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Bone Impairment in Phenylketonuria Is Characterized by Circulating Osteoclast Precursors and Activat...

Bone Impairment in Phenylketonuria Is Characterized by Circulating Osteoclast Precursors and Activat...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1292425074

Bone Impairment in Phenylketonuria Is Characterized by Circulating Osteoclast Precursors and Activated T Cell Increase

About this item

Full title

Bone Impairment in Phenylketonuria Is Characterized by Circulating Osteoclast Precursors and Activated T Cell Increase

Publisher

United States: Public Library of Science

Journal title

PloS one, 2010-11, Vol.5 (11), p.e14167-e14167

Language

English

Formats

Publication information

Publisher

United States: Public Library of Science

Subjects

Subjects and topics

More information

Scope and Contents

Contents

Phenylketonuria (PKU) is a rare inborn error of metabolism often complicated by a progressive bone impairment of uncertain etiology, as documented by both ionizing and non- ionizing techniques.
Peripheral blood mononuclear cell (PBMC) cultures were performed to study osteoclastogenesis, in the presence or absence of recombinant human monocyte-co...

Alternative Titles

Full title

Bone Impairment in Phenylketonuria Is Characterized by Circulating Osteoclast Precursors and Activated T Cell Increase

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_1292425074

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1292425074

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0014167

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