1. A mild clinical and neuropsychological phenotype of Renpenning syndrome: A new case report with a maternally inherited PQBP1 missense mutation. Issue 4 (2nd October 2022) Authors: Lopez-Martín, Sara; Albert, Jacobo; Peña Vila-Belda, Mᵃ del Mar; Liu, Xian; Zhang, Zi-Chao; Han, Junhai; Jiménez de Domingo, Ana; Fernández-Mayoralas, Daniel Martín; Fernández-Perrone, Ana Laura; Calleja-Pérez, Beatriz; Álvarez, Sara; Fernández-Jaén, Alberto Journal: Applied neuropsychology Issue: Volume 11:Issue 4(2022) Page Start: 921 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Altered hydroxymethylome in the substantia nigra of Parkinson's disease. Issue 20 (4th June 2022) Authors: Min, Shishi; Xu, Qian; Qin, Lixia; Li, Yujing; Li, Ziyi; Chen, Chao; Wu, Hao; Han, Junhai; Zhu, Xiongwei; Jin, Peng; Tang, Beisha Journal: Human molecular genetics Issue: Volume 31:Issue 20(2022) Page Start: 3494 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Bidirectional regulation of fragile X mental retardation protein phosphorylation controls rhodopsin homoeostasis. (31st October 2016) Authors: Wang, Xiao; Mu, Yawen; Sun, Mengshi; Han, Junhai Journal: Journal of molecular cell biology Issue: Volume 9:Number 2(2017:Apr.) Page Start: 104 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Group 1 Metabotropic Glutamate Receptors in Neurological and Psychiatric Diseases: Mechanisms and Prospective. (October 2022) Authors: Su, Li-Da; Wang, Na; Han, Junhai; Shen, Ying Journal: Neuroscientist Issue: Volume 28:Number 5(2022) Page Start: 453 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Mutations of PQBP1 in Renpenning syndrome promote ubiquitin-mediated degradation of FMRP and cause synaptic dysfunction. (10th January 2017) Authors: Zhang, Xiao-Yan; Qi, Junxia; Shen, Yu-Qian; Liu, Xian; Liu, An; Zhou, Zikai; Han, Junhai; Zhang, Zi Chao Journal: Human molecular genetics Issue: Volume 26:Number 5(2017:Mar. 01) Page Start: 955 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Novel regulation of the eEF2K/eEF2 pathway: prospects of 'PQBP1 promotes translational elongation and regulates hippocampal mGluR-LTD by suppressing eEF2 phosphorylation'. (18th March 2021) Authors: Shen, Yuqian; Han, Junhai; Zhang, Zi Chao Journal: Journal of molecular cell biology Issue: Volume 13:Number 5(2021) Page Start: 392 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. TDP‐43 loss of function increases TFEB activity and blocks autophagosome–lysosome fusion. (23rd December 2015) Authors: Xia, Qin; Wang, Hongfeng; Hao, Zongbing; Fu, Cheng; Hu, Qingsong; Gao, Feng; Ren, Haigang; Chen, Dong; Han, Junhai; Ying, Zheng; Wang, Guanghui Journal: EMBO journal Issue: Volume 35:Number 2(2016) Page Start: 121 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. The role of PQBP1 in neural development and function. (27th February 2023) Authors: Cheng, Shanshan; Liu, Xian; Yuan, Linjuan; Wang, Nan; Zhang, Zi Chao; Han, Junhai Journal: Biochemical Society transactions Issue: Volume 51:Number 1(2023) Page Start: 363 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