Hasil Pencarian - Neil V Morgan

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  1. 1
    Editorial: Case reports in cardiovascular genetics and systems medicine: 2022

    Editorial: Case reports in cardiovascular genetics and systems medicine: 2022 oleh Neil V. Morgan

    Diterbitkan 2023-09-01
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  2. 2
    Gene of the issue: RUNX1 mutations and inherited bleeding

    Gene of the issue: RUNX1 mutations and inherited bleeding oleh Neil V. Morgan, Martina E. Daly

    Diterbitkan 2017-02-01
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  3. 3
    New insights into glycoprotein Ibα desialylation-mediated platelet clearance

    New insights into glycoprotein Ibα desialylation-mediated platelet clearance oleh Jack Yule, Neil V. Morgan, Natalie S. Poulter

    Diterbitkan 2020-07-01
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  4. 4
    Inherited Thrombocytopenia: Update on Genes and Genetic Variants Which may be Associated With Bleeding

    Inherited Thrombocytopenia: Update on Genes and Genetic Variants Which may be Associated With Bleeding oleh Ibrahim Almazni, Rachel Stapley, Neil V. Morgan

    Diterbitkan 2019-06-01
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  5. 5
    Inherited platelet disorders: Insight from platelet genomics using next-generation sequencing

    Inherited platelet disorders: Insight from platelet genomics using next-generation sequencing oleh Annabel Maclachlan, Steve P. Watson, Neil V. Morgan

    Diterbitkan 2017-01-01
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  6. 6
    Inherited ADAMTS13 mutations associated with Thrombotic Thrombocytopenic Purpura: a short review and update

    Inherited ADAMTS13 mutations associated with Thrombotic Thrombocytopenic Purpura: a short review and update oleh Zoe Markham-Lee, Neil V. Morgan, Jonas Emsley

    Diterbitkan 2023-01-01
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  7. 7
    SLFN14 gene mutations associated with bleeding

    SLFN14 gene mutations associated with bleeding oleh Rachel J. Stapley, Vera P. Pisareva, Andrey V. Pisarev, Neil V. Morgan

    Diterbitkan 2020-04-01
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  8. 8
    Prevalence and natural history of variants in the ANKRD26 gene: a short review and update of reported cases

    Prevalence and natural history of variants in the ANKRD26 gene: a short review and update of reported cases oleh Hrushikesh Vyas, Ahmad Alcheikh, Gillian Lowe, William S Stevenson, Neil V Morgan, David J Rabbolini

    Diterbitkan 2022-11-01
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  9. 9
    CRISPR-Cas9 Mediated Labelling Allows for Single Molecule Imaging and Resolution

    CRISPR-Cas9 Mediated Labelling Allows for Single Molecule Imaging and Resolution oleh Abdullah O. Khan, Victoria A. Simms, Jeremy A. Pike, Steven G. Thomas, Neil V. Morgan

    Diterbitkan 2017-08-01
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  10. 10
    Whole exome sequencing identifies a mutation in thrombomodulin as the genetic cause of a suspected platelet disorder in a family with normal platelet function

    Whole exome sequencing identifies a mutation in thrombomodulin as the genetic cause of a suspected platelet disorder in a family with normal platelet function oleh Annabel Maclachlan, Gerry Dolan, Charlotte Grimley, Steve P. Watson, Neil V. Morgan, on behalf of the UK GAPP Study Group

    Diterbitkan 2017-08-01
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  11. 11
    A novel RUNX1 exon 3 - 7 deletion causing a familial platelet disorder

    A novel RUNX1 exon 3 - 7 deletion causing a familial platelet disorder oleh Ibrahim Almazni, Pavel Chudakou, Alison Dawson-Meadows, Kate Downes, Kathleen Freson, Joanne Mason, Paula Page, Kim Reay, Bethan Myers, Neil V Morgan

    Diterbitkan 2022-02-01
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  12. 12
    Evaluation of the Total Thrombus-Formation System (T-TAS): application to human and mouse blood analysis

    Evaluation of the Total Thrombus-Formation System (T-TAS): application to human and mouse blood analysis oleh Rashid Al Ghaithi, Jun Mori, Zoltan Nagy, Annabel Maclachlan, Lewis Hardy, Helen Philippou, Emma Hethershaw, Neil V. Morgan, Yotis A. Senis, Paul Harrison

    Diterbitkan 2019-10-01
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  13. 13
    An adaptable analysis workflow for characterization of platelet spreading and morphology

