Published in Blood on July 20, 2004
Tetraspanins: push and pull in suppressing and promoting metastasis. Nat Rev Cancer (2008) 3.04
Next-generation sequencing of a 40 Mb linkage interval reveals TSPAN12 mutations in patients with familial exudative vitreoretinopathy. Am J Hum Genet (2010) 2.26
Tetraspanin CD151 plays a key role in skin squamous cell carcinoma. Oncogene (2012) 2.16
Targeting of tetraspanin proteins--potential benefits and strategies. Nat Rev Drug Discov (2008) 1.91
Kidney failure in mice lacking the tetraspanin CD151. J Cell Biol (2006) 1.85
CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency. J Clin Invest (2010) 1.79
Blood pressure influences end-stage renal disease of Cd151 knockout mice. J Clin Invest (2011) 1.75
Gain of glycosylation in integrin α3 causes lung disease and nephrotic syndrome. J Clin Invest (2012) 1.66
CD151 accelerates breast cancer by regulating alpha 6 integrin function, signaling, and molecular organization. Cancer Res (2008) 1.64
Deletion of tetraspanin Cd151 results in decreased pathologic angiogenesis in vivo and in vitro. Blood (2006) 1.53
Multiple functions of the integrin alpha6beta4 in epidermal homeostasis and tumorigenesis. Mol Cell Biol (2006) 1.51
A critical role for tetraspanin CD151 in alpha3beta1 and alpha6beta4 integrin-dependent tumor cell functions on laminin-5. Mol Biol Cell (2006) 1.47
Potentiation of the ligand-binding activity of integrin alpha3beta1 via association with tetraspanin CD151. Proc Natl Acad Sci U S A (2005) 1.44
Widespread balancing selection and pathogen-driven selection at blood group antigen genes. Genome Res (2008) 1.40
Deletion of CD151 results in a strain-dependent glomerular disease due to severe alterations of the glomerular basement membrane. Am J Pathol (2008) 1.36
Laminin-binding integrins and their tetraspanin partners as potential antimetastatic targets. Expert Rev Mol Med (2010) 1.30
Review series: The cell biology of renal filtration. J Cell Biol (2015) 1.25
Wound healing is defective in mice lacking tetraspanin CD151. J Invest Dermatol (2006) 1.22
Alport syndrome--insights from basic and clinical research. Nat Rev Nephrol (2012) 1.14
Subfractionation, characterization, and in-depth proteomic analysis of glomerular membrane vesicles in human urine. Kidney Int (2013) 1.04
Deficiency of the tetraspanin CD63 associated with kidney pathology but normal lysosomal function. Mol Cell Biol (2008) 1.04
Tetraspanin CD151 regulates growth of mammary epithelial cells in three-dimensional extracellular matrix: implication for mammary ductal carcinoma in situ. Cancer Res (2010) 1.03
Cell-matrix adhesion of podocytes in physiology and disease. Nat Rev Nephrol (2013) 1.02
Tetraspanins as regulators of the tumour microenvironment: implications for metastasis and therapeutic strategies. Br J Pharmacol (2014) 1.01
Structure-function analysis of tetraspanin CD151 reveals distinct requirements for tumor cell behaviors mediated by α3β1 versus α6β4 integrin. J Biol Chem (2010) 1.00
Integrin-associated CD151 drives ErbB2-evoked mammary tumor onset and metastasis. Neoplasia (2012) 0.99
CD151 restricts the α6 integrin diffusion mode. J Cell Sci (2012) 0.95
Integrins in kidney disease. J Am Soc Nephrol (2013) 0.95
Finding new genes for non-syndromic hearing loss through an in silico prioritization study. PLoS One (2010) 0.90
Tetraspanins and vascular functions. Cardiovasc Res (2009) 0.90
Focal segmental glomerulosclerosis: molecular genetics and targeted therapies. BMC Nephrol (2015) 0.90
The importance of podocyte adhesion for a healthy glomerulus. Front Endocrinol (Lausanne) (2014) 0.89
Molecular identification of collagen 17a1 as a major genetic modifier of laminin gamma 2 mutation-induced junctional epidermolysis bullosa in mice. PLoS Genet (2014) 0.89
Regulatory network decoded from epigenomes of surface ectoderm-derived cell types. Nat Commun (2014) 0.88
The tetraspanins CD9 and CD81 regulate CD9P1-induced effects on cell migration. PLoS One (2010) 0.88
Blood Groups in Infection and Host Susceptibility. Clin Microbiol Rev (2015) 0.88
The role of cell-extracellular matrix interactions in glomerular injury. Exp Cell Res (2012) 0.84
Molecular architecture and function of the hemidesmosome. Cell Tissue Res (2014) 0.83
