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  • 1
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    Genes coding for histone proteins in man are located on the distal end of the long arm of chromosome 7 (1979)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1979-08-31
    Description: Tritium-labeled complementary RNA's to two cloned sea urchin DNA sequences, one coding for histones H1, H2B, and H4 and the other for H2A and H3, were hybridized in situ to high resolution human chromosomes. Evidence is presented showing that the histone genes in man are localized in bands q32-36 on the long arm of chromosome 7.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Chandler, M E -- Kedes, L H -- Cohn, R H -- Yunis, J J -- New York, N.Y. -- Science. 1979 Aug 31;205(4409):908-10.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/472711" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Chromosome Mapping ; Chromosomes/ultrastructure ; *Chromosomes, Human, 6-12 and X ; *Genes ; Histones/*genetics ; Humans ; Lymphocytes/ultrastructure ; Nucleic Acid Hybridization ; Sea Urchins/genetics
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Published by American Association for the Advancement of Science (AAAS)
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  • 2
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    Regional assignment of genes for human esterase D and retinoblastoma to chromosome band 13q14 (1980)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1980-05-30
    Description: The expression of human esterase D was evaluated quantitatively and qualitatively in five persons with partial deletions or duplications of chromosome 13. The results showed that the locus of this enzyme is at band 13q14. Deletion of this same band in other subjects has been found previously to indicate a predisposition to the development of retinoblastoma, which was present in the four individuals in this study who had partial deletions of chromosome 13. Because of this close synteny, esterase D evaluation should aid in the diagnosis and genetic counseling of retinoblastoma.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Sparkes, R S -- Sparkes, M C -- Wilson, M G -- Towner, J W -- Benedict, W -- Murphree, A L -- Yunis, J J -- New York, N.Y. -- Science. 1980 May 30;208(4447):1042-4.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7375916" target="_blank"〉PubMed〈/a〉
    Keywords: Chromosome Deletion ; Chromosome Mapping ; *Chromosomes, Human, 13-15 ; Esterases/*genetics ; Female ; Genes ; Humans ; Intellectual Disability/enzymology/genetics ; Male ; Retinoblastoma/enzymology/*genetics
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Published by American Association for the Advancement of Science (AAAS)
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  • 3
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    The origin of man: a chromosomal pictorial legacy (1982)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1982-03-19
    Description: Man, gorilla, and chimpanzee likely shared an ancestor in whom the fine genetic organization of chromosomes was similar to that of present man. A comparative analysis of high-resolution chromosomes from orangutan, gorilla, chimpanzee, and man suggests that 18 or 23 pairs of chromosomes of modern man are virtually identical to those of our "common hominoid ancestor", with the remaining pairs slightly different. From this lineage, gorilla separated fist, and three major chromosomal rearrangements presumably occurred in a progenitor of chimpanzee and man before the final divergence of these tow species. A precursor of the hominoid ancestor and orangutan is also assumed.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yunis, J J -- Prakash, O -- New York, N.Y. -- Science. 1982 Mar 19;215(4539):1525-30.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7063861" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biological Evolution ; Chromosome Banding ; Chromosomes, Human/*ultrastructure ; Humans ; Karyotyping/methods ; Primates/*genetics
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Published by American Association for the Advancement of Science (AAAS)
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  • 4
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    The chromosomal basis of human neoplasia (1983)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1983-07-15
