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The molecular chaperone cysteine string protein is required for monomeric SNARE proteins to assemble in trans-complexes during human sperm acrosomal exocytosis

Biology of reproduction, 2023-02, Vol.108 (2), p.1-12

2023

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The Role of Cysteine String Protein α Phosphorylation at Serine 10 and 34 by Protein Kinase Cγ for Presynaptic Maintenance

The Journal of neuroscience, 2018-01, Vol.38 (2), p.278-290

2018

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Palmitoylation of the synaptic vesicle fusion machinery

Journal of neurochemistry, 2009-08, Vol.110 (4), p.1135-1149

2009

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CSPα-chaperoning presynaptic proteins

Frontiers in cellular neuroscience, 2014-04, Vol.8, p.116-116

2014

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CSPα, a Molecular Co-chaperone Essential for Short and Long-Term Synaptic Maintenance

Frontiers in neuroscience, 2017-02, Vol.11, p.39-39

2017

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A single-cross, RNA interference-based genetic tool for examining the long-term maintenance of homeostatic plasticity

Frontiers in cellular neuroscience, 2015-03, Vol.9, p.107-107

2015

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Abnormal triaging of misfolded proteins by adult neuronal ceroid lipofuscinosis-associated DNAJC5/CSPα mutants causes lipofuscin accumulation

Autophagy, 2023-01, Vol.19 (1), p.204-223

2023

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Overexpression of Cysteine-String Proteins in Drosophila Reveals Interactions with Syntaxin

The Journal of neuroscience, 1999-12, Vol.19 (23), p.10270-10279

1999

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Aggregation of mutant cysteine string protein-α via Fe-S cluster binding is mitigated by iron chelators

Nature structural & molecular biology, 2020-02, Vol.27 (2), p.192

2020

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Tissue distribution of cysteine string protein/DNAJC5 in C. elegans analysed by CRISPR/Cas9-mediated tagging of endogenous DNJ-14

Cell and tissue research, 2024-04, Vol.396 (1), p.41-55

2024

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Neurons Export Extracellular Vesicles Enriched in Cysteine String Protein and Misfolded Protein Cargo

Scientific reports, 2017-04, Vol.7 (1), p.956-12, Article 956

2017

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The 15q11.2 BP1-BP2 Microdeletion ( Burnside-Butler ) Syndrome: In Silico Analyses of the Four Coding Genes Reveal Functional Associations with Neurodevelopmental Phenotypes

International journal of molecular sciences, 2020-05, Vol.21 (9), p.3296

2020

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Neuronal ceroid lipofuscinosis with DNAJC5/CSPα mutation has PPT1 pathology and exhibit aberrant protein palmitoylation

Acta neuropathologica, 2016-04, Vol.131 (4), p.621-637

2016

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Adult-Onset Neuronal Ceroid Lipofuscinosis With a Novel DNAJC5 Mutation Exhibits Aberrant Protein Palmitoylation

Frontiers in aging neuroscience, 2022-04, Vol.14, p.829573-829573

2022

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Loss of postnatal quiescence of neural stem cells through mTOR activation upon genetic removal of cysteine string protein-α

Proceedings of the National Academy of Sciences - PNAS, 2019-04, Vol.116 (16), p.8000-8009

2019

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Phosphorylation of cysteine string protein-α up-regulates the frequency of cholinergic waves via starburst amacrine cells

Visual neuroscience, 2022-05, Vol.39, p.E003-E003, Article E003

2022

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Exploring pathway interactions to detect molecular mechanisms of disease: 22q11.2 deletion syndrome

Orphanet journal of rare diseases, 2023-10, Vol.18 (1), p.335-335, Article 335

2023

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Systems Biology in Chronic Heart Failure-Identification of Potential miRNA Regulators

International journal of molecular sciences, 2022-12, Vol.23 (23), p.15226

2022

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Proteomic Analysis of the Excretory and Secretory Proteins of Haemonchus contortus (HcESP) Binding to Goat PBMCs In Vivo Revealed Stage-Specific Binding Profiles

PloS one, 2016-07, Vol.11 (7), p.e0159796-e0159796

2016

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Pharmacological attenuation of melanoma by tryptanthrin pertains to the suppression of MITF-M through MEK/ERK signaling axis

Cellular and molecular life sciences : CMLS, 2022-09, Vol.79 (9), p.478-478, Article 478

