The immunohistochemical analysis of pendrin in the mouse inner ear

Pendred's syndrome (PS) is an autosomal recessive disorder characterized by deafness and goiter, which are caused by mutations in the Pendred's syndrome gene ( PDS). PDS encodes a membrane protein named pendrin that is considered to act as an anion transporter. An expression pattern of the...

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Veröffentlicht in:	Hearing research 2004-09, Vol.195 (1), p.9-16
Hauptverfasser:	Yoshino, Takahiko, Sato, Eisuke, Nakashima, Tsutomu, Nagashima, Wataru, Teranishi, Masa-aki, Nakayama, Atsuo, Mori, Naoyoshi, Murakami, Hideki, Funahashi, Hiroomi, Imai, Tsuneo
Format:	Artikel
Sprache:	eng
Schlagworte:	Animals Anion Transport Proteins Biological and medical sciences Brain - metabolism Ear, auditive nerve, cochleovestibular tract, facial nerve: diseases, semeiology Ear, Inner - metabolism Endocrinopathies Humans Immunohistochemical analysis Immunohistochemistry Inner ear Kidney - metabolism Medical sciences Membrane Transport Proteins - genetics Mice Mice, Inbred C57BL Mouse Non tumoral diseases Non tumoral diseases. Target tissue resistance. Benign neoplasms Otorhinolaryngology. Stomatology Pendred's syndrome Pendrin Thyroid Gland - cytology Thyroid Gland - metabolism Thyroid. Thyroid axis (diseases)
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