Published in Lancet Infect Dis on August 01, 2004
Distinct clones of Yersinia pestis caused the black death. PLoS Pathog (2010) 2.48
High throughput, multiplexed pathogen detection authenticates plague waves in medieval Venice, Italy. PLoS One (2011) 1.19
A decade of plague in Mahajanga, Madagascar: insights into the global maritime spread of pandemic plague. MBio (2013) 0.93
Immuno-PCR--a new tool for paleomicrobiology: the plague paradigm. PLoS One (2012) 0.78
Body lice, Yersinia pestis Orientalis, and Black Death. Emerg Infect Dis (2010) 0.75
Yersinia seeks pardon for Black Death. Lancet Infect Dis (2002) 4.43
Was the Black Death caused by Yersinia pestis? Lancet Infect Dis (2004) 1.91
Yersinia pestis genome sequencing identifies patterns of global phylogenetic diversity. Nat Genet (2010) 4.35
Multiple antimicrobial resistance in plague: an emerging public health risk. PLoS One (2007) 4.21
Plague: past, present, and future. PLoS Med (2008) 3.23
New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencing. Nat Commun (2012) 3.18
Development and testing of a rapid diagnostic test for bubonic and pneumonic plague. Lancet (2003) 2.68
GJB2 mutations and degree of hearing loss: a multicenter study. Am J Hum Genet (2005) 2.63
Plague. Lancet (2007) 2.17
Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4). Am J Hum Genet (2004) 1.67
The structure of salmochelins: C-glucosylated enterobactins of Salmonella enterica. Biometals (2004) 1.60
Parity violating energetic difference and enantiomorphous crystalsp-caveats; reinvestigation of tyrosine crystallization. Orig Life Evol Biosph (2006) 1.40
Thyroid hormone deficiency affects postnatal spiking activity and expression of Ca2+ and K+ channels in rodent inner hair cells. J Neurosci (2007) 1.39
A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations. Cell Physiol Biochem (2004) 1.32
Epidemiologic features of four successive annual outbreaks of bubonic plague in Mahajanga, Madagascar. Emerg Infect Dis (2002) 1.29
First isolation and direct evidence for the existence of large small-mammal reservoirs of Leptospira sp. in Madagascar. PLoS One (2010) 1.25
Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations. Hum Genet (2002) 1.23
Epidemiological trends for human plague in Madagascar during the second half of the 20th century: a survey of 20,900 notified cases. Trop Med Int Health (2006) 1.21
Differential expression of otoferlin in brain, vestibular system, immature and mature cochlea of the rat. Eur J Neurosci (2006) 1.21
Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell. Hum Mol Genet (2009) 1.21
Phylogeography and molecular epidemiology of Yersinia pestis in Madagascar. PLoS Negl Trop Dis (2011) 1.19
A 4-bp insertion in the eya-homologous region (eyaHR) of EYA4 causes hearing impairment in a Hungarian family linked to DFNA10. Mol Med (2002) 1.14
A genomic screening approach to the structure-guided identification of drug candidates from natural sources. Chembiochem (2007) 1.13
Technical note: a rapid diagnostic test detects plague in ancient human remains: an example of the interaction between archeological and biological approaches (southeastern France, 16th-18th centuries). Am J Phys Anthropol (2008) 1.08
Genetic heterogeneity of deafness phenotypes linked to DFNA4. Am J Med Genet A (2005) 1.05
Loss of heterozygosity and promoter methylation, but not mutation, may underlie loss of TFF1 in gastric carcinoma. Lab Invest (2002) 1.05
IL-4 and IL-13 up-regulate intestinal trefoil factor expression: requirement for STAT6 and de novo protein synthesis. J Immunol (2004) 1.04
Intestinal expression of TFF and related genes during postnatal development in a piglet probiotic trial. Cell Physiol Biochem (2009) 1.03
Aberrant epigenetic patterns in the etiology of gastrointestinal cancers. J Appl Genet (2008) 1.01
Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients. Hum Mutat (2002) 1.01
Comment on "The brain of LB1, Homo floresiensis". Science (2005) 1.00
Planktocyclin, a cyclooctapeptide protease inhibitor produced by the freshwater cyanobacterium Planktothrix rubescens. J Nat Prod (2007) 1.00
Lessons learned about pneumonic plague diagnosis from two outbreaks, Democratic Republic of the Congo. Emerg Infect Dis (2011) 0.99
High frequency of ENG and ALK1/ACVRL1 mutations in German HHT patients. Hum Mutat (2005) 0.99
Down-regulation of TFF expression in gastrointestinal cell lines by cytokines and nuclear factors. Cell Physiol Biochem (2002) 0.98
Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping. Int J Mol Med (2008) 0.98
Arylomycins A and B, new biaryl-bridged lipopeptide antibiotics produced by Streptomyces sp. Tü 6075. II. Structure elucidation. J Antibiot (Tokyo) (2002) 0.95
Study on the movement of Rattus rattus and evaluation of the plague dispersion in Madagascar. Vector Borne Zoonotic Dis (2010) 0.95
Development and evaluation of two simple, rapid immunochromatographic tests for the detection of Yersinia pestis antibodies in humans and reservoirs. PLoS Negl Trop Dis (2009) 0.94
Detection of Yersinia pestis using real-time PCR in patients with suspected bubonic plague. Mol Cell Probes (2010) 0.94
[A rapid diagnostic test for plague detects Yersinia pestis F1 antigen in ancient human remains]. C R Biol (2007) 0.94
A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindness. Am J Ophthalmol (2003) 0.93
Bromobalhimycin and chlorobromobalhimycins--illuminating the potential of halogenases in glycopeptide antibiotic biosyntheses. Chembiochem (2003) 0.93
Second family with hearing impairment linked to 19q13 and refined DFNA4 localisation. Eur J Hum Genet (2002) 0.92
The CpG island methylator phenotype correlates with long-range epigenetic silencing in colorectal cancer. Mol Cancer Res (2008) 0.92
Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma cases. Cancer Genet Cytogenet (2004) 0.92
Coincidence of mutations in different connexin genes in Hungarian patients. Int J Mol Med (2007) 0.92
Cytokine regulation of the trefoil factor family binding protein GKN2 (GDDR/TFIZ1/blottin) in human gastrointestinal epithelial cells. Cell Physiol Biochem (2007) 0.91
The biosynthesis of vancomycin-type glycopeptide antibiotics--a model for oxidative side-chain cross-linking by oxygenases coupled to the action of peptide synthetases. Chembiochem (2005) 0.91
Rab8b GTPase, a protein transport regulator, is an interacting partner of otoferlin, defective in a human autosomal recessive deafness form. Hum Mol Genet (2008) 0.90
Mutasynthesis of glycopeptide antibiotics: variations of vancomycin's AB-ring amino acid 3,5-dihydroxyphenylglycine. J Am Chem Soc (2004) 0.89
Otoferlin couples to clathrin-mediated endocytosis in mature cochlear inner hair cells. J Neurosci (2013) 0.89
FISH of supernumerary marker chromosomes (SMCs) identifies six diagnostically relevant intervals on chromosome 22q and a novel type of bisatellited SMC(22). Eur J Hum Genet (2005) 0.89
Clinical features and etiology of pneumonia in acid-fast bacillus sputum smear-negative HIV-infected patients hospitalized in Asia and Africa. AIDS (2008) 0.89
Identification of blottin: a novel gastric trefoil factor family-2 binding protein. Proteomics (2006) 0.87
Evaluation of a standardized F1 capsular antigen capture ELISA test kit for the rapid diagnosis of plague. FEMS Immunol Med Microbiol (2004) 0.87
Trefoil factor 2 (TFF2) deficiency in murine digestive tract influences the immune system. Cell Physiol Biochem (2005) 0.86
Frequencies of GJB2 mutations in German control individuals and patients showing sporadic non-syndromic hearing impairment. Hum Mutat (2002) 0.86
Polymorphism in nucleotide excision repair gene XPC correlates with bleomycin-induced chromosomal aberrations. Environ Mol Mutagen (2007) 0.85
Intermediate- and low-methylation epigenotypes do not correspond to CpG island methylator phenotype (low and -zero) in colorectal cancer. Cancer Epidemiol Biomarkers Prev (2012) 0.85
Epigenetic alterations by methylation of RASSF1A and DAPK1 promoter sequences in mammary carcinoma detected in extracellular tumor DNA. Cancer Genet Cytogenet (2010) 0.85
Fluorobalhimycin--a new chapter in glycopeptide antibiotic research. Angew Chem Int Ed Engl (2002) 0.85
Epigenetic control of the E-cadherin gene (CDH1) by CpG methylation in colectomy samples of patients with ulcerative colitis. Genes Chromosomes Cancer (2002) 0.84
Inactivation of the cyclin-dependent kinase inhibitor 2A (CDKN2A) gene in squamous cell carcinoma of the larynx. Mol Carcinog (2004) 0.84
Basics in paleodemography: a comparison of age indicators applied to the early medieval skeletal sample of Lauchheim. Am J Phys Anthropol (2008) 0.83
Three distinct regions of deletion on 13q in squamous cell carcinoma of the larynx. Oncol Rep (2006) 0.83
Active succinate dehydrogenase (SDH) and lack of SDHD mutations in sporadic paragangliomas. Anticancer Res (2005) 0.83
