J. Peters

发表

Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment

E. Fisher, D. Rogers, S.D.M. Brown, 1997, Mammalian Genome.

Identification of an imprinting control region affecting the expression of all transcripts in the Gnas cluster

P. Glenister, G. Kelsey, M. Maconochie, 2006, Nature Genetics.

A Mouse Model for Osseous Heteroplasia

R. Cox, M. Warren, T. Hough, 2012, PloS one.

Mapping of the structural gene for S-adenosyl homocysteine hydrolase to mouse Chromosome 2, and related sequences to Chromosomes 8 and X

C. Abbott, J. Peters, P. Tissier, 2004, Mammalian Genome.

Tmed 9 and IKBKE cluster and miR-296 targets Gnas / GNAS MicroRNAs 296 and 298 are imprinted and part of the Material Supplemental

J. Peters, Joan E. Robson, S. Eaton, 2011 .

The molecular characterization of an A:T to G:C transition in theHbb-b1 gene of the murine homologue of hemoglobin Rainier

J. Peters, Janet Jones, 1991, Biochemical Genetics.

The molecular characterization of an A:T to G:C transition in theHbb-b1 gene of the murine homologue of hemoglobin Rainier

J. Peters, Janet Jones, 1991, Biochemical Genetics.

Explorer Regulation of alternative polyadenylation by genomic imprinting

A. Wood, D. Bourc’his, Reiner Schulz, 2017 .

Regulation of alternative polyadenylation by genomic imprinting.

Reiner Schulz, Colin V Beechey, A. Wood, 2008, Genes & development.

The kinesin light chain gene: its mapping and exclusion in mouse and human forms of inherited motor neuron degeneration

E. Fisher, F. Baas, M. Hafezparast, 1999, Neuroscience Letters.

Great times for mouse genetics: getting ready for large-scale ENU-mutagenesis

Steve D. M. Brown, M. Justice, R. Balling, 2000, Mammalian Genome.

Explorer KATNAL 1 regulation of sertoli cell microtubule dynamics is essential for spermiogenesis and male fertility

Lee B. Smith, S. Wells, P. Nolan, 2017 .

KATNAL 1 regulation of sertoli cell microtubule dynamics is essential for spermiogenesis and male fertility

Lee B. Smith, S. Wells, P. Nolan, 2012 .

KATNAL1 Regulation of Sertoli Cell Microtubule Dynamics Is Essential for Spermiogenesis and Male Fertility

Lee B. Smith, S. Wells, P. Nolan, 2012, PLoS genetics.

Overview of Mammalian Genome special issue on epigenetics

J. Peters, 2009, Mammalian Genome.

The imprinted signaling protein XL alpha s is required for postnatal adaptation to feeding.

G. Kelsey, W. Dean, S. Cinti, 2004, Nature genetics.

Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy.

S. Rastan, E. Fisher, K. Davies, 2001, Human molecular genetics.

Death of mouse embryos that lack a functional gene for glucose phosphate isomerase.

J. Peters, S. Ball, J. West, 1990, Genetical research.

Biochemical and recessive visible specific locus responses of C3H/HeH to fractionated, acute radiation.

J. Peters, S. Ball, 2003, Mutation research.

A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse

Steve D. M. Brown, Ian C. Gray, Zuzanna Tymowska-Lalanne, 2000, Nature Genetics.

Collagen dysregulation in the dermis of the Sagg/+ mouse: a loose skin model.

L. Soslowsky, M. Yamauchi, J. Peters, 2006, The Journal of investigative dermatology.

Towards a mutant map of the mouse – new models of neurological, behavioural, deafness, bone, renal and blood disorders

S. Rastan, E. Fisher, S. Greenaway, 2004, Genetica.

Identification of two novel mutations in the murine Nsdhl sterol dehydrogenase gene and development of a functional complementation assay in yeast.

