Kaliziri extract upregulates tyrosinase, TRP-1, TRP-2 and MITF expression in murine B16 melanoma cells

por Tuerxuntayi, Adila, Liu, Yong-qiang, Tulake, Ablajan, Kabas, Maidina, Eblimit, Aiden, Aisa, Haji Akber
Publicado 2014

Next-generation sequencing-based molecular diagnosis of 12 inherited retinal disease probands of Uyghur ethnicity

por Tajiguli, Abulikemu, Xu, Mingchu, Fu, Qing, Yiming, Rouzimaimaiti, Wang, Keqing, Li, Yumei, Eblimit, Aiden, Sui, Ruifang, Chen, Rui, Aisa, Haji Akber
Publicado 2016

Co-Injection of Sulfotyrosine Facilitates Retinal Uptake of Hyaluronic Acid Nanospheres Following Intravitreal Injection

por Eblimit, Aiden, Makia, Mustafa S., Strayve, Daniel, Crane, Ryan, Conley, Shannon M., Sinha, Tirthankar, Acharya, Ghanashyam, Al-Ubaidi, Muayyad R., Naash, Muna I.
Publicado 2021

Hypomorphic mutations identified in candidate Leber congenital amaurosis disease gene CLUAP1

por Soens, Zachry T., Li, Yuanyuan, Zhao, Li, Eblimit, Aiden, Dharmat, Rachayata, Li, Yumei, Chen, Yiyun, Naqeeb, Mohammed, Fajardo, Norma, Lopez, Irma, Sun, Zhaoxia, Koenekoop, Robert K., Chen, Rui
Publicado 2016

Integrative subcellular proteomic analysis allows accurate prediction of human disease-causing genes

por Zhao, Li, Chen, Yiyun, Bajaj, Amol Onkar, Eblimit, Aiden, Xu, Mingchu, Soens, Zachry T., Wang, Feng, Ge, Zhongqi, Jung, Sung Yun, He, Feng, Li, Yumei, Wensel, Theodore G., Qin, Jun, Chen, Rui
Publicado 2016

SPATA7 maintains a novel photoreceptor-specific zone in the distal connecting cilium

por Dharmat, Rachayata, Eblimit, Aiden, Robichaux, Michael A., Zhang, Zhixian, Nguyen, Thanh-Minh T., Jung, Sung Yun, He, Feng, Jain, Antrix, Li, Yumei, Qin, Jun, Overbeek, Paul, Roepman, Ronald, Mardon, Graeme, Wensel, Theodore G., Chen, Rui
Publicado 2018

REEP6 deficiency leads to retinal degeneration through disruption of ER homeostasis and protein trafficking

por 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.
Publicado 2017

Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa

por Arno, Gavin, Agrawal, Smriti A., Eblimit, Aiden, Bellingham, James, Xu, Mingchu, Wang, Feng, Chakarova, Christina, Parfitt, David A., Lane, Amelia, Burgoyne, Thomas, Hull, Sarah, Carss, Keren J., Fiorentino, Alessia, Hayes, Matthew J., Munro, Peter M., Nicols, Ralph, Pontikos, Nikolas, Holder, Graham E., Asomugha, Chinwe, Raymond, F. Lucy, Moore, Anthony T., Plagnol, Vincent, Michaelides, Michel, Hardcastle, Alison J., Li, Yumei, Cukras, Catherine, Webster, Andrew R., Cheetham, Michael E., Chen, Rui
Publicado 2016