BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 37365821)

  • 1. First case of very late-onset FHL2 in Spain with two variants in the PRF1 gene.
    Sienes Bailo P; Goñi Ros N; Menéndez Jándula B; Álvarez Alegret R; González Gómez E; González Tarancón R; Izquierdo Álvarez S
    Ann Clin Biochem; 2023 Sep; 60(5):356-364. PubMed ID: 37365821
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic subtypes of familial hemophagocytic lymphohistiocytosis: correlations with clinical features and cytotoxic T lymphocyte/natural killer cell functions.
    Ishii E; Ueda I; Shirakawa R; Yamamoto K; Horiuchi H; Ohga S; Furuno K; Morimoto A; Imayoshi M; Ogata Y; Zaitsu M; Sako M; Koike K; Sakata A; Takada H; Hara T; Imashuku S; Sasazuki T; Yasukawa M
    Blood; 2005 May; 105(9):3442-8. PubMed ID: 15632205
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A case report of novel mutation in PRF1 gene, which causes familial autosomal recessive hemophagocytic lymphohistiocytosis.
    Bordbar MR; Modarresi F; Farazi Fard MA; Dastsooz H; Shakib Azad N; Faghihi MA
    BMC Med Genet; 2017 May; 18(1):49. PubMed ID: 28468610
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis (FHL) patients in India.
    Mhatre S; Madkaikar M; Desai M; Ghosh K
    Blood Cells Mol Dis; 2015 Mar; 54(3):250-7. PubMed ID: 25577959
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Expression of porforin and granzyme B in familial hemophagocytic lymphohistiocytosis].
    Zhou XH; Luo JM; Bin Q; Huang XH
    Zhonghua Xue Ye Xue Za Zhi; 2016 Mar; 37(3):227-32. PubMed ID: 27033761
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Correlation between phenotypic heterogeneity and gene mutational characteristics in familial hemophagocytic lymphohistiocytosis (FHL).
    Ueda I; Ishii E; Morimoto A; Ohga S; Sako M; Imashuku S
    Pediatr Blood Cancer; 2006 Apr; 46(4):482-8. PubMed ID: 16365863
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Search for the potential "second-hit" mechanism underlying the onset of familial hemophagocytic lymphohistiocytosis type 2 by whole-exome sequencing analysis.
    Gao L; Dang X; Huang L; Zhu L; Fang M; Zhang J; Xu X; Zhu L; Li T; Zhao L; Wei J; Zhou J
    Transl Res; 2016 Apr; 170():26-39. PubMed ID: 26739415
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Down-regulation of CD5 expression on activated CD8+ T cells in familial hemophagocytic lymphohistiocytosis with perforin gene mutations.
    Wada T; Sakakibara Y; Nishimura R; Toma T; Ueno Y; Horita S; Tanaka T; Nishi M; Kato K; Yasumi T; Ohara O; Yachie A
    Hum Immunol; 2013 Dec; 74(12):1579-85. PubMed ID: 24051121
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Spectrum of Atypical Clinical Presentations in Patients with Biallelic PRF1 Missense Mutations.
    Tesi B; Chiang SC; El-Ghoneimy D; Hussein AA; Langenskiöld C; Wali R; Fadoo Z; Silva JP; Lecumberri R; Unal S; Nordenskjöld M; Bryceson YT; Henter JI; Meeths M
    Pediatr Blood Cancer; 2015 Dec; 62(12):2094-100. PubMed ID: 26184781
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Case Report: Chronic inflammatory demyelinating polyradiculoneuropathy rather than hemophagocytic lymphohistiocytosis-the initial phenotype of PRF1 gene mutation.
    Hu LY; Wan L; Wang QH; Shi XY; Meng Y; Yang XF; Yang G; Zou LP
    Front Immunol; 2023; 14():1306338. PubMed ID: 38149249
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic predisposition to hemophagocytic lymphohistiocytosis: Report on 500 patients from the Italian registry.
    Cetica V; Sieni E; Pende D; Danesino C; De Fusco C; Locatelli F; Micalizzi C; Putti MC; Biondi A; Fagioli F; Moretta L; Griffiths GM; Luzzatto L; Aricò M
    J Allergy Clin Immunol; 2016 Jan; 137(1):188-196.e4. PubMed ID: 26342526
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rare cause of Hemophagocytic Lymphohistiocytosis due to mutation in PRF1 and SH2D1A genes in two children - a case report with a review.
    Sheth J; Patel A; Shah R; Bhavsar R; Trivedi S; Sheth F
    BMC Pediatr; 2019 Mar; 19(1):73. PubMed ID: 30849948
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis in ethnic Omani patients.
    Muralitharan S; Wali YA; Dennison D; Lamki ZA; Zachariah M; Nagwa el B; Pathare A; Krishnamoorthy R
    Am J Hematol; 2007 Dec; 82(12):1099-102. PubMed ID: 17674359
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial Hemophagocytic Lymphohistiocytosis secondary to UNC13D mutation: a report of two cases.
    Sadeghi P; Esslami GG; Rokni-Zadeh H; Changi-Ashtiani M; Mohsenipour R
    BMC Pediatr; 2022 Nov; 22(1):667. PubMed ID: 36401200
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Review of hemophagocytic lymphohistiocytosis (HLH) in children with focus on Japanese experiences.
    Ishii E; Ohga S; Imashuku S; Kimura N; Ueda I; Morimoto A; Yamamoto K; Yasukawa M
    Crit Rev Oncol Hematol; 2005 Mar; 53(3):209-23. PubMed ID: 15718147
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Late-onset cases of familial hemophagocytic lymphohistiocytosis with missense perforin gene mutations.
    Ueda I; Kurokawa Y; Koike K; Ito S; Sakata A; Matsumora T; Fukushima T; Morimoto A; Ishii E; Imashuku S
    Am J Hematol; 2007 Jun; 82(6):427-32. PubMed ID: 17266056
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.