BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 27033761)

  • 41. [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]  

  • 42. Bone marrow derived mesenchymal stem cells ameliorate inflammatory response in an in vitro model of familial hemophagocytic lymphohistiocytosis 2.
    Sevim H; Kocaefe YÇ; Onur MA; Uçkan-Çetinkaya D; Gürpınar ÖA
    Stem Cell Res Ther; 2018 Jul; 9(1):198. PubMed ID: 30021624
    [TBL] [Abstract][Full Text] [Related]  

  • 43. A CD57
    Hori M; Yasumi T; Shimodera S; Shibata H; Hiejima E; Oda H; Izawa K; Kawai T; Ishimura M; Nakano N; Shirakawa R; Nishikomori R; Takada H; Morita S; Horiuchi H; Ohara O; Ishii E; Heike T
    J Clin Immunol; 2017 Jan; 37(1):92-99. PubMed ID: 27896523
    [TBL] [Abstract][Full Text] [Related]  

  • 44. 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]  

  • 45. [Screening for cytotoxic defects with flow cytometric detection of CD107α on natural killer cells and cytotoxic lymphocyte cells].
    Wang J; Liu Z; Jiang LP; An YF; Zhao XD
    Zhonghua Er Ke Za Zhi; 2012 May; 50(5):386-91. PubMed ID: 22883044
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Korean Infant With Compound Heterozygous PRF1 Defects Involving a PRF1 Mutation, c.1091T>G.
    Kim MS; Cho YU; Jang S; Seo EJ; Im HJ; Park CJ
    Ann Lab Med; 2017 Mar; 37(2):162-165. PubMed ID: 28029005
    [No Abstract]   [Full Text] [Related]  

  • 47. Germline heterozygous variants in genes associated with familial hemophagocytic lymphohistiocytosis as a cause of increased bleeding.
    Fager Ferrari M; Leinoe E; Rossing M; Norström E; Strandberg K; Steen Sejersen T; Qvortrup K; Zetterberg E
    Platelets; 2018 Jan; 29(1):56-64. PubMed ID: 28399723
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Immunologic difference between hypersensitivity to mosquito bite and hemophagocytic lymphohistiocytosis associated with Epstein-Barr virus infection.
    Lee WI; Lin JJ; Hsieh MY; Lin SJ; Jaing TH; Chen SH; Hung IJ; Yang CP; Chen CJ; Huang YC; Li SP; Huang JL
    PLoS One; 2013; 8(10):e76711. PubMed ID: 24204658
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Adult onset type 2 familial hemophagocytic lymphohistiocytosis with
    Liu XY; Nie YB; Chen XJ; Gao XH; Zhai LJ; Min FL
    World J Clin Cases; 2021 Apr; 9(10):2289-2295. PubMed ID: 33869605
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Hemophagocytic lymphohistiocytosis with a hemizygous PRF1 c.674G>A mutation.
    Xin X; Wang N; Zhang Y
    Am J Med Sci; 2023 Nov; 366(5):387-394. PubMed ID: 37467895
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Analysis of natural killer-cell function in familial hemophagocytic lymphohistiocytosis (FHL): defective CD107a surface expression heralds Munc13-4 defect and discriminates between genetic subtypes of the disease.
    Marcenaro S; Gallo F; Martini S; Santoro A; Griffiths GM; Aricó M; Moretta L; Pende D
    Blood; 2006 Oct; 108(7):2316-23. PubMed ID: 16778144
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Serglycin determines secretory granule repertoire and regulates natural killer cell and cytotoxic T lymphocyte cytotoxicity.
    Sutton VR; Brennan AJ; Ellis S; Danne J; Thia K; Jenkins MR; Voskoboinik I; Pejler G; Johnstone RW; Andrews DM; Trapani JA
    FEBS J; 2016 Mar; 283(5):947-61. PubMed ID: 26756195
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Pathology of the liver in familial hemophagocytic lymphohistiocytosis.
    Chen JH; Fleming MD; Pinkus GS; Pinkus JL; Nichols KE; Mo JQ; Perez-Atayde AR
    Am J Surg Pathol; 2010 Jun; 34(6):852-67. PubMed ID: 20442642
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Late Onset of Primary Hemophagocytic Lymphohistiocytosis (HLH) with a Novel Constellation of Compound Heterozygosity Involving Two Missense Variants in the
    Stadermann A; Haar M; Riecke A; Mayer T; Neumann C; Bauer A; Schulz A; Nagarathinam K; Gebauer N; Böhm S; Groß M; Grunert M; Müller M; Witte H
    Int J Mol Sci; 2024 Feb; 25(5):. PubMed ID: 38474010
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Whole-Exome Sequencing Reveals Mutations in Genes Linked to Hemophagocytic Lymphohistiocytosis and Macrophage Activation Syndrome in Fatal Cases of H1N1 Influenza.
    Schulert GS; Zhang M; Fall N; Husami A; Kissell D; Hanosh A; Zhang K; Davis K; Jentzen JM; Napolitano L; Siddiqui J; Smith LB; Harms PW; Grom AA; Cron RQ
    J Infect Dis; 2016 Apr; 213(7):1180-8. PubMed ID: 26597256
    [TBL] [Abstract][Full Text] [Related]  

  • 56. [Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis in Chinese children: a primary study on clinical characteristics and gene mutations].
    Liu R; Shi X; Li J; Hu T; Cao J; Sun Y; Tong C; Liu H
    Zhonghua Yi Xue Za Zhi; 2014 Jul; 94(25):1941-6. PubMed ID: 25253006
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. STX11 mutations and clinical phenotypes of familial hemophagocytic lymphohistiocytosis in North America.
    Marsh RA; Satake N; Biroschak J; Jacobs T; Johnson J; Jordan MB; Bleesing JJ; Filipovich AH; Zhang K
    Pediatr Blood Cancer; 2010 Jul; 55(1):134-40. PubMed ID: 20486178
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Type 2 familial hemophagocytic lymphohistiocytosis in half brothers: A case report.
    Liu C; Li M; Wu X; Yao X; Zhao L
    Medicine (Baltimore); 2018 Jul; 97(30):e11577. PubMed ID: 30045285
    [TBL] [Abstract][Full Text] [Related]  

  • 60. [Analysis of clinical phenotype and genetic mutations of a pedigree of familial hemophagocytic lymphohistiocytosis].
    Sun S; Guo X; Zhu Y; Yang X; Li Q; Gao J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):570-3. PubMed ID: 25297583
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.