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Springer Nature5
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Human Genetics5
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Brunhilde Wirth results 5 · Newest (Page 1/1, per page 25)
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Author: Brunhilde Wirth ×Clear All Filters
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Nonsense-mediated messenger RNA decay of survival motor neuron 1 causes spinal muscular atrophyNARA Subscribed
Human Genetics · 2008 · Vol. 123 · Issue 2 · Springer
Lars Brichta; Lutz Garbes; Maria Jedrzejowska; Sushma-Nagaraja Grellscheid; Irmgard Holker; Katharina Zimmermann; Brunhilde Wirth
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The benzamide M344, a novel histone deacetylase inhibitor, significantly increases SMN2 RNA/protein levels in spinal muscular atrophy cellsNARA Subscribed
Human Genetics · 2006 · Vol. 120 · Issue 1 · Springer
Markus Riessland; Lars Brichta; Eric Hahnen; Brunhilde Wirth
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Evidence for a modifying pathway in SMA discordant families: reduced SMN level decreases the amount of its interacting partners and Htra2-beta1NARA Subscribed
Human Genetics · 2003 · Vol. 114 · Issue 1 · Springer
Claudia Helmken; Yvonne Hofmann; Frank Schoenen; Gabriela Oprea; Heidrun Raschke; Sabine Rudnik-Sch�neborn; Klaus Zerres; Brunhilde Wirth
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No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approachNARA Subscribed
Human Genetics · 2003 · Vol. 114 · Issue 1 · Springer
Johannes Schumacher; Andreas C. J. Otte; Tim Becker; Yuli Sun; Thomas F. Wienker; Brunhilde Wirth; Petra Franke; Rami Abou Jamra; Peter Propping; J�rgen Deckert; Markus M. N�then; Sven Cichon
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Exclusion of Htra2-β1, an up-regulator of full-length SMN2 transcript, as a modifying gene for spinal muscular atrophyNARA Subscribed
Human Genetics · 2000 · Vol. 107 · Issue 6 · Springer
Claudia Helmken; Brunhilde Wirth
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