Markus Storbeck und Brunhilde Wirth - Info zur Person

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VAMP1 mutations cause a new type of congenital CMMCwww.cmmc-uni-koeln.de › show-news-detail › vam...

www.cmmc-uni-koeln.de

· Dr. Markus Storbeck (l.), Andreas delle Vedove MD/PhD (r.) and Prof. Dr. Brunhilde Wirth, Foto: Uniklinik Köln. The research group of Prof.

Plastin 3 is upregulated in iPSC-derived motoneurons from ...ScienceOpen

www.scienceopen.com

... Seyyed Mohsen Hosseini-Barkooie , Markus Storbeck , Noemi Fusaki , Renata Lonigro Raoul Heller , Min Jeong Kye , Oliver Brüstle Brunhilde Wirth.

Vol 99, Issue 6, Pages (1 December 2016)ScienceDirect

www.sciencedirect.com

Andrea Delle Vedove, Markus Storbeck, Raoul Heller, Irmgard Hölker, ... Brunhilde Wirth. Pages : Download PDF · Previous vol/issue · Next vol/issue.

CAPRIN1 P512L causes aberrant protein aggregation and ...

link.springer.com

von A Delle Vedove · — Andrea Delle Vedove, Anixa Muiños-Bühl, Markus Storbeck, Irmgard Hölker & Brunhilde Wirth. Center for Molecular and Cellular Bioengineering, ... › article

Publications | Human Genetics Uniklinik Köln - uk-koeln.de

humangenetik.uk-koeln.de

WebMarkus Storbeck, Kristina Hupperich, John Antonydas Gaspar, Kesavan Meganathan, Lilian Martínez Carrera, Radu Wirth, Agapios Sachinidis, Brunhilde Wirth Neuronal …

Expanding the phenotype of BICD2 mutations toward skeletal muscle...

n.neurology.org

... Wolfgang A. Linke, Lilian Martinez-Carrera, Markus Storbeck, Brunhilde Wirth, Sabine Hoffjan, Matthias Vorgerd. First published October 26, ...

Exon mapping | PLOS ONE

journals.plos.org

Markus Storbeck, Kristina Hupperich, [ ... ], Brunhilde Wirth. Gene Expression, Single Nucleotide Variant and Fusion Transcript Discovery in Archival ... › browse

RNA processing | PLOS ONE

journals.plos.org

Markus Storbeck, Kristina Hupperich, [ ... ], Brunhilde Wirth. A Pan-Cancer Analysis of Transcriptome Changes Associated with Somatic Mutations in U2AF › browse

Altmetric – Plastin 3 is upregulated in iPSC-derived motoneurons from...

springeropen.altmetric.com

... Eckert, Seyyed Mohsen Hosseini-Barkooie, Markus Storbeck, Noemi Fusaki, Renata Lonigro, Raoul Heller, Min Jeong Kye, Oliver Brüstle, Brunhilde Wirth.

PRUNE1: a disease-causing gene for secondary microcephaly

oxfordjournals.altmetric.com

Authors. Mert Karakaya, Sanem Yilmaz, Markus Storbeck, Irmgard Hoelker, Raoul Heller, Gül Serdaroglu, Sarenur Gökben, Uluc Yis, Brunhilde Wirth[show] ... › ...

Neue Art von Muskelatrophie entdeckt - BVOU

www.bvou.net

— Dr. Markus Storbeck, Postdoktorand in der Forschungsgruppe um Humangenetikerin Prof. Dr. Brunhilde Wirth, hat Sequenzdaten von mehr als ... › neue-art-von-muskelatrophie-e...

Novel insights into SMALED2: BICD2 mutations increase ...Sigma-Aldrich

www.sigmaaldrich.com

— ... Colin D Donohoe, Irmgard Hölker, Aruljothi Mariappan, Markus Storbeck, Mirka Uhlirova, Jay Gopalakrishnan, Brunhilde Wirth.

ukk_lab_wirth_webBVOU

www.bvou.net

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Markus Storbeck und Brunhilde Wirth Person-Info