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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 34 (1976), S. 171-174 
    ISSN: 1432-0533
    Keywords: Brain tumor ; Meningiomas ; Papova-Virus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Human meningiomas show characteristic chromosome aberrations very similar to those reported in human cell cultures experimentally transformed by Simian virus 40 (SV 40). Three out of eight meningiomas tested showed SV 40 specific tumor antigen but no virus capsid antigen. Experiments to rescue virus were successfully performed. Electron microscopic studies of these cell cultures revealed cytoplasmic inclusions containing virus particles which corresponded in size and morphology to Papova viruses.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 56 (1978), S. 7-16 
    ISSN: 1432-1440
    Keywords: Chromosome aberrations ; Neoplasms ; Leukaemia ; Meningioma ; Lymphoma ; Animal neoplasm ; Chromosomenaberrationen ; Tumoren ; Leukämie ; Meningeom ; Lymphom ; Tiertumor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung In den letzten Jahren wurden von zwei relativ unterschiedlichen zytogenetischen Forschungsrichtungen Hinweise auf Zusammenhänge zwischen Chromosomenanomalien und der Entstehung von Tumoren gefunden: 1. Es stellte sich heraus, daß Patienten mit exogen oder genetisch bedingter Chromosomenbrüchigkeit ein stark erhöhtes Tumorrisiko haben. Das gleiche gilt in abgeschwächter Form für Patienten mit angeborenen Chromosomenanomalien. 2. Bei einigen tierischen und menschlichen Tumoren wurden Chromosomenveränderungen gefunden, die für den jeweiligen Tumor relativ typisch sind. Unter den menschlichen Tumoren ist die chronisch myeloische Leukämie das bekannteste Beispiel, aber auch für andere tumoröse Erkrankungen des Knochenmarks wurden Anomalien einiger weniger Chromosomen besonders häufig festgestellt. Unter den soliden menschlichen Tumoren sind bisher nur für das Meningeom und die malignen Lymphome spezifische Chromosomenaberrationen beschrieben worden. Anhand dieser Befunde werden verschiedene Theorien über die Bedeutung von Chromosomenanomalien für die Tumorentstehung diskutiert, insbesondere, ob chromosomale Störungen ganz allgemein und unspezifisch die Zellen für tumorauslösende Faktoren empfänglicher machen, oder ob nur der Verlust oder Zugewinn bestimmter Chromosomen bzw. Chromosomenabschnitte bei der Tumorentstehung eine Rolle spielt. Es wird jedoch auch die Möglichkeit erörtert, daß die Chromosomenanomalien eine Begleiterscheinung der Onkogenese darstellen könnten und mit der Tumorentstehung in keinem direkten Zusammenhang stehen.
    Notes: Summary In the last few years new facts concerning the relations between chromosomal aberrations and oncogenesis have been gathered from two different areas of cytogenetic research: 1. It could be shown that the tumor risk is dramatically increased in patients with chromosome breakage, caused by exogen or genetic factors. The same is mostly true in patients with congenital chromosome aberrations. 2. In some animal and human tumors chromosomal anomalies were detected which were relatively typical for the tumor in question. Among the human tumors the chronic myeloic leukaemia is the most common example, but also in other tumorous disorders of the bone marrow certain chromosomal aberrations have been observed unexpectedly often. Under the human solid tumors only the meningioma and the malignant lymphomas show specific aberrations of the karyotype. Considering these new facts, different theories about the importance of chromosomal disturbances in oncogenesis are discussed. Special interest is paid to the question whether chromosome aberrations make the cells susceptible for oncogenic agents in an unspecific way, or if only the loss or gain of specific chromosomes or parts of chromosomes facilitate the occurrence of malignancy in human or animal cells. On the contrary, attention must be paid to the possibility that the chromosomal aberrations are only an accompanying phenomenon with no direct relation to oncogenesis.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 47 (1969), S. 237-244 
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary The first case of atypical Klinefelter's syndrome with supernumerary X-iso-chromosome of the long arm is described. (Karyotype 47,XXqiY). The patient has only supernumerary long arms of X-chromosome. However the clinical picture does not show differences from the typical Klinefelter's syndrome with the chromosomal complement 47,XXY. In dermatoglyphics, the total ridge count was lower than expected. But this finding can be explained by possible genetic influences from the side of the father who has an extremely low total ridge count. The discussion deals with the possible origin of the supernumerary chromosome and his genetical activity in connection with the Lyon hypothesis.
