Zobrazeno 1 - 9
of 9
pro vyhledávání: '"H O Sweet"'
Autor:
Roderick T. Bronson, H. O. Sweet
Publikováno v:
Journal of Heredity. 82:140-144
Osteochondrodystrophy (ocd) is a new autosomal recessive mouse mutation characterized by a short, slightly domed head, reduced body size, disproportionately shortened long bones of the legs, supination of the forefeet, and short thickened tail. Histo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccef9d971ac090dfff7454041687ffcd
https://doi.org/10.1093/oxfordjournals.jhered.a111048
https://doi.org/10.1093/oxfordjournals.jhered.a111048
Publikováno v:
Mammalian Genome. 7:555-557
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f8860c4514a763a8367ae52f06158ac
https://doi.org/10.1007/s003359900166
https://doi.org/10.1007/s003359900166
Publikováno v:
The Journal of heredity. 89(6)
A new allelic series at the underwhite gene is described. Three of the alleles in the series--uw, uwd, and Uwdbr--arose as spontaneous mutations on different genetic backgrounds at The Jackson Laboratory. We report here the visible phenotypes and dom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::189b0c086e64a8a2f804634f8d92b1df
https://pubmed.ncbi.nlm.nih.gov/9864865
https://pubmed.ncbi.nlm.nih.gov/9864865
Autor:
M. J. van Vugt, Richard P. Woychik, Scott J. Bultman, H O Sweet, Edward J. Michaud, M T Davisson
Publikováno v:
Genesdevelopment. 8(12)
The agouti gene normally confers the wild-type coat color of mice. Dominant mutations at the agouti locus result in a pleiotropic syndrome that is characterized by excessive amounts of yellow pigment in the coat, obesity, a non-insulin-dependent diab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f1f3722066979a220efaae32374c6ba
https://pubmed.ncbi.nlm.nih.gov/7926745
https://pubmed.ncbi.nlm.nih.gov/7926745
Autor:
O Ben-Zeev, H. O. Sweet, C A Langner, M T Davisson, M C Schotz, Jeffrey I. Gordon, E H Birkenmeier
Publikováno v:
Journal of Biological Chemistry. 264:7994-8003
An autosomal recessive mutation, termed fatty liver dystrophy (fld), can be identified in neonatal mice by their enlarged and fatty liver (Sweet, H. O., Birkenmeier, E. H., and Davisson, M. T. (1988) Mouse News Letter 81, 69). We have examined the un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4baa696ba99728a25a3a934ce8bcf22f
https://doi.org/10.1016/s0021-9258(18)83141-6
https://doi.org/10.1016/s0021-9258(18)83141-6
Publikováno v:
Nature. 297:402-404
Research into the basic mechanisms underlying the development of complex multi-system diseases has been facilitated by the study of single gene mutations in experimental animals. Ataxia telangiectasia is such a multifaceted genetically determined dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18e52d446010d3c483f39eff3e05a90b
https://doi.org/10.1038/297402a0
https://doi.org/10.1038/297402a0
Autor:
L. D. Shultz, H. O. Sweet, Melvin J. Bosma, Norman R. Ruetsch, Muriel T. Davisson, Gayle C. Bosma
Publikováno v:
Immunogenetics. 29(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1180c59773763cecc397f39ae686ed51
https://pubmed.ncbi.nlm.nih.gov/2908877
https://pubmed.ncbi.nlm.nih.gov/2908877
Autor:
C A, Langner, E H, Birkenmeier, O, Ben-Zeev, M C, Schotz, H O, Sweet, M T, Davisson, J I, Gordon
Publikováno v:
The Journal of biological chemistry. 264(14)
An autosomal recessive mutation, termed fatty liver dystrophy (fld), can be identified in neonatal mice by their enlarged and fatty liver (Sweet, H. O., Birkenmeier, E. H., and Davisson, M. T. (1988) Mouse News Letter 81, 69). We have examined the un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::be6b364dbbec00519c9cc1a2efe71be7
https://pubmed.ncbi.nlm.nih.gov/2722772
https://pubmed.ncbi.nlm.nih.gov/2722772
Publikováno v:
Immunogenetics. 29:224-224
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41d724db84dcba931c769d0b9e6022b5
https://doi.org/10.1007/bf00373654
https://doi.org/10.1007/bf00373654