Tetralogy of Fallot is an Uncommon Manifestation of Warts, Hypogammaglobulinemia, Infections, and Myelokathexis Syndrome
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L. Dotta | R. Badolato | F. Locatelli | Y. Bertrand | F. Bachelerie | L. Notarangelo | J. Donadieu | L. Tassone | F. Porta | G. Amendola
[1] T. Fleisher,et al. The CXCR4 antagonist plerixafor corrects panleukopenia in patients with WHIM syndrome. , 2011, Blood.
[2] B. Wood,et al. The CXCR4 antagonist plerixafor is a potential therapy for myelokathexis, WHIM syndrome. , 2011, Blood.
[3] T. Sakmar,et al. CXCR7/CXCR4 Heterodimer Constitutively Recruits β-Arrestin to Enhance Cell Migration* , 2011, The Journal of Biological Chemistry.
[4] L. Dotta,et al. Clinical and genetic features of Warts, Hypogammaglobulinemia, Infections and Myelokathexis (WHIM) syndrome. , 2011, Current molecular medicine.
[5] S. Cai,et al. The role of CXCR7 on the adhesion, proliferation and angiogenesis of endothelial progenitor cells , 2011, Journal of cellular and molecular medicine.
[6] D. Srivastava,et al. The chemokine receptor CXCR7 functions to regulate cardiac valve remodeling , 2011, Developmental dynamics : an official publication of the American Association of Anatomists.
[7] F. Bachelerie. CXCL12/CXCR4-Axis Dysfunctions: Markers of the Rare Immunodeficiency Disorder WHIM Syndrome , 2010, Disease markers.
[8] Y. Zou,et al. An Essential Role of the Cytoplasmic Tail of CXCR4 in G-Protein Signaling and Organogenesis , 2010, PloS one.
[9] Joanne P. Starr,et al. Tetralogy of Fallot: Yesterday and Today , 2010, World Journal of Surgery.
[10] U. Naumann,et al. CXCR7 Functions as a Scavenger for CXCL12 and CXCL11 , 2010, PloS one.
[11] A. Redington,et al. Tetralogy of Fallot , 2009, The Lancet.
[12] F. Baleux,et al. CXCR7 heterodimerizes with CXCR4 and regulates CXCL12-mediated G protein signaling. , 2009, Blood.
[13] F. Baleux,et al. CXCR4 dimerization and beta-arrestin-mediated signaling account for the enhanced chemotaxis to CXCL12 in WHIM syndrome. , 2008, Blood.
[14] Richard P. Harvey,et al. Disrupted cardiac development but normal hematopoiesis in mice deficient in the second CXCL12/SDF-1 receptor, CXCR7 , 2007, Proceedings of the National Academy of Sciences.
[15] Kevin Wei,et al. A novel chemokine receptor for SDF-1 and I-TAC involved in cell survival, cell adhesion, and tumor development , 2006, The Journal of experimental medicine.
[16] M. Thelen,et al. The Chemokine SDF-1/CXCL12 Binds to and Signals through the Orphan Receptor RDC1 in T Lymphocytes* , 2005, Journal of Biological Chemistry.
[17] G. Diaz,et al. WHIM syndrome: A defect in CXCR4 signaling , 2005, Current allergy and asthma reports.
[18] Alain Dupuy,et al. WHIM syndromes with different genetic anomalies are accounted for by impaired CXCR4 desensitization to CXCL12. , 2005, Blood.
[19] R. Gorlin,et al. Mutations in the chemokine receptor gene CXCR4 are associated with WHIM syndrome, a combined immunodeficiency disease , 2003, Nature Genetics.
[20] T. Nagasawa. Role of Chemokine SDF‐1/PBSF and Its Receptor CXCR4 in Blood Vessel Development , 2001, Annals of the New York Academy of Sciences.
[21] T. Nagasawa,et al. A chemokine, SDF-1/PBSF, and its receptor, CXC chemokine receptor 4, as mediators of hematopoiesis. , 2000, International journal of hematology.
[22] B. Gelb,et al. WHIM syndrome, an autosomal dominant disorder: clinical, hematological, and molecular studies. , 2000, American journal of medical genetics.
[23] Masahiko Kuroda,et al. Function of the chemokine receptor CXCR4 in haematopoiesis and in cerebellar development , 1998, Nature.
[24] T. Springer,et al. Molecular cloning and characterization of a murine pre-B-cell growth-stimulating factor/stromal cell-derived factor 1 receptor, a murine homolog of the human immunodeficiency virus 1 entry coreceptor fusin. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[25] C. Krill,et al. CHRONIC IDIOPATHIC GRANULOCYTOPENIA. , 1964, The New England journal of medicine.
[26] W. Zuelzer,et al. "MYELOKATHEXIS"--A NEW FORM OF CHRONIC GRANULOCYTOPENIA. REPORT OF A CASE. , 1964, The New England journal of medicine.
[27] A. Bassett,et al. Patterns of cardiac and extracardiac anomalies in adults with tetralogy of fallot. , 2011, American heart journal.
[28] N. Naumann,et al. WHIM syndrome myelokathexis reproduced in the NOD/SCID mouse xenotransplant model engrafted with healthy human stem cells transduced with C-terminus-truncated CXCR4. , 2007, Blood.