Dinesh C. Soares

Edinburgh, SCT EH42XU, United Kingdom

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 45 publications

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

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

Journal: Bioscience reports

Published: December 10, 2019

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

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

Journal: Investigative ophthalmology & visual science

Published: July 03, 2019

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

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

Journal: mBio

Published: March 29, 2018

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

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

Journal: Journal of cell science

Published: October 03, 2017

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

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

Journal: Nature communications

Published: May 24, 2017

Novel pathogenic mutations in C1QTNF5 support a dominant negative disease mechanism in late-onset retinal degeneration.

Novel pathogenic mutations in C1QTNF5 support a dominant negative disease mechanism in late-onset retinal degeneration.

Journal: Scientific reports

Published: April 04, 2017

A recurrent de novo mutation in ACTG1 causes isolated ocular coloboma.

A recurrent de novo mutation in ACTG1 causes isolated ocular coloboma.

Journal: Human mutation

Published: February 14, 2017

PLAA Mutations Cause a Lethal Infantile Epileptic Encephalopathy by Disrupting Ubiquitin-Mediated Endolysosomal Degradation of Synaptic Proteins.

PLAA Mutations Cause a Lethal Infantile Epileptic Encephalopathy by Disrupting Ubiquitin-Mediated Endolysosomal Degradation of Synaptic Proteins.

Journal: American journal of human genetics

Published: January 01, 2017

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.

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.

Journal: The Journal of biological chemistry

Published: December 22, 2016

HpARI Protein Secreted by a Helminth Parasite Suppresses Interleukin-33.

HpARI Protein Secreted by a Helminth Parasite Suppresses Interleukin-33.

Journal: Immunity

Published: December 12, 2016

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

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

Journal: Scientific reports

Published: November 02, 2016

Rare disruptive variants in the DISC1 Interactome and Regulome: association with cognitive ability and schizophrenia.

Rare disruptive variants in the DISC1 Interactome and Regulome: association with cognitive ability and schizophrenia.

Journal: Molecular psychiatry

Published: October 26, 2016

Showing 1-12 of 45

Last Updated: 09/26/2026