List of works - Brent W. Weston

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

scientific article published on July 1999

A fluorescent bisboronic acid compound that selectively labels cells expressing oligosaccharide Lewis X.

scientific article published on 28 April 2015

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

scientific article published in January 2004

Catheter-associated thrombosis in children: single-institution experience and review of pediatric venous thromboembolic disease

scientific article published on March 2014

Childhood non-Hodgkin lymphoma presenting as hemophagocytic syndrome

scientific article published on 01 January 2002

Diboronic acids as fluorescent probes for cells expressing sialyl Lewis X.

scientific article

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

scientific article published on 11 October 2002

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

scientific article published on May 1999

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

scientific article

Familial deficiency of vitamin K-dependent clotting factors

scientific article

Fatigue as marker of thrombocytopenia in childhood idiopathic thrombocytopenic purpura

scientific article published in February 2010

Fluorescent conjugate of sLe(x)-selective bisboronic acid for imaging application.

scientific article published in October 2013

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

scientific article published on 01 June 2000

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

scientific article published on 01 September 2000

Granulomatous-Lymphocytic Interstitial Lung Disease in 22q11.2 Deletion Syndrome: a Case Report and Literature Review

scientific article published on 22 February 2018

Histo-blood group gene polymorphisms as potential genetic modifiers of infection and cystic fibrosis lung disease severity

scientific article

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

scientific article

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

scientific article (publication date: 19 August 1994)

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

scientific article

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

scientific article

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

scientific article

Rare Co-occurrence of Eosinophilic Esophagitis and Type 2B von Willebrand Disease: Implications for Endoscopic Surveillance and Esophageal Dilation

scientific article published on 14 May 2019

Spindle cell lesions of the head and neck mimicking rhabdomyosarcoma in children

scientific article published in March 2002

The first fluorescent diboronic acid sensor specific for hepatocellular carcinoma cells expressing sialyl Lewis X.

scientific article published on April 2004

The incidence of catheter-associated venous thrombosis in noncritically ill children

scientific article

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

scientific article published in April 2000

Tyrosine kinase inhibitor therapy induces remission in a patient with refractory EBF1-PDGFRB-positive acute lymphoblastic leukemia.

scientific article

List of works by Brent W. Weston

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

A fluorescent bisboronic acid compound that selectively labels cells expressing oligosaccharide Lewis X.

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

Catheter-associated thrombosis in children: single-institution experience and review of pediatric venous thromboembolic disease

Childhood non-Hodgkin lymphoma presenting as hemophagocytic syndrome

Diboronic acids as fluorescent probes for cells expressing sialyl Lewis X.

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

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

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

Familial deficiency of vitamin K-dependent clotting factors

Fatigue as marker of thrombocytopenia in childhood idiopathic thrombocytopenic purpura

Fluorescent conjugate of sLe(x)-selective bisboronic acid for imaging application.

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

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

Granulomatous-Lymphocytic Interstitial Lung Disease in 22q11.2 Deletion Syndrome: a Case Report and Literature Review

Histo-blood group gene polymorphisms as potential genetic modifiers of infection and cystic fibrosis lung disease severity

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

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

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

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

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

Rare Co-occurrence of Eosinophilic Esophagitis and Type 2B von Willebrand Disease: Implications for Endoscopic Surveillance and Esophageal Dilation

Spindle cell lesions of the head and neck mimicking rhabdomyosarcoma in children

The first fluorescent diboronic acid sensor specific for hepatocellular carcinoma cells expressing sialyl Lewis X.

The incidence of catheter-associated venous thrombosis in noncritically ill children

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

Tyrosine kinase inhibitor therapy induces remission in a patient with refractory EBF1-PDGFRB-positive acute lymphoblastic leukemia.