The role of pendrin in health and disease : molecular and functional aspects of the SLC26A4 anion exchanger

This book reviews the current state of knowledge on the genetics, molecular biology and physiology of pendrin, with a particular focus on pendrin dysfunction and the consequences for human health. Pendrin is a membrane transport protein expressed in the thyroid, inner ear, kidney and airways, and wa...

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Bibliographic Details
Other Authors: Dossena, Silvia, (Editor), Paulmichl, Markus, (Editor)
Format: eBook
Language: English
Published: Cham, Switzerland : Springer, 2017.
Subjects:
membránové bílkoviny
buněčné membrány
biochemie
membrane proteins
cell membranes
biochemistry
elektronické knihy
sborníky
electronic books
papers of several authors
ISBN: 9783319432878
9783319432854
Physical Description: 1 online resource (x, 226 pages) : illustrations (some color)

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024 7 |a 10.1007/978-3-319-43287-8  |2 doi 
024 8 |a 10.1007/978-3-319-43 
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072 7 |a 577  |x Biochemie. Molekulární biologie. Biofyzika  |2 Konspekt  |9 2 
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080 |a 577.1  |2 MRF 
080 |a (0.034.2:08)   |2 MRF 
080 |a (082)  |2 MRF 
245 0 4 |a The role of pendrin in health and disease :  |b molecular and functional aspects of the SLC26A4 anion exchanger /  |c Silvia Dossena, Markus Paulmichl, editors. 
264 1 |a Cham, Switzerland :  |b Springer,  |c 2017. 
300 |a 1 online resource (x, 226 pages) :  |b illustrations (some color) 
336 |a text  |b txt  |2 rdacontent 
337 |a počítač  |b c  |2 rdamedia 
338 |a online zdroj  |b cr  |2 rdacarrier 
500 |a Includes index. 
504 |a Includes bibliographical references and index. 
506 |a Plný text je dostupný pouze z IP adres počítačů Univerzity Tomáše Bati ve Zlíně nebo vzdáleným přístupem pro zaměstnance a studenty 
520 |a This book reviews the current state of knowledge on the genetics, molecular biology and physiology of pendrin, with a particular focus on pendrin dysfunction and the consequences for human health. Pendrin is a membrane transport protein expressed in the thyroid, inner ear, kidney and airways, and was recently found in a variety of other tissues and organs. Pendrin malfunction may cause a genetic disease called Pendred syndrome or non-syndromic deafness. The book provides a thorough description of the multifaceted role of pendrin in human health and disease. As such, it offers an invaluable tool for physiology and pathology researchers, while also providing essential guidance for otorhinolaryngologists and endocrinologists in the diagnosis of Pendred syndrome and pendrin-related deafness.- Resumé vydavatel 
590 |a SpringerLink  |b Springer Complete eBooks 
650 0 7 |a membránové bílkoviny  |2 czenas  |7 ph569184 
650 0 7 |a buněčné membrány  |2 czenas  |7 ph170663 
650 0 7 |a biochemie  |2 czenas  |7 ph114149 
650 0 9 |a membrane proteins  |2 eczenas 
650 0 9 |a cell membranes  |2 eczenas 
650 0 9 |a biochemistry  |2 eczenas 
655 7 |a elektronické knihy  |7 fd186907  |2 czenas 
655 7 |a sborníky  |7 fd163935   |2 czenas 
655 9 |a electronic books  |2 eczenas 
655 9 |a papers of several authors  |2 eczenas 
700 1 |a Dossena, Silvia,  |e editor. 
700 1 |a Paulmichl, Markus,  |e editor. 
776 0 8 |i Print version:  |t Role of pendrin in health and disease.  |d Cham, Switzerland : Springer, 2017  |z 9783319432854  |z 3319432850  |w (OCoLC)952981282 
856 4 0 |u https://proxy.k.utb.cz/login?url=https://link.springer.com/10.1007/978-3-319-43287-8  |y Plný text 
942 |2 udc 
992 |c NTK-SpringerBLS 
993 |x NEPOSILAT  |y EIZ 

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