Page last updated: 2024-10-28

hydroxyurea and Monosomy

hydroxyurea has been researched along with Monosomy in 3 studies

Monosomy: The condition in which one chromosome of a pair is missing. In a normally diploid cell it is represented symbolically as 2N-1.

Research Excerpts

ExcerptRelevanceReference
"Hydroxyurea induces mitotic gene conversion, mitotic crossing-over, reverse mutation, respiration-deficient petite mutants and aneuploidy in growing cultures of Saccharomyces cerevisiae."7.67Aneuploidy and other genetic effects induced by hydroxyurea in Saccharomyces cerevisiae. ( Goin, CJ; Mayer, VW; Zimmermann, FK, 1986)
"Monosomy 7 variant childhood chronic myelogenous leukemia (CML) is a rare, fatal leukemia that usually terminates in blast crisis."5.28Establishment of donor hematopoiesis after hydroxyurea-induced aplasia following allograft failure in a patient with monosomy 7 variant of childhood chronic myelogenous leukemia. ( Cassano, WF, 1989)
"Hydroxyurea induces mitotic gene conversion, mitotic crossing-over, reverse mutation, respiration-deficient petite mutants and aneuploidy in growing cultures of Saccharomyces cerevisiae."3.67Aneuploidy and other genetic effects induced by hydroxyurea in Saccharomyces cerevisiae. ( Goin, CJ; Mayer, VW; Zimmermann, FK, 1986)
"Monosomy 7 variant childhood chronic myelogenous leukemia (CML) is a rare, fatal leukemia that usually terminates in blast crisis."1.28Establishment of donor hematopoiesis after hydroxyurea-induced aplasia following allograft failure in a patient with monosomy 7 variant of childhood chronic myelogenous leukemia. ( Cassano, WF, 1989)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19902 (66.67)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Coccaro, N1
Tota, G1
Anelli, L1
Zagaria, A1
Casieri, P1
Cellamare, A1
Minervini, A1
Minervini, CF1
Brunetti, C1
Ricco, A1
Orsini, P1
Cumbo, C1
Specchia, G1
Albano, F1
Cassano, WF1
Mayer, VW1
Goin, CJ1
Zimmermann, FK1

Other Studies

3 other studies available for hydroxyurea and Monosomy

ArticleYear
Centromeric fragment of chromosome 7 in atypical chronic myeloid leukemia with the SET binding protein 1 gene mutation.
    Leukemia & lymphoma, 2015, Volume: 56, Issue:3

    Topics: Antineoplastic Agents; Carrier Proteins; Centromere; Chromosomes, Human, Pair 7; Humans; Hydroxyurea

2015
Establishment of donor hematopoiesis after hydroxyurea-induced aplasia following allograft failure in a patient with monosomy 7 variant of childhood chronic myelogenous leukemia.
    Bone marrow transplantation, 1989, Volume: 4, Issue:2

    Topics: Bone Marrow; Bone Marrow Transplantation; Chimera; Chromosome Deletion; Chromosomes, Human, Pair 7;

1989
Aneuploidy and other genetic effects induced by hydroxyurea in Saccharomyces cerevisiae.
    Mutation research, 1986, Volume: 160, Issue:1

    Topics: Aneuploidy; Cell Survival; Cycloheximide; Drug Resistance, Microbial; Gene Conversion; Hydroxyurea;

1986