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thymidine and Abnormalities, Sex Chromosome

thymidine has been researched along with Abnormalities, Sex Chromosome in 32 studies

Research Excerpts

ExcerptRelevanceReference
"Folate metabolism and the effects of folic acid on chromosome stability were studied in four related patients with the fragile X syndrome."3.67Folate metabolism and chromosomal stability in the fragile X syndrome. ( Arthur, DC; Branda, RF; Danzl, TJ; King, RA; Woods, WG, 1984)

Research

Studies (32)

TimeframeStudies, this research(%)All Research%
pre-199030 (93.75)18.7374
1990's1 (3.13)18.2507
2000's1 (3.13)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Di Berardino, D1
Coppola, G1
Verdoliva, C1
Coppola, GF1
Ramunno, L1
Enne, G1
Di Meo, GP1
Iannuzzi, L1
ATKINS, L1
BOEOEK, JA1
GUSTAVSON, KH2
HANSSON, O1
HJELM, M1
Ockey, CH1
Wennström, J1
De la Chapelle, A3
Gardiner, GB1
Wenger, SL1
Steele, MW1
Glover, TW1
Branda, RF1
Arthur, DC1
Woods, WG1
Danzl, TJ1
King, RA1
Snyder, FF1
Harasym, CA1
Lin, CC1
Scher, I1
Ahmed, A1
Strong, DM1
Steinberg, AD1
Paul, WE1
Leisti, JT1
Kaback, MM1
Rimoin, DL1
Kuwano, A1
Murano, I1
Kajii, T1
Sutherland, GR1
Baker, E1
Purvis-Smith, S1
Hockey, A1
Krumins, E1
Eichenbaum, SZ1
Hori, T1
Takahashi, E1
Tsuji, H1
Tsuji, S1
Murata, M1
Nussbaum, RL1
Ledbetter, DH1
Therman, E2
Sarto, GE2
Patau, K2
Mikkelsen, M1
Dahl, G1
Andersson, L1
Bergman, S1
Reitalu, J1
Ansehn, S1
Voorhees, JJ1
Hayes, E1
Wilkins, J1
Harrell, ER1
Santesson, B2
BOOK, JA2
Kjessler, B1
Schröder, J1
Tal'vik, TA1
Mikel'saar, AV2
Mikel'saar, RV2
Kask, VA1
Blyumina, MG1
Kuznetsova, LI1
Cooke, P1
Black, JA1
Curtis, DJ1
Bocian, M1
Krmpotic, E1
Szego, K1
Rosenthal, IM1
Weber, FM1
Sparkes, RS1
Muller, H1
Siniscalco, M1
Knowles, BB1
Steplewski, Z1
Schwinger, E1
Citoler, P1
Gropp, A1
Polani, PE1
Angell, R1
Giannelli, F1
Race, RR1
Sanger, R1
Neuhäuser, G1
Back, F1
Higure, M1
De Capoa, A1
Allen, FH1
Gold, AP1
Koenigsberger, R1
Miller, OJ1

Reviews

1 review available for thymidine and Abnormalities, Sex Chromosome

ArticleYear
Fragile X syndrome: a unique mutation in man.
    Annual review of genetics, 1986, Volume: 20

    Topics: Caffeine; Chromosome Fragility; Female; Fragile X Syndrome; Genetic Counseling; Genetic Linkage; Gen

1986

Other Studies

31 other studies available for thymidine and Abnormalities, Sex Chromosome

ArticleYear
Onset and sequence of RBA-band replication on the inactive X-chromosomes of cattle (Bos taurus L.), river buffalo (Bubalus bubalis L.) and goat (Capra hircus L.).
    Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology, 2002, Volume: 10, Issue:8

    Topics: Animals; Bromodeoxyuridine; Buffaloes; Cattle; Cells, Cultured; Chromosome Banding; DNA Replication;

2002
A CASE OF XXXXY SEX CHROMOSOME ANOMALY WITH AUTORADIOGRAPHIC STUDIES.
    Cytogenetics, 1963, Volume: 2

    Topics: Autoradiography; Biopsy; Bone Diseases; Cell Division; Chromosome Aberrations; Chromosome Disorders;

1963
Isochromosome-X in man. II.
    Hereditas, 1966, Volume: 54, Issue:3

    Topics: Autoradiography; Chromosome Aberrations; DNA; DNA Replication; Female; Humans; Leukocytes; Male; Mit

