Joie Davis

Joie Davis

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Joie Davis

Joie Davis

Publications by authors named "Joie Davis"

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West Nile virus encephalitis in GATA2 deficiency.

Allergy Asthma Clin Immunol 2019 24;15. Epub 2019 Jan 24.

1Division of Allergy, Immunology, and Rheumatology, Department of Pediatrics, Stanford University School of Medicine, 269 Campus Drive, CCSR 3215, MC 5366, Stanford, CA 94305 USA.

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http://dx.doi.org/10.1186/s13223-019-0321-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346581PMC
January 2019

Comprehensive RNAi-based screening of human and mouse TLR pathways identifies species-specific preferences in signaling protein use.

Sci Signal 2016 Jan 5;9(409):ra3. Epub 2016 Jan 5.

Signaling Systems Unit, Laboratory of Systems Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1126/scisignal.aab2191DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381726PMC
January 2016

Natural history of autoimmune lymphoproliferative syndrome associated with FAS gene mutations.

Blood 2014 Mar 7;123(13):1989-99. Epub 2014 Jan 7.

Molecular Development Section, Laboratory of Immunology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD;

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http://www.bloodjournal.org/lookup/doi/10.1182/blood-2013-10
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http://dx.doi.org/10.1182/blood-2013-10-535393DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3968385PMC
March 2014

Lung parenchyma surgery in autosomal dominant hyper-IgE syndrome.

J Clin Immunol 2013 Jul 13;33(5):896-902. Epub 2013 Apr 13.

Laboratory of Clinical Infectious Diseases, NIAID, NIH, NIH Building 10 Room 11 N234, 9000 Rockville Pike, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1007/s10875-013-9890-5DOI Listing
July 2013

Intermediate phenotypes in patients with autosomal dominant hyper-IgE syndrome caused by somatic mosaicism.

J Allergy Clin Immunol 2013 Jun 25;131(6):1586-93. Epub 2013 Apr 25.

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

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http://dx.doi.org/10.1016/j.jaci.2013.02.038DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4103905PMC
June 2013

A rapid ex vivo clinical diagnostic assay for fas receptor-induced T lymphocyte apoptosis.

J Clin Immunol 2013 Feb 11;33(2):479-88. Epub 2012 Oct 11.

Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1007/s10875-012-9811-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3567298PMC
February 2013

Cutaneous manifestations of DOCK8 deficiency syndrome.

Arch Dermatol 2012 Jan 19;148(1):79-84. Epub 2011 Sep 19.

Dermatology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, USA.

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http://dx.doi.org/10.1001/archdermatol.2011.262DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4103903PMC
January 2012

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

A Markov model to analyze cost-effectiveness of screening for severe combined immunodeficiency (SCID).

Mol Genet Metab 2011 Nov 12;104(3):383-9. Epub 2011 Jul 12.

Department of Health Sciences, College of Health and Rehabilitation Sciences: Sargent College, Boston University, Boston, MA 02215, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S109671921100233
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http://dx.doi.org/10.1016/j.ymgme.2011.07.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3205197PMC
November 2011

Coronary artery abnormalities in Hyper-IgE syndrome.

J Clin Immunol 2011 Jun 15;31(3):338-45. Epub 2011 Apr 15.

Immunopathogenesis Section, Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases (NIAID), 10 Center Drive, Bethesda, MD 20892-1899, USA.

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http://link.springer.com/content/pdf/10.1007/s10875-011-9515
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http://link.springer.com/10.1007/s10875-011-9515-9
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http://dx.doi.org/10.1007/s10875-011-9515-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091041PMC
June 2011

FAS haploinsufficiency is a common disease mechanism in the human autoimmune lymphoproliferative syndrome.

J Immunol 2011 May 13;186(10):6035-43. Epub 2011 Apr 13.

Department of Laboratory Medicine, Clinical Center, National Institutes of Health, Bethesda, MD 20814, USA.

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http://dx.doi.org/10.4049/jimmunol.1100021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3725553PMC
May 2011

Paucity of genotype-phenotype correlations in STAT3 mutation positive Hyper IgE Syndrome (HIES).

Clin Immunol 2011 Apr 14;139(1):75-84. Epub 2011 Jan 14.

Laboratory of Clinical Infectious Diseases, Immunopathogenesis Section, National Institute of Allergy and Infectious Disease/NIH, Bethesda, MD 20892, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S152166161100008
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http://dx.doi.org/10.1016/j.clim.2011.01.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3065511PMC
April 2011

Combined immunodeficiency associated with DOCK8 mutations.

N Engl J Med 2009 Nov 23;361(21):2046-55. Epub 2009 Sep 23.

Laboratory of Host Defenses, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1056/NEJMoa0905506DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2965730PMC
November 2009

The spectrum of parkinsonian manifestations associated with glucocerebrosidase mutations.

