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Items: 1 to 50 of 116

1.

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

Chatterjee D, Fatah M, Akdis D, Spears DA, Koopmann TT, Mittal K, Rafiq MA, Cattanach BM, Zhao Q, Healey JS, Ackerman MJ, Bos JM, Sun Y, Maynes JT, Brunckhorst C, Medeiros-Domingo A, Duru F, Saguner AM, Hamilton RM.

Eur Heart J. 2018 Nov 21;39(44):3932-3944. doi: 10.1093/eurheartj/ehy567.

PMID:
30239670
2.

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

Cattanach BM, Dukes-McEwan J, Wotton PR, Stephenson HM, Hamilton RM.

Vet Rec. 2015 May 9;176(19):492. doi: 10.1136/vr.102821. Epub 2015 Feb 6.

3.

Gene Dosage Effects at the Imprinted Gnas Cluster.

Ball ST, Kelly ML, Robson JE, Turner MD, Harrison J, Jones L, Napper D, Beechey CV, Hough T, Plagge A, Cattanach BM, Cox RD, Peters J.

PLoS One. 2013 Jun 18;8(6):e65639. doi: 10.1371/journal.pone.0065639. Print 2013.

4.

A -defensin mutation causes black coat color in domestic dogs.

Candille SI, Kaelin CB, Cattanach BM, Yu B, Thompson DA, Nix MA, Kerns JA, Schmutz SM, Millhauser GL, Barsh GS.

Science. 2007 Nov 30;318(5855):1418-23. Epub 2007 Oct 18.

5.

Interactions between imprinting effects: summary and review.

Cattanach BM, Beechey CV, Peters J.

Cytogenet Genome Res. 2006;113(1-4):17-23. Review.

PMID:
16575158
6.

Interactions between imprinting effects in the mouse.

Cattanach BM, Beechey CV, Peters J.

Genetics. 2004 Sep;168(1):397-413.

7.

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

Nitta Y, Yoshida K, Satoh K, Senba K, Nakagata N, Peters J, Cattanach BM.

J Radiat Res. 2004 Jun;45(2):245-51.

8.

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

Mok H, Jelinek J, Pai S, Cattanach BM, Prchal JT, Youssoufian H, Schumacher A.

Development. 2004 Apr;131(8):1859-68.

9.
10.

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

Takada S, Paulsen M, Tevendale M, Tsai CE, Kelsey G, Cattanach BM, Ferguson-Smith AC.

Hum Mol Genet. 2002 Jan 1;11(1):77-86.

PMID:
11773001
11.

Two imprinted gene mutations: three phenotypes.

Cattanach BM, Peters J, Ball S, Rasberry C.

Hum Mol Genet. 2000 Sep 22;9(15):2263-73.

PMID:
11001929
12.

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

Li LL, Szeto IY, Cattanach BM, Ishino F, Surani MA.

Genomics. 2000 Feb 1;63(3):333-40.

PMID:
10704281
13.

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

Banerjee S, Singh PB, Rasberry C, Cattanach BM.

Mech Dev. 2000 Feb;90(2):217-26.

14.

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

Cattanach BM, Papworth D, Patrick G, Goodhead DT, Hacker T, Cobb L, Whitehill E.

Mutat Res. 1998 Jul 17;403(1-2):1-12.

PMID:
9726000
15.

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

Williamson CM, Beechey CV, Ball ST, Dutton ER, Cattanach BM, Tease C, Ishino F, Peters J.

Cytogenet Cell Genet. 1998;81(1):73-8.

PMID:
9691180
16.

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

Cattanach BM, Shibata H, Hayashizaki Y, Townsend KM, Ball S, Beechey CV.

Cytogenet Cell Genet. 1998;80(1-4):41-7.

PMID:
9678333
17.

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.

Mahadevaiah SK, Odorisio T, Elliott DJ, Rattigan A, Szot M, Laval SH, Washburn LL, McCarrey JR, Cattanach BM, Lovell-Badge R, Burgoyne PS.

Hum Mol Genet. 1998 Apr;7(4):715-27.

PMID:
9499427
18.

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

Kikyo N, Williamson CM, John RM, Barton SC, Beechey CV, Ball ST, Cattanach BM, Surani MA, Peters J.

Dev Biol. 1997 Oct 1;190(1):66-77.

19.

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

Albrecht U, Sutcliffe JS, Cattanach BM, Beechey CV, Armstrong D, Eichele G, Beaudet AL.

Nat Genet. 1997 Sep;17(1):75-8.

PMID:
9288101
20.

Hindshaker, a novel myelin mutant showing hypomyelination preferentially affecting the spinal cord.

King H, McCulloch MC, Barrie JA, Kyriakides E, Beechey CV, Cattanach BM, Griffiths IR.

J Neurocytol. 1997 Aug;26(8):557-66.

PMID:
9350807
21.

A candidate model for Angelman syndrome in the mouse.

Cattanach BM, Barr JA, Beechey CV, Martin J, Noebels J, Jones J.

Mamm Genome. 1997 Jul;8(7):472-8. Erratum in: Mamm Genome 1997;8(11):877.

PMID:
9195990
22.

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

Cattanach BM, Beechey CV, Rasberry C, Jones J, Papworth D.

Genet Res. 1996 Aug;68(1):35-44.

PMID:
8772424
23.

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

Laval SH, Glenister PH, Rasberry C, Thornton CE, Mahadevaiah SK, Cooke HJ, Burgoyne PS, Cattanach BM.