    Notes: Zusammenfassung Es wird der bisher erste Fall eines atypischen Klinefelter-Syndroms mit überzähligem X-Isochromosom des langen Arms beschrieben (Karyotyp: 47,XXqiY in allen untersuchten Zellen). Der Patient besitzt nur überzählige lange X-Chromosomenarme; trotzdem unterscheidet er sich klinisch nicht von dem typischen Syndrom mit dem Chromosomensatz 47,XXY. Im Bereich der Papillarleisten läßt sich die hinter dem Erwartungswert zurückbleibende Gesamtleistenzahl durch mögliche genetische Einflüsse von seiten des Vaters erklären, der eine außerordentlich geringe GLZ aufweist. Die mögliche Herkunft des überzähligen Chromosoms wird diskutiert und seine genetische Expressivität im Zusammenhang mit der Lyon-Hypothese betrachtet.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Human genetics 〈Berlin〉 8 (1969), S. 47-52 
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The association pattern of the acrocentric chromosomes shows no significant difference between a population of mothers of mongoloid children and male and female controls of the same age-group. It could only be demonstrated that the associations of the mothers were interconnected by thread-like structures in a higher percentage. However, no significance could be deduced from for this phenomenon (P ≊ 0.1).
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Human genetics 〈Berlin〉 9 (1970), S. 172-184 
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Description / Table of Contents: Zusammenfassung Die cytogenetische Untersuchung einer Reihe von 40 kurzzeit-gezüchteten menschlichen Meningeomen ergab als Hauptbefund den Verlust eines kleinen akrozentrischen Chromosoms der Gruppe 21–22 bei 32 Tumoren. 6 Tumoren hatten einen offensichtlich normalen Chromosomensatz, 2 Tumoren eine numerische Chromosomenveränderung ohne Beteiligung eines G-Chromosoms. Bei 18 Meningeomen war der G-Chromosomenverlust die einzige Veränderung; sie bestand entweder bei allen untersuchten Mitosen oder neben einer zusätzlichen normalen Zellinie. Histologisch entsprach diese Gruppe dem typischen endotheliomatösen Meningeom mit unterschiedlich ausgeprägten Sekundärstrukturen und regressiven Veränderungen. Bei 14 Tumoren fehlten neben dem fehlenden G-Chromosom 1–5 weitere Chromosomen; der jeweilige Karyotyp war dabei für den betreffenden Tumor konstant. Die Gruppe mit 44-43 Chromosomen entsprach histologisch überwiegend einem fibromatösen Meningeom, diejenige mit 42-40 Chromosomen einem atypischen endotheliomatösen Meningeom. Tumoren mit mehr als 46 und weniger als 40 Chromosomen fehlten in unserem Material. Bei einigen Meningeomen existierte eine Stammlinie mit einem deletierten Chromosom, in der Regel waren jedoch strukturelle Veränderungen selten. Es konnte lediglich eine Tendenz zur Assoziation von Zentromeren und Telomeren nachgewiesen werden, wobei gelegentlich die Unterscheidung von dizentrischen Chromosomen nicht mehr möglich war. Es wird auf die Ähnlichkeit zwischen dem Befund des Ph1-Chromosoms bei der chronischen myeloischen Leukämie und der G-Monosomie bei den Meningeomen hingewiesen, sowie auf die Tatsache, daß bei Virusinfektion menschlicher Zellkulturen oft als initiale Veränderung der Verlust eines G-Chromosoms zu verzeichnen ist. Es wird die Möglichkeit diskutiert, daß diese Chromosomenveränderung eine unlimitierte Zellvermehrung induziert.
