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1

6-phosphogluconolactonase Deficiency, a Hereditary Erythrocyte Enzyme Deficiency: Possible Interaction with Glucose-6-phosphate Dehydrogenase Deficiency

Ernest Beutler, Wanda Kuhl and Terri Gelbart

Journal:

Proceedings of the National Academy of Sciences

Year:

1985

Language:

english

File:

PDF, 414 KB

english, 1985

2

Mutation analysis of glucose-6-phosphate dehydrogenase (G6PD) variants in Costa Rica

Ernest Beutler, Wanda Kuhl, German F. R. Sáenz, R. Walter Rodríguez

Journal:

Year:

1991

Language:

english

File:

PDF, 301 KB

english, 1991

3

Some Mexican glucose-6-phosphate dehydrogenase variants revisited

Ernest Beutler, Wanda Kuhl, Eva Ramirez, Ruben Lisker

Journal:

Year:

1991

Language:

english

File:

PDF, 369 KB

english, 1991

4

Linkage between a PvuII restriction fragment length polymorphism and G6PD A-202A/376G: evidence for a single origin of the common G6PD A — mutation

Ernest Beutler, Wanda Kuhl

Journal:

Year:

1990

Language:

english

File:

PDF, 288 KB

english, 1990

5

Blood cell phosphogluconolactonase: assay and properties

Ernest Beutler, Wanda Kuhl, Terri Gelbart

Journal:

British Journal of Haematology

Year:

1986

Language:

english

File:

PDF, 459 KB

english, 1986

6

The tissue distribution of hexosaminidase S and hexosaminidase C

ERNEST BEUTLEE, WANDA KUHL

Journal:

Annals of Human Genetics

Year:

1977

Language:

english

File:

PDF, 517 KB

english, 1977

7

A Strategy for Cloning the Hereditary Hemochromatosis Gene

Ernest Beutler, Terri Gelbart, Carol West, Wanda Kuhl, Pauline Lee

Journal:

Blood Cells, Molecules, and Diseases

Year:

1995

Language:

english

File:

PDF, 1.86 MB

english, 1995

8

Homology between a Human Protein and a Protein of the Green Garden Pea

Pauline Lee, Wanda Kuhl, Terri Gelbart, Takashi Kamimura, Carol West, Ernest Beutler

Journal:

Year:

1994

File:

PDF, 421 KB

1994

9

Guanosine triphosphatase activity in human erythrocyte membranes

Ernest Beutler, Wanda Kuhl

Journal:

Biochimica et Biophysica Acta (BBA) - Biomembranes

Year:

1980

Language:

english

File:

PDF, 393 KB

english, 1980

10

Human red cell glucose-6-phosphate dehydrogenase: All active enzyme has sequence predicted by the X chromosome-encoded cDNA

Ernest Beutler, Terri Gelbart, Wanda Kuhl

Journal:

Year:

1990

Language:

english

File:

PDF, 661 KB

english, 1990

11

Studying X inactivation

Curnutte, JohnT., Hopkins, PenelopeJ., Kuhl, Wanda, Beutler, Ernest

Journal:

Year:

1992

Language:

english

File:

PDF, 179 KB

english, 1992

12

DETECTION OF THE DEFECT OF GAUCHER'S DISEASE AND ITS CARRIER STATE IN PERIPHERAL-BLOOD LEUCOCYTES

Beutler, Ernest, Kuhl, Wanda

Journal:

Year:

1970

Language:

english

File:

PDF, 278 KB

english, 1970

13

Glucocerebrosidase Processing in Normal Fibroblasts and in Fibroblasts from Patients with Type I, Type II, and Type III Gaucher Disease

Ernest Beutler and Wanda Kuhl

Journal:

Proceedings of the National Academy of Sciences

Year:

1986

Language:

english

File:

PDF, 738 KB

english, 1986

14

Complete Correction of the Enzymatic Defect of Type I Gaucher Disease Fibroblasts by Retroviral-Mediated Gene Transfer

Joseph Sorge, Wanda Kuhl, Carol West and Ernest Beutler

Journal:

Proceedings of the National Academy of Sciences

Year:

1987

Language:

english

File:

PDF, 584 KB

english, 1987

15

Identification of the Binding Domain for NADP+of Human Glucose-6-phosphate Dehydrogenase by Sequence Analysis of Mutants

Akira Hirono, Wanda Kuhl, Terri Gelbart, Linda Forman, Virgil F. Fairbanks and Ernest Beutler

Journal:

Proceedings of the National Academy of Sciences

Year:

1989

Language:

english

File:

PDF, 537 KB

english, 1989

16

Galactokinase Deficiency as a Cause of Cataracts

Beutler, Ernest, Matsumoto, Florinda, Kuhl, Wanda, Krill, Alex, Levy, Norman, Sparkes, Robert, Degnan, Mark

Journal:

Boston Medical and Surgical Journal

Year:

1973

File:

PDF, 3.46 MB

1973

17

Masking of Macrocytosis by α-Thalassemia in Blacks with Pernicious Anemia

Green, Ralph, Kuhl, Wanda, Jacobson, Robert, Johnson, Cage, Carmel, Ralph, Beutler, Ernest

Journal:

Boston Medical and Surgical Journal

Year:

1982

File:

PDF, 1.11 MB

1982

18

Definition of the Mutations of G6PD Wayne, G6PD Viangchan, G6PD Jammu, and G6PD ‘Lejeune’

Beutler, Ernest, Westwood, Beryl, Kuhl, Wanda

Journal:

Acta Haematologica

Year:

1991

File:

PDF, 1.65 MB

1991

19

An Assay for Terminal Deoxynucleotidyl Transferase in Leukocytes and Bone Marrow

Beutler, Ernest, Kuhl, Wanda

Journal:

American Journal of Clinical Pathology

Year:

1978

Language:

english

File:

PDF, 422 KB

english, 1978

20

Detection of the 1226 (Jewish) Mutation for Gaucher's Disease by Color PCR: A Means for Studying the Gene Frequency of the Disorder

Zimran, Ari, Kuhl, Wanda C., Beutler, Ernest

Journal:

American Journal of Clinical Pathology

Year:

1990

Language:

english

File:

PDF, 761 KB

english, 1990

21

Prenatal Diagnosis of Glucose-6-Phosphate-Dehydrogenase Deficiency

Beutler, Ernest, Kuhl, Wanda, Fox, Michelle, Tabsh, Khalil, Crandall, Barbara F.

Journal:

Acta Haematologica

Year:

2009

File:

PDF, 698 KB

2009

22

Sodium-Potassium-ATPase Activity Is Influenced by Ethnic Origin and Not by Obesity

Beutler, Ernest, Kuhl, Wanda, Sacks, Peter

Journal:

Boston Medical and Surgical Journal

Year:

1983

Language:

english

File:

PDF, 712 KB

english, 1983

23

Failure of Alglucerase Infused into Gaucher Disease Patients to Localize in Marrow Macrophages

Beutler, Ernest, Kuhl, Wanda, Vaughan, Luke M.

Journal:

Molecular Medicine

Year:

1995

Language:

english

File:

PDF, 663 KB

english, 1995

24

An Assay for Terminal Deoxynucleotidyl Transferase in Leukocytes and Bone Marrow

Beutler, Ernest, Kuhl, Wanda

Journal:

American Journal of Clinical Pathology

Year:

1978

Language:

english

File:

PDF, 495 KB

english, 1978

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