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Acta Biochimica Et Biophysica Sinica|September 16, 2017
Isochlorogenic acid A promotes melanin synthesis in B16 cell through the β-catenin signal pathwayNuramina Mamat, Jun Dou, Xueying Lu, et al.
The FEBS Journal|June 4, 2016
Conditional knockout of retinal determination genes in differentiating cells in DrosophilaMeng Jin, Aiden Eblimit, Merlyn Pulikkathara, et al.
BMC Complementary and Alternative Medicine|June 3, 2014
Kaliziri extract upregulates tyrosinase, TRP-1, TRP-2 and MITF expression in murine B16 melanoma cellsAdila Tuerxuntayi, Yong-qiang Liu, Ablajan Tulake, et al.
Experimental Eye Research|November 5, 2017
Conditional loss of Spata7 in photoreceptors causes progressive retinal degeneration in miceAiden Eblimit, Smriti Akshay Agrawal, Kandace Thomas, et al.
Experimental Eye Research|April 21, 2018
NMNAT1 E257K variant, associated with Leber Congenital Amaurosis (LCA9), causes a mild retinal degeneration phenotypeAiden Eblimit, Smriti Agrawal Zaneveld, Wei Liu, et al.
Scientific Reports|February 10, 2016
Next-generation sequencing-based molecular diagnosis of 12 inherited retinal disease probands of Uyghur ethnicityAbulikemu Tajiguli, Mingchu Xu, Qing Fu, et al.
Pharmaceutics|September 28, 2021
Co-Injection of Sulfotyrosine Facilitates Retinal Uptake of Hyaluronic Acid Nanospheres Following Intravitreal InjectionAiden Eblimit, Mustafa S Makia, Daniel Strayve, et al.
Human Gene Therapy|August 14, 2018
Gene Therapy Rescues Retinal Degeneration in Receptor Expression-Enhancing Protein 6 Mutant MiceSmriti Agrawal Zaneveld, Aiden Eblimit, Qingnan Liang, et al.
Human Mutation|December 15, 2015
ADIPOR1 Is Mutated in Syndromic Retinitis PigmentosaMingchu Xu, Aiden Eblimit, Jing Wang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 29, 2016
Hypomorphic mutations identified in the candidate Leber congenital amaurosis gene CLUAP1Zachry T Soens, Yuanyuan Li, Li Zhao, et al.
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