Page last updated: 2024-08-21

ethylnitrosourea and Low Bone Density

ethylnitrosourea has been researched along with Low Bone Density in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Benet-Pagès, A; Calzada-Wack, J; Cohrs, CM; Eck, S; Esposito, I; Favor, J; Fuchs, H; Hans, W; Hrabě de Angelis, M; Klaften, M; Lorenz-Depiereux, B; Rathkolb, B; Rubio-Aliaga, I; Sabrautzki, S; Seedorf, H; Strom, TM; Wolf, E	1
Barbaric, I; Brown, SD; Cheeseman, M; Dear, TN; Hough, T; Hunter, AJ; Marusic, A; Perry, MJ; Rodrigues Da Costa, A; Salopek, D; Wells, S	1

Other Studies

2 other study(ies) available for ethylnitrosourea and Low Bone Density

Article	Year
New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis. Mammalian genome : official journal of the International Mammalian Genome Society, 2012, Volume: 23, Issue:7-8 Topics: Alkaline Phosphatase; Amino Acid Sequence; Animals; Base Sequence; Bone Diseases, Metabolic; Calcium; Chromosomes, Mammalian; Disease Models, Animal; DNA Mutational Analysis; Ethylnitrosourea; Female; Male; Mice; Mice, Inbred C3H; Mice, Inbred C57BL; Mutagenesis; Mutagens; Mutation; Phenotype; PHEX Phosphate Regulating Neutral Endopeptidase; Phosphates; Polymorphism, Single Nucleotide; Receptors, Calcium-Sensing; Statistics, Nonparametric; X Chromosome	2012
An ENU-induced mutation in the Ankrd11 gene results in an osteopenia-like phenotype in the mouse mutant Yoda. Physiological genomics, 2008, Feb-19, Volume: 32, Issue:3 Topics: Abnormalities, Multiple; Amino Acid Sequence; Amino Acid Substitution; Animals; Bone Density; Bone Diseases, Metabolic; Conserved Sequence; Craniofacial Abnormalities; DNA-Binding Proteins; Ethylnitrosourea; Female; Genes, Lethal; Kyphosis; Male; Mice; Mice, Inbred BALB C; Mice, Inbred C3H; Mice, Mutant Strains; Molecular Sequence Data; Mutagenesis; Mutation, Missense; Phenotype; Point Mutation; Repressor Proteins; Sequence Alignment; Sequence Homology, Amino Acid	2008

Article

Year

New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis.

Mammalian genome : official journal of the International Mammalian Genome Society, 2012, Volume: 23, Issue:7-8

Topics: Alkaline Phosphatase; Amino Acid Sequence; Animals; Base Sequence; Bone Diseases, Metabolic; Calcium; Chromosomes, Mammalian; Disease Models, Animal; DNA Mutational Analysis; Ethylnitrosourea; Female; Male; Mice; Mice, Inbred C3H; Mice, Inbred C57BL; Mutagenesis; Mutagens; Mutation; Phenotype; PHEX Phosphate Regulating Neutral Endopeptidase; Phosphates; Polymorphism, Single Nucleotide; Receptors, Calcium-Sensing; Statistics, Nonparametric; X Chromosome

2012

An ENU-induced mutation in the Ankrd11 gene results in an osteopenia-like phenotype in the mouse mutant Yoda.

Physiological genomics, 2008, Feb-19, Volume: 32, Issue:3

Topics: Abnormalities, Multiple; Amino Acid Sequence; Amino Acid Substitution; Animals; Bone Density; Bone Diseases, Metabolic; Conserved Sequence; Craniofacial Abnormalities; DNA-Binding Proteins; Ethylnitrosourea; Female; Genes, Lethal; Kyphosis; Male; Mice; Mice, Inbred BALB C; Mice, Inbred C3H; Mice, Mutant Strains; Molecular Sequence Data; Mutagenesis; Mutation, Missense; Phenotype; Point Mutation; Repressor Proteins; Sequence Alignment; Sequence Homology, Amino Acid

2008