X. Bing

发表

A missense mutation in pstpip2 is associated with the murine autoinflammatory disorder chronic multifocal osteomyelitis.

P. Ferguson, T. Waldschmidt, H. El-Shanti, 2006, Bone.

An autoinflammatory disease with deficiency of the interleukin-1-receptor antagonist.

P. Gregersen, P. Babyn, E. Remmers, 2009, The New England journal of medicine.

A Common Genetic Variant in TLR1 Enhances Human Neutrophil Priming and Impacts Length of Intensive Care Stay in Pediatric Sepsis

H. Wong, P. Ferguson, C. Ahn, 2016, The Journal of Immunology.

Recessive coding and regulatory mutations in FBLIM1 underlie the pathogenesis of chronic recurrent multifocal osteomyelitis (CRMO)

G. Velez, A. Bassuk, V. Mahajan, 2017, PloS one.

PHAGOCYTES , GRANULOCYTES , AND MYELOPOIESIS The F-BAR protein PSTPIP 1 controls extracellular matrix degradation and fi lopodia formation in macrophages

P. Ferguson, J. Eickhoff, A. Huttenlocher, 2014 .

PHAGOCYTES , GRANULOCYTES , AND MYELOPOIESIS The F-BAR protein PSTPIP 1 controls extracellular matrix degradation and fi lopodia formation in macrophages

P. Ferguson, J. Eickhoff, A. Huttenlocher, 2014 .

Neutrophil dysfunction in a family with a SAPHO syndrome-like phenotype.

P. Ferguson, Leah S. Muhle, M. Lokuta, 2008, Arthritis and rheumatism.

Effect of treatment of diabetic rats with dehydroepiandrosterone on vascular and neural function.

E. Davidson, M. Yorek, L. Coppey, 2002, American journal of physiology. Endocrinology and metabolism.

Inflammasome-independent IL-1β mediates autoinflammatory disease in Pstpip2-deficient mice

A. Bassuk, F. Sutterwala, T. Burns, 2014, Proceedings of the National Academy of Sciences.

Impacts Length of Intensive Care Stay in Enhances Human Neutrophil Priming and A Common Genetic Variant in TLR1

Wong, X. Bing, J. Moreland, 2016 .

Dehydroepiandrosterone inhibits intracellular calcium release in β-cells by a plasma membrane-dependent mechanism

L. Love-Homan, Dongmin Liu, S. Deorah, 2006, Steroids.

Efficacy of anti-IL-1 treatment in Majeed syndrome

P. Ferguson, M. Bjerre, H. Hasle, 2012, Annals of the rheumatic diseases.

CASE REPORT: PYELONEPHRITIS CAUSED SOLELY BY ESCHERICHIA HERMANII

Sun Qing, X. Bing, Tong Qing, 2014 .

Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction

T. Wassink, A. Bassuk, D. Mohapatra, 2013, Molecular Psychiatry.

Phenotypic Variability in Majeed Syndrome

P. Ferguson, D. Gopalakrishna, X. Bing, 2016, The Journal of Rheumatology.

Exome Sequencing Reveals RAG1 Mutations in a Child with Autoimmunity and Sterile Chronic Multifocal Osteomyelitis Evolving into Disseminated Granulomatous Disease

A. Bassuk, J. Church, P. Ferguson, 2013, Journal of Clinical Immunology.

Mutations in Extracellular Matrix Genes NID1 and LAMC1 Cause Autosomal Dominant Dandy–Walker Malformation and Occipital Cephaloceles

Alberto Maria Segre, J. Cremer, A. Bassuk, 2013, Human mutation.

Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction

T. Wassink, A. Bassuk, D. Mohapatra, 2014, Molecular Psychiatry.

Erratum: Disruption of the non-canonical Wnt gene PRICKLE2 leads to autism-like behaviors with evidence for hippocampal synaptic dysfunction (Molecular Psychiatry (2013) 18 (1077-1089) DOI: 10.1038/mp.2013.71)

T. Wassink, A. Bassuk, D. Mohapatra, 2014 .

Correction: Recessive coding and regulatory mutations in FBLIM1 underlie the pathogenesis of chronic recurrent multifocal osteomyelitis (CRMO)

G. Velez, A. Bassuk, V. Mahajan, 2017, PLoS ONE.

Exome Sequencing Reveals RAG1 Mutations in a Child with Autoimmunity and Sterile Chronic Multifocal Osteomyelitis Evolving into Disseminated Granulomatous Disease

A. Bassuk, J. Church, P. Ferguson, 2013, Journal of Clinical Immunology.

The F-BAR protein PSTPIP1 controls extracellular matrix degradation and filopodia formation in macrophages.

A. Huttenlocher, C. Seroogy, David A Bennin, 2014, Blood.