M. Keighren

发表

Palmitoylation Regulates Epidermal Homeostasis and Hair Follicle Differentiation

I. Jackson, M. Fukata, Y. Fukata, 2009, PLoS Genetics.

A cell/cilia cycle biosensor for single cell kinetics reveals persistence of cilia after the G1/ S transition is a general property in cells and mice

A. Miyawaki, Asako Sakaue-Sawano, I. Jackson, 2022 .

Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function

S. Cross, S. Wells, I. Jackson, 2020, Scientific Reports.

PLAA Mutations Cause a Lethal Infantile Epileptic Encephalopathy by Disrupting Ubiquitin-Mediated Endolysosomal Degradation of Synaptic Proteins

Mark T. Handley, I. Jackson, R. Ribchester, 2017, American journal of human genetics.

Mutations in PLAA cause a lethal infantile epileptic encephalopathy by disrupting ubiquitin-mediated endolysosomal degradation of synaptic proteins

Mark T. Handley, R. Ribchester, C. Woods, 2017 .

Fluorescent in vivo editing reporter (FIVER): A novel multispectral reporter of in vivo genome editing

S. Hart, P. Tennant, M. Pearson, 2020, bioRxiv.

Evaluation of triploid↔diploid and trisomy-3↔diploid mouse chimeras as models for investigating how lineage restriction occurs in confined placental mosaicism

M. Keighren, J. West, C. A. Everett, 2007, Reproduction.

A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathy.

S. Wells, I. Jackson, P. Potter, 2013, Investigative ophthalmology & visual science.

Murine submucosal glands are clonally derived and show a cystic fibrosis gene-dependent distribution pattern.

J. Dorin, M. Keighren, J. West, 1999, American journal of respiratory cell and molecular biology.

Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis.

Martin A. M. Reijns, P. Lockhart, I. Jackson, 2011, American journal of human genetics.

Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse.

S. Cross, I. Jackson, L. Sánchez-Pulido, 2019, Investigative ophthalmology & visual science.

Robust Genetic Analysis of the X-Linked Anophthalmic (Ie) Mouse

I. Jackson, D. Adams, D. Fitzpatrick, 2022, bioRxiv.

A Trans-Acting Protein Effect Causes Severe Eye Malformation in the Mp Mouse

I. Jackson, M. Fisher, D. Fitzpatrick, 2013, PLoS genetics.

Explorer Acute Versus Chronic Loss of Mammalian Azi 1 / Cep 131 Results in Distinct Ciliary Phenotypes

Lee B. Smith, I. Jackson, A. Jarman, 2017 .

Acute Versus Chronic Loss of Mammalian Azi1/Cep131 Results in Distinct Ciliary Phenotypes

Lee B. Smith, I. Jackson, A. Jarman, 2013, PLoS genetics.

Clonal analysis of patterns of growth, stem cell activity, and cell movement during the development and maintenance of the murine corneal epithelium

B. Dhillon, R. Hill, J. Collinson, 2002, Developmental dynamics : an official publication of the American Association of Anatomists.

Dopachrome tautomerase variants in patients with oculocutaneous albinism

I. Jackson, P. Pennamen, D. Lacombe, 2020, Genetics in Medicine.

ZMYND10 functions in a chaperone relay during axonemal dynein assembly

A. von Kriegsheim, A. García-Muñoz, A. Jarman, 2017, bioRxiv.

Humanized MC1R transgenic mice reveal human specific receptor function.

I. Jackson, M. Keighren, P. Budd, 2007, Human molecular genetics.

A study of the role of the reactive thiol group of rabbit muscle creatine kinase with a chromophoric reporter group.

N. C. Price, M. Keighren, 1978, The Biochemical journal.

Analysis of cell ploidy in histological sections of mouse tissues by DNA-DNA in situ hybridization with digoxigenin-labelled probes

M. Keighren, J. West, 2004, The Histochemical Journal.

Survival of glucose phosphate isomerase null somatic cells and germ cells in adult mouse chimaeras

M. Keighren, J. West, Jean H. Flockhart, 2016, Biology Open.

BIO017111 596..610

M. Keighren, J. West, Jean H. Flockhart, 2016 .

Lessons from mouse chimaera experiments with a reiterated transgene marker: revised marker criteria and a review of chimaera markers

M. Keighren, J. Birtley, J. West, 2015, Transgenic Research.

Enzymatic Removal of Ribonucleotides from DNA Is Essential for Mammalian Genome Integrity and Development

Martin A. M. Reijns, Martin S. Taylor, S. Boyle, 2012, Cell.

Quantitative analysis of mid-gestation mouse aggregation chimaeras: non-random composition of the placenta

M. Keighren, R. James, J. West, 1993, Roux's archives of developmental biology.

Restricted distribution of tetraploid cells in mouse tetraploid<==>diploid chimaeras.

M. Keighren, R. James, A. Klerkx, 1995, Developmental biology.

Selection against BALB/c strain cells in mouse chimaeras

M. Keighren, J. West, P. Tang, 2018, Biology Open.

Re-evaluation of the causes of variation among mouse aggregation chimaeras

M. Keighren, J. West, P. Tang, 2019, Biology Open.

Evaluation of the mouse TgTP6.3 tauGFP transgene as a lineage marker in chimeras

D. Price, J. Mason, T. Pratt, 2005, Journal of anatomy.

Biochemical evidence for cell fusion in placentas of mouse aggregation chimeras.

