B. Cattanach

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Gonadotrophin-releasing hormone deficiency in a mutant mouse with hypogonadism

G. Fink, B. Cattanach, C. Iddon, 1977, Nature.

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.

R. Lovell-Badge, D. Elliott, S. Laval, 1998, Human molecular genetics.

The radiosensitivity of spermatogonial stem cells in C3H/101 F1 hybrid mice.

D. D. de Rooij, B. Cattanach, Y. van der Meer, 1993, Mutation research.

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

M. Azim Surani, Hiroyuki Sasaki, Bruce M. Cattanach, 1993, Nature.

Activation of an imprinted Igf 2 gene in mouse somatic cell cultures

M. Surani, A. Ferguson-Smith, P. Eversole-Cire, 1993 .

Large deletions and other gross forms of chromosome imbalance compatible with viability and fertility in the mouse

E. P. Evans, B. Cattanach, M. Burtenshaw, 1993, Nature Genetics.

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

J. Healey, M. Rafiq, M. Ackerman, 2018, European heart journal.

Abnormally high variability in the uncrossed retinofugal pathway of mice with albino mosaicism.

R. Guillery, G. Jeffery, B. Cattanach, 1987, Development.

The response of spontaneous and transplantable murine tumors to vasoactive agents measured by 31P magnetic resonance spectroscopy.

G. Adams, I. Stratford, P. Wood, 1992, International journal of radiation oncology, biology, physics.

Genetic imprinting in the mouse: Implications for gene regulation

B. Cattanach, J. Jones, 1994, Journal of Inherited Metabolic Disease.

Activation of an imprinted Igf 2 gene in mouse somatic cell cultures

M. Surani, A. Ferguson-Smith, P. Eversole-Cire, 1993, Molecular and cellular biology.

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.

Embryonic inheritance of the chromatin organisation of the imprinted H19 domain in mouse spermatozoa

Prim B. Singh, Subhasis Banerjee, B. Cattanach, 2000, Mechanisms of Development.

Association of a redefined proximal mouse chromosome 11 imprinting region and U2afbp-rs/U2af1-rs1 expression

Y. Hayashizaki, S. Ball, B. Cattanach, 1998, Cytogenetic and Genome Research.

A candidate model for angelman syndrome in the mouse

J. Noebels, B. Cattanach, C. Beechey, 1997, Mammalian Genome.

Parental origin effects in mice.

B. Cattanach, 1986, Journal of embryology and experimental morphology.

OP-EHEA180582 1..13

J. Healey, M. Rafiq, M. Ackerman, 2018 .

Induction of specific locus mutations in mouse spermatogonial stem cells by combined chemical X-ray treatments.

J. Peters, B. Cattanach, C. Rasberry, 1989, Mutation research.

Analysis of mouse conceptuses with uniparental duplication/deficiency for distal chromosome 12: comparison with chromosome 12 uniparental disomy and implications for genomic imprinting

A. Ferguson-Smith, B. Cattanach, M. Watkins, 2006, Cytogenetic and Genome Research.

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.

Snaker: A dominant abnormality caused by chromosomal imbalance

B. Cattanach, 1965, Zeitschrift für Vererbungslehre.

Haematopoietic role for Patch (Ph) revealed by new W mutant (Wct) in mice.

B. Cattanach, J. Loutit, 1983, Genetical research.

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.

Autosomal and X-chromosome imprinting.

B. Cattanach, C. Beechey, 1990, Development (Cambridge, England). Supplement.

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

S. Rastan, R. Lovell-Badge, C. Bishop, 1993, Nature Genetics.

Enzyme levels in testis and other tissues of genetically sex-reversed mice.

J. T. Jones, B. Cattanach, S. Andrews, 1979, Journal of reproduction and fertility.

A genetically determined variant of the a-subunit of lactic dehydrogenase in the deer mouse

B. Cattanach, J. N. Perez, 1969, Biochemical Genetics.

Y chromosome short arm-Sxr recombination in XSxr/Y males causes deletion of Rbm and XY female sex reversal.

