thymidine has been researched along with Deficiency, Mental in 43 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 42 (97.67) | 18.7374 |
1990's | 1 (2.33) | 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 |
---|---|
ATKINS, L | 1 |
BOEOEK, JA | 1 |
GUSTAVSON, KH | 2 |
HANSSON, O | 1 |
HJELM, M | 1 |
GERMAN, J | 2 |
LEJEUNE, J | 1 |
MACINTYRE, MN | 1 |
DE GROUCHY, J | 1 |
Warburton, D | 1 |
Miller, DA | 1 |
Miller, OJ | 1 |
Breg, WR | 1 |
De Capoa, A | 1 |
Shaw, MW | 1 |
Ockey, CH | 1 |
De la Chapelle, A | 1 |
Glover, TW | 1 |
Barinsky, IF | 1 |
Dementiev, IV | 1 |
Shvetsova, TP | 1 |
Ugryumov, EP | 1 |
Ryabova, MV | 1 |
Bugbee, SJ | 1 |
Sutnick, AI | 2 |
Millman, I | 1 |
Blumberg, BS | 2 |
Schmickel, RD | 1 |
Chu, EH | 1 |
Trosko, JE | 1 |
Chang, CC | 1 |
Leisti, JT | 1 |
Kaback, MM | 1 |
Rimoin, DL | 1 |
Webb, T | 1 |
Jacobs, PA | 1 |
Nussbaum, RL | 1 |
Ledbetter, DH | 1 |
Mikkelsen, M | 2 |
Dahl, G | 1 |
Crandall, BF | 3 |
Carrel, RE | 1 |
Howard, J | 1 |
Schroeder, WA | 1 |
Müller, H | 2 |
Agarwal, SS | 1 |
Gerstley, BJ | 1 |
London, WT | 1 |
Loeb, LA | 1 |
Venetianer, A | 1 |
Dallmann, L | 1 |
László, A | 1 |
Burg, K | 1 |
Fowler, I | 1 |
Hollingsworth, DR | 1 |
Traurig, H | 1 |
Tal'vik, TA | 2 |
Mikel'saar, AV | 3 |
Mikel'saar, RV | 3 |
Buhl, SN | 1 |
Setlow, RB | 1 |
Regan, JD | 1 |
Pfeiffer, RA | 1 |
Bier, L | 1 |
Majewski, F | 1 |
Rager, K | 1 |
Kask, VA | 1 |
Kleijer, WJ | 1 |
de Weerd-Kastelein, EA | 1 |
Sluyter, ML | 1 |
Keijzer, W | 1 |
de Wit, J | 1 |
Bootsma, D | 1 |
Blyumina, MG | 1 |
Kuznetsova, LI | 1 |
Levenson, JE | 1 |
Sparkes, RS | 3 |
Santesson, B | 1 |
Böök, JA | 1 |
Francke, U | 1 |
Campbell, MA | 1 |
Cooke, P | 2 |
Black, JA | 1 |
Curtis, DJ | 1 |
De Chieri, PR | 1 |
Albores, JM | 1 |
Cosín, A | 1 |
Cosín, JM | 1 |
Cohen, MM | 1 |
Lin, CC | 1 |
Sybert, V | 1 |
Orecchio, EJ | 1 |
Reiss, JA | 1 |
Wyandt, HE | 2 |
Magenis, RE | 1 |
Lovrien, EW | 2 |
Hecht, F | 2 |
Weber, FM | 1 |
Stewart, RE | 1 |
McHugh, J | 1 |
Wright, T | 1 |
Genest, P | 1 |
Lachance, R | 1 |
Poty, J | 1 |
Jacob, D | 1 |
Webb, GC | 1 |
Garson, M | 1 |
Robson, MK | 1 |
Pitt, DB | 1 |
Siniscalco, M | 1 |
Klinger, HP | 1 |
Eagle, H | 1 |
Koprowski, H | 1 |
Fujimoto, WY | 1 |
Seegmiller, JE | 1 |
Ferrier, PE | 1 |
Ferrier, SA | 1 |
Niebuhr, E | 1 |
Ricci, N | 1 |
Dallapiccola, B | 1 |
Ventimiglia, B | 1 |
Preto, G | 1 |
Bijlsma, JB | 1 |
de France, H | 1 |
Bleeker-Wagemakers, EM | 1 |
Kasahara, S | 1 |
Reisman, LE | 1 |
Walker, ME | 1 |
Stiefel, FH | 1 |
Allen, FH | 1 |
Emerit, I | 1 |
Vernant, P | 1 |
Lubs, HA | 1 |
Dekaban, AS | 1 |
1 review available for thymidine and Deficiency, Mental
Article | Year |
---|---|
Fragile X syndrome: a unique mutation in man.
