Mutations in HYAL1, a member of a tandemly distributed multigene family encoding disparate hyaluronidase activities, cause a newly described lysosomal disorder, mucopolysaccharidosis IX (Q24654385)

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English	Mutations in HYAL1, a member of a tandemly distributed multigene family encoding disparate hyaluronidase activities, cause a newly described lysosomal disorder, mucopolysaccharidosis IX	scientific article

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instance of

scholarly article

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title

Mutations in HYAL1, a member of a tandemly distributed multigene family encoding disparate hyaluronidase activities, cause a newly described lysosomal disorder, mucopolysaccharidosis IX (English)

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main subject

mucopolysaccharidosis IX

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based on heuristic

inferred from title

author

Barbara Triggs-Raine

object named as

B Triggs-Raine

series ordinal

1

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author name string

T J Salo

series ordinal

2

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H Zhang

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3

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B A Wicklow

series ordinal

4

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M R Natowicz

series ordinal

5

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language of work or name

English

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publication date

25 May 1999

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published in

Proceedings of the National Academy of Sciences of the United States of America

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volume

96

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issue

11

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page(s)

6296-300

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cites work

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HYAL2, a human gene expressed in many cells, encodes a lysosomal hyaluronidase with a novel type of specificity

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7 April 2017

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

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The hyaluronidase gene HYAL1 maps to chromosome 3p21.2-p21.3 in human and 9F1-F2 in mouse, a conserved candidate tumor suppressor locus

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Purification and microsequencing of hyaluronidase isozymes from human urine

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Clinical and biochemical manifestations of hyaluronidase deficiency

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7 April 2017

Construction of a 600-kilobase cosmid clone contig and generation of a transcriptional map surrounding the lung cancer tumor suppressor gene (TSG) locus on human chromosome 3p21.3: progress toward the isolation of a lung cancer TSG

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Structures and mechanisms of glycosyl hydrolases

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Hyaluronan: its nature, distribution, functions and turnover

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Hyaluronidases--a group of neglected enzymes

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The human sperm protein PH-20 has hyaluronidase activity.

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Analysis of glycosaminoglycan-degrading enzymes by substrate gel electrophoresis (zymography).

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Enzymic pathways of hyaluronan catabolism

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Human serum hyaluronidase: characterization of a clinical assay.

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Hyaluronan in morphogenesis

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In Vitro Mutagenesis of PH-20 Hyaluronidase from Human Sperm

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reference URL

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based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1073/PNAS.96.11.6296

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ADS bibcode

1999PNAS...96.6296T

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PMC publication ID

26875

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PubMed publication ID

10339581

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ResearchGate publication ID

12958447

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