P. Glenister, S. Laval, H. Cooke, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Paris Conference (1971): Standardization in human cytogenetics.

J. F. Lasley, B. N. Day, H. Klinger, 1972, Cytogenetics.

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

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

The mouse mutation ulnaless on chromosome 2.

M. Davisson, B. Cattanach, 1990, The Journal of heredity.

A chemically-induced variegated-type position effect in the mouse

B. Cattanach, 2004, Zeitschrift für Vererbungslehre.

Induction of specific-locus mutations in female mice by triethylenemelamine (TEM).

B. Cattanach, 1982, Mutation research.

Sterile period, translocation and specific locus mutation in the mouse following fractionated x-ray treatments with different fractionation intervals.

B. Cattanach, H. Moseley, 1974, Mutation research.

Specific Locus Mutation in Mice

B. Cattanach, 1971 .

Induction of paternal sex-chromosome losses and deletions and of autosomal gene mutations by the treatment of mouse post-meiotic germ cells with triethylenemelamine.

B. Cattanach, 1967, Mutation research.

Chemically induced mutations in mice.

B. Cattanach, 1966, Mutation research.

Controlling elements in the mouse X-chromosome. I. Interaction with the X-linked genes.

B. Cattanach, C. E. Pollard, J. N. Perez, 1969, Genetical research.

Crossover suppression in mice heterozygous for tobacco mouse metacentrics.

B. Cattanach, 1978, Cytogenetics and cell genetics.

Enhanced spermatogonial stem cell killing and reduced translocation yield from X-irradiated 101/H mice.

B. Cattanach, M. Kirk, 1987, Mutation research.

Sex‐Reversed Mice and Sex Determination

B. Cattanach, BRUCE M. CATTANACH, 1987, Annals of the New York Academy of Sciences.

Sex-reversed mice: XX and XO males.

B. Cattanach, C. E. Pollard, S. Hawker, 1971, Cytogenetics.

Genetical effects of caffeine in mice

B. Cattanach, 2004, Zeitschrift für Vererbungslehre.

Differential activity of maternally and paternally derived chromosome regions in mice

B. Cattanach, B. M. Cattanach, M. Kirk, 1985, Nature.

Information on the Y chromosome and sex determination from mutants and other variants of sexual development.

B. Cattanach, 1985, Archives d'anatomie microscopique et de morphologie experimentale.

Male, female and intersex development in mice of identical chromosome constitution

E. P. Evans, B. Cattanach, J. Barlow, 1982, Nature.

Meitoic crossing-over between the X and Y chromosomes of male mice carrying the sex-reversing (Sxr) factor

E. P. Evans, B. Cattanach, M. Burtenshaw, 1982, Nature.

Controlling elements in the mouse. IV. Evidence of non-random X-inactivation.

B. Cattanach, P. Johnston, 1981, Genetical research.

Serological evidence for H–Y antigen in Sxr, XX sex-reversed phenotypic males

S. Wachtel, D. Bennett, B. Cattanach, 1977, Nature.

Position effect variegation in the mouse.

B. Cattanach, 1974, Genetical research.

Genetic disorders of sex determination in mice and other mammals, p. 129-141. In a. G. Motulsky and w. Lentz (ed.) Internat. Cong. Ser. NO. 310- -birth Defects-(proc. Fourth internat. Conf. Vienna, austria, 2-8

B. Cattanach, 1973 .

Controlling elements in the mouse X chromosome.

B. Cattanach, J. Isaacson, 1967, Genetics.

Canine homolog of the T-box transcription factor T; failure of the protein to bind to its DNA target leads to a short-tail phenotype

M. Breen, M. Binns, B. Cattanach, 2001, Mammalian Genome.

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

Steve D. M. Brown, E. Fisher, K. Steel, 2003, Current Biology.

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

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

A test of distributive pairing between two specific non-homologous chromosomes in the mouse.

