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Manuel Mark

Researcher at University of Strasbourg

Publications -  22
Citations -  9931

Manuel Mark is an academic researcher from University of Strasbourg. The author has contributed to research in topics: Retinoic acid & Retinoic acid receptor. The author has an hindex of 14, co-authored 22 publications receiving 9340 citations. Previous affiliations of Manuel Mark include Centre national de la recherche scientifique & French Institute of Health and Medical Research.

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High-throughput discovery of novel developmental phenotypes

Mary E. Dickinson, +85 more
- 22 Sep 2016 - 
TL;DR: It is shown that human disease genes are enriched for essential genes, thus providing a dataset that facilitates the prioritization and validation of mutations identified in clinical sequencing efforts and reveals that incomplete penetrance and variable expressivity are common even on a defined genetic background.
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FUNCTION OF RETINOID NUCLEAR RECEPTORS: Lessons from Genetic and Pharmacological Dissections of the Retinoic Acid Signaling Pathway During Mouse Embryogenesis

TL;DR: Genetic and pharmacological studies in the mouse demonstrate that RXR/RAR heterodimers in which RXR is either transcriptionally active or silent are involved in the transduction of the RA signal during prenatal development, and the physiological role of RA and its receptors cannot be extrapolated from teratogenesis studies using retinoids in excess.
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Homeotic transformation of the occipital bones of the skull by ectopic expression of a homeobox gene.

TL;DR: This work has expressed the Hox-4.2 gene more rostrally than its normal mesoderm anterior boundary of expression, which results in a homeotic transformation of the occipital bones towards a more posterior phenotype into structures that resemble cervical vertebrae, which supports the 'posterior prevalence' model.
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Mice deficient in cellular retinoic acid binding protein II (CRABPII) or in both CRABPI and CRABPII are essentially normal

TL;DR: The present results demonstrate that CRABP are not critically involved in the retinoic acid signaling pathway, and that none of the functions previously proposed for CRABPs are important enough to account for their evolutionary conservation.