These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

264 related articles for article (PubMed ID: 21937013)

  • 21. Birt-Hogg-Dubé renal tumors are genetically distinct from other renal neoplasias and are associated with up-regulation of mitochondrial gene expression.
    Klomp JA; Petillo D; Niemi NM; Dykema KJ; Chen J; Yang XJ; Sääf A; Zickert P; Aly M; Bergerheim U; Nordenskjöld M; Gad S; Giraud S; Denoux Y; Yonneau L; Méjean A; Vasiliu V; Richard S; MacKeigan JP; Teh BT; Furge KA
    BMC Med Genomics; 2010 Dec; 3():59. PubMed ID: 21162720
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [The Birt-Hogg-Dube Syndrome].
    Schweizer S; Krayenbühl PA
    Praxis (Bern 1994); 2014 Nov; 103(23):1359-66; quiz 1367-8. PubMed ID: 25391741
    [No Abstract]   [Full Text] [Related]  

  • 23. 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]  

  • 24. Pathology of Birt-Hogg-Dubé syndrome: A special reference of pulmonary manifestations in a Japanese population with a comprehensive analysis and review.
    Furuya M; Nakatani Y
    Pathol Int; 2019 Jan; 69(1):1-12. PubMed ID: 30632664
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Primary spontaneous pneumothorax and the Birt-Hogg-Dubé syndrome.
    Koul PA
    J Postgrad Med; 2013; 59(4):324-5. PubMed ID: 24430303
    [No Abstract]   [Full Text] [Related]  

  • 27. Birt-Hogg-Dubé syndrome. State-of-the-art review with emphasis on pulmonary involvement.
    Dal Sasso AA; Belém LC; Zanetti G; Souza CA; Escuissato DL; Irion KL; Guimarães MD; Marchiori E
    Respir Med; 2015 Mar; 109(3):289-96. PubMed ID: 25519092
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Novel germline mutations in FLCN gene identified in two Chinese patients with Birt-Hogg-Dubé syndrome.
    Li T; Ning X; He Q; Gong K
    Chin J Cancer; 2017 Jan; 36(1):4. PubMed ID: 28069055
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Birt-Hogg-Dubé syndrome in Korean: clinicoradiologic features and long term follow-up.
    Lee JH; Jeon MJ; Song JS; Chae EJ; Choi JH; Kim GH; Song JW
    Korean J Intern Med; 2019 Jul; 34(4):830-840. PubMed ID: 30360018
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Birt-Hogg-Dubé syndrome with simultaneous hyperplastic polyposis of the gastrointestinal tract: case report and review of the literature.
    Balsamo F; Cardoso PAS; do Amaral Junior SA; Theodoro TR; de Sousa Gehrke F; da Silva Pinhal MA; Bianco B; Waisberg J
    BMC Med Genet; 2020 Mar; 21(1):52. PubMed ID: 32171268
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The impact of germline BHD mutation on histological concordance and clinical treatment of patients with bilateral renal masses and known unilateral oncocytoma.
    Boris RS; Benhammou J; Merino M; Pinto PA; Linehan WM; Bratslavsky G
    J Urol; 2011 Jun; 185(6):2050-5. PubMed ID: 21496834
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Birt-Hogg-Dube syndrome: clinicopathological features of the lung.
    Furuya M; Nakatani Y
    J Clin Pathol; 2013 Mar; 66(3):178-86. PubMed ID: 23223565
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Haploinsufficiency of the folliculin gene leads to impaired functions of lung fibroblasts in patients with Birt-Hogg-Dubé syndrome.
    Hoshika Y; Takahashi F; Togo S; Hashimoto M; Nara T; Kobayashi T; Nurwidya F; Kataoka H; Kurihara M; Kobayashi E; Ebana H; Kikkawa M; Ando K; Nishino K; Hino O; Takahashi K; Seyama K
    Physiol Rep; 2016 Nov; 4(21):. PubMed ID: 27905298
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Birt-Hogg-Dubé syndrome].
    Rehfeld A; van Steensel MA; Friis-Hansen L
    Ugeskr Laeger; 2010 Jul; 172(29):2085-90. PubMed ID: 20633341
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Isolated familial pneumothorax in a Taiwanese family with Birt-Hogg-Dubé syndrome.
    Yang CY; Wang HC; Chen JS; Yu CJ
    J Postgrad Med; 2013; 59(4):321-3. PubMed ID: 24346394
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Unique mutation, accelerated mTOR signaling and angiogenesis in the pulmonary cysts of Birt-Hogg-Dubé syndrome.
    Nishii T; Tanabe M; Tanaka R; Matsuzawa T; Okudela K; Nozawa A; Nakatani Y; Furuya M
    Pathol Int; 2013 Jan; 63(1):45-55. PubMed ID: 23356225
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Intratumoral peripheral small papillary tufts: a diagnostic clue of renal tumors associated with Birt-Hogg-Dubé syndrome.
    Kuroda N; Furuya M; Nagashima Y; Gotohda H; Moritani S; Kawakami F; Imamura Y; Bando Y; Takahashi M; Kanayama HO; Ota S; Michal M; Hes O; Nakatani Y
    Ann Diagn Pathol; 2014 Jun; 18(3):171-6. PubMed ID: 24767893
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Birt-Hogg-Dubé syndrome in two Chinese families with mutations in the FLCN gene.
    Hou X; Zhou Y; Peng Y; Qiu R; Xia K; Tang B; Zhuang W; Jiang H
    BMC Med Genet; 2018 Jan; 19(1):14. PubMed ID: 29357828
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Renal cancer and pneumothorax risk in Birt-Hogg-Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families.
    Houweling AC; Gijezen LM; Jonker MA; van Doorn MB; Oldenburg RA; van Spaendonck-Zwarts KY; Leter EM; van Os TA; van Grieken NC; Jaspars EH; de Jong MM; Bongers EM; Johannesma PC; Postmus PE; van Moorselaar RJ; van Waesberghe JH; Starink TM; van Steensel MA; Gille JJ; Menko FH
    Br J Cancer; 2011 Dec; 105(12):1912-9. PubMed ID: 22146830
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.