Page last updated: 2024-10-16

quinacrine and Autosomal Chromosome Disorders

quinacrine has been researched along with Autosomal Chromosome Disorders in 62 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Quinacrine: An acridine derivative formerly widely used as an antimalarial but superseded by chloroquine in recent years.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
"The total incidence of major chromosome aberrations including numerical changes of the sex chromosomes, and structural changes of autosomes, was 0."1.26Chromosome analysis on 930 consecutive newborn children using quinacrine fluorescent banding technique. ( Gedeon, MM; Griffith, P; Lin, CC; Newton, DR; Sewell, LM; Smink, WK; Wilkie, L, 1976)
"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 (62)

TimeframeStudies, this research(%)All Research%
pre-199062 (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
Fowler, G1
Kaiser-McCaw, B1
Hecht, F4
Verma, RS1
Dosik, H1
Penchaszadeh, VB1
Coco, R1
Gutierrez, AC1
Salamanca, F1
Lisker, R1
Segovia, A1
Kulikov, RI1
Mashkova, MV1
Verlinskaia, DK1
Bondarev, GN1
Lin, CC1
Gedeon, MM1
Griffith, P1
Smink, WK1
Newton, DR1
Wilkie, L1
Sewell, LM1
Fraccaro, M1
Zuffardi, O1
Buhler, EM1
Jurik, LP1
Garson, OM1
Bocian, M2
Mohandas, T1
Noël, B2
Ayraud, N1
Levy, M1
Cau, D1
McConnell, HD1
Carr, DH1
Naritomi, K1
Hirayama, K1
Nielsen, H1
Skakkebaek, NE1
Philip, J1
Retief, AE1
van Niekerk, WA1
Franceschini, P1
Fabris, C1
Bogetti, G1
Santoro, MA1
Chaippo, G1
Yanagisawa, S1
Distèche, C1
Hagemeijer, A1
Frederic, J1
Progneaux, D1
Peterson, WD1
Simpson, WF1
Ecklund, PS1
Stulberg, CS1
Magenis, RE3
McCaw, BK1
Caspersson, T2
Lindsten, J2
Lomakka, G1
Moller, A1
Zech, L3
Miller, OJ3
Miller, DA3
Warburton, D1
Baserga, A1
Castoldi, GL1
Rowley, JD1
Jacobsen, P1
Mikkelsen, M1
Rosleff, F1
Zeuthen, E1
Nielsen, J2
De la Chapelle, A1
Koivisto, M1
Schröder, J1
Hreidarsson, AB1
Christensen, KR1
Shaw, MW1
Porter, IH1
McKusick, VA1
Chase, GA1
del Solar, C1
Uchida, IA1
Mitelman, F1
Hsia, YE1
Appadorai, V1
Breg, WR5
Howard, RO1
Allderdice, PW1
Warren, RJ1
Rimoin, DL1
Summitt, RL1
Toomey, K1
Bartuska, D1
Alderdice, PW1
Armendares, S1
Weleber, RG1
Overton, K1
Atkins, L1
Miller, WL1
Salam, M1
Baughman, FA1
Mann, JD1
Borgaonkar, DS1
Ebenezer, L1
Scott, CI1
Golomb, HM1
Bahr, GF1
Falk, RE1
Carrel, RE1
Valente, M1
Crandall, BF2
Sparkes, RS1
Van den Berghe, H1
Fryns, JP1
David, G1
Rosenthal, IM1
Krmpotic, E1
Szego, K1
Mayeda, K1
Weiss, L1
Lindahl, R1
Dully, M1
Traut, H1
Scheid, W1
Becker, KL1
Schnedl, W1
Gustavson, KH1
Hitrec, V1
Santesson, B1
Weber, F1
Muller, HM1
Burwell, JK1
Reiss, JA1
Wyandt, HE1
Lovrien, EW1
Short, EM1
Solitare, GB1
Emerit, I1
Luciani, JM1
Quack, B1
Berger, R1
Gagné, R1
Francke, U1
Nesbitt, M1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Randomised Multicentre Phase IV Study to Compare Glivec® (Imatinib Mesylate, STI571) in Monotherapy Versus Glivec® in Combination With Interferon Alpha at Low Doses in the Treatment of Newly-Diagnosed Chronic-Phase Chronic Myeloid Leukaemia[NCT00390897]Phase 4360 participants Interventional2003-07-31Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Reviews