Paleopathological features of the cervical spine in the early middle ages: natural history of degenerative diseases. Neurosurgery (2003) 0.83
Lateral angle: a method for sexing using the petrous bone. Am J Phys Anthropol (2005) 0.82
A novel IRF6 nonsense mutation (Y67X) in a German family with Van der Woude syndrome. Int J Mol Med (2007) 0.82
Influence of polymorphisms in xenobiotic-metabolizing genes and DNA-repair genes on diepoxybutane-induced SCE frequency. Environ Mol Mutagen (2006) 0.82
Epigenetic control of E-cadherin (CDH1) by CpG methylation in metastasising laryngeal cancer. Oncol Rep (2003) 0.82
Transcriptional control of TFF3 (intestinal trefoil factor) via promoter binding sites for the nuclear factor kappaB and C/EBPbeta. Peptides (2004) 0.82
Immune responses to plague infection in wild Rattus rattus, in Madagascar: a role in foci persistence? PLoS One (2012) 0.81
Aspochalamins A-D and aspochalasin Z produced by the endosymbiotic Fungus Aspergillus niveus LU 9575. II. Structure elucidation. J Antibiot (Tokyo) (2004) 0.81
The 48 bp centromeric repeat is a functionally conserved motif in great apes and man showing protein-binding properties. Electrophoresis (2002) 0.80
Population haplotypes of exon ORF15 of the retinitis pigmentosa GTPase regulator gene in Germany : implications for screening for inherited retinal disorders. Mol Diagn Ther (2006) 0.80
Molecular mass of macromolecules and subunits and the quaternary structure of hemoglobin from the microcrustacean Daphnia magna. FEBS J (2006) 0.79
Factors associated with negative direct sputum examination in Asian and African HIV-infected patients with tuberculosis (ANRS 1260). PLoS One (2011) 0.79
The intestinal factor Tff3 and a miRNA network regulate murine caloric metabolism. RNA Biol (2011) 0.79
Plague circulation and population genetics of the reservoir Rattus rattus: the influence of topographic relief on the distribution of the disease within the Madagascan focus. PLoS Negl Trop Dis (2013) 0.79
GJB2 mutations in patients with non-syndromic hearing loss from Northeastern Hungary. Hum Mutat (2004) 0.79
The otoferlin interactome in neurosensory hair cells: significance for synaptic vesicle release and trans-Golgi network (Review). Int J Mol Med (2011) 0.79
A set of specific miRNAs is connected with murine and human gastric cancer. Genes Chromosomes Cancer (2012) 0.79
The expression of the carboxyl ester lipase gene in pancreas and pancreatic adenocarcinomas. Int J Oncol (2006) 0.78
Trefoil factor family member 2 (Tff2) KO mice are protected from high-fat diet-induced obesity. Obesity (Silver Spring) (2013) 0.78
Lack of Tff3 peptide results in hearing impairment and accelerated presbyacusis. Cell Physiol Biochem (2008) 0.78
Functional analysis of a novel I71N mutation in the GJB2 gene among Southern Egyptians causing autosomal recessive hearing loss. Cell Physiol Biochem (2011) 0.78
Fossil record of meningioma. Lancet (2003) 0.78
Mutational risk in highly repetitive exon ORF15 of the RPGR multidisease gene is not associated with haplotype background. Int J Mol Med (2005) 0.78
Paleopathological examination of medieval spines with exceptional thoracic kyphosis most likely secondary to spinal tuberculosis. Historical vignette. J Neurosurg Spine (2004) 0.78
TFF1 is membrane-associated in breast carcinoma cell line MCF-7. Peptides (2004) 0.77
Increased susceptibility to Yersinia enterocolitica Infection of Tff2 deficient mice. Cell Physiol Biochem (2012) 0.77
Ergic2, a brain specific interacting partner of Otoferlin. Cell Physiol Biochem (2012) 0.77
Promoter selection for the cytosine deaminase suicide gene constructs in gastric cancer. Eur J Gastroenterol Hepatol (2004) 0.77
Molecular phylogenetics employing modern and ancient DNA. J Appl Genet (2003) 0.77
Hirschsprung, RET-SOX and beyond: the challenge of examining non-mendelian traits (Review). Int J Mol Med (2002) 0.76
Analysis of candidate genes for genotypic diagnosis in the long QT syndrome. J Appl Genet (2004) 0.76
Archaeology and prevalence of Paget's disease. J Bone Miner Res (2005) 0.75
Contrasted patterns of selection on MHC-linked microsatellites in natural populations of the Malagasy plague reservoir. PLoS One (2012) 0.75
Temporal expression pattern of Fkbp8 in rodent cochlea. Cell Physiol Biochem (2011) 0.75
Altered miRNA expression patterns in Tff2 knock-out mice correlate with cellular pathways of neoplastic development and caloric metabolism. Int J Mol Med (2012) 0.75