A novel candidate gene to rescue misprocessing of ΔF508 CFTR present in most patients with cystic fibrosis

被引:0
|
作者
Okiyoneda, T
Jono, H
Wada, I
Shuto, T
Yoshitake, K
Shibata, Y
Nagayama, S
Riordan, JR
Isohama, Y
Miyata, T
Kai, H
机构
[1] Kumamoto Univ, Kumamoto 8620973, Japan
[2] Sapporo Med Coll, Sapporo, Hokkaido, Japan
[3] Mayo Clin Scottsdale, Johnson Med Res Ctr, Scottsdale, AZ 85251 USA
关键词
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
2175
引用
收藏
页码:419A / 419A
页数:1
相关论文
共 50 条
  • [1] Removal of multiple arginine-framed trafficking signals overcomes misprocessing of ΔF508 CFTR present in most patients with cystic fibrosis
    Chang, XB
    Cui, LY
    Hou, YX
    Jensen, TJ
    Aleksandrov, AA
    Mengos, A
    Riordan, JR
    MOLECULAR CELL, 1999, 4 (01) : 137 - 142
  • [2] ∆F508 CFTR interactome remodelling promotes rescue of cystic fibrosis
    Sandra Pankow
    Casimir Bamberger
    Diego Calzolari
    Salvador Martínez-Bartolomé
    Mathieu Lavallée-Adam
    William E. Balch
    John R. Yates
    Nature, 2015, 528 : 510 - 516
  • [3] ΔF508 CFTR interactome remodelling promotes rescue of cystic fibrosis
    Pankow, Sandra
    Bamberger, Casimir
    Calzolari, Diego
    Martinez-Bartolome, Salvador
    Lavallee-Adam, Mathieu
    Balch, William E.
    Yates, John R., III
    NATURE, 2015, 528 (7583) : 510 - +
  • [4] MICRORNAS FUNCTIONALLY RESCUE [ΔF508]-CFTR IN CYSTIC FIBROSIS CELLS
    Kumar, P.
    Bhattacharyya, A.
    Kundu, S.
    Bhattacharyya, S.
    Peters, K.
    Sen, A.
    Frizzell, R. A.
    Cox, R.
    Guggino, W. B.
    Caohuy, H.
    Pollard, H. B.
    Biswas, R.
    PEDIATRIC PULMONOLOGY, 2013, 48 : 218 - 218
  • [5] The ΔF508 Mutation Causes CFTR Misprocessing and Cystic Fibrosis-Like Disease in Pigs
    Ostedgaard, Lynda S.
    Meyerholz, David K.
    Chen, Jeng-Haur
    Pezzulo, Alejandro A.
    Karp, Philip H.
    Rokhlina, Tatiana
    Ernst, Sarah E.
    Hanfland, Robert A.
    Reznikov, Leah R.
    Ludwig, Paula S.
    Rogan, Mark P.
    Davis, Greg J.
    Dohrn, Cassie L.
    Wohlford-Lenane, Christine
    Taft, Peter J.
    Rector, Michael V.
    Hornick, Emma
    Nassar, Boulos S.
    Samuel, Melissa
    Zhang, Yuping
    Richter, Sandra S.
    Uc, Aliye
    Shilyansky, Joel
    Prather, Randall S.
    McCray, Paul B., Jr.
    Zabner, Joseph
    Welsh, Michael J.
    Stoltz, David A.
    SCIENCE TRANSLATIONAL MEDICINE, 2011, 3 (74)
  • [6] ΔF508 CFTR protein expression in tissues from patients with cystic fibrosis
    Kälin, N
    Claass, A
    Sommer, M
    Puchelle, E
    Tümmler, B
    JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (10): : 1379 - 1389
  • [7] High Mortality in Cardiomyopathy Patients Heterozygous for the CFTR ΔF508 Cystic Fibrosis Mutation
    London, Barry
    Boudreau, Ryan
    Haider, Indrani
    -Estrada, Andres Vargas
    Comellas, Alejandro
    Johnson, Frances L.
    Zabner, Joseph
    Gutmann, Rebecca A.
    Bloom, Heather L.
    Dudley, Samuel C.
    Ellinor, Patrick T.
    Shalaby, Alaa
    Weiss, Raul
    CIRCULATION, 2015, 132
  • [8] Aquagenic wrinkling of the palms in patients with cystic fibrosis homozygous for the ΔF508 CFTR mutation
    Katz, KA
    Yan, AC
    Turner, ML
    ARCHIVES OF DERMATOLOGY, 2005, 141 (05) : 621 - 624
  • [9] Glucose homeostasis and genotype-phenotype interplay in cystic fibrosis patients with CFTR gene ΔF508 mutation
    Preumont, Vanessa
    Hermans, Michel P.
    Lebecque, Patrick
    Buysschaert, Martin
    DIABETES CARE, 2007, 30 (05) : 1187 - 1192
  • [10] Frequency of Genotype With ΔF508 Mutation in CFTR Gene Among Iranian Cystic Fibrosis Patients With Pancreatic Insufficiency
    Khodadad, Ahmad
    Elahi, Elaheh
    Hassani, Setareh Sadat Bani
    Rouhani, Pejman
    Sadeghi, Bamdad
    Rezaei, Nima
    IRANIAN JOURNAL OF PEDIATRICS, 2015, 25 (06)