Publications by authors named "Mark Screen"

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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition).
Daniel J Klionsky, Kotb Abdelmohsen, Akihisa Abe, Md Joynal Abedin, Hagai Abeliovich, Mark Screen

Autophagy· October 2016

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Gene expression profiling in tibial muscular dystrophy reveals unfolded protein response and altered autophagy.
Mark Screen, Olayinka Raheem, Jeanette Holmlund-Hampf, Per Harald Jonson, Sanna Huovinen

PLoS One· May 2015

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Abnormal splicing of NEDD4 in myotonic dystrophy type 2: possible link to statin adverse reactions.
Mark Screen, Per Harald Jonson, Olayinka Raheem, Johanna Palmio, Reijo Laaksonen

Am J Pathol· August 2014

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Atypical phenotypes in titinopathies explained by second titin mutations.
Anni Evilä, Anna Vihola, Jaakko Sarparanta, Olayinka Raheem, Johanna Palmio, Mark Screen

Ann Neurol· February 2014

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Welander distal myopathy is caused by a mutation in the RNA-binding protein TIA1.
Peter Hackman, Jaakko Sarparanta, Sara Lehtinen, Anna Vihola, Anni Evilä, Mark Screen

Ann Neurol· April 2013

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Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy.
Jaakko Sarparanta, Per Harald Jonson, Christelle Golzio, Satu Sandell, Helena Luque, Mark Screen

Nat Genet· February 2012

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Cathepsin proteases have distinct roles in trophoblast function and vascular remodelling.
Mark Screen, Wendy Dean, James C Cross, Myriam Hemberger

Development· October 2008

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