Page last updated: 2024-08-21

ethylnitrosourea and Congenital Myasthenia

ethylnitrosourea has been researched along with Congenital Myasthenia in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bouriez-Jones, T; Bull, KR; Chaudhry, S; Cornall, RJ; Crockford, TL; Goodnow, CC; Hough, TA; Mason, T; Rimmer, AJ; Roberts, IS; Silver, KL	1

Other Studies

1 other study(ies) available for ethylnitrosourea and Congenital Myasthenia

Article	Year
Next-generation sequencing to dissect hereditary nephrotic syndrome in mice identifies a hypomorphic mutation in Lamb2 and models Pierson's syndrome. The Journal of pathology, 2014, Volume: 233, Issue:1 Topics: Abnormalities, Multiple; Animals; Disease Models, Animal; DNA Mutational Analysis; Ethylnitrosourea; Eye Abnormalities; Genetic Association Studies; Genetic Predisposition to Disease; High-Throughput Nucleotide Sequencing; Kidney Tubules; Laminin; Mice; Mice, 129 Strain; Mice, Inbred C57BL; Mice, Mutant Strains; Mutation; Myasthenic Syndromes, Congenital; Nephrotic Syndrome; Pedigree; Phenotype; Proteinuria; Pupil Disorders	2014

Article

Year

Next-generation sequencing to dissect hereditary nephrotic syndrome in mice identifies a hypomorphic mutation in Lamb2 and models Pierson's syndrome.

The Journal of pathology, 2014, Volume: 233, Issue:1

Topics: Abnormalities, Multiple; Animals; Disease Models, Animal; DNA Mutational Analysis; Ethylnitrosourea; Eye Abnormalities; Genetic Association Studies; Genetic Predisposition to Disease; High-Throughput Nucleotide Sequencing; Kidney Tubules; Laminin; Mice; Mice, 129 Strain; Mice, Inbred C57BL; Mice, Mutant Strains; Mutation; Myasthenic Syndromes, Congenital; Nephrotic Syndrome; Pedigree; Phenotype; Proteinuria; Pupil Disorders

2014