Investigating the properties of rare, cystic fibrosis causing mutations of the CFTR chloride channel

被引:0
|
作者
Zavoti, O. [1 ]
Simon, M. A. [1 ]
Csanady, L. [1 ]
机构
[1] Semmelweis Univ, Dept Biochem, Budapest, Hungary
来源
FEBS OPEN BIO | 2022年 / 12卷
关键词
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
P-04.1-055
引用
收藏
页码:238 / 239
页数:2
相关论文
共 50 条
  • [1] Clinical characteristics of rare CFTR mutations causing cystic fibrosis in Polish population
    Zybert, Katarzyna
    Wozniacki, Lukasz
    Tomaszewska-Sobczynska, Agnieszka
    Wertheim-Tysarowska, Katarzyna
    Czerska, Kamila
    Oltarzewski, Mariusz
    Sands, Dorota
    [J]. PEDIATRIC PULMONOLOGY, 2020, 55 (08) : 2097 - 2107
  • [2] CFTR, the chloride channel defective in cystic fibrosis
    Riordan, JR
    Kiser, GL
    Aleksandrov, AA
    Chang, XB
    [J]. NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1998, 358 (01) : R380 - R380
  • [3] DRUG REPURPOSING FOR CYSTIC FIBROSIS SUBJECTS WITH RARE CFTR MUTATIONS
    Hagemeijer, M. C.
    de Poel, E.
    van Mourik, P.
    Vonk, A. M.
    Oppelaar, H.
    de Winter-de Groot, K. M.
    Heida-Michel, S.
    Geerdink, M.
    van der Ent, C. K.
    Beekman, J. M.
    [J]. PEDIATRIC PULMONOLOGY, 2017, 52 : S316 - S317
  • [4] The cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel.
    Hanrahan, JW
    Zhu, T
    Dahan, D
    Fung, S
    Meredith, J
    Phillips, JE
    [J]. AMERICAN ZOOLOGIST, 2000, 40 (06): : 1046 - 1046
  • [5] MOLECULAR MECHANISMS OF CFTR CHLORIDE CHANNEL DYSFUNCTION IN CYSTIC-FIBROSIS
    WELSH, MJ
    SMITH, AE
    [J]. CELL, 1993, 73 (07) : 1251 - 1254
  • [6] CFTR - MUTATIONS, ION-CHANNEL FUNCTION AND CYSTIC-FIBROSIS
    DAWSON, DC
    MANSOURA, MK
    WILKINSON, DJ
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1995, 489P : S2 - S2
  • [7] Sweat chloride concentrations and CFTR gene mutations in late diagnosed cystic fibrosis
    Bradley, D. T.
    Beattie, D.
    Graham, C. A.
    Magee, A. C.
    Mckee, S. A.
    Patterson, C. C.
    Rendall, J.
    Elborn, J. S.
    [J]. THORAX, 2007, 62 : A104 - A105
  • [8] Cystic fibrosis: Channel, catalytic, and folding properties of the CFTR protein
    Seibert, FS
    Loo, TW
    Clarke, DM
    Riordan, JR
    [J]. JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1997, 29 (05) : 429 - 442
  • [9] Cystic Fibrosis: Channel, Catalytic, and Folding Properties of the CFTR Protein
    Fabian S. Seibert
    Tip W. Loo
    David M. Clarke
    John R. Riordan
    [J]. Journal of Bioenergetics and Biomembranes, 1997, 29 : 429 - 442
  • [10] ANALYSIS OF THE EFFECTS OF RARE CYSTIC FIBROSIS MUTATIONS ON CFTR EXPRESSION, STABILITY AND FUNCTION
    Cai, Z.
    Millen, L.
    Gottschalk, L. B.
    Cutting, G. R.
    Hong, J. S.
    Lukacs, G. L.
    Sheppard, D. N.
    Sorscher, E. J.
    Thomas, P. J.
    Tuggle, K. L.
    [J]. PEDIATRIC PULMONOLOGY, 2015, 50 : 193 - 194