Ngā hua rapu - Birgit Stallmeyer
- E whakaatu ana i te 1 - 20 hua o te 27
- Haere ki te Whārangi Whai Ake
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Nitric oxide triggers enhanced induction of vascular endothelial growth factor expression in cultured keratinocytes (HaCaT) and during cutaneous wound repair mā Stefan L. Frank, Birgit Stallmeyer, Heiko Kämpfer, Nicole Kolb, Josef Pfeilschifter
I whakaputaina 1999Artigo -
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Large and Sustained Induction of Chemokines during Impaired Wound Healing in the Genetically Diabetic Mouse: Prolonged Persistence of Neutrophils and Macrophages during the Late Ph... mā Christian Wetzler, Heiko Kämpfer, Birgit Stallmeyer, Josef Pfeilschifter, Stefan L. Frank
I whakaputaina 2000Artigo -
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Molybdenum co‐factor biosynthesis: the <i>Arabidopsis thaliana</i> cDNA <i>cnx1</i> encodes a multifunctional two‐domain protein homologous to a mammalian neuroprotein, the insect... mā Birgit Stallmeyer, Michael Nerlich, Jochen Schiemann, Henner Brinkmann, Ralf R. Mendel
I whakaputaina 1995Artigo -
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Overlapping Cardiac Phenotype Associated with a Familial Mutation in the Voltage Sensor of the KCNQ1 Channel mā Ulrike Henrion, Sven Zumhagen, Katja Steinke, Nathalie Strutz‐Seebohm, Birgit Stallmeyer, Florian Läng, Eric Schulze‐Bahr, Guiscard Seebohm
I whakaputaina 2012Artigo -
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Gain‐of‐function mutation in <scp>TASK</scp>‐4 channels and severe cardiac conduction disorder mā Corinna Friedrich, Susanne Rinné, Sven Zumhagen, Aytuğ K. Kiper, Nicole Silbernagel, Michael F. Netter, Birgit Stallmeyer, Eric Schulze‐Bahr, Niels Decher
I whakaputaina 2014Artigo -
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Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type I mā Martin Kruse, Eric Schulze‐Bahr, Valerie A. Corfield, Alf Beckmann, Birgit Stallmeyer, Güven Kurtbay, Iris Ohmert, Ellen Schulze-Bahr, Paul A. Brink, Olaf Pongs
I whakaputaina 2009Artigo -
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Familial Sinus Node Disease Caused by a Gain of GIRK (G-Protein Activated Inwardly Rectifying K <sup>+</sup> Channel) Channel Function mā Johanna Kuß, Birgit Stallmeyer, Matthias Goldstein, Susanne Rinné, Christiane Pees, Sven Zumhagen, Guiscard Seebohm, Niels Decher, Lutz Pott, Marie‐Cécile Kienitz, Eric Schulze‐Bahr
I whakaputaina 2019Artigo -
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Mutational spectrum in the Ca2+-activated cation channel gene TRPM4 in patients with cardiac conductance disturbances mā Birgit Stallmeyer, Sven Zumhagen, Isabelle Denjoy, Guillaume Duthoit, Jean‐Louis Hébert, Xavier Ferrer, Svetlana Maugenre, Wilhelm Schmitz, Uwe Kirchhefer, Ellen Schulze-Bahr, Pascale Guicheney, Eric Schulze‐Bahr
I whakaputaina 2011Artigo -
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A Mutation in the G-Protein Gene <i>GNB2</i> Causes Familial Sinus Node and Atrioventricular Conduction Dysfunction mā Birgit Stallmeyer, Johanna Kuß, S. Kotthoff, Sven Zumhagen, Kirsty Vowinkel, Susanne Rinné, Lina A. Matschke, Corinna Friedrich, Ellen Schulze-Bahr, Stephan Rust, Guiscard Seebohm, Niels Decher, Eric Schulze‐Bahr
I whakaputaina 2017Artigo -
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DDX3Y is likely the key spermatogenic factor in the AZFa region that contributes to human non-obstructive azoospermia mā Ann‐Kristin Dicke, Adrian Pilatz, Margot J. Wyrwoll, Margus Punab, Christian Rückert, Liina Nagirnaja, Kenneth I. Aston, Donald F. Conrad, Sara Di Persio, Nina Neuhaus, Daniela Fietz, Maris Laan, Birgit Stallmeyer, Frank Tüttelmann
I whakaputaina 2023Artigo -
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Sodium permeable and “hypersensitive” <scp>TREK</scp> ‐1 channels cause ventricular tachycardia mā Niels Decher, Beatriz Ortiz‐Bonnin, Corinna Friedrich, Marcus Schewe, Aytuğ K. Kiper, Susanne Rinné, Gunnar Seemann, Rémi Peyronnet, Sven Zumhagen, Daniel Bustos, Jens Kockskämper, Peter Köhl, Steffen Just, Wendy González, Thomas Baukrowitz, Birgit Stallmeyer, Eric Schulze‐Bahr
I whakaputaina 2017Artigo -
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Estradiol regulates human QT-interval: acceleration of cardiac repolarization by enhanced KCNH2 membrane trafficking mā Lars Anneken, Stefan Baumann, Patrick Vigneault, Péter Biliczki, Corinna Friedrich, Ling Xiao, Zenawit Girmatsion, Ina Takac, Ralf P. Brandes, Stefan Kissler, Inka Wiegratz, Sven Zumhagen, Birgit Stallmeyer, Stefan H. Hohnloser, Thomas Klingenheben, Eric Schulze‐Bahr, Stanley Nattel, Joachim R. Ehrlich
I whakaputaina 2015Artigo -
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Cardiac α-Actin ( <i>ACTC1</i> ) Gene Mutation Causes Atrial-Septal Defects Associated With Late-Onset Dilated Cardiomyopathy mā Derk Frank, Ashraf Yusuf Rangrez, Corinna Friedrich, Sven Dittmann, Birgit Stallmeyer, Pankaj Yadav, Alexander Bernt, Ellen Schulze-Bahr, Ankush Borlepawar, Wolfram‐Hubertus Zimmermann, Stefan Peischard, Guiscard Seebohm, Wolfgang A. Linke, Hideo A. Baba, Marcus Krüger, Andreas Unger, Philip Usinger, Norbert Frey, Eric Schulze‐Bahr
I whakaputaina 2019Artigo -
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Human fertilization in vivo and in vitro requires the CatSper channel to initiate sperm hyperactivation mā Samuel Young, Christian Schiffer, Alice Wagner, Jannika Patz, A. Potapenko, Leonie Herrmann, Verena Nordhoff, Tim Pock, Claudia Krallmann, Birgit Stallmeyer, Albrecht Röpke, Michelina Kierzek, Cristina Biagioni, Tao Wang, Lars Haalck, Dirk Deuster, Jan N. Hansen, Dagmar Wachten, Benjamin Risse, Hermann M. Behre, Stefan Schlatt, Sabine Kliesch, Frank Tüttelmann, Christoph Brenker, Timo Strünker
I whakaputaina 2024Artigo
Ngā utauta rapu:
Ngā marau whai pānga
Biology
Genetics
Medicine
Gene
Internal medicine
Cell biology
Endocrinology
Chemistry
Mutation
QT interval
Cardiology
Long QT syndrome
Biochemistry
Receptor
Brugada syndrome
Environmental health
Exome sequencing
Genotype
Immunology
Keratinocyte
Molecular biology
Organic chemistry
Phenotype
Population
Single-nucleotide polymorphism
Sodium
Sodium channel
Wound healing
Allele
Bioinformatics