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SAFER model: Strategic allocation of fundamental epidemic resources

Journal of public health (Oxford, England), 2022-06, Vol.44 (2), p.228-233

2022

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Saving Lives with Tourniquets: A Review of Penetrating Injury Medical Examiner Cases

Prehospital emergency care, 2020-07, Vol.24 (4), p.494-499

2020

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Does an individualized feedback mechanism improve quality of out-of-hospital CPR?

Resuscitation, 2017-04, Vol.113, p.96-100

2017

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Isolation of a novel human alpha (1,3)fucosyltransferase gene and molecular comparison to the human Lewis blood group alpha (1,3/1,4)fucosyltransferase gene. Syntenic, homologous, nonallelic genes encoding enzymes with distinct acceptor substrate specificities

The Journal of biological chemistry, 1992-02, Vol.267 (6), p.4152-4160

1992

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Molecular cloning of a fourth member of a human alpha (1,3)fucosyltransferase gene family. Multiple homologous sequences that determine expression of the Lewis x, sialyl Lewis x, and difucosyl sialyl Lewis x epitopes

The Journal of biological chemistry, 1992-12, Vol.267 (34), p.24575-24584

1992

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Familial deficiency of vitamin K-dependent clotting factors

Haemophilia : the official journal of the World Federation of Hemophilia, 2008-11, Vol.14 (6), p.1209-1213

2008

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Association of the Lewis genotype with cardiovascular risk factors and subclinical carotid atherosclerosis: the Atherosclerosis Risk in Communities (ARIC) study

Journal of internal medicine, 2004-01, Vol.255 (1), p.40-51

2004

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Expression of human α(1,3)fucosyltransferase antisense sequences inhibits selectin-mediated adhesion and liver metastasis of colon carcinoma cells

Cancer research (Chicago, Ill.), 1999-05, Vol.59 (9), p.2127-2135

1999

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Molecular basis for Lewis alpha(1,3/1,4)-fucosyltransferase gene deficiency (FUT3) found in Lewis-negative Indonesian pedigrees

The Journal of biological chemistry, 1994-08, Vol.269 (33), p.20987-20994

1994

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Genetic background of Lewis negative blood group phenotype and its association with atherosclerotic disease in the NHLBI Family Heart Study

Journal of internal medicine, 2000-06, Vol.247 (6), p.689-698

2000

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Distribution of Lewis (FUT3)genotype and allele: frequencies in a biethnic United States population

Annals of hematology, 2002-10, Vol.81 (10), p.558-565

2002

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Molecular basis for plasma alpha(1,3)-fucosyltransferase gene deficiency (FUT6)

The Journal of biological chemistry, 1994-04, Vol.269 (17), p.12662-12671

1994

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Glucose-6-phosphatase mutation G188R confers an atypical glycogen storage disease type 1b phenotype

Pediatric research, 2000-09, Vol.48 (3), p.329-334

2000

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Leukocyte infection by the granulocytic ehrlichiosis agent is linked to expression of a selectin ligand

The Journal of clinical investigation, 1999-02, Vol.103 (3), p.407-412

1999

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A cloned CD15s-negative variant of HL60 cells is deficient in expression of FUT7 and does not adhere to cytokine-stimulated endothelial cells

European journal of haematology, 1999-07, Vol.63 (1), p.42-49

1999

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Chronic active Epstein-Barr virus infection and virus-associated hemophagocytic syndrome

Archives of pathology & laboratory medicine (1976), 1991-05, Vol.115 (5), p.470

1991

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Transfection of α(1,3)fucosyltransferase antisense sequences impairs the proliferative and tumorigenic ability of human colon carcinoma cells

Molecular carcinogenesis, 2000-04, Vol.27 (4), p.280-288

2000

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Physical maps of human α(1,3)fucosyltransferase genes FUT3–FUT6 on chromosomes 19p13.3 and 11q21

Genomics (San Diego, Calif.), 1995-03, Vol.26 (1), p.142-146

1995

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Self-Assessment Feedback Form Improves Quality of Out-of-Hospital CPR

Prehospital emergency care, 2019-01, Vol.23 (1), p.66-73

2019

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Expression of human chromosome 19p alpha(1,3)-fucosyltransferase genes in normal tissues. Alternative splicing, polyadenylation, and isoforms

