Human HspB1, HspB3, HspB5 and HspB8: Shaping these disease factors during vertebrate evolution

Structural aspects of the human small heat shock proteins related to their functional activities

(2020) Wilbert C. Boelens   CELL STRESS & CHAPERONES

Mutations in HspB1 and hereditary neuropathies

(2020) Lydia K. Muranova et al.   CELL STRESS & CHAPERONES

Small heat shock proteins in neurodegenerative diseases

(2020) Leen Vendredy et al.   CELL STRESS & CHAPERONES

N- and C-terminal regions of αB-crystallin and Hsp27 mediate inhibition of amyloid nucleation, fibril binding, and fibril disaggregation

(2020) Emily E. Selig et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Mutations in heat shock protein beta-1 (HSPB1) are associated with a range of clinical phenotypes related to different patterns of motor neuron dysfunction: A case series

(2020) Matthew Katz et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Distal hereditary motor neuropathies: Mutation spectrum and genotype–phenotype correlation

(2020) Marina Frasquet et al.   EUROPEAN JOURNAL OF NEUROLOGY

Small heat shock proteins: multifaceted proteins with important implications for life

(2019) Serena Carra et al.   CELL STRESS & CHAPERONES

Neuropathy-causing mutations in HSPB1 impair autophagy by disturbing the formation of SQSTM1/p62 bodies

(2019) Mansour Haidar et al.   Autophagy

Small Heat Shock Proteins, Big Impact on Protein Aggregation in Neurodegenerative Disease

(2019) Jack M. Webster et al.   Frontiers in Pharmacology

Characterization of human small heat shock protein HSPB1 α-crystallin domain localized mutants associated with hereditary motor neuron diseases

(2018) Stephen D. Weeks et al.   Scientific Reports

Axonal Neuropathies due to Mutations in Small Heat Shock Proteins: Clinical, Genetic, and Functional Insights into Novel Mutations

(2017) Andoni Echaniz-Laguna et al.   HUMAN MUTATION

Charcot-Marie-Tooth type 2 and distal hereditary motor neuropathy: Clinical, neurophysiological and genetic findings from a single-centre experience

(2016) Marco Luigetti et al.   CLINICAL NEUROLOGY AND NEUROSURGERY

Incorporating tree-thinking and evolutionary time scale into developmental biology

(2016) Shigehiro Kuraku et al.   DEVELOPMENT GROWTH & DIFFERENTIATION

Trends in substitution models of molecular evolution

(2015) Miguel Arenas   Frontiers in Genetics

Neuropathy- and myopathy-associated mutations in human small heat shock proteins: Characteristics and evolutionary history of the mutation sites

(2014) Rainer Benndorf et al.   MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH

Mutations of small heat shock proteins and human congenital diseases

(2013) P. N. Datskevich et al.   BIOCHEMISTRY-MOSCOW

Computational methods for Gene Orthology inference

(2011) D. M. Kristensen et al.   BRIEFINGS IN BIOINFORMATICS

HSPB1 and HSPB8 in inherited neuropathies: study of an Italian cohort of dHMN and CMT2 patients

(2011) Simona Capponi et al.   JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM

HDAC6 inhibitors reverse axonal loss in a mouse model of mutant HSPB1–induced Charcot-Marie-Tooth disease

(2011) Constantin d'Ydewalle et al.   NATURE MEDICINE

Large Potentials of Small Heat Shock Proteins

(2011) Evgeny V. Mymrikov et al.   PHYSIOLOGICAL REVIEWS

The role played by natural selection on Mendelian traits in humans

(2010) Lluis Quintana-Murci et al.   Annals of the New York Academy of Sciences

Independent evolution of the core domain and its flanking sequences in small heat shock proteins

(2010) Thomas Kriehuber et al.   FASEB JOURNAL

Increased Monomerization of Mutant HSPB1 Leads to Protein Hyperactivity in Charcot-Marie-Tooth Neuropathy

(2010) Leonardo Almeida-Souza et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

FastTree 2 – Approximately Maximum-Likelihood Trees for Large Alignments

(2010) Morgan N. Price et al.   PLoS One

Correcting the Bias of Empirical Frequency Parameter Estimators in Codon Models

(2010) Sergei Kosakovsky Pond et al.   PLoS One

Why proteins without an α-crystallin domain should not be included in the human small heat shock protein family HSPB

(2009) Guido Kappé et al.   CELL STRESS & CHAPERONES

A generalized model of gene dosage and dominant negative effects in macromolecular complexes

(2009) Reiner A. Veitia   FASEB JOURNAL

Dominance and gene dosage balance in health and disease: why levels matter!

(2009) Reiner A. Veitia et al.   JOURNAL OF PATHOLOGY

Guidelines for the nomenclature of the human heat shock proteins

(2008) Harm H. Kampinga et al.   CELL STRESS & CHAPERONES

Natural Selection on Genes that Underlie Human Disease Susceptibility

(2008) Ran Blekhman et al.   CURRENT BIOLOGY