Topics: Caffeine; Chromosome Fragility; Female; Fragile X Syndrome; Genetic Counseling; Genetic Linkage; Gen | 1986 |
42 other studies available for thymidine and Deficiency, Mental
Article | Year |
---|---|
A CASE OF XXXXY SEX CHROMOSOME ANOMALY WITH AUTORADIOGRAPHIC STUDIES.
Topics: Autoradiography; Biopsy; Bone Diseases; Cell Division; Chromosome Aberrations; Chromosome Disorders; | 1963 |
CHROMOSOMAL AUTORADIOGRAPHY IN THE CRI DU CHAT SYNDROME.
Topics: Autoradiography; Chromosome Aberrations; Chromosome Disorders; Chromosomes; Cri-du-Chat Syndrome; DN | 1964 |
Distinction between chromosome 4 and chromosome 5 by replication pattern and length of long and short arms.
Topics: Autoradiography; Chromosome Aberrations; Chromosome Disorders; Humans; Intellectual Disability; Kary | 1967 |
Autoradiographic re-appraisal of an XXXxY male as a probable XXXXY with a 4-11 translocation.
Topics: Adult; Autoradiography; Chromosome Aberrations; Chromosome Disorders; DNA; Humans; Intellectual Disa | 1967 |
FUdR induction of the X chromosome fragile site: evidence for the mechanism of folic acid and thymidine inhibition.
Topics: Cells, Cultured; DNA; Female; Floxuridine; Folic Acid; Humans; Intellectual Disability; Lymphocytes; | 1981 |
Investigation of the nature of Australia antigen. I: The absence of biological activity of Australia antigen in human blood leukocyte culture.
Topics: Adolescent; Adult; Chromosome Aberrations; DNA Nucleotidyltransferases; Down Syndrome; Female; Hepat | 1975 |
Cockayne syndrome: a cellular sensitivity to ultraviolet light.
Topics: Abnormalities, Multiple; Child, Preschool; Chromosomes, Human, 6-12 and X; Dwarfism; Female; Fibrobl | 1977 |
Human X-autosome translocations: differential inactivation of the X chromosome in a kindred with an X-9 translocation.
Topics: Adolescent; Adult; Amenorrhea; Autoradiography; Body Height; Child; Chromosome Aberrations; Chromoso | 1975 |
Fragile Xq27.3 in female heterozygotes for the Martin-Bell syndrome.
Topics: Bromodeoxyuridine; Chromosome Fragility; Dosage Compensation, Genetic; Female; Fragile X Syndrome; G | 1990 |
Unbalanced X-autosomal translocation with inactivation of the normal X chromosome.
Topics: Abnormalities, Multiple; ABO Blood-Group System; Adult; Autoradiography; Chromosome Aberrations; Chr | 1973 |
Trisomy 13 with a 13-X translocation.
Topics: Autoradiography; Chromosomes, Human, 13-15; Dermatoglyphics; Female; Humans; Infant, Newborn; Intell | 1974 |
DNA polymerase activity as an index of lymphocyte stimulation: studies in Down's syndrome.
Topics: Adolescent; Adult; Antigens; Blood Proteins; DNA Nucleotidyltransferases; Down Syndrome; Female; gam | 1970 |
Detection of mucopolysaccharidoses by sulphate incorporation into stimulated lymphocytes.
Topics: Chondroitin; Diagnosis, Differential; Humans; Intellectual Disability; Lectins; Lymphocytes; Mucopol | 1974 |
Response to stimulation in vitro of lymphocytes from patients with Down's syndrome.
Topics: Down Syndrome; Humans; Intellectual Disability; Lectins; Lymphocyte Activation; Lymphocytes; Thymidi | 1973 |
Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+).
Topics: Abnormalities, Multiple; Adult; Autoradiography; Child, Preschool; Chromosome Aberrations; Chromosom | 1974 |
Recovery of the ability to synthesize DNA in segments of normal size at long times after ultraviolet irradiation of human cells.
Topics: Cell Line; Centrifugation, Density Gradient; Chromosome Aberrations; Chromosome Disorders; DNA; DNA | 1973 |
De novo translocation t(Yq-; 15p+) in a malformed boy.
Topics: Abnormalities, Multiple; Autoradiography; Child; Child, Preschool; Chromosome Aberrations; Chromosom | 1973 |
Ring heterosome in a two-and-a-half year old girl (46, XXr or 46, XYr).
Topics: ABO Blood-Group System; Child, Preschool; Chromatin; Chromosomes; Dermatoglyphics; DNA Replication; | 1973 |
UV-induced DNA repair synthesis in cells of patients with different forms of xeroderma pigmentosum and of heterozygotes.
