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Sexual isolation and speciation in bacteria.
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Report of the ad hoc committee for the re-evaluation of the species definition in bacteriology.
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The refined 1.9 A crystal structure of human alpha-thrombin: interaction with D-Phe-Pro-Arg chloromethylketone and significance of the Tyr-Pro-Pro-Trp insertion segment.
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DNA Mismatch Repair: Functions and Mechanisms
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1984 Nature
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1996
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The Complete Amino Acid Sequence of Low Molecular Mass Urokinase from Human Urine
1982
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Genetic Dissection of Complex Traits
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1994
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2005 StandoutNobel
Covalent structure of human haptoglobin: a serine protease homolog.
1980
[29] Synthesis and sequence-specific proteolysis of hybrid proteins produced in Escherichia coli
1987
EcoK selection vectors for shotgun cloning into M13 and deletion mutagenesls
1985 StandoutNobel
Biodegradable Long-Circulating Polymeric Nanospheres
1994 StandoutScience
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1998 StandoutScience
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2003
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2003
Phospholipid binding properties of human placental anticoagulant protein-I, a member of the lipocortin family
1989
Archaic African and Asian lineages in the genetic ancestry of modern humans.
1997
Declining stroke rates in Californian children with sickle cell disease
2004
Two novel annexins from Drosophila melanogaster. Cloning, characterization, and differential expression in development.
1990 StandoutNobel
Microbiological and Clinical Aspects of Infection Associated with Stenotrophomonas maltophilia
1998 Standout
Sexual Isolation and Speciation in Bacteria
2002
Molecular Origin of Blood‐Based Infrared Spectroscopic Fingerprints**
2021 StandoutNobel
Systematic Review: Hydroxyurea for the Treatment of Adults with Sickle Cell Disease
2008
Expression of embryonic zeta-globin and epsilon-globin chains in a 10- year-old girl with congenital anemia
1993
Safety of hydroxyurea in children with sickle cell anemia: results of the HUG-KIDS study, a phase I/II trial. Pediatric Hydroxyurea Group.
1999
Sustained long-term hematologic efficacy of hydroxyurea at maximum tolerated dose in children with sickle cell disease
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Extended-Spectrum β-Lactamase-ProducingKlebsiellapneumoniaein a Neonatal Intensive Care Unit in the High-Prevalence Area of Athens, Greece
2002
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1996
Neurodevelopmental Outcomes in Children With Congenital Heart Disease: Evaluation and Management
2012 Standout
Long-term hydroxyurea treatment in children with sickle cell disease: tolerance and clinical outcomes.
2006
Random amplified polymorphic DNA and plasmid analyses used in investigation of an outbreak of multiresistant Klebsiella pneumoniae
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Association of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemia.
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Bases physiopathologiques moléculaires et cellulaires du traitement de la drépanocytose
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Drépanocytose et adhérence cellulaire
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Three-Year Follow-Up of Hydroxyurea Treatment in Severely Ill Children with Sickle Cell Disease
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Association between Duffy antigen receptor for chemokines expression and levels of inflammation markers in sickle cell anemia patients
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Erythroid adhesion molecules in sickle cell disease: Effect of hydroxyurea
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Nucleotide sequence evidence of the unicentric origin of the ?C mutation in Africa
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The relative importance of the X‐linked FCP locus and β‐globin haplotypes in determining haemoglobin F levels: a study of SS patients homozygous for βS haplotypes
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Mutation of SFTPC in infantile pulmonary alveolar proteinosis with or without fibrosing lung disease
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Comparative study of Mycobacterium paratuberculosis strains isolated from Crohn's disease and Johne's disease using restriction fragment length polymorphism and arbitrarily primed polymerase chain reaction
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A rare FokI RFLP in the human dopamine D2 receptor gene (DRD2)
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Sex in Escherichia coli does not disrupt the clonal structure of the population: evidence from random amplified polymorphic DNA and restriction-fragment-length polymorphism
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Molecular Analysis of Multiply Recurrent Meningitis Due to Escherichia coli K1 in an Infant
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Strong association between a new marker of hemolysis and glomerulopathy in sickle cell anemia
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Phylogenetic Analysis ofEscherichia coliStrains Causing Neonatal Meningitis Suggests Horizontal Gene Transfer from a Predominant Pool of Highly Virulent B2 Group Strains
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Differential modulation of adhesion molecule expression by hydroxycarbamide in human endothelial cells from the micro- and macrocirculation: potential implications in sickle cell disease vasoocclusive events
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Genetic polymorphism of the mannose-binding protein gene in children with sickle cell disease: identification of three new variant alleles and relationship to infections
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Acute clinical events in 299 homozygous sickle cell patients living in France
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UGT1A1 polymorphism outweighs the modest effect of deletional (−3.7 kb) α‐thalassemia on cholelithogenesis in sickle cell anemia
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Complete sequence of the major outer membrane protein-encoding gene of Chlamydia trachomatis serovar Da
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Long-term hydroxyurea treatment in young sickle cell patients
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Evolutionary Implications of the Frequent Horizontal Transfer of Mismatch Repair Genes
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Left heart opacification with peripheral venous injection of a new saccharide echo contrast agent in dogs
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Commensal Escherichia coli isolates are phylogenetically distributed among geographically distinct human populations
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Genotyping May Provide Rapid Identification of Escherichia coli K1 Organisms That Cause Neonatal Meningitis
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Covalent structures of beta and gamma autolytic derivatives of human alpha-thrombin.
