C. West

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The osmotic fragility of erythrocytes after prolonged liquid storage and after reinfusion.

E. Beutler, W. Kuhl, C. West, 1982, Blood.

An improved assay and some properties of phosphoglycolate phosphatase.

E. Beutler, C. West, 1980, Analytical biochemistry.

Hematologic differences between African-Americans and whites: the roles of iron deficiency and alpha-thalassemia on hemoglobin levels and mean corpuscular volume.

Carol West, Ernest Beutler, E. Beutler, 2005, Blood.

Gaucher disease: gene frequencies in the Ashkenazi Jewish population.

R. Mcpherson, E. Beutler, C. West, 1993, American journal of human genetics.

Comment concerning a fluorometric assay for glutathione.

E. Beutler, C. West, 1977, Analytical biochemistry.

Genetic polymorphisms and susceptibility to lung disease

Pauline L. Lee, C. West, K. Crain, 2006, Journal of Negative Results in BioMedicine.

Mutations in the gene encoding cytosolic β-glucosidase in Gaucher disease

E. Beutler, C. West, L. Beutler, 2004 .

Synergy between TLR2 and TLR4: a safety mechanism.

E. Beutler, C. West, T. Gelbart, 2001, Blood cells, molecules & diseases.

Glucosephosphate isomerase (GPI) deficiency mutations associated with hereditary nonspherocytic hemolytic anemia (HNSHA).

L. Forman, E. Beutler, C. West, 1997, Blood cells, molecules & diseases.

Mutations in Jewish patients with Gaucher disease.

E. Beutler, A. Zimran, W. Kuhl, 1992, Blood.

Polymorphisms in the human glucocerebrosidase gene.

E. Beutler, C. West, T. Gelbart, 1992, Genomics.

Autosomal dominant hereditary hemochromatosis associated with a novel ferroportin mutation and unique clinical features.

E. Beutler, C. Andrews, Pauline L. Lee, 2005, Blood cells, molecules & diseases.

SLC40A1 c.1402G→A Results in Aberrant Splicing, Ferroportin Truncation after Glycine 330, and an Autosomal Dominant Hemochromatosis Phenotype

J. Barton, Pauline L. Lee, C. West, 2007, Acta Haematologica.

Ferroportin 1 (SCL40A1) variant associated with iron overload in African-Americans.

C. Vulpe, V. Felitti, J. Barton, 2003, Blood cells, molecules & diseases.

A previously undescribed nonsense mutation of the HFE gene

E. Beutler, C. West, T. Gelbart, 2002, Clinical genetics.

A strategy for cloning the hereditary hemochromatosis gene.

E. Beutler, W. Kuhl, C. West, 1995, Blood cells, molecules & diseases.

Polymorphisms in the 5' flanking region of the HFE gene: linkage disequilibrium and relationship to iron homeostasis.

E. Beutler, C. West, 2002, Blood cells, molecules & diseases.

New diallelic markers in the HLA region of chromosome 6.

E. Beutler, C. West, 1997, Blood cells, molecules & diseases.

Erythrocytosis due to bisphosphoglycerate mutase deficiency with concurrent glucose‐6‐phosphate dehydrogenase (G‐6‐PD) deficiency

J. Hoyer, E. Beutler, C. West, 2004, American journal of hematology.

Effect of oxalate and malonate on red cell metabolism.

L. Forman, E. Beutler, C. West, 1987, Blood.

Mutation analysis of the transferrin receptor-2 gene in patients with iron overload.

E. Beutler, C. West, P. Lee, 2001, Blood cells, molecules & diseases.

The hHFE gene of browsing and grazing rhinoceroses: a possible site of adaptation to a low-iron diet.

I. Wilson, J. Speir, E. Beutler, 2001, Blood cells, molecules & diseases.

Iron overload and prolonged ingestion of iron supplements: Clinical features and mutation analysis of hemochromatosis‐associated genes in four cases

J. Barton, Pauline L. Lee, C. West, 2006, American journal of hematology.

The human glucocerebrosidase gene has two functional ATG initiator codons.

E. Beutler, W. Kuhl, C. West, 1987, American journal of human genetics.

The facile detection of the nt 1226 mutation of glucocerebrosidase by 'mismatched' PCR.

E. Beutler, C. West, T. Gelbart, 1990, Clinica chimica acta; international journal of clinical chemistry.

The effect of additives on red cell 2,3 diphosphoglycerate levels in CPDA preservatives

E. Beutler, C. West, S. Vora, 1989, Transfusion.

FusionGeneinGaucherDisease Implications fortheMolecular Anatomy,Pathogenesis, andDiagnosis ofthisDisorder

A. Zimran, C. West, J. Sorge, 1990 .

High level transcription of the glucocerebrosidase pseudogene in normal subjects and patients with Gaucher disease.

