Citation Impact
Citing Papers
Piezo1 ion channel pore properties are dictated by C-terminal region
2015 StandoutNobel
Molecular Cloning and Characterization of an Aquaporin cDNA from Salivary, Lacrimal, and Respiratory Tissues
1995 StandoutNobel
Human genetic disorders of sphingolipid biosynthesis
2014
The MyD88-Dependent, but Not the MyD88-Independent, Pathway of TLR4 Signaling Is Important in Clearing Nontypeable Haemophilus influenzae from the Mouse Lung
2005 StandoutNobel
Fibroblast growth factor 15 functions as an enterohepatic signal to regulate bile acid homeostasis
2005 Standout
The Mechanosensitive Ion Channel Piezo Inhibits Axon Regeneration
2019 StandoutNobel
The FGF family: biology, pathophysiology and therapy
2009 Standout
Altered Structure and Anion Transport Properties of Band 3 (AE1, SLC4A1) in Human Red Cells Lacking Glycophorin A
2004
Human red cell Aquaporin CHIP. II. Expression during normal fetal development and in a novel form of congenital dyserythropoietic anemia.
1994 StandoutNobel
Murine monoclonal antibody MB‐2D10 recognizes Rh‐related glycoproteins in the human red cell membrane
1990
Sphingolipids and their metabolism in physiology and disease
2017 Standout
Hereditary stomatocytosis and cation leaky red cells — Recent developments
2009
Aquaporin water channels: molecular mechanisms for human diseases1
2003 StandoutNobel
Aquaporin Water Channels in Kidney
2000 StandoutNobel
Complement regulatory proteins and autoimmunity
2006
Impaired PIEZO1 function in patients with a novel autosomal recessive congenital lymphatic dysplasia
2015 StandoutNobel
Regulation of Fibroblastic Growth Factor 23 Expression but Not Degradation by PHEX
2003
Membrane Dynamics of the Water Transport Protein Aquaporin-1 in Intact Human Red Cells
1999 StandoutNobel
The aquaporin family of water channels in kidney
1995 StandoutNobel
Functional Analysis of Aquaporin-1 Deficient Red Cells
1996 StandoutNobel
Complement: a key system for immune surveillance and homeostasis
2010 Standout
Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels
2013 StandoutNobel
Mechanically Activated Ion Channels
2015 StandoutNobel
Piezos thrive under pressure: mechanically activated ion channels in health and disease
2017 StandoutNobel
A role of PIEZO1 in iron metabolism in mice and humans
2021 StandoutNobel
Immune Thrombocytopenic Purpura
2002 Standout
Membrane complement regulatory proteins
2005
The immune gene repertoire encoded in the purple sea urchin genome
2006 Standout
Structure of the mechanically activated ion channel Piezo1
2017 StandoutNatureNobel
Defective Urinary Concentrating Ability Due to a Complete Deficiency of Aquaporin-1
2001 StandoutNobel
Aquaporin water channels: unanswered questions and unresolved controversies
1995 StandoutNobel
AnAQP1null allele in an Indian woman with Co(a–b–) phenotype and high‐titer anti‐Co3 associated with mild HDN
2001
Progress on the Structure and Function of Aquaporin 1
1998 StandoutNobel
Molecular determinants of the pathogenesis of disease due to non-typableHaemophilus influenzae
1999
Chemical approaches to the investigation of cellular systems
2002 StandoutNobel
Aquaporin water channels – from atomic structure to clinical medicine
2002 StandoutNobel
Human red cell aquaporin CHIP. I. Molecular characterization of ABH and Colton blood group antigens.
