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Use of nuclear magnetic resonance to study the three-dimensional structureof rhodopsin
G PROTEIN PATHWAYS, PT A, RECEPTORS
Three-dimensional representations of G protein-coupled receptor structuresand mechanisms
G PROTEIN PATHWAYS, PT A, RECEPTORS
Envelope glycoprotein cytoplasmic domains from diverse lentiviruses interact with the prenylated Rab acceptor
JOURNAL OF VIROLOGY
Can a place of origin of the main cystic fibrosis mutations be identified?
AMERICAN JOURNAL OF HUMAN GENETICS
Endothelin- and sarafotoxin-induced receptor-mediated calcium mobilizationin a clonal murine osteoblast-like cell line, MC3T3-E1/B
BONE
Down-regulation of regulatory proteins for differentiation and proliferation in murine fetal hypoplastic lungs: Altered mesenchymal-epithelial interactions
PEDIATRIC PULMONOLOGY
European Epidemiologic Registry of Cystic Fibrosis (ERCF): Comparison of major disease manifestations between patients with different classes of mutations
PEDIATRIC PULMONOLOGY
Liquid transport properties of porcine tracheal epithelium
JOURNAL OF APPLIED PHYSIOLOGY
Protection of T cells from radiation-induced apoptosis by Cepharanthin (R)
INTERNATIONAL IMMUNOPHARMACOLOGY
Human genetics: Lessons from Quebec populations
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
Challenges and strategies for cystic fibrosis lung gene therapy
MOLECULAR THERAPY
Regulated expression of the human CFTR gene in epithelial cells
MOLECULAR THERAPY
Use of perfluorochemical liquid allows earlier detection of gene expression and use of less vector in normal lung and enhances gene expression in acutely injured lung
MOLECULAR THERAPY
Host responses and persistence of vector genome following intrabronchial administration of an E1(-)E3(-) adenovirus gene transfer vector to normal individuals
MOLECULAR THERAPY
Desensitization of chemokine receptor CCR5 in dendritic cells at the earlystage of differentiation by activation of formyl peptide receptors
CLINICAL IMMUNOLOGY
Intra- and intercellular distribution of mitochondrial probes and changes after treatment with MDR modulators
IUBMB LIFE
Oligomeric antigen receptors: a new view on signaling for the selection oflymphocytes
TRENDS IN IMMUNOLOGY
MICA and MICB genes: can the enigma of their polymorphism be resolved?
TRENDS IN IMMUNOLOGY
Multiple roles of Eph receptors and ephrins in neural development
NATURE REVIEWS NEUROSCIENCE
Non-specific activation of the epithelial sodium channel by the CFTR chloride channel
EMBO REPORTS
'CFTR-opathies': disease phenotypes associated with cystic fibrosis transmembrane regulator gene mutations
RESPIRATORY RESEARCH
Glycosylation and the cystic fibrosis transmembrane conductance regulator
RESPIRATORY RESEARCH
Increased filamin binding to beta-integrin cytoplasmic domains inhibits cell migration
NATURE CELL BIOLOGY
The Hsc70 co-chaperone CHIP targets immature CFTR for proteasomal degradation
NATURE CELL BIOLOGY
Binding of the non-typeable Haemophilus influenzae lipooligosaccharide to the PAF receptor initiates host cell signalling
CELLULAR MICROBIOLOGY
Self-assembling organic nanotubes
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
An artificial ion channel formed by a macrocyclic resorcin[4]arene with amphiphilic cholic acid ether groups
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Implicit two-phase solvation model as a tool to assess conformation and energetics of proteins in membrane-mimetic media
THEORETICAL CHEMISTRY ACCOUNTS
Tetraspanins
CELLULAR AND MOLECULAR LIFE SCIENCES
The unfolded protein response: No longer just a special teams player
TRAFFIC
Strategies for prokaryotic expression of eukaryotic membrane proteins
TRAFFIC
Targeting of C-terminal (tail)-anchored proteins: Understanding how cytoplasmic activities are anchored to intracellular membranes
TRAFFIC
Optimized aminolysis conditions for cleavage of N-protected hydrophobic peptides from solid-phase resins
JOURNAL OF PEPTIDE RESEARCH
N-terminal myristylation of HBV preS1 domain enhances receptor recognition
JOURNAL OF PEPTIDE RESEARCH
Artificial ion channels formed by a synthetic cyclic peptide