    Description: High-resolution banding techniques for the study of human chromosomes have revealed that the malignant cells of most tumors analyzed have characteristic chromosomal defects. Translocations of the same chromosome segments with precise breakpoints occur in many leukemias and lymphomas, and a specific chromosome band is deleted in several carcinomas. Trisomy, or the occurrence of a particular chromosome in triplicate, is the only abnormality observed in a few neoplasias. It is proposed that chromosomal rearrangements play a central role in human neoplasia and may exert their effects through related genomic mechanisms. Thus, a translocation could serve to place an oncogene next to an activating DNA sequence, a deletion to eliminate an oncogene repressor, and trisomy to carry extra gene dosage.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yunis, J J -- CA31024/CA/NCI NIH HHS/ -- CA33314/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1983 Jul 15;221(4607):227-36.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6336310" target="_blank"〉PubMed〈/a〉
    Keywords: Carcinogens/pharmacology ; Carcinoma/genetics ; Chromosome Aberrations/genetics ; Chromosome Banding ; Chromosome Disorders ; Chromosome Fragility ; Chromosomes, Human/drug effects/*physiology ; Humans ; Leukemia/genetics ; Lymphoma/genetics ; Neoplasms/*genetics ; Oncogenes ; Translocation, Genetic
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Published by American Association for the Advancement of Science (AAAS)
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  • 5
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    The striking resemblance of high-resolution G-banded chromosomes of man and chimpanzee (1980)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1980-06-06
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yunis, J J -- Sawyer, J R -- Dunham, K -- New York, N.Y. -- Science. 1980 Jun 6;208(4448):1145-8.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7375922" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Azure Stains ; Centromere/ultrastructure ; Chromosome Banding ; Chromosome Inversion ; Chromosomes/*ultrastructure ; Chromosomes, Human/*ultrastructure ; Heterochromatin/ultrastructure ; Humans ; Pan troglodytes/*genetics ; Prophase
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Published by American Association for the Advancement of Science (AAAS)
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  • 6
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    Amplification and rearrangement of Hu-ets-1 in leukemia and lymphoma with involvement of 11q23 (1986)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1986-04-18
    Description: The Hu-ets-1 oncogene was found to be rearranged and amplified 30-fold in one case of acute myelomonocytic leukemia in which a homogeneously staining region occurred on 11q23; the oncogene was rearranged and amplified approximately tenfold in a case of small lymphocytic cell lymphoma with an inverted insertion that also involved band 11q23. This work suggests that Hu-ets-1 is an unusual oncogene that can help explain the common involvement of chromosome band 11q23 in various subtypes of hematopoietic malignancies.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rovigatti, U -- Watson, D K -- Yunis, J J -- CA-31024/CA/NCI NIH HHS/ -- CA-33314/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1986 Apr 18;232(4748):398-400.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/3457468" target="_blank"〉PubMed〈/a〉
    Keywords: Chromosome Aberrations/genetics ; Chromosome Banding ; Chromosome Disorders ; Chromosome Mapping ; Chromosomes, Human, 13-15/ultrastructure ; *Chromosomes, Human, 6-12 and X/ultrastructure ; DNA, Neoplasm/genetics/isolation & purification ; Humans ; Leukemia, Myeloid, Acute/*genetics ; Lymphoma, Non-Hodgkin/*genetics ; Nucleic Acid Hybridization ; *Oncogenes ; Translocation, Genetic
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 7
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    Molecular cloning of the chromosomal breakpoint of B-cell lymphomas and leukemias with the t(11;14) chromosome translocation (1984)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1984-06-29
    Description: The chromosomal breakpoint of chronic lymphocytic leukemia (CLL) cells of the B-cell type carrying the translocated long arms of chromosomes 11 and 14 [t(11;14) (q13;q32)] was cloned. The breakpoint was found to be within the joining segment of the human heavy chain locus on the translocated long arm of chromosome 14. A probe that is specific for chromosome 11 and that maps immediately 5' to the breakpoint on the 14q+ chromosome was isolated. The probe detected a rearrangement of the homologous genomic DNA segment in the parental CLL cells and also in DNA from a diffuse large cell lymphoma with the t(11;14) translocation. This rearranged DNA segment was not present in Burkitt lymphoma cells with the t(8;14) translocation or in nonneoplastic human lymphoblastoid cells. The probe can thus be used to identify and characterize a gene located on band q13 of chromosome 11 that appears to be involved in the malignant transformation of human B cells carrying the t(11;14) translocation. This gene, named bcl -1, appears to be unrelated to any of the known retrovirus oncogenes described to date.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tsujimoto, Y -- Yunis, J -- Onorato-Showe, L -- Erikson, J -- Nowell, P C -- Croce, C M -- CA15882/CA/NCI NIH HHS/ -- CA16685/CA/NCI NIH HHS/ -- CA20034/CA/NCI NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1984 Jun 29;224(4656):1403-6.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6610211" target="_blank"〉PubMed〈/a〉
