Page last updated: 2024-08-21

ethylnitrosourea and Syndrome

ethylnitrosourea has been researched along with Syndrome in 2 studies

Research

Studies (2)

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

Authors

Authors	Studies
Bachman, S; Breyer, MD; Davis, LS; Dikov, MM; Dunn, SR; Harris, RC; Ishibashi, K; Kadkina, V; Khuchua, Z; Rinchik, EM; Tchekneva, EE	1
Carpenter, DA; Handel, MA; Rinchik, EM	1

Other Studies

2 other study(ies) available for ethylnitrosourea and Syndrome

Article	Year
Single amino acid substitution in aquaporin 11 causes renal failure. Journal of the American Society of Nephrology : JASN, 2008, Volume: 19, Issue:10 Topics: Amino Acid Substitution; Animals; Aquaporins; Disease Models, Animal; Ethylnitrosourea; Female; Male; Mice; Mice, Mutant Strains; Point Mutation; Polymorphism, Single Nucleotide; Renal Insufficiency; Syndrome	2008
Pleiotropy in microdeletion syndromes: neurologic and spermatogenic abnormalities in mice homozygous for the p6H deletion are likely due to dysfunction of a single gene. Proceedings of the National Academy of Sciences of the United States of America, 1995, Jul-03, Volume: 92, Issue:14 Topics: Animals; Chromosome Mapping; Crosses, Genetic; Ethylnitrosourea; Female; Gene Deletion; Genes, Recessive; Genetic Carrier Screening; Genetic Markers; Genotype; Homozygote; Infertility, Male; Male; Mice; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, Mutant Strains; Mutagenesis; Mutagens; Nervous System Diseases; Phenotype; Spermatogenesis; Spermatozoa; Syndrome; Testis	1995

Article

Year

Single amino acid substitution in aquaporin 11 causes renal failure.

Journal of the American Society of Nephrology : JASN, 2008, Volume: 19, Issue:10

Topics: Amino Acid Substitution; Animals; Aquaporins; Disease Models, Animal; Ethylnitrosourea; Female; Male; Mice; Mice, Mutant Strains; Point Mutation; Polymorphism, Single Nucleotide; Renal Insufficiency; Syndrome

2008

Pleiotropy in microdeletion syndromes: neurologic and spermatogenic abnormalities in mice homozygous for the p6H deletion are likely due to dysfunction of a single gene.

Proceedings of the National Academy of Sciences of the United States of America, 1995, Jul-03, Volume: 92, Issue:14

Topics: Animals; Chromosome Mapping; Crosses, Genetic; Ethylnitrosourea; Female; Gene Deletion; Genes, Recessive; Genetic Carrier Screening; Genetic Markers; Genotype; Homozygote; Infertility, Male; Male; Mice; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, Mutant Strains; Mutagenesis; Mutagens; Nervous System Diseases; Phenotype; Spermatogenesis; Spermatozoa; Syndrome; Testis

1995