M. Bard, G. Herman, J. Peters, 2003, Molecular genetics and metabolism.

A Mouse Model for Osseous

R. Cox, M. Warren, T. Hough, 2019 .

New Mutations at the Imprinted Gnas Cluster Show Gene Dosage Effects of Gsα in Postnatal Growth and Implicate XLαs in Bone and Fat Metabolism but Not in Suckling

L. Moir, L. Teboul, M. Maconochie, 2012, Molecular and Cellular Biology.

Bone and Fat Metabolism but Not in s in α in Postnatal Growth and Implicate XL α Cluster Show Gene Dosage Effects of Gs Gnas New Mutations at the Imprinted

L. Moir, L. Teboul, J. Peters, 2012 .

Transcriptional activation of the α1(I) procollagen gene and up-regulation of α1(I) and α1(III) procollagen messenger RNA in dermal fibroblasts from tight skin 2 mice

S. Jimenez, J. Peters, R. McGrath, 1998 .

Testing of SHIRPA, a mouse phenotypic assessment protocol, on Dmdmdx and Dmdmdx3cv dystrophin-deficient mice

K. Davies, J. Peters, Y. Nitta, 2000, Mammalian Genome.

Novel phenotypes identified by plasma biochemical screening in the mouse

Steve D. M. Brown, S. Rastan, E. Fisher, 2002, Mammalian Genome.

Mouse chromosome 2

D. Pomp, C. Abbott, L. Siracusa, 1996, Mammalian Genome.

Polymorphism of esterase 11 in Mus musculus, a further esterase locus on chromosome 8

J. Peters, H. Nash, H. R. Nash, 1977, Biochemical Genetics.

Rare electrophoretic variants of glycerol‐3‐phosphate dehydrogenase: evidence for two structural gene loci (GPD1 and GPD2)

H. Harris, J. Peters, H. Harris, 1974, Annals of human genetics.

Deficiency of adenosine deaminase in the wasted mouse.

C. Abbott, J. Peters, C. Skidmore, 1986, Proceedings of the National Academy of Sciences of the United States of America.

The genes for endothelin 3, vitamin D 24-hydroxylase, and melanocortin 3 receptor map to distal mouse Chromosome 2, in the region of conserved synteny with human Chromosome 20

C. Abbott, J. Peters, S. Malas, 1994, Mammalian Genome.

Localisation of the imprinted gene neuronatin, Nnat, confirms and refines the location of a second imprinting region on mouse chromosome 2

F. Ishino, J. Peters, C. Williamson, 1998, Cytogenetic and Genome Research.

The scurfy mouse mutant has previously unrecognized hematological abnormalities and resembles Wiskott-Aldrich syndrome.

M. Lyon, P. Glenister, J. Peters, 1990, Proceedings of the National Academy of Sciences of the United States of America.

The Pk-3 gene determines both the heart, M1, and the kidney, M2, pyruvate kinase isozymes in the mouse; and a simple electrophoretic method for separating phosphoglucomutase-3

J. Peters, S. Andrews, 1984, Biochemical Genetics.

Alternative non-coding splice variants of Nespas, an imprinted gene antisense to Nesp in the Gnas imprinting cluster

G. Kelsey, J. Peters, C. Williamson, 2002, Mammalian Genome.

Comparative mapping of mouse Chromosome 4 and human Chromosome 9: Lv, Orm, and Hxb are closely linked on mouse Chromosome 4

C. Abbott, J. Peters, A. Pilz, 2004, Mammalian Genome.

A cis-acting control region is required exclusively for the tissue-specific imprinting of Gnas

W. Fraser, T. Hough, M. Maconochie, 2004, Nature Genetics.

Identification and characterisation of imprinted genes in the mouse.

J. Peters, C. Beechey, 2004, Briefings in functional genomics & proteomics.

Maternal inheritance of the Gnas cluster mutation Ex1A-T affects size, implicating NESP55 in growth

T. Hough, J. Peters, R. Fischer‐Colbrie, 2013, Mammalian Genome.

Gene Dosage Effects at the Imprinted Gnas Cluster

R. Cox, T. Hough, J. Harrison, 2013, PloS one.

Interactions between imprinting effects: summary and review

J. Peters, B. Cattanach, C. Beechey, 2006, Cytogenetic and Genome Research.

A missense mutation in the non-neural G-protein α-subunit isoforms modulates susceptibility to obesity

R. Cox, L. Moir, J. Jansson, 2009, International Journal of Obesity.

DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressed

G. Kelsey, P. Stanier, D. Monk, 2002, Mammalian Genome.

Transcriptional activation of α1(III) procollagen gene in Tsk2/+ dermal fibroblasts

S. Jimenez, J. Peters, R. McGrath, 2003 .

Demonstration of Autoimmunity in the Tight Skin-2 Mouse: A Model for Scleroderma1

Laura J. McCloskey, S. Jimenez, J. Peters, 2005, The Journal of Immunology.