Arch Neurol 2008 Oct;65(10):1353-7

Section on Molecular Neurogenetics, National Human Genome Research Institute, National Institutes of Health, 35 Convent Dr, MSC 3708, Bldg 35, Room 1A213, Bethesda, MD 20892-3708, USA.

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http://dx.doi.org/10.1001/archneur.65.10.1353DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2629407PMC
October 2008

Gene therapy improves immune function in preadolescents with X-linked severe combined immunodeficiency.

Blood 2007 Jul 16;110(1):67-73. Epub 2007 Mar 16.

Genetics and Molecular Biology Branch, National Human Genome Research Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, MD 20892-1456, USA.

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http://dx.doi.org/10.1182/blood-2006-11-058933DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1896128PMC
July 2007

Causes of death in hyper-IgE syndrome.

J Allergy Clin Immunol 2007 May 1;119(5):1234-40. Epub 2007 Mar 1.

National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892-1684, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S009167490700232
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http://dx.doi.org/10.1016/j.jaci.2006.12.666DOI Listing
May 2007

Brain abnormalities in patients with hyperimmunoglobulin E syndrome.

Pediatrics 2007 May 16;119(5):e1121-5. Epub 2007 Apr 16.

National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.

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http://pediatrics.aappublications.org/content/pediatrics/119
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http://pediatrics.aappublications.org/cgi/doi/10.1542/peds.2
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http://dx.doi.org/10.1542/peds.2006-2649DOI Listing
May 2007

Pneumocystis jiroveci infection in patients with hyper-immunoglobulin E syndrome.

Pediatrics 2006 Oct 28;118(4):e1271-5. Epub 2006 Aug 28.

National Institute of Allergy and Infectious Disease, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD 20892, USA.

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http://pediatrics.aappublications.org/cgi/doi/10.1542/peds.2
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http://dx.doi.org/10.1542/peds.2006-0311DOI Listing
October 2006

Genetic alterations in caspase-10 may be causative or protective in autoimmune lymphoproliferative syndrome.

Hum Genet 2006 Apr 31;119(3):284-94. Epub 2006 Jan 31.

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

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http://dx.doi.org/10.1007/s00439-006-0138-9DOI Listing
April 2006

HLA B44 is associated with decreased severity of autoimmune lymphoproliferative syndrome in patients with CD95 defects (ALPS type Ia).

Clin Immunol 2006 Jan 27;118(1):59-65. Epub 2005 Oct 27.

Genetics and Molecular Biology Branch, National Human Genome Research Institute, National Institutes of Health, 49 Convent Drive, Building 49, Room 4A14, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1016/j.clim.2005.09.006DOI Listing
January 2006

Stickler syndrome: clinical characteristics and diagnostic criteria.

Am J Med Genet A 2005 Oct;138A(3):199-207

Warren Magnuson Grant Clinical Center, National Institutes of Health, Bethesda, Maryland, USA.

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http://dx.doi.org/10.1002/ajmg.a.30955DOI Listing
October 2005

Use of mycophenolate mofetil for chronic, refractory immune cytopenias in children with autoimmune lymphoproliferative syndrome.

Br J Haematol 2005 May;129(4):534-8

Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases/NIH, 10 Center Drive, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1111/j.1365-2141.2005.05496.xDOI Listing
May 2005

Dermatitis and the newborn rash of hyper-IgE syndrome.

Arch Dermatol 2004 Sep;140(9):1119-25

Dermatology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892-1908, USA.

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http://dx.doi.org/10.1001/archderm.140.9.1119DOI Listing
September 2004

Familial immunodeficiency with cutaneous vasculitis, myoclonus, and cognitive impairment.

Am J Med Genet A 2004 Mar;125A(2):145-51

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

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http://dx.doi.org/10.1002/ajmg.a.20595DOI Listing
March 2004

Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity.

J Pediatr 2004 Jan;144(1):93-9

Department of Infectious Diseases and Clinical Immunology, University Children's Hospital, Dr v. Haunersches Kinderspital, Munich, Germany.

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http://dx.doi.org/10.1016/S0022-3476(03)00449-9DOI Listing
January 2004

Mutant deoxynucleotide carrier is associated with congenital microcephaly.

Nat Genet 2002 Sep 19;32(1):175-9. Epub 2002 Aug 19.

National Human Genome Research Institute, National Institutes of Health, 49 Convent Drive, Bethesda, Maryland 20892-4472, USA.

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http://dx.doi.org/10.1038/ng948DOI Listing
September 2002

Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiency.

Nature 2002 Sep;419(6905):395-9

Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.

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http://dx.doi.org/10.1038/nature01063DOI Listing
September 2002

The role of the nurse in cancer genetics.

Cancer Nurs 2002 Jun;25(3):196-206

Urology Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Md. 20892-1873, USA.

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June 2002