Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Nikolai Dicke"'
Autor:
Rebekka Vogtmann, Elisabeth Kühnel, Nikolai Dicke, Rikst Nynke Verkaik-Schakel, Torsten Plösch, Hubert Schorle, Violeta Stojanovska, Florian Herse, Angela Köninger, Rainer Kimmig, Elke Winterhager, Alexandra Gellhaus
Publikováno v:
Frontiers in Endocrinology, Vol 10 (2019)
The anti-angiogenic soluble fms-like tyrosine kinase 1 (sFLT1) is one of the candidates in the progression of preeclampsia, often associated with fetal growth restriction (FGR). Therapeutic agents against preeclampsia with/without FGR, as well as ade
Externí odkaz:
https://doaj.org/article/69b6b9d0a8f84f35aadf653ac1b94b86
Autor:
Oliver Tress, Marta Maglione, Armin Zlomuzica, Dennis May, Nikolai Dicke, Joachim Degen, Ekrem Dere, Helmut Kettenmann, Dieter Hartmann, Klaus Willecke
Publikováno v:
PLoS Genetics, Vol 7, Iss 7, p e1002146 (2011)
Gap junction channels are intercellular conduits that allow diffusional exchange of ions, second messengers, and metabolites. Human oligodendrocytes express the gap junction protein connexin47 (Cx47), which is encoded by the GJC2 gene. The autosomal
Externí odkaz:
https://doaj.org/article/8c5580de9b074600841a02b4205d381a
Autor:
Rikst Nynke Verkaik-Schakel, Angela Kon¨inger, Torsten Plos¨ch, Alexandra Gellhaus, Mahsa Matin, Elisabeth Kuh¨nel, Jacqueline Heupel, Rainer Kimmig, Florian Herse, Rebekka Vogtmann, Violeta Stojanovska, Nikolai Dicke, Henning Hagmann, Elke Winterhager, Hubert Schorle
Publikováno v:
Pregnancy Hypertension. 17:S30-S31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60eae2306ee9be4c535ac31e6fd66444
https://doi.org/10.1016/j.preghy.2019.08.153
https://doi.org/10.1016/j.preghy.2019.08.153
Autor:
Alexander V. Gourine, Robert Eason, Nikolai Dicke, Klaus Willecke, Nephtali Marina, Nicholas Dale, Rachid id Bihi, Robert T. R. Huckstepp, K. Michael Spyer
Publikováno v:
The Journal of Physiology. 588:3901-3920
Arterial PCO2, a major determinant of breathing, is detected by chemosensors located in the brainstem. These are important for maintaining physiological levels of PCO2 in the blood and brain, yet the mechanisms by which the brain senses CO(2) remain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad64993689c566c2dca94df1c7ef2f5f
https://doi.org/10.1113/jphysiol.2010.192088
https://doi.org/10.1113/jphysiol.2010.192088
Autor:
Oliver Tress, Julia Hecker, Alexandra Gellhaus, Nikolai Dicke, Nicole Pielensticker, Klaus Willecke, Tobias Bald, Elke Winterhager, Joachim Degen
In order to study the specific function of connexin-26 (Cx26, also known as gap junction beta-2 protein; Gjb2), we generated knockin mice that expressed either a floxed lacZ reporter or, after Cre-mediated deletion, connexin-32 (Cx32)-coding DNA, bot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d994f58e361da43b441e871c9229350f
https://www.ncbi.nlm.nih.gov/pubmed/21807945
https://www.ncbi.nlm.nih.gov/pubmed/21807945
Autor:
Klaus Willecke, Joachim Degen, Nikolai Dicke, Melanie Jokwitz, Nicola Strenzke, Tobias Moser, Melanie Schütz
Publikováno v:
European journal of cell biology. 90(10)
Functional gap junction channels composed of certain connexin proteins are essential for the function of the cochlea. Homozygous deficiency in the Gjb2 (mice) or GJB2 (human) gene coding for connexin26 (Cx26) in the cochlea leads to hearing impairmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef023aa9a7993546aa6352370dbc9011
https://pubmed.ncbi.nlm.nih.gov/21813206
https://pubmed.ncbi.nlm.nih.gov/21813206
Autor:
Klaus Willecke, Nikolai Dicke, Alexander V. Gourine, Robert Timothy Richard Huckstepp, K. Michael Spyer, Nicholas Dale, Rachid id Bihi, Robert Eason
Publikováno v:
The FASEB Journal. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::651353f77834ac9f2cb0df3b62065aa5
https://doi.org/10.1096/fasebj.24.1_supplement.1026.2
https://doi.org/10.1096/fasebj.24.1_supplement.1026.2
Autor:
Klaus Willecke, Philipp Wörsdörfer, Dawid Eckert, Volker Wulf, Reinhard Bauer, Nikolai Dicke, Radoslaw Dobrowolski, Hubert Schorle, Hildegard Lechner, Gerda Hertig
Publikováno v:
Human molecular genetics. 18(15)
Mutations in the GJA1 gene coding for connexin43 (Cx43) cause oculodentodigital dysplasia (ODDD), a pleiotropic human disorder with characteristic morphologic anomalies of face, teeth, bones and digits. Interdigital webbings, also called syndactylies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ebedc5e68a1ec39cfcb811099f7dfcd
https://pubmed.ncbi.nlm.nih.gov/19439426
https://pubmed.ncbi.nlm.nih.gov/19439426