Zobrazeno 1 - 3
of 3
pro vyhledávání: '"E. L. Hassemer"'
Autor:
Duska J. Sidjanin, Bradley T. Endres, E. L. Hassemer, Adam Ronchetti, Richard R. Dubielzig, Joseph A. Toonen
Publikováno v:
Investigative ophthalmologyvisual science. 54(1)
During mammalian embryonic eyelid closure ADAM17 has been proposed to play a role as a transactivator of epidermal growth factor receptor (EGFR) signaling by shedding membrane bound EGFR ligands. However, ADAM17 also sheds numerous other ligands, thu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a69c1b5724c5aaa8c9afa5a726bf0efc
https://pubmed.ncbi.nlm.nih.gov/23211830
https://pubmed.ncbi.nlm.nih.gov/23211830
Autor:
Duska J. Sidjanin, C. J. Zeiss, S. M. Le Gall, Yasunori Okada, Tokuhiro Kimura, Mark T. McNally, R. Liegel, R. D. Dubielzig, B. Chang, E. L. Hassemer, Keisuke Horiuchi, Carl P. Blobel
The waved with open eyes (woe) locus is a spontaneous recessive mouse mutation that exhibits wavy fur, eyelids open at birth, and enlarged heart and esophagus. In this study, we confirmed the previously identified woe phenotypes and additionally iden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a60bc7d40142aea6b676f6b3c4db1d9
https://europepmc.org/articles/PMC2870960/
https://europepmc.org/articles/PMC2870960/
Juvenile retinoschisis is a rare retinal dystrophy caused by RS1 gene mutations. 1 Clinical examinations and molecular testing definitively diagnosed juvenile retinoschisis in 2 male infants, one of whom had a novel mutation not previously reported i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9b4e34984cc11a808b04f0839cd1812
https://europepmc.org/articles/PMC3926297/
https://europepmc.org/articles/PMC3926297/