Zobrazeno 1 - 10
of 54
pro vyhledávání: '"M F, Lyon"'
Autor:
V J, Buckle, J H, Edwards, E P, Evans, J A, Jonasson, M F, Lyon, J, Peters, A G, Searle, N S, Wedd
Publikováno v:
Clinical Genetics. 26:1-11
Chromosome displays and listings are presented showing loci whose position is known in both man and mouse, in similar manner to our previous report (Dalton et al. 1981). There is now evidence for at least 27 conserved autosomal segments with two or m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e42e605ab716677a77f0ea8ca0a2dbfd
https://doi.org/10.1111/j.1399-0004.1984.tb00780.x
https://doi.org/10.1111/j.1399-0004.1984.tb00780.x
Publikováno v:
Genetics. 126:1103-1114
The t-complex is located on the proximal third of chromosome 17 in the house mouse. Naturally occurring variant forms of the t-complex, known as complete t-haplotypes, are found in wild mouse populations. The t-haplotypes contain at least four nonove
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bd02617901dd5314b1221edf4d99f03
https://doi.org/10.1093/genetics/126.4.1103
https://doi.org/10.1093/genetics/126.4.1103
Autor:
M F Lyon
Publikováno v:
Genetics. 125:231-236
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f932676cba35bc8bdbad46e25f4d2d0d
https://doi.org/10.1093/genetics/125.2.231
https://doi.org/10.1093/genetics/125.2.231
Publikováno v:
Molecular vision. 6
The work forms part of a major project to study the genetics of mouse cataract mutants found during the course of mutagenesis experiments. The long-term aim is to find the underlying gene mutation in each cataract mutant. Here we report further studi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f4b96895d33ecf1750d6fa292d941db4
https://pubmed.ncbi.nlm.nih.gov/11062307
https://pubmed.ncbi.nlm.nih.gov/11062307
Autor:
K R, Willison, M F, Lyon
Publikováno v:
The International journal of developmental biology. 44(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a11b0352cf30b366a52bdbacf6ed8e95
https://pubmed.ncbi.nlm.nih.gov/10761848
https://pubmed.ncbi.nlm.nih.gov/10761848
Autor:
M. F. Lyon, M. C. Brown, M. P. Coleman, A. Tarlton, E. A. Buckmaster, V.H. Perry, L. Conforti
Publikováno v:
Mammalian genome : official journal of the International Mammalian Genome Society. 10(6)
Kinesin and kinesin superfamily proteins are molecular motors involved in important intracellular functions such as organelle transport and cell division. They are microtubule-activated ATPases composed of a motor domain that binds to microtubules an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::589bdacffbf8876f45d320a86c201838
https://pubmed.ncbi.nlm.nih.gov/10341097
https://pubmed.ncbi.nlm.nih.gov/10341097
Autor:
M. F. Lyon, M. C. Brown, L. Conforti, V. H. Perry, E. A. Buckmaster, M. P. Coleman, Rob M. Ewing, A. Tarlton
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 95(17)
Wallerian degeneration is the degeneration of the distal stump of an injured axon. It normally occurs over a time course of around 24 hr but it is delayed in the slow Wallerian degeneration mutant mouse (C57BL/ Wld s ) for up to 3 weeks. The gene, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68a0fb8f7a5e2c03af3b55d5d9b75de6
https://pubmed.ncbi.nlm.nih.gov/9707587
https://pubmed.ncbi.nlm.nih.gov/9707587
Publikováno v:
Molecular vision. 3
Lim2, the gene encoding the second most abundant lens specific integral membrane protein, MP19, has recently been proposed as an ideal candidate gene for the cataractous mouse mutant, To3. The aim of this study was to screen the Lim2 gene in the To3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bff0ad9f861d98f17c0bd528107eae79
https://pubmed.ncbi.nlm.nih.gov/9238094
https://pubmed.ncbi.nlm.nih.gov/9238094
Autor:
M. F. Lyon, M. C. Brown, M. P. Coleman, V.H. Perry, E. A. Buckmaster, B. W. Ogunkolade, A. Tarlton
Publikováno v:
Mammalian genome : official journal of the International Mammalian Genome Society. 7(7)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47042666a25d84f2a314d1ce5a297932
https://pubmed.ncbi.nlm.nih.gov/8672149
https://pubmed.ncbi.nlm.nih.gov/8672149
Autor:
M F, Lyon
Publikováno v:
The Turkish journal of pediatrics. 37(2)
This paper represents the text of two lectures given on the occasion of a Workshop on the X-Chromosome held at Hacettepe University, Ankara, in September 1994. The history of the development of ideas concerning the mechanism of X-chromosome inactivat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ca13bd2d71d89fedeac2ebee4c8a0f47
https://pubmed.ncbi.nlm.nih.gov/7597763
https://pubmed.ncbi.nlm.nih.gov/7597763