Literature DB >> 7094698

Spontaneous cell fusion and PCC formation in Bloom's syndrome.

P G Otto, E Therman.   

Abstract

Corresponding to 4,633 diploid lymphocytes 64 tetraploid or near-tetraploid (including one octoploid) metaphases were found in two sibs with Bloom's syndrome. Eight of the polyploid cells had resulted from cell fusion with half the chromosomes representing PCC. One similar fibroblast was also observed. In 13,584 untreated cells from persons without a chromosome-breakage syndrome no such cells were encountered (P = 0.0000176). This seems to be the first description of spontaneous fusion of nonmalignant cells. The extended segments in the G2 type PCC which correspond to the Q-bright, late-replicating chromosome parts are less tightly spiralized than other chromosome regions which renders the chromosomes similar to those which have incorporated BrdU late in the S period. Obviously the chromosome segments which replicate last also are the last to spiralize.

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Year:  1982        PMID: 7094698     DOI: 10.1007/BF00344601

Source DB:  PubMed          Journal:  Chromosoma        ISSN: 0009-5915            Impact factor:   4.316


  11 in total

1.  "Hybrid" type cells in combined cultures of two different mammalian cell strains.

Authors:  G BARSKI; S SORIEUL; F CORNEFERT
Journal:  J Natl Cancer Inst       Date:  1961-05       Impact factor: 13.506

2.  Cytogenetic investigations in a new case of Bloom's syndrome.

Authors:  K Sperling; U Goll; J Kunze; E K Lüdtke; M Tolksdorf; G Obe
Journal:  Hum Genet       Date:  1976-01-28       Impact factor: 4.132

3.  Bloom's syndrome. V. Surveillance for cancer in affected families.

Authors:  J German; D Bloom; E Passarge
Journal:  Clin Genet       Date:  1977-09       Impact factor: 4.438

4.  Premature chromosome condensation in carcinoma of the bladder: presumptive evidence for fusion of normal and malignant cells.

Authors:  N B Atkin
Journal:  Cytogenet Cell Genet       Date:  1979

5.  Asynchrony of DNA replication and mitotic spiralization along heterochromatic portions of Chinese hamster chromosomes.

Authors:  A F Zakharov; N A Egolina
Journal:  Chromosoma       Date:  1968       Impact factor: 4.316

6.  Bloom's syndrome. I. Genetical and clinical observations in the first twenty-seven patients.

Authors:  J German
Journal:  Am J Hum Genet       Date:  1969-03       Impact factor: 11.025

Review 7.  Mitotic crossing-over and segregation in man.

Authors:  E Therman; E M Kuhn
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

8.  The behavior of allocyclic chromosomes in Bloom's syndrome.

Authors:  P G Otto; P A Otto; E Therman
Journal:  Chromosoma       Date:  1981       Impact factor: 4.316

9.  X chromosome constitution and the human female phenotype.

Authors:  E Therman; C Denniston; G E Sarto; M Ulber
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

10.  Cytological demonstration of mitotic crossing-over in man.

Authors:  E Therman; E M Kuhn
Journal:  Cytogenet Cell Genet       Date:  1976
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  6 in total

1.  Premature chromosome condensation in a child with trisomy 21.

Authors:  K Prabhakara; B Kar; S K Murthy
Journal:  J Med Genet       Date:  1992-10       Impact factor: 6.318

2.  Do individual allocyclic chromosomes in metaphase reflect their interphase domains?

Authors:  E M Kuhn; E Therman; D A Buchler
Journal:  Hum Genet       Date:  1987-11       Impact factor: 4.132

3.  47,XXX females, sex chromosomes, and tooth crown structure.

Authors:  L Alvesalo; E Tammisalo; E Therman
Journal:  Hum Genet       Date:  1987-12       Impact factor: 4.132

4.  What causes the abnormal phenotype in a 49,XXXXY male?

Authors:  G E Sarto; P G Otto; E M Kuhn; E Therman
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

5.  Replication variants of the human inactive X chromosome. II. Frequency and replication rate relative to the other chromosomes of the complement.

Authors:  M Schmidt; W M Stolzmann
Journal:  Chromosoma       Date:  1984       Impact factor: 4.316

6.  The similarity of phenotypic effects caused by Xp and Xq deletions in the human female: a hypothesis.

Authors:  E Therman; B Susman
Journal:  Hum Genet       Date:  1990-07       Impact factor: 4.132

  6 in total

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