Page last updated: 2024-10-16

quinacrine and Chromosomal Triplication

quinacrine has been researched along with Chromosomal Triplication in 39 studies

Quinacrine: An acridine derivative formerly widely used as an antimalarial but superseded by chloroquine in recent years. It has also been used as an anthelmintic and in the treatment of giardiasis and malignant effusions. It is used in cell biological experiments as an inhibitor of phospholipase A2.
quinacrine : A member of the class of acridines that is acridine substituted by a chloro group at position 6, a methoxy group at position 2 and a [5-(diethylamino)pentan-2-yl]nitrilo group at position 9.

Research Excerpts

ExcerptRelevanceReference
"These chromosome abnormalities were compared to previous cytogenic analyses on the transplantable Shay chloroleukemia, in which new fluorescent banding techniques were not utilized."1.26Chromosome studies of the transplantable Shay chloroleukemia in rats. ( Alt, B, 1977)
"2 had total and partial No."1.26Reproducible chromosome changes of polycyclic hydrocarbon-induced rat leukemia: incidence and chromosome banding pattern. ( Fukuhara, S; Maeda, S; Sugiyama, T; Ueda, N; Uenaka, H, 1978)
"Chromosomal abnormalities were detected in 59% of the specimens."1.25Recent advances in the cytogenetic study of human spontaneous abortions. ( Carr, DH; McConnell, HD, 1975)

Research

Studies (39)

TimeframeStudies, this research(%)All Research%
pre-199039 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Moser, GC1
Müller, H2
Robbins, E1
Penchaszadeh, VB1
Coco, R1
Korenberg, JR1
Therman, E1
Denniston, C1
Habedank, M1
Faust, J1
Alt, B1
Hunter, AG1
Ray, M1
Langston, C1
Sugiyama, T1
Uenaka, H1
Ueda, N1
Fukuhara, S1
Maeda, S1
Pérez-Castillo, A1
Abrisqueta, JA1
Robson, EB1
Hopkinson, DA1
Buckton, KE3
Robinson, J1
Polani, PE1
McConnell, HD1
Carr, DH1
O'Riordan, ML1
Robinson, JA1
Evans, HJ1
Bühler, EM1
Stalder, GR1
Werder, E1
Pawlowitzki, IH1
Caspersson, T2
Lindsten, J2
Zech, L2
Price, WH1
Pearson, P1
White, BJ1
Tjio, JH1
Van de Water, LC1
Crandall, C1
Uchida, IA1
Lin, CC1
De la Chapelle, A3
Schröder, J3
Vuopio, P1
Lomakka, G1
Moller, A1
Miller, OJ4
Miller, DA4
Warburton, D1
Koivisto, M1
Shaw, MW1
Holbek, S1
Friedrich, U1
Lauritsen, JG1
Therkelsen, J1
Fujita, H1
Abe, T1
Yamamoto, K1
Furuyama, J1
Breg, WR5
Allderdice, PW3
Benirschike, K1
Bogart, MH1
McClure, HM1
Nelson-Rees, WA1
Cohen, MM1
Finch, AB1
Lubs, HA1
Falk, RE1
Carrel, RE1
Valente, M1
Crandall, BF1
Sparkes, RS1
Van den Berghe, H1
Van Eygen, M1
Fryns, JP1
Tanghe, W1
Verresen, H1
Franceschini, HP1
Fabris, C1
Ponzone, A1
Rosenthal, IM1
Krmpotic, E1
Bocian, M1
Szego, K1
Traut, H1
Scheid, W1
Francke, U1
Gustavson, KH1
Hitrec, V1
Santesson, B1
Short, EM1
Solitare, GB1
Kaski, U1
Forsius, H1
Gendel, E1
Zelson, C1

Reviews

3 reviews available for quinacrine and Chromosomal Triplication

ArticleYear
The use of new staining techniques for human chromosome identification.
    Journal of medical genetics, 1972, Volume: 9, Issue:3

    Topics: Binding Sites; Cell Nucleus; Chromosomes; DNA; Evaluation Studies as Topic; Female; Fluoresceins; Hu

1972
The use of fluorescence techniques for the recognition of mammalian chromosomes and chromosome regions.
    International review of experimental pathology, 1972, Volume: 11

    Topics: Animals; Chromosome Aberrations; Chromosome Disorders; Chromosomes; Chromosomes, Human, 16-18; Chrom

1972
Application of new staining techniques to the study of human chromosomes.
    Progress in medical genetics, 1973, Volume: 9

    Topics: Base Sequence; Burkitt Lymphoma; Cell Line; Chromosome Aberrations; Chromosome Disorders; Chromosome

1973

Other Studies

36 other studies available for quinacrine and Chromosomal Triplication

ArticleYear
Differential nuclear fluorescence during the cell cycle.
    Experimental cell research, 1975, Mar-01, Volume: 91, Issue:1

    Topics: Autoradiography; Cell Line; Chromatin; Embryo, Mammalian; Female; Fibroblasts; HeLa Cells; Humans; M

