Zobrazeno 1 - 10
of 50
pro vyhledávání: '"B. M. Cattanach"'
Publikováno v:
The Veterinary Record
The objective of this paper was to investigate by pedigree-based genetic means the origins and inheritance of arrhythmogenic right ventricular cardiomyopathy (ARVC) in UK Boxers and assess the role of the proposed causal mutation in the gene, Striati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a092db5adbab2fe387ef4549256fe0e
https://eprints.gla.ac.uk/107045/1/107045.pdf
https://eprints.gla.ac.uk/107045/1/107045.pdf
Autor:
Beechey Cv, E. Kyriakides, B. M. Cattanach, Jennifer A. Barrie, Ian R. Griffiths, M. C. McCulloch, King H
Publikováno v:
Journal of Neurocytology. 26:557-566
Animals with spontaneous mutations affecting myelin formation have provided useful information about the genetic and cellular mechanisms regulating normal and abnormal myelination. In this paper we describe a novel murine mutation termed hindshaker (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0874d987b02e82b6edc02bc6ca06f74c
https://doi.org/10.1023/a:1015486508111
https://doi.org/10.1023/a:1015486508111
Autor:
P, Eversole-Cire, A C, Ferguson-Smith, H, Sasaki, K D, Brown, B M, Cattanach, F A, Gonzales, M A, Surani, P A, Jones
Publikováno v:
Molecular and Cellular Biology. 13:4928-4938
The mouse insulin-like growth factor II gene (Igf 2), located on distal chromosome 7, is parentally imprinted such that the paternal allele is expressed while the maternal allele is transcriptionally silent. We derived a cell line from a mouse embryo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b46fd4664b559f41c88149820ed077f3
https://doi.org/10.1128/mcb.13.8.4928-4938.1993
https://doi.org/10.1128/mcb.13.8.4928-4938.1993
Autor:
B M Cattanach, H Sasaki, K D Brown, Anne C. Ferguson-Smith, Peter A. Jones, Felicidad A. Gonzales, M A Surani, P Eversole-Cire
Publikováno v:
Molecular and Cellular Biology. 13:4928-4938
The mouse insulin-like growth factor II gene (Igf 2), located on distal chromosome 7, is parentally imprinted such that the paternal allele is expressed while the maternal allele is transcriptionally silent. We derived a cell line from a mouse embryo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8576a1eec0ef55aa4a833e62102ddfef
https://doi.org/10.1128/mcb.13.8.4928
https://doi.org/10.1128/mcb.13.8.4928
Autor:
B. M. Cattanach
Publikováno v:
Clinical Genetics. 8:389-390
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0055285d1d12241c37db4d14d028391b
https://doi.org/10.1111/j.1399-0004.1975.tb01524.x
https://doi.org/10.1111/j.1399-0004.1975.tb01524.x
Autor:
C M, Williamson, C V, Beechey, S T, Ball, E R, Dutton, B M, Cattanach, C, Tease, F, Ishino, J, Peters
Publikováno v:
Cytogenetics and cell genetics. 81(1)
Nine regions on six mouse autosomes are subject to imprinting and uniparental inheritance of any one of these regions results in mice with phenotypic anomalies. So far on distal Chromosome (Chr) 2 there is a unique imprinting region between 2H3 and 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3b65433cee94d0e8479413448b950d36
https://pubmed.ncbi.nlm.nih.gov/9691180
https://pubmed.ncbi.nlm.nih.gov/9691180
Publikováno v:
Cytogenetics and cell genetics. 80(1-4)
Mice with maternal and paternal disomy for chromosome 11 (Chr 11) show growth retarded and overgrowth phenotypes, respectively, which can be attributed to genomic imprinting. Previous studies have defined the region of Chr 11 responsible (the Chr 11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::677a2518f39f11367999331bc4e10197
https://pubmed.ncbi.nlm.nih.gov/9678333
https://pubmed.ncbi.nlm.nih.gov/9678333
Autor:
H, King, M C, McCulloch, J A, Barrie, E, Kyriakides, C V, Beechey, B M, Cattanach, I R, Griffiths
Publikováno v:
Journal of neurocytology. 26(8)
Animals with spontaneous mutations affecting myelin formation have provided useful information about the genetic and cellular mechanisms regulating normal and abnormal myelination. In this paper we describe a novel murine mutation termed hindshaker (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::043113a02107a19f9f052b38339cec23
https://pubmed.ncbi.nlm.nih.gov/9350807
https://pubmed.ncbi.nlm.nih.gov/9350807
Autor:
B. M. Cattanach, J. Jones
Publikováno v:
Journal of inherited metabolic disease. 17(4)
Genetic imprinting specifies a germline marking that subsequently results in the repression of one or other parental allele at some point in development. Genetic manipulations to generate maternal and paternal duplications of specific chromosome regi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc51922c486217089dc2583b740d099d
https://pubmed.ncbi.nlm.nih.gov/7967491
https://pubmed.ncbi.nlm.nih.gov/7967491
Autor:
M. L. Fanarraga, Jennifer A. Barrie, Peter G. E. Kennedy, Ian R. Griffiths, B. M. Cattanach, M. C. McCulloch, Peter J. Brophy
Publikováno v:
Neuropathology and applied neurobiology. 17(4)
This study examines the myelin deficits found in the spinal cord and optic nerves of female mice heterozygotes for rumpshaker (rsh), an X-linked mutation causing hypomyelination. No clinical abnormalities were detected but morphological changes were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49363e05af9124eb8f8da86cbc2da61e
https://pubmed.ncbi.nlm.nih.gov/1944806
https://pubmed.ncbi.nlm.nih.gov/1944806