Ulla Hass
Brunel University London
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Featured researches published by Ulla Hass.
Endocrinology | 2015
Walter Lichtensteiger; Catherine Bassetti-Gaille; Oliver Faass; Marta Axelstad; Julie Boberg; Sofie Christiansen; Hubert Rehrauer; Jelena Kühn Georgijevic; Ulla Hass; Andreas Kortenkamp; Margret Schlumpf
The study addressed the question whether gene expression patterns induced by different mixtures of endocrine disrupting chemicals (EDCs) administered in a higher dose range, corresponding to 450×, 200×, and 100× high-end human exposure levels, could be characterized in developing brain with respect to endocrine activity of mixture components, and which developmental processes were preferentially targeted. Three EDC mixtures, A-Mix (anti-androgenic mixture) with 8 antiandrogenic chemicals (di-n-butylphthalate, diethylhexylphthalate, vinclozolin, prochloraz, procymidone, linuron, epoxiconazole, and DDE), E-Mix (estrogenic mixture) with 4 estrogenic chemicals (bisphenol A, 4-methylbenzylidene camphor, 2-ethylhexyl 4-methoxycinnamate, and butylparaben), a complex mixture, AEP-Mix, containing the components of A-Mix and E-Mix plus paracetamol, and paracetamol alone, were administered by oral gavage to rat dams from gestation day 7 until weaning. General developmental endpoints were not affected by EDC mixtures or paracetamol. Gene expression was analyzed on postnatal day 6, during sexual brain differentiation, by exon microarray in medial preoptic area in the high-dose group, and by real-time RT-PCR in medial preoptic area and ventromedial hypothalamus in all dose groups. Expression patterns were mixture, sex, and region specific. Effects of the analgesic drug paracetamol, which exhibits antiandrogenic activity in peripheral systems, differed from those of A-Mix. All mixtures had a strong, mixture-specific impact on genes encoding for components of excitatory glutamatergic synapses and genes controlling migration and pathfinding of glutamatergic and GABAergic neurons, as well as genes linked with increased risk of autism spectrum disorders. Because development of glutamatergic synapses is regulated by sex steroids also in hippocampus, this may represent a general target of ECD mixtures.
Archive | 2015
Sofie Christiansen; Ulla Hass
SETAC Europe 24th Annual Meeting | 2014
Henrik Holbech; Poul Bjerregaard; Ulla Hass; Sofie Christiansen
Archive | 2014
Sofie Christiansen; Ulla Hass
Archive | 2013
Karen Mandrup; Julie Boberg; Kirsten Pilegaard; Ulla Hass
Archive | 2013
Pernille Rosenskjold Jacobsen; Sofie Christiansen; Ulla Hass
15th European Congress of Endocrinology | 2013
Julie Boberg; Louise Krag Isling; Sofie Christiansen; Marta Axelstad; Pernille Rosenskjold Jacobsen; Ulla Hass
Archive | 2012
Ulla Hass; Sofie Christiansen; Julie Broberg; Anne Marie Vinggaard; Anna-Maria Andersson; Niels Erik Skakkebæk; Katrine Bay; Henrik Holbech; Karin Lund Kinnberg; Poul Bjerregaard
Archive | 2012
Dorthe Nørgaard Andersen; Lise Møller; Helle Buchardt Boyd; Julie Boberg; Marta Axelstad Petersen; Sofie Christiansen; Ulla Hass; Pia Bruun Poulsen; Maria Strandesen; Daniela Bach
Archive | 2012
Ulla Hass; Sofie Christiansen; Marta Axelstad Petersen; Julie Boberg; Anna-Maria Andersson; Niels Erik Skakkebæk; Katrine Bay; Henrik Holbech; Karin Lund Kinnberg; Poul Bjerregaard