1975
Trisomy 22. Two new cases and delineation of the phenotype.
    Journal of medical genetics, 1975, Volume: 12, Issue:2

    Topics: Abnormalities, Multiple; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 21-22 and

1975
Hot spots and functional organization of human chromosomes.
    Human genetics, 1978, Jul-12, Volume: 43, Issue:1

    Topics: Abortion, Spontaneous; Chromosomes; Chromosomes, Human; Crossing Over, Genetic; Female; Genes; Human

1978
Trisomy 9p and unusual translocation mongolism in siblings due to different 3:1 segregations of maternal translocation rcp(9;21)(p11;q11).
    Human genetics, 1978, Jun-27, Volume: 42, Issue:3

    Topics: Adolescent; Adult; Azure Stains; Child, Preschool; Chromosomes; Chromosomes, Human, 21-22 and Y; Chr

1978
Chromosome studies of the transplantable Shay chloroleukemia in rats.
    Journal of the National Cancer Institute, 1977, Volume: 58, Issue:5

    Topics: Animals; Chromosome Aberrations; Chromosome Deletion; Fluorescent Dyes; Leukemia, Experimental; Leuk

1977
Cebocephaly in an infant with trisomy 18.
    Journal of medical genetics, 1977, Volume: 14, Issue:4

    Topics: Brain; Chromosomes, Human; Chromosomes, Human, 16-18; Cytological Techniques; Eye Abnormalities; Gen

1977
Reproducible chromosome changes of polycyclic hydrocarbon-induced rat leukemia: incidence and chromosome banding pattern.
    Journal of the National Cancer Institute, 1978, Volume: 60, Issue:1

    Topics: 9,10-Dimethyl-1,2-benzanthracene; Anemia; Animals; Benz(a)Anthracenes; Chromosome Aberrations; Femal

1978
Patau's syndrome and 13q21q translocation.
    Human genetics, 1978, Jun-27, Volume: 42, Issue:3

    Topics: Azure Stains; Chromosomes; Chromosomes, Human, 13-15; Chromosomes, Human, 21-22 and Y; Humans; Infan

1978
Family studies on esterase D and chromosome 13 in man.
    Birth defects original article series, 1976, Volume: 12, Issue:7

    Topics: Chromosomes; Chromosomes, Human, 13-15; Esterases; Female; Genes; Genetic Linkage; Humans; Male; Qui

1976
Recent advances in the cytogenetic study of human spontaneous abortions.
    Obstetrics and gynecology, 1975, Volume: 45, Issue:5

    Topics: Abortion, Spontaneous; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 1-3; Chromo

1975
Distinguishing between the chromosomes involved in Down's syndrome (trisomy 21) and cronic myeloid leukaemia (Ph1) by fluorescence.
    Nature, 1971, Mar-19, Volume: 230, Issue:5290

    Topics: Chromosomes; Chromosomes, Human, 21-22 and Y; Down Syndrome; Female; Fluorescent Dyes; Humans; Karyo

1971
A strongly fluorescing abnormal chromosome in a malformed child.
    Humangenetik, 1971, Volume: 12, Issue:1

    Topics: Abnormalities, Multiple; Child; Chromosome Aberrations; Female; Fluorescence; Humans; Quinacrine; Se

1971
[Fluorography of human chromosomes. A photoelectric procedure for the differentiation of somatic metaphase chromosomes through their fluorescence pattern].
    Humangenetik, 1971, Volume: 13, Issue:3

    Topics: Chromosomes; Chromosomes, Human, 13-15; Chromosomes, Human, 16-18; Chromosomes, Human, 19-20; Chromo

1971
Four patients with trisomy 8 identified by the fluorescence and Giemsa banding techniques.
    Journal of medical genetics, 1972, Volume: 9, Issue:1

    Topics: Abnormalities, Multiple; Adolescent; Blood Cells; Child; Child, Preschool; Chromosomes, Human, 6-12

1972
Trisomy for the smallest autosome of the mouse and identification of the T1Wh translocation chromosome.
    Cytogenetics, 1972, Volume: 11, Issue:5

    Topics: Animals; Chromosome Aberrations; Chromosomes; Cleft Palate; Female; Genotype; Hybridization, Genetic

1972
Identification of partial 12 trisomy by quinacrine fluorescence.
    The Journal of pediatrics, 1973, Volume: 82, Issue:2

    Topics: Chromosome Aberrations; Chromosomes, Human, 6-12 and X; Cytogenetics; Dermatoglyphics; Down Syndrome

1973
8-Trisomy in the bone marrow. Report of two cases.
    Clinical genetics, 1972, Volume: 3, Issue:6

    Topics: Adult; Agranulocytosis; Bone Marrow; Chromosomes, Human, 6-12 and X; Female; Humans; Karyotyping; Ma

1972
Segregating reciprocal (4;21) (q21;q21) translocation with proposita trisomic for parts of 4q and 21.
    Journal of medical genetics, 1973, Volume: 10, Issue:4

    Topics: Abnormalities, Multiple; Amino Acids; Blood Protein Electrophoresis; Body Height; Body Weight; Child