JOURNAL OF PEPTIDE RESEARCH
The leucine zipper motif of the envelope glycoprotein ectodomain of human immunodeficiency virus type 1 contains conformationally flexible regions asrevealed by NMR and circular dichroism studies in different media
JOURNAL OF PEPTIDE RESEARCH
New procedures for glycophorin A purification with high yield and high purity
JOURNAL OF CHROMATOGRAPHY B
Support vector machine approach for protein subcellular localization prediction
BIOINFORMATICS
Concepts of ventricular defibrillation
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES
Mutation screening of the Wolfram syndrome gene in psychiatric patients
MOLECULAR PSYCHIATRY
Basis for regulated RNA cleavage by functional analysis of RNase L and Ire1p
RNA-A PUBLICATION OF THE RNA SOCIETY
Protective effect of glutathione in HIV-1 lytic peptide 1-induced cell death in human neuronal cells
JOURNAL OF NEUROVIROLOGY
Pharmacological treatment of the ion transport defect in cystic fibrosis
EXPERT OPINION ON INVESTIGATIONAL DRUGS
Gene therapy for cystic fibrosis
EXPERT OPINION ON THERAPEUTIC PATENTS
Vertebrate photoreceptors
PROGRESS IN RETINAL AND EYE RESEARCH
Serine/threonine protein kinases PknF and PknG of Mycobacterium tuberculosis: characterization and localization
MICROBIOLOGY-SGM
Perspectives on gene therapy for cystic fibrosis airway disease
BIODRUGS
Docking of transmembrane helices into four helix bundles in the high affinity IgE receptor
INTERNET JOURNAL OF CHEMISTRY
Gene therapy for cystic fibrosis
JOURNAL OF GENE MEDICINE
Translational control is required for the unfolded protein response and invivo glucose homeostasis
MOLECULAR CELL
Molecular genetics of type 1 glycogen storage disease
MOLECULAR GENETICS AND METABOLISM
Glycoconjugate metabolism in a cystic fibrosis knockout mouse model
MOLECULAR GENETICS AND METABOLISM
Presence of a major WFS1 mutation in Spanish wolfram syndrome pedigrees
MOLECULAR GENETICS AND METABOLISM
Different activation mechanisms of cystic fibrosis transmembrane conductance regulator expressed in Xenopus laevis oocytes
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-MOLECULAR AND INTEGRATIVE PHYSIOLOGY
Molecular physiology of osmoregulation in eels and other teleosts: the role of transporter isoforms and gene duplication
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-MOLECULAR AND INTEGRATIVE PHYSIOLOGY
Gene targeting in hemostasis. Hepsin
FRONTIERS IN BIOSCIENCE
Designer cancer vaccines made easy: Protein transfer of immunostimulatory molecules for use in therapeutic tumor vaccines
FRONTIERS IN BIOSCIENCE
CFTR and pseudomonas infections in cystic fibrosis
FRONTIERS IN BIOSCIENCE
Structure and function analysis of the calcium-related gene spray in Neurospora crassa
FUNGAL GENETICS AND BIOLOGY
Protein solubility and folding monitored in vivo by structural complementation of a genetic marker protein
NATURE BIOTECHNOLOGY
Molecular genetic analysis and biochemical characterization of mammalian P-glycoproteins involved in multidrug resistance
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
Lipid distribution and transport across cellular membranes
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
CD44-mediated oncogenic signaling and cytoskeleton activation during mammary tumor progression
JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA
Erythrocyte membrane ATP binding cassette (ABC) proteins: MRP1 and CFTR aswell as CD39 (ecto-apyrase) involved in RBC ATP transport and elevated blood plasma ATP of cystic fibrosis
BLOOD CELLS MOLECULES AND DISEASES
Cellular and biophysical evidence for interactions between adenosine triphosphate and P-glycoprotein substrates: functional implications for adenosine triphosphate/drug cotransport in P-glycoprotein overexpressing tumor cells and in P-glycoprotein low-level expressing erythrocytes
BLOOD CELLS MOLECULES AND DISEASES
The neglected ion: HCO3-
NATURE MEDICINE
Control of the proinflammatory state in cystic fibrosis lung epithelial cells by genes from the TNF-alpha R/NF kappa B pathway
MOLECULAR MEDICINE
The truncated cytoplasmic tail of HLA-G serves a quality-control function in post-ER compartments
