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Agre, P.
Agre, Peter
Agre, Peter C.
Agre, Peter Courtland
Peter Agre (Amerikaans moleculair bioloog en Nobelprijswinnaar)
Peter Agre (amerykański, biochemik)
Peter Agre (biologo statunitense)
Peter Agre (Nobel Prize winner in chemistry, Distinguished Eagle Scout)
Peter Agre (US-amerikanischer Molekularbiologe und Nobelpreisträger für Chemie)
Peter Courtland Agre
Питер Агре
Питър Агре
Пітер Егр
Пітэр Эгр
Эгр, Питер
פיטר אגרה
بيتر أغري
پیتر آگره
پیتەر ئەگری
پیٹر اگری
پیٹر ایجر
पीटर एग्रे
পিটার অ্যাগর (Nobel Prize winner in chemistry, Distinguished Eagle Scout)
Creation class: 
Language material
Creation role: 
Related names: 
Beitz, Eric (1968-)
Cartron, Jean Pierre
Hohmann, Stefan (1956-)
Nielsen, Søren (1962-)
Parker, John C. (1935-)
3.7 A projection map of the glycerol facilitator GlpF: a variant of the aquaporin tetramer., The
ABH and Colton blood group antigens on aquaporin-1, the human red cell water channel protein.
Abnormal Distribution of Aquaporin-5 Water Channel Protein in Salivary Glands from Sjögren's Syndrome Patients
Action at a distance: another lesson from the red cell.
Adenovirus-mediated expression of aquaporin-5 in epithelial cells
Alpha-syntrophin deletion removes the perivascular but not endothelial pool of aquaporin-4 at the blood--brain barrier and delays the development of brain edema in an experimental model of acute hyponatremia
alpha -syntrophin-dependent pool of AQP4 in astroglial end-feet confers bidirectional water flow between blood and brain, An
Alteration of the erythrocyte membrane skeletal ultrastructure in hereditary spherocytosis, hereditary elliptocytosis, and pyropoikilocytosis.
Altered ubiquitination and stability of aquaporin-1 in hypertonic stress.
Appearance of water channels in Xenopus oocytes expressing red cell CHIP28 protein.
Aqp1 expression in erythroleukemia cells: genetic regulation of glucocorticoid and chemical induction.
Aquaglyceroporin AQP9: solute permeation and metabolic control of expression in liver.
Aquaglyceroporin PbAQP during intraerythrocytic development of the malaria parasite Plasmodium berghei
Aquaporin-1 and endothelial nitric oxide synthase expression in capillary endothelia of human peritoneum.
Aquaporin-1 is expressed by vascular smooth muscle cells and mediates rapid water transport across vascular cell membranes.
Aquaporin-1 water channel expression in human kidney.
Aquaporin-1 water channel protein in lung. Ontogeny, steroid-induced expression, and distribution in rat
Aquaporin-1 water channels in short and long loop descending thin limbs and in descending vasa recta in rat kidney.
Aquaporin-4 water channel protein in the rat retina and optic nerve: polarized expression in Müller cells and fibrous astrocytes.
Aquaporin-6: An intracellular vesicle water channel protein in renal epithelia.
Aquaporin 9 is the major pathway for glycerol uptake by mouse erythrocytes, with implications for malarial virulence.
Aquaporin CHIP: the archetypal molecular water channel.
aquaporin family of water channel proteins in clinical medicine., The
aquaporin family of water channels in kidney: an update on physiology and pathophysiology of aquaporin-2., The
Aquaporin in Candida: characterization of a functional water channel protein
Aquaporin null phenotypes: The importance of classical physiology
Aquaporin Sidedness Revisited, The
Aquaporin water channels: atomic structure molecular dynamics meet clinical medicine.
Aquaporin water channels--from atomic structure to clinical medicine.
Aquaporin water channels: molecular mechanisms for human diseases.
Aquaporin water channels (Nobel Lecture).
Aquaporin water channels: unanswered questions and unresolved controversies.
aquaporin-Z water channel gene of Escherichia coli: Structure, organization and phylogeny, The
Aquaporins: a family of water channel proteins.
Aquaporins and ion conductance
Aquaporins and the respiratory system: advice for a lung investigator.
Aquaporins in complex tissues: distribution of aquaporins 1-5 in human and rat eye.
Aquaporins in complex tissues. I. Developmental patterns in respiratory and glandular tissues of rat.
Aquaporins in complex tissues. II. Subcellular distribution in respiratory and glandular tissues of rat.
Aquaporins in Saccharomyces: Characterization of a second functional water channel protein
Aquaporins in the kidney: from molecules to medicine.
