Page last updated: 2024-08-21

ethylnitrosourea and Disease, Pulmonary

ethylnitrosourea has been researched along with Disease, Pulmonary 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
Adelstein, RS; Bhagwat, AM; Buettner, C; Graumann, J; Grohmann, B; Guenther, A; Guenther, S; Gunawan, F; Jin, YJ; Kim, HT; Kostin, S; Looso, M; Ma, X; Offermanns, S; Panza, P; Preussner, J; Ruppert, C; Sokol, AM; Stainier, DYR; Yin, W	1
Hagarman, JA; O'Brien, TP	1

Other Studies

2 other study(ies) available for ethylnitrosourea and Disease, Pulmonary

Article	Year
Myh10 deficiency leads to defective extracellular matrix remodeling and pulmonary disease. Nature communications, 2018, 11-02, Volume: 9, Issue:1 Topics: Amino Acid Sequence; Animals; Down-Regulation; Emphysema; Ethylnitrosourea; Extracellular Matrix; Female; Lung Diseases; Male; Matrix Metalloproteinase 2; Mesoderm; Mice, Inbred C57BL; Mutagenesis; Mutation, Missense; Myosin Heavy Chains; Nonmuscle Myosin Type IIB; Organogenesis; Phenotype; Pulmonary Alveoli; Up-Regulation	2018
An essential gene mutagenesis screen across the highly conserved piebald deletion region of mouse chromosome 14. Genesis (New York, N.Y. : 2000), 2009, Volume: 47, Issue:6 Topics: Alkylating Agents; Amino Acid Sequence; Animals; Animals, Newborn; Base Sequence; Carrier Proteins; Chromosome Deletion; Chromosome Mapping; Chromosomes, Mammalian; DNA Mutational Analysis; Ethylnitrosourea; Female; Genes, Essential; Genes, Lethal; Genotype; Lung Diseases; Male; Mice; Mice, Inbred C3H; Mice, Inbred C57BL; Molecular Sequence Data; Mutagenesis; Phenotype; Ubiquitin-Protein Ligases	2009

Article

Year

Myh10 deficiency leads to defective extracellular matrix remodeling and pulmonary disease.

Nature communications, 2018, 11-02, Volume: 9, Issue:1

Topics: Amino Acid Sequence; Animals; Down-Regulation; Emphysema; Ethylnitrosourea; Extracellular Matrix; Female; Lung Diseases; Male; Matrix Metalloproteinase 2; Mesoderm; Mice, Inbred C57BL; Mutagenesis; Mutation, Missense; Myosin Heavy Chains; Nonmuscle Myosin Type IIB; Organogenesis; Phenotype; Pulmonary Alveoli; Up-Regulation

2018

An essential gene mutagenesis screen across the highly conserved piebald deletion region of mouse chromosome 14.

Genesis (New York, N.Y. : 2000), 2009, Volume: 47, Issue:6

Topics: Alkylating Agents; Amino Acid Sequence; Animals; Animals, Newborn; Base Sequence; Carrier Proteins; Chromosome Deletion; Chromosome Mapping; Chromosomes, Mammalian; DNA Mutational Analysis; Ethylnitrosourea; Female; Genes, Essential; Genes, Lethal; Genotype; Lung Diseases; Male; Mice; Mice, Inbred C3H; Mice, Inbred C57BL; Molecular Sequence Data; Mutagenesis; Phenotype; Ubiquitin-Protein Ligases

2009