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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 186 (1960), S. 990-991 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] In Table 1 the variety of crosses and detected double cross-overs are listed. Most exceptional individuals were found among the progeny of females heterozygous either for y* su-wa wa spt (su-wa = suppressor of wa; wa=whiteapricot eye colour) or y ac wch spl (ac = acheate bristles; wch=white -cherry ...
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 184 (1959), S. 294-294 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Experiments were designed as follows to determine whether the wild-type isoalleles could differentially influence the frequency of crossing-over in their vicinity. Three marker genes, yellow body (y), white-cherry eye (wch) and split bristles (spl) were selected and crossing-over studied among the ...
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  • 3
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Genetics 14 (1980), S. 109-120 
    ISSN: 0066-4197
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 85 (1953), S. 435-449 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary 1. A genetic analysis of the mutant Bx r49k (herein designated as Bx r2) in D. melanogaster is reported. 2. Crossing-over occurs between Bx r 2 and Bx 1. From the analysis of the crossover types recovered, it is concluded that Bx r 2 is associated with a tandem duplication in which the Bx + locus as well as unknown gene loci to the right and left of Bx + are duplicated. The sy + and fu + loci are not duplicated in Bx r 2 as previously reported for Bx r . 3. The duplication nature of Bx r 2 has been confirmed by a salivary gland chromosome analysis. 4. In ♀ ♀ homozygous Bx r 2 unequal crossing over occurs by which means triplications of the Bx + locus have been recovered. This occurrence of unequal crossing over is in sharp contrast to the absence of unequal crossing over previously reported for ♀ ♀ homozygous Bx r . 5. Unequal crossing over also occurs in ♀ ♀ homozygous for the Bx + triplication and as a consequence quadruplications of the Bx + locus have been recovered. 6. It is concluded that the phenotypes associated with duplication, triplication and quadruplication of the Bx + locus are the result of position effect.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 87 (1956), S. 708-721 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary 1. A cytogenetic analysis of 18 independent lz mutants is presented. 2. On a phenotypic basis the mutants can be separated into three classes. 3. The results of a recombination analysis show that each of the 18 mutants can be assigned to one of three loci. No case where a lz mutant involved more than one locus was found. 4. Both phenotypic and recombination evidence place the amx mutant outside the lz pseudoallelic system. 5. Cytologically the lz pseudoalleles have been localized to section 8D of the salivary X chromosome. 6. The relevance of the data presented to the nature of pseudoallelism is discussed.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 90 (1959), S. 375-384 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary 1. From ⧫⧫ heterozygous for the mutantsw a /w a4 white-eyed progeny are recovered in association with crossing over. On the basis of the marker gene distribution to the white-eyed exceptions, the left segment of theirw locus comes from thew a4 chromosome, the right segment from thew a chromosome. 2. No exceptions reciprocal to the white-eyed exceptions were found. 3. Evidence is presented which demonstrates that the white-eyed exceptions are associated with a cytologically undetectable loss. 4. The occurrence of the white-eyed exceptions is dependent not on thew a mutant but rather on tightly linked factors to the right ofw a . 5. It is suggested that the white-eyed exceptions occur as a consequence of crossing over within not strictly homologusly paired component segments of thewhite region of the chromosome.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 94 (1963), S. 200-214 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Unequal crossing over occurs in females heterozygousw a /w a4 such that a deficiency and duplication can be recovered regularly. A triplication was also found following crossing over in the homozygous duplication. Genetic analysis of the duplication showed that of the several knownw loci only thew e andsp-w loci are duplicated. By means of crossing overw e andsp-w were introduced separately into the left half of the duplication andw e into the right half. The phenotypic consequences of such substitutions are interpreted in terms of the loci which are included in specific functional units or genes. They suggest thatw e andsp-w are in distinctive functional units. The fact that these duplications and deficiencies are without obvious affect on salivary gland band morphology suggests that the gene loci constitute only a small portion of the band structure.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 36 (1972), S. 391-412 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract A detailed cytogenetic study of male-viable and lethal deficiencies affecting the w-spl interval in Drosophila melanogaster has revealed the existence of genetic duplication such that, for example, the consequences of the loss of salivary chromosome band 3C3 are essentially compensated for by the presence of band 3C5-6, and vice versa. Although each of the duplicate elements possesses rst + and vt + activity, rst and vt phenotypes appear in males when 3C3 and part, but not all, of 3C5-6 are deleted. The degree of rst and vt expression can be correlated with the amount of material lost from 3C5-6. Deletions removing the entire 3C3-6 interval are male lethal. Despite the duplicate elements, at least one EMS-induced, presumptive point mutation expressing only rst is known; two others express both rst and vt. No loci other than rst and vt occur between W and spl. Band 3C2 appears to be associated with the w locus, which probably extends into the interband space between 3C1 and 3C2. The w locus is not involved in the rst-vt duplication in the 3C3-6 region. — The cytogenetic characteristics of the 3C region—a high coefficient of crossing over, frequent induced chromosome breakage, ectopic pairing, constriction, and an extended replication period—can be correlated with the fact that in 3C a relatively long stretch of DNA, nearly 2% of the entire X chromosome, is highly compacted into but few adjacent bands. These characteristics do not necessarily represent special properties of intercalary heterochromatin; they can be interpreted as reflecting the properties of any similarly organized euchromatic region.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 74 (1979), S. 329-335 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Two tandem duplications of the X chromosome associated with the white eye color locus are described. In heterozygous females both revert to a nonduplicated chromosome without detectable meiotic recombination. Clustering of revertants suggests the reversion event occurs in the germ line prior to meiosis. Similarly in males one duplication also reverts with clustering implying a premeiotic event. Revertant X chromosomes derived from males are either nonduplicated or deleted. Intrastrand exchange can account for some but not all revertants recovered.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 82 (1981), S. 259-266 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The third chromosome, mutagen sensitive mutant mus(3)312D1 impairs the meiotic process in females by increasing the frequency of first division nondisjunction and decreasing the frequency of meiotic crossing over. These genetic properties connote 312 to be defective in DNA replication and/or repair intimately associated with the crossing over exchange process. The mutant maps to the left arm of chromosome III between ru and h, and represents a new genetic site for a meiotic mutant.
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