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Astrid Novosel

Researcher at Ludwig Maximilian University of Munich

Publications -  6
Citations -  3737

Astrid Novosel is an academic researcher from Ludwig Maximilian University of Munich. The author has contributed to research in topics: microRNA & Leishmaniasis. The author has an hindex of 3, co-authored 6 publications receiving 3531 citations.

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Journal ArticleDOI

A mammalian microRNA expression atlas based on small RNA library sequencing.

TL;DR: A relatively small set of miRNAs, many of which are ubiquitously expressed, account for most of the differences in miRNA profiles between cell lineages and tissues.
Journal ArticleDOI

Congenital visceral leishmaniasis.

TL;DR: A case of VL in a German infant, who never had been to a VL-endemic area, is described, most likely, the parasite was congenitally transmitted from the asymptomatic mother to her child.
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Multiple pheochromocytomas and paragangliomas in a young patient carrying a SDHD gene mutation.

TL;DR: Investigations including dopamine-positron emission tomography demonstrated bilateral adrenal tumours, a further right-sided paravertebral tumour as well as bilateral cervical glomus tumours and genetic testing revealed a germline mutation in the succinate dehydrogenase subunit D gene.
Journal Article

Congenital visceral leishmaniasis [letter]

TL;DR: A case of VL is described in a German infant who never had been to a VL-endemic area and who had a 4-week history of intermittent fever recurrent upper respiratory tract infections and failure to thrive.
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The impact of T(h)1/T(h)2 response variations on risk of developing childhood leukaemia: A pilot study.

TL;DR: The aims in this study are to collect and catalogue archived paediatric ALL and non-ALL control DNA samples from centres around Europe; to expand the collected stocks by whole genome amplification (WGA); and to determine the combination of immune response gene-related SNPs in paediatricall patients while piloting a high-throughput protocol for determining patterns of single nucleotide polymorphisms in multiple genes.