The Journal of biological chemistry, 1995-08, Vol.270 (34), p.20112-20122

1995

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Specificity, inhibition, and synthetic utility of a recombinant human .alpha.-1,3-fucosyltransferase

Journal of the American Chemical Society, 1992-08, Vol.114 (18), p.7321-7322

1992

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Synthesis and structural analysis using 2-D NMR of sialyl Lewis X (SLex) and Lewis X (Lex) oligosaccharides: ligands related to E-selectin [ELAM-1] binding

Journal of the American Chemical Society, 1992-06, Vol.114 (13), p.5449-5451

1992

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SPINDLE CELL LESIONS OF THE HEAD AND NECK MIMICKING RHABDOMYOSARCOMA IN CHILDREN

Pediatric hematology and oncology, 2002, Vol.19 (2), p.129-134

2002

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S2.1 Structure and function of mammalian glycosyltransferase genes

Glycoconjugate journal, 1993-08, Vol.10 (4), p.232-232

1993

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Steel in war time

Manufacturers Record, 1918-07, Vol.74, p.85-86

Weston, W B

1918

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SAFER model: Strategic allocation of fundamental epidemic resources

Saving Lives with Tourniquets: A Review of Penetrating Injury Medical Examiner Cases

Does an individualized feedback mechanism improve quality of out-of-hospital CPR?

Isolation of a novel human alpha (1,3)fucosyltransferase gene and molecular comparison to the human Lewis blood group alpha (1,3/1,4)fucosyltransferase gene. Syntenic, homologous, nonallelic genes encoding enzymes with distinct acceptor substrate specificities

Molecular cloning of a fourth member of a human alpha (1,3)fucosyltransferase gene family. Multiple homologous sequences that determine expression of the Lewis x, sialyl Lewis x, and difucosyl sialyl Lewis x epitopes

Familial deficiency of vitamin K-dependent clotting factors

Association of the Lewis genotype with cardiovascular risk factors and subclinical carotid atherosclerosis: the Atherosclerosis Risk in Communities (ARIC) study

Expression of human α(1,3)fucosyltransferase antisense sequences inhibits selectin-mediated adhesion and liver metastasis of colon carcinoma cells

Molecular basis for Lewis alpha(1,3/1,4)-fucosyltransferase gene deficiency (FUT3) found in Lewis-negative Indonesian pedigrees

Genetic background of Lewis negative blood group phenotype and its association with atherosclerotic disease in the NHLBI Family Heart Study

Distribution of Lewis (FUT3)genotype and allele: frequencies in a biethnic United States population

Molecular basis for plasma alpha(1,3)-fucosyltransferase gene deficiency (FUT6)

Glucose-6-phosphatase mutation G188R confers an atypical glycogen storage disease type 1b phenotype

Leukocyte infection by the granulocytic ehrlichiosis agent is linked to expression of a selectin ligand

A cloned CD15s-negative variant of HL60 cells is deficient in expression of FUT7 and does not adhere to cytokine-stimulated endothelial cells

Chronic active Epstein-Barr virus infection and virus-associated hemophagocytic syndrome

Transfection of α(1,3)fucosyltransferase antisense sequences impairs the proliferative and tumorigenic ability of human colon carcinoma cells

Physical maps of human α(1,3)fucosyltransferase genes FUT3–FUT6 on chromosomes 19p13.3 and 11q21

Self-Assessment Feedback Form Improves Quality of Out-of-Hospital CPR

Expression of human chromosome 19p alpha(1,3)-fucosyltransferase genes in normal tissues. Alternative splicing, polyadenylation, and isoforms

Specificity, inhibition, and synthetic utility of a recombinant human .alpha.-1,3-fucosyltransferase

Synthesis and structural analysis using 2-D NMR of sialyl Lewis X (SLex) and Lewis X (Lex) oligosaccharides: ligands related to E-selectin [ELAM-1] binding

SPINDLE CELL LESIONS OF THE HEAD AND NECK MIMICKING RHABDOMYOSARCOMA IN CHILDREN

S2.1 Structure and function of mammalian glycosyltransferase genes

Steel in war time

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