IMMUNITY
Membrane structure and fusion-triggering conformational change of the fusion domain from influenza hemagglutinin
NATURE STRUCTURAL BIOLOGY
Interhelical hydrogen bonds in the CFTR membrane domain
NATURE STRUCTURAL BIOLOGY
Nitroxide radicals. Controlled release from and transport through biomimetic and hollow fibre membranes
FREE RADICAL RESEARCH
A critical role for the branched sidechain adjacent to the third arginine of the sodium channel voltage sensor
IEEE TRANSACTIONS ON DIELECTRICS AND ELECTRICAL INSULATION
Regulation of red cell membrane protein interactions: implications for redcell function
CURRENT OPINION IN HEMATOLOGY
A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy
NATURE GENETICS
Molecular model of the Escherichia coli Na-1/H-1 antiporter NhaA
RECEPTORS & CHANNELS
ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: Role in diagnosis and clinical correlations
HUMAN MUTATION
Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness
HUMAN MUTATION
WFS1/Wolframin mutations, Wolfram syndrome, and associated diseases
HUMAN MUTATION
Topological and mutational analysis of Saccharomyces cerevisiae Ste14p, founding member of the isoprenylcysteine carboxyl methyltransferase family
MOLECULAR BIOLOGY OF THE CELL
An intact dilysine-like motif in the carboxyl terminus of MAL is required for normal apical transport of the influenza virus hemagglutinin cargo protein in epithelial Madin-Darby canine kidney cells
MOLECULAR BIOLOGY OF THE CELL
Layilin, a novel integral membrane protein, is a hyaluronan receptor
MOLECULAR BIOLOGY OF THE CELL
Differential expression of plexin-A subfamily members in the mouse nervoussystem
DEVELOPMENTAL DYNAMICS
Review: Protein secondary structure prediction continues to rise
JOURNAL OF STRUCTURAL BIOLOGY
Role of CFTR in autosomal recessive polycystic kidney disease
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
Roles of line stimulation-induced virtual electrodes and action potential prolongation in arrhythmic propagation
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY
Effect of strength and timing of transmembrane current pulses on isolated ventricular myocytes
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY
Theoretical and experimental study of sawtooth effect in isolated cardiac cell-pairs
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY
Structure of ligand-gated ion channels: Critical assessment of biochemicaldata supports novel topology
MOLECULAR AND CELLULAR NEUROSCIENCE
Cocaine-induced expression of the tetraspanin CD81 and its relation to hypothalamic function
MOLECULAR AND CELLULAR NEUROSCIENCE
Chinks in the armor of the airway - Pseudomonas infection in the cystic fibrosis lung
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY
Ontogeny of CLCN3 chloride channel gene expression in human pulmonary epithelium
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY
Infliximab downregulates interferon-gamma production in activated gut T-lymphocytes from patients with Crohn's disease
CYTOKINE
Molecular properties of the PTH/PTHrP receptor
TRENDS IN ENDOCRINOLOGY AND METABOLISM
A phase I study of aerosolized administration of tgAAVCF to cystic fibrosis subjects with mild lung disease
HUMAN GENE THERAPY
Aerosol and lobar administration of a recombinant adenovirus to individuals with cystic fibrosis. I. Methods, safety, and clinical implications
HUMAN GENE THERAPY
Aerosol and lobar administration of a recombinant adenovirus to individuals with cystic fibrosis. II. Transfection efficiency in airway epithelium
HUMAN GENE THERAPY
Radioisotopic imaging allows optimization of adenovirus lung deposition for cystic fibrosis gene therapy
HUMAN GENE THERAPY
Multidrug resistance-like genes of Arabidopsis required for auxin transport and auxin-mediated development
PLANT CELL
Chlorzoxazone or 1-EBIO increases Na+ absorption across cystic fibrosis airway epithelial cells
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY
Partial correction of defective Cl- secretion in cystic fibrosis epithelial cells by an analog of squalamine
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY