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

Neuropeptide PACAP promotes sweat secretion

神经肽PACAP促进汗液分泌

Cui, C-Y; Schlessinger, D

No evidence of association between subclinical thyroid disorders and common carotid intima medial thickness or atherosclerotic plaque

没有证据表明亚临床甲状腺疾病与颈总动脉内膜中层厚度或动脉粥样硬化斑块之间存在关联。

Delitala, A P; Filigheddu, F; Orrù, M; AlGhatrif, M; Steri, M; Pilia, M G; Scuteri, A; Lobina, M; Piras, M G; Delitala, G; Lakatta, E G; Schlessinger, D; Cucca, F

Meta-analysis of genome-wide association studies for personality

人格全基因组关联研究的荟萃分析

de Moor, M H M; Costa, P T; Terracciano, A; Krueger, R F; de Geus, E J C; Toshiko, T; Penninx, B W J H; Esko, T; Madden, P A F; Derringer, J; Amin, N; Willemsen, G; Hottenga, J-J; Distel, M A; Uda, M; Sanna, S; Spinhoven, P; Hartman, C A; Sullivan, P; Realo, A; Allik, J; Heath, A C; Pergadia, M L; Agrawal, A; Lin, P; Grucza, R; Nutile, T; Ciullo, M; Rujescu, D; Giegling, I; Konte, B; Widen, E; Cousminer, D L; Eriksson, J G; Palotie, A; Peltonen, L; Luciano, M; Tenesa, A; Davies, G; Lopez, L M; Hansell, N K; Medland, S E; Ferrucci, L; Schlessinger, D; Montgomery, G W; Wright, M J; Aulchenko, Y S; Janssens, A C J W; Oostra, B A; Metspalu, A; Abecasis, G R; Deary, I J; Räikkönen, K; Bierut, L J; Martin, N G; van Duijn, C M; Boomsma, D I

Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking

全基因组关联研究的荟萃分析发现,CTNNA2 中的常见变异与寻求刺激有关

Terracciano, A; Esko, T; Sutin, A R; de Moor, M H M; Meirelles, O; Zhu, G; Tanaka, T; Giegling, I; Nutile, T; Realo, A; Allik, J; Hansell, N K; Wright, M J; Montgomery, G W; Willemsen, G; Hottenga, J-J; Friedl, M; Ruggiero, D; Sorice, R; Sanna, S; Cannas, A; Räikkönen, K; Widen, E; Palotie, A; Eriksson, J G; Cucca, F; Krueger, R F; Lahti, J; Luciano, M; Smoller, J W; van Duijn, C M; Abecasis, G R; Boomsma, D I; Ciullo, M; Costa, P T Jr; Ferrucci, L; Martin, N G; Metspalu, A; Rujescu, D; Schlessinger, D; Uda, M

The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data

人格与重度抑郁症或双相情感障碍的遗传关联:基于全基因组关联数据的多基因评分分析

Middeldorp, C M; de Moor, M H M; McGrath, L M; Gordon, S D; Blackwood, D H; Costa, P T; Terracciano, A; Krueger, R F; de Geus, E J C; Nyholt, D R; Tanaka, T; Esko, T; Madden, P A F; Derringer, J; Amin, N; Willemsen, G; Hottenga, J-J; Distel, M A; Uda, M; Sanna, S; Spinhoven, P; Hartman, C A; Ripke, S; Sullivan, P F; Realo, A; Allik, J; Heath, A C; Pergadia, M L; Agrawal, A; Lin, P; Grucza, R A; Widen, E; Cousminer, D L; Eriksson, J G; Palotie, A; Barnett, J H; Lee, P H; Luciano, M; Tenesa, A; Davies, G; Lopez, L M; Hansell, N K; Medland, S E; Ferrucci, L; Schlessinger, D; Montgomery, G W; Wright, M J; Aulchenko, Y S; Janssens, A C J W; Oostra, B A; Metspalu, A; Abecasis, G R; Deary, I J; Räikkönen, K; Bierut, L J; Martin, N G; Wray, N R; van Duijn, C M; Smoller, J W; Penninx, B W J H; Boomsma, D I

Canadian College of Neuropsychopharmacology: 2010 Award Winners

加拿大神经精神药理学会:2010 年获奖者

Terracciano, A; Sanna, S; Uda, M; Deiana, B; Usala, G; Busonero, F; Maschio, A; Scally, M; Patriciu, N; Chen, W-M; Distel, M A; Slagboom, E P; Boomsma, D I; Villafuerte, S; Sliwerska, E; Burmeister, M; Amin, N; Janssens, A C J W; van Duijn, C M; Schlessinger, D; Abecasis, G R; Costa, P T Jr

High neuroticism and low conscientiousness are associated with interleukin-6.

高神经质和低尽责性与白细胞介素-6相关

Sutin A R, Terracciano A, Deiana B, Naitza S, Ferrucci L, Uda M, Schlessinger D, Costa P T Jr

Eleven densely clustered genes, six of them novel, in 176 kb of mouse t-complex DNA

在小鼠t复合体DNA的176 kb区域内,发现了11个密集聚集的基因,其中6个是新发现的基因。

Kargul, G J; Nagaraja, R; Shimada, T; Grahovac, M J; Lim, M K; Nakashima, H; Waeltz, P; Ma, P; Chen, E; Schlessinger, D; Ko, M S

Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27

X连锁隐性遗传性特发性甲状旁腺功能减退症定位于Xq26-q27上的1.5 Mb区域

Trump, D; Dixon, P H; Mumm, S; Wooding, C; Davies, K E; Schlessinger, D; Whyte, M P; Thakker, R V

The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains

Tabby表型是由EDA基因的小鼠同源基因突变引起的,该突变揭示了新的小鼠和人类外显子,并编码一种具有胶原结构域的蛋白质(外胚层发育不良蛋白-A)。

Srivastava, A K; Pispa, J; Hartung, A J; Du, Y; Ezer, S; Jenks, T; Shimada, T; Pekkanen, M; Mikkola, M L; Ko, M S; Thesleff, I; Kere, J; Schlessinger, D