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A long noncoding RNA influences the choice of the X chromosome to be inactivated

Proceedings of the National Academy of Sciences - PNAS, 2022-07, Vol.119 (28), p.e2118182119-e2118182119

2022

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An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesis

European heart journal, 2018-11, Vol.39 (44), p.3932-3944

2018

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β-Defensin Mutation Causes Black Coat Color in Domestic Dogs

Science (American Association for the Advancement of Science), 2007-11, Vol.318 (5855), p.1418-1423

2007

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Gene Dosage Effects at the Imprinted Gnas Cluster

PloS one, 2013-06, Vol.8 (6), p.e65639-e65639

2013

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Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse

Current biology, 2003-07, Vol.13 (13), p.1129-1133

2003

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Epigenetic analysis of the Dlk1-Gtl2 imprinted domain on mouse chromosome 12: implications for imprinting control from comparison with Igf2-H19

Human molecular genetics, 2002, Vol.11 (1), p.77-86

2002

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Imprinted expression of the murine Angelman syndrome gene, Ube3a , in hippocampal and Purkinje neurons

Nature genetics, 1997-09, Vol.17 (1), p.75-78

1997

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Disruption of ferroportin 1 regulation causes dynamic alterations in iron homeostasis and erythropoiesis in polycythaemia mice

Development (Cambridge), 2004-04, Vol.131 (8), p.1859-1868

2004

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Interactions Between Imprinting Effects in the Mouse

Genetics (Austin), 2004-09, Vol.168 (1), p.397-413

2004

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Parental-origin-specific epigenetic modification of the mouse H19 gene

Nature (London), 1993-04, Vol.362 (6422), p.751-755

1993

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The Imprinted Oedematous-Small Mutation on Mouse Chromosome 2 Identifies New Roles for Gnas and Gnasxl in Development

Genomics (San Diego, Calif.), 2002-10, Vol.80 (4), p.373-375

2002

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Bob Edwards tribute

Reproductive biomedicine online, 2011, Vol.23, p.9-9

Cattanach, Bruce

2011

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Disruption of mesodermal enhancers for Igf2 in the minute mutant

Development (Cambridge), 2002-04, Vol.129 (7), p.1657-1668

2002

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Deletion of Y chromosome sequences located outside the testis determining region can cause XY female sex reversal

Nature genetics, 1993-11, Vol.5 (3), p.301-307

1993

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A candidate model for Angelman syndrome in the mouse

Mammalian genome, 1997-07, Vol.8 (7), p.472-478

1997

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A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression

Nature genetics, 1992-12, Vol.2 (4), p.270-274

1992

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Stem cell factor is encoded at the SI locus of the mouse and is the ligand for the c- kit tyrosine kinase receptor

Cell, 1990-10, Vol.63 (1), p.213-224

1990

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Mapping the murine Xce locus with (CA)n repeats

Mammalian genome, 1993-09, Vol.4 (9), p.523-530

1993

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Spontaneous and Radiation-induced Leukemogenesis of the Mouse Small Eye Mutant, Pax6Sey3H

JOURNAL OF RADIATION RESEARCH, 2004, Vol.45 (2), p.245-251

2004

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

Journal of radiation research, 2004-06, Vol.45 (2), p.245

2004

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Organization and Parent-of-Origin-Specific Methylation of Imprinted Peg3 Gene on Mouse Proximal Chromosome 7

Genomics (San Diego, Calif.), 2000-02, Vol.63 (3), p.333-340

2000

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Autosomal and X-chromosome imprinting

Development (Cambridge), 1990-04, Vol.108 (Supplement), p.63-72

1990

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Mouse Homologues of the Human AZF Candidate Gene RBM Are Expressed in Spermatogonia and Spermatids, and Map to a Y Chromosome Deletion Interval Associated with a High Incidence of Sperm Abnormalities

Human molecular genetics, 1998-04, Vol.7 (4), p.715-727

1998

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Two imprinted gene mutations : three phenotypes

Human molecular genetics, 2000-09, Vol.9 (15), p.2263-2273

2000

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

Nature genetics, 1999-06, Vol.22 (2), p.182-187

1999

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A long noncoding RNA influences the choice of the X chromosome to be inactivated

An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesis

β-Defensin Mutation Causes Black Coat Color in Domestic Dogs

Gene Dosage Effects at the Imprinted Gnas Cluster

Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse

Epigenetic analysis of the Dlk1-Gtl2 imprinted domain on mouse chromosome 12: implications for imprinting control from comparison with Igf2-H19

Imprinted expression of the murine Angelman syndrome gene, Ube3a , in hippocampal and Purkinje neurons

Disruption of ferroportin 1 regulation causes dynamic alterations in iron homeostasis and erythropoiesis in polycythaemia mice

Interactions Between Imprinting Effects in the Mouse

Parental-origin-specific epigenetic modification of the mouse H19 gene

The Imprinted Oedematous-Small Mutation on Mouse Chromosome 2 Identifies New Roles for Gnas and Gnasxl in Development

Bob Edwards tribute

Disruption of mesodermal enhancers for Igf2 in the minute mutant

Deletion of Y chromosome sequences located outside the testis determining region can cause XY female sex reversal

A candidate model for Angelman syndrome in the mouse

A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression

Stem cell factor is encoded at the SI locus of the mouse and is the ligand for the c- kit tyrosine kinase receptor

Mapping the murine Xce locus with (CA)n repeats

Spontaneous and Radiation-induced Leukemogenesis of the Mouse Small Eye Mutant, Pax6Sey3H

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

Organization and Parent-of-Origin-Specific Methylation of Imprinted Peg3 Gene on Mouse Proximal Chromosome 7

Autosomal and X-chromosome imprinting

Mouse Homologues of the Human AZF Candidate Gene RBM Are Expressed in Spermatogonia and Spermatids, and Map to a Y Chromosome Deletion Interval Associated with a High Incidence of Sperm Abnormalities

Two imprinted gene mutations : three phenotypes

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

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