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P-200 Human Hematopoietic Stem Cells with a Defined Immunodeficiency Transfer Clinical Phenotype to...

P-200 Human Hematopoietic Stem Cells with a Defined Immunodeficiency Transfer Clinical Phenotype to...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_3169801111

P-200 Human Hematopoietic Stem Cells with a Defined Immunodeficiency Transfer Clinical Phenotype to Novel Humanized Mouse Strain

About this item

Full title

P-200 Human Hematopoietic Stem Cells with a Defined Immunodeficiency Transfer Clinical Phenotype to Novel Humanized Mouse Strain

Publisher

Oxford, UK: Oxford University Press

Journal title

Inflammatory bowel diseases, 2013-12, Vol.19 (suppl_1), p.S105-S105

Language

English

Formats

Publication information

Publisher

Oxford, UK: Oxford University Press

More information

Scope and Contents

Contents

Immunopathologies resulting from immunodeficiencies can be caused by a single mutation in a critical regulatory gene as seen in immunodysregulation polyendocrinopathy enteropathy X-linked (IPEX) which harbors a mutation in the forkhead transcription factor, foxP3. One remaining hurdle for advances in personalized medicine is the lack of a robust mo...

Alternative Titles

Full title

P-200 Human Hematopoietic Stem Cells with a Defined Immunodeficiency Transfer Clinical Phenotype to Novel Humanized Mouse Strain

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_3169801111

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_3169801111

Other Identifiers

ISSN

1078-0998

E-ISSN

1536-4844

DOI

10.1097/01.MIB.0000438942.02091.00

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