Author

N. V. Morgan

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Cell Biology· 3

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 3 Research Focus:cell type annotation· 3 Approach:experimental assay· 3 Organism:human· 3 Research Focus:differential expression· 1 Assay:metabolomics· 1 Organism:mouse· 1 Research Focus:protein folding & dynamics· 1

Frequent Co-Authors

A. O. Khan· 2 shared A. J. Murphy· 1 shared A. Khan· 1 shared A. Maclachlan· 1 shared A. Slater· 1 shared A. Tcherepanov· 1 shared A. V. Pisarev· 1 shared D. Freire· 1 shared

Activity by Year

2018-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 16 mutual co-author links

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2 shared papersCell Biology

A. O. Khan

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Cell BiologybioRxivFeb 12, 2023

Efficient megakaryopoiesis and platelet production require phospholipid remodeling and PUFA uptake through CD36

M. N. Barrachina, G. Pernes, I. C. Becker…·K. R. Machlus

This study identifies the role of phospholipid remodeling and PUFA uptake via CD36 in megakaryopoiesis and platelet production, showing dietary fatty acids impact platelet counts.

DOI 10.1038/s44161-023-00305-y

mousehuman

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Cell BiologyHaematologicaPeer-reviewedDec 17, 2020

Post-translational polymodification of β1 tubulin regulates motor protein localisation in platelet production and function

A. O. Khan, A. Slater, A. Maclachlan…·N. V. Morgan

The paper investigates how post-translational polymodifications of β1 tubulin regulate motor protein localization in platelet production and function using patient data, iPSC-derived megakaryocytes, and platelets.

DOI 10.3324/haematol.2020.270793

humanproteomics

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Cell BiologybioRxivFeb 18, 2018

Role of the novel endoribonuclease SLFN14 and its disease causing mutations in ribosomal degradation

S. J. Fletcher, V. P. Pisareva, A. Khan…·A. V. Pisarev

This study investigates the role of SLFN14 and its disease-causing mutations in ribosomal degradation and platelet dysfunction.

DOI 10.1261/rna.066415.118

humanexperimental assay

𝕏 PostBluesky