quinacrine has been researched along with Abnormalities, Multiple in 16 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Quinacrine: An acridine derivative formerly widely used as an antimalarial but superseded by chloroquine in recent years.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.
Abnormalities, Multiple: Congenital abnormalities that affect more than one organ or body structure.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 16 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Fowler, G | 1 |
| Kaiser-McCaw, B | 1 |
| Hecht, F | 3 |
| Penchaszadeh, VB | 1 |
| Coco, R | 1 |
| Naritomi, K | 1 |
| Hirayama, K | 1 |
| Bühler, EM | 1 |
| Müller, H | 1 |
| Stalder, GR | 1 |
| Werder, E | 1 |
| Caspersson, T | 1 |
| Lindsten, J | 1 |
| Zech, L | 1 |
| Buckton, KE | 1 |
| Price, WH | 1 |
| Distèche, C | 1 |
| Hagemeijer, A | 1 |
| Frederic, J | 1 |
| Progneaux, D | 1 |
| De la Chapelle, A | 1 |
| Koivisto, M | 1 |
| Schröder, J | 1 |
| Hsia, YE | 1 |
| Appadorai, V | 1 |
| Breg, WR | 2 |
| Howard, RO | 1 |
| Zackai, EH | 1 |
| Magenis, RE | 2 |
| Armendares, S | 1 |
| Weleber, RG | 1 |
| Overton, K | 1 |
| Cohen, MM | 1 |
| Putnam, TI | 1 |
| Van den Berghe, H | 1 |
| Van Eygen, M | 1 |
| Fryns, JP | 1 |
| Tanghe, W | 1 |
| Verresen, H | 1 |
| Mayeda, K | 1 |
| Weiss, L | 1 |
| Lindahl, R | 1 |
| Dully, M | 1 |
| Gustavson, KH | 1 |
| Hitrec, V | 1 |
| Santesson, B | 1 |
| Crandall, BF | 1 |
| Weber, F | 1 |
| Muller, HM | 1 |
| Burwell, JK | 1 |
| Reiss, JA | 1 |
| Wyandt, HE | 1 |
| Lovrien, EW | 1 |
16 other studies available for quinacrine and Abnormalities, Multiple
| Article | Year |
|---|---|
The use of sequential silver and quinacrine staining to determine the parental origin and breakpoints of a ring-22 human chromosome.
Topics: Abnormalities, Multiple; Child, Preschool; Chromosome Aberrations; Chromosome Deletion; Chromosome D | 1980 |
Trisomy 22. Two new cases and delineation of the phenotype.
Topics: Abnormalities, Multiple; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 21-22 and | 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.
Topics: Abnormalities, Multiple; Chromosome Aberrations; Chromosome Banding; Chromosome Disorders; Chromosom | 1988 |
A strongly fluorescing abnormal chromosome in a malformed child.
Topics: Abnormalities, Multiple; Child; Chromosome Aberrations; Female; Fluorescence; Humans; Quinacrine; Se | 1971 |
Four patients with trisomy 8 identified by the fluorescence and Giemsa banding techniques.
Topics: Abnormalities, Multiple; Adolescent; Blood Cells; Child; Child, Preschool; Chromosomes, Human, 6-12 | 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.
Topics: Abnormalities, Multiple; Adolescent; Blood; Chromosome Aberrations; Chromosome Disorders; Chromosome | 1972 |
Segregating reciprocal (4;21) (q21;q21) translocation with proposita trisomic for parts of 4q and 21.
Topics: Abnormalities, Multiple; Amino Acids; Blood Protein Electrophoresis; Body Height; Body Weight; Child | 1973 |
Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndrome.
Topics: Abnormalities, Multiple; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 1-3; Chro | 1974 |
Ring chromosome 7 with variable phenotypic expression.
Topics: Abnormalities, Multiple; Blepharoptosis; Child; Chromosome Aberrations; Chromosomes, Human, 6-12 and | 1973 |
Identification by fluorescence of two G rings: (46,XY,21r) G deletion syndrome I and (46, XX, 22r) G deletion syndrome II.
Topics: Abnormalities, Multiple; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 21-22 and | 1972 |
An 18p21q translocation in a patient with presumptive "monosomy G".
Topics: Abnormalities, Multiple; Aneuploidy; Child, Preschool; Chromosome Aberrations; Chromosomes, Human, 1 | 1972 |
Partial Trisomy 1, Karyotype 46,XY,12-,t(1q,12p)+.
Topics: Abnormalities, Multiple; Adult; Chromosome Aberrations; Chromosomes, Human, 1-3; Chromosomes, Human, | 1973 |
Localization of the human lactate dehydrogenase B gene on the short arm of chromosome 12.
Topics: Abnormalities, Multiple; Child; Chromosome Aberrations; Chromosome Disorders; Chromosome Mapping; Ch | 1974 |
Three non-mongoloid patients of similar phenotype with an extra G-like chromosome.
Topics: Abnormalities, Multiple; Autoradiography; Child; Child, Preschool; Chromosome Aberrations; Chromosom | 1972 |
Identification of 21r and 22r chromosomes by quinacrine fluorescence.
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-).
Topics: Abnormalities, Multiple; Adult; Aneuploidy; Autoradiography; Blood Group Antigens; Child; Chromosome | 1972 |