Investigation of anion transport by artificial ionophores to bypass loss of CFTR function in cystic fibrosis

Bibliographic Details
Main Author:	Hughes, Lauren Kimberley
Published:	University of Bristol 2007
Subjects:	616.372060724
Online Access:	http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.442200

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spelling	ndltd-bl.uk-oai-ethos.bl.uk-4422002015-03-19T08:54:49ZInvestigation of anion transport by artificial ionophores to bypass loss of CFTR function in cystic fibrosisHughes, Lauren Kimberley2007616.372060724University of Bristolhttp://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.442200Electronic Thesis or Dissertation
collection	NDLTD
sources	NDLTD
topic	616.372060724
spellingShingle	616.372060724 Hughes, Lauren Kimberley Investigation of anion transport by artificial ionophores to bypass loss of CFTR function in cystic fibrosis
author	Hughes, Lauren Kimberley
author_facet	Hughes, Lauren Kimberley
author_sort	Hughes, Lauren Kimberley
title	Investigation of anion transport by artificial ionophores to bypass loss of CFTR function in cystic fibrosis
title_short	Investigation of anion transport by artificial ionophores to bypass loss of CFTR function in cystic fibrosis
title_full	Investigation of anion transport by artificial ionophores to bypass loss of CFTR function in cystic fibrosis
title_fullStr	Investigation of anion transport by artificial ionophores to bypass loss of CFTR function in cystic fibrosis
title_full_unstemmed	Investigation of anion transport by artificial ionophores to bypass loss of CFTR function in cystic fibrosis
title_sort	investigation of anion transport by artificial ionophores to bypass loss of cftr function in cystic fibrosis
publisher	University of Bristol
publishDate	2007
url	http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.442200
work_keys_str_mv	AT hugheslaurenkimberley investigationofaniontransportbyartificialionophorestobypasslossofcftrfunctionincysticfibrosis
_version_	1716768097282555904

Investigation of anion transport by artificial ionophores to bypass loss of CFTR function in cystic fibrosis

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