PubRank

Markus Moser

Author PubWeight™ 87.89‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 SILAC mouse for quantitative proteomics uncovers kindlin-3 as an essential factor for red blood cell function. Cell 2008 5.02
2 Stable isotope labeling by amino acids in cell culture (SILAC) and proteome quantitation of mouse embryonic stem cells to a depth of 5,111 proteins. Mol Cell Proteomics 2007 3.60
3 Kindlin-2 controls bidirectional signaling of integrins. Genes Dev 2008 3.15
4 Leukocyte adhesion deficiency-III is caused by mutations in KINDLIN3 affecting integrin activation. Nat Med 2009 2.51
5 Loss of talin1 in platelets abrogates integrin activation, platelet aggregation, and thrombus formation in vitro and in vivo. J Exp Med 2007 2.43
6 Mutations in SIL1 cause Marinesco-Sjögren syndrome, a cerebellar ataxia with cataract and myopathy. Nat Genet 2005 2.38
7 The Kindlins: subcellular localization and expression during murine development. Exp Cell Res 2006 2.36
8 LAD-1/variant syndrome is caused by mutations in FERMT3. Blood 2008 2.22
9 Novel function for blood platelets and podoplanin in developmental separation of blood and lymphatic circulation. Blood 2010 2.04
10 The RGD motif in fibronectin is essential for development but dispensable for fibril assembly. J Cell Biol 2007 1.81
11 Loss of Kindlin-1 causes skin atrophy and lethal neonatal intestinal epithelial dysfunction. PLoS Genet 2008 1.78
12 Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1). J Am Soc Nephrol 2003 1.70
13 Distinct roles for talin-1 and kindlin-3 in LFA-1 extension and affinity regulation. Blood 2012 1.64
14 Bone morphogenic proteins are overexpressed in malignant melanoma and promote cell invasion and migration. Cancer Res 2005 1.49
15 Identification and characterization of Pkhd1, the mouse orthologue of the human ARPKD gene. J Am Soc Nephrol 2002 1.41
16 Impaired channel targeting and retinal degeneration in mice lacking the cyclic nucleotide-gated channel subunit CNGB1. J Neurosci 2005 1.40
17 PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD). Hum Mutat 2004 1.40
18 PINCH1 regulates cell-matrix and cell-cell adhesions, cell polarity and cell survival during the peri-implantation stage. J Cell Sci 2005 1.34
19 Loss of Swiss cheese/neuropathy target esterase activity causes disruption of phosphatidylcholine homeostasis and neuronal and glial death in adult Drosophila. J Neurosci 2005 1.33
20 Kindlin-3-mediated signaling from multiple integrin classes is required for osteoclast-mediated bone resorption. J Cell Biol 2011 1.32
21 Redundant function of the heparan sulfate 6-O-endosulfatases Sulf1 and Sulf2 during skeletal development. Dev Dyn 2008 1.30
22 The molecular basis of leukocyte recruitment and its deficiencies. Mol Immunol 2012 1.30
23 The transcription factor TCFAP2C/AP-2gamma cooperates with CDX2 to maintain trophectoderm formation. Mol Cell Biol 2010 1.23
24 The mechanism of kindlin-mediated activation of integrin αIIbβ3. Curr Biol 2013 1.22
25 Loss of Kindlin-3 in LAD-III eliminates LFA-1 but not VLA-4 adhesiveness developed under shear flow conditions. Blood 2009 1.21
26 Effect of apolipoprotein M on high density lipoprotein metabolism and atherosclerosis in low density lipoprotein receptor knock-out mice. J Biol Chem 2007 1.19
27 Lentivector-mediated RNAi efficiently suppresses prion protein and prolongs survival of scrapie-infected mice. J Clin Invest 2006 1.19
28 PINCH2 is a new five LIM domain protein, homologous to PINCHand localized to focal adhesions. Exp Cell Res 2003 1.16
29 RAGE and ICAM-1 cooperate in mediating leukocyte recruitment during acute inflammation in vivo. Blood 2010 1.14
30 Proper synaptic vesicle formation and neuronal network activity critically rely on syndapin I. EMBO J 2011 1.11
31 CCR7-mediated LFA-1 functions in T cells are regulated by 2 independent ADAP/SKAP55 modules. Blood 2011 1.10
32 Consequences of loss of PINCH2 expression in mice. J Cell Sci 2005 1.08
33 PKHD1 mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease (ARPKD). Hum Mutat 2004 1.06
34 Novel highly sensitive IL-10-beta-lactamase reporter mouse reveals cells of the innate immune system as a substantial source of IL-10 in vivo. J Immunol 2011 1.03
35 The ARF-like GTPase ARFRP1 is essential for lipid droplet growth and is involved in the regulation of lipolysis. Mol Cell Biol 2009 1.03
36 Fussel-15, a novel Ski/Sno homolog protein, antagonizes BMP signaling. Mol Cell Neurosci 2007 1.03