    Keywords: Aged ; Animals ; B-Lymphocytes ; Burkitt Lymphoma/genetics ; Cell Line ; *Chromosomes, Human, 13-15 ; *Cloning, Molecular ; DNA, Neoplasm/genetics ; DNA, Recombinant/metabolism ; Humans ; Hybrid Cells/metabolism ; Leukemia/*genetics ; Leukemia, Lymphoid/genetics ; Lymphoma/*genetics ; Male ; Mice ; Nucleic Acid Hybridization ; *Translocation, Genetic
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 8
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    Cloning of the chromosome breakpoint of neoplastic B cells with the t(14;18) chromosome translocation (1984)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1984-11-30
    Description: From an acute B-cell leukemia cell line, a DNA probe was obtained that was specific for chromosome 18 and flanked the heavy chain joining region of the immunoglobulin heavy chain locus on chromosome 14. This probe detected rearrangement of the homologous DNA segment in the leukemic cells and in follicular lymphoma cells with the t(14:18) chromosome translocation but not in other neoplastic or normal B or T cells. The probe appears to identify bcl-2, a gene locus on chromosome 18 (band q21) that is unrelated to known oncogenes and may be important in the pathogenesis of B-cell neoplasms with this translocation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tsujimoto, Y -- Finger, L R -- Yunis, J -- Nowell, P C -- Croce, C M -- CA15822/CA/NCI NIH HHS/ -- CA16685/CA/NCI NIH HHS/ -- CA20034/CA/NCI NIH HHS/ -- etc. -- New York, N.Y. -- Science. 1984 Nov 30;226(4678):1097-9.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6093263" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; B-Lymphocytes/*cytology ; Chromosome Banding ; *Chromosomes, Human, 13-15 ; *Chromosomes, Human, 16-18 ; *Cloning, Molecular ; Cricetinae ; Cricetulus ; DNA Restriction Enzymes ; DNA, Recombinant/analysis ; Humans ; Hybrid Cells/cytology ; Karyotyping ; Leukemia/*genetics ; Mice ; *Translocation, Genetic
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 9
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    Constitutive fragile sites and cancer (1984)
    American Association for the Advancement of Science (AAAS)
    Details
    Publication Date: 1984-12-07
    Description: Breaks were observed at 51 sites in homologous chromosomes in lymphocytes from ten humans and two great apes when cells were deprived of thymidine. The incidence of breaks was enhanced by caffeine, a substance that inhibits DNA repair in replicating cells. The locations of 20 sites were correlated with breakpoints that have been related to human malignancy.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Yunis, J J -- Soreng, A L -- New York, N.Y. -- Science. 1984 Dec 7;226(4679):1199-204.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6239375" target="_blank"〉PubMed〈/a〉
    Keywords: Adolescent ; Adult ; Animals ; Caffeine/pharmacology ; Cells, Cultured ; Child ; Chromosome Fragile Sites ; *Chromosome Fragility ; Chromosome Mapping ; Female ; Floxuridine/pharmacology ; Folic Acid/metabolism ; Gorilla gorilla ; Humans ; Male ; Middle Aged ; Neoplasms/*genetics ; Pan troglodytes ; Thymidine/metabolism
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Published by American Association for the Advancement of Science (AAAS)
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  • 10
    Electronic Resource
    Electronic Resource
    G-banding patterns of high-resolution human chromosomes 6–22, X, and Y (1979)
    Springer
    Human genetics 〈Berlin〉 49 (1979), S. 291-306 
    Details
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary A precise schematic representation of the number, height, position, and staining intensity of the Giemsa bands of late prophase, prometaphase, early metaphase, and mid-metaphase chromosomes 6–22, X, and Y is presented. Late prophase chromosomes were found to have 2–21/2 times the length and 3–31/2 times the number of bands previously observed in mid-metaphase, whereas prometaphases and early metaphases were intermediate in length and number of bands. In this work, the maximum number of bands observed per haploid set in late prophase was 1353, while more than 350 were generally found in mid-metaphase.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00569349
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    Paper (German National Licenses)
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