mitomycin has been researched along with Abnormalities, Multiple in 11 studies
Mitomycin: An antineoplastic antibiotic produced by Streptomyces caespitosus. It is one of the bi- or tri-functional ALKYLATING AGENTS causing cross-linking of DNA and inhibition of DNA synthesis.
mitomycin : A family of aziridine-containing natural products isolated from Streptomyces caespitosus or Streptomyces lavendulae.
Abnormalities, Multiple: Congenital abnormalities that affect more than one organ or body structure.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Seckel syndrome is a rare autosomal recessive disorder." | 5.30 | Normal expression of the Fanconi anemia proteins FAA and FAC and sensitivity to mitomycin C in two patients with Seckel syndrome. ( Abou-Zahr, F; Bacino, C; Bejjani, B; Kruyt, FA; Kurg, R; Shapira, SK; Youssoufian, H, 1999) |
| "Seckel syndrome is a rare autosomal recessive disorder." | 1.30 | Normal expression of the Fanconi anemia proteins FAA and FAC and sensitivity to mitomycin C in two patients with Seckel syndrome. ( Abou-Zahr, F; Bacino, C; Bejjani, B; Kruyt, FA; Kurg, R; Shapira, SK; Youssoufian, H, 1999) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (27.27) | 18.7374 |
| 1990's | 5 (45.45) | 18.2507 |
| 2000's | 2 (18.18) | 29.6817 |
| 2010's | 1 (9.09) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bharti, SK | 1 |
| Khan, I | 1 |
| Banerjee, T | 1 |
| Sommers, JA | 1 |
| Wu, Y | 1 |
| Brosh, RM | 1 |
| Bobabilla-Morales, L | 1 |
| Corona-Rivera, A | 1 |
| Corona-Rivera, JR | 1 |
| Buenrostro, C | 1 |
| García-Cobián, TA | 1 |
| Corona-Rivera, E | 1 |
| Cantú-Garza, JM | 1 |
| García-Cruz, D | 1 |
| Saricaoglu, MS | 1 |
| Sengun, A | 1 |
| Karakurt, A | 1 |
| Colluoglu, Z | 1 |
| Allingham-Hawkins, DJ | 2 |
| Tomkins, DJ | 3 |
| Van den Berg, DJ | 1 |
| Francke, U | 1 |
| Abou-Zahr, F | 1 |
| Bejjani, B | 1 |
| Kruyt, FA | 1 |
| Kurg, R | 1 |
| Bacino, C | 1 |
| Shapira, SK | 1 |
| Youssoufian, H | 1 |
| Kraakman-van der Zwet, M | 1 |
| Overkamp, WJ | 1 |
| Friedl, AA | 1 |
| Klein, B | 1 |
| Verhaegh, GW | 1 |
| Jaspers, NG | 1 |
| Midro, AT | 1 |
| Eckardt-Schupp, F | 1 |
| Lohman, PH | 1 |
| Zdzienicka, MZ | 1 |
| Burns, MA | 1 |
| Uehara, M | 1 |
| Kida, M | 1 |
| Butler, MG | 1 |
| Hall, BD | 1 |
| Maclean, RN | 1 |
| Lozzio, CB | 1 |
1 review available for mitomycin and Abnormalities, Multiple
| Article | Year |
|---|---|
Molecular functions and cellular roles of the ChlR1 (DDX11) helicase defective in the rare cohesinopathy Warsaw breakage syndrome.
Topics: Abnormalities, Multiple; DEAD-box RNA Helicases; DNA Breaks; DNA Helicases; G-Quadruplexes; Genomic | 2014 |
10 other studies available for mitomycin and Abnormalities, Multiple
| Article | Year |
|---|---|
Chromosome instability induced in vitro with mitomycin C in five Seckel syndrome patients.
Topics: Abnormalities, Multiple; Adolescent; Adult; Child, Preschool; Chromosomal Instability; Cytogenetic A | 2003 |
Autosomal dominant Weill-Marchesani syndrome and glaucoma management.
Topics: Abnormalities, Multiple; Adolescent; Chromosome Disorders; Dwarfism; Eye Abnormalities; Follow-Up St | 2005 |
Heterogeneity in Roberts syndrome.
Topics: Abnormalities, Multiple; Cell Line; Developmental Disabilities; Female; Genetic Heterogeneity; Growt | 1995 |
Sensitivity of Roberts syndrome cells to gamma radiation, mitomycin C, and protein synthesis inhibitors.
Topics: Abnormalities, Multiple; Cell Cycle; Cell Division; Cell Line; Demecolcine; Dose-Response Relationsh | 1993 |
Normal expression of the Fanconi anemia proteins FAA and FAC and sensitivity to mitomycin C in two patients with Seckel syndrome.
Topics: Abnormalities, Multiple; Blotting, Western; Cell Cycle Proteins; Child; Child, Preschool; DNA-Bindin | 1999 |
Immortalization and characterization of Nijmegen Breakage syndrome fibroblasts.
Topics: Abnormalities, Multiple; Antineoplastic Agents; Bleomycin; Camptothecin; Cell Line; Cell Line, Trans | 1999 |
Somatic cell hybridization of Roberts syndrome and normal lymphoblasts resulting in correction of both the cytogenetic and mutagen hypersensitivity cellular phenotypes.
Topics: Abnormalities, Multiple; Child, Preschool; Dose-Response Relationship, Drug; Female; Genes, Recessiv | 1991 |
Hypersensitivity to mitomycin C cell-killing in Roberts syndrome fibroblasts with, but not without, the heterochromatin abnormality.
Topics: Abnormalities, Multiple; Cells, Cultured; Fibroblasts; Heterochromatin; Humans; Mitomycin; Mitomycin | 1989 |
A complex mosaic with tdic(13;18) (p11;p11), +13p-, +18p-, r(13) etc. in a male infant. II. Increased dissociation of dicentric chromosome by mitomycin C.
Topics: Abnormalities, Multiple; Bromodeoxyuridine; Cells, Cultured; Centromere; Chromosome Aberrations; Chr | 1986 |
Do some patients with Seckel syndrome have hematological problems and/or chromosome breakage?
Topics: Abnormalities, Multiple; Adolescent; Child; Chromosome Aberrations; Chromosome Fragility; Chromosome | 1987 |