162 related articles for article (PubMed ID: 17573253)
21. WHIM syndrome: Immunopathogenesis, treatment and cure strategies.
McDermott DH; Murphy PM
Immunol Rev; 2019 Jan; 287(1):91-102. PubMed ID: 30565238
[TBL] [Abstract][Full Text] [Related]
22. Genotype-phenotype correlations in WHIM syndrome: a systematic characterization of CXCR4
Zmajkovicova K; Pawar S; Maier-Munsa S; Maierhofer B; Wiest I; Skerlj R; Taveras AG; Badarau A
Genes Immun; 2022 Sep; 23(6):196-204. PubMed ID: 36089616
[TBL] [Abstract][Full Text] [Related]
23. Altered leukocyte response to CXCL12 in patients with warts hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome.
Gulino AV; Moratto D; Sozzani S; Cavadini P; Otero K; Tassone L; Imberti L; Pirovano S; Notarangelo LD; Soresina R; Mazzolari E; Nelson DL; Notarangelo LD; Badolato R
Blood; 2004 Jul; 104(2):444-52. PubMed ID: 15026312
[TBL] [Abstract][Full Text] [Related]
24. CXCR4 dimerization and beta-arrestin-mediated signaling account for the enhanced chemotaxis to CXCL12 in WHIM syndrome.
Lagane B; Chow KY; Balabanian K; Levoye A; Harriague J; Planchenault T; Baleux F; Gunera-Saad N; Arenzana-Seisdedos F; Bachelerie F
Blood; 2008 Jul; 112(1):34-44. PubMed ID: 18436740
[TBL] [Abstract][Full Text] [Related]
25. WHIM syndrome caused by a single amino acid substitution in the carboxy-tail of chemokine receptor CXCR4.
Liu Q; Chen H; Ojode T; Gao X; Anaya-O'Brien S; Turner NA; Ulrick J; DeCastro R; Kelly C; Cardones AR; Gold SH; Hwang EI; Wechsler DS; Malech HL; Murphy PM; McDermott DH
Blood; 2012 Jul; 120(1):181-9. PubMed ID: 22596258
[TBL] [Abstract][Full Text] [Related]
26. Clinical and Hematologic Effects of Endotoxin in Warts, Hypogammaglobulinemia, Infections, and Myelokathexis Syndrome Model Mice.
Majumdar S; Gao JL; Pontejo SM; Balabanian K; Bachelerie F; Murphy PM
Immunohorizons; 2022 Jul; 6(7):543-558. PubMed ID: 35882421
[TBL] [Abstract][Full Text] [Related]
27. CXCL12/CXCR4-axis dysfunctions: Markers of the rare immunodeficiency disorder WHIM syndrome.
Bachelerie F
Dis Markers; 2010; 29(3-4):189-98. PubMed ID: 21178277
[TBL] [Abstract][Full Text] [Related]
28. WHIM Syndrome Caused by Waldenström's Macroglobulinemia-Associated Mutation CXCR4 (L329fs).
Liu Q; Pan C; Lopez L; Gao J; Velez D; Anaya-O'Brien S; Ulrick J; Littel P; Corns JS; Ellenburg DT; Malech HL; Murphy PM; McDermott DH
J Clin Immunol; 2016 May; 36(4):397-405. PubMed ID: 27059040
[TBL] [Abstract][Full Text] [Related]
29. [WHIM syndrome: presumptive diagnosis based on myelokathexis on bone marrow smear].
Bock I; Dugué F; Loppinet E; Bellanné-Chantelot C; Bénet B
Ann Biol Clin (Paris); 2014; 72(1):111-9. PubMed ID: 24492099
[TBL] [Abstract][Full Text] [Related]
30. Sporadic case of warts, hypogammaglobulinemia, immunodeficiency, and myelokathexis syndrome.
Tarzi MD; Jenner M; Hattotuwa K; Faruqi AZ; Diaz GA; Longhurst HJ
J Allergy Clin Immunol; 2005 Nov; 116(5):1101-5. PubMed ID: 16275383
[TBL] [Abstract][Full Text] [Related]
31. CXCR4 mutations in WHIM syndrome: a misguided immune system?
Diaz GA
Immunol Rev; 2005 Feb; 203():235-43. PubMed ID: 15661033
[TBL] [Abstract][Full Text] [Related]
32. A Sherlock Approach to a Kindred With a Variable Immunohematologic Phenotype.
Walkovich K; Grunebaum E
J Allergy Clin Immunol Pract; 2022 Jul; 10(7):1714-1722. PubMed ID: 35470097
[TBL] [Abstract][Full Text] [Related]
33. Live imaging of neutrophil motility in a zebrafish model of WHIM syndrome.
Walters KB; Green JM; Surfus JC; Yoo SK; Huttenlocher A
Blood; 2010 Oct; 116(15):2803-11. PubMed ID: 20592249
[TBL] [Abstract][Full Text] [Related]
34. WHIM Syndrome With a Novel CXCR4 Variant in a Korean Child.
Shin DW; Park SN; Kim SM; Im K; Kim JA; Hong KT; Choi JY; Hong CR; Park KD; Shin HY; Kang HJ; Kim HK; Lee DS
Ann Lab Med; 2017 Sep; 37(5):446-449. PubMed ID: 28643496
[No Abstract] [Full Text] [Related]
35. Adaptive Immunodeficiency in WHIM Syndrome.
Majumdar S; Murphy PM
Int J Mol Sci; 2018 Dec; 20(1):. PubMed ID: 30577453
[TBL] [Abstract][Full Text] [Related]
36. [Picture in clinical hematology no. 40: Infant case of neutropenia due to WHIM syndrome(myelokathexis)].
Ueda K; Nakagawa S; Osono S; Inada H
Rinsho Ketsueki; 2009 Aug; 50(8):591. PubMed ID: 19915371
[No Abstract] [Full Text] [Related]
37. Oligoclonality, impaired class switch and B-cell memory responses in WHIM syndrome.
Mc Guire PJ; Cunningham-Rundles C; Ochs H; Diaz GA
Clin Immunol; 2010 Jun; 135(3):412-21. PubMed ID: 20226738
[TBL] [Abstract][Full Text] [Related]
38. WHIM syndrome: a genetic disorder of leukocyte trafficking.
Gulino AV
Curr Opin Allergy Clin Immunol; 2003 Dec; 3(6):443-50. PubMed ID: 14612668
[TBL] [Abstract][Full Text] [Related]
39. The negative charge of the 343 site is essential for maintaining physiological functions of CXCR4.
Wang L; Xiong Q; Li P; Chen G; Tariq N; Wu C
BMC Mol Cell Biol; 2021 Jan; 22(1):8. PubMed ID: 33485325
[TBL] [Abstract][Full Text] [Related]
40. [WHIM syndrome: a case report and literature review].
Chen XJ; Yang WY; Wang SC; Guo Y; Liu F; Qi BQ; Chang LX; Zhou JF; An WB; Wei W; Wan Y; Zhu XF
Zhonghua Er Ke Za Zhi; 2013 Mar; 51(3):178-82. PubMed ID: 23751577
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