5 reviews available for quinacrine and Autosomal Chromosome Disorders

ArticleYear
Chromosome-banding techniques and their implication in hematology.
    Progress in hematology, 1979, Volume: 11

    Topics: Acute Disease; Azure Stains; Cell Transformation, Neoplastic; Chromosome Aberrations; Chromosome Ban

1979
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
The Philadelphia chromosome.
    Biomedicine / [publiee pour l'A.A.I.C.I.G.], 1973, Volume: 18, Issue:2

    Topics: Alkaline Phosphatase; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 21-22 and Y;

1973
Human genetics.
    Annual review of genetics, 1973, Volume: 7

    Topics: Animals; Chromosome Aberrations; Chromosome Disorders; Chromosome Mapping; Chromosomes; Crossing Ove

1973

Other Studies

57 other studies available for quinacrine and Autosomal Chromosome Disorders

ArticleYear
The use of sequential silver and quinacrine staining to determine the parental origin and breakpoints of a ring-22 human chromosome.
    Clinical genetics, 1980, Volume: 18, Issue:4

    Topics: Abnormalities, Multiple; Child, Preschool; Chromosome Aberrations; Chromosome Deletion; Chromosome D

1980
Heteromorphisms of the Philadelphia (Ph1) chromosome in patients with chronic melogenous leukaemia (CML). I. Classification and clinical significance.
    British journal of haematology, 1980, Volume: 45, Issue:2

    Topics: Acridine Orange; Aged; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 21-22 and Y

1980
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
Supernumerary bisatellited chromosome in a family ascertained through a patient with Sturge-Weber syndrome.
    Annales de genetique, 1975, Volume: 18, Issue:1

    Topics: Angiomatosis; Cells, Cultured; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Fluor

1975
[Identification of several chromosome aberrations in man by the fluorescent method using quinacrine yprite].
    Tsitologiia, 1976, Volume: 18, Issue:2

    Topics: Adolescent; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Cytodiagnosis; Disorders

1976
Chromosome analysis on 930 consecutive newborn children using quinacrine fluorescent banding technique.
    Human genetics, 1976, Mar-12, Volume: 31, Issue:3

    Topics: Chromosome Aberrations; Chromosome Disorders; Chromosome Inversion; Chromosomes, Human, 1-3; Chromos

1976
15/15 translocation in Prader-Willi syndrome.
    Journal of medical genetics, 1977, Volume: 14, Issue:4

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

1977
Recent cytogenetic advances and implications for pediatric practice.
    Pediatric clinics of North America, 1978, Volume: 25, Issue:3

    Topics: Abortion, Spontaneous; Azure Stains; Chromosome Aberrations; Chromosome Banding; Chromosome Disorder

1978
[Cat eye syndrome: chromosome study and genetic counseling].
    Journal de genetique humaine, 1976, Volume: 24 Suppl

    Topics: Adult; Aneuploidy; Bromodeoxyuridine; Chromosome Aberrations; Chromosome Disorders; Chromosomes; Col

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
Determination of the breakpoints and the parental origin of a ring 22 chromosome: an analysis by high-resolution banding technique, quinacrine and silver stainings.
    Jinrui idengaku zasshi. The Japanese journal of human genetics, 1988, Volume: 33, Issue:1

    Topics: Abnormalities, Multiple; Chromosome Aberrations; Chromosome Banding; Chromosome Disorders; Chromosom

1988
Dyeing the Y chromosome.
    Lancet (London, England), 1971, Feb-06, Volume: 1, Issue:7693

    Topics: Acridines; Animals; Chromosome Aberrations; Chromosome Disorders; Cricetinae; Flavins; Fluorescence;

1971
[Fluorescence microscopy of Y chromatin. A method for the study of Y-chromosome abnormalities].
    Ugeskrift for laeger, 1971, Apr-09, Volume: 133, Issue:14

    Topics: Amnion; Chromosome Aberrations; Chromosome Disorders; Fibroblasts; Humans; Lymphocytes; Male; Method

1971
[A new technic for the analysis of human chromosomes].
    South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 1971, Sep-04, Volume: 45, Issue:35

    Topics: Chromosome Aberrations; Chromosome Disorders; Chromosomes; Cytogenetics; Female; Fluorescent Antibod

