Moira Crosier
| SRPK3 Is Essential for Cognitive and Ocular Development in Humans and Zebrafish, Explaining X-Linked Intellectual Disability | 2024 |
|
Professor Bob Anderson Dr Simon Bamforth Dr Bill Chaudhry Dr Lorraine Eley Dr Janet Kerwin et al. | Development of the arterial roots and ventricular outflow tracts | 2024 |
|
Dr Joseph Collin Dr Agata Rozanska Zerti Zerti Adrienne Unsworth Moira Crosier et al. | Single-cell analyses reveal transient retinal progenitor cells in the ciliary margin of developing human retina | 2024 |
|
Dr Angela Pyle Dr Brendan Payne Dr Jonathan Coxhead Professor Gavin Hudson Moira Crosier et al. | Author Correction: Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos (Nature Cell Biology, (2018), 20, 2, (144-151), 10.1038/s41556-017-0017-8) | 2023 |
|
Dr Rachel Queen Moira Crosier Dr Lorraine Eley Dr Janet Kerwin Jasmin Turner et al. | Spatial transcriptomics reveals novel genes during the remodelling of the embryonic human arterial valves | 2023 |
|
Dr Ayman Alzu'bi Niveditha Sankar Moira Crosier Dr Janet Kerwin Dr Gavin Clowry et al. | Tyramide signal amplification coupled with multiple immunolabeling and RNAScope in situ hybridization in formaldehyde-fixed paraffin-embedded human fetal brain | 2022 |
|
Moira Crosier
| Transcriptome-Wide Analysis Reveals a Role for Extracellular Matric and Integrin Receptor Genes in Otic Neurosensory Differntiation from Human iPSCs | 2021 |
|
Dr Vasileios Floros Dr Angela Pyle Dr Wei Wei Dr Brendan Payne Dr Jonathan Coxhead et al. | Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos | 2018 |
|
Moira Crosier
| Whole Exome Sequencing Identifies a New Splicing Factor Gene Causative of X-linked Spinocerebellar Ataxia | 2015 |
|
Moira Crosier Emerita Professor Susan Lindsay
| Abnormal retinal development associated with FRMD7 mutations | 2014 |
|
Dr Ralf Kist Michelle Watson Moira Crosier Dr Max Robinson Dr Julie Reichelt et al. | The Formation of Endoderm-Derived Taste Sensory Organs Requires a Pax9-Dependent Expansion of Embryonic Taste Bud Progenitor Cells | 2014 |
|
Dr Ingrid Ehrmann Caroline Dalgliesh Dr Marina Danilenko Moira Crosier Lynne Overman et al. | The Tissue-Specific RNA Binding Protein T-STAR Controls Regional Splicing Patterns of Neurexin Pre-mRNAs in the Brain | 2013 |
|
Dr YuZhu Cheng Lynne Overman Moira Crosier Dr Steven Lisgo Emerita Professor Susan Lindsay et al. | Assisting research into human embryonic and fetal development | 2012 |
|
Shaun Haigh Gavin Cuthbert Moira Crosier Fiona Harding Dr John Wolstenholme et al. | Origin of trisomy: no evidence to support the ovarian mosaicism theory | 2012 |
|
Dr YuZhu Cheng Lynne Overman Moira Crosier Dr Steven Lisgo Emerita Professor Susan Lindsay et al. | Assisting research into human embryonic and fetal development | 2011 |
|
Moira Crosier Emerita Professor Susan Lindsay
| The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus | 2011 |
|
Moira Crosier Dr Steven Lisgo Emerita Professor Susan Lindsay
| The Essential Role of Centrosomal NDE1 in Human Cerebral Cortex Neurogenesis | 2011 |
|
Moira Crosier Emerita Professor Susan Lindsay
| Expression of PLA2G6 in human fetal development: Implications for infantile neuroaxonal dystrophy | 2010 |
|
Dr Alison Trainer Moira Crosier
| Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome | 2010 |
|
Moira Crosier Emerita Professor Susan Lindsay
| The nystagmus-associated FRMD7 gene regulates neuronal outgrowth and development | 2010 |
|
Moira Crosier
| A Truncating Mutation of TRAPPC9 Is Associated with Autosomal-Recessive Intellectual Disability and Postnatal Microcephaly | 2009 |
|
Moira Crosier Emerita Professor Susan Lindsay
| Human CHN1 mutations hyperactivate α2-chimaerin and cause Duane's retraction syndrome | 2008 |
|
Moira Crosier Dr Alison Trainer
| Esco1, a candidate gene for TAR syndrome | 2006 |
|
Moira Crosier Dr Vikki Rand Dr Margaret Jackson
| DNA sequence and analysis of human chromosome 9 | 2004 |
|
Emerita Professor Susan Lindsay Mark Scott Dr Subrot Sarma Moira Crosier Dr Steven Lisgo et al. | Human developmental gene expression: an important link between disorder and understanding | 2004 |
|
Moira Crosier Dr Michael Jackson
| Human paralogs of KIAA0187 were created through independent pericentromeric-directed and chromosome-specific duplication mechanisms | 2002 |
|
Moira Crosier Dr Debbie Scott Dr Felicity May Professor Bruce Westley
| High expression of the trefoil protein TFF1 in interval breast cancers | 2001 |
|
Dr Michael Jackson Moira Crosier
| Characterisation of the heterochromatin/euchromatin boundary at 10q11 and identification of novel transcripts formed by repeat induced instability | 1999 |
|