Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Choco Michael Gorospe"'
Publikováno v:
Methods in Molecular Biology ISBN: 9781071629215
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a8906f6df285d4ce520c197d82123242
https://doi.org/10.1007/978-1-0716-2922-2_21
https://doi.org/10.1007/978-1-0716-2922-2_21
Autor:
Choco Michael Gorospe, Bruno Marçal Repolês, Phong Tran, Paulina H. Wanrooij, Anna Karin Nilsson
Publikováno v:
Mitochondrion. 61:179-187
The integrity of mitochondrial DNA (mtDNA) isolated from solid tissues is critical for analyses such as long-range PCR, but is typically assessed under conditions that fail to provide information on the individual mtDNA strands. Using denaturing gel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6bbc71aeadb2f1b23c51d12460f8d76
https://doi.org/10.1016/j.mito.2021.10.005
https://doi.org/10.1016/j.mito.2021.10.005
Publikováno v:
Molecular & Cellular Toxicology. 18:39-45
Leucine prototrophic yeast exhibits extended longevity and related phenotypes similar to yeast grown under calorie restriction (CR) condition. The extended longevity of leucine prototrophic yeast is thought to be a function of abundant cellular leuci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::129d7dd20514e5661ede940c5bc0d267
https://doi.org/10.1007/s13273-021-00166-1
https://doi.org/10.1007/s13273-021-00166-1
Autor:
Mi-Sun Kang, Sung-Lim Yu, Ho-Yeol Kim, Choco Michael Gorospe, Byung Hyune Choi, Sung Haeng Lee, Sung-Keun Lee
Publikováno v:
Biology Open, Vol 3, Iss 1, Pp 29-41 (2013)
Summary Mutations in the human XPG gene cause Cockayne syndrome (CS) and xeroderma pigmentosum (XP). Transcription defects have been suggested as the fundamental cause of CS; however, defining CS as a transcription syndrome is inconclusive. In partic
Externí odkaz:
https://doaj.org/article/a3f8c5560b79435789a48275f9c9ccbb
Autor:
Choco Michael Gorospe, Alicia Herrera Curbelo, Gustavo Carvalho, Lisa Marchhart, Katarzyna Niedźwiecka, Paulina H. Wanrooij
Mitochondria are central to numerous anabolic and catabolic pathways whereby mitochondrial dysfunction has a profound impact on metabolism and can manifest in disease. The consequences of mitochondrial dysfunction can be ameliorated by adaptive respo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::528285d92f830bbb7bcd5be599798b41
https://doi.org/10.1101/2022.02.18.480979
https://doi.org/10.1101/2022.02.18.480979
Autor:
Kwan Young Kim, Choco Michael Gorospe, Su Yeon Jeong, Seong Geun Kim, Da-Yeon Jung, Jae-Seong So, Sang-Hyun Han
Publikováno v:
KSBB Journal. 34:54-60
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::833a9426cd59d35f3ddb229033abefe3
https://doi.org/10.7841/ksbbj.2019.34.1.54
https://doi.org/10.7841/ksbbj.2019.34.1.54
Autor:
Katarzyna Niedźwiecka, Choco Michael Gorospe, Vinod Kumar Singh, Kerryn Elliott, Alicia Herrera Curbelo, Gustavo Carvalho, Lisa Marchhart, Erik Larsson, Paulina H. Wanrooij
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1863:148897
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::502e4f0499b46d7530c654bbe49dc7b3
https://doi.org/10.1016/j.bbabio.2022.148897
https://doi.org/10.1016/j.bbabio.2022.148897
Publikováno v:
Molecular & Cellular Toxicology. 15:65-73
Backgrounds Leucine is involved in various cellular mechanisms, including protein metabolism, insulin signaling, and longevity control. Nevertheless, the contribution of leucine metabolism genes to longevity have not been thoroughly studied.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b906d0da5af77fd6bdb2802ce9526589
https://doi.org/10.1007/s13273-019-0008-x
https://doi.org/10.1007/s13273-019-0008-x
Autor:
Sung Haeng Lee, Sung-Lim Yu, Mi-Sun Kang, Sung-Keun Lee, Ho-Yeol Kim, Byung Hyune Choi, Choco Michael Gorospe
Publikováno v:
Biology Open
Biology Open, Vol 3, Iss 1, Pp 29-41 (2013)
Biology Open, Vol 3, Iss 1, Pp 29-41 (2013)
Summary Mutations in the human XPG gene cause Cockayne syndrome (CS) and xeroderma pigmentosum (XP). Transcription defects have been suggested as the fundamental cause of CS; however, defining CS as a transcription syndrome is inconclusive. In partic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c46f85fe7ece8c80c97089f1bffcfa43
http://europepmc.org/articles/PMC3892158
http://europepmc.org/articles/PMC3892158
Autor:
Joo-Young Park, Choco Michael Gorospe, Sang-Hyun Han, Jae-Seong So, Seong-Geun Kim, Jin-Hoon Jeong, Chang-Ho Kang
Publikováno v:
Biotechnology and Bioprocess Engineering. 18:903-908
We examined the effectiveness of using different calcium salts for bioconsolidation. Four calcium salts were chosen based on their applicability and solubility. Initial experiments demonstrated that the addition of any calcium salt had a negative eff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de7bf99e46fd2904ed8475f28c17be18
https://doi.org/10.1007/s12257-013-0030-0
https://doi.org/10.1007/s12257-013-0030-0