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The Link between Phylogeny and Virulence in Escherichia coli Extraintestinal Infection
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DNA sequence variation in a negative control region 5' to the beta- globin gene correlates with the phenotypic expression of the beta s mutation
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Value and limitations of computer analysis of digital subtraction angiography in the assessment of coronary flow reserve.
1986
The Spectrum of Cardiac Anomalies in Noonan Syndrome as a Result of Mutations in the PTPN11 Gene
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Identification of Regions of the Escherichia coli Chromosome Specific for Neonatal Meningitis-Associated Strains
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Monosaccharides Bound to Hemoglobins in Normal and Diabetic Individuals. Evidence for Glucose, Mannose ansd Galactose as Sugars Released by Methanolysis of the Different Hemoglobin Components
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Molecular epidemiology unravels the complexity of neonatal Escherichia coli acquisition in twins
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A novel sickle cell mutation of yet another origin in Africa: the Cameroon type
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Strategy linking several analytical methods of neonatal screening for sickle cell disease
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Cross-species characterization of the promoter region of the cystic fibrosis transmembrane conductance regulator gene reveals multiple levels of regulation
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Anthropological approach to the heterogeneity of beta-thalassemia mutations in northern Africa.
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Loss of heterozygosity in the chromosomal region 12p12-13 is very common in childhood acute lymphoblastic leukemia and permits the precise localization of a tumor-suppressor gene distinct from p27KIP1
1995
Description and partial characterization of a new chlamydia-like microorganism
1993
Inter-ethnic polymorphism of the ?-globin gene locus control region (LCR) in sickle-cell anemia patients
1993
Fetal Hemoglobin and F-Cell Responses to Long-Term Hydroxyurea Treatment in Young Sickle Cell Patients
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Primary structure of human prethrombin 2 and alpha-thrombin.
1977
Hydroxyurea corrects the dysregulated L-selectin expression and increased H2O2 production of polymorphonuclear neutrophils from patients with sickle cell anemia
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Molecular epidemiology of plasmid spread among extended broad-spectrum beta-lactamase-producing Klebsiella pneumoniae isolates in a pediatric hospital
1993
DNA restriction fragment length polymorphism differentiates crossed from independent infections in nosocomial Xanthomonas maltophilia bacteremia
1991
Haplotypes in tribal Indians bearing the sickle gene: evidence for the unicentric origin of the beta S mutation and the unicentric origin of the tribal populations of India.
1989
Use of ribotyping in epidemiological surveillance of nosocomial outbreaks
1994
Evidence for the genetic unrelatedness of nosocomial vancomycin-resistant Enterococcus faecium strains in a pediatric hospital
1991
A novel δβ fusion gene expresses hemoglobin A (HbA) not Hb Lepore: Senegalese δ0β+thalassemia
2001
Arbitrarily primed polymerase chain reaction provides rapid differentiation of Proteus mirabilis isolates from a pediatric hospital
1993
Origin and spread of beta-globin gene mutations in India, Africa, and Mediterranea: analysis of the 5' flanking and intragenic sequences of beta S and beta C genes.
1991
Transcriptional regulation of rat alpha 1-acid glycoprotein gene by phenobarbital.
1994