1966
In vitro reversal of fragile-X expression by exogenous thymidine.
    Clinical genetics, 1984, Volume: 25, Issue:2

    Topics: Culture Media; Floxuridine; Fragile X Syndrome; Humans; In Vitro Techniques; Lymphocytes; Male; Sex

1984
FUdR induction of the X chromosome fragile site: evidence for the mechanism of folic acid and thymidine inhibition.
    American journal of human genetics, 1981, Volume: 33, Issue:2

    Topics: Cells, Cultured; DNA; Female; Floxuridine; Folic Acid; Humans; Intellectual Disability; Lymphocytes;

1981
Folate metabolism and chromosomal stability in the fragile X syndrome.
    The American journal of medicine, 1984, Volume: 77, Issue:4

    Topics: Adult; Bone Marrow; Cells, Cultured; Chromosome Fragile Sites; Chromosome Fragility; DNA; Erythrocyt

1984
Purine, thymidylate and amino acid requirements for human lymphocyte transformation and fragile chromosome site expression.
    Advances in experimental medicine and biology, 1984, Volume: 165 Pt A

    Topics: Amino Acids; Cells, Cultured; Female; Folic Acid; Humans; Hypoxanthine; Hypoxanthines; Lymphocyte Ac

1984
X-linked B-lymphocyte immune defect in CBA/HN mice. I. Studies of the function and composition of spleen cells.
    The Journal of experimental medicine, 1975, Apr-01, Volume: 141, Issue:4

    Topics: Animals; Antigen-Antibody Reactions; Autoradiography; B-Lymphocytes; Complement System Proteins; Con

1975
Human X-autosome translocations: differential inactivation of the X chromosome in a kindred with an X-9 translocation.
    American journal of human genetics, 1975, Volume: 27, Issue:4

    Topics: Adolescent; Adult; Amenorrhea; Autoradiography; Body Height; Child; Chromosome Aberrations; Chromoso

1975
Cell type-dependent difference in the distribution and frequency of excess thymidine-induced common fragile sites: T lymphocytes and skin fibroblasts.
    Human genetics, 1990, Volume: 84, Issue:6

    Topics: Adolescent; Adult; Cells, Cultured; Child; Child, Preschool; Chromosome Fragile Sites; Chromosome Fr

1990
Prenatal diagnosis of the fragile X using thymidine induction.
    Prenatal diagnosis, 1987, Volume: 7, Issue:3

    Topics: Adult; Amniocentesis; Australia; Chorionic Villi; Female; Floxuridine; Fragile X Syndrome; Humans; M

1987
Fragile X expression in thymidine-prototrophic and auxotrophic human-mouse somatic cell hybrids under low and high thymidylate stress conditions.
    Cytogenetics and cell genetics, 1988, Volume: 47, Issue:4

    Topics: Animals; Bromodeoxyuridine; Cell Cycle; Deoxycytosine Nucleotides; Fragile X Syndrome; Gene Expressi

1988
Apparently isodicentric but functionally monocentric X chromosome in man.
    American journal of human genetics, 1974, Volume: 26, Issue:1

    Topics: Amenorrhea; Crossing Over, Genetic; Female; Fibroblasts; Heterochromatin; Humans; Karyotyping; Lymph

1974
Unbalanced X-autosomal translocation with inactivation of the normal X chromosome.
    Cytogenetics and cell genetics, 1973, Volume: 12, Issue:5

    Topics: Abnormalities, Multiple; ABO Blood-Group System; Adult; Autoradiography; Chromosome Aberrations; Chr

1973
A case of XX male.--Cytogenetic findings by autoradiography and fluorescence microscopy.
    Hereditas, 1972, Volume: 70, Issue:2

    Topics: Adult; Autoradiography; Humans; Karyotyping; Male; Microscopy, Fluorescence; Sex Chromatin; Sex Chro

1972
The XYY chromosomal complement and nodulocystic acne.
    Annals of internal medicine, 1970, Volume: 73, Issue:2

    Topics: Acne Vulgaris; Adolescent; Autoradiography; Back; Child; Child, Preschool; Facial Dermatoses; Humans

1970
Increased Q fluorescence of an inactive Xq-chromosome in man.
    Clinical genetics, 1974, Volume: 6, Issue:4

    Topics: Adult; Amenorrhea; Autoradiography; Chromosome Aberrations; Chromosomes, Human, 16-18; Deafness; Fem

