viktoria A. Pfeifle, Stefan Holland-Cunz, Susanna H. M. Sluka, Beat Thöny, Gabor Szinnai, Martina Huemer, Marianne Rohrbach, Ralph Fingerhut
Publikováno v:
International Journal of Neonatal Screening, Vol 3, Iss 3, p 24 (2017)
We describe a term born boy of non-consanguineous Swiss parents with tetrahydrobiopterine (BH4)-responsive Phenylketonuria (PKU) and Hirschsprung disease with unusual neonatal presentation. The child presented with floppiness, irritability, recurrent
Externí odkaz:
https://doaj.org/article/7e4f58b2270547e7b03b66b1442f151a
Autor:
Ralph Fingerhut, Susanna H. M. Sluka
Publikováno v:
International Journal of Neonatal Screening, Vol 2, Iss 4, p 11 (2016)
The Perkin Elmer Genetic Screening Processor (GSP)™ is a fully automated system for the processing of immunoassays for thyroid stimulating hormone (TSH), 17-hydroxyprogesterone (17-OHP), immuno reactive trypsin (IRT), biotinidase, and total T4, as
Externí odkaz:
https://doaj.org/article/94c70bcae07845bf85bc4bef696b1ad9
Autor:
Bernhard G. Herrmann, Bernd Timmermann, Susanna H. M. Sluka, Jiri Forejt, Ralf Herwig, Heiner Kuhl, Marta Caparros, Matthias Lienhard, Markus Morkel, Christina Grimm, Alexandra L. Farrall
Publikováno v:
Cancer research : an official organ of the American Association for Cancer Research
Genetic predisposition affects the penetrance of tumor-initiating mutations, such as APC mutations that stabilize β-catenin and cause intestinal tumors in mice and humans. However, the mechanisms involved in genetically predisposed penetrance are no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ef41112547d481f0d3a206ff447172a
https://doi.org/10.1158/0008-5472.can-20-1480
https://doi.org/10.1158/0008-5472.can-20-1480
Autor:
Alexandra L, Farrall, Matthias, Lienhard, Christina, Grimm, Heiner, Kuhl, Susanna H M, Sluka, Marta, Caparros, Jiri, Forejt, Bernd, Timmermann, Ralf, Herwig, Bernhard G, Herrmann, Markus, Morkel
Publikováno v:
Cancer research. 81(1)
Genetic predisposition affects the penetrance of tumor-initiating mutations, such as APC mutations that stabilize β-catenin and cause intestinal tumors in mice and humans. However, the mechanisms involved in genetically predisposed penetrance are no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9d5f2a9d191a736d92f5a6bb1b952a1b
https://pubmed.ncbi.nlm.nih.gov/33154092
https://pubmed.ncbi.nlm.nih.gov/33154092
Autor:
Wolfram Ruf, Johannes Beckers, Marion Horsch, Felix C. Tanner, Tanja Klein-Rodewald, Thomas F. Lüscher, Andrea S. Rothmeier, Frauke Neff, Birgit Rathkolb, Martin Hrabě de Angelis, Simon F. Stämpfli, Anja Schrewe, Helmut Fuchs, Susanna H. M. Sluka, Alexander Akhmedov, Paula Grest, Valerie Gailus-Durner, Adrián Sanz-Moreno, Giovanni G. Camici, Eckhard Wolf
Publikováno v:
Haematologica
Haematologica 105, 2484-2495 (2019)
Haematologica 105, 2484-2495 (2019)
Tissue factor is highly expressed in sub-endothelial tissue. The extracellular allosteric disulfide bond Cys186-Cys209 of human tissue factor shows high evolutionary conservation and in vitro evidence suggests that it significantly contributes to tis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d62206c901495c434a28961bc17b765
https://pubmed.ncbi.nlm.nih.gov/33054088
https://pubmed.ncbi.nlm.nih.gov/33054088
Autor:
Ralph Fingerhut, Martin Girsberger, Silvia Azzarello-Burri, Niels J. Rupp, Anita Rauch, Susanna H. M. Sluka, Theresia Herget, Matthias R. Baumgartner, Pascal Joset
Publikováno v:
International Journal of Neonatal Screening, Vol 3, Iss 3, p 21 (2017)
Medium-chain acyl-CoA dehydrogenase deficiency (MCADD) is an autosomal recessively inherited disorder of fatty acid oxidation with a potentially fatal outcome in undiagnosed patients. The introduction of tandem mass spectrometry into newborn screenin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35fa3677afb1477cc27ba6b5f03fc5c7
https://www.mdpi.com/2409-515X/3/3/21
https://www.mdpi.com/2409-515X/3/3/21
Publikováno v:
Frontiers in Pediatrics
Congenital adrenal hyperplasia (CAH) is one of the most frequent autosomal recessive diseases in Europe. Treatment is a challenge for pediatric endocrinologists. Important parameters to judge the outcome are adult height and menstrual cycle. We repor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08fe54953f9adda7738487a0da1b9273
https://doi.org/10.3389/fped.2017.00035
https://doi.org/10.3389/fped.2017.00035
Autor:
Stefan Holland-Cunz, Gabor Szinnai, Viktoria A. Pfeifle, Beat Thöny, Susanna H. M. Sluka, Nina Lenherr, Martina Huemer, Ralph Fingerhut, Marianne Rohrbach
Publikováno v:
International Journal of Neonatal Screening, Vol 3, Iss 3, p 24 (2017)
We describe a term born boy of non-consanguineous Swiss parents with tetrahydrobiopterine (BH4)-responsive Phenylketonuria (PKU) and Hirschsprung disease with unusual neonatal presentation. The child presented with floppiness, irritability, recurrent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2384617bf42ea38e9a2f3c73301020a
https://doi.org/10.3390/ijns3030024
https://doi.org/10.3390/ijns3030024
Autor:
Anders Hallenberg, Nicolle Kränkel, Lubor Borsig, Thomas F. Lüscher, Izabela Rozenberg, Jan Borén, Ulf Landmesser, Susanna H. M. Sluka, Einar E. Eriksson, Felix C. Tanner, Pierre Rotzius, Pavani Mocharla
Publikováno v:
PLoS ONE
PloS one
PLoS ONE, Vol 6, Iss 7, p e21675 (2011)
PloS one
PLoS ONE, Vol 6, Iss 7, p e21675 (2011)
Atherosclerosis is an inflammatory disease characterized by accumulation of leukocytes in the arterial intima. Members of the selectin family of adhesion molecules are important mediators of leukocyte extravasation. However, it is unclear whether L-s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::340d7cf69773f11694cfe80af0a5b19a
http://europepmc.org/articles/PMC3132176
http://europepmc.org/articles/PMC3132176