1994 StandoutNobel
The Human Aquaporin-5 Gene
1996 StandoutNobel
Refinement of the hereditary xerocytosis locus on chromosome 16q in a large Canadian kindred
2011
Disorders of red cell volume regulation
2013
Biofortification of crops with seven mineral elements often lacking in human diets – iron, zinc, copper, calcium, magnesium, selenium and iodine
2009 Standout
Missense mutations in the ABCB6 transporter cause dominant familialpseudohyperkalemia
2012
Integrating Molecular Technologies for Red Blood Cell Typing and Compatibility Testing Into Blood Centers and Transfusion Services
2008
Microglia Sculpt Postnatal Neural Circuits in an Activity and Complement-Dependent Manner
2012 Standout
The human AQP4 gene: definition of the locus encoding two water channel polypeptides in brain.
1996 StandoutNobel
Mutations in aquaporin-1 in Phenotypically Normal Humans Without Functional CHIP Water Channels
1994 StandoutScienceNobel
Piezo1 links mechanical forces to red blood cell volume
2015 StandoutNobel
Chemical camouflage of antigenic determinants: Stealth erythrocytes
1997
Transfusion-related mortality: the ongoing risks of allogeneic blood transfusion and the available strategies for their prevention
2009 Standout
Aqp1 expression in erythroleukemia cells: genetic regulation of glucocorticoid and chemical induction
1997 StandoutNobel
Aquaporin water channels: atomic structure molecular dynamics meet clinical medicine
2002 StandoutNobel
Decreased pulmonary vascular permeability in aquaporin-1-null humans
2002 StandoutNobel
Piezo1, a mechanically activated ion channel, is required for vascular development in mice
2014 StandoutNobel
FGF23, PHEX, and MEPE regulation of phosphate homeostasis and skeletal mineralization
2003
Aquaporin-1 water channel protein in lung: ontogeny, steroid-induced expression, and distribution in rat.
1996 StandoutNobel
Aquaporin water channels: atomic structure molecular dynamics meet clinical medicine
2002 StandoutNobel
Aquaporin water channels: atomic structure molecular dynamics meet clinical medicine
2002 StandoutNobel
Mechanically activated ion channel PIEZO1 is required for lymphatic valve formation
2018 StandoutNobel
Disorders of erythrocyte volume homeostasis
2015
The Aquaporin Family of Water Channel Proteins in Clinical Medicine
1997 StandoutNobel
Cellular and Molecular Biology of the Aquaporin Water Channels
1999 StandoutNobel
Molecular biology of the Rh antigens
1991 StandoutNobel
Targeted deletion of the CD59 gene causes spontaneous intravascular hemolysis and hemoglobinuria
2001
Chemical activation of the mechanotransduction channel Piezo1
2015 StandoutNobel
Aquaporins in the Kidney: From Molecules to Medicine
2002 StandoutNobel
Aquaporin-6: An intracellular vesicle water channel protein in renal epithelia
1999 StandoutNobel
Works of Joyce Poole being referenced
The monovalent cation leak in overhydrated stomatocytic red blood cells results from amino acid substitutions in the Rh-associated glycoprotein
2008
Molecular Basis of the Globoside-deficient Pk Blood Group Phenotype
2002
Molecular Defects Underlying the Kell Null Phenotype
2001
Acquired and transient RBC CD55 deficiency (Inab phenotype) and anti‐IFC
2002
Additional molecular bases of the clinically important p blood group phenotype
2003
The blood group antigen factsbook
1997
Biochemical studies on red blood cells from a patient with the Inab phenotype (decay-accelerating factor deficiency)
1991
A novel form of congenital dyserythropoietic anemia associated with deficiency of erythroid CD44 and a unique blood group phenotype [In(a-b- ), Co(a-b-)]
1994
A review of the ISBT rare blood donor program
2004
The Anton blood group antigen is the erythrocyte receptor forHaemophilus influenzae
1986
Molecular basis of reduced or absent expression of decay-accelerating factor in Cromer blood group phenotypes
1994
TWO APPARENTLY HEALTHY JAPANESE INDIVIDUALS OF TYPE MkMk HAVE ERYTHROCYTES WHICH LACK BOTH THE BLOOD GROUP MN AND Ss‐ACTIVE SIALOGLYCOPROTEINS
1979