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Results of search for 'au:"BEUTLER, E"', page 30 of 37
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Authors
ALVING, A S
BEUTLER, E
Beutler, E
Blume, K G
Carrera, C J
Carson, D A
DERN, R J
Dale, G L
Forman, L
Gelbart, T
Koziol, J A
Kuhl, W
Matsumoto, F
McMillan, R
Piro, L D
Saven, A
Srivastava, S K
West, C
Westwood, B
Zimran, A
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Erythrocytes
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Gaucher Disease
Glucosephosphate Dehydrogenase
Glucosephosphate Dehydrogenase Deficiency
Glucosylceramidase
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581.
Mutations in Jewish patients with Gaucher disease.
[electronic resource]
by
Beutler, E
Gelbart, T
Kuhl, W
Zimran, A
West, C
Producer:
19920514
In:
Blood
vol. 79
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582.
Studying X inactivation.
[electronic resource]
by
Curnutte, J T
Hopkins, P J
Kuhl, W
Beutler, E
Producer:
19920415
In:
Lancet (London, England)
vol. 339
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583.
The genetics of galactose-1-phosphate uridyl transferase deficiency.
[electronic resource]
by
Beutler, E
Baluda, M C
Sturgeon, P
Day, R W
Producer:
19670126
In:
The Journal of laboratory and clinical medicine
vol. 68
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584.
Prolonged remissions in acute myelocytic leukemia in adults.
[electronic resource]
by
Fairbanks, V F
Shanbrom, E
Steinfeld, J L
Beutler, E
Producer:
19680625
In:
JAMA
vol. 204
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585.
A method for the establishment and long-term maintenance of in vitro monocytic cultures with functional and morphological homogeneity.
[electronic resource]
by
Packard, B S
Tavassoli, M
Dale, G L
Beutler, E
Producer:
19821021
In:
Blood
vol. 60
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586.
A strategy for cloning the hereditary hemochromatosis gene.
[electronic resource]
by
Beutler, E
Gelbart, T
West, C
Kuhl, W
Lee, P
Producer:
19960815
In:
Blood cells, molecules & diseases
vol. 21
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587.
The effect of transferrin polymorphisms on iron metabolism.
[electronic resource]
by
Lee, P L
Ho, N J
Olson, R
Beutler, E
Producer:
20000328
In:
Blood cells, molecules & diseases
vol. 25
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588.
Immunological difference between glucose-6-P dehydrogenase and hexose-6-P dehydrogenase from human liver.
[electronic resource]
by
Srivastava, S K
Blume, K G
Beutler, E
Yoshida, A
Producer:
19721214
In:
Nature: New biology
vol. 238
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589.
Studies on human beta-D-N-acetylhexosaminidases. II. Kinetic and structural properties.
[electronic resource]
by
Srivastava, S K
Yoshida, A
Awasthi, Y C
Beutler, E
Producer:
19740529
In:
The Journal of biological chemistry
vol. 249
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590.
Five new Gaucher disease mutations.
[electronic resource]
by
Beutler, E
Gelbart, T
Demina, A
Zimran, A
LeCoutre, P
Producer:
19951005
In:
Blood cells, molecules & diseases
vol. 21
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591.
Commentary on HFE S65C variant is not associated with increased transferrin saturation in voluntary blood donors by Naveen Arya, Subrata Chakrabrati, Robert A. Hegele, Paul C. Adams.
[electronic resource]
by
Beutler, E
Felitti, V J
Ho, N J
Gelbart, T
Producer:
20000328
In:
Blood cells, molecules & diseases
vol. 25
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592.
A previously undescribed frameshift deletion mutation of HFE (c.del277; G93fs) associated with hemochromatosis and iron overload in a C282Y heterozygote.
[electronic resource]
by
Barton, J C
West, C
Lee, P L
Beutler, E
Producer:
20050308
In:
Clinical genetics
vol. 66
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593.
The hemolytic effect of primaquine. VII. Biochemical studies of drug-sensitive erythrocytes.
[electronic resource]
by
BEUTLER, E
DERN, R J
FLANAGAN, C L
ALVING, A S
Producer:
20030501
In:
The Journal of laboratory and clinical medicine
vol. 45
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594.
Erythrocyte fragility and chronic intermittent pigmenturia in a dog.
[electronic resource]
by
LeGrange, S N
Breitschwerdt, E B
Grindem, C B
Beutler, E
Producer:
19950706
In:
Journal of the American Veterinary Medical Association
vol. 206
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595.
The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms.
[electronic resource]
by
Lee, P L
Gelbart, T
West, C
Halloran, C
Beutler, E
Producer:
19981123
In:
Blood cells, molecules & diseases
vol. 24
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596.
Prenatal diagnosis of glucose-6-phosphate-dehydrogenase deficiency.
[electronic resource]
by
Beutler, E
Kuhl, W
Fox, M
Tabsh, K
Crandall, B F
Producer:
19920618
In:
Acta haematologica
vol. 87
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597.
Lasting remissions in hairy-cell leukemia induced by a single infusion of 2-chlorodeoxyadenosine.
[electronic resource]
by
Piro, L D
Carrera, C J
Carson, D A
Beutler, E
Producer:
19900509
In:
The New England journal of medicine
vol. 322
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598.
Molecular abnormalities of a phosphoglycerate kinase variant generated by spontaneous mutation.
[electronic resource]
by
Maeda, M
Bawle, E V
Kulkarni, R
Beutler, E
Yoshida, A
Producer:
19920619
In:
Blood
vol. 79
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599.
Large scale purification of glucocerebrosidase from human placentas.
[electronic resource]
by
Dale, G L
Beutler, E
Fournier, P
Blanc, P
Liautaud, J
Producer:
19810317
In:
Birth defects original article series
vol. 16
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600.
Demonstration of HLA antigens on human skin fibroblasts by the peroxidase-antiperoxidase method.
[electronic resource]
by
Schmidt, G M
Bross, K J
Blume, K G
Beutler, E
Producer:
19800625
In:
Transplantation
vol. 29
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