Compounds > bromodeoxyuridine
Page last updated: 2024-08-17

bromodeoxyuridine and Hyperdactyly

bromodeoxyuridine has been researched along with Hyperdactyly in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19901 (20.00)18.7374
1990's1 (20.00)18.2507
2000's2 (40.00)29.6817
2010's1 (20.00)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
DIPAOLO, JA1
Ishizuya-Oka, A; Koibuchi, N; Saitoh, Y; Ueda, S1
Fujioka, M; Mori, C; Nakamura, N1
Albrecht, AN; Böddrich, A; Mundlos, S; Schwabe, GC; Stricker, S; Wanker, EE1

Other Studies

5 other study(ies) available for bromodeoxyuridine and Hyperdactyly

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
POLYDACTYLISM IN THE OFFSPRING OF MICE INJECTED WITH 5-BROMODEOXYURIDINE.
    Science (New York, N.Y.), 1964, Jul-31, Volume: 145, Issue:3631

    Topics: Abnormalities, Drug-Induced; Animals; Blood Chemical Analysis; Bromodeoxyuridine; Family; Female; Fluorouracil; Foot; Foot Diseases; Humans; Mice; Nucleosides; Polydactyly; Pregnancy; Pregnancy, Animal; Research; Toxicology

1964
Local disturbance of neuronal migration in the S-100beta-retarded mutant mouse.
    Cell and tissue research, 1997, Volume: 289, Issue:3

    Topics: Animals; Animals, Newborn; Antimetabolites; Bromodeoxyuridine; Calcium-Binding Proteins; Cell Movement; Cerebral Cortex; Female; Glial Fibrillary Acidic Protein; Immunohistochemistry; Male; Mice; Mice, Neurologic Mutants; Nerve Growth Factors; Neuroglia; Neurons; Polydactyly; Pregnancy; S100 Calcium Binding Protein beta Subunit; S100 Proteins

1997
Alteration of programmed cell death and gene expression by 5-bromodeoxyuridine during limb development in mice.
    Toxicology and applied pharmacology, 2000, Sep-01, Volume: 167, Issue:2

    Topics: Abnormalities, Drug-Induced; Animals; Apoptosis; Bromodeoxyuridine; Embryonic and Fetal Development; Female; Fibroblast Growth Factor 8; Fibroblast Growth Factors; Gene Expression Regulation, Developmental; Hindlimb; Homeodomain Proteins; In Situ Hybridization; Male; Mice; Mice, Inbred ICR; Polydactyly; Pregnancy; Reverse Transcriptase Polymerase Chain Reaction; Teratogens; Transcription Factors

2000
The synpolydactyly homolog (spdh) mutation in the mouse -- a defect in patterning and growth of limb cartilage elements.
    Mechanisms of development, 2002, Volume: 112, Issue:1-2

    Topics: Animals; Apoptosis; Bromodeoxyuridine; Cartilage; Cell Differentiation; Cell Division; Chondrocytes; COS Cells; Disease Models, Animal; DNA, Complementary; Extremities; Gene Expression Regulation, Developmental; Homeodomain Proteins; Homozygote; In Situ Hybridization; Mice; Mice, Mutant Strains; Mutation; Phenotype; Polydactyly; Reverse Transcriptase Polymerase Chain Reaction; Transcription Factors

2002