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pro vyhledávání: '"Erin M Itza"'
Autor:
Tao Wu, Joel D. Sanneman, Rajanikanth J Maganti, Kazuhiro Nakaya, Donald G. Harbidge, Philine Wangemann, Sara E. Billings, Erin M Itza, Daniel C. Marcus
Publikováno v:
American journal of physiology. Renal physiology. 292(5)
Pendred syndrome, characterized by childhood deafness and postpuberty goiter, is caused by mutations of SLC26A4, which codes for the anion exchanger pendrin. The goal of the present study was to determine how loss of pendrin leads to hair cell degene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebbf7529e4e074ccd355d2f5989fed6e
https://pubmed.ncbi.nlm.nih.gov/17299139
https://pubmed.ncbi.nlm.nih.gov/17299139
Autor:
Erin M. Itza, Nancy M. Mozingo
Publikováno v:
Zygote (Cambridge, England). 13(3)
In sea urchin embryos, blastula formation occurs between the seventh and tenth cleavage and is associated with changes in the permeability properties of the epithelium although the structures responsible for mediating these changes are not known. Tig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e177bfd32fd0df705ba5a63d63a20521
https://pubmed.ncbi.nlm.nih.gov/16261771
https://pubmed.ncbi.nlm.nih.gov/16261771
Autor:
Erin M Itza, Philine Wangemann, Lorraine A. Everett, Beatrice Albrecht, Daniel C. Marcus, Tao Wu, Eric D. Green, Ines E. Royaux, Rajanikanth J Maganti, Sairam V. Jabba, Susan M. Wall, Jun Ho Lee
Publikováno v:
BMC Medicine
BMC Medicine, Vol 2, Iss 1, p 30 (2004)
BMC Medicine, Vol 2, Iss 1, p 30 (2004)
Background Pendred syndrome, a common autosomal-recessive disorder characterized by congenital deafness and goiter, is caused by mutations of SLC26A4, which codes for pendrin. We investigated the relationship between pendrin and deafness using mice t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2183c940a5516b8866153966af726f41