Hasil Pencarian - Neil V Morgan
- Menampilkan 1 - 20 hasil dari 22
- Ke Halaman Berikutnya
-
1
Editorial: Case reports in cardiovascular genetics and systems medicine: 2022 oleh Neil V. Morgan
Diterbitkan 2023-09-01
Artikel -
2
Gene of the issue: RUNX1 mutations and inherited bleeding oleh Neil V. Morgan, Martina E. Daly
Diterbitkan 2017-02-01
Artikel -
3
New insights into glycoprotein Ibα desialylation-mediated platelet clearance oleh Jack Yule, Neil V. Morgan, Natalie S. Poulter
Diterbitkan 2020-07-01
Artikel -
4
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
Artikel -
5
Inherited platelet disorders: Insight from platelet genomics using next-generation sequencing oleh Annabel Maclachlan, Steve P. Watson, Neil V. Morgan
Diterbitkan 2017-01-01
Artikel -
6
-
7
SLFN14 gene mutations associated with bleeding oleh Rachel J. Stapley, Vera P. Pisareva, Andrey V. Pisarev, Neil V. Morgan
Diterbitkan 2020-04-01
Artikel -
8
-
9
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
Artikel -
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 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
Artikel -
11
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
Artikel -
12
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
Artikel -
13
-
14
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
Artikel -
15
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
Artikel -
16
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
Artikel -
17
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
Artikel -
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 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
Artikel -
19
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
Artikel -
20
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
Artikel