A.Jeanne Hymes: search on Z-Library

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1

Assay of galactosyltransferase by high-performance liquid chromatography

A.Jeanne Hymes, Franklin Mullinax

Journal:

Analytical Biochemistry

Year:

1984

Language:

english

File:

PDF, 369 KB

english, 1984

2

Biotinylation of biotinidase following incubation with biocytin

Jeanne Hymes, Kristin Fleischhauer, Barry Wolf

Journal:

Clinica Chimica Acta

Year:

1995

Language:

english

File:

PDF, 433 KB

english, 1995

3

Delayed-onset profound biotinidase deficiency

Barry Wolf, Robert J. Pomponio, Karen J. Norrgard, Ira T. Lott, E.Regula Baumgartner, Terttu Suormala, Vincent Th. Ramaekers, Turgay Coskun, Aysegul Tokatli, Imran Ozalp, Jeanne Hymes

Journal:

The Journal of Pediatrics

Year:

1998

Language:

english

File:

PDF, 35 KB

english, 1998

4

[Methods in Enzymology] Vitamins and Coenzymes Part I Volume 279 || [44] Biotinidase in serum and tissues

Year:

1997

Language:

english

File:

PDF, 642 KB

english, 1997

5

Mutations in BTD causing biotinidase deficiency

Jeanne Hymes, Christine M. Stanley, Barry Wolf

Journal:

Year:

2001

Language:

english

File:

PDF, 289 KB

english, 2001

6

Arg538 to Cys mutation in a CpG dinucleotide of the human biotinidase gene is the second most common cause of profound biotinidase deficiency in symptomatic children

Robert J. Pomponio, Karen J. Norrgard, Jeanne Hymes, Thomas R. Reynolds, Gregory A. Buck, Regula Baumgartner, Terttu Suormala, B. Wolf

Journal:

Year:

1997

Language:

english

File:

PDF, 192 KB

english, 1997

7

Biochemical and Immunologic Characterization of Serum Biotinidase in Partial Biotinidase

Hart, P Suzanne, Hymes, Jeanne, Wolf, Barry

Journal:

Pediatric Research

Year:

1992

Language:

english

File:

PDF, 525 KB

english, 1992

8

Human Biotinidase Isn't Just for Recycling Biotin

Hymes, Jeanne, Wolf, Barry

Journal:

Journal of Nutrition

Year:

1999

Language:

english

File:

PDF, 217 KB

english, 1999

9

Double mutation (A171T) and (D444H) is a common cause of profound biotinidase deficiency in children ascertained by newborn screening in the United States

Karen J. Norrgard, Robert J. Pomponio, Katie L. Swango, Jeanne Hymes, Thomas Reynolds, Gregory A. Buck, Barry Wolf

Journal:

Year:

1998

Language:

english

File:

PDF, 356 KB

english, 1998

10

Immunological comparison of biotinidase in serum from normal and biotinidase-deficient individuals

Barry Wolf, James B. Miller, Jeanne Hymes, Julie Secor McVoy, Yuka Ishikawa, Emmanuel Shapira

Journal:

Clinica Chimica Acta

Year:

1987

Language:

english

File:

PDF, 617 KB

english, 1987

11

Examination of the Signal Peptide Region of Human Biotinidase Using a Baculovirus Expression System

Karen J. Norrgard, Jeanne Hymes, Barry Wolf

Journal:

Molecular Genetics and Metabolism

Year:

2000

Language:

english

File:

PDF, 164 KB

english, 2000

12

Biotinidase and its roles in biotin metabolism

Jeanne Hymes, Barry Wolf

Journal:

Clinica Chimica Acta

Year:

1996

Language:

english

File:

PDF, 678 KB

english, 1996

13

Mutation (Q456H) Is the Most Common Cause of Profound Biotinidase Deficiency in Children Ascertained by Newborn Screening in the United States

Karen J. Norrgard, Robert J. Pomponio, Katie L. Swango, Jeanne Hymes, Thomas R. Reynolds, Gregory A. Buck, Barry Wolf

Journal:

Biochemical and Molecular Medicine

Year:

1997

Language:

english

File:

PDF, 166 KB

english, 1997

14

Profound biotinidase deficiency in two asymptomatic adults

Wolf, Barry, Norrgard, Karen, Pomponio, Robert J., Mock, Donald M., Secor McVoy, Julie R., Fleischhauer, Kristin, Shapiro, Steven, Blitzer, Miriam G., Hymes, Jeanne

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 36 KB

english, 1997

15

Identification of alternatively spliced human biotinidase mRNAs and putative localization of endogenous biotinidase

Christine M Stanley, Jeanne Hymes, Barry Wolf

Journal:

Molecular Genetics and Metabolism

Year:

2004

Language:

english

File:

PDF, 4.02 MB

english, 2004

16

Mutation in a Putative Glycosylation Site (N489T) of Biotinidase in the Only Known Japanese Child with Biotinidase Deficiency

Robert J. Pomponio, Akihiro Yamaguchi, Shinichiro Arashima, Jeanne Hymes, Barry Wolf

Journal:

Molecular Genetics and Metabolism

Year:

1998

Language:

english

File:

PDF, 58 KB

english, 1998

17

Isoforms of human serum biotinidase

P.Suzanne Hart, Jeanne Hymes, Barry Wolf

Journal:

Clinica Chimica Acta

Year:

1991

Language:

english

File:

PDF, 699 KB

english, 1991

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