Crystal Structure of a Full-Length Human Tetraspanin Reveals a Cholesterol-Binding Pocket. Cell (2016) 0.81
Podocytes. F1000Res (2016) 0.81
Age-related changes in cochlear gene expression in normal and shaker 2 mice. J Assoc Res Otolaryngol (2006) 0.80
Tetraspanins CD81 and CD82 facilitate α4β1-mediated adhesion of human erythroblasts to vascular cell adhesion molecule-1. PLoS One (2013) 0.79
Tetraspanins and Transmembrane Adaptor Proteins As Plasma Membrane Organizers-Mast Cell Case. Front Cell Dev Biol (2016) 0.78
Hold tight or you'll fall off: CD151 helps podocytes stick in high-pressure situations. J Clin Invest (2011) 0.78
CD151 represses mammary gland development by maintaining the niches of progenitor cells. Cell Cycle (2014) 0.78
Molecular architecture and function of the hemidesmosome. Cell Tissue Res (2015) 0.77
Reduced susceptibility to two-stage skin carcinogenesis in mice with epidermis-specific deletion of CD151. J Invest Dermatol (2013) 0.77
Do cell junction protein mutations cause an airway phenotype in mice or humans? Am J Respir Cell Mol Biol (2011) 0.77
Generation and characterization of a tetraspanin CD151/integrin α6β1-binding domain competitively binding monoclonal antibody for inhibition of tumor progression in HCC. Oncotarget (2016) 0.76
Histochemical and immunoelectron microscopic analysis of ganglioside GM3 in human kidney. Clin Exp Nephrol (2014) 0.76
Tetraspanin, CD151, is required for maintenance of trigeminal placode identity. J Neurochem (2011) 0.76
CD151: Basis Sequence: Mouse. AFCS Nat Mol Pages (2015) 0.75
The Emerging Role of Tetraspanins in the Proteolytic Processing of the Amyloid Precursor Protein. Front Mol Neurosci (2016) 0.75
The Players: Cells Involved in Glomerular Disease. Clin J Am Soc Nephrol (2016) 0.75
CD151 expression is frequent but unrelated to clinical outcome in head and neck cancer. Clin Oral Investig (2016) 0.75
Scissor sisters: regulation of ADAM10 by the TspanC8 tetraspanins. Biochem Soc Trans (2017) 0.75
EMAGE: a spatial database of gene expression patterns during mouse embryo development. Nucleic Acids Res (2006) 3.48
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach. Nat Genet (2011) 2.51
A band 3-based macrocomplex of integral and peripheral proteins in the RBC membrane. Blood (2003) 2.24
Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype. Blood (2008) 2.23
EMAGE mouse embryo spatial gene expression database: 2010 update. Nucleic Acids Res (2009) 2.16
X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" study. J Am Soc Nephrol (2003) 2.12
Maturing reticulocytes internalize plasma membrane in glycophorin A-containing vesicles that fuse with autophagosomes before exocytosis. Blood (2012) 2.03
The Mouse Limb Anatomy Atlas: an interactive 3D tool for studying embryonic limb patterning. BMC Dev Biol (2008) 1.89
Blood group antibodies and their significance in transfusion medicine. Transfus Med Rev (2007) 1.70
EMAGE--Edinburgh Mouse Atlas of Gene Expression: 2008 update. Nucleic Acids Res (2007) 1.66
Altered expression and allelic association of the hypervariable membrane mucin MUC1 in Helicobacter pylori gastritis. Gastroenterology (2002) 1.63
Targeted gene deletion demonstrates that the cell adhesion molecule ICAM-4 is critical for erythroblastic island formation. Blood (2006) 1.63
Preimplantation genetic diagnosis. Nat Rev Genet (2002) 1.62
The human P(k) histo-blood group antigen provides protection against HIV-1 infection. Blood (2009) 1.55
Expert guidelines for the management of Alport syndrome and thin basement membrane nephropathy. J Am Soc Nephrol (2013) 1.52
The Virtual Fly Brain browser and query interface. Bioinformatics (2011) 1.44
Additional molecular bases of the clinically important p blood group phenotype. Transfusion (2003) 1.43
Legalizing the sale of kidneys for transplantation: suggested guidelines. Isr Med Assoc J (2002) 1.39
The majority of the in vitro erythroid expansion potential resides in CD34(-) cells, outweighing the contribution of CD34(+) cells and significantly increasing the erythroblast yield from peripheral blood samples. Haematologica (2010) 1.39
Web tools for large-scale 3D biological images and atlases. BMC Bioinformatics (2012) 1.38
