日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Sry-modified laboratory rat lines to study sex-chromosome effects underlying sex differences in physiology and disease: Four Core Genotypes and more

利用Sry基因改造的实验大鼠品系研究性染色体对生理和疾病性别差异的影响:四种核心基因型及其他

Arnold, Arthur P; Chen, Xuqi; Grzybowski, Michael N; Ryan, Janelle M; Sengelaub, Dale R; Mohanroy, Tara; Furlan, V Andree; Schmidtke, Helen R; Prokop, Jeremy W; Tutaj, Monika; Ciosek, Julia L; Kalbfleisch, Theodore S; O'Donnell, Liza; Grisham, William; Landen, Shanie; Malloy, Lynn; Takizawa, Akiko; Li, Kai; Barseghyan, Hayk; Wiese, Carrie B; Vergnes, Laurent; Reue, Karen; Wanagat, Jonathan; Skaletsky, Helen; Page, David C; Harley, Vincent R; Dwinell, Melinda R; Geurts, Aron M

Muscle metabolic resilience and enhanced exercise adaptation by Esr1-induced remodeling of mitochondrial cristae-nucleoid architecture in males.

Esr1诱导的线粒体嵴-核样体结构重塑增强了男性肌肉代谢韧性和运动适应能力

Zhou Zhenqi, Moore Timothy M, Strumwasser Alexander R, Ribas Vicent, Iwasaki Hirotaka, Morrow Noelle, Ma Alice, Tran Peter H, Wanagat Jonathan, de Aguiar Vallim Thomas Q, Clifford Bethan, Zhang Zhengyi, Sallam Tamer, Parks Brian W, Reue Karen, Shirihai Orian, Acin-Perez Rebeca, Morselli Marco, Pellegrini Matteo, Mahata Sushil K, Norheim Frode, Zhou Mingqi, Seldin Marcus M, Lusis Aldons J, Lee Cathy C, Goodarzi Mark O, Rotter Jerome I, Hansen Joshua R, Drucker Ben, Sagendorf Tyler J, Adkins Joshua N, Sanford James A, DeMayo Francesco J, Hewitt Sylvia C, Korach Kenneth S, Hevener Andrea L

Increased mitochondrial mutation heteroplasmy induces aging phenotypes in pluripotent stem cells and their differentiated progeny.

线粒体突变异质性的增加会诱导多能干细胞及其分化后代出现衰老表型

Vandiver Amy R, Torres Alejandro Jr, Sanden Amberly, Nguyen Thang L, Gasilla Jasmine, Doan Mary T, Martirosian Vahan, Hoang Austin, Wanagat Jonathan, Teitell Michael A

Chimeric mitochondrial RNA transcripts predict mitochondrial genome deletion mutations in mitochondrial genetic diseases and aging

嵌合线粒体RNA转录本可预测线粒体遗传疾病和衰老过程中线粒体基因组缺失突变

Vandiver, Amy R; Herbst, Allen; Stothard, Paul; Wanagat, Jonathan

Age-induced changes in skeletal muscle mitochondrial DNA synthesis, quantity, and quality in genetically unique rats

年龄对遗传独特大鼠骨骼肌线粒体DNA合成、数量和质量的影响

Musci, Robert V; Fuqua, Jordan D; Peelor, Frederick F 3rd; Nguyen, Hoang Van Michelle; Richardson, Arlan; Choi, Solbie; Miller, Benjamin F; Wanagat, Jonathan

Mitochondrial haplotype and sex modulate responses to endurance exercise training

线粒体单倍型和性别调节对耐力运动训练的反应

Ahn, Bumsoo; Wei, Tianhao; Pettit-Mee, Ryan; Kim, Eunyoung; Musci, Robert V; Wanagat, Jonathan; Nguyen, Hoang Van M; Richardson, Arlan; Kim, Hyunyoung

Cognitive Impairment Highly Prevalent and Associated With Reduced Physical Function in Older Veteran Clinical Exercise Program

认知障碍在老年退伍军人临床运动计划中普遍存在,且与身体机能下降相关

Wilkins, Stacy Schantz; Zhou, Jin J; Melrose, Rebecca J; Delgadillo, Mia; Ogawa, Elisa F; Castle, Steven C; Pearson, Megan; Harris, Rebekah; Wanagat, Jonathan; Giffuni, Jamie; Alexander, Neil; Gepner, Adam D; Abbate, Lauren M; Forman, Daniel E; Addison, Odessa; Serra, Monica C; Hall, Katherine S; Lee, Cathy C

Unacylated Ghrelin Counteracts Contractile and Mitochondrial Dysfunction in Cancer Cachexia

非酰化生长素释放肽可对抗癌症恶病质中的收缩功能障碍和线粒体功能障碍

Ahn, Bumsoo; Wanagat, Jonathan; Cleary, Caroline; Ainsworth, Hannah C; Kim, Eunyoung; Kim, Hyunyoung

Sry -modified laboratory rat lines to study sex-chromosome effects underlying sex differences in physiology and disease: Four Core Genotypes and more

利用 Sry 基因改造的实验室大鼠品系研究性染色体对生理和疾病性别差异的影响:四种核心基因型及其他

Arnold, Arthur P; Chen, Xuqi; Grzybowski, Michael N; Ryan, Janelle M; Sengelaub, Dale R; Mohanroy, Tara; Furlan, V Andree; Schmidtke, Helen R; Prokop, Jeremy W; Tutaj, Monika; Grisham, William; Landen, Shanie; Malloy, Lynn; Takizawa, Akiko; Ciosek, Julia L; Li, Kai; Kalbfleisch, Theodore S; Barseghyan, Hayk; Wiese, Carrie B; Vergnes, Laurent; Reue, Karen; Wanagat, Jonathan; Skaletsky, Helen; Page, David C; Harley, Vincent R; Dwinell, Melinda R; Geurts, Aron M

Nanopore sequencing identifies a higher frequency and expanded spectrum of mitochondrial DNA deletion mutations in human aging

纳米孔测序技术发现,人类衰老过程中线粒体DNA缺失突变的频率更高,谱系更广。

Vandiver, Amy R; Hoang, Austin N; Herbst, Allen; Lee, Cathy C; Aiken, Judd M; McKenzie, Debbie; Teitell, Michael A; Timp, Winston; Wanagat, Jonathan