267 related articles for article (PubMed ID: 17087743)
1. Recurrent CXCR4 sequence variation in a girl with WHIM syndrome.
Alapi K; Erdos M; Kovács G; Maródi L
Eur J Haematol; 2007 Jan; 78(1):86-8. PubMed ID: 17087743
[TBL] [Abstract][Full Text] [Related]
2. Mutations in the chemokine receptor gene CXCR4 are associated with WHIM syndrome, a combined immunodeficiency disease.
Hernandez PA; Gorlin RJ; Lukens JN; Taniuchi S; Bohinjec J; Francois F; Klotman ME; Diaz GA
Nat Genet; 2003 May; 34(1):70-4. PubMed ID: 12692554
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Enhanced function with decreased internalization of carboxy-terminus truncated CXCR4 responsible for WHIM syndrome.
Kawai T; Choi U; Whiting-Theobald NL; Linton GF; Brenner S; Sechler JM; Murphy PM; Malech HL
Exp Hematol; 2005 Apr; 33(4):460-8. PubMed ID: 15781337
[TBL] [Abstract][Full Text] [Related]
5. WHIM syndrome myelokathexis reproduced in the NOD/SCID mouse xenotransplant model engrafted with healthy human stem cells transduced with C-terminus-truncated CXCR4.
Kawai T; Choi U; Cardwell L; DeRavin SS; Naumann N; Whiting-Theobald NL; Linton GF; Moon J; Murphy PM; Malech HL
Blood; 2007 Jan; 109(1):78-84. PubMed ID: 16946301
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [WHIM syndrome].
Erdos M; Maródi L
Orv Hetil; 2007 Jun; 148(25):1173-9. PubMed ID: 17573253
[TBL] [Abstract][Full Text] [Related]
8. Clinical and genetic features of Warts, Hypogammaglobulinemia, Infections and Myelokathexis (WHIM) syndrome.
Dotta L; Tassone L; Badolato R
Curr Mol Med; 2011 Jun; 11(4):317-25. PubMed ID: 21506920
[TBL] [Abstract][Full Text] [Related]
9. Familial occurrence of warts, hypogammaglobulinemia, infections, and myelokathexis (WHIM) syndrome.
Siedlar M; Rudzki Z; Strach M; Trzyna E; Pituch-Noworolska A; Błaut-Szlósarczyk A; Bukowska-Strakova K; Lenart M; Grodzicki T; Zembala M
Arch Immunol Ther Exp (Warsz); 2008; 56(6):419-25. PubMed ID: 19043667
[TBL] [Abstract][Full Text] [Related]
10. The role of a mutation of the CXCR4 gene in WHIM syndrome.
Taniuchi S; Masuda M; Fujii Y; Izawa K; Kanegane H; Kobayashi Y
Haematologica; 2005 Sep; 90(9):1271-2. PubMed ID: 16154852
[TBL] [Abstract][Full Text] [Related]
11. A case of WHIM syndrome associated with diabetes and hypothyroidism.
Takaya J; Fujii Y; Higashino H; Taniuchi S; Nakamura M; Kaneko K
Pediatr Diabetes; 2009 Nov; 10(7):484-6. PubMed ID: 19476565
[TBL] [Abstract][Full Text] [Related]
12. Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients.
Geier CB; Ellison M; Cruz R; Pawar S; Leiss-Piller A; Zmajkovicova K; McNulty SM; Yilmaz M; Evans MO; Gordon S; Ujhazi B; Wiest I; Abolhassani H; Aghamohammadi A; Barmettler S; Bhar S; Bondarenko A; Bolyard AA; Buchbinder D; Cada M; Cavieres M; Connelly JA; Dale DC; Deordieva E; Dorsey MJ; Drysdale SB; Ehl S; Elfeky R; Fioredda F; Firkin F; Förster-Waldl E; Geng B; Goda V; Gonzalez-Granado L; Grunebaum E; Grzesk E; Henrickson SE; Hilfanova A; Hiwatari M; Imai C; Ip W; Jyonouchi S; Kanegane H; Kawahara Y; Khojah AM; Kim VH; Kojić M; Kołtan S; Krivan G; Langguth D; Lau YL; Leung D; Miano M; Mersyanova I; Mousallem T; Muskat M; Naoum FA; Noronha SA; Ouederni M; Ozono S; Richmond GW; Sakovich I; Salzer U; Schuetz C; Seeborg FO; Sharapova SO; Sockel K; Volokha A; von Bonin M; Warnatz K; Wegehaupt O; Weinberg GA; Wong KJ; Worth A; Yu H; Zharankova Y; Zhao X; Devlin L; Badarau A; Csomos K; Keszei M; Pereira J; Taveras AG; Beaussant-Cohen SL; Ong MS; Shcherbina A; Walter JE
J Clin Immunol; 2022 Nov; 42(8):1748-1765. PubMed ID: 35947323
[TBL] [Abstract][Full Text] [Related]
13. Successful umbilical cord blood stem cell transplantation in a child with WHIM syndrome.
Kriván G; Erdos M; Kállay K; Benyó G; Tóth A; Sinkó J; Goda V; Tóth B; Maródi L
Eur J Haematol; 2010 Mar; 84(3):274-5. PubMed ID: 19878273
[No Abstract] [Full Text] [Related]
14. 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]
15. Cerebellar involvement in warts Hypogammaglobulinemia immunodeficiency myelokathexis patients: neuroimaging and clinical findings.
Galli J; Pinelli L; Micheletti S; Palumbo G; Notarangelo LD; Lougaris V; Dotta L; Fazzi E; Badolato R
Orphanet J Rare Dis; 2019 Feb; 14(1):61. PubMed ID: 30819232
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. CXCR4-Specific Nanobodies as Potential Therapeutics for WHIM syndrome.
de Wit RH; Heukers R; Brink HJ; Arsova A; Maussang D; Cutolo P; Strubbe B; Vischer HF; Bachelerie F; Smit MJ
J Pharmacol Exp Ther; 2017 Oct; 363(1):35-44. PubMed ID: 28768817
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. 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]
20. 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]
[Next] [New Search]