Proc Natl Acad Sci U S A. 1995 Oct 24;92(22):10403-7.

24.

Ubiquitous expression and imprinting of Snrpn in the mouse.

Barr JA, Jones J, Glenister PH, Cattanach BM.

Mamm Genome. 1995 Jun;6(6):405-7.

PMID:
7647462
25.

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

Cattanach BM, Patrick G, Papworth D, Goodhead DT, Hacker T, Cobb L, Whitehill E.

Int J Radiat Biol. 1995 May;67(5):607-15.

PMID:
7775836
26.

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

Hustad CM, Perry WL, Siracusa LD, Rasberry C, Cobb L, Cattanach BM, Kovatch R, Copeland NG, Jenkins NA.

Genetics. 1995 May;140(1):255-65.

27.

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

Cattanach BM, Rasberry C.

Mutat Res. 1994 Nov 1;311(1):77-84.

PMID:
7526177
28.

Genetic imprinting in the mouse: implications for gene regulation.

Cattanach BM, Jones J.

J Inherit Metab Dis. 1994;17(4):403-20. Review.

PMID:
7967491
29.

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

van der Meer Y, Cattanach BM, de Rooij DG.

Mutat Res. 1993 Dec;290(2):201-10.

PMID:
7694111
30.

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

Capel B, Rasberry C, Dyson J, Bishop CE, Simpson E, Vivian N, Lovell-Badge R, Rastan S, Cattanach BM.

Nat Genet. 1993 Nov;5(3):301-7.

PMID:
8275095
31.

Mapping the murine Xce locus with (CA)n repeats.

Simmler MC, Cattanach BM, Rasberry C, Rougeulle C, Avner P.

Mamm Genome. 1993 Sep;4(9):523-30.

PMID:
8118102
32.

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

Eversole-Cire P, Ferguson-Smith AC, Sasaki H, Brown KD, Cattanach BM, Gonzales FA, Surani MA, Jones PA.

Mol Cell Biol. 1993 Aug;13(8):4928-38.

33.

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

Ferguson-Smith AC, Sasaki H, Cattanach BM, Surani MA.

Nature. 1993 Apr 22;362(6422):751-5.

PMID:
8469285
34.

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

Cattanach BM, Burtenshaw MD, Rasberry C, Evans EP.

Nat Genet. 1993 Jan;3(1):56-61.

PMID:
8490655
35.

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

Cattanach BM, Barr JA, Evans EP, Burtenshaw M, Beechey CV, Leff SE, Brannan CI, Copeland NG, Jenkins NA, Jones J.

Nat Genet. 1992 Dec;2(4):270-4.

PMID:
1303278
36.

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

Wood PJ, Stratford IJ, Sansom JM, Cattanach BM, Quinney RM, Adams GE.

Int J Radiat Oncol Biol Phys. 1992;22(3):473-6.

PMID:
1735681
37.

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

Fanarraga ML, Griffiths IR, McCulloch MC, Barrie JA, Cattanach BM, Brophy PJ, Kennedy PG.

Neuropathol Appl Neurobiol. 1991 Aug;17(4):323-34.

PMID:
1944806
38.

Embryological and molecular investigations of parental imprinting on mouse chromosome 7.

Ferguson-Smith AC, Cattanach BM, Barton SC, Beechey CV, Surani MA.

Nature. 1991 Jun 20;351(6328):667-70.

PMID:
2052093
39.

Testicular steroidogenesis in X/X sex-reversed mice.

O'Shaughnessy PJ, Abbott DH, Leigh AJ, Cattanach BM.

Int J Androl. 1991 Apr;14(2):140-8.

PMID:
1869316
40.

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

Cattanach BM, Rasberry C, Evans EP, Dandolo L, Simmler MC, Avner P.

Cytogenet Cell Genet. 1991;56(3-4):137-43.

PMID:
2055107
41.

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

Brockdorff N, Kay G, Cattanach BM, Rastan S.

Mamm Genome. 1991;1(3):152-7.

PMID:
1797229
42.

Illegitimate pairing of the X and Y chromosomes in Sxr mice.

Cattanach BM, Rasberry C, Burtenshaw MD, Evans EP.

Genet Res. 1990 Oct-Dec;56(2-3):121-8.

PMID:
2272501
43.

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

Griffiths IR, Scott I, McCulloch MC, Barrie JA, McPhilemy K, Cattanach BM.

J Neurocytol. 1990 Apr;19(2):273-83.

PMID:
1694232
44.

The mouse mutation ulnaless on chromosome 2.

Davisson MT, Cattanach BM.

J Hered. 1990 Mar-Apr;81(2):151-3.

PMID:
2338491
45.

Autosomal and X-chromosome imprinting.

Cattanach BM, Beechey CV.

Dev Suppl. 1990:63-72. Review.

PMID:
2090432
46.

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

Jones J, Peters J, Rasberry C, Cattanach BM.

Genet Res. 1989 Jun;53(3):193-9.

PMID:
2767429
47.
48.

Sex chromosome pairing patterns in male mice of novel Sxr genotypes.

Tease C, Cattanach BM.

Chromosoma. 1989 Mar;97(5):390-5.

PMID:
2721310
49.

Mammalian chromosome imprinting.

Cattanach BM.

Genome. 1989;31(2):1083-4. No abstract available.

PMID:
2632335
50.

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

Guillery RW, Jeffery G, Cattanach BM.

Development. 1987 Dec;101(4):857-67.

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