Spontaneous and radiation-induced leukemogenesis of the mouse small eye mutant, Pax6(Sey3H).

K. Satoh, N. Nakagata, J. Peters, 2004, Journal of radiation research.

Characterisation of the growth regulating gene IMP3, a candidate for Silver-Russell syndrome

M. Preece, P. Stanier, D. Monk, 2002, Journal of medical genetics.

An XXY mouse, the result of a rearrangement between one X and a Y chromosome.

J. Peters, E. P. Evans, G. Breckon, 1990, Genetical research.

Comparative mapping of mouse chromosome 2 and human chromosome 9q: the genes for gelsolin and dopamine beta-hydroxylase map to mouse chromosome 2.

C. Abbott, J. Peters, A. Pilz, 1992, Genomics.

An allele at the triose phosphate isomerase, Tpi-1 locus on chromosome 6 recovered from feral mice.

G. Bulfield, J. Peters, S. Ball, 1987, Genetical research.

Prader-Willi and snoRNAs

J. Peters, 2008, Nature Genetics.

A high-resolution linkage map of the tight skin 2 (Tsk2) locus: A mouse model for scleroderma (SSc) and other cutaneous fibrotic diseases

S. Jimenez, L. Siracusa, J. Peters, 1996, Mammalian Genome.

Mapping studies of the distal imprinting region of mouse chromosome 2.

J. Peters, S. Ball, E. P. Evans, 1994, Genetical research.

Alternately spliced WT1 antisense transcripts interact with WT1 sense RNA and show epigenetic and splicing defects in cancer.

K. Pritchard-Jones, A. Ward, K. Moorwood, 2007, RNA.

Chromosome maps of man and mouse. IV

M. Lyon, J. Edwards, V. Buckle, 1989, Annals of human genetics.

The gene mutated in bare patches and striated mice encodes a novel 3β-hydroxysteroid dehydrogenase

W. Miller, A. Mallon, M. Botcherby, 1999, Nature Genetics.

Novel ENU-induced eye mutations in the mouse: models for human eye disease.

Steve D. M. Brown, S. Cross, I. Jackson, 2002, Human molecular genetics.

Polymorphism of kidney pyruvate kinase in the mouse is determined by a gene, Pk-3, on chromosome 9

G. Bulfield, J. Peters, E. Eicher, 1981, Biochemical Genetics.

Implementation of a large-scale ENU mutagenesis program: towards increasing the mouse mutant resource

Steve D. M. Brown, Steve D.M. Brown, Mark Strivens, 2000, Mammalian Genome.

Nondisjunction of chromosome 21: comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin.

H. Willard, T. Hassold, J. Peters, 1992, American journal of human genetics.

Sequence characterization of alleles Gpi1-sa and Gpi1-sb at the glucose phosphate isomerase structural locus

S. Pearce, J. Peters, S. Ball, 1995, Mammalian Genome.

Chromosome maps of man and mouse

M. Lyon, J. Edwards, J. Peters, 1981, Clinical genetics.

Nonspecific esterases of Mus musculus

J. Peters, 1982, Biochemical Genetics.

Esterases of Mus musculus: Substrate and inhibition characteristics, new isozymes, and homologies with man

J. Peters, H. Nash, H. R. Nash, 1978, Biochemical Genetics.

Polymorphism of esterase-10 in Mus musculus

J. Peters, H. Nash, H. R. Nash, 1976, Biochemical Genetics.

MicroRNAs 296 and 298 are imprinted and part of the GNAS/Gnas cluster and miR-296 targets IKBKE and Tmed9.

