PubRank

Sabine Krause

Author PubWeight™ 36.00‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Imaging of amyloid beta in Alzheimer's disease with 18F-BAY94-9172, a novel PET tracer: proof of mechanism. Lancet Neurol 2008 3.67
2 TraG-like proteins of DNA transfer systems and of the Helicobacter pylori type IV secretion system: inner membrane gate for exported substrates? J Bacteriol 2002 2.04
3 The ubiquitin-selective chaperone CDC-48/p97 links myosin assembly to human myopathy. Nat Cell Biol 2007 2.04
4 5' trans-splicing repair of the PLEC1 gene. J Invest Dermatol 2007 1.77
5 Pathological consequences of VCP mutations on human striated muscle. Brain 2006 1.68
6 Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect. Am J Hum Genet 2011 1.39
7 Curcumin-derived pyrazoles and isoxazoles: Swiss army knives or blunt tools for Alzheimer's disease? ChemMedChem 2008 1.32
8 Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts. Neuromuscul Disord 2009 1.23
9 The phenotypic spectrum of neutral lipid storage myopathy due to mutations in the PNPLA2 gene. J Neurol 2011 1.21
10 No overall hyposialylation in hereditary inclusion body myopathy myoblasts carrying the homozygous M712T GNE mutation. Biochem Biophys Res Commun 2005 1.16
11 The p.G154S mutation of the alpha-B crystallin gene (CRYAB) causes late-onset distal myopathy. Neuromuscul Disord 2010 1.08
12 UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) binds to alpha-actinin 1: novel pathways in skeletal muscle? PLoS One 2008 0.98
13 Influence of UDP-GlcNAc 2-epimerase/ManNAc kinase mutant proteins on hereditary inclusion body myopathy. Biochemistry 2006 0.95
14 ANO5 gene analysis in a large cohort of patients with anoctaminopathy: confirmation of male prevalence and high occurrence of the common exon 5 gene mutation. Hum Mutat 2013 0.95
15 Late-onset autosomal dominant limb girdle muscular dystrophy and Paget's disease of bone unlinked to the VCP gene locus. J Neurol Sci 2010 0.95
16 Preclinical characterization of a novel class of 18F-labeled PET tracers for amyloid-β. J Nucl Med 2012 0.93
17 Dystrophin-deficient pigs provide new insights into the hierarchy of physiological derangements of dystrophic muscle. Hum Mol Genet 2013 0.93
18 Distinctive differences in DNA double-strand break repair between normal urothelial and urothelial carcinoma cells. Mutat Res 2007 0.91
19 CHRND mutation causes a congenital myasthenic syndrome by impairing co-clustering of the acetylcholine receptor with rapsyn. Brain 2006 0.90
20 Severe nemaline myopathy caused by mutations of the stop codon of the skeletal muscle alpha actin gene (ACTA1). Neuromuscul Disord 2006 0.85
21 Proteomic characterization of aggregate components in an intrafamilial variable FHL1-associated myopathy. Neuromuscul Disord 2013 0.85
22 Doxycycline regulation in a single retroviral vector by an autoregulatory loop facilitates controlled gene expression in liver cells. Nucleic Acids Res 2004 0.84
23 Divergent molecular effects of desmin mutations on protein assembly in myofibrillar myopathy. J Neuropathol Exp Neurol 2010 0.83
24 Antigen processing and presentation in human muscle: cathepsin S is critical for MHC class II expression and upregulated in inflammatory myopathies. J Neuroimmunol 2003 0.82
25 In vitro characterization of [18F]-florbetaben, an Aβ imaging radiotracer. Nucl Med Biol 2012 0.82
26 A novel mutation in the myotilin gene (MYOT) causes a severe form of limb girdle muscular dystrophy 1A (LGMD1A). J Neurol 2011 0.80
27 Antisense-mediated VEGF suppression in bladder and breast cancer cells. Cancer Lett 2004 0.79
28 Severe nemaline myopathy associated with consecutive mutations E74D and H75Y on a single ACTA1 allele. Neuromuscul Disord 2009 0.79
29 A new web-based method for automated analysis of muscle histology. BMC Musculoskelet Disord 2013 0.79
30 Novel missense mutation p.A310P in the GNE gene in autosomal-recessive hereditary inclusion-body myopathy/distal myopathy with rimmed vacuoles in an Italian family. Neuromuscul Disord 2010 0.79
31 Analysis of HLA class I and II alleles in sporadic inclusion-body myositis. J Neurol 2003 0.77
32 In vitro supplementation with deoxynucleoside monophosphates rescues mitochondrial DNA depletion. Mol Genet Metab 2012 0.76