Compounds > bromodeoxyuridine
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bromodeoxyuridine and Syndrome

bromodeoxyuridine has been researched along with Syndrome in 9 studies

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19904 (44.44)18.7374
1990's1 (11.11)18.2507
2000's2 (22.22)29.6817
2010's2 (22.22)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Adams, C; Bonthron, DT; Boycot, KM; Braun, KPJ; Dobyns, WB; Faivre, L; Fry, AE; Giamanco, KA; Gripp, KW; Hevner, RF; Hodge, RD; Johnson, CA; Kholmanskikh, SS; Logan, CV; Majewski, J; Mancini, GM; Mirzaa, G; Pang, K; Parry, DA; Pilz, DT; Rivière, JB; Roberts, N; Ross, ME; Schwartzentruber, J; Sheridan, EG; Singh, S; St-Onge, J; Steinraths, M; Sweeney, E; van Esch, H; Vanstone, M; Verbeek, N; Wieczorek, D1
Buturak, A; Gorgulu, S; Norgaz, T1
Dobyns, WB; Fukuda, T; Iizuka-Kogo, A; Kamiirisa, K; Kamijo, S; Kasahara, M; Kato, M; Kato-Fukui, Y; Kitamura, K; Kondo, I; Kusaka, M; Matsuo, M; Miura, H; Morohashi, K; Ogata, T; Omichi, K; Sugiyama, N; Suzuki, R; Yanazawa, M; Yokoyama, M; Yoshioka, H1
Beechey, C; Bentley, L; Hitchins, MP; Ishino, F; Kelsey, G; Monk, D; Moore, GE; Peters, J; Preece, MA; Stanier, P1
Francke, U; Jones, KL; Monheit, A; Saunders, B1
Dewald, G; Dicken, CH; Gordon, H1
Sandberg, AA; Shiraishi, Y1
Bartram, CR; Koske-Westphal, T; Passarge, E1
Knuutila, S; Larramendy, M1

Other Studies

9 other study(ies) available for bromodeoxyuridine and Syndrome

ArticleYear
De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome.
    Nature genetics, 2014, Volume: 46, Issue:5

    Topics: Abnormalities, Multiple; Animals; Base Sequence; Blotting, Western; Bromodeoxyuridine; Cyclin D2; Electroporation; Exome; Female; HEK293 Cells; Humans; Hydrocephalus; Immunohistochemistry; Malformations of Cortical Development; Megalencephaly; Mice; Microscopy, Fluorescence; Molecular Sequence Data; Mutagenesis, Site-Directed; Polydactyly; Sequence Analysis, DNA; Syndrome

2014
Brivudine induced coronary vasospasm as a manifestation of Kounis syndrome: First report.
    International journal of cardiology, 2015, Apr-15, Volume: 185

    Topics: Antiviral Agents; Bromodeoxyuridine; Coronary Vasospasm; Herpes Zoster; Humans; Male; Middle Aged; Syndrome

2015
Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans.
    Nature genetics, 2002, Volume: 32, Issue:3

    Topics: Alleles; Amino Acid Sequence; Animals; Apoptosis; Base Sequence; Brain; Bromodeoxyuridine; Cell Differentiation; Cell Division; Cell Movement; DNA, Complementary; Doublecortin Protein; Epithelial Cells; Genetic Linkage; Genetic Vectors; Genitalia; Homeodomain Proteins; Humans; Immunohistochemistry; Male; Mice; Mice, Knockout; Microscopy, Fluorescence; Models, Genetic; Molecular Sequence Data; Mutation; Neurons; Phenotype; Prosencephalon; Syndrome; Testis; Transcription Factors; Transfection; X Chromosome

2002
DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressed.
    Mammalian genome : official journal of the International Mammalian Genome Society, 2002, Volume: 13, Issue:12

    Topics: Alleles; Animals; Bromodeoxyuridine; Cell Cycle; Cell Division; Cells, Cultured; Chromosomes, Human, Pair 7; Cytoskeletal Proteins; DNA Primers; DNA, Complementary; Dopa Decarboxylase; ErbB Receptors; Female; Fetal Growth Retardation; Fetus; Gene Duplication; Genomic Imprinting; GRB10 Adaptor Protein; Humans; Male; Mice; Microfilament Proteins; Polymerase Chain Reaction; Proteins; Syndrome; Transcription, Genetic

2002
The penta-X syndrome.
    Journal of medical genetics, 1980, Volume: 17, Issue:5

    Topics: Abnormalities, Multiple; Bromodeoxyuridine; Chromosome Banding; Female; Humans; Infant, Newborn; Karyotyping; Phenotype; Sex Chromosome Aberrations; Sex Chromosomes; Syndrome; X Chromosome

1980
Sister chromatid exchanges in Bloom's syndrome.
    Archives of dermatology, 1978, Volume: 114, Issue:5

    Topics: Abnormalities, Multiple; Adult; Bromodeoxyuridine; Child; Child, Preschool; Chromatids; Erythema; Facial Dermatoses; Female; Genetic Techniques; Growth Disorders; Humans; Infant; Infant, Newborn; Male; Middle Aged; Neoplasms; Photosensitivity Disorders; Pregnancy; Syndrome; Telangiectasis

1978
Evaluation of sister chromatid exchanges in Bloom's syndrome.
    Cytobios, 1978, Volume: 21, Issue:83-84

    Topics: Adult; Bromodeoxyuridine; Caffeine; Chromatids; Chromosome Aberrations; Culture Techniques; Facial Dermatoses; Humans; Male; Skin; Syndrome

1978
Chromatid exchanges in ataxia telangiectasia, Bloom syndrome, Werner syndrome, and xeroderma pigmentosum.
    Annals of human genetics, 1976, Volume: 40, Issue:1

    Topics: Abnormalities, Multiple; Adolescent; Adult; Aged; Ataxia Telangiectasia; Bromodeoxyuridine; Cells, Cultured; Child; Chromatids; Facial Dermatoses; Female; Humans; Infant, Newborn; Lectins; Lymphocytes; Male; Middle Aged; Radiation Effects; Syndrome; Telangiectasis; Ultraviolet Rays; Werner Syndrome; Xeroderma Pigmentosum

1976
Sister chromatid differentiation and chromosomal in situ suppression hybridization: a combined methodology for analyzing cell proliferation and SCEs in individual chromosomes.
    Cytogenetics and cell genetics, 1992, Volume: 61, Issue:2

    Topics: Bromodeoxyuridine; Cell Division; Cells, Cultured; Chromosomes, Human, Pair 12; Fibroblasts; Genetic Diseases, Inborn; Humans; In Situ Hybridization; Kinetics; Metaphase; Mitosis; Mosaicism; Sister Chromatid Exchange; Syndrome

1992