BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 21129284)

  • 1. [Etiology analysis of 38 patients with hemophagocytic syndrome].
    Wang JS; Wang Z; Wu L; Chen X; Feng CC
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2010 Oct; 18(5):1316-20. PubMed ID: 21129284
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A.
    Zur Stadt U; Beutel K; Kolberg S; Schneppenheim R; Kabisch H; Janka G; Hennies HC
    Hum Mutat; 2006 Jan; 27(1):62-8. PubMed ID: 16278825
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Screening the PRF1, UNC13D, STX11, SH2D1A, XIAP, and ITK gene mutations in Chinese children with Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis.
    Zhizhuo H; Junmei X; Yuelin S; Qiang Q; Chunyan L; Zhengde X; Kunling S
    Pediatr Blood Cancer; 2012 Mar; 58(3):410-4. PubMed ID: 21674762
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Perforin gene analaysis in an Iranian family with familial hemophagocytic lymphohistiocytosis.
    Galehdari H; Mohammadi E; Andashti B; Naderi A; Molavi MA
    Iran J Immunol; 2007 Jun; 4(2):122-6. PubMed ID: 17652853
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Characterization of PRF1, STX11 and UNC13D genotype-phenotype correlations in familial hemophagocytic lymphohistiocytosis.
    Horne A; Ramme KG; Rudd E; Zheng C; Wali Y; al-Lamki Z; Gürgey A; Yalman N; Nordenskjöld M; Henter JI
    Br J Haematol; 2008 Oct; 143(1):75-83. PubMed ID: 18710388
    [TBL] [Abstract][Full Text] [Related]  

  • 6. UNC13D is the predominant causative gene with recurrent splicing mutations in Korean patients with familial hemophagocytic lymphohistiocytosis.
    Yoon HS; Kim HJ; Yoo KH; Sung KW; Koo HH; Kang HJ; Shin HY; Ahn HS; Kim JY; Lim YT; Bae KW; Lee KO; Shin JS; Lee ST; Chung HS; Kim SH; Park CJ; Chi HS; Im HJ; Seo JJ
    Haematologica; 2010 Apr; 95(4):622-6. PubMed ID: 20015888
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Advances in studies on hemophagocytic lymphohistiocytosis].
    Luo Z; Tang Y
    Zhonghua Er Ke Za Zhi; 2014 Apr; 52(4):267-70. PubMed ID: 24915913
    [No Abstract]   [Full Text] [Related]  

  • 8. Spectrum and clinical implications of syntaxin 11 gene mutations in familial haemophagocytic lymphohistiocytosis: association with disease-free remissions and haematopoietic malignancies.
    Rudd E; Göransdotter Ericson K; Zheng C; Uysal Z; Ozkan A; Gürgey A; Fadeel B; Nordenskjöld M; Henter JI
    J Med Genet; 2006 Apr; 43(4):e14. PubMed ID: 16582076
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosis.
    Rudd E; Bryceson YT; Zheng C; Edner J; Wood SM; Ramme K; Gavhed S; Gürgey A; Hellebostad M; Bechensteen AG; Ljunggren HG; Fadeel B; Nordenskjöld M; Henter JI
    J Med Genet; 2008 Mar; 45(3):134-41. PubMed ID: 17993578
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [The study of gene mutations in unknown refractory viral infection and primary hemophagocytic lymphohistiocytosis].
    Tong CR; Liu HX; Xie JJ; Wang F; Cai P; Wang H; Zhu J; Teng W; Zhang X; Yang JF; Zhang YL; Fei XH; Zhao J; Yin YM; Wu T; Wang JB; Sun Y; Liu R; Shi XD; Lu DP
    Zhonghua Nei Ke Za Zhi; 2011 Apr; 50(4):280-3. PubMed ID: 21600143
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Defective cytotoxic lymphocyte degranulation in syntaxin-11 deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients.
    Bryceson YT; Rudd E; Zheng C; Edner J; Ma D; Wood SM; Bechensteen AG; Boelens JJ; Celkan T; Farah RA; Hultenby K; Winiarski J; Roche PA; Nordenskjöld M; Henter JI; Long EO; Ljunggren HG
    Blood; 2007 Sep; 110(6):1906-15. PubMed ID: 17525286
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Unusual clinical presentations of familial hemophagocytic lymphohistiocytosis type-2.
    Mhatre S; Madkaikar M; Jijina F; Ghosh K
    J Pediatr Hematol Oncol; 2014 Nov; 36(8):e524-7. PubMed ID: 24390453
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial hemophagocytic lymphohistiocytosis in an adult patient homozygous for A91V in the perforin gene, with tuberculosis infection.
    Mancebo E; Allende LM; Guzmán M; Paz-Artal E; Gil J; Urrea-Moreno R; Fernández-Cruz E; Gayà A; Calvo J; Arbós A; Durán MA; Canet R; Balanzat J; Udina MA; Vercher FJ
    Haematologica; 2006 Sep; 91(9):1257-60. PubMed ID: 16956828
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Perforin gene mutations in adult-onset hemophagocytic lymphohistiocytosis.
    Nagafuji K; Nonami A; Kumano T; Kikushige Y; Yoshimoto G; Takenaka K; Shimoda K; Ohga S; Yasukawa M; Horiuchi H; Ishii E; Harada M
    Haematologica; 2007 Jul; 92(7):978-81. PubMed ID: 17606450
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Subtypes of familial hemophagocytic lymphohistiocytosis in Japan based on genetic and functional analyses of cytotoxic T lymphocytes.
    Nagai K; Yamamoto K; Fujiwara H; An J; Ochi T; Suemori K; Yasumi T; Tauchi H; Koh K; Sato M; Morimoto A; Heike T; Ishii E; Yasukawa M
    PLoS One; 2010 Nov; 5(11):e14173. PubMed ID: 21152410
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Spectrum mutations of PRF1, UNC13D, STX11, and STXBP2 genes in Vietnamese patients with hemophagocytic lymphohistiocytosis.
    Xinh PT; Chuong HQ; Diem TPH; Nguyen TM; Van ND; Mai Anh NH; Nghia H; Vu HA
    Int J Lab Hematol; 2021 Dec; 43(6):1524-1530. PubMed ID: 34339548
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Prognostic Factors and Long-Term Outcome in 52 Turkish Children With Hemophagocytic Lymphohistiocytosis.
    Kaya Z; Bay A; Albayrak M; Kocak U; Yenicesu I; Gursel T
    Pediatr Crit Care Med; 2015 Jul; 16(6):e165-73. PubMed ID: 25901543
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [An analysis of etiological and genetic factors of a patient with familial hemophagocytic lymphohistiocytosis].
    Liu HX; Tong CR; Wang H; Zhu J; Wang F; Cai P; Teng W; Yang JF; Zhang YL; Lu DP
    Zhonghua Nei Ke Za Zhi; 2011 Feb; 50(2):132-5. PubMed ID: 21418834
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial hemophagocytic lymphohistiocytosis in a 6-week-old male infant.
    Jakovljević G; Kardum-Skelin I; Rogosić S; Culić S; Stepan J; Gagro A; Skarić I; Mikecin L; Bonevski A; Barisić I; Nakić M
    Coll Antropol; 2010 Jun; 34(2):631-4. PubMed ID: 20698142
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Synergistic defects of different molecules in the cytotoxic pathway lead to clinical familial hemophagocytic lymphohistiocytosis.
    Zhang K; Chandrakasan S; Chapman H; Valencia CA; Husami A; Kissell D; Johnson JA; Filipovich AH
    Blood; 2014 Aug; 124(8):1331-4. PubMed ID: 24916509
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.