2022

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Autosomal dominant neuronal ceroid lipofuscinosis: Clinical features and molecular basis

Clinical genetics, 2021-01, Vol.99 (1), p.111-118

2021

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Identification, characterization, and prognosis investigation of pivotal genes shared in different stages of breast cancer

Scientific reports, 2023-05, Vol.13 (1), p.8447-8447, Article 8447

Rommasi, Foad

2023

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High Functioning Autism with Missense Mutations in Synaptotagmin-Like Protein 4 (SYTL4) and Transmembrane Protein 187 (TMEM187) Genes: SYTL4- Protein Modeling, Protein-Protein Interaction, Expression Profiling and MicroRNA Studies

International journal of molecular sciences, 2019-07, Vol.20 (13), p.3358

2019

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Analysis of genome-wide knockout mouse database identifies candidate ciliopathy genes

Scientific reports, 2022-12, Vol.12 (1), p.20791-17, Article 20791

2022

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A cluster of palmitoylated cysteines are essential for aggregation of cysteine-string protein mutants that cause neuronal ceroid lipofuscinosis

Scientific reports, 2017-01, Vol.7 (1), p.10-10, Article 10

2017

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The molecular chaperone cysteine string protein is required for monomeric SNARE proteins to assemble in trans-complexes during human sperm acrosomal exocytosis

The Role of Cysteine String Protein α Phosphorylation at Serine 10 and 34 by Protein Kinase Cγ for Presynaptic Maintenance

Palmitoylation of the synaptic vesicle fusion machinery

CSPα-chaperoning presynaptic proteins

CSPα, a Molecular Co-chaperone Essential for Short and Long-Term Synaptic Maintenance

A single-cross, RNA interference-based genetic tool for examining the long-term maintenance of homeostatic plasticity

Abnormal triaging of misfolded proteins by adult neuronal ceroid lipofuscinosis-associated DNAJC5/CSPα mutants causes lipofuscin accumulation

Overexpression of Cysteine-String Proteins in Drosophila Reveals Interactions with Syntaxin

Aggregation of mutant cysteine string protein-α via Fe-S cluster binding is mitigated by iron chelators

Tissue distribution of cysteine string protein/DNAJC5 in C. elegans analysed by CRISPR/Cas9-mediated tagging of endogenous DNJ-14

Neurons Export Extracellular Vesicles Enriched in Cysteine String Protein and Misfolded Protein Cargo

The 15q11.2 BP1-BP2 Microdeletion ( Burnside-Butler ) Syndrome: In Silico Analyses of the Four Coding Genes Reveal Functional Associations with Neurodevelopmental Phenotypes

Neuronal ceroid lipofuscinosis with DNAJC5/CSPα mutation has PPT1 pathology and exhibit aberrant protein palmitoylation

Adult-Onset Neuronal Ceroid Lipofuscinosis With a Novel DNAJC5 Mutation Exhibits Aberrant Protein Palmitoylation

Loss of postnatal quiescence of neural stem cells through mTOR activation upon genetic removal of cysteine string protein-α

Phosphorylation of cysteine string protein-α up-regulates the frequency of cholinergic waves via starburst amacrine cells

Exploring pathway interactions to detect molecular mechanisms of disease: 22q11.2 deletion syndrome

Systems Biology in Chronic Heart Failure-Identification of Potential miRNA Regulators

Proteomic Analysis of the Excretory and Secretory Proteins of Haemonchus contortus (HcESP) Binding to Goat PBMCs In Vivo Revealed Stage-Specific Binding Profiles

Pharmacological attenuation of melanoma by tryptanthrin pertains to the suppression of MITF-M through MEK/ERK signaling axis

Autosomal dominant neuronal ceroid lipofuscinosis: Clinical features and molecular basis

Identification, characterization, and prognosis investigation of pivotal genes shared in different stages of breast cancer

High Functioning Autism with Missense Mutations in Synaptotagmin-Like Protein 4 (SYTL4) and Transmembrane Protein 187 (TMEM187) Genes: SYTL4- Protein Modeling, Protein-Protein Interaction, Expression Profiling and MicroRNA Studies

Analysis of genome-wide knockout mouse database identifies candidate ciliopathy genes

A cluster of palmitoylated cysteines are essential for aggregation of cysteine-string protein mutants that cause neuronal ceroid lipofuscinosis

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