Stacie M Anderson

Stacie M Anderson

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Stacie M Anderson

Stacie M Anderson

Publications by authors named "Stacie M Anderson"

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24Publications

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Molecular convergence in ex vivo models of Diamond-Blackfan anemia.

Blood 2017 06 4;129(23):3111-3120. Epub 2017 Apr 4.

Genetics and Molecular Biology Branch, National Human Genome Research Institute (NHGRI), National Institutes of Health, Bethesda, MD.

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http://dx.doi.org/10.1182/blood-2017-01-760462DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465839PMC
June 2017

Age-Dependent Defects of Regulatory B Cells in Wiskott-Aldrich Syndrome Gene Knockout Mice.

PLoS One 2015 8;10(10):e0139729. Epub 2015 Oct 8.

Genetics and Molecular Biology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America; Division of Immunology and Allergy, University Hospital of Lausanne, Lausanne, Switzerland.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0139729PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598155PMC
June 2016

Itk is required for Th9 differentiation via TCR-mediated induction of IL-2 and IRF4.

Nat Commun 2016 Mar 3;7:10857. Epub 2016 Mar 3.

National Human Genome Research Institute, National Institutes of Health, 49 Convent Drive, Bethesda, Maryland 20892, USA.

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http://dx.doi.org/10.1038/ncomms10857DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782063PMC
March 2016

A somatic cell defect is associated with the onset of neurological symptoms in a lysosomal storage disease.

Mol Genet Metab 2013 Sep-Oct;110(1-2):188-90. Epub 2013 Jun 21.

Genetic Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1016/j.ymgme.2013.06.010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3775472PMC
March 2014

Molecular and phenotypic abnormalities of B lymphocytes in patients with Wiskott-Aldrich syndrome.

J Allergy Clin Immunol 2014 Mar 8;133(3):896-9.e4. Epub 2013 Nov 8.

Genetics and Molecular Biology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Md. Electronic address:

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http://dx.doi.org/10.1016/j.jaci.2013.08.050DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3943658PMC
March 2014

Itk-mediated integration of T cell receptor and cytokine signaling regulates the balance between Th17 and regulatory T cells.

J Exp Med 2014 Mar 17;211(3):529-43. Epub 2014 Feb 17.

National Human Genome Research Institute, 2 National Institute of Allergy and Infectious Diseases, 3 National Institute of Arthritis and Musculoskeletal and Skin Diseases, and 4 National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892.

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http://dx.doi.org/10.1084/jem.20131459DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3949578PMC
March 2014

Autoimmune lymphoproliferative syndrome due to FAS mutations outside the signal-transducing death domain: molecular mechanisms and clinical penetrance.

Genet Med 2012 Jan 7;14(1):81-9. Epub 2011 Oct 7.

Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.

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http://dx.doi.org/10.1038/gim.0b013e3182310b7dDOI Listing
January 2012

Defective inhibition of B-cell proliferation by Wiskott-Aldrich syndrome protein-deficient regulatory T cells.

Blood 2011 Jun 22;117(24):6608-11. Epub 2011 Apr 22.

Genetics and Molecular Biology Branch, National Human Genome Research Institute, National Institutes of Health, 49 Convent Drive, Bethesda, MD, USA.

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http://dx.doi.org/10.1182/blood-2010-12-322834DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3123025PMC
June 2011

Requirements for selection of conventional and innate T lymphocyte lineages.

Immunity 2007 Nov;27(5):775-85

National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1016/j.immuni.2007.09.012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2377064PMC
November 2007

Wnt5a inhibits canonical Wnt signaling in hematopoietic stem cells and enhances repopulation.

Proc Natl Acad Sci U S A 2007 Sep 19;104(39):15436-41. Epub 2007 Sep 19.

Genetics and Molecular Biology Branch, National Human Genome Research Institute, Bethesda, MD 20892-4442, USA.

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http://dx.doi.org/10.1073/pnas.0704747104DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1986571PMC
September 2007

Impaired in vitro regulatory T cell function associated with Wiskott-Aldrich syndrome.

Clin Immunol 2007 Jul 18;124(1):41-8. Epub 2007 May 18.

Genetics and Molecular Biology Branch, National Human Genome Research Institute, National Institutes of Health, 49 Convent Dr., Blg. 49, Rm 3A20, Bethesda, MD 20892-4442, USA.

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http://dx.doi.org/10.1016/j.clim.2007.02.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1986664PMC
July 2007

Improved transduction of human sheep repopulating cells by retrovirus vectors pseudotyped with feline leukemia virus type C or RD114 envelopes.

Blood 2005 Jul 17;106(1):51-8. Epub 2005 Mar 17.

Genetics and Molecular Biology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1182/blood-2004-11-4491DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1895126PMC
July 2005

Hmgb3 deficiency deregulates proliferation and differentiation of common lymphoid and myeloid progenitors.

Blood 2005 Jan 9;105(2):627-34. Epub 2004 Sep 9.

Hematopoiesis Section, Genetics and Molecular Biology Branch, National Human Genome Research Institute, Bethesda, MD 20892-4442, USA

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http://dx.doi.org/10.1182/blood-2004-07-2551DOI Listing
January 2005

Differential contribution of Wiskott-Aldrich syndrome protein to selective advantage in T- and B-cell lineages.

Blood 2004 Jan 22;103(2):676-8. Epub 2003 Sep 22.

Disorders of Immunity Section, Genetics and Molecular Biology Branch, National Human Genome Research Institute, National Institutes of Health, 49 Convent Dr, 49/3A20, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1182/blood-2003-05-1739DOI Listing
January 2004

Second-site mutation in the Wiskott-Aldrich syndrome (WAS) protein gene causes somatic mosaicism in two WAS siblings.

J Clin Invest 2003 May;111(9):1389-97

Genetics and Molecular Biology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892-4442, USA.

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http://dx.doi.org/10.1172/JCI15485DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC154438PMC
May 2003