Aquaporins: Water channel proteins of plant and animal cells
Arsenic trioxide uptake by human and rat aquaglyceroporins.
Arsenite transport by mammalian aquaglyceroporins AQP7 and AQP9
Association between human erythrocyte calmodulin and the cytoplasmic surface of human erythrocyte membranes.
Atomic Architecture of a Gas Channel, The
Cellular and molecular biology of the aquaporin water channels.
Characterization of aquaporin-6 as a nitrate channel in mammalian cells. Requirement of pore-lining residue threonine 63.
CHIP28 water channels are localized in constitutively water-permeable segments of the nephron.
Cholangiocytes express the aquaporin CHIP and transport water via a channel-mediated mechanism
Clinical disorders of the erythrocyte membrane skeleton.
Clinical relevance of basic research on red cell membranes.
Cognate DNA binding specificity retained after leucine zipper exchange between GCN4 and C/EBP.
Concurrent expression of erythroid and renal aquaporin CHIP and appearance of water channel activity in perinatal rats.
Conversion of aquaporin 6 from an anion channel to a water-selective channel by a single amino acid substitution
Cultured bovine corneal endothelial cells express CHIP28 water channels.
Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis.
Decreased pulmonary vascular permeability in aquaporin-1-null humans.
Defective cellular trafficking of lacrimal gland aquaporin-5 in Sjogren's syndrome
Defective glycerol metabolism in aquaporin 9 (AQP9) knockout mice.
Defective urinary concentrating ability due to a complete deficiency of aquaporin-1
Deficient red-cell spectrin in severe, recessively inherited spherocytosis.
Delayed K+ clearance associated with aquaporin-4 mislocalization: phenotypic defects in brains of alpha-syntrophin-null mice.
Delayed onset of brain edema and mislocalization of aquaporin-4 in dystrophin-null transgenic mice.
Developmental gene expression and tissue distribution of the CHIP28 water-channel protein.
Differential control of band 3 lateral and rotational mobility in intact red cells.
distribution of erythrocyte phospholipids in hereditary spherocytosis demonstrates a minimal role for erythrocyte spectrin on phospholipid diffusion and asymmetry., The
Distribution of the aquaporin CHIP in secretory and resorptive epithelia and capillary endothelia.
Effects of microtubule disruption on endocytosis, membrane recycling and polarized distribution of Aquaporin-1 and gp330 in proximal tubule cells.
Expression of aquaporin isoforms during human and mouse tooth development.
Expression of aquaporins-1 and -2 during nephrogenesis and in autosomal dominant polycystic kidney disease.
Expression of multiple water channel activities in Xenopus oocytes injected with mRNA from rat kidney.
Fast and Selective Ammonia Transport by Aquaporin-8
From Structure to Disease: the Evolving Tale of Aquaporin Biology
Functional analysis of aquaporin-1 deficient red cells. The Colton-null phenotype.
Functional Expression and Characterization of an Archaeal Aquaporin -- aqpM From Methanothermobacter marburgensis
Functional impairment of lens aquaporin in two families with dominantly inherited cataracts
Functional Reconstitution and Characterization of AqpZ, the E. coli Water Channel Protein
Functional requirement of aquaporin-5 in plasma membranes of sweat glands.
Genomic organization and developmental expression of aquaporin-5 in lung.
Heterotetrameric composition of aquaporin-4 water channels.
High resolution AFM topographs of the Escherichia coli water channel aquaporin Z
Highly selective water channel activity measured by voltage clamp: analysis of planar lipid bilayers reconstituted with purified AqpZ.
Homer W. Smith award lecture. Aquaporin water channels in kidney.
Hourglass pore-forming domains restrict aquaporin-1 tetramer assembly.
human Aquaporin-5 gene. Molecular characterization and chromosomal localization., The
human aquaporin-CHIP gene. Structure, organization, and chromosomal localization., The
Human red cell aquaporin CHIP. I. Molecular characterization of ABH and Colton blood group antigens.
Human red cell Aquaporin CHIP. II. Expression during normal fetal development and in a novel form of congenital dyserythropoietic anemia.
human tumor cloning assay in cancer drug development. A review., The
Hypertonic Induction of Aquaporin-5 Expression through an ERK-dependent Pathway
Identification of AQP5 in lipid rafts and its translocation to apical membranes by activation of M3 mAChRs in interlobular ducts of rat parotid gland.
Immunolocalization of AQP-5 in rat parotid and submandibular salivary glands after stimulation or inhibition of secretion in vivo.
importance of aquaporin water channel protein structures, The
Inheritance pattern and clinical response to splenectomy as a reflection of erythrocyte spectrin deficiency in hereditary spherocytosis.
