J. Hymes

发表

Amino acid homologies between human biotinidase and bacterial aliphatic amidases: putative identification of the active site of biotinidase.

B. Wolf, K. L. Swango, J. Hymes, 2000, Molecular genetics and metabolism.

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

G. Buck, B. Wolf, K. L. Swango, 1998 .

Mutation (Q456H) is the most common cause of profound biotinidase deficiency in children ascertained by newborn screening in the United States.

G. Buck, B. Wolf, K. L. Swango, 1997, Biochemical and molecular medicine.

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

C. Stanley, B. Wolf, J. Hymes, 2004, Molecular genetics and metabolism.

Examination of the signal peptide region of human biotinidase using a baculovirus expression system.

B. Wolf, J. Hymes, K. Norrgard, 2000, Molecular genetics and metabolism.

Biotinylation of biotinidase following incubation with biocytin.

B. Wolf, J. Hymes, K. Fleischhauer, 1995, Clinica chimica acta; international journal of clinical chemistry.

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

T. Suormala, G. Buck, B. Wolf, 1997, Human Genetics.

Delayed-onset profound biotinidase deficiency.

T. Suormala, E. R. Baumgartner, V. Ramaekers, 1998, The Journal of pediatrics.

Human serum biotinidase. cDNA cloning, sequence, and characterization.

G. Buck, B. Wolf, J. Hymes, 1994, The Journal of biological chemistry.

Mutations in BTD causing biotinidase deficiency

C. Stanley, B. Wolf, J. Hymes, 2001, Human mutation.

Mutation in a putative glycosylation site (N489T) of biotinidase in the only known Japanese child with biotinidase deficiency.

B. Wolf, J. Hymes, A. Yamaguchi, 1998, Molecular genetics and metabolism.

Mutations in the Human Biotinidase Gene That Cause Profound Biotinidase Deficiency in Symptomatic Children: Molecular, Biochemical, and Clinical Analysis

G. Buck, B. Wolf, J. Hymes, 1997, Pediatric Research.

Biotinidase and its roles in biotin metabolism.

B. Wolf, J. Hymes, Barry Wolf, 1996, Clinica chimica acta; international journal of clinical chemistry.

Human biotinidase isn't just for recycling biotin.

B. Wolf, J. Hymes, Barry Wolf, 1999, The Journal of nutrition.

Biotinylation of histones by human serum biotinidase: assessment of biotinyl-transferase activity in sera from normal individuals and children with biotinidase deficiency.

B. Wolf, J. Hymes, K. Fleischhauer, 1995, Biochemical and molecular medicine.

Mutations Causing Profound Biotinidase Deficiency in Children Ascertained by Newborn Screening in the United States Occur at Different Frequencies than in Symptomatic Children

B. Wolf, J. Hymes, K. Norrgard, 1999, Pediatric Research.

Profound biotinidase deficiency in two asymptomatic adults.

M. Blitzer, D. Mock, B. Wolf, 1997, American journal of medical genetics.

Double mutation (A171T and D444H) is a common cause of profound biotinidase deficiency in children ascertained by newborn screening the the United States. Mutations in brief no. 128. Online.

G. Buck, B. Wolf, K. L. Swango, 1998, Human mutation.

Biochemical and immunological characterization of serum biotinidase in profound biotinidase deficiency.

B. Wolf, J. Hymes, P. Hart, 1992, American journal of human genetics.

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

J. Miller, B. Wolf, J. S. Secor McVoy, 1987, Clinica chimica acta; international journal of clinical chemistry.

Biotinidase in serum and tissues.

B. Wolf, J. Hymes, K. Fleischhauer, 1997, Methods in enzymology.

Isoforms of human serum biotinidase.

B. Wolf, J. Hymes, P. Hart, 1991, Clinica chimica acta; international journal of clinical chemistry.

Prenatal diagnosis of heterozygosity for biotinidase deficiency by enzymatic and molecular analyses

A. Pandya, G. Buck, P. Melone, 1998, Prenatal diagnosis.

Biochemical and Immunologic Characterization of Serum Biotinidase in Partial Biotinidase

B. Wolf, J. Hymes, P. Hart, 1992, Pediatric Research.

The use of biotinylated compounds or reagents is much more complicated than originally thought

B. Wolf, J. Hymes, 2000, Journal of Neuroscience Methods.

Pneumaturia: Report of a Case in a Diabetic With Review of the Literature

J. Hymes, M. Spring, 1952, Diabetes.

Neurogenic Bladder Dysfunction as a Complication of Diabetes: Report of Seven Cases

J. Hymes, M. Spring, 1953, Diabetes.