Publications by Moira Crosier - ePrints

Browsing publications by Moira Crosier.

Newcastle Authors	Title	Year
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