Topics: Adolescent; Adult; Cells, Cultured; Child; Child, Preschool; Chromosome Aberrations; Chromosome Diso | 1973 |
Children with an XYY sex chromosome constitution.
Topics: Anthropometry; Child; Chromosomes; Colchicine; Dermatoglyphics; Humans; Intellectual Disability; Kar | 1973 |
Partial deletion syndromes of chromosome 18.
Topics: Autoradiography; Child; Chromosome Aberrations; Chromosomes, Human, 16-18; Eye Abnormalities; Eye Di | 1971 |
DNA synthesis of human XYY cells. Autoradiography and fluorescence pattern.
Topics: Adult; Autoradiography; Child; DNA; DNA Replication; Fluorescence; Humans; Intellectual Disability; | 1972 |
Inherited t(13q14q) in two retarded sisters.
Topics: Adolescent; Autoradiography; Blood Group Antigens; Body Height; Body Weight; Chromosome Aberrations; | 1972 |
Comparative clinical studies and X chromosome behaviour in a case of XXXX-XXXXX mosaicism.
Topics: Abnormalities, Multiple; Autoradiography; Dermatoglyphics; Female; Humans; Infant; Intellectual Disa | 1972 |
A human ring C chromosome associated with multiple congenital abnormalities.
Topics: Abnormalities, Multiple; Autoradiography; Blood Protein Electrophoresis; Bone Marrow Cells; Chromoso | 1972 |
Two human X-autosome translocations identified by autoradiography and fluorescence.
Topics: Autoradiography; Child; Chromosome Aberrations; Chromosomes, Human, 6-12 and X; Congenital Abnormali | 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 |
Double monosomy mosaicism (45,X-45, XX,21-) in a retarded child with multiple congenital malformations.
Topics: Abnormalities, Multiple; Aneuploidy; Autoradiography; Blood Protein Electrophoresis; Bone Marrow Cel | 1971 |
Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+).
Topics: Acid Phosphatase; Analysis of Variance; Aneuploidy; Autoradiography; Blood Group Antigens; Child, Pr | 1971 |
A family showing transmission of a translocation t(3porq-;Cq+).
Topics: Abnormalities, Multiple; Adolescent; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Huma | 1971 |
Autosomal translocation in a mentally retarded male child with 46,XY,t(2q-;13q+) complement. Case report and review.
Topics: Autoradiography; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, | 1971 |
A partial D-trisomy-normal mosaic female.
Topics: Autoradiography; Bone Marrow Cells; Child; Chromosome Aberrations; Chromosomes, Human, 13-15; Chromo | 1971 |
Evidence for intergenic complementation in hybrid cells derived from two human diploid strains each carrying an X-linked mutation.
Topics: Autoradiography; Chromosomes; Culture Techniques; Cytogenetics; Diploidy; Female; Fibroblasts; Gluco | 1969 |
XXYY Klinefelter's syndrome: case report and a study of the Y chromosomes' DNA replication pattern.
Topics: Adolescent; Autoradiography; Dermatoglyphics; DNA Replication; Humans; Intellectual Disability; Kary | 1968 |
A ring chromosome (46,XY,13r) occurring in a family with a D-D translocation 13-,14-, t(13q 14q).
Topics: Abnormalities, Multiple; Autoradiography; Blood Group Antigens; Child; Chromosome Aberrations; Chrom | 1969 |
[Ring chromosome 18].
Topics: Autoradiography; Child; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 16-18; Der | 1970 |
Duplication deficiency syndrome in familial translocation (2q-;5p+).
Topics: Abnormalities, Multiple; Anthropometry; Autoradiography; Blood Group Antigens; Child; Child, Prescho | 1971 |
Short arm deletion of chromosome 18.
Topics: Agenesis of Corpus Callosum; Autoradiography; Chromosome Aberrations; Chromosome Disorders; Chromoso | 1967 |
MN blood-group locus: data concerning the possible chromosomal location.
Topics: Autoradiography; Blood Group Antigens; Child, Preschool; Chromosome Aberrations; Chromosome Disorder | 1968 |
[Abnormal C group chromosome in several members of the same family].
Topics: Abnormalities, Multiple; Adult; Autoradiography; Blood Group Antigens; Child; Child, Preschool; Chro | 1968 |
A marker X chromosome.
Topics: Adolescent; Adult; Autoradiography; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; | 1969 |
Transmission of a D/D reciprocal translocation in a family with high incidence of mental retardation.
Topics: Autoradiography; Chromosome Aberrations; Chromosome Disorders; Chromosomes; Culture Techniques; Derm | 1966 |