BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 31419955)

  • 1. A novel single amino acid deletion impairs fibronectin function and causes familial glomerulopathy with fibronectin deposits: case report of a family.
    Dos Reis Monteiro MLG; Custódio FB; de Menezes Neves PDM; Ferreira FM; Watanabe EH; Lerário AM; de Araújo LS; Balbo BEP; Pinto VCD; Barbosa LMG; de Paiva Marques V; Machado JR; Reis MA; Onuchic LF
    BMC Nephrol; 2019 Aug; 20(1):322. PubMed ID: 31419955
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A case of familial glomerulopathy with fibronectin deposits caused by the Y973C mutation in fibronectin.
    Ertoy Baydar D; Kutlugun AA; Bresin E; Piras R
    Am J Kidney Dis; 2013 Mar; 61(3):514-8. PubMed ID: 23219110
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of mutations in FN1 leading to glomerulopathy with fibronectin deposits.
    Ohtsubo H; Okada T; Nozu K; Takaoka Y; Shono A; Asanuma K; Zhang L; Nakanishi K; Taniguchi-Ikeda M; Kaito H; Iijima K; Nakamura S
    Pediatr Nephrol; 2016 Sep; 31(9):1459-67. PubMed ID: 27056061
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A child with genetic FN1 mutation in the absence of classic glomerulopathy with fibronectin deposits(GFND) findings on biopsy.
    Yang XQ; Shen T
    BMC Nephrol; 2022 Jul; 23(1):250. PubMed ID: 35836154
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations in FN1 cause glomerulopathy with fibronectin deposits.
    Castelletti F; Donadelli R; Banterla F; Hildebrandt F; Zipfel PF; Bresin E; Otto E; Skerka C; Renieri A; Todeschini M; Caprioli J; Caruso RM; Artuso R; Remuzzi G; Noris M
    Proc Natl Acad Sci U S A; 2008 Feb; 105(7):2538-43. PubMed ID: 18268355
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prednisone-induced sustained remission in a patient with familial fibronectin glomerulopathy (GFND).
    Goldman BI; Panner BJ; Welle SL; Gross MD; Gray DA
    CEN Case Rep; 2021 Nov; 10(4):510-514. PubMed ID: 33837952
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fibronectin Glomerulopathy Caused by the Y973C Mutation in Fibronectin: A Case Report and Literature Review.
    Li C; Wen YB; Li H; Li MX; Li XW; Li XM
    Chin Med Sci J; 2018 Mar; 33(1):60-63. PubMed ID: 29620516
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical and morphological features of fibronectin glomerulopathy: a report of ten patients from a single institution.
    Chen H; Bao H; Xu F; Zhu X; Zhu M; He Q; Zeng C; Liu Z
    Clin Nephrol; 2015 Feb; 83(2):93-9. PubMed ID: 25601194
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fibronectin glomerulopathy complicated with persistent cloaca and congenital esophageal atresia: a case report and literature review.
    Takii M; Suehiro T; Shima A; Yotsueda H; Hisano S; Katafuchi R
    BMC Nephrol; 2017 Sep; 18(1):288. PubMed ID: 28877681
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pathologic-genomic correlation identified a novel variant in FN1 and established the diagnosis of recurrent fibronectin glomerulopathy in the kidney allograft.
    Batal I; Nasr SH; Dasari S; Weins A; Vena N; Stokes MB; Kiryluk K; Appel GB
    Am J Transplant; 2024 Mar; 24(3):498-502. PubMed ID: 37852577
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Extraglomerular Vascular Involvement of Glomerulopathy with Fibronectin Deposits.
    Hara M; Kusaba T; Ono K; Masuzawa N; Nakamura I; Urata N; Shiraishi H; Hara S; Konishi E; Matoba S; Shiotsu Y; Tamagaki K
    Intern Med; 2021 Jul; 60(13):2103-2107. PubMed ID: 33551409
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Generation of the integration-free induced pluripotent stem cell line (FHUSTCi001-A) from a patient with glomerulopathy with fibronectin deposits harboring FN1 mutation.
    Yu X; Wang H; Xiao F; Jiang S; Li K; Chen Q; Wang G; Kong F; Zhao S
    Stem Cell Res; 2022 May; 61():102751. PubMed ID: 35395622
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Glomerulopathy associated with predominant fibronectin deposits: exclusion of the genes for fibronectin, villin and desmin as causative genes.
    Hildebrandt F; Strahm B; Prochoroff A; Cybulla M; Gemperle O; Krapf R; Brandis M
    Am J Med Genet; 1996 May; 63(1):323-7. PubMed ID: 8723129
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel variant in
    Aslam N; Singh A; Cortese C; Riegert-Johnson DL
    Hum Genome Var; 2019; 6():11. PubMed ID: 30820325
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Glomerulopathy associated with predominant fibronectin deposits: a newly recognized hereditary disease.
    Strøm EH; Banfi G; Krapf R; Abt AB; Mazzucco G; Monga G; Gloor F; Neuweiler J; Riess R; Stosiek P
    Kidney Int; 1995 Jul; 48(1):163-70. PubMed ID: 7564073
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A case of unexpected diagnosis of fibronectin glomerulopathy with histological features of membranoproliferative glomerulonephritis.
    Hata M; Mori T; Hirose Y; Nishida Y; Mandai S; Ando F; Susa K; Iimori S; Naito S; Sohara E; Rai T; Taguchi T; Tomii S; Ohashi K; Uchida S
    BMC Nephrol; 2024 Jan; 25(1):25. PubMed ID: 38254040
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Detection of a Splice Site Variant in a Patient with Glomerulopathy and Fibronectin Deposits.
    Tsuji Y; Nozu K; Sofue T; Hara S; Nakanishi K; Yamamura T; Minamikawa S; Nozu Y; Kaito H; Fujimura J; Horinouchi T; Morisada N; Morioka I; Taniguchi-Ikeda M; Matsuo M; Iijima K
    Nephron; 2018; 138(2):166-171. PubMed ID: 29131116
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A high-impact FN1 variant correlates with fibronectin-mediated glomerulopathy via decreased binding to collagen type IV.
    Qiu J; Chi H; Gan C; Zhou X; Chen D; Yang Q; Chen Y; Wang M; Yang H; Jiang W; Li Q
    Pathology; 2023 Jun; 55(4):498-507. PubMed ID: 36774238
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinicopathological analysis of glomerulopathy with fibronectin deposits (GFND): a case of sporadic, elderly-onset GFND with codeposition of IgA, C1q, and fibrinogen.
    Yoshino M; Miura N; Ohnishi T; Suzuki K; Kitagawa W; Nishikawa K; Imai H
    Intern Med; 2013; 52(15):1715-20. PubMed ID: 23903505
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Case Report: Recurrent Deposition in Renal Allografts: A Rare Case of Fibronectin Glomerulopathy Overlooked in Native Kidneys.
    Wei X; Wang X; Zhang R; Liang P; Liu B; Wang L; Yue S; Li X; Chen W; Yang Q
    Front Genet; 2022; 13():839703. PubMed ID: 35774511
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.