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A multi‐property assessment of intensity of use provides a functional understanding of animal movement

Methods in ecology and evolution, 2024-02, Vol.15 (2), p.345-357

2024

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Long-term treatment with oral N-acetylcysteine: Affects lung function but not sputum inflammation in cystic fibrosis subjects. A phase II randomized placebo-controlled trial

Journal of cystic fibrosis, 2015-03, Vol.14 (2), p.219-227

2015

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Sensitivity of a Renal K+ Channel (ROMK2) to the Inhibitory Sulfonylurea Compound Glibenclamide is Enhanced by Coexpression with the ATP-Binding Cassette Transporter Cystic Fibrosis Transmembrane Regulator

Proceedings of the National Academy of Sciences - PNAS, 1996-07, Vol.93 (15), p.8083-8088

1996

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In vitro pharmacologic restoration of CFTR-mediated chloride transport with sodium 4-phenylbutyrate in cystic fibrosis epithelial cells containing delta F508-CFTR

The Journal of clinical investigation, 1997-11, Vol.100 (10), p.2457-2465

1997

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Differential expression of ORCC and CFTR induced by low temperature in CF airway epithelial cells

American Journal of Physiology: Cell Physiology, 1995-01, Vol.268 (1), p.C243-C251

1995

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CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP

Cell, 1995-06, Vol.81 (7), p.1063-1073

1995

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Diagnosis of vaginitis

American family physician, 2000-09, Vol.62 (5), p.1095-1104

2000

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Relationships Among Ara-CTP Pools, Formation of (Ara-C)DNA, and Cytotoxicity of Human Leukemic Cells

Blood, 1984-07, Vol.64 (1), p.54-58

1984

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Genetic modifiers of liver disease in cystic fibrosis

JAMA : the journal of the American Medical Association, 2009-09, Vol.302 (10), p.1076

2009

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Chloride Channel and Chloride Conductance Regulator Domains of CFTR, the Cystic Fibrosis Transmembrane Conductance Regulator

Proceedings of the National Academy of Sciences - PNAS, 1998-03, Vol.95 (5), p.2674-2679

1998

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Lethality of Human Myeloblasts Correlates with the Incorporation of Arabinofuranosylcytosine into DNA

Proceedings of the National Academy of Sciences - PNAS, 1981-05, Vol.78 (5), p.3235-3239

1981

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Continuous Detection of Extracellular ATP on Living Cells by Using Atomic Force Microscopy

Proceedings of the National Academy of Sciences - PNAS, 1999-10, Vol.96 (21), p.12180-12185

1999

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Effects of the Serine/Threonine Kinase SGK1 on the Epithelial Na+ Channel (ENaC) and CFTR: Implications for Cystic Fibrosis

Cellular physiology and biochemistry, 2001-01, Vol.11 (4), p.209-218

2001

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CFTR Is a Conductance Regulator as well as a Chloride Channel

Physiological reviews, 1999-01, Vol.79 (1), p.145-S166

1999

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Correlation of cytotoxicity with incorporation of ara-C into DNA

The Journal of biological chemistry, 1980-10, Vol.255 (19), p.8997-9000

1980

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Curcumin, a Major Constituent of Turmeric, Corrects Cystic Fibrosis Defects

Science (American Association for the Advancement of Science), 2004-04, Vol.304 (5670), p.600-602

2004

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A functional CFTR-NBF1 is required for ROMK2-CFTR interaction

American journal of physiology. Renal physiology, 1997-11, Vol.273 (5), p.843-F848

1997

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The Adult Calfactant in Acute Respiratory Distress Syndrome Trial

Chest, 2015-08, Vol.148 (2), p.356-364

2015

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5-Fluoro-2'-deoxyuridine incorporation in L1210 DNA

The Journal of biological chemistry, 1981-09, Vol.256 (17), p.8885-8888

1981

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Identification of the Cystic Fibrosis Transmembrane Conductance Regulator Domains That Are Important for Interactions with ROMK2

The Journal of biological chemistry, 2000-06, Vol.275 (22), p.16697-16701

2000

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Lethal effects of 1-beta-D-arabinofuranosylcytosine incorporation into deoxyribonucleic acid during ultraviolet repair

Molecular pharmacology, 1984-03, Vol.25 (2), p.322-326

1984

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Assessment of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Activity in CFTR-Null Mice after Bone Marrow Transplantation

Proceedings of the National Academy of Sciences - PNAS, 2006-02, Vol.103 (8), p.2965-2970

2006

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Genetics of Cystic Fibrosis

Clinics in chest medicine, 2016-03, Vol.37 (1), p.9-16

Egan, Marie E., MD

2016

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Calcium-pump inhibitors induce functional surface expression of ΔF508-CFTR protein in cystic fibrosis epithelial cells

Nature medicine, 2002-05, Vol.8 (5), p.485-492

2002

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Cloning, expression and in vitro evaluation of recombinant canine Tum5, an angiostatic domain of mammalian type IV collagen

Veterinary & comparative oncology, 2003-03, Vol.1 (1), p.36-47

2003

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A multi‐property assessment of intensity of use provides a functional understanding of animal movement

Long-term treatment with oral N-acetylcysteine: Affects lung function but not sputum inflammation in cystic fibrosis subjects. A phase II randomized placebo-controlled trial

Sensitivity of a Renal K+ Channel (ROMK2) to the Inhibitory Sulfonylurea Compound Glibenclamide is Enhanced by Coexpression with the ATP-Binding Cassette Transporter Cystic Fibrosis Transmembrane Regulator

In vitro pharmacologic restoration of CFTR-mediated chloride transport with sodium 4-phenylbutyrate in cystic fibrosis epithelial cells containing delta F508-CFTR

Differential expression of ORCC and CFTR induced by low temperature in CF airway epithelial cells

CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP

Diagnosis of vaginitis

Relationships Among Ara-CTP Pools, Formation of (Ara-C)DNA, and Cytotoxicity of Human Leukemic Cells

Genetic modifiers of liver disease in cystic fibrosis

Chloride Channel and Chloride Conductance Regulator Domains of CFTR, the Cystic Fibrosis Transmembrane Conductance Regulator

Lethality of Human Myeloblasts Correlates with the Incorporation of Arabinofuranosylcytosine into DNA

Continuous Detection of Extracellular ATP on Living Cells by Using Atomic Force Microscopy

Effects of the Serine/Threonine Kinase SGK1 on the Epithelial Na+ Channel (ENaC) and CFTR: Implications for Cystic Fibrosis

CFTR Is a Conductance Regulator as well as a Chloride Channel

Correlation of cytotoxicity with incorporation of ara-C into DNA

Curcumin, a Major Constituent of Turmeric, Corrects Cystic Fibrosis Defects

A functional CFTR-NBF1 is required for ROMK2-CFTR interaction

The Adult Calfactant in Acute Respiratory Distress Syndrome Trial

5-Fluoro-2'-deoxyuridine incorporation in L1210 DNA

Identification of the Cystic Fibrosis Transmembrane Conductance Regulator Domains That Are Important for Interactions with ROMK2

Lethal effects of 1-beta-D-arabinofuranosylcytosine incorporation into deoxyribonucleic acid during ultraviolet repair

Assessment of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Activity in CFTR-Null Mice after Bone Marrow Transplantation

Genetics of Cystic Fibrosis

Calcium-pump inhibitors induce functional surface expression of ΔF508-CFTR protein in cystic fibrosis epithelial cells

Cloning, expression and in vitro evaluation of recombinant canine Tum5, an angiostatic domain of mammalian type IV collagen

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