PG/16/103/32650/BHF_/British Heart Foundation/United Kingdom[Grants and Funding] - Search Results

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Subject: PG/16/103/32650/BHF_/British Heart Foundation/Uni - PubMed

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Introduction of an ancient founder glycoprotein VI mutation into the Chilean population.

Dalby A, Mezzano D, Rivera J, Watson SP, Morgan NV. Dalby A, et al. Blood Adv. 2022 Nov 22;6(22):5866-5869. doi: 10.1182/bloodadvances.2022008531. Blood Adv. 2022. PMID: 35994634 Free PMC article. No abstract available.

Prevalence and natural history of variants in the ANKRD26 gene: a short review and update of reported cases.

Vyas H, Alcheikh A, Lowe G, Stevenson WS, Morgan NV, Rabbolini DJ. Vyas H, et al. Platelets. 2022 Nov 17;33(8):1107-1112. doi: 10.1080/09537104.2022.2071853. Epub 2022 May 19. Platelets. 2022. PMID: 35587581 Free PMC article. Review.

Rare missense variants in Tropomyosin-4 (TPM4) are associated with platelet dysfunction, cytoskeletal defects, and excessive bleeding.

Stapley RJ, Poulter NS, Khan AO, Smith CW, Bignell P, Fratter C, Lester W, Lowe G, Morgan NV; UK GAPP Study Group. Stapley RJ, et al. J Thromb Haemost. 2022 Feb;20(2):478-485. doi: 10.1111/jth.15584. Epub 2021 Nov 21. J Thromb Haemost. 2022. PMID: 34758189 Free article.

A novel RUNX1 exon 3 - 7 deletion causing a familial platelet disorder.

Almazni I, Chudakou P, Dawson-Meadows A, Downes K, Freson K, Mason J, Page P, Reay K, Myers B, Morgan NV; UK GAPP Study Group. Almazni I, et al. Platelets. 2022 Feb 17;33(2):320-323. doi: 10.1080/09537104.2021.1887470. Epub 2021 Feb 22. Platelets. 2022. PMID: 33616470

Heterozygous mutation SLFN14 K208N in mice mediates species-specific differences in platelet and erythroid lineage commitment.

Stapley RJ, Smith CW, Haining EJ, Bacon A, Lax S, Pisareva VP, Pisarev AV, Watson SP, Khan AO, Morgan NV. Stapley RJ, et al. Blood Adv. 2021 Jan 26;5(2):377-390. doi: 10.1182/bloodadvances.2020002404. Blood Adv. 2021. PMID: 33496736 Free PMC article.

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

Khan AO, Slater A, Maclachlan A, Nicolson PLR, Pike JA, Reyat JS, Yule J, Stapley R, Rayes J, Thomas SG, Morgan NV. Khan AO, et al. Haematologica. 2022 Jan 1;107(1):243-259. doi: 10.3324/haematol.2020.270793. Haematologica. 2022. PMID: 33327716 Free PMC article.

Novel gene variants in patients with platelet-based bleeding using combined exome sequencing and RNAseq murine expression data.

Khan AO, Stapley RJ, Pike JA, Wijesinghe SN, Reyat JS, Almazni I, Machlus KR, Morgan NV; UK GAPP Study Group. Khan AO, et al. J Thromb Haemost. 2021 Jan;19(1):262-268. doi: 10.1111/jth.15119. Epub 2020 Oct 28. J Thromb Haemost. 2021. PMID: 33021027 Free article.

A comprehensive bioinformatic analysis of 126 patients with an inherited platelet disorder to identify both sequence and copy number genetic variants.

Almazni I, Stapley RJ, Khan AO, Morgan NV. Almazni I, et al. Hum Mutat. 2020 Nov;41(11):1848-1865. doi: 10.1002/humu.24114. Epub 2020 Oct 8. Hum Mutat. 2020. PMID: 32935436

New insights into glycoprotein Ibα desialylation-mediated platelet clearance.

Yule J, Morgan NV, Poulter NS. Yule J, et al. Platelets. 2020 Jul 3;31(5):621-623. doi: 10.1080/09537104.2020.1764922. Epub 2020 Jun 4. Platelets. 2020. PMID: 32498669 Free PMC article. No abstract available.

SLFN14 gene mutations associated with bleeding.

Stapley RJ, Pisareva VP, Pisarev AV, Morgan NV. Stapley RJ, et al. Platelets. 2020;31(3):407-410. doi: 10.1080/09537104.2019.1648781. Epub 2019 Aug 4. Platelets. 2020. PMID: 31378119 Free PMC article. Review. No abstract available.

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