Zobrazeno 1 - 10
of 13
pro vyhledávání: '"A O, Ruvinskiĭ"'
Publikováno v:
Genetika. 29(2)
The aberrant chromosome 1 with two large homogeneously staining insertions was isolated from wild populations of Mus musculus. Specific features of aberrant chromosome were described elsewhere. These include preferential entry of the chromosome into
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0ad740d91e79774068e3c4d937acf96b
https://pubmed.ncbi.nlm.nih.gov/8486257
https://pubmed.ncbi.nlm.nih.gov/8486257
Publikováno v:
Genetika. 28(12)
An aberrant chromosome 1 carrying an inverted fragment with two amplified DNA regions was isolated from natural populations of Mus musculus. A meiotic drive favouring the aberrant chromosome was previously demonstrated for heterozygous females. The c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3ed1627ad55d323028cd9285d06d7fd3
https://pubmed.ncbi.nlm.nih.gov/1338195
https://pubmed.ncbi.nlm.nih.gov/1338195
Publikováno v:
Genetika. 28(5)
The t complex in the proximal part of chromosome 17 is one of the most thoroughly studied regions of the mouse genome. We determined the sequence of Tu80, a molecular clone derived from microdissected fragments of chromosome 17. The sequence data dem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f7c1a98180fcf4d99c1d48106c380cf3
https://pubmed.ncbi.nlm.nih.gov/1639255
https://pubmed.ncbi.nlm.nih.gov/1639255
Publikováno v:
Genetika. 26(11)
Analysis of the functional nature of mutations can be based on their manifestation in organisms with a deletion or a duplication of a particular chromosome segment. With the use of reciprocal translocation T(16;17)43H it is feasible to produce mice w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aab8e260c666cfa7d8dc990b927293f5
https://pubmed.ncbi.nlm.nih.gov/2074009
https://pubmed.ncbi.nlm.nih.gov/2074009
Publikováno v:
Genetika. 26(10)
The properties of the t haplotypes, specific mutant states of the proximal region of chromosome 17 in the house mouse keep renewing interest. One such property is increased transmission of the t haplotype from heterozygous t/+ males to their offsprin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e4988425d7af9fa14d724f611b3009ac
https://pubmed.ncbi.nlm.nih.gov/2283048
https://pubmed.ncbi.nlm.nih.gov/2283048
Publikováno v:
Genetika. 26(8)
Screening of wild male mice trapped in Turkmenistan (Middle Asia) revealed a mouse with a mutation causing strong increase in expressivity of T mutation (Brachyury). A novel mutation was designated tctN-t complex tail interaction Novosibirsk. Compoun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c4cfea0730190fd65eca1562e3338883
https://pubmed.ncbi.nlm.nih.gov/2258033
https://pubmed.ncbi.nlm.nih.gov/2258033
Publikováno v:
Genetika. 26(4)
Animals with aberrant chromosome 1 carrying one or two large insertions were earlier described in natural populations of Mus musculus. In the present work, inheritance of the aberrant chromosome 1 from the Yakutsk population was investigated. It was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e4947079004e6d6fb9b11067f218cb41
https://pubmed.ncbi.nlm.nih.gov/2373357
https://pubmed.ncbi.nlm.nih.gov/2373357
Autor:
A O, Ruvinskiĭ
Publikováno v:
Genetika. 23(6)
According to up-to-date literature, one of the approaches to elucidating the essence of evolutionary events consists in admitting the importance of events which change genome activity. A crucial way of reorganization of gene activity is the inhetrite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a5dbee55722fe7122991654bc513116d
https://pubmed.ncbi.nlm.nih.gov/3305163
https://pubmed.ncbi.nlm.nih.gov/3305163
Publikováno v:
Genetika. 23(1)
The influence of some t-haplotypes on the phenotypic manifestation of fused and kinky genes located on chromosome 17 of the house mouse was studied. It was shown that t12-haplotype decreases the penetrance of these genes to 59-70%. The effect was obs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f791a49ed0e2b20807237478fac93eab
https://pubmed.ncbi.nlm.nih.gov/3817466
https://pubmed.ncbi.nlm.nih.gov/3817466
Publikováno v:
Genetika. 22(10)
It was demonstrated that mutations T, Fu, Ki, t6 of chromosome 17 cause preferential transmission of the acrocentric homologues to the progeny from female Rb heterozygotes. The results indicate that the effects of these mutations on segregation are r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::73d51d501511c3589af6d5d9ef300af6
https://pubmed.ncbi.nlm.nih.gov/3792838
https://pubmed.ncbi.nlm.nih.gov/3792838