    An adaptable analysis workflow for characterization of platelet spreading and morphology oleh Jeremy A. Pike, Victoria A. Simms, Christopher W. Smith, Neil V. Morgan, Abdullah O. Khan, Natalie S. Poulter, Iain B. Styles, Steven G. Thomas

    Diterbitkan 2021-01-01
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  14. 14
    Investigation of the contribution of an underlying platelet defect in women with unexplained heavy menstrual bleeding

    Investigation of the contribution of an underlying platelet defect in women with unexplained heavy menstrual bleeding oleh Gillian C. Lowe, Roksana Fickowska, Rashid Al Ghaithi, Annabel Maclachlan, Paul Harrison, Will Lester, Steve P. Watson, Bethan Myers, Justin Clark, Neil V. Morgan

    Diterbitkan 2019-01-01
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  15. 15
    High-throughput platelet spreading analysis: a tool for the diagnosis of platelet-based bleeding disorders

    High-throughput platelet spreading analysis: a tool for the diagnosis of platelet-based bleeding disorders oleh Abdullah O. Khan, Annabel Maclachlan, Gillian C. Lowe, Phillip L.R. Nicolson, Rashid Al Ghaithi, Steven G. Thomas, Steve P. Watson, Jeremy A. Pike, Neil V. Morgan

    Diterbitkan 2020-03-01
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  16. 16
    Post-translational polymodification of β1-tubulin regulates motor protein localization in platelet production and function

    Post-translational polymodification of β1-tubulin regulates motor protein localization in platelet production and function oleh Abdullah O. Khan, Alexandre Slater, Annabel Maclachlan, Phillip L.R. Nicolson, Jeremy A. Pike, Jasmeet S. Reyat, Jack Yule, Rachel Stapley, Julie Rayes, Steven G. Thomas, Neil V. Morgan

    Diterbitkan 2020-12-01
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  17. 17
    Sorting nexin 24 is required for α-granule biogenesis and cargo delivery in megakaryocytes

    Sorting nexin 24 is required for α-granule biogenesis and cargo delivery in megakaryocytes oleh Joanne Lacey, Simon J. Webster, Paul R. Heath, Chris J. Hill, Lucinda Nicholson-Goult, Bart E. Wagner, Abdullah O. Khan, Neil V. Morgan, Michael Makris, Martina E. Daly

    Diterbitkan 2022-01-01
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  18. 18
    A Novel GATA1 Variant in the C-Terminal Zinc Finger Compared with the Platelet Phenotype of Patients with A Likely Pathogenic Variant in the N-Terminal Zinc Finger

    A Novel GATA1 Variant in the C-Terminal Zinc Finger Compared with the Platelet Phenotype of Patients with A Likely Pathogenic Variant in the N-Terminal Zinc Finger oleh José M. Bastida, Stefano Malvestiti, Doris Boeckelmann, Verónica Palma-Barqueros, Mira Wolter, María L. Lozano, Hannah Glonnegger, Rocío Benito, Carlo Zaninetti, Felix Sobotta, Freimut H. Schilling, Neil V. Morgan, Kathleen Freson, José Rivera, Barbara Zieger

    Diterbitkan 2022-10-01
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  19. 19
    Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease.

    Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease. oleh Neil V Morgan, Mark R Morris, Hakan Cangul, Diane Gleeson, Anna Straatman-Iwanowska, Nicholas Davies, Stephen Keenan, Shanaz Pasha, Fatimah Rahman, Dean Gentle, Maaike P G Vreeswijk, Peter Devilee, Margaret A Knowles, Serdar Ceylaner, Richard C Trembath, Carlos Dalence, Erol Kismet, Vedat Köseoğlu, Hans-Christoph Rossbach, Paul Gissen, David Tannahill, Eamonn R Maher

    Diterbitkan 2010-02-01
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  20. 20
    Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders

    Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders oleh José M. Bastida, María L. Lozano, Rocío Benito, Kamila Janusz, Verónica Palma-Barqueros, Mónica Del Rey, Jesús M. Hernández-Sánchez, Susana Riesco, Nuria Bermejo, Hermenegildo González-García, Agustín Rodriguez-Alén, Carlos Aguilar, Teresa Sevivas, María F. López-Fernández, Anna E. Marneth, Bert A. van der Reijden, Neil V. Morgan, Steve P. Watson, Vicente Vicente, Jesús M. Hernández-Rivas, José Rivera, José R. González-Porras

    Diterbitkan 2018-01-01
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