    Notes: Summary The chromosomal investigation of a series of 40 short term cultured human meningiomas revealed as main finding the loss of a short acrocentric chromosome of the 21–22 group in 32 tumors. 6 tumors had an apparantly normal chromosome complement, 2 tumors had a numerical chromosome aberration without G-chromosome loss involved. In 18 meningiomas the G-chromosome loss was the only finding either in all mitoses investigated or besides a normal accessory cell line. Histologically this group corresponded with the typical endotheliomatous meningioma with more or less secondary structures and regressive alterations. 14 tumors showed a loss of 1–5 chromosomes besides the missing G-group chromosome, but without variation of the karyotypes. The group with 44-43 chromosomes corresponded histologically mostly with a fibromatous meningioma, the group with 42-40 chromosomes with an atypical endotheliomatous meningioma. Tumors with more than 46 and less than 40 chromosomes were absent. In some meningiomas a stemline with a deleted chromosome could be found, but in general structural aberrations were few. Only a tendency to centromere and telomere associations, occasionally not distinguishable from dicentric chromosomes, has been found. The similarity between the Ph1-chromosome in chronic myelogenic leukemia and the G-monosomy in the meningiomas as possible inducer of unlimited cell propagation was discussed. Furthermore the attention was drawn to the often found initial G-chromosome loss in human virus infected cell cultures.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Human genetics 〈Berlin〉 86 (1991), S. 487-490 
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary A classical minisatellite family, the M13 tandem repeat, is shown here to be spread over all human chromosomes. M13 shows an R-band-like pattern, in contrast to the 33.15 family of Jeffreys, which preferentially clusters in the telomeric regions.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 118 (1975), S. 303-313 
    ISSN: 1432-1076
    Keywords: Cyproheptadin ; Nuran® ; Human fibroblast cultures ; Chromosome studies ; Cytotoxic effects
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Zellkulturen kindlicher Fibroblasten wurden auf eine chromosomenmutagene Wirkung von Cyproheptadin untersucht. Weder bei 24stündiger Belastung mit Konzentrationen von 16,0 bis 32,0 mg/l Nährmedium noch bei Dauerbelastung mit einer Konzentration von 8,0 mg/l über einen Zeitraum von 8 bis 11 Wochen konnte eine Chromosomenmutagenität beobachtet werden. Reversible, cytomorphologische und cytochemische Veränderungen (8,0–16,0 mg/l), verbunden mit einer Zellteilungshemmung (32,0 mg/l) und irreversible Veränderungen mit Zelluntergang bei höchsten Konzentrationen (64,0–128,0 mg/l) werden als unspezifischer cytotoxischer in vitro-Effekt gedeutet.
    Notes: Abstract Cyproheptadin was tested on chromosomes in fibroblast cultures of children for its possible mutagenic efficacy. Neither 24-hour exposure to Cyproheptadin at concentrations of 8–16 mg/l medium nor a chronic exposure for 8–11 weeks at a concentration of 8 mg/l caused any discernable chromosomal mutations. At concentrations between 8–16 mg/l reversible cytomorphological and cytochemical changes occured; 32 mg/l suppressed cell division and higher concentrations (64–128 mg/l) brought about irreversible changes leading to cell death. These reactions were rather in vitro cytotoxic effects of unspecific nature.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0942-0940
    Keywords: Meningioma ; grading ; Ki-67 ; computerized image processing ; morphometry ; cytogenetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary With regard to meningioma grading and the recently introduced “atypical” meningioma, we evaluated 160 cases retrospectively by conventional histology and image analysis. For that, the cell nuclei were stained with a Ki-67 (MIB1)/Feulgen-method on paraffin sections, thus enabling the assessment of both the Ki-67 proliferation index and nuclear morphometric features, such as tumour cell arrangement, nuclear pleomorphism, and cellularity. It could be demonstrated that the Ki-67 proliferation index is the most important criterion for distinguishing anaplastic meningiomas (WHO “grade” III) (mean Ki-67 index: 11%) from those of common type (WHO “grade” I) (mean Ki-67 index: 0.7%). The parameter for the “relative volume weighted mean nuclear volume” is another valuable morphometric feature. The “atypical” meningioma (WHO “grade” II) which should represent an intermediate category between common type and anaplastic meningiomas is characterized by a mean Ki-67 proliferation index of 2.1%. Common type meningiomas which comprise almost 50% of the cases of this series have a relapse rate of 9%. “Atypical” and anaplastic meningiomas recurred in 29% and 50%, respectively. Since the term “atypical” meningioma is confusing in the context of tumour grading, the term “intermediate type meningioma” is proposed. Furthermore, the results of cytogenetic analyses of 142 cases of this series were evaluated and compared with the meningioma grades. Thereby, 25 cases disclosed, independent of the typical loss of one chromosome 22, cytogenetic features assumed to be progression-associated, e.g., the gain or loss of different chromosomes and the deletion of the short arm of one chromosome 1 (hyperdiploidy, increased hypodiploidy, Ip-), when correlated to the histological and morphometric findings or the high relapse rate. For meningioma diagnosis and grading, a practical guideline is proposed based upon histology, morphometry (Ki-67), and cytogenetics.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 216 (1967), S. 84-85 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The tumours were cultured by the method of Kersting1. The medium used for 600 brain tumour cultures did not allow excessive growth of connective tissue. Chromosome analysis was carried out on primary particle cultures in roller tubes. Cultures grown for 5-9 days were subjected to a hypotonic ...
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Cancer Genetics and Cytogenetics 77 (1994), S. 155 
    ISSN: 0165-4608
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine
    Type of Medium: Electronic Resource
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