Page last updated: 2024-08-21

ethylnitrosourea and Aura

ethylnitrosourea has been researched along with Aura in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's2 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kuramoro, T; Mashimo, T; Ohno, Y; Sasa, M; Serikawa, T; Voigt, B1
Baulac, S; Ishida, S; Kaneko, S; Kuwamura, M; Mashimo, T; Nishio, T; Ohno, Y; Sakamoto, Y; Serikawa, T; Takizawa, A1
Bergren, SK; Beyer, B; Claes, L; Dejonghe, P; Frankel, WN; Kearney, JA; Yang, Y1

Reviews

1 review(s) available for ethylnitrosourea and Aura

ArticleYear
Advances on genetic rat models of epilepsy.
    Experimental animals, 2015, Volume: 64, Issue:1

    Topics: Animals; Disease Models, Animal; Epilepsy; Ethylnitrosourea; Genetic Engineering; Genetic Predisposition to Disease; Genome; Intercellular Signaling Peptides and Proteins; Kv1.1 Potassium Channel; Models, Genetic; Mutagenesis; Mutation, Missense; NAV1.1 Voltage-Gated Sodium Channel; Phenotype; Proteins; Rats

2015

Other Studies

2 other study(ies) available for ethylnitrosourea and Aura

ArticleYear
Kcna1-mutant rats dominantly display myokymia, neuromyotonia and spontaneous epileptic seizures.
    Brain research, 2012, Jan-30, Volume: 1435

    Topics: Animals; Antiemetics; Biophysical Phenomena; Biotinylation; Body Weight; Carbamazepine; Cells, Cultured; Chromosome Mapping; Disease Models, Animal; DNA Mutational Analysis; Electric Stimulation; Electroencephalography; Electromyography; Epilepsy; Ethylnitrosourea; Gene Transfer Techniques; Humans; Isaacs Syndrome; Kv1.1 Potassium Channel; Male; Membrane Potentials; Mice; Models, Molecular; Mutagenesis; Mutagens; Mutation, Missense; Myokymia; Oocytes; Patch-Clamp Techniques; Protein Transport; Psychomotor Performance; Rats; Rats, Inbred F344; Rats, Mutant Strains; Sequence Analysis; Serine; Survival Analysis; Swimming; Threonine; Time Factors; Xenopus

2012
Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2.
    Human molecular genetics, 2006, Mar-15, Volume: 15, Issue:6

    Topics: Amino Acid Sequence; Animals; Epilepsy; Ethylnitrosourea; Genetic Testing; Humans; KCNQ2 Potassium Channel; Male; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Mice, Transgenic; Molecular Sequence Data; Mutation, Missense; NAV1.1 Voltage-Gated Sodium Channel; NAV1.2 Voltage-Gated Sodium Channel; Nerve Tissue Proteins; Sodium Channels

2006