Citation Impact
Citing Papers
Platelet gene expression and function in patients with COVID-19
2020 Standout
Jinx , an MCMV susceptibility phenotype caused by disruption of Unc13d : a mouse model of type 3 familial hemophagocytic lymphohistiocytosis
2007 StandoutNobel
Podocin and MEC-2 bind cholesterol to regulate the activity of associated ion channels
2006 StandoutNobel
Molecular evolution of the nuclear von Willebrand factor gene in mammals and the phylogeny of rodents
1999
Functional redundancy of Rab27 proteins and the pathogenesis of Griscelli syndrome
2002
Molecular cloning of a novel human PAPS synthetase which is differentially expressed in metastatic and non-metastatic colon carcinoma cells
1999
Rab GTPases, intracellular traffic and disease
2002
Signals from the lysosome: a control centre for cellular clearance and energy metabolism
2013 Standout
Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression
2008
MEC-2 Is Recruited to the Putative Mechanosensory Complex in C. elegans Touch Receptor Neurons through Its Stomatin-like Domain
2004 StandoutNobel
Cellular and molecular mechanisms of fibrosis
2007 Standout
Lysosomes: fusion and function
2007 Standout
Regulation and Functions of the ER-Associated Nrf1 Transcription Factor
2022 StandoutNobel
Rab27a and Rab27b control different steps of the exosome secretion pathway
2009 Standout
Lysosome biogenesis and lysosomal membrane proteins: trafficking meets function
2009 Standout
Conserved synteny between the Fugu and human PTEN locus and the evolutionary conservation of vertebrate PTEN function
2001 StandoutNobel
Fibrin deposition in tissues from endotoxin-treated mice correlates with decreases in the expression of urokinase-type but not tissue-type plasminogen activator.
1996
Rab proteins as membrane organizers
2001 Standout
Shiga-toxin-producing Escherichia coli and haemolytic uraemic syndrome
2005 Standout
Pentoxifylline
1987 Standout
Extracellular Proteins Organize the Mechanosensory Channel Complex in C. elegans Touch Receptor Neurons
2004 StandoutNobel
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura
2001 StandoutNature
Rab GTPases as coordinators of vesicle traffic
2009 Standout
Hermansky–Pudlak syndrome: a disease of protein trafficking and organelle function
2006
Thrombin signalling and protease-activated receptors
2000 StandoutNature
Platelet α-granules: Basic biology and clinical correlates
2009
Versatile Role of Rab27 in Membrane Trafficking: Focus on the Rab27 Effector Families
2005
The mechanosensory protein MEC-6 is a subunit of the C. elegans touch-cell degenerin channel
2002 StandoutNatureNobel
Diclofenac residues as the cause of vulture population decline in Pakistan
2004 StandoutNature
Platelet Activation and Atherothrombosis
2007 Standout
A Munc13/RIM/Rab3 tripartite complex: from priming to plasticity?
2005 StandoutNobel
The regulation of E2F by pRB-family proteins
1998 Standout
The ATP-gated P2X1 Receptor Plays a Pivotal Role in Activation of Aspirin-treated Platelets by Thrombin and Epinephrine
2008 StandoutNobel
The MEC-4 DEG/ENaC channel of Caenorhabditis elegans touch receptor neurons transduces mechanical signals
2004 StandoutNobel
Expressional Regulation of Angiopoietin-1 and -2 and the Tie-1 and -2 Receptor Tyrosine Kinases during Cutaneous Wound Healing: A Comparative Study of Normal and Impaired Repair
2001
A dual thrombin receptor system for platelet activation
1998 Nature
Expression of Factor VIII by Murine Liver Sinusoidal Endothelial Cells
1999
Characterization of BLOC‐2, a Complex Containing the Hermansky–Pudlak Syndrome Proteins HPS3, HPS5 and HPS6
2004
A Complete Genetic Analysis of Neuronal Rab3 Function
2004 StandoutNobel
Local force and geometry sensing regulate cell functions
2006 Standout
CTL secretory lysosomes: biogenesis and secretion of a harmful organelle
2004
Megakaryocytes and beyond: the birth of platelets
2003
Prenylation of Rab GTPases: molecular mechanisms and involvement in genetic disease
2001
Endosome maturation
2011 Standout
Rabphilin regulates SNARE‐dependent re‐priming of synaptic vesicles for fusion
2006 StandoutNobel
COX-2 inhibitors
1999 Standout
Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)
2003
Munc13-4 Is a GTP-Rab27-binding Protein Regulating Dense Core Granule Secretion in Platelets
2004
Neurosensory mechanotransduction
2008 StandoutNobel
Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse
1998
Antibodies to von Willebrand Factor–Cleaving Protease in Acute Thrombotic Thrombocytopenic Purpura
1998 Standout
Guidelines for the Early Management of Adults With Ischemic Stroke
2007 Standout
Hemostasis in the Mouse (Mus musculus): A Review
1999
Slc15a4, AP-3, and Hermansky-Pudlak syndrome proteins are required for Toll-like receptor signaling in plasmacytoid dendritic cells