J. Peters, Joan E. Robson, S. Eaton, 2012, RNA.

Imprinted noncoding RNAs

J. Peters, Joan E. Robson, 2008, Mammalian Genome.

The role of genomic imprinting in biology and disease: an expanding view

J. Peters, 2014, Nature Reviews Genetics.

The spatial and temporal expression pattern of Nesp and its antisense Nespas, in mid-gestation mouse embryos

J. Peters, C. Williamson, S. Ball, 2001, Mechanisms of Development.

The lethal mutation of the mouse wasted (wst) is a deletion that abolishes expression of a tissue-specific isoform of translation elongation factor 1alpha, encoded by the Eef1a2 gene.

C. Abbott, J. Peters, J. Peters, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Imprinted methylation profiles for proximal mouse Chromosomes 11 and 7 as revealed by methylation-sensitive representational difference analysis

G. Kelsey, P. Stanier, D. Monk, 2003, Mammalian Genome.

Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark.

Philip Stanier, Philippe Arnaud, David Monk, 2003, Human molecular genetics.

Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal development

S. Cross, I. Jackson, T. Webb, 2008, Journal of Cell Science.

Linkage mapping around the ragged (Ra) and wasted (wst) loci on distal mouse chromosome 2.

C. Abbott, J. Peters, A. Pilz, 1994, Genomics.

Interactions Between Imprinting Effects in the Mouse

Josephine Peters, Colin V. Beechey, Bruce M. Cattanach, 2004, Genetics.

The imprinted signaling protein XLαs is required for postnatal adaptation to feeding

G. Kelsey, W. Dean, S. Cinti, 2004, Nature Genetics.

Epigenetic Properties and Identification of an Imprint Mark in the Nesp-Gnasxl Domain of the Mouse Gnas Imprinted Locus

G. Kelsey, W. Dean, R. Feil, 2003, Molecular and Cellular Biology.

Chromosome maps of man and mouse, III.

M. Lyon, J. Edwards, V. Buckle, 1987, Genomics.

Genetic linkage analysis of the Ak1, Col5a1, Epb7.2, Fpgs, Grp78, Pbx3, and Notch1 genes in the region of mouse chromosome 2 homologous to human chromosome 9q.

C. Abbott, J. Peters, R. Prohaska, 1994, Genomics.

Localization of Blvr, biliverdin reductase, on mouse chromosome 2.

A. von Deimling, J. Peters, S. Ball, 1989, Genomics.

The localization of G6pd, glucose-6-phosphate dehydrogenase, and mdx, muscular dystrophy in the mouse X chromosome.

V. Chapman, G. Bulfield, J. Peters, 1988, Genetical research.

MouseBook: an integrated portal of mouse resources

John M. Hancock, Steve D. M. Brown, Ann-Marie Mallon, 2009, Nucleic Acids Res..

Control of Imprinting at the Gnas Cluster

J. Peters, C. Williamson, 2007, Epigenetics.

Imprinting control within the compact Gnas locus

D. Monk, J. Peters, C. Williamson, 2006, Cytogenetic and Genome Research.

A comprehensive transcript map of the mouse Gnas imprinted complex.

Paul Denny, C. Wells, P. Denny, 2003, Genome research.

The imprinted oedematous-small mutation on mouse chromosome 2 identifies new roles for Gnas and Gnasxl in development.

J. Peters, B. Cattanach, J. Skinner, 2002, Genomics.

Two imprinted gene mutations: three phenotypes.

J. Peters, S. Ball, B. Cattanach, 2000, Human molecular genetics.

An imprinted transcript, antisense to Nesp, adds complexity to the cluster of imprinted genes at the mouse Gnas locus.

G. Kelsey, J. Peters, C. Williamson, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Identification of imprinted loci by methylation-sensitive representational difference analysis: application to mouse distal chromosome 2.

G. Kelsey, H. J. Miller, J. Peters, 1999, Genomics.

A cluster of oppositely imprinted transcripts at the Gnas locus in the distal imprinting region of mouse chromosome 2.

