Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kiyoka Kobayashi"'
Autor:
Akira Wada, Mika Nakamura, Kiyoka Kobayashi, Akiyoshi Kuroda, Daisuke Harada, Satoshi Kido, Masashi Kuwahata
Publikováno v:
Journal of Parenteral and Enteral Nutrition. 47:399-407
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a8f5394a40fa247f94c1a1c4ded299c
https://doi.org/10.1002/jpen.2472
https://doi.org/10.1002/jpen.2472
Autor:
Iori Ohmori, Mamoru Ouchida, Masakazu Shinohara, Kiyoka Kobayashi, Saeko Ishida, Tomoji Mashimo
Publikováno v:
Epilepsia. 63
Thioredoxin, encoded by Txn1, is a critical antioxidant that protects against oxidative damage by regulating the dithiol/disulfide balance of interacting proteins. We recently discovered the Adem rat, an epileptic rat harboring the Txn1-F54L mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a1314a7f6874eb48dfa6577d5d43f34
https://doi.org/10.1111/epi.17295
https://doi.org/10.1111/epi.17295
Publikováno v:
Experimental Animals
Homozygous Groggy dams, which carry a Cacna1a missense mutation, often show no interest in their offspring, leading to frequent offspring deaths due to lack of nurturing. The present study aimed to clarify whether the Cacna1a mutation contributes to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0434b3003d1a29b6e58727f798176e7e
https://ousar.lib.okayama-u.ac.jp/61313
https://ousar.lib.okayama-u.ac.jp/61313
Publikováno v:
Experimental Animals. 69:153-160
Homozygous Groggy dams, which carry a Cacna1a missense mutation, often show no interest in their offspring, leading to frequent offspring deaths due to lack of nurturing. The present study aimed to clarify whether the Cacna1a mutation contributes to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::afca49f2f5cb9e618b33a9784eb97a2a
https://doi.org/10.1538/expanim.19-0086
https://doi.org/10.1538/expanim.19-0086
Publikováno v:
Neurochemistry international. 141
This study aimed to examine the effects of Cacna1a mutation on the phenotype of Scn1a-associated epilepsy in rats. We used rats with an N1417H missense mutation in the Scn1a gene and others with an M251K mutation in the Cacna1a gene. Scn1a/Cacna1a do
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dec9f3b93bedbe0a9dc9815ae2aaf135
https://pubmed.ncbi.nlm.nih.gov/33045260
https://pubmed.ncbi.nlm.nih.gov/33045260