Ion permeation of AQP6 water channel protein. Single channel recordings after Hg2+ activation.
Isolation of the cDNA for erythrocyte integral membrane protein of 28 kilodaltons: member of an ancient channel family.
Keratinocyte growth factor modulates alveolar epithelial cell phenotype in vitro: expression of aquaporin 5.
Linkage of dominant hereditary spherocytosis to the gene for the erythrocyte membrane-skeleton protein ankyrin.
Localization of aquaporin CHIP in the human eye: implications in the pathogenesis of glaucoma and other disorders of ocular fluid balance.
Loss of perivascular aquaporin 4 may underlie deficient water and K+ homeostasis in the human epileptogenic hippocampus.
Mammalian red cell membrane Rh polypeptides are selectively palmitoylated subunits of a macromolecular complex.
Man is not a rodent: Aquaporins in the airways
Membrane topology of aquaporin CHIP. Analysis of functional epitope-scanning mutants by vectorial proteolysis.
Membrane water transport and aquaporins: looking back.
mercury-sensitive residue at cysteine 189 in the CHIP28 water channel., The
Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. I. Biochemical identification of rearrangements in the spectrin/actin binding domain and functional characterizations.
Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. II. Determination of molecular genetic origins of rearrangements.
Molecular basis of water selectivity on aquaporin-1
Molecular characterization of an aquaporin cDNA from brain: Candidate osmoreceptor and regulator of water balance
Molecular cloning and characterization of an aquaporin cDNA from salivary, lacrimal, and respiratory tissues
Molecular cloning and characterization of AqpZ a water channel from Escherichia coli
molecular defect in two families with hemolytic poikilocytic anemia: reduction of high affinity membrane binding sites for ankyrin., A
Molecular genetics of the human beta-spectrin gene.
Molecular structure of the water channel through aquaporin CHIP. The hourglass model.
Mutant forms of spectrin alpha-subunits in hereditary elliptocytosis.
Mutations in aquaporin-1 in phenotypically normal humans without functional CHIP water channels.
new face of the Rhesus antigen, A
Ontogeny of water transport in rat brain: postnatal expression of the aquaporin-4 water channel
Partial deficiency of erythrocyte spectrin in hereditary spherocytosis.
Polymorphism in the Mr 32,000 Rh protein purified from Rh(D)-positive and -negative erythrocytes.
Progress on the structure and function of aquaporin 1.
Projection map of aquaporin-1 determined by electron crystallography.
proposal to standardize terminology for weak D antigen., A
Protein blood group antigens of tahe human red cell, c1992:
Protein Blood Group Antigens of the Human Red Cell: Structure, Function, and the Clinical
Proteomic analysis of lithium-induced nephrogenic diabetes insipidus: Mechanisms for aquaporin 2 down-regulation and cellular proliferation
Purification and functional characterization of aquaporin-8.
Quantification of Aquaporin-CHIP water channel protein in microdissected renal tubules by fluorescence-based ELISA.
Rapid gating and anion permeability of an intracellular aquaporin
Reconstitution and functional comparison of purified GlpF and AqpZ, the glycerol and water channels from Escherichia coli
Reconstitution of functional water channels in liposomes containing purified red cell CHIP28 protein.
Reconstitution of water channel function of aquaporins 1 and 2 by expression in yeast secretory vesicles.
Red blood cell membranes : structure, function, clinical implications
red cell membrane skeleton: a model with general biological relevance but pathological significance for blood., The
Reduced arsenic clearance and increased toxicity in aquaglyceroporin-9-null mice
Regulation of the Escherichia coli water channel gene aqpZ.
Respiratory aquaporins in lung inflammation: The night is young
Secretin induces the apical insertion of aquaporin-1 water channels in rat cholangiocytes.
Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis.
Specialized membrane domains for water transport in glial cells: High-resolution immunogold cytochemistry of aquaporin-4 in rat brain
Structural biology. The atomic architecture of a gas channel.
Structural determinants of water permeation through aquaporin-1.
Structure of the Water Channel AqpZ from Escherichia coli Revealed by Electron Crystallography
Surface topographies at subnanometer-resolution reveal asymmetry and sidedness of aquaporin-1.
Syntrophin-dependent expression and localization of Aquaporin-4 water channel protein
Targeted disruption of the Cl super(-)/HCO sub(3) super(-) exchanger Ae2 results in osteopetrosis in mice
three-dimensional structure of aquaporin-1., The
Towards a molecular understanding of water homeostasis in the brain
Water and ion permeation of aquaporin-1 in planar lipid bilayers. Major differences in structural determinants and stoichiometry.
Water channel properties of major intrinsic protein of lens.
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