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Browsing publications by Moira Crosier.

Newcastle AuthorsTitleYearFull text
Moira Crosier
Transcriptome-Wide Analysis Reveals a Role for Extracellular Matric and Integrin Receptor Genes in Otic Neurosensory Differntiation from Human iPSCs2021
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 embryos2018
Moira Crosier
Whole Exome Sequencing Identifies a New Splicing Factor Gene Causative of X-linked Spinocerebellar Ataxia2015
Moira Crosier
Emerita Professor Susan Lindsay
Abnormal retinal development associated with FRMD7 mutations2014
Dr Ralf Kist
Michelle Watson
Moira Crosier
Dr Max Robinson
Dr Julia Reichelt
et al.
The Formation of Endoderm-Derived Taste Sensory Organs Requires a Pax9-Dependent Expansion of Embryonic Taste Bud Progenitor Cells2014
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 Brain2013
Dr YuZhu Cheng
Lynne Overman
Moira Crosier
Dr Steven Lisgo
Emerita Professor Susan Lindsay
et al.
Assisting research into human embryonic and fetal development2012
Shaun Haigh
Gavin Cuthbert
Moira Crosier
Fiona Harding
Dr John Wolstenholme
et al.
Origin of trisomy: no evidence to support the ovarian mosaicism theory2012
Dr YuZhu Cheng
Lynne Overman
Moira Crosier
Dr Steven Lisgo
Emerita Professor Susan Lindsay
et al.
Assisting research into human embryonic and fetal development2011
Moira Crosier
Emerita Professor Susan Lindsay
The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus2011
Moira Crosier
Dr Steven Lisgo
Emerita Professor Susan Lindsay
The Essential Role of Centrosomal NDE1 in Human Cerebral Cortex Neurogenesis2011
Moira Crosier
Emerita Professor Susan Lindsay
Expression of PLA2G6 in human fetal development: Implications for infantile neuroaxonal dystrophy2010
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 syndrome2010
Moira Crosier
Emerita Professor Susan Lindsay
The nystagmus-associated FRMD7 gene regulates neuronal outgrowth and development2010
Moira Crosier
A Truncating Mutation of TRAPPC9 Is Associated with Autosomal-Recessive Intellectual Disability and Postnatal Microcephaly2009
Moira Crosier
Emerita Professor Susan Lindsay
Human CHN1 mutations hyperactivate α2-chimaerin and cause Duane's retraction syndrome2008
Moira Crosier
Dr Alison Trainer
Esco1, a candidate gene for TAR syndrome2006
Moira Crosier
Dr Vikki Rand
Dr Margaret Jackson
DNA sequence and analysis of human chromosome 92004
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 understanding2004
Moira Crosier
Dr Michael Jackson
Human paralogs of KIAA0187 were created through independent pericentromeric-directed and chromosome-specific duplication mechanisms2002
Moira Crosier
Dr Debbie Scott
Dr Felicity May
Professor Bruce Westley
High expression of the trefoil protein TFF1 in interval breast cancers2001
Dr Michael Jackson
Moira Crosier
Characterisation of the heterochromatin/euchromatin boundary at 10q11 and identification of novel transcripts formed by repeat induced instability1999