B. Cattanach, 1967, Cytogenetics.

Induction of Translocations in Mice by Triethylenemelamine

B. Cattanach, 1957, Nature.

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

David A. Williams, S. Galli, K. Zsebo, 1990, Cell.

The sensitivity of the mouse testis to the mutagenic action of triethylenemelamine

B. Cattanach, 2004, Zeitschrift für Vererbungslehre.

Mutagenicity of Selected Chemicals in Mammals: The Heritable Translocation Test

B. Cattanach, W. Generoso, A. Malashenko, 1981 .

Ethyl methanesulfonate-induced chromosome breakage in the mouse.

B. Cattanach, J. Isaacson, C. E. Pollard, 1968, Mutation research.

The effect of triethylene-melamine on the ferility of female mice.

B. Cattanach, 1959, International journal of radiation biology and related studies in physics, chemistry, and medicine.

IV.—The Effects of Triethylenemelamine on the Fertility of Male Mice

B. Cattanach, R. Edwards, 1958 .

A β-Defensin Mutation Causes Black Coat Color in Domestic Dogs

G. Barsh, G. Millhauser, J. Kerns, 2007, Science.

Books received for review

J. F. Lasley, B. N. Day, H. Klinger, 1923, The Mathematical Gazette.

Comparison of the Mutagenic Effect of Chemicals and Ionizing Radiation in the Spermatogenic Cells of the Mouse1

B. Cattanach, 1975 .

AUTOSOMAL TRISOMY IN THE MOUSE.

B. Cattanach, 1964, Cytogenetics.

Testicular steroidogenesis in X/X sex-reversed mice.

P. O’Shaughnessy, D. Abbott, B. Cattanach, 1991, International journal of andrology.

An XYY sex-chromosome constitution in the mouse.

B. Cattanach, C. E. Pollard, 1969, Cytogenetics.

Enhanced specific-locus mutation response of 101/H male mice to single, acute X-irradiation.

B. Cattanach, C. Rasberry, 1994, Mutation research.

X-inactivation of the Sts locus in the mouse: an anomaly of the dosage compensation mechanism.

B. Cattanach, C. Rasberry, J. Jones, 1989, Genetical research.

The E6-Ap ubiquitin-protein ligase (UBE3A) gene is localized within a narrowed Angelman syndrome critical region.

J. Bressler, D. Ledbetter, J. Sutcliffe, 1997, Genome research.

Control of chromosome inactivation.

B. Cattanach, 1975, Annual review of genetics.

Embryological and molecular investigations of parental imprinting on mouse chromosome 7

M. Surani, A. Ferguson-Smith, S. Barton, 1991, Nature.

Sex chromosome pairing patterns in male mice of novel Sxr genotypes

B. Cattanach, C. Tease, 1989, Chromosoma.

Interactions Between Imprinting Effects in the Mouse

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

X-ray induction of translocations in mice carrying metacentrics (Robertsonian fusions); detection of whole arm chromosome exchanges.

B. Cattanach, M. Crocker, 1981, Mutation research.

Genetic imprinting map.

B. Cattanach, C. Beechey, A. Searle, 1990 .

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.

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.

Time of initiation and site of action of the mouse chromosome 11 imprinting effects.

B. Cattanach, D. Papworth, C. Beechey, 1996, Genetical research.

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

S. Leff, N. Copeland, N. Jenkins, 1992, Nature Genetics.

Nodisjunction and reduced fertility caused by the tobacco mouse metacentric chromosomes.

B. Cattanach, H. Moseley, 1973, Cytogenetics and cell genetics.

Evidence of non-random X chromosome activity in the mouse.

B. Cattanach, C. E. Williams, 1972, Genetical research.

Xce genotype has no impact on the effect of imprinting on X-chromosome expression in the mouse yolk sac endoderm.

B. Cattanach, T. Bücher, J. West, 1986, Genetical research.

Mary Lyon: an appreciation.

