Anton Enright

Group Leader - University Lecturer

University of Cambridge

United Kingdom

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Anton Enright is a Group Leader and University Lecturer at the University of Cambridge, UK. His research focuses on malignant germ cell tumors, hematopoietic lineages, and computational genomics, as evidenced by his recent publications. His work includes the exploration of microRNA dynamics and their implications in tumor growth inhibition and cell cycle disruption.

Positions (1)

Anton Enright

University Name

Cambridge University

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Microbiome exploration

No summary provided for this position.

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Articles (17)

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2024

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2020

Collaborators (14)

Attila Molnar

University of Edinburgh

UNITED KINGDOM

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Catherine J Merrick

University of Cambridge

UNITED KINGDOM

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Paul Janssen

Tufts University School of Medicine

UNITED STATES

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Ben Skinner

Lecturer

University of Essex

UNITED KINGDOM

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Pier Paolo D'Avino

University of Cambridge

UNITED KINGDOM

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José Afonso Guerra-Assunção

University College London

UNITED KINGDOM

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Jun Wang

Senior Lecturer in Bioinformatics

Barts Cancer Institute

UNITED KINGDOM

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Jude Fitzgibbon

Professor in Personalised Cancer Medicine

Queen Mary University of London

UNITED KINGDOM

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Jessica Okosun

Clinical Senior Lecturer

Barts Cancer Institute

UNITED KINGDOM

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Miriam Maiellaro

Istituto Dermatologico San Gallicano

ITALY

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Christos Ouzounis

Professor

Aristotle University of Thessaloniki

GREECE

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David Kelsell

Queen Mary University of London

UNITED KINGDOM

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Brian Ferguson

Professor of Viral Immunity

University of Cambridge

UNITED KINGDOM

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Geoffrey L Smith

Professor

University of Oxford

UNITED KINGDOM

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Anton Enright

Research Interests

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About

Positions (1)

Microbiome exploration

Articles (17)

Population Structure and Genomic Characterisation of the Ashanti Dwarf Pig of Ghana.

Replenishing co-downregulated miR-100-5p and miR-125b-5p in malignant germ cell tumors causes growth inhibition through cell cycle disruption.

Deciphering Transcriptomic Variations in Hematopoietic Lineages: HSCs, EBs, and MKs.

CGG toolkit: Software components for computational genomics.

Correction: Targeting oncogenic microRNAs from the miR-371~373 and miR-302/367 clusters in malignant germ cell tumours causes growth inhibition through cell cycle disruption.

Targeting oncogenic microRNAs from the miR-371~373 and miR-302/367 clusters in malignant germ cell tumours causes growth inhibition through cell cycle disruption.

Testicular germ cell tumour cells release microRNA-containing extracellular vesicles that induce phenotypic and genotypic changes in cells of the tumour microenvironment.

RNA sequencing and lipidomics uncovers novel pathomechanisms in recessive X-linked ichthyosis.

Smallpox vaccination induces a substantial increase in commensal skin bacteria that promote pathology and influence the host response

Midbody Proteins Display Distinct Dynamics during Cytokinesis

The in vivo RNA structurome of the malaria parasite Plasmodium falciparum, a protozoan with an A/U-rich transcriptome

Small non-coding RNA sequencing reveals global dysregulation of piwi-interacting RNA (piRNA) expression in gonadal malignant germ cell tumours.

Correction: MiR-277/4989 regulate transcriptional landscape during juvenile to adult transition in the parasitic helminth Schistosoma mansoni.

Identification of Recurrent Mutations in the microRNA-Binding Sites of B-Cell Lymphoma-Associated Genes in Follicular Lymphoma.

3D model of harlequin ichthyosis reveals inflammatory therapeutic targets

Locating patterns in Nanopore currents using time-warped signal representation of consensus nucleotides for demultiplexing and motif detection.

Schwann cell reprogramming into repair cells increases miRNA-21 expression in exosomes promoting axonal growth.

Collaborators (14)

Attila Molnar

Catherine J Merrick

Paul Janssen

Ben Skinner

Pier Paolo D'Avino

José Afonso Guerra-Assunção

Jun Wang

Jude Fitzgibbon

Jessica Okosun

Miriam Maiellaro

Christos Ouzounis

David Kelsell

Brian Ferguson

Geoffrey L Smith

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