M. Keighren, J. West, J. Flockhart, 1995, Developmental biology.

Quantitative and spatial information on the composition of chimaeric fetal mouse eyes from single histological sections

M. Keighren, J. West, B. Hodson, 1997, Development, growth & differentiation.

A quantitative test for developmental neutrality of a transgenic lineage marker in mouse chimaeras.

M. Keighren, J. West, J. Flockhart, 1996, Genetical research.

Analysis of cell ploidy in histological mouse tissues by DNA-DNA in situ with digoxigenin-labelled probes sections of hybridization

M. Keighren, J. West, 1993 .

Evaluation of methods for one-dimensional spatial analysis of two-dimensional patterns in mouse chimaeras

M. Keighren, J. West, A. Springbett, 2011, Journal of anatomy.

Genomic localization of a Dct-LacZ transgene locus: a simple assay for transgene status.

I. Jackson, M. Keighren, Hiroaki Yamamoto, 2006, Pigment cell research.

A WDR35-dependent coat protein complex transports ciliary membrane cargo vesicles to cilia

E. Lorentzen, Weihua Leng, G. Pigino, 2021, eLife.

Correction: A Dominant-Negative Mutation of Mouse Lmx1b Causes Glaucoma and Is Semi-lethal via LBD1-Mediated Dimerisation

S. Cross, I. Jackson, Richard S. Smith, 2014, PLoS Genetics.

Cloning of the am (glutamate dehydrogenase) gene of Neurospora crassa through the use of a synthetic DNA probe.

J. Fincham, J. Kinsey, M. Keighren, 1982, Gene.

Missense Mutations in the Human Nanophthalmos Gene TMEM98 Cause Retinal Defects in the Mouse

S. Cross, I. Jackson, L. Sánchez-Pulido, 2019, bioRxiv.

Involvement of the Melanocortin-1 Receptor in Acute Pain and Pain of Inflammatory but Not Neuropathic Origin

I. Jackson, S. Fleetwood-Walker, A. Delaney, 2010, PloS one.

A Dominant-Negative Mutation of Mouse Lmx1b Causes Glaucoma and Is Semi-lethal via LBD1-Mediated Dimerisation

S. Cross, I. Jackson, Richard S. Smith, 2014, PLoS genetics.

Reconciling diverse mammalian pigmentation patterns with a fundamental mathematical model

Ruth E. Baker, Christian A. Yates, Gabriel Landini, 2016, Nature Communications.

Comparison of two related lines of tauGFP transgenic mice designed for lineage tracing

D. Price, J. Mason, T. Pratt, 2017, BMC Developmental Biology.

Comparison of two related lines of tauGFP transgenic mice designed for lineage tracing

D. Price, J. Mason, T. Pratt, 2017, BMC Developmental Biology.

Manuscript submitted to eLife

J. Marsh, Weihua Leng, G. Pigino, 2020 .

Ex vivo culture of mouse embryonic skin and live-imaging of melanoblast migration.

I. Jackson, R. Mort, M. Keighren, 2014, Journal of visualized experiments : JoVE.

Fucci2a: A bicistronic cell cycle reporter that allows Cre mediated tissue specific expression in mice

Atsushi Miyawaki, Asako Sakaue-Sawano, Peter Hohenstein, 2014, Cell cycle.

Genetically engineered multicistronic allele of Pmel yielding highly specific CreERT2‐mediated recombination in the melanocyte lineage

Emma L. Wilkinson, I. Jackson, S. Allinson, 2022, Pigment cell & melanoma research.

Fucci 2 a : A bicistronic cell cycle reporter that allows Cre mediated tissue speci fi c expression in mice

A. Miyawaki, Asako Sakaue-Sawano, I. Jackson, 2014 .

A Cell/Cilia Cycle Biosensor for Single-Cell Kinetics Reveals Persistence of Cilia after G1/S Transition Is a General Property in Cells and Mice

Asako Sakaue-Sawano, I. Jackson, R. Meehan, 2018, Developmental cell.

Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function

S. Cross, I. Jackson, J. Marsh, 2018, Disease Models & Mechanisms.

A Trans-Acting Protein Effect Causes Severe Eye Malformation in the Mp Mouse

I. Jackson, M. Fisher, D. Keene, 2013, PLoS genetics.

Palmitoylation Regulates Epidermal Homeostasis and Hair Follicle Differentiation

I. Jackson, M. Fukata, Y. Fukata, 2009, PLoS genetics.

Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis.

Martin A. M. Reijns, P. Lockhart, I. Jackson, 2011, American journal of human genetics.

Frameshift mutations affecting the N-terminal sequence of Neurospora NADP-specific glutamate dehydrogenase.

J. Fincham, J. Kinsey, M. Keighren, 1980, Journal of molecular biology.

Lessons from mouse chimaera experiments with a reiterated transgene marker: revised marker criteria and a review of chimaera markers

M. Keighren, Jean H. Flockhart, Benjamin A. Hodson, 2015, Transgenic Research.

Lessons from mouse chimaera experiments with a reiterated transgene marker

M. Keighren, Jean H. Flockhart, Benjamin A. Hodson, 2016 .

Polyploid cells in the mouse ovary

E. Telfer, M. Keighren, L. Macfadyen, 2003, Journal of anatomy.

A WDR35-dependent coatomer transports ciliary membrane proteins from the Golgi to the cilia

J. Marsh, Weihua Leng, G. Pigino, 2020, bioRxiv.

Newcastle University Eprints Date Deposited: 3 This Work Is Licensed under a Creative Commons Attribution 4.0 International License Acute versus Chronic Loss of Mammalian Azi1/cep131 Results in Distinct Ciliary Phenotypes

Lee B. Smith, I. Jackson, A. Jarman, 2022 .