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Zsuzsa Bebők

Fahrenheit universities

H指数:36

被引数:4,802

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miR-200b downregulates CFTR during hypoxia in human lung epithelial cells

CELLULAR & MOLECULAR BIOLOGY LETTERS

IF10.2

2017-11-1543

OAAI

Targets for cystic fibrosis therapy: proteomic analysis and correction of mutant cystic fibrosis transmembrane conductance regulator

囊性纤维化治疗的靶点: 蛋白质组学分析和突变囊性纤维化跨膜传导调节因子的校正

EXPERT REVIEW OF PROTEOMICS

IF2.8

2014-01-0937

OAAI

Cigarette smoke and CFTR: implications in the pathogenesis of COPD

AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY

IF3.5

2013-10-15146

OAAI

Regulation of angiogenesis by hypoxia: the role of microRNA

CELLULAR & MOLECULAR BIOLOGY LETTERS

IF10.2

2013-01-0170

OAAI

The CFTR and ENaC debate: how important is ENaC in CF lung disease?

AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY

IF3.5

2012-06-0172

OAAI

Dab2 is a key regulator of endocytosis and post-endocytic trafficking of the cystic fibrosis transmembrane conductance regulator

Dab2是囊性纤维化跨膜传导调节因子的内吞作用和内吞后运输的关键调节因子

BIOCHEMICAL JOURNAL

IF4.3

2011-12-2142

OAAI

The Unfolded Protein Response (UPR)-activated Transcription Factor X-box-binding Protein 1 (XBP1) Induces MicroRNA-346 Expression That Targets the Human Antigen Peptide Transporter 1 (TAP1) mRNA and Governs Immune Regulatory Genes

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2011-12-01139

OAAI

A Synonymous Single Nucleotide Polymorphism in ΔF508 CFTR Alters the Secondary Structure of the mRNA and the Expression of the Mutant Protein

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2010-09-01188

OAAI

Functional Stability of Rescued ΔF508 Cystic Fibrosis Transmembrane Conductance Regulator in Airway Epithelial Cells

气道上皮细胞中拯救的 ΔF508囊性纤维化跨膜传导调节因子的功能稳定性

AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY

IF5.3

2010-03-0156

OAAI

Search and Rescue Finding Ways to Correct ΔF508 CFTR

AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY

IF5.3

2009-04-0112

PREAI

Activation of the unfolded protein response by ΔF508 CFTR

AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY

IF5.3

2008-10-0192

OAAI

Somatic mosaicism for copy number variation in differentiated human tissues

IF3.7

2008-09-01194

OAAI

The mechanism of cystic fibrosis transmembrane conductance regulator transcriptional repression during the unfolded protein response

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2008-05-0169

OAAI

Enhanced cell-surface stability of rescued ΔF508 cystic fibrosis transmembrane conductance regulator (CFTR) by pharmacological chaperones

BIOCHEMICAL JOURNAL

IF4.3

2008-02-27110

OAAI

Bioelectric effects of quinine on polarized airway epithelial cells

JOURNAL OF CYSTIC FIBROSIS

IF6

2007-09-015

OAAI

Restoration of W1282X CFTR activity by enhanced expression

AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY

IF5.3

2007-09-0164

OAAI

No detectable improvements in cystic fibrosis transmembrane conductance regulator by nasal aminoglycosides in patients with cystic fibrosis with stop mutations

AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY

IF5.3

2007-07-0187

OAAI

VCP/p97 AAA-ATPase does not interact with the endogenous wild-type cystic fibrosis transmembrane conductance regulator

AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY

IF5.3

2007-06-0115

OA

Endoplasmic reticulum stress and the unfolded protein response regulate genomic cystic fibrosis transmembrane conductance regulator expression

AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY

IF4.7

2007-02-0165

PREAI

Mutations in the amino terminus of the cystic fibrosis transmembrane conductance regulator enhance endocytosis

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2006-02-0138

OAAI