Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Lee Ling Yang"'
Publikováno v:
Advances in experimental medicine and biology. 1185
Retinal degenerative diseases are genetically diverse and rare inherited disorders that cause the death of rod and cone photoreceptors, resulting in progressive vision loss and blindness. This review will focus on two retinal degeneration-causing gen
Publikováno v:
Retinal Degenerative Diseases ISBN: 9783030273774
Retinal degenerative diseases are genetically diverse and rare inherited disorders that cause the death of rod and cone photoreceptors, resulting in progressive vision loss and blindness. This review will focus on two retinal degeneration-causing gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18de327ba314db7712522bc31bdf8b12
https://doi.org/10.1007/978-3-030-27378-1_79
https://doi.org/10.1007/978-3-030-27378-1_79
Publikováno v:
Langmuir. 26:11609-11614
We present a novel bonding technique for poly(dimethylsiloxane) (PDMS)-based devices employing chemical surface modifications at room temperature. PDMS surfaces were functionalized to present primary amine groups, and glass or gold substrates were fu
Autor:
Lee Ling Yang, Bradford Ross, Garnet Martens, Tami H. Bogėa, Orson L. Moritz, Beatrice M. Tam
Publikováno v:
Experimental eye research. 136
Transmission electron microscopy is the gold standard for examination of photoreceptor outer segment morphology and photoreceptor outer segment abnormalities in transgenic animal models of retinal disease. Small vertebrates such as zebrafish and Xeno
Autor:
Lee Ling, Yang
Protocadherin-21 (pcdh-21) is a transmembrane protein concentrated at nascent disks in mouse photoreceptors and thought to regulate disk synthesis. PCDH-21 mutations are associated with retinal degenerative diseases. Pcdh-21 undergoes proteolytic cle
Externí odkaz:
http://hdl.handle.net/2429/43594
Autor:
Lee Ling Yang, Beatrice M. Tam, Jenny S. Wong, Robert E. Anderson, Martin-Paul Agbaga, Orson L. Moritz
Publikováno v:
Investigative Opthalmology & Visual Science. 55:3669
PURPOSE Autosomal dominant Stargardt macular dystrophy caused by mutations in the Elongation of Very Long Chain fatty acids (ELOVL4) gene results in macular degeneration, leading to early childhood blindness. Transgenic mice and pigs expressing mutan