1971
[Value of the use of fluorescent substances in the study of normal and pathologic human karyotypes. I. Identification of the Y chromosome].
    Minerva pediatrica, 1972, Jun-09, Volume: 24, Issue:21

    Topics: Chromosome Aberrations; Chromosome Disorders; Chromosomes; Fluorescence; Humans; Karyotyping; Method

1972
Immunoglobulin abnormality in a girl with a large chromosome 18.
    Journal of medical genetics, 1972, Volume: 9, Issue:3

    Topics: Adolescent; Child; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 16-18; Dermatog

1972
An abnormal large human chromosome identified as an end-to-end fusion of two X's by combined results of the new banding techniques and microdensitometry.
    Clinical genetics, 1972, Volume: 3, Issue:5

    Topics: Abnormalities, Multiple; Adolescent; Blood; Chromosome Aberrations; Chromosome Disorders; Chromosome

1972
Diploid and heteroploid human cell lines surveyed for Y chromosome fluorescence.
    Nature: New biology, 1973, Mar-07, Volume: 242, Issue:114

    Topics: Cell Line; Cell Transformation, Neoplastic; Cells, Cultured; Chromosome Aberrations; Chromosome Diso

1973
Clinical cytogenetics. Dawn breaks on a new era.
    American journal of diseases of children (1960), 1973, Volume: 125, Issue:3

    Topics: Child; Chromosome Aberrations; Chromosome Disorders; Cytogenetics; Female; Humans; Infant, Newborn;

1973
Letter: A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining.
    Nature, 1973, Jun-01, Volume: 243, Issue:5405

    Topics: Adolescent; Adult; Aged; Bone Marrow Cells; Chromosome Aberrations; Chromosome Disorders; Chromosome

1973
A ring chromosome, diagnosed by quinacrine fluorescence as No. 9, in a mentally retarded girl.
    Clinical genetics, 1973, Volume: 4, Issue:5

    Topics: Adult; Amino Acids; Body Height; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 6

1973
D-D translocations in males examined for military service.
    Journal of medical genetics, 1973, Volume: 10, Issue:4

    Topics: Adult; Body Height; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 13-15; Denmark

1973
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
D-D translocations in patients with mental illness.
    Hereditas, 1973, Volume: 75, Issue:1

    Topics: Adolescent; Adult; Child; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 13-15; F

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
Human cytogenetics: trends and techniques.
    Progress in clinical pathology, 1973, Volume: 5

    Topics: Autoradiography; Chromosome Aberrations; Chromosome Disorders; Chromosome Mapping; Chromosomes; Cyto

1973
Identification of chromosomal abnormalities by quinacrine-staining technique in patients with normal karyotypes by conventional analysis.
    The Journal of pediatrics, 1974, Volume: 84, Issue:4

    Topics: Adolescent; Adult; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Chromosome

1974
Heterogeneity of Ph1 in chronic myeloid leukaemia.
    Hereditas, 1974, Volume: 76, Issue:2

    Topics: Bone Marrow Cells; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 21-22 and Y; Ch

1974
Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndrome.
    Birth defects original article series, 1974, Volume: 10, Issue:8

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

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
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
Identification by fluorescent microscopy of the abnormal chromosomes associated with the G-deletion syndromes.
    American journal of human genetics, 1973, Volume: 25, Issue:1

    Topics: Blepharoptosis; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Chromosomes,

1973
Clinical application of fluorescent staining of chromosomes.
    Journal of the American Medical Women's Association (1972), 1973, Volume: 26, Issue:6

    Topics: Alkylating Agents; Chromosome Aberrations; Chromosome Disorders; Female; Fluoresceins; Fluorescence;

1973
Quinacrine fluorescence patterns and terminal DNA labelling of human C group chromosomes.
    Nature: New biology, 1972, Mar-22, Volume: 236, Issue:64

    Topics: Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 6-12 and X; DNA; Female; Fluoresce

1972
Identification by fluorescence of two G rings: (46,XY,21r) G deletion syndrome I and (46, XX, 22r) G deletion syndrome II.
    Annales de genetique, 1972, Volume: 15, Issue:4

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

1972
A ring-20 chromosome.
    Journal of medical genetics, 1972, Volume: 9, Issue:3

    Topics: Child; Child Behavior Disorders; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 1