EMAGE mouse embryo spatial gene expression database: 2014 update. Nucleic Acids Res (2013) 1.37
Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height. Oncotarget (2011) 1.31
Refined genotype-phenotype correlations in cases of chromosome 6p deletion syndromes. Eur J Hum Genet (2004) 1.31
A de novo peptide hexamer with a mutable channel. Nat Chem Biol (2011) 1.30
Chorein detection for the diagnosis of chorea-acanthocytosis. Ann Neurol (2004) 1.28
The BloodGen project: toward mass-scale comprehensive genotyping of blood donors in the European Union and beyond. Transfusion (2007) 1.24
eMouseAtlas, EMAGE, and the spatial dimension of the transcriptome. Mamm Genome (2012) 1.21
The monovalent cation leak in overhydrated stomatocytic red blood cells results from amino acid substitutions in the Rh-associated glycoprotein. Blood (2008) 1.17
The Moraxella adhesin UspA1 binds to its human CEACAM1 receptor by a deformable trimeric coiled-coil. EMBO J (2008) 1.13
Investigating the key membrane protein changes during in vitro erythropoiesis of protein 4.2 (-) cells (mutations Chartres 1 and 2). Haematologica (2010) 1.12
Genetic dysfunction of MT-ATP6 causes axonal Charcot-Marie-Tooth disease. Neurology (2012) 1.11
A clinical service in the UK to predict fetal Rh (Rhesus) D blood group using free fetal DNA in maternal plasma. Ann N Y Acad Sci (2004) 1.09
The value of clinical criteria in identifying patients with X-linked Alport syndrome. Clin J Am Soc Nephrol (2010) 1.07
Fetal genotyping for the K (Kell) and Rh C, c, and E blood groups on cell-free fetal DNA in maternal plasma. Transfusion (2007) 1.06
Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype. Am J Med Genet A (2013) 1.04
Annexin A2 tetramer activates human and murine macrophages through TLR4. Blood (2009) 1.03
A basis set of de novo coiled-coil peptide oligomers for rational protein design and synthetic biology. ACS Synth Biol (2012) 1.00
Autophagy facilitates organelle clearance during differentiation of human erythroblasts: evidence for a role for ATG4 paralogs during autophagosome maturation. Autophagy (2013) 0.98
New mutations in C1GALT1C1 in individuals with Tn positive phenotype. Br J Haematol (2008) 0.97
The ins and outs of human reticulocyte maturation: autophagy and the endosome/exosome pathway. Autophagy (2012) 0.96
Identification and activity of a series of azole-based compounds with lactate dehydrogenase-directed anti-malarial activity. J Biol Chem (2004) 0.96
Phenotypic features in patients with 15q11.2(BP1-BP2) deletion: further delineation of an emerging syndrome. Am J Med Genet A (2014) 0.95
Goodbye to agglutination and all that? Transfusion (2005) 0.95
Mutations in the second zinc finger of human EKLF reduce promoter affinity but give rise to benign and disease phenotypes. Blood (2011) 0.95
Structural basis of substrate specificity in human glyoxylate reductase/hydroxypyruvate reductase. J Mol Biol (2006) 0.94
Clinical utility gene card for: Alport syndrome. Eur J Hum Genet (2011) 0.94
Identification of critical amino-acid residues on the erythroid intercellular adhesion molecule-4 (ICAM-4) mediating adhesion to alpha V integrins. Blood (2003) 0.94
Identification of the components of a glycolytic enzyme metabolon on the human red blood cell membrane. J Biol Chem (2012) 0.93
Identification of six new alleles at the FUT1 and FUT2 loci in ethnically diverse individuals with Bombay and Para-Bombay phenotypes. Transfusion (2006) 0.93
Novel secreted isoform of adhesion molecule ICAM-4: potential regulator of membrane-associated ICAM-4 interactions. Blood (2002) 0.90
Cloning, sequence and expression of the lactate dehydrogenase gene from the human malaria parasite, Plasmodium vivax. Biotechnol Lett (2004) 0.90
AQP3 deficiency in humans and the molecular basis of a novel blood group system, GIL. J Biol Chem (2002) 0.90
Causes of fetal anemia in hemolytic disease due to anti-K. Transfusion (2003) 0.90
Plasmodium falciparum: stage specific effects of a selective inhibitor of lactate dehydrogenase. Exp Parasitol (2005) 0.90
DNA variant databases improve test accuracy and phenotype prediction in Alport syndrome. Pediatr Nephrol (2013) 0.89
Normal prion protein trafficking in cultured human erythroblasts. Blood (2007) 0.89
