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Patricia Ruiz Noppinger

Researcher at Charité

Publications -  12
Citations -  1839

Patricia Ruiz Noppinger is an academic researcher from Charité. The author has contributed to research in topics: Estrogen receptor & Regulation of gene expression. The author has an hindex of 12, co-authored 12 publications receiving 1705 citations. Previous affiliations of Patricia Ruiz Noppinger include Max Planck Society.

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Hdac2 regulates the cardiac hypertrophic response by modulating Gsk3 beta activity.

TL;DR: It is shown that histone deacetylase-2 (Hdac2) regulates expression of many fetal cardiac isoforms and that Hdac1 and Gsk3β are components of a regulatory pathway providing an attractive therapeutic target for the treatment of cardiac hypertrophy and heart failure.
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The mammalian gene function resource: the international knockout mouse consortium

Allan Bradley, +83 more
- 12 Sep 2012 - 
TL;DR: The IKMC materials considerably enhance functional gene annotation of the mammalian genome and will have a major impact on future biomedical research.
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Female sex and estrogen receptor-β attenuate cardiac remodeling and apoptosis in pressure overload

TL;DR: Both female sex and ERbeta attenuate the development of fibrosis and apoptosis, thus slowing the progression to heart failure, and the number of apoptotic nuclei was increased in both sexes of ERbeta(-/-)/TAC mice, most prominent in males.
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A critical review of fundamental controversies in the field of GPR30 research.

TL;DR: This review revisits the inconsistencies that still exist in the literature and focuses on selected publications that basically address the following two questions: what is the evidence for and against the hypothesis that GPR30 acts as an estrogen receptor?
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Expression Pattern of G Protein-Coupled Receptor 30 in LacZ Reporter Mice

TL;DR: The objective of this study was to identify cell types that express GPR30 in vivo by analyzing a mutant mouse model that harbors a lacZ reporter (Gpr30-lacZ) in the Gpr30 locus leading to a partial deletion of the G PR30 coding sequence.