B. Cattanach, J. Peters, T. Searle, 1990, Genetical research.

Interaction between the Xce locus and imprinting of the paternal X chromosome in mouse yolk-sac endoderm

S. Rastan, B. Cattanach, 1983, Nature.

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

S. Takada, A. Ferguson-Smith, G. Kelsey, 2002, Human molecular genetics.

Ubiquitous expression and imprinting of Snrpn in the mouse

P. Glenister, B. Cattanach, J. Jones, 1995, Mammalian Genome.

From M. R. C. Mutagenesis Research Group, Institute of Animal Genetics, Edinburgh, 9 GENETICAL EFFECTS OF CAFFEINE IN MICE

B. Cattanach, 1962 .

Investigation of lung tumour induction in BALB/cJ mice following paternal X-irradiation.

L. M. Cobb, D. Goodhead, B. Cattanach, 1995, International journal of radiation biology.

Genetic effects of combined chemical-X-ray treatments in male mouse germ cells.

B. Cattanach, C. Rasberry, 1987, International journal of radiation biology and related studies in physics, chemistry, and medicine.

Evidence for the re-establishment of a heterogeneity in radiosensitivity among spermatogonial stem cells repopulating the mouse testis following depletion by X-rays.

B. Cattanach, J. Barlow, 1984, Mutation research.

Modified genetic response to X-irradiation of mouse spermatogonial stem cells surviving treatment with TEM.

B. Cattanach, A. Crocker, 1980, Mutation research.

Translocation yield from mouse spermatogonial stem cells following unequal-sized x-ray fractionations: evidence of radiation-induced loss of heterogeneity.

B. Cattanach, A. Crocker, 1979, Mutation research.

Translocation yield from the mouse spermatogonial stem cell following fractionated X-ray treatments: influence of unequal fraction size and of increasing fractionation interval.

B. Cattanach, C. M. Heath, J. M. Tracey, 1976, Mutation research.

Spermatogonial stem cell killing in the mouse following single and fractionated x-ray doses, as assessed by length of sterile period.

B. Cattanach, 1974, Mutation research.

Investigation of lung tumour induction in C3H/HeH mice, with and without tumour promotion with urethane, following paternal X-irradiation.

D. Goodhead, B. Cattanach, D. Papworth, 1998, Mutation research.

Translocation yield from the immature mouse testis and the nature of spermatogonial stem cell heterogeneity.

B. Cattanach, J. M. Tracey, I. Murray, 1977, Mutation research.

Genetic tests for autosomal non-disjunction and chromosome loss in mice.

B. Cattanach, D. Papworth, M. Kirk, 1984, Mutation research.

An attempt to distinguish a modified genetic response of the mouse testis to X-ray exposure by the action of a spermatogonial chalone.

B. Cattanach, J. Jones, S. Andrews, 1979, Mutation research.

Specific-locus mutation response to unequal, 1 + 9 Gy X-ray fractionations at 24-h and 4-day fraction intervals.

B. Cattanach, D. Papworth, C. Jones, 1985, Mutation research.

Selected bibliography of Susumu Ohno

C. Disteche, B. Migeon, B. Kerem, 1998, Cytogenetic and Genome Research.

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

J. Sutcliffe, G. Eichele, A. Beaudet, 1997, Nature Genetics.

Genetic control over the inactivation of autosomal genes attached to the X-chromosome

B. Cattanach, J. Isaacson, 2004, Zeitschrift für Vererbungslehre.

Controlling elements in the mouse. V. Linkage tests with X-linked genes.

B. Cattanach, D. Papworth, 1981, Genetical research.

Mapping the murine Xce locus with (CA)n repeats

P. Avner, C. Rougeulle, B. Cattanach, 1993, Mammalian Genome.

Controlling elements in the mouse X-chromosome. II. Location in the linkage map.

B. Cattanach, C. E. Pollard, J. N. Perez, 1970, Genetical research.

The location of Cattanach's translocation in the X-chromosome linkage map of the mouse.

B. Cattanach, 1966, Genetical research.

Cytological study of an X-autosome translocation in Mus musculus.