Molecular basis of the JAHK (RH53) antigen. Transfusion (2005) 0.89
The RKIP (Raf-1 Kinase Inhibitor Protein) conserved pocket binds to the phosphorylated N-region of Raf-1 and inhibits the Raf-1-mediated activated phosphorylation of MEK. Cell Signal (2008) 0.89
Structure of lactate dehydrogenase from Plasmodium vivax: complexes with NADH and APADH. Biochemistry (2005) 0.89
Aortic abnormalities in males with Alport syndrome. Nephrol Dial Transplant (2010) 0.88
The Laminin 511/521-binding site on the Lutheran blood group glycoprotein is located at the flexible junction of Ig domains 2 and 3. Blood (2007) 0.88
A cryptic mitochondrial targeting motif in Atg4D links caspase cleavage with mitochondrial import and oxidative stress. Autophagy (2012) 0.87
McLeod syndrome resulting from a novel XK mutation. Br J Haematol (2003) 0.87
The use of maternal plasma for prenatal RhD blood group genotyping. Methods Mol Biol (2009) 0.87
Fetal RHD genotyping in maternal plasma at 11-13 weeks of gestation. Fetal Diagn Ther (2011) 0.86
Structure, function and significance of Rh proteins in red cells. Curr Opin Hematol (2008) 0.86
Two missense mutations in the CD44 gene encode two new antigens of the Indian blood group system. Transfusion (2007) 0.85
The recognition of local DNA conformation by the human papillomavirus type 6 E2 protein. Nucleic Acids Res (2006) 0.85
Towards universal red blood cells. Nat Biotechnol (2007) 0.85
Adhesive activity of Lu glycoproteins is regulated by interaction with spectrin. Blood (2008) 0.85
Protein flexibility directs DNA recognition by the papillomavirus E2 proteins. Nucleic Acids Res (2010) 0.84
The molecular diversity of Sema7A, the semaphorin that carries the JMH blood group antigens. Transfusion (2007) 0.84
Y chromosome detection by Real Time PCR and pyrophosphorolysis-activated polymerisation using free fetal DNA isolated from maternal plasma. Prenat Diagn (2007) 0.83
Blood group phenotypes resulting from mutations in erythroid transcription factors. Curr Opin Hematol (2012) 0.83
Accessibility, reactivity, and selectivity of side chains within a channel of de novo peptide assembly. J Am Chem Soc (2013) 0.82
Mapping the binding site for gossypol-like inhibitors of Plasmodium falciparum lactate dehydrogenase. Mol Biochem Parasitol (2005) 0.82
An N-terminal GFP tag does not alter the functional expression to the plasma membrane of red cell and kidney anion exchanger (AE1) in mammalian cells. Mol Membr Biol (2002) 0.82
A KEL gene encoding serine at position 193 of the Kell glycoprotein results in expression of KEL1 antigen. Transfusion (2006) 0.82
The internet is parents' main source of information about psychiatric manifestations of 22q11.2 deletion syndrome (22q11.2DS). Eur J Med Genet (2013) 0.82
Clinical and genetic features in autosomal recessive and X-linked Alport syndrome. Pediatr Nephrol (2013) 0.82
Noninvasive genotyping fetal Kell blood group (KEL1) using cell-free fetal DNA in maternal plasma by MALDI-TOF mass spectrometry. Prenat Diagn (2008) 0.81
Correlation of in situ mechanosensitive responses of the Moraxella catarrhalis adhesin UspA1 with fibronectin and receptor CEACAM1 binding. Proc Natl Acad Sci U S A (2011) 0.81
A novel deletion in proximal 22q associated with cardiac septal defects and microcephaly: a case report. Mol Cytogenet (2009) 0.81
Nonsyndromic mental retardation and cryptogenic epilepsy in women with doublecortin gene mutations. Ann Neurol (2003) 0.81
Partial D and weak D: can they be distinguished? Transfus Med (2007) 0.81
alpha-Hemoglobin stabilizing protein is not a suitable marker for a screening test for variant Creutzfeldt-Jakob disease. Transfusion (2008) 0.80
Molecular structure of the extracellular region of Lutheran blood group glycoprotein and location of the laminin binding site. Blood Cells Mol Dis (2008) 0.80
Differential proteomic analysis of human erythroblasts undergoing apoptosis induced by epo-withdrawal. PLoS One (2012) 0.80
The gene involved in X-linked agammaglobulinaemia is a member of the Src family of protein-tyrosine kinases. 1993. J Immunol (2012) 0.80
Tetraspanins CD81 and CD82 facilitate α4β1-mediated adhesion of human erythroblasts to vascular cell adhesion molecule-1. PLoS One (2013) 0.79