37 Inactivation of anoctamin-6/Tmem16f, a regulator of phosphatidylserine scrambling in osteoblasts, leads to decreased mineral deposition in skeletal tissues. J Bone Miner Res 2013 1.02
38 Disruption of the latent transforming growth factor-beta binding protein-1 gene causes alteration in facial structure and influences TGF-beta bioavailability. Biochim Biophys Acta 2007 1.01
39 GLUT1 messenger RNA and protein induction relates to the malignant transformation of cervical cancer. Am J Clin Pathol 2003 0.98
40 Identification and embryonic expression of a new AP-2 transcription factor, AP-2 epsilon. Dev Dyn 2004 0.98
41 Talin-1 and kindlin-3 regulate alpha4beta1 integrin-mediated adhesion stabilization, but not G protein-coupled receptor-induced affinity upregulation. J Immunol 2011 0.97
42 LMX1B is essential for the maintenance of differentiated podocytes in adult kidneys. J Am Soc Nephrol 2013 0.97
43 Specific expression and regulation of the new melanoma inhibitory activity-related gene MIA2 in hepatocytes. J Biol Chem 2003 0.95
44 Comparative expression analysis of the murine palladin isoforms. Dev Dyn 2008 0.94
45 GLUT1 mRNA and protein expression in ovarian borderline tumors and cancer. Oncology 2004 0.94
46 Cloning and functional characterization of a new Ski homolog, Fussel-18, specifically expressed in neuronal tissues. Lab Invest 2005 0.93
47 Targeted disruption of Slc2a8 (GLUT8) reduces motility and mitochondrial potential of spermatozoa. Mol Membr Biol 2008 0.90
48 Biological role of prolyl 3-hydroxylation in type IV collagen. Proc Natl Acad Sci U S A 2013 0.88
49 A heart-hand syndrome gene: Tfap2b plays a critical role in the development and remodeling of mouse ductus arteriosus and limb patterning. PLoS One 2011 0.88
50 Two biochemically distinct and tissue-specific twinfilin isoforms are generated from the mouse Twf2 gene by alternative promoter usage. Biochem J 2009 0.88
51 The vinculin-DeltaIn20/21 mouse: characteristics of a constitutive, actin-binding deficient splice variant of vinculin. PLoS One 2010 0.87
52 The cartilage-specific transcription factor Sox9 regulates AP-2epsilon expression in chondrocytes. FEBS J 2009 0.86
53 The integrin coactivator Kindlin-3 is not required for lymphocyte diapedesis. Blood 2013 0.86
54 The GTPase ARFRP1 controls the lipidation of chylomicrons in the Golgi of the intestinal epithelium. Hum Mol Genet 2012 0.85
55 Regulation of integrin alpha10 expression in chondrocytes by the transcription factors AP-2epsilon and Ets-1. Biochem Biophys Res Commun 2006 0.85
56 Kindlin-3 regulates integrin activation and adhesion reinforcement of effector T cells. Proc Natl Acad Sci U S A 2013 0.85
57 Altered GLUT4 trafficking in adipocytes in the absence of the GTPase Arfrp1. Biochem Biophys Res Commun 2010 0.82
58 β1 integrin-mediated signals are required for platelet granule secretion and hemostasis in mouse. Blood 2013 0.81
59 Targeted disruption of the mouse Csrp2 gene encoding the cysteine- and glycine-rich LIM domain protein CRP2 result in subtle alteration of cardiac ultrastructure. BMC Dev Biol 2008 0.81
60 Enhanced selection for homologous-recombinant embryonic stem cell clones by Cre recombinase-mediated deletion of the positive selection marker. Transgenic Res 2011 0.80
61 The small RNA expression profile of the developing murine urinary and reproductive systems. FEBS Lett 2010 0.80
62 Bral2 is indispensable for the proper localization of brevican and the structural integrity of the perineuronal net in the brainstem and cerebellum. J Comp Neurol 2012 0.79
63 Validation of a luminescence immunoassay for the detection of PrP(Sc) in brain homogenate. J Virol Methods 2002 0.78
64 Cloning, expression and characterization of the murine orthologue of SBF2, the gene mutated in Charcot-Marie-Tooth disease type 4B2. Gene Expr Patterns 2006 0.78
65 The murine latent transforming growth factor-beta binding protein (Ltbp-1) is alternatively spliced, and maps to a region syntenic to human chromosome 2p21-22. Gene 2003 0.77
66 Twinfilin-2a is dispensable for mouse development. PLoS One 2011 0.77
67 AP-2δ is a crucial transcriptional regulator of the posterior midbrain. PLoS One 2011 0.77
68 Diagnosis, pathogenesis, and treatment prospects in cystic kidney disease. Mol Diagn Ther 2006 0.77
69 MST1-dependent vesicle trafficking regulates neutrophil transmigration through the vascular basement membrane. J Clin Invest 2016 0.75
70 Leukocyte adhesion deficiency-III: when leukocytes cannot stop. Pediatr Res 2010 0.75