E. Beutler, C. West, J. Sorge, 1990, The Journal of clinical investigation.

Glycolytic enzymes of stored granulocytes

E. Beutler, T. Lane, C. West, 1984, Transfusion.

Measurement of the viability of stored red cells by the single‐isotope technique using 51Cr. Analysis of validity

E. Beutler, C. West, 1984, Transfusion.

The storage of hard-packed red blood cells in citrate-phosphate-dextrose (CPD) and CPD-adenine (CPDA-1).

E. Beutler, C. West, 1979, Blood.

A simple rapid radiometric assay for pyrimidine-5'-nucleotidase.

E. Beutler, C. West, J. Torrance, 1977, The Journal of laboratory and clinical medicine.

Sequence of a cDNA clone encoding a rat Reg-2 protein.

E. Beutler, C. West, T. Kamimura, 1992, Gene.

PREDICTION OF SEVERITY OF GAUCHER'S DISEASE BY IDENTIFICATION OF MUTATIONS AT DNA LEVEL

E. Beutler, A. Zimran, C. West, 1989, The Lancet.

The removal of leukocytes and platelets from whole blood.

E. Beutler, C. West, C West, 1976, The Journal of laboratory and clinical medicine.

A Chimeric Mouse Model of Gaucher Disease

B. Torbett, E. Beutler, C. West, 2002, Molecular medicine.

E. Beutler, C. West, 1983, Clinical chemistry.

Identification of the second common Jewish Gaucher disease mutation makes possible population-based screening for the heterozygous state.

E. Beutler, W. Kuhl, C. West, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Molecular cloning and nucleotide sequence of human glucocerebrosidase cDNA.

E. Beutler, C. West, J. Sorge, 1985, Proceedings of the National Academy of Sciences of the United States of America.

Polymorphisms in glucosylceramide (glucocerebroside) synthase and the Gaucher disease phenotype.

E. Beutler, C. West, 2002, The Israel Medical Association journal : IMAJ.

Metabolic compensation for profound erythrocyte adenylate kinase deficiency. A hereditary enzyme defect without hemolytic anemia.

L. Forman, E. Beutler, W. Kuhl, 1983, The Journal of clinical investigation.

Three genes encoding zinc finger proteins on human chromosome 6p21.3: members of a new subclass of the Kruppel gene family containing the conserved SCAN box domain.

E. Beutler, C. West, T. Gelbart, 1997, Genomics.

A study of genes that may modulate the expression of hereditary hemochromatosis: transferrin receptor-1, ferroportin, ceruloplasmin, ferritin light and heavy chains, iron regulatory proteins (IRP)-1 and -2, and hepcidin.

V. Felitti, E. Beutler, Pauline L. Lee, 2001, Blood cells, molecules & diseases.

Erythrocyte Viability in Blood Salvaged During Total Joint Arthroplasty with Cement

C. Colwell, B. Morris, E. Beutler, 2002, The Journal of bone and joint surgery. American volume.

Mutations in Jewish patients with Gaucher disease

E. Beutler, C. West, T. Gelbart, 1992 .

Large-scale molecular screening for galactosemia alleles in a pan-ethnic population

E. Beutler, C. West, Makoto Suzuki, 2001, Human Genetics.

Seeking candidate mutations that affect iron homeostasis.

E. Beutler, Pauline L. Lee, C. West, 2002, Blood cells, molecules & diseases.

Involvement of the erythroid series in acute myeloid leukemia

E. Beutler, Cage S. Johnson, C. West, 1979 .

G6PD Capetown, a variant of glucose-6-phosphate dehydrogenase.

R. J. Dern, E. Beutler, C. West, 1969, American journal of human genetics.

Electrophoretic polymorphism of glutathione peroxidase

E. Beutler, C. West, B. Beutler, 1974, Annals of human genetics.

Glucosephosphate-isomerase (GPI) deficiency: GPI elyria.

E. Beutler, C. West, W. Muir, 1974, Annals of internal medicine.

Genotypic and phenotypic heterogeneity of African Americans with primary iron overload.

J. Barton, E. Beutler, R. Acton, 2003, Blood cells, molecules & diseases.

Complete correction of the enzymatic defect of type I Gaucher disease fibroblasts by retroviral-mediated gene transfer.

E. Beutler, W. Kuhl, C. West, 1987, Proceedings of the National Academy of Sciences of the United States of America.

Mutation analysis in hereditary hemochromatosis.

