Abnormal interaction of motor neuropathy-associated mutant HspB8 (Hsp22) forms with the RNA helicase Ddx20 (gemin3)
Open Access
- 1 September 2010
- journal article
- research article
- Published by Elsevier BV in Cell Stress and Chaperones
- Vol. 15 (5), 567-582
- https://doi.org/10.1007/s12192-010-0169-y
Abstract
No abstract availableKeywords
This publication has 80 references indexed in Scilit:
- Why proteins without an α-crystallin domain should not be included in the human small heat shock protein family HSPBCell Stress and Chaperones, 2010
- The pivotal role of the β7 strand in the intersubunit contacts of different human small heat shock proteinsCell Stress and Chaperones, 2010
- Chaperone Hsp27, a Novel Subunit of AUF1 Protein Complexes, Functions in AU-Rich Element-Mediated mRNA DecayMolecular and Cellular Biology, 2008
- DEAD-Box Protein-103 (DP103, Ddx20) Is Essential for Early Embryonic Development and Modulates Ovarian Morphology and FunctionEndocrinology, 2008
- Recruitment of phosphorylated small heat shock protein Hsp27 to nuclear speckles without stressExperimental Cell Research, 2007
- DExD/H box RNA helicases: multifunctional proteins with important roles in transcriptional regulationNucleic Acids Research, 2006
- αB-Crystallin mutation in dilated cardiomyopathies: Low prevalence in a consecutive series of 200 unrelated probandsBiochemical and Biophysical Research Communications, 2006
- αB-crystallin mutation in dilated cardiomyopathyBiochemical and Biophysical Research Communications, 2006
- Hsp27 Enhances Recovery of Splicing as well as Rephosphorylation of SRp38 after Heat ShockMolecular Biology of the Cell, 2006
- Some properties of human small heat shock protein Hsp22 (H11 or HspB8)Biochemical and Biophysical Research Communications, 2004