Contrasts in scientific style: research groups in the chemical and biochemical sciences

por Morgan, Neil
Publicado 1991

The shaping of Cambridge botany

por Morgan, Neil
Publicado 1982

History of clinical chemistry

por Morgan, Neil
Publicado 1984

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

por Morgan, Neil V.
Publicado 2023

Gene of the issue: RUNX1 mutations and inherited bleeding

por Morgan, Neil V., Daly, Martina E.
Publicado 2017

Inherited Thrombocytopenia: Update on Genes and Genetic Variants Which may be Associated With Bleeding

por Almazni, Ibrahim, Stapley, Rachel, Morgan, Neil V.
Publicado 2019

New insights into glycoprotein Ibα desialylation-mediated platelet clearance

por Yule, Jack, Morgan, Neil V., Poulter, Natalie S.
Publicado 2020

Inherited thrombocytopenia: novel insights into megakaryocyte maturation, proplatelet formation and platelet lifespan

por Johnson, Ben, Fletcher, Sarah J., Morgan, Neil V.
Publicado 2016

Inherited platelet disorders: Insight from platelet genomics using next-generation sequencing

por Maclachlan, Annabel, Watson, Steve P., Morgan, Neil V.
Publicado 2017

Development of a New Dislodgeable Foliar Residue Analytical Laboratory Method for Pesticides

por Badawy, Mohamed H, Murnane, Darragh, Lewis, Kathleen A, Morgan, Neil
Publicado 2022

SLFN14 gene mutations associated with bleeding

por Stapley, Rachel J., Pisareva, Vera P., Pisarev, Andrey V., Morgan, Neil V.
Publicado 2019

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

por Dalby, Amanda, Mezzano, Diego, Rivera, José, Watson, Steve P., Morgan, Neil V.
Publicado 2022

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

por Vyas, Hrushikesh, Alcheikh, Ahmad, Lowe, Gillian, Stevenson, William S, Morgan, Neil V, Rabbolini, David J
Publicado 2022

CRISPR-Cas9 Mediated Labelling Allows for Single Molecule Imaging and Resolution

por Khan, Abdullah O., Simms, Victoria A., Pike, Jeremy A., Thomas, Steven G., Morgan, Neil V.
Publicado 2017

Whole exome sequencing identifies a mutation in thrombomodulin as the genetic cause of a suspected platelet disorder in a family with normal platelet function

por Maclachlan, Annabel, Dolan, Gerry, Grimley, Charlotte, Watson, Steve P., Morgan, Neil V., on behalf of the UK GAPP Study Group
Publicado 2017

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

por Fletcher, Sarah J., Pisareva, Vera P., Khan, Abdullah O., Tcherepanov, Andrew, Morgan, Neil V., Pisarev, Andrey V.
Publicado 2018

Cell-Free DNA in the Investigation of Miscarriage

por Colley, Emily, Devall, Adam J., Williams, Helen, Hamilton, Susan, Smith, Paul, Morgan, Neil V., Quenby, Siobhan, Coomarasamy, Arri, Allen, Stephanie
Publicado 2020

Initiation codon mutation in βB1-crystallin (CRYBB1) associated with autosomal recessive nuclear pulverulent cataract

por Meyer, Esther, Rahman, Fatimah, Owens, Jessica, Pasha, Shanaz, Morgan, Neil V., Trembath, Richard C., Stone, Edwin M., Moore, Anthony T., Maher, Eamonn R.
Publicado 2009

Investigation of the contribution of an underlying platelet defect in women with unexplained heavy menstrual bleeding

por Lowe, Gillian C., Fickowska, Roksana, Al Ghaithi, Rashid, Maclachlan, Annabel, Harrison, Paul, Lester, Will, Watson, Steve P., Myers, Bethan, Clark, Justin, Morgan, Neil V.
Publicado 2018

An adaptable analysis workflow for characterization of platelet spreading and morphology

por Pike, Jeremy A., Simms, Victoria A., Smith, Christopher W., Morgan, Neil V., Khan, Abdullah O., Poulter, Natalie S., Styles, Iain B., Thomas, Steven G.
Publicado 2020