Literature DB >> 1192363

Abnormalities of chromosome 1 in myeloproliferative disorders.

J D Rowley.   

Abstract

Three patients with myeloproliferative disorders showed a similar chromosome abnormality, accompanied by other abnormalities that were different in each case. Marrow cells from all three patients were trisomic either for the entire chromosome 1 or for its long arm. Patient 1 had a brief period of anemia and thrombocytopenia which preceded a terminal acute leukemia; Patient 2 had polycythemia vera (P.V.) that terminated in acute leukemia; and Patient 3 has P.V. The detection of an abnormal karyotype in Patients 1 and 2 was an important factor in establishing the diagnosis of acute leukemia. Preliminary evidence supports the suggestion that some chromosomal changes are nonrandom in myeloproliferative diseases. Nonrandom abnormalities involving the same chromosome have been observed in several human neoplastic disorders.

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Year:  1975        PMID: 1192363     DOI: 10.1002/1097-0142(197511)36:5<1748::aid-cncr2820360530>3.0.co;2-n

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  13 in total

1.  RABGAP1L gene rearrangement resulting from a der(Y)t(Y;1)(q12;q25) in acute myeloid leukemia arising in a child with Klinefelter syndrome.

Authors:  Maria Cristina Roberti; Roberta La Starza; Cecilia Surace; Pietro Sirleto; Rita Maria Pinto; Valentina Pierini; Barbara Crescenzi; Cristina Mecucci; Adriano Angioni
Journal:  Virchows Arch       Date:  2009-01-28       Impact factor: 4.064

2.  Chromosomes 1 in 14 ovarian cancers. Heterochromatin variants and structural changes.

Authors:  N B Atkin; V J Pickthall
Journal:  Hum Genet       Date:  1977-08-31       Impact factor: 4.132

3.  Partial trisomy of the long arm of human chromosome 1 as demostrated by in situ hybridization with 5S ribosomal RNA.

Authors:  D M Steffensen; E H Chu; D P Speert; P M Wall; K Meilinger; R P Kelch
Journal:  Hum Genet       Date:  1977-04-07       Impact factor: 4.132

4.  A case of myelodysplastic syndrome with a der(1;18)(q10;q10) translocation.

Authors:  Jung-Sook Ha; Dong-Suk Jeon
Journal:  Blood Res       Date:  2014-06-25

5.  Pure red cell hypoplasia associated with long-arm deletion of chromosome 5.

Authors:  J DiBenedetto; T Padre-Mendoza; M M Albala
Journal:  Hum Genet       Date:  1979-02-15       Impact factor: 4.132

6.  The pattern of radiation-induced transmissible aberrations in a human cell culture.

Authors:  C L Lee; O P Kamra
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

7.  Monosomy 1pter.

Authors:  E Yunis; L Quintero; M Leibovici
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

8.  Multiple cytogenetically abnormal clones in two polycythemia vera patients.

Authors:  J R Testa; J R Kanofsky; J D Rowley; J M Baron
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

9.  Karyotype analysis of a human mammary sarcoma explant in vitro.

Authors:  T R Chen; G Seman
Journal:  Breast Cancer Res Treat       Date:  1981       Impact factor: 4.872

Review 10.  [Chromosomal abnormalities in human neoplasia (author's transl)].

Authors:  C R Bartram; H W Rüdiger
Journal:  Klin Wochenschr       Date:  1978-08-01
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