1974
The mortality of human XO embryos.
    Journal of reproduction and fertility, 1973, Volume: 34, Issue:1

    Topics: Abortion, Spontaneous; Animals; Autoradiography; DNA; Embryo, Mammalian; Female; Fetus; Glucosephosp

1973
Autoradiographically identified karyotype 49,XXXXY, t(4; 11) (q35; q23) confirmed by banding.
    Hereditas, 1973, Volume: 74, Issue:2

    Topics: Chromosome Aberrations; Humans; Karyotyping; Male; Sex Chromosome Aberrations; Thymidine; Tritium

1973
Ring heterosome in a two-and-a-half year old girl (46, XXr or 46, XYr).
    Soviet genetics, 1973, Nov-15, Volume: 7, Issue:7

    Topics: ABO Blood-Group System; Child, Preschool; Chromatin; Chromosomes; Dermatoglyphics; DNA Replication;

1973
Children with an XYY sex chromosome constitution.
    Soviet genetics, 1973, Dec-01, Volume: 7, Issue:8

    Topics: Anthropometry; Child; Chromosomes; Colchicine; Dermatoglyphics; Humans; Intellectual Disability; Kar

1973
DNA synthesis of human XYY cells. Autoradiography and fluorescence pattern.
    Clinical genetics, 1972, Volume: 3, Issue:1

    Topics: Adult; Autoradiography; Child; DNA; DNA Replication; Fluorescence; Humans; Intellectual Disability;

1972
Comparative clinical studies and X chromosome behaviour in a case of XXXX-XXXXX mosaicism.
    Journal of medical genetics, 1972, Volume: 9, Issue:2

    Topics: Abnormalities, Multiple; Autoradiography; Dermatoglyphics; Female; Humans; Infant; Intellectual Disa

1972
Somatic stigmata of Turner's syndrome in a patient with 46,XXq-.
    Journal of medical genetics, 1971, Volume: 8, Issue:3

    Topics: Adult; Autoradiography; Chromosomes; Chromosomes, Human, 6-12 and X; Dermatoglyphics; DNA Replicatio

1971
Double monosomy mosaicism (45,X-45, XX,21-) in a retarded child with multiple congenital malformations.
    Cytogenetics, 1971, Volume: 10, Issue:6

    Topics: Abnormalities, Multiple; Aneuploidy; Autoradiography; Blood Protein Electrophoresis; Bone Marrow Cel

1971
Hybridization of human diploid strains carrying X-linked mutants and its potential in studies of somatic cell genetics.
    The Wistar Institute symposium monograph, 1969, Volume: 9

    Topics: Anemia, Hemolytic, Congenital Nonspherocytic; Autoradiography; Cell Fusion; Cell Line; Cell Nucleus;

1969
[DNA replication pattern of the supernumerary sex chromosome in "XYY" constitution].
    Klinische Wochenschrift, 1969, May-15, Volume: 47, Issue:10

    Topics: Adult; Autoradiography; DNA Replication; Humans; Karyometry; Male; Sex Chromosome Aberrations; Sex C

1969
Evidence that the Xg locus is inactivated in structurally abnormal X chromosomes.
    Nature, 1970, Aug-08, Volume: 227, Issue:5258

    Topics: ABO Blood-Group System; Autoradiography; Blood Group Antigens; Chromosome Aberrations; Female; Gene

1970
[Cytogenetic variation of the Ullrich-Turner syndrome].
    Medizinische Klinik, 1968, May-24, Volume: 63, Issue:21

    Topics: Adolescent; Adult; Autoradiography; Female; Humans; Karyotyping; Mosaicism; Sex Chromosome Aberratio

1968
[Application of autoradiography to chromosome analysis. 3. Study of congenital abnormalities due to chromosome abnormality].
    Nihon Shonika Gakkai zasshi. Acta paediatrica Japonica, 1968, Sep-01, Volume: 72, Issue:9

    Topics: Autoradiography; Chromosome Aberrations; Chromosome Disorders; Chromosomes; Female; Humans; Karyotyp

1968
Presumptive C-15 translocation and familial large Y identified by autoradiography.
    Journal of medical genetics, 1969, Volume: 6, Issue:1

    Topics: Abnormalities, Multiple; Adult; Autoradiography; Blood Group Antigens; Chromosome Aberrations; Chrom

1969