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

Plasma Allopregnanolone and Sex Hormone Responses to Stress Induction: Contributors to the Formation of Intrusive Memories

血浆别孕烯醇酮和性激素对压力诱导的反应:侵入性记忆形成的促成因素

Amir Hamzah, Khalisa; Jarvis, Madeline; Turner, Natalie P; Lipp, Ottmar V; Flintoff, Jonathan M; Schmidt, Luke; Ney, Luke J

Predictive biomarkers of performance under stress: a two-phase study protocol to develop a wearable monitoring system

预测压力下表现的生物标志物:开发可穿戴监测系统的两阶段研究方案

Flintoff, Jonathan M; Pattinson, Cassandra; Ahamed, Sarah; Ali, Shahnewaz; Bagley, Angus; Broszczak, Daniel; Crewther, Blair; de Waal, Louis; Edmed, Shannon L; Fernando, Tharindu; Fookes, Clinton; Frentiu, Francesca D; Hunt, Andrew P; Lipp, Ottmar V; McMaster, Ben; Mengersen, Kerrie; Ney, Luke; Oon, Senn L; Pandey, Ajay; Pandit, Parth; Peake, Jonathan M; Perera, Muthukuttige Madusha Nuwanthi; Perlo, Virginie; Punyadeera, Chamindie; Schmidt, Luke; Smith, Simon S; Spann, Kirsten; Stewart, Ian; Sullivan, Karen A; Young, Danielle; Kerr, Graham; Parker, Tony J

The dynamic strategy shifting task: Optimisation of an operant task for assessing cognitive flexibility in rats

动态策略转换任务:优化操作性任务以评估大鼠的认知灵活性

Flintoff, Jonathan Martin; Alexander, Suzy; Kesby, James Paul; Burne, Thomas Henry

Conjugated linoleic acid modulation of risk factors associated with atherosclerosis

共轭亚油酸对动脉粥样硬化相关风险因素的调节

Nakamura, Yukiko K; Flintoff-Dye, Nichole; Omaye, Stanley T

Clinical and molecular phenotype of Aicardi-Goutieres syndrome

Aicardi-Goutieres综合征的临床和分子表型

Rice, Gillian; Patrick, Teresa; Parmar, Rekha; Taylor, Claire F; Aeby, Alec; Aicardi, Jean; Artuch, Rafael; Montalto, Simon Attard; Bacino, Carlos A; Barroso, Bruno; Baxter, Peter; Benko, Willam S; Bergmann, Carsten; Bertini, Enrico; Biancheri, Roberta; Blair, Edward M; Blau, Nenad; Bonthron, David T; Briggs, Tracy; Brueton, Louise A; Brunner, Han G; Burke, Christopher J; Carr, Ian M; Carvalho, Daniel R; Chandler, Kate E; Christen, Hans-Jurgen; Corry, Peter C; Cowan, Frances M; Cox, Helen; D'Arrigo, Stefano; Dean, John; De Laet, Corinne; De Praeter, Claudine; Dery, Catherine; Ferrie, Colin D; Flintoff, Kim; Frints, Suzanna G M; Garcia-Cazorla, Angels; Gener, Blanca; Goizet, Cyril; Goutieres, Francoise; Green, Andrew J; Guet, Agnes; Hamel, Ben C J; Hayward, Bruce E; Heiberg, Arvid; Hennekam, Raoul C; Husson, Marie; Jackson, Andrew P; Jayatunga, Rasieka; Jiang, Yong-Hui; Kant, Sarina G; Kao, Amy; King, Mary D; Kingston, Helen M; Klepper, Joerg; van der Knaap, Marjo S; Kornberg, Andrew J; Kotzot, Dieter; Kratzer, Wilfried; Lacombe, Didier; Lagae, Lieven; Landrieu, Pierre Georges; Lanzi, Giovanni; Leitch, Andrea; Lim, Ming J; Livingston, John H; Lourenco, Charles M; Lyall, E G Hermione; Lynch, Sally A; Lyons, Michael J; Marom, Daphna; McClure, John P; McWilliam, Robert; Melancon, Serge B; Mewasingh, Leena D; Moutard, Marie-Laure; Nischal, Ken K; Ostergaard, John R; Prendiville, Julie; Rasmussen, Magnhild; Rogers, R Curtis; Roland, Dominique; Rosser, Elisabeth M; Rostasy, Kevin; Roubertie, Agathe; Sanchis, Amparo; Schiffmann, Raphael; Scholl-Burgi, Sabine; Seal, Sunita; Shalev, Stavit A; Corcoles, C Sierra; Sinha, Gyan P; Soler, Doriette; Spiegel, Ronen; Stephenson, John B P; Tacke, Uta; Tan, Tiong Yang; Till, Marianne; Tolmie, John L; Tomlin, Pam; Vagnarelli, Federica; Valente, Enza Maria; Van Coster, Rudy N A; Van der Aa, Nathalie; Vanderver, Adeline; Vles, Johannes S H; Voit, Thomas; Wassmer, Evangeline; Weschke, Bernhard; Whiteford, Margo L; Willemsen, Michel A A; Zankl, Andreas; Zuberi, Sameer M; Orcesi, Simona; Fazzi, Elisa; Lebon, Pierre; Crow, Yanick J

Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndrome

TREX1基因的杂合突变会导致家族性冻疮性狼疮和显性遗传性艾卡迪-古蒂埃综合征。

Rice, Gillian; Newman, William G; Dean, John; Patrick, Teresa; Parmar, Rekha; Flintoff, Kim; Robins, Peter; Harvey, Scott; Hollis, Thomas; O'Hara, Ann; Herrick, Ariane L; Bowden, Andrew P; Perrino, Fred W; Lindahl, Tomas; Barnes, Deborah E; Crow, Yanick J

The importance of seeking ALMS1 mutations in infants with dilated cardiomyopathy

对患有扩张型心肌病的婴儿进行ALMS1基因突变检测的重要性

Bond, J; Flintoff, K; Higgins, J; Scott, S; Bennet, C; Parsons, J; Mannon, J; Jafri, H; Rashid, Y; Barrow, M; Trembath, R; Woodruff, G; Rossa, E; Lynch, S; Sheilds, J; Newbury-Ecob, R; Falconer, A; Holland, P; Cockburn, D; Karbani, G; Malik, S; Ahmed, M; Roberts, E; Taylor, G; Woods, C G

Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locus

长段型和短段型家族性先天性巨结肠:RET基因位点的临床表现多样性

Edery, P; Pelet, A; Mulligan, L M; Abel, L; Attié, T; Dow, E; Bonneau, D; David, A; Flintoff, W; Jan, D

Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremia

从 DXS165 位点发生的染色体跳跃可以对四种微缺失和一种与脉络膜萎缩症相关的新生 X/13 染色体易位进行分子表征。

Cremers, F P; van de Pol, D J; Wieringa, B; Collins, F S; Sankila, E M; Siu, V M; Flintoff, W F; Brunsmann, F; Blonden, L A; Ropers, H H

Complementation of a methotrexate uptake defect in Chinese hamster ovary cells by DNA-mediated gene transfer

利用DNA介导的基因转移技术补偿中国仓鼠卵巢细胞中甲氨蝶呤摄取缺陷

Underhill, T M; Flintoff, W F