C. Wells, G. Kelsey, H. J. Miller, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Glomerular-specific imprinting of the mouse gsalpha gene: how does this relate to hormone resistance in albright hereditary osteodystrophy?

J. Peters, C. Williamson, Y. Edwards, 1996, Genomics.

Thirteen genes (Cebpb, E2f1, Tcf4, Cyp24, Pck1, Acra4, Edn3, Kcnb1, Mc3r, Ntsr, Cd40, Plcg1 and Rcad) that probably lie in the distal imprinting region of mouse chromosome 2 are not monoallelically expressed.

C. Abbott, J. Peters, C. Williamson, 1995, Genetical research.

The imprinted region on human chromosome 7q32 extends to the carboxypeptidase A gene cluster: an imprinted candidate for Silver-Russell syndrome

Z Birjandi, L Bentley, K Nakabayashi, 2003, Journal of medical genetics.

Control of imprinting at the Gnas cluster.

J. Peters, C. Williamson, 2007, Advances in experimental medicine and biology.

Imprinting of distal mouse chromosome 2 is associated with phenotypic anomalies in utero.

C. Wells, J. Peters, C. Williamson, 1998, Genetical research.

Chromosome maps of man and mouse.

J Peters, M. Lyon, J. Edwards, 1981, Clinical genetics.

Parental influences on expression of glucose-6-phosphate dehydrogenase, G6pd, in the mouse; a case of imprinting.

J. Peters, S. Ball, 1990, Genetical research.

A transcript map encompassing the multiple endocrine neoplasia type-1 (MEN1) locus on chromosome 11q13.

M. Sawicki, H. Weier, E. Srivatsan, 1997, Genomics.

A mouse beta-globin mutant that is an exact model of hemoglobin Rainier in man.

J. Clegg, J. Peters, J. Loutit, 1985, Genetics.

Combining mutagenesis and genomics in the mouse--closing the phenotype gap.

J. Peters, S. Brown, 1996, Trends in genetics : TIG.

Sequence characterization of ENU-induced mutants of glucose phosphate isomerase in mouse

S. Pearce, J. Peters, S. Ball, 1995, Mammalian Genome.

Linkage of lactate dehydrogenase-2, Ldh-2, in the mouse

J. Peters, S. Andrews, 1985, Biochemical Genetics.

Mapping of mouse carbonic anhydrase-3, Car-3: another locus in the homologous region of mouse chromosome 3 and human chromosome 8.

S. Tweedie, N. Spurr, J. Peters, 1990, Genomics.

The tight skin 2 mouse

S. Jimenez, L. Siracusa, J. Peters, 1995 .

The tight skin 2 mouse. An animal model of scleroderma displaying cutaneous fibrosis and mononuclear cell infiltration.

S. Jimenez, L. Siracusa, J. Peters, 1995, Arthritis and rheumatism.

Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy

Steve D. M. Brown, S. Rastan, E. Fisher, 2000 .

Uncoupling Antisense-Mediated Silencing and DNA Methylation in the Imprinted Gnas Cluster

Lydia Teboul, Christine M. Williamson, Colin V. Beechey, 2011, PLoS genetics.

An integrated genetic, radiation hybrid, physical and transcription map of a region of distal mouse chromosome 12, including an imprinted locus and the 'Legs at odd angles' (Loa) mutation.

E. Fisher, M. Sergot, H. Hummerich, 2002, Gene.

Mouse Chromosome 7

T. Magnuson, G. Kelsey, C. Conti, 2004, Mammalian Genome.

Mouse chromosome 7

A. Saunders, J. Peters, M. Sutcliffe, 2004, Mammalian Genome.

Adenosine deaminase,Ada, is in mouse chromosome 2H3, and is not allelic with wasted,wst

C. Abbott, J. Peters, C. Skidmore, 1991, Biochemical Genetics.

Adenosine deaminase,Ada, is in mouse chromosome 2H3, and is not allelic with wasted,wst

C. Abbott, J. Peters, C. Skidmore, 1991, Biochemical Genetics.

Loss of Gnas Imprinting Differentially Affects REM/NREM Sleep and Cognition in Mice

G. Colonna, A. Bartolomucci, T. Nieus, 2012, PLoS genetics.

Antisense Activity across the Nesp Promoter is Required for Nespas-Mediated Silencing in the Imprinted Gnas Cluster

G. Kelsey, L. Teboul, Charlotte Tibbit, 2015, Non-coding RNA.

Imprinting: silently crossing the boundary

J. Peters, 2000, Genome Biology.

Structural characterization of Rasgrf1 and a novel linked imprinted locus.