1972
Ascertainment of seven YY males in a private neurology practice.
    JAMA, 1972, Volume: 222, Issue:4

    Topics: Adolescent; Adult; Antisocial Personality Disorder; Child, Preschool; Chromosome Aberrations; Chromo

1972
Identification of a D-E(15-18) translocation chromosome by quinacrine fluorescence and urea banding techniques.
    Humangenetik, 1973, Volume: 17, Issue:4

    Topics: Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 13-15; Chromosomes, Human, 16-18;

1973
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
Renovascular hypertension. Prospective diagnostic yield in a random access population.
    Humangenetik, 1973, Dec-20, Volume: 20, Issue:4

    Topics: Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 1-3; Fluorescence; Humans; Hypogon

1973
A (15;18) translocation, unbalanced, 45 chromosomes. Human Genetic Mutant Cell Repository, Camden, N.J., identification No. GM-17.
    Cytogenetics and cell genetics, 1973, Volume: 12, Issue:5

    Topics: Cells, Cultured; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human,

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
Localization of the human lactate dehydrogenase B gene on the short arm of chromosome 12.
    American journal of human genetics, 1974, Volume: 26, Issue:1

    Topics: Abnormalities, Multiple; Child; Chromosome Aberrations; Chromosome Disorders; Chromosome Mapping; Ch

1974
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
The human karyotype.
    Postgraduate medicine, 1972, Volume: 52, Issue:1

    Topics: Chromosome Aberrations; Chromosome Disorders; Humans; Karyotyping; Methods; Microscopy, Fluorescence

1972
[The atebrin fluorescence method in human cytogenetics].
    Wiener klinische Wochenschrift, 1972, Jun-16, Volume: 84, Issue:24

    Topics: Chromosome Aberrations; Chromosome Disorders; Cytogenetics; Female; Fluorescence; Fluorescent Dyes;

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
Identification of 21r and 22r chromosomes by quinacrine fluorescence.
    Clinical genetics, 1972, Volume: 3, Issue:4

    Topics: Abnormalities, Multiple; Adult; Chromosome Aberrations; Chromosome Disorders; Chromosome Mapping; Ch

1972
Mosaicism with translocation: autoradiographic and fluorescent studies of an inherited reciprocal translocation t(2q+;14q-).
    Journal of medical genetics, 1972, Volume: 9, Issue:3

    Topics: Abnormalities, Multiple; Adult; Aneuploidy; Autoradiography; Blood Group Antigens; Child; Chromosome

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
A familial Y-autosome translocation in man.
    Clinical genetics, 1971, Volume: 2, Issue:1

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

1971
[Constitutional chromosome abnormalities].
    La Presse medicale, 1971, Oct-23, Volume: 79, Issue:44

    Topics: Chromosome Aberrations; Chromosome Disorders; Cytogenetics; DNA; Fluoresceins; Humans; Karyotyping;

1971
[New perspectives in human cytogenetics].
    L'union medicale du Canada, 1971, Volume: 100, Issue:11

    Topics: Acridines; Chromosome Aberrations; Chromosome Disorders; Cytogenetics; DNA; Humans; Methods; Nucleic

1971
The identification of human chromosomes by fluorescence technics.
    The Biochemical journal, 1971, Volume: 124, Issue:5

    Topics: Animals; Burkitt Lymphoma; Chromosome Aberrations; Chromosome Disorders; Chromosomes; Crossing Over,

1971
Cattanach's translocation: cytological characterization by quinacrine mustard staining.
    Proceedings of the National Academy of Sciences of the United States of America, 1971, Volume: 68, Issue:12

    Topics: Animals; Chromosome Aberrations; Chromosome Disorders; Female; Fluorescence; Genetic Linkage; Hetero

1971
Identification of the abnormal B group chromosome in the "cri du chat" syndrome by QM-fluorescence.
    Experimental cell research, 1970, Volume: 61, Issue:2

    Topics: Autoradiography; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 4-5; Cri-du-Chat

1970
Chromosome identification.
    Canadian Medical Association journal, 1971, May-22, Volume: 104, Issue:10

    Topics: Chromosome Aberrations; Chromosome Disorders; Chromosomes; Female; Humans; Male; Methods; Microscopy

1971