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

Dietary Micronutrient Supplementation for 12 Days in Obese Male Mice Restores Sperm Oxidative Stress.

对肥胖雄性小鼠进行 12 天的膳食微量营养素补充可恢复精子氧化应激

McPherson Nicole O, Shehadeh Helana, Fullston Tod, Zander-Fox Deirdre L, Lane Michelle

It takes a community to conceive: an analysis of the scope, nature and accuracy of online sources of health information for couples trying to conceive

孕育新生命需要整个社群的共同努力:对备孕夫妇在线健康信息来源的范围、性质和准确性进行分析

Kedzior, Sophie G E; Bianco-Miotto, Tina; Breen, James; Diener, Kerrilyn R; Donnelley, Martin; Dunning, Kylie R; Penno, Megan A S; Schjenken, John E; Sharkey, David J; Hodyl, Nicolette A; Fullston, Tod; Gardiner, Maria; Brown, Hannah M; Rumbold, Alice R

Sperm microRNA Content Is Altered in a Mouse Model of Male Obesity, but the Same Suite of microRNAs Are Not Altered in Offspring's Sperm

在雄性肥胖小鼠模型中,精子微RNA含量发生改变,但子代精子中相同的微RNA组合并未发生改变。

Fullston, Tod; Ohlsson-Teague, E Maria C; Print, Cristin G; Sandeman, Lauren Y; Lane, Michelle

Paternal obesity induces metabolic and sperm disturbances in male offspring that are exacerbated by their exposure to an "obesogenic" diet.

父亲肥胖会导致男性后代出现代谢和精子紊乱,而接触“致肥胖”饮食会加剧这种情况

Fullston Tod, McPherson Nicole O, Owens Julie A, Kang Wan Xian, Sandeman Lauren Y, Lane Michlle

Impact of obesity on male fertility, sperm function and molecular composition

肥胖对男性生育能力、精子功能和分子组成的影响

Palmer, Nicole O; Bakos, Hassan W; Fullston, Tod; Lane, Michelle

Fine-scale survey of X chromosome copy number variants and indels underlying intellectual disability

对与智力障碍相关的X染色体拷贝数变异和插入缺失进行精细调查

Whibley, Annabel C; Plagnol, Vincent; Tarpey, Patrick S; Abidi, Fatima; Fullston, Tod; Choma, Maja K; Boucher, Catherine A; Shepherd, Lorraine; Willatt, Lionel; Parkin, Georgina; Smith, Raffaella; Futreal, P Andrew; Shaw, Marie; Boyle, Jackie; Licata, Andrea; Skinner, Cindy; Stevenson, Roger E; Turner, Gillian; Field, Michael; Hackett, Anna; Schwartz, Charles E; Gecz, Jozef; Stratton, Michael R; Raymond, F Lucy

Ohtahara syndrome in a family with an ARX protein truncation mutation (c.81C>G/p.Y27X)

大田原综合征与 ARX 蛋白截断突变 (c.81C>G/p.Y27X) 家族相关

Fullston, Tod; Brueton, Louise; Willis, Tracey; Philip, Sunny; MacPherson, Lesley; Finnis, Merran; Gecz, Jozef; Morton, Jenny

Mutations in the nuclear localization sequence of the Aristaless related homeobox; sequestration of mutant ARX with IPO13 disrupts normal subcellular distribution of the transcription factor and retards cell division

Aristaless相关同源异型盒的核定位序列发生突变;突变型ARX与IPO13的结合破坏了转录因子的正常亚细胞分布,并阻碍了细胞分裂。

Shoubridge, Cheryl; Tan, May Huey; Fullston, Tod; Cloosterman, Desiree; Coman, David; McGillivray, George; Mancini, Grazia M; Kleefstra, Tjitske; Gécz, Jozef