Yue-zhong Wu, C. Plass, G. Leone, 2002, Gene.

Three Novel Pigmentation Mutants Generated by Genome-Wide Random ENU Mutagenesis in the Mouse

Steve D. M. Brown, S. Rastan, E. Fisher, 2004, Comparative and functional genomics.

Transcription Driven Somatic DNA Methylation within the Imprinted Gnas Cluster

Charlotte Tibbit, J. Peters, M. Fray, 2015, PloS one.

Two ENU-induced mutations in Rasgrf1 and early mouse growth retardation

P. Orban, R. Brambilla, J. Peters, 2003, Mammalian Genome.

Biochemical genetics of a new glucosephosphate isomerase allele (Gpi-1c) from wild mice

G. Bulfield, J. Peters, R. Padua, 1978, Biochemical Genetics.

A gene (Neu-1) on chromosome 17 of the mouse affects acid alpha-glucosidase and codes for neuraminidase.

J. Peters, D. Swallow, S. Andrews, 1981, Genetical research.

Mor2, supernatant malate dehydrogenase, is linked to wa2 and Hba on mouse chromosome 11 in a region of homology with human chromosome 2p.

J. Peters, S. Ball, H. Moseley, 1994, Genomics.

Linkage analyses and biochemical genetics of sorbitol dehydrogenase-1 (Sdh-1) in the mouse

J. Peters, S. Andrews, 1983, Biochemical Genetics.

A presumed deletion covering the W and Ph loci of the mouse.

M. Lyon, P. Glenister, J. Peters, 1984, Genetical research.

Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged mice

C. Abbott, G. Muscat, P. Koopman, 2000, Nature Genetics.

Progressive loss of motor neuron function in wasted mice: effects of a spontaneous null mutation in the gene for the eEF1 A2 translation factor.

R. Ribchester, H. Newbery, C. Abbott, 2005, Journal of neuropathology and experimental neurology.

Deletion of the Snord116/SNORD116 Alters Sleep in Mice and Patients with Prader-Willi Syndrome.

A. Mauro, A. Gozzi, L. Priano, 2016, Sleep.

Deletion of the Snord 116 / SNORD 116 Alters Sleep in Mice and Patients with Prader-Willi Syndrome

A. Mauro, A. Gozzi, L. Priano, 2016 .

Mouse Chromosome 2

D. Church, J. Peters, A. Zuberi, 1999, Mammalian Genome.

Maternal inheritance of the Gnas cluster mutation Ex1A-T affects size, implicating NESP55 in growth

T. Hough, J. Peters, R. Fischer‐Colbrie, 2013, Mammalian Genome.

ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis

Steve D. M. Brown, K. Steel, J. Guénet, 2002, Mammalian Genome.

Linkage mapping of the Aldo-2, Pax-5, Ambp, and D4h9S3E loci on mouse chromosome 4 in the region of homology with human chromosome 9.

C. Abbott, J. Peters, J. Fountain, 1993, Genomics.

Xylose dehydrogenase-1, a new gene on mouse chromosome 7

J. Peters, M. Newton, S. Andrews, 1982, Biochemical Genetics.

Linkage relationships of peptidase-7, Pep-7, in the mouse

S. Povey, S. Jeremiah, J. Peters, 1983, Biochemical Genetics.

Chromosome maps of man and mouse II

M. Lyon, J. Edwards, V. Buckle, 1984 .

Genetic and functional analysis of neuronatin in mice with maternal or paternal duplication of distal Chr 2.

M. Surani, S. Barton, J. Peters, 1997, Developmental biology.

A presumed deletion covering the W and Ph loci of the mouse.

M. Lyon, P. Glenister, J. Peters, 1984, Genetical research.