REEP6 deficiency leads to retinal degeneration through disruption of ER homeostasis and protein trafficking by Agrawal, Smriti A, Burgoyne, Thomas, Eblimit, Aiden, Bellingham, James, Parfitt, David A, Lane, Amelia, Nichols, Ralph, Asomugha, Chinwe, Hayes, Matthew J, Munro, Peter M, Xu, Mingchu, Wang, Keqing, Futter, Clare E, Li, Yumei, Chen, Rui, Cheetham, Michael E

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ATF6 Is Mutated in Early Onset Photoreceptor Degeneration With Macular Involvement by Xu, Mingchu, Gelowani, Violet, Eblimit, Aiden, Wang, Feng, Young, Marielle P, Sawyer, Briana L, Zhao, Li, Jenkins, Glen, Creel, Donnell J, Wang, Keqing, Ge, Zhongqi, Wang, Hui, Li, Yumei, Hartnett, M Elizabeth, Chen, Rui

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Angiopoietin-1 promotes atherosclerosis by increasing the proportion of circulating Gr1+ monocytes by Fujisawa, Takeshi, Wang, Keqing, Niu, Xi-Lin, Egginton, Stuart, Ahmad, Shakil, Hewett, Peter, Kontos, Christopher D, Ahmed, Asif

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A Dipeptide‐Based Hierarchical Nanoarchitecture with Enhanced Catalytic Activity by Wang, Chenlei, Fei, Jinbo, Wang, Keqing, Li, Junbai

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iPlacenta - A PhD program to drive innovation in modelling placenta for Maternal and Fetal Health by Murdoch, Colin, iPlacenta consortium, Khalil, Asma, Lanz, Henriette, Ng, Chee, Bussolati, Benedetta, de Windt, Leon, Vaiman, Daniel, McCarthy, Cathal, Wolkenhauer, Olaf, van der Merwe, Hannes, Deprest, Jan, Wang, Keqing, Bircsak, Kristin, Thilaganathan, Basky, Krstajic, Nikola, McCarthy, Fergus

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A missense mutation in HK1 leads to autosomal dominant retinitis pigmentosa by Wang, Feng, Wang, Yandong, Zhang, Bin, Zhao, Li, Lyubasyuk, Vera, Wang, Keqing, Xu, Mingchu, Li, Yumei, Wu, Frances, Wen, Cindy, Bernstein, Paul S, Lin, Danni, Zhu, Susanna, Wang, Hui, Zhang, Kang, Chen, Rui

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Heterodimerisation between VEGFR-1 and VEGFR-2 and not the homodimers of VEGFR-1 inhibit VEGFR-2 activity by Cai, Meng, Wang, Keqing, Murdoch, Colin E, Gu, Yuchun, Ahmed, Asif

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Electrochemical determination of pyrophosphate at nanomolar levels using a gold electrode covered with a cysteine nanofilm and based on competitive coordination of Cu(II) ion to cy... by Lin, Yuqing, Hu, Lianglu, Li, Linbo, Wang, Keqing, Ji, Yunfei, Zou, Hong

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Lactate Dehydrogenase/Albumin To-Urea Ratio: A Novel Prognostic Maker for Fatal Clinical Complications in Patients with COVID-19 Infection by Shokr, Hala, Marwah, Mandeep Kaur, Siddiqi, Hisam, Wandroo, Farooq, Sanchez-Aranguren, Lissette, Ahmad, Shakil, Wang, Keqing, Marwah, Sukhjinder

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Front Cover by Liao, Ziyan, Zhang, Lin, Nobis, Michael P., Wu, Xiaogang, Pan, Kaiwen, Wang, Keqing, Dakhil, Mohammed A., Du, Mingxi, Xiong, Qinli, Pandey, Bikram, Tian, Xianglin

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Noncoding mutation in RPGRIP1 contributes to inherited retinal degenerations by Zou, Gang, Zhang, Tao, Cheng, Xuesen, Igelman, Austin D, Wang, Jun, Qian, Xinye, Fu, Shangyi, Wang, Keqing, Koenekoop, Robert K, Fishman, Gerald A, Yang, Paul, Li, Yumei, Pennesi, Mark E, Chen, Rui

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Novel microneedle patches for transdermal delivery of AP39, a hydrogen sulphide donor, in the treatment of scenarios mimicking neurological disorders by Balakrishnan, Pavanjeeth, Junaid, Sarah, Ahmad, Shakil, Wang, Keqing, Hindalekar, Yukta Sameer, Shokr, Hala, Upadhya, Manoj, Hopkins, Sarah, Sacharczuk, Jakub, Singh Rana, Karan, Anas Al Tahan, Mohamad, Juvale, Parag, Chan, Felix, Sanchez-Aranguren, Lissette, Marwah, Mandeep

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Tunable Fluorescent Silica-Coated Carbon Dots: A Synergistic Effect for Enhancing the Fluorescence Sensing of Extracellular Cu 2+ in Rat Brain by Lin, Yuqing, Wang, Chao, Li, Linbo, Wang, Hao, Liu, Kangyu, Wang, Keqing, Li, Bo

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S100P enhances the motility and invasion of human trophoblast cell lines by Tabrizi, Maral E. A., Lancaster, Tara L., Ismail, Thamir M., Georgiadou, Athina, Ganguly, Ankana, Mistry, Jayna J., Wang, Keqing, Rudland, Philip S., Ahmad, Shakil, Gross, Stephane R.

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Next-generation sequencing-based molecular diagnosis of 12 inherited retinal disease probands of Uyghur ethnicity by Tajiguli, Abulikemu, Xu, Mingchu, Fu, Qing, Yiming, Rouzimaimaiti, Wang, Keqing, Li, Yumei, Eblimit, Aiden, Sui, Ruifang, Chen, Rui, Aisa, Haji Akber

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A homozygous missense mutation in NEUROD1 is associated with nonsyndromic autosomal recessive retinitis pigmentosa by Wang, Feng, Li, Huajin, Xu, Mingchu, Li, Hui, Zhao, Li, Yang, Lizhu, Zaneveld, Jacques E, Wang, Keqing, Li, Yumei, Sui, Ruifang, Chen, Rui

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WSGM-SD： An Approach to RESTful Service Discovery Based on Weighted Service Goal Model by Zhang, Neng, He, Keqing, Wang, Jian, Li, Zheng

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Dysregulation of placental cystathionine-β-synthase promotes fetal growth restriction by Wang, Keqing, Cai, Meng, Abu-Alkheir, Wijdan, Ahmad, Shakil, Ahmed, Asif

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PP36 - Hydrogen sulphide rescues preeclampsia-like phenotype aggravated by high sFlt-1 in placenta growth factor (PlGF) deficiency by Ahmad, Shakil, Wang, Keqing, Egginton, Stuart, Hewett, Peter W., Ahmed, Asif

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PP108 - Dysregulation of placental cystathionine-β-synthase promotes fetal growth restriction by Wang, Keqing, Cai, Meng, Abu-Alkheir, Wijdan, Ahmad, Shakil, Ahmed, Asif

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