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HpARI Protein Secreted by a Helminth Parasite Suppresses Interleukin-33

Immunity (Cambridge, Mass.), 2017-10, Vol.47 (4), p.739-751.e5

2017

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A structurally distinct TGF-β mimic from an intestinal helminth parasite potently induces regulatory T cells

Nature communications, 2017-11, Vol.8 (1), p.1741-13, Article 1741

2017

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Ablation of EYS in zebrafish causes mislocalisation of outer segment proteins, F-actin disruption and cone-rod dystrophy

Scientific reports, 2017-04, Vol.7 (1), p.46098-46098, Article 46098

2017

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Translation elongation factor 1A2 is encoded by one of four closely related eef1a genes and is dispensable for survival in zebrafish

Bioscience reports, 2020-01, Vol.40 (1)

2020

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HIV-1 Uncoating and Reverse Transcription Require eEF1A Binding to Surface-Exposed Acidic Residues of the Reverse Transcriptase Thumb Domain

mBio, 2018-03, Vol.9 (2)

2018

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Open Science at ACS: Present and Future Opportunities for ACS Omega as We Celebrate 200 Issues

ACS omega, 2022-10, Vol.7 (41), p.36050-36051

2022

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Structural models of human eEF1A1 and eEF1A2 reveal two distinct surface clusters of sequence variation and potential differences in phosphorylation

PloS one, 2009-07, Vol.4 (7), p.e6315

2009

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DISC1: Structure, Function, and Therapeutic Potential for Major Mental Illness

ACS chemical neuroscience, 2011-11, Vol.2 (11), p.609-632

2011

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Characterization of a novel RP2-OSTF1 interaction and its implication for actin remodelling

Journal of cell science, 2018-02, Vol.131 (4), p.jcs211748-jcs211748

2018

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A structural organization for the Disrupted in Schizophrenia 1 protein, identified by high-throughput screening, reveals distinctly folded regions, which are bisected by mental illness-related mutations

The Journal of biological chemistry, 2017-04, Vol.292 (16), p.6468-6477

2017

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Specific Interaction between eEF1A and HIV RT Is Critical for HIV-1 Reverse Transcription and a Potential Anti-HIV Target

PLoS pathogens, 2015-12, Vol.11 (12), p.e1005289-e1005289

2015

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Structural analysis of the C-terminal region (modules 18-20) of complement regulator factor H (FH)

PloS one, 2012-02, Vol.7 (2), p.e32187-e32187

2012

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A Cytogenetic Abnormality and Rare Coding Variants Identify ABCA13 as a Candidate Gene in Schizophrenia, Bipolar Disorder, and Depression

American journal of human genetics, 2009-12, Vol.85 (6), p.833-846

2009

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RPGR: Its role in photoreceptor physiology, human disease, and future therapies

Experimental eye research, 2015-09, Vol.138, p.32-41

2015

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SAF-A Regulates Interphase Chromosome Structure through Oligomerization with Chromatin-Associated RNAs

Cell, 2017-06, Vol.169 (7), p.1214-1227.e18

2017

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NDE1 and NDEL1: twin neurodevelopmental proteins with similar ‘nature’ but different ‘nurture’

Biomolecular concepts, 2013-10, Vol.4 (5), p.447-464

2013

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eEF1A2 and neuronal degeneration

Biochemical Society transactions, 2009-12, Vol.37 (Pt 6), p.1293

2009

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Structure of the N-terminal Region of Complement Factor H and Conformational Implications of Disease-linked Sequence Variations

The Journal of biological chemistry, 2008-04, Vol.283 (14), p.9475-9487

2008

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ARABIDOPSIS CRINKLY4 Function, Internalization, and Turnover Are Dependent on the Extracellular Crinkly Repeat Domain

The Plant cell, 2005-04, Vol.17 (4), p.1154-1166

2005

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Energy Research at ACS in the Age of Open Access

ACS omega, 2021-03, Vol.6 (12), p.7967-7969

2021

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NDE1 and NDEL1: Multimerisation, alternate splicing and DISC1 interaction

Neuroscience letters, 2009-01, Vol.449 (3), p.228-233

2009

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The evolution of TEP1, an exceptionally polymorphic immunity gene in Anopheles gambiae

BMC evolutionary biology, 2008-10, Vol.8, p.274

2008

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Celebrating 5 Years of Open Access with ACS Omega

ACS omega, 2020-07, Vol.5 (28), p.16986-16986

2020

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Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse

Investigative ophthalmology & visual science, 2019-07, Vol.60 (8), p.2875-2887

2019

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The intermediate filament protein, vimentin, is a regulator of NOD2 activity

Gut, 2013-05, Vol.62 (5), p.695-707

2013

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HpARI Protein Secreted by a Helminth Parasite Suppresses Interleukin-33

A structurally distinct TGF-β mimic from an intestinal helminth parasite potently induces regulatory T cells

Ablation of EYS in zebrafish causes mislocalisation of outer segment proteins, F-actin disruption and cone-rod dystrophy

Translation elongation factor 1A2 is encoded by one of four closely related eef1a genes and is dispensable for survival in zebrafish

HIV-1 Uncoating and Reverse Transcription Require eEF1A Binding to Surface-Exposed Acidic Residues of the Reverse Transcriptase Thumb Domain

Open Science at ACS: Present and Future Opportunities for ACS Omega as We Celebrate 200 Issues

Structural models of human eEF1A1 and eEF1A2 reveal two distinct surface clusters of sequence variation and potential differences in phosphorylation

DISC1: Structure, Function, and Therapeutic Potential for Major Mental Illness

Characterization of a novel RP2-OSTF1 interaction and its implication for actin remodelling

A structural organization for the Disrupted in Schizophrenia 1 protein, identified by high-throughput screening, reveals distinctly folded regions, which are bisected by mental illness-related mutations

Specific Interaction between eEF1A and HIV RT Is Critical for HIV-1 Reverse Transcription and a Potential Anti-HIV Target

Structural analysis of the C-terminal region (modules 18-20) of complement regulator factor H (FH)

A Cytogenetic Abnormality and Rare Coding Variants Identify ABCA13 as a Candidate Gene in Schizophrenia, Bipolar Disorder, and Depression

RPGR: Its role in photoreceptor physiology, human disease, and future therapies

SAF-A Regulates Interphase Chromosome Structure through Oligomerization with Chromatin-Associated RNAs

NDE1 and NDEL1: twin neurodevelopmental proteins with similar ‘nature’ but different ‘nurture’

eEF1A2 and neuronal degeneration

Structure of the N-terminal Region of Complement Factor H and Conformational Implications of Disease-linked Sequence Variations

ARABIDOPSIS CRINKLY4 Function, Internalization, and Turnover Are Dependent on the Extracellular Crinkly Repeat Domain

Energy Research at ACS in the Age of Open Access

NDE1 and NDEL1: Multimerisation, alternate splicing and DISC1 interaction

The evolution of TEP1, an exceptionally polymorphic immunity gene in Anopheles gambiae

Celebrating 5 Years of Open Access with ACS Omega

Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse

The intermediate filament protein, vimentin, is a regulator of NOD2 activity

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