Page last updated: 2024-11-04

streptonigrin and Autosomal Chromosome Disorders

streptonigrin has been researched along with Autosomal Chromosome Disorders in 3 studies

Research Excerpts

ExcerptRelevanceReference
"Nijmegen breakage syndrome is characterized by a variable T cell and B cell immunodeficiency, growth failure, and an increased risk of malignancy."1.30Cell cycle checkpoints and DNA repair in Nijmegen breakage syndrome. ( Lederman, H; Lees-Miller, SP; Sullivan, KE; Veksler, E, 1997)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19901 (33.33)18.7374
1990's2 (66.67)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Nasjleti, CE1
Spencer, HH1
Sullivan, KE1
Veksler, E1
Lederman, H1
Lees-Miller, SP1
Wolff, DJ1
Needleman, BW1
Wasserman, SS1
Schwartz, S1

Other Studies

3 other studies available for streptonigrin and Autosomal Chromosome Disorders

ArticleYear
Chromosome polyploidization in human leukocyte cultures treated with streptonigrin and cyclophosphamide.
    Cancer, 1967, Volume: 20, Issue:1

    Topics: Antibiotics, Antineoplastic; Cell Division; Chromosome Aberrations; Chromosome Disorders; Cyclophosp

1967
Cell cycle checkpoints and DNA repair in Nijmegen breakage syndrome.
    Clinical immunology and immunopathology, 1997, Volume: 82, Issue:1

    Topics: Abnormalities, Multiple; Antigens, Nuclear; Ataxia Telangiectasia; Cell Cycle; Cell Line; Chromosome

1997
Spontaneous and clastogen induced chromosomal breakage in scleroderma.
    The Journal of rheumatology, 1991, Volume: 18, Issue:6

    Topics: 4-Nitroquinoline-1-oxide; Adult; Aged; Bleomycin; Cells, Cultured; Chromosome Aberrations; Chromosom

1991