2010 StandoutNobel
Rab3 Superprimes Synaptic Vesicles for Release: Implications for Short-Term Synaptic Plasticity
2006 StandoutNobel
Rab27a Is Required for Regulated Secretion in Cytotoxic T Lymphocytes
2001
Rab7: roles in membrane trafficking and disease
2009
Mice deficient in LMAN1 exhibit FV and FVIII deficiencies and liver accumulation of α1-antitrypsin
2011 StandoutNobel
Mice with mutations of Dock7 have generalized hypopigmentation and white-spotting but show normal neurological function
2009 StandoutNobel
Tissue Distribution and Regulation of Murine von Willebrand Factor Gene Expression In Vivo
1998
The Roles of Rab27 and Its Effectors in the Regulated Secretory Pathways
2003
The small GTPase Rab27B regulates amylase release from rat parotid acinar cells
2004
Programmed DNA destruction by miniature CRISPR-Cas14 enzymes
2018 StandoutScienceNobel
The Murine Misty Mutation: Phenotypic Effects on Melanocytes, Platelets and Brown Fat
1998
Rab27b localizes to zymogen granules and regulates pancreatic acinar exocytosis
2004
Pleistocene North African genomes link Near Eastern and sub-Saharan African human populations
2018 StandoutScienceNobel
Functional redundancy of Rab27 proteins and the pathogenesis of Griscelli syndrome
2002
A member of a family of sulfate-activating enzymes causes murine brachymorphism
1998
The KEAP1-NRF2 System: a Thiol-Based Sensor-Effector Apparatus for Maintaining Redox Homeostasis
2018 Standout
Wound Healing: A Cellular Perspective
2018 Standout
Molecular phylogenetics and the origins of placental mammals
2001 StandoutNature
Coexpression of IL-5 and Eotaxin-2 in Mice Creates an Eosinophil-Dependent Model of Respiratory Inflammation with Characteristics of Severe Asthma
2007
Putting polyphosphates to the test: evidence against platelet-induced activation of factor XII
2013 StandoutNobel
A dual mechanism controlling the localization and function of exocytic v-SNAREs
2003
TRP ION CHANNELS AND TEMPERATURE SENSATION
2006 StandoutNobel
Occurrence of drugs in German sewage treatment plants and rivers
1998 Standout
Endothelial cells in physiology and in the pathophysiology of vascular disorders.
1998 Standout
Rab27a is a key component of the secretory machinery of azurophilic granules in granulocytes
2007 StandoutNobel
Transcription factor NF-E2 is required for platelet formation independent of the actions of thrombopoeitin/MGDF in megakaryocyte development
1995
A mutation in Rab27a causes the vesicle transport defects observed in ashen mice
2000
Rab27b regulates number and secretion of platelet dense granules
2007
Effects of Disturbed Flow on Vascular Endothelium: Pathophysiological Basis and Clinical Perspectives
2011 Standout
Regulation of Wound Healing by Growth Factors and Cytokines
2003 Standout
E2F-1 Blocks Terminal Differentiation and Causes Proliferation in Transgenic Megakaryocytes
1996
Genetics of Sensory Mechanotransduction
2002 StandoutNobel
Works of M Reddington being referenced
Cocoa: a new mouse model for platelet storage pool deficiency
1988
Survival and Lung Pathology of Mouse Models of Hermansky‐ Pudlak Syndrome and Chediak‐Higashi Syndrome
1999
Molecular markers near the mouse brachymorphic (bm) gene, which affects connective tissues and bleeding time
1996
Sandy: a new mouse model for platelet storage pool deficiency
1991
Inherited prolonged bleeding time and platelet storage pool deficiency in the subtle gray (sut) mouse.
1996
Platelet storage pool deficiency associated with inherited abnormalities of the inner ear in the mouse pigment mutants muted and mocha
1991
Inherited thrombocytopenia caused by reduced platelet production in mice with the gunmetal pigment gene mutation
1995
The RIIIS/J inbred mouse strain as a model for von Willebrand disease
1990
von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor gene [published erratum appears in Blood 1995 Sep 15;86(6):2461]
1994
von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor gene [published erratum appears in Blood 1995 Sep 15;86(6):2461]
1994
The regulation of platelet-dense granules by Rab27a in the ashen mouse, a model of Hermansky-Pudlak and Griscelli syndromes, is granule-specific and dependent on genetic background
2002
von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor gene
1995
Immature dense granules in platelets from mice with platelet storage pool disease
1987
Red Cell Flexibility and Platelet Aggregation in Patients with Chronic Obstructive Vascular Disease (COAD) and Study of Therapeutic Approaches
1984
Inherited abnormalities in platelet organelles and platelet formation and associated altered expression of low molecular weight guanosine triphosphate-binding proteins in the mouse pigment mutant gunmetal
1993
Immature dense granules in platelets from mice with platelet storage pool disease
1987