Literature DB >> 20080601

CFTR: break a pump, make a channel.

Christopher Miller1.   

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Year:  2010        PMID： 20080601      PMCID： PMC2824264          DOI： 10.1073/pnas.0913576107

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN： 0027-8424            Impact factor:   11.205


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  8 in total

Review 1.  The ABC protein turned chloride channel whose failure causes cystic fibrosis.

Authors:  David C Gadsby; Paola Vergani; László Csanády
Journal:  Nature       Date:  2006-03-23       Impact factor: 49.962

2.  Conformational states of CFTR associated with channel gating: the role ATP binding and hydrolysis.

Authors:  K L Gunderson; R R Kopito
Journal:  Cell       Date:  1995-07-28       Impact factor: 41.582

Review 3.  CFTR (ABCC7) is a hydrolyzable-ligand-gated channel.

Authors:  Andrei A Aleksandrov; Luba A Aleksandrov; John R Riordan
Journal:  Pflugers Arch       Date:  2006-09-26       Impact factor: 3.657

4.  The non-hydrolytic pathway of cystic fibrosis transmembrane conductance regulator ion channel gating.

Authors:  A A Aleksandrov; X Chang; L Aleksandrov; J R Riordan
Journal:  J Physiol       Date:  2000-10-15       Impact factor: 5.182

5.  Coupling of CFTR Cl- channel gating to an ATP hydrolysis cycle.

Authors:  T Baukrowitz; T C Hwang; A C Nairn; D C Gadsby
Journal:  Neuron       Date:  1994-03       Impact factor: 17.173

6.  The two nucleotide-binding domains of cystic fibrosis transmembrane conductance regulator (CFTR) have distinct functions in controlling channel activity.

Authors:  M R Carson; S M Travis; M J Welsh
Journal:  J Biol Chem       Date:  1995-01-27       Impact factor: 5.157

7.  The antioxidant role of thiocyanate in the pathogenesis of cystic fibrosis and other inflammation-related diseases.

Authors:  Yanping Xu; Szilvia Szép; Zhe Lu
Journal:  Proc Natl Acad Sci U S A       Date:  2009-11-16       Impact factor: 11.205

Review 8.  ABC transporters: the power to change.

Authors:  Douglas C Rees; Eric Johnson; Oded Lewinson
Journal:  Nat Rev Mol Cell Biol       Date:  2009-03       Impact factor: 94.444
  8 in total
  6 in total

1.  Alternating access to the transmembrane domain of the ATP-binding cassette protein cystic fibrosis transmembrane conductance regulator (ABCC7).

Authors:  Wuyang Wang; Paul Linsdell
Journal:  J Biol Chem       Date:  2012-02-01       Impact factor: 5.157

2.  Changes in accessibility of cytoplasmic substances to the pore associated with activation of the cystic fibrosis transmembrane conductance regulator chloride channel.

Authors:  Yassine El Hiani; Paul Linsdell
Journal:  J Biol Chem       Date:  2010-07-30       Impact factor: 5.157

3.  Cystic fibrosis transmembrane conductance regulator in the gills of the climbing perch, Anabas testudineus, is involved in both hypoosmotic regulation during seawater acclimation and active ammonia excretion during ammonia exposure.

Authors:  Yuen K Ip; Jonathan M Wilson; Ai M Loong; Xiu L Chen; Wai P Wong; Inês L S Delgado; Siew H Lam; Shit F Chew
Journal:  J Comp Physiol B       Date:  2012-04-22       Impact factor: 2.200

4.  Full-open and closed CFTR channels, with lateral tunnels from the cytoplasm and an alternative position of the F508 region, as revealed by molecular dynamics.

Authors:  Jean-Paul Mornon; Brice Hoffmann; Slavica Jonic; Pierre Lehn; Isabelle Callebaut
Journal:  Cell Mol Life Sci       Date:  2014-10-07       Impact factor: 9.261

5.  Identification of a lipid scrambling domain in ANO6/TMEM16F.

Authors:  Kuai Yu; Jarred M Whitlock; Kyleen Lee; Eric A Ortlund; Yuan Yuan Cui; H Criss Hartzell
Journal:  Elife       Date:  2015-06-09       Impact factor: 8.140

Review 6.  A Pore Idea: the ion conduction pathway of TMEM16/ANO proteins is composed partly of lipid.

Authors:  Jarred M Whitlock; H Criss Hartzell
Journal:  Pflugers Arch       Date:  2016-01-06       Impact factor: 3.657
  6 in total

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