C. Venditti, E. Beutler, M. Kosty, 1996, Blood cells, molecules & diseases.

Mechanism of improved maintenance of 2,3-diphosphoglycerate in stored blood by the xanthone compound 2-(2-hydroxyethoxy)-6-(1-H-tetrazole-5-yl)xanthen-9-one (BW A440C).

L. Forman, E. Beutler, C. West, 1988, Biochemical pharmacology.

The effect of 2,3-DPG on the sickling phenomenon.

E. Beutler, C. West, N. Paniker, 1971, Blood.

Prevalence of glucose-6-phosphate dehydrogenase deficiency in sickle-cell disease.

E. Beutler, D. Powars, C. West, 1974, The New England journal of medicine.

Glucose-6-phosphate dehydrogenase deficiency and chronic haemolysis in an English family

E. Huskisson, C. West, B. Murphy, 1970, Journal of clinical pathology.

A glucocerebrosidase fusion gene in Gaucher disease. Implications for the molecular anatomy, pathogenesis, and diagnosis of this disorder.

E. Beutler, A. Zimran, C. West, 1990, The Journal of clinical investigation.

Characterization of two new variants of glucose-phosphate-isomerase deficiency with hereditary nonspherocytic hemolytic anemia.

E. Beutler, D. Powars, C. West, 1972, The Journal of laboratory and clinical medicine.

The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms.

E. Beutler, Pauline L. Lee, C. West, 1998, Blood cells, molecules & diseases.

Uric acid metabolism in starvation.

I. Gilliland, C. West, R. Lloyd‐Mostyn, 1970, Annals of the rheumatic diseases.

SLC40A1 Q248H allele frequencies and Q248H-associated risk of non-HFE iron overload in persons of sub-Saharan African descent.

J. Barton, R. Acton, Pauline L. Lee, 2007, Blood cells, molecules & diseases.

Homology between a human protein and a protein of the green garden pea.

E. Beutler, Pauline L. Lee, W. Kuhl, 1994, Genomics.

The reversibility of N-ethylmaleimide (NEM) alkylation of red cell glutathione.

E. Beutler, C. West, S. Srivastava, 1970, Biochemical and biophysical research communications.

Gaucher disease: retrovirus-mediated correction of the enzymatic defect in cultured cells.

E. Beutler, W. Kuhl, C. West, 1986, Cold Spring Harbor symposia on quantitative biology.

Identification of six new Gaucher disease mutations.

E. Beutler, C. West, T. Gelbart, 1993, Genomics.

The Molecular Biology of Gaucher Disease

E. Beutler, C. West, J. Sorge, 1988 .

Heterogeneity in type I Gaucher disease demonstrated by restriction mapping of the gene.

E. Beutler, C. West, J. Sorge, 1985, Proceedings of the National Academy of Sciences of the United States of America.

Simplified determination of carboxyhemoglobin.

E. Beutler, C. West, 1984, Clinical chemistry.

Glucose-6-phosphate dehydrogenase variants in the chimpanzee.

E. Beutler, C. West, 1978, Biochemical medicine.

Pyridoxine administration in sickle cell disease: an unsuccessful attempt to influence the properties of sickle hemoglobin.

E. Beutler, C. West, N. Paniker, 1972, Biochemical medicine.

Polymorphisms in iron‐responsive binding protein 2 and lack of association with sporadic Parkinson's disease

E. Beutler, Pauline L. Lee, C. West, 2002, Movement disorders : official journal of the Movement Disorder Society.

Red cell glutathione peroxidase polymorphism in Afro-Americans.

E. Beutler, C. West, 1974, American journal of human genetics.

HLA-H and Associated Proteins in Patients with Hemochromatosis

E. Beutler, C. West, T. Gelbart, 1997, Molecular medicine.

Red cell adenylate kinase deficiency: molecular study of 3 new mutations (118G>A, 190G>A, and GAC deletion) associated with hereditary nonspherocytic hemolytic anemia.

E. Beutler, K. Varughese, C. West, 2003, Blood.

Storage of red cell concentrates in CPD-A2 for 42 and 49 days.

E. Beutler, C. West, 1983, The Journal of laboratory and clinical medicine.

Red cell adenylate kinase deficiency: molecular study of 3 new mutations (118G>A, 190G>A, and GAC deletion) associated with hereditary nonspherocytic hemolytic anemia.

E. Beutler, K. Varughese, C. West, 2003, Blood.

hereditary nonspherocytic hemolytic anemia mutations (118G>A, 190G>A, and GAC deletion) associated with Red cell adenylate kinase deficiency: molecular study of 3 new

E. Beutler, K. Varughese, C. West, 2013 .

Tissue distribution of pyrimidine-5'-nucleotidase.

E. Beutler, C. West, 1982, Biochemical medicine.