S. Ohno, B. Cattanach, 1962, Cytogenetics.

Controlling elements in the mouse X-chromosome. 3. Influence upon both parts of an X divided by rearrangement.

B. Cattanach, 1970, Genetical research.

Parental influence on X-autosome translocation-induced variegation in the mouse.

B. Cattanach, J. N. Perez, 1970, Genetical research.

Molecular genetic analysis of the Ta25H deletion: Evidence for additional deleted loci

S. Rastan, G. Kay, N. Brockdorff, 2004, Mammalian Genome.

A pedigree-based genetic appraisal of Boxer ARVC and the role of the Striatin mutation

R. Hamilton, B. Cattanach, J. Dukes-McEwan, 2015, Veterinary Record.

The mutagenicity of cyclamates and their metabolites.

B. Cattanach, 1976, Mutation research.

Molecular genetic characterization of six recessive viable alleles of the mouse agouti locus.

N. Copeland, N. Jenkins, L. Siracusa, 1995, Genetics.

Disruption of mesodermal enhancers for Igf2 in the minute mutant.

W. Reik, W. Dean, PaulR . Smith, 2002, Development.

Genetic and molecular evidence of an X-chromosome deletion spanning the tabby (Ta) and testicular feminization (Tfm) loci in the mouse.

P. Avner, L. Dandolo, E. P. Evans, 1991, Cytogenetics and cell genetics.

Organization and parent-of-origin-specific methylation of imprinted Peg3 gene on mouse proximal chromosome 7.

M. Surani, F. Ishino, B. Cattanach, 2000, Genomics.

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

J. Jelinek, J. Prchal, H. Youssoufian, 2004, Development.

Location of xce in the mouse x chromosome and effects on pgk-1 expression. Abstr.

B. Cattanach, S. Andrews, T. Bucher, 1982 .

Lack of effect of nicotine on the fertility of male and female mice

B. Cattanach, 1962, Zeitschrift für Vererbungslehre.

A search for chromosome aberrations induced in mouse spermatogonia by chemical mutagens.

B. Cattanach, C. E. Williams, 1971, Mutation research.

Hindshaker, a Novel Myelin Mutant Showing Hypomyelination Preferentially Affecting the Spinal Cord

I. Griffiths, B. Cattanach, M. McCulloch, 1997, Journal of neurocytology.

Genetic Mechanisms Determining the Central Visual Pathways of Mice

R. Guillery, B. Cattanach, G. Scott, 1973, Science.

Identification of the linkage groups carried by the metacentric chromosomes of the tobacco mouse (Mus poschiavinus).

B. Cattanach, C. E. Williams, H. Bailey, 1972, Cytogenetics.

A comparative study of the coats of chimaeric mice and those of heterozygotes for X-linked genes.

M. Lyon, B. Cattanach, H. G. Wolfe, 1972, Genetical research.

Mutagenicity tests with cyclohexylamine in the mouse.

B. Cattanach, C. E. Pollard, 1971, Mutation research.

The genetics of Sleek: a possible regulatory mutation of the tabby-crinkled-downless syndrome.

B. Cattanach, M. Crocker, 1979, Genetical research.

Control scheme for familial nephropathy in cocker spaniels

B. Cattanach, D F Macdougall, A S Nash, 1987, Veterinary Record.

Rumpshaker mouse: A new X-linked mutation affecting myelination: Evidence for a defect in PLP expression

I. Griffiths, I. Scott, B. Cattanach, 1990, Journal of neurocytology.

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

P. Avner, M. Nireekshan Kumar, A. Cerase, 2022, Proceedings of the National Academy of Sciences of the United States of America.

Mammalian chromosome imprinting.

B. Cattanach, 1989, Genome.

Rumpshaker: an X‐linked mutation affecting CNS myelination. A study of the female heterozygote

I. Griffiths, M. Fanarraga, P. Kennedy, 1991, Neuropathology and applied neurobiology.