1973
Uses of banding techniques for the identification of human diseases of cytogenetic origin.
    Environmental health perspectives, 1973, Volume: 6

    Topics: Burkitt Lymphoma; Chromosome Aberrations; Chromosome Disorders; Genetic Techniques; Humans; Leukemia

1973
Marker chromosomes in parents of spontaneous abortuses.
    Humangenetik, 1974, Volume: 25, Issue:1

    Topics: Abortion, Spontaneous; Chromosome Aberrations; Chromosomes, Human, 1-3; Chromosomes, Human, 13-15; C

1974
Possible complex translocation t(9;14;13) (q12;pl?;Q31) in mother of a child with 9-p trisomy syndrome.
    Humangenetik, 1974, Volume: 25, Issue:2

    Topics: Adult; Autoradiography; Child; Chromosome Aberrations; Chromosomes, Human, 13-15; Chromosomes, Human

1974
Updating advances in cytogenetics. Applications of the new chromosome banding methods.
    Birth defects original article series, 1974, Volume: 10, Issue:8

    Topics: Chromosome Aberrations; Chromosome Disorders; Chromosome Inversion; Chromosomes; Chromosomes, Human,

1974
Distinctive fluorescence of quinacrine-labelled human G group chromosomes.
    Nature: New biology, 1971, Jun-30, Volume: 231, Issue:26

    Topics: Chromosomes, Human, 21-22 and Y; Down Syndrome; Fluorescence; Humans; Karyotyping; Male; Quinacrine;

1971
Quinacrine fluorescence patterns of human D group chromosomes.
    Nature, 1971, Jul-02, Volume: 232, Issue:5305

    Topics: Autoradiography; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 13-15; Down Syndr

1971
Fluorescence of the trisomic chimpanzee chromosomes.
    Journal of medical primatology, 1974, Volume: 3, Issue:5

    Topics: Animals; Chromosomes; Down Syndrome; Female; Fluorescence; Humans; Karyotyping; Pan troglodytes; Qui

1974
Trisomy 18 with an E-G translocation (46,XY,21-t(21q18q)+). Identification of the component chromosomes by several laboratory techniques.
    Annales de genetique, 1972, Volume: 15, Issue:1

    Topics: Autoradiography; Chromosome Aberrations; Chromosomes, Human, 16-18; Chromosomes, Human, 21-22 and Y;

1972
Partial trisomy of chromosome 11: a case report.
    American journal of mental deficiency, 1973, Volume: 77, Issue:4

    Topics: Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 6-12 and

1973
Partial Trisomy 1, Karyotype 46,XY,12-,t(1q,12p)+.
    Humangenetik, 1973, May-25, Volume: 18, Issue:3

    Topics: Abnormalities, Multiple; Adult; Chromosome Aberrations; Chromosomes, Human, 1-3; Chromosomes, Human,

1973
[Fluorescence and non-disjonction].
    La Nouvelle presse medicale, 1973, Sep-15, Volume: 2, Issue:32

    Topics: Chromosomes; Chromosomes, Human, 13-15; Chromosomes, Human, 16-18; Chromosomes, Human, 21-22 and Y;

1973
Trisomy of the short arm of chromosome 8: association with translocation between chromosomes 8 and 22 46,XY,22-,t(8p22q) plus.
    Clinical genetics, 1973, Volume: 4, Issue:6

    Topics: Adult; Autoradiography; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Chrom

1973
The production of monosomic-trisomic individuals in Drosophila melanogaster by x-irradiation of immature oocytes.
    Mutation research, 1971, Volume: 13, Issue:4

    Topics: Aneuploidy; Animals; Brain; Chromosome Aberrations; Chromosome Disorders; Cytogenetics; Drosophila m

1971
Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations.
    American journal of human genetics, 1972, Volume: 24, Issue:2

    Topics: Adult; Autoradiography; Child; Child, Preschool; Chromosome Aberrations; Chromosomes, Human, 1-3; Ch

1972
Three non-mongoloid patients of similar phenotype with an extra G-like chromosome.
    Clinical genetics, 1972, Volume: 3, Issue:2

    Topics: Abnormalities, Multiple; Autoradiography; Child; Child, Preschool; Chromosome Aberrations; Chromosom

1972
A case of partial 14 trisomy 47,XY,(14q-)+ and translocation t(9p+;14q-) in mother and brother.
    Journal of medical genetics, 1972, Volume: 9, Issue:3

    Topics: Adult; Blood Group Antigens; Child; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human

1972
[Fluorescence microscopy--a simple test for XYY].
    Duodecim; laaketieteellinen aikakauskirja, 1971, Volume: 87, Issue:21

    Topics: Cell Nucleus; Child; Humans; Karyotyping; Male; Methods; Microscopy, Fluorescence; Mosaicism; Mouth

1971
Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescence.
    Humangenetik, 1971, Volume: 13, Issue:3

    Topics: Cell Division; Child, Preschool; Chromosome Aberrations; Chromosomes, Human, 13-15; Chromosomes, Hum

1971