Publications by authors named "Astrid Grimme"

2Publications

ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity.

Authors:
Hiromi Hirata Indrajit Nanda Anne van Riesen Gai McMichael Hao Hu Melanie Hambrock Marie-Amélie Papon Ute Fischer Sylviane Marouillat Can Ding Servane Alirol Melanie Bienek Sabine Preisler-Adams Astrid Grimme Dominik Seelow Richard Webster Eric Haan Alastair MacLennan Werner Stenzel Tzu Ying Yap Alison Gardner Lam Son Nguyen Marie Shaw Nicolas Lebrun Stefan A Haas Wolfram Kress Thomas Haaf Elke Schellenberger Jamel Chelly Géraldine Viot Lisa G Shaffer Jill A Rosenfeld Nancy Kramer Rena Falk Dima El-Khechen Luis F Escobar Raoul Hennekam Peter Wieacker Christoph Hübner Hans-Hilger Ropers Jozef Gecz Markus Schuelke Frédéric Laumonnier Vera M Kalscheuer

Am J Hum Genet 2013 May 25;92(5):681-95. Epub 2013 Apr 25.

Center for Frontier Research, National Institute of Genetics, Precursory Research for Embryonic Science and Technology, Japan Science and Technology Agency, Mishima 411-8540, Japan.

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May 2013

Common pathological mutations in PQBP1 induce nonsense-mediated mRNA decay and enhance exclusion of the mutant exon.

Authors:
Luciana Musante Stella-Amrei Kunde Tina O Sulistio Ute Fischer Astrid Grimme Suzanna G M Frints Charles E Schwartz Francisco Martínez Corrado Romano Hans-Hilger Ropers Vera M Kalscheuer

Hum Mutat 2010 Jan;31(1):90-8

Max-Planck-Institute for Molecular Genetics, D-14195 Berlin, Germany.

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January 2010