Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 25 to 26 of 26 entries
Sorted by: Best Match Show Resources per page
Reversible impairment of the ku80 gene by a recyclable marker in Aspergillus aculeatus.

AMB Express

Tani S, Tsuji A, Kunitake E, Sumitani J, Kawaguchi T.
PMID: 23311774
AMB Express. 2013 Jan 12;3(1):4. doi: 10.1186/2191-0855-3-4.

Auxotrophic mutants of Aspergillus can be isolated in the presence of counter-selective compounds, but the process is laborious. We developed a method to enable reversible impairment of the ku80 gene (Aaku80) in the imperfect fungus Aspergillus aculeatus. Aaku80 was...

Cite
Tani S, Tsuji A, Kunitake E, et al. Reversible impairment of the ku80 gene by a recyclable marker in Aspergillus aculeatus. AMB Express. 2013;3(1):4doi: 10.1186/2191-0855-3-4.
Tani, S., Tsuji, A., Kunitake, E., Sumitani, J., & Kawaguchi, T. (2013). Reversible impairment of the ku80 gene by a recyclable marker in Aspergillus aculeatus. AMB Express, 3(1), 4. https://doi.org/10.1186/2191-0855-3-4
Tani, Shuji, et al. "Reversible impairment of the ku80 gene by a recyclable marker in Aspergillus aculeatus." AMB Express vol. 3,1 (2013): 4. doi: https://doi.org/10.1186/2191-0855-3-4
Tani S, Tsuji A, Kunitake E, Sumitani J, Kawaguchi T. Reversible impairment of the ku80 gene by a recyclable marker in Aspergillus aculeatus. AMB Express. 2013 Jan 12;3(1):4. doi: 10.1186/2191-0855-3-4. PMID: 23311774; PMCID: PMC3598690.
Copy Download .nbib Format: NLM
Late-onset ornithine transcarbamylase deficiency: a rare cause of recurrent abnormal behavior in adults.

Acute medicine & surgery

Hidaka M, Higashi E, Uwatoko T, Uwatoko K, Urashima M, Takashima H, Watanabe Y, Kitazono T, Sugimori H.
PMID: 32995020
Acute Med Surg. 2020 Sep 08;7(1):e565. doi: 10.1002/ams2.565. eCollection 2020.

BACKGROUND: Ornithine transcarbamylase is an enzyme of the urea cycle, which produces urea from ammonia. Although ornithine transcarbamylase deficiency mainly occurs as a severe neonatal-onset disease, a late-onset form that could become symptomatic from infancy to adulthood is also...

Cite
Hidaka M, Higashi E, Uwatoko T, et al. Late-onset ornithine transcarbamylase deficiency: a rare cause of recurrent abnormal behavior in adults. Acute Med Surg. 2020;7(1):e565doi: 10.1002/ams2.565.
Hidaka, M., Higashi, E., Uwatoko, T., Uwatoko, K., Urashima, M., Takashima, H., Watanabe, Y., Kitazono, T., & Sugimori, H. (2020). Late-onset ornithine transcarbamylase deficiency: a rare cause of recurrent abnormal behavior in adults. Acute medicine & surgery, 7(1), e565. https://doi.org/10.1002/ams2.565
Hidaka, Masaoki, et al. "Late-onset ornithine transcarbamylase deficiency: a rare cause of recurrent abnormal behavior in adults." Acute medicine & surgery vol. 7,1 (2020): e565. doi: https://doi.org/10.1002/ams2.565
Hidaka M, Higashi E, Uwatoko T, Uwatoko K, Urashima M, Takashima H, Watanabe Y, Kitazono T, Sugimori H. Late-onset ornithine transcarbamylase deficiency: a rare cause of recurrent abnormal behavior in adults. Acute Med Surg. 2020 Sep 08;7(1):e565. doi: 10.1002/ams2.565. eCollection 2020. PMID: 32995020; PMCID: PMC7507316.
Copy Download .nbib Format: NLM
Showing 25 to 26 of 26 entries