BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

233 related articles for article (PubMed ID: 12471204)

  • 21. Birt-Hogg-Dubé syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2.
    Schmidt LS; Warren MB; Nickerson ML; Weirich G; Matrosova V; Toro JR; Turner ML; Duray P; Merino M; Hewitt S; Pavlovich CP; Glenn G; Greenberg CR; Linehan WM; Zbar B
    Am J Hum Genet; 2001 Oct; 69(4):876-82. PubMed ID: 11533913
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Distinctive expression patterns of glycoprotein non-metastatic B and folliculin in renal tumors in patients with Birt-Hogg-Dubé syndrome.
    Furuya M; Hong SB; Tanaka R; Kuroda N; Nagashima Y; Nagahama K; Suyama T; Yao M; Nakatani Y
    Cancer Sci; 2015 Mar; 106(3):315-23. PubMed ID: 25594584
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Fluorescent and chromogenic in situ hybridization of CEN17q as a potent useful diagnostic marker for Birt-Hogg-Dubé syndrome-associated chromophobe renal cell carcinomas.
    Kato I; Iribe Y; Nagashima Y; Kuroda N; Tanaka R; Nakatani Y; Hasumi H; Yao M; Furuya M
    Hum Pathol; 2016 Jun; 52():74-82. PubMed ID: 26980015
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Familial multiple discoid fibromas: a look-alike of Birt-Hogg-Dubé syndrome not linked to the FLCN locus.
    Starink TM; Houweling AC; van Doorn MB; Leter EM; Jaspars EH; van Moorselaar RJ; Postmus PE; Johannesma PC; van Waesberghe JH; Ploeger MH; Kramer MT; Gille JJ; Waisfisz Q; Menko FH
    J Am Acad Dermatol; 2012 Feb; 66(2):259.e1-9. PubMed ID: 21794948
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Birt-Hogg-Dubé syndrome: novel FLCN frameshift deletion in daughter and father with renal cell carcinomas.
    Näf E; Laubscher D; Hopfer H; Streit M; Matyas G
    Fam Cancer; 2016 Jan; 15(1):127-32. PubMed ID: 26342594
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Novel mutations in the BHD gene and absence of loss of heterozygosity in fibrofolliculomas of Birt-Hogg-Dubé patients.
    van Steensel MA; Verstraeten VL; Frank J; Kelleners-Smeets NW; Poblete-Gutiérrez P; Marcus-Soekarman D; Bladergroen RS; Steijlen PM; van Geel M
    J Invest Dermatol; 2007 Mar; 127(3):588-93. PubMed ID: 17124507
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Birt-Hogg-Dubé syndrome: a novel marker of kidney neoplasia.
    Toro JR; Glenn G; Duray P; Darling T; Weirich G; Zbar B; Linehan M; Turner ML
    Arch Dermatol; 1999 Oct; 135(10):1195-202. PubMed ID: 10522666
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Nonsense mutations in folliculin presenting as isolated familial spontaneous pneumothorax in adults.
    Graham RB; Nolasco M; Peterlin B; Garcia CK
    Am J Respir Crit Care Med; 2005 Jul; 172(1):39-44. PubMed ID: 15805188
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genetic, epidemiologic and clinicopathologic studies of Japanese Asian patients with Birt-Hogg-Dubé syndrome.
    Furuya M; Yao M; Tanaka R; Nagashima Y; Kuroda N; Hasumi H; Baba M; Matsushima J; Nomura F; Nakatani Y
    Clin Genet; 2016 Nov; 90(5):403-412. PubMed ID: 27220747
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Birt-Hogg-Dubé syndrome: a literature review and case study of a Chinese woman presenting a novel FLCN mutation.
    Hao S; Long F; Sun F; Liu T; Li D; Jiang S
    BMC Pulm Med; 2017 Feb; 17(1):43. PubMed ID: 28222720
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Lung cysts in Birt-Hogg-Dubé syndrome: histopathological characteristics and aberrant sequence repeats.
    Koga S; Furuya M; Takahashi Y; Tanaka R; Yamaguchi A; Yasufuku K; Hiroshima K; Kurihara M; Yoshino I; Aoki I; Nakatani Y
    Pathol Int; 2009 Oct; 59(10):720-8. PubMed ID: 19788617
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Alterations of the Birt-Hogg-Dubé gene (BHD) in sporadic colorectal tumours.
    Kahnoski K; Khoo SK; Nassif NT; Chen J; Lobo GP; Segelov E; Teh BT
    J Med Genet; 2003 Jul; 40(7):511-5. PubMed ID: 12843323
    [No Abstract]   [Full Text] [Related]  

  • 33. A 4-bp deletion in the Birt-Hogg-Dubé gene (FLCN) causes dominantly inherited spontaneous pneumothorax.
    Painter JN; Tapanainen H; Somer M; Tukiainen P; Aittomäki K
    Am J Hum Genet; 2005 Mar; 76(3):522-7. PubMed ID: 15657874
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Birt-Hogg-Dubé syndrome: a large single family cohort.
    Skolnik K; Tsai WH; Dornan K; Perrier R; Burrowes PW; Davidson WJ
    Respir Res; 2016 Feb; 17():22. PubMed ID: 26928018
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Birt-Hogg-Dubé syndrome: mapping of a novel hereditary neoplasia gene to chromosome 17p12-q11.2.
    Khoo SK; Bradley M; Wong FK; Hedblad MA; Nordenskjöld M; Teh BT
    Oncogene; 2001 Aug; 20(37):5239-42. PubMed ID: 11526515
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A germ-line insertion in the Birt-Hogg-Dubé (BHD) gene gives rise to the Nihon rat model of inherited renal cancer.
    Okimoto K; Sakurai J; Kobayashi T; Mitani H; Hirayama Y; Nickerson ML; Warren MB; Zbar B; Schmidt LS; Hino O
    Proc Natl Acad Sci U S A; 2004 Feb; 101(7):2023-7. PubMed ID: 14769940
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Inactivation of BHD in sporadic renal tumors.
    Khoo SK; Kahnoski K; Sugimura J; Petillo D; Chen J; Shockley K; Ludlow J; Knapp R; Giraud S; Richard S; Nordenskjöld M; Teh BT
    Cancer Res; 2003 Aug; 63(15):4583-7. PubMed ID: 12907635
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Partial pleural covering for intractable pneumothorax in patients with Birt-Hogg-Dubé Syndrome.
    Okada A; Hirono T; Watanabe T; Hasegawa G; Tanaka R; Furuya M
    Clin Respir J; 2017 Mar; 11(2):224-229. PubMed ID: 26073198
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Clinical and Genetic Comparison of Birt-Hogg-Dubé Syndrome (Hornstein-Knickenberg Syndrome) in Chinese: A Systemic Review of Reported Cases.
    Zhou W; Liu K; Xu KF; Liu Y; Tian X
    Int J Gen Med; 2022; 15():5111-5121. PubMed ID: 35637701
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Birt-Hogg-Dubé syndrome in a patient with cutaneous symptoms and a c.1429 C > T;p.R477X mutation in exon 12 of the folliculin gene].
    Fuertes I; Mascaró-Galy JM; Ferrando J
    Actas Dermosifiliogr; 2009 Apr; 100(3):227-30. PubMed ID: 19457309
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.