BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 15864829)

  • 1. Birt-Hogg-Dubé syndrome: germline mutation in the (C)8 mononucleotide tract of the BHD gene in a German patient.
    Lamberti C; Schweiger N; Hartschuh W; Schulz T; Becker-Wegerich P; Küster W; Rütten A; Sauerbruch T; Ruzicka T; Kruse R
    Acta Derm Venereol; 2005; 85(2):172-3. PubMed ID: 15864829
    [No Abstract]   [Full Text] [Related]  

  • 2. A novel familial germline mutation in the initiator codon of the BHD gene in a patient with Birt-Hogg-Dubé syndrome.
    Bessis D; Giraud S; Richard S
    Br J Dermatol; 2006 Nov; 155(5):1067-9. PubMed ID: 17034545
    [No Abstract]   [Full Text] [Related]  

  • 3. Analysis of the Birt-Hogg-Dubé (BHD) tumour suppressor gene in sporadic renal cell carcinoma and colorectal cancer.
    da Silva NF; Gentle D; Hesson LB; Morton DG; Latif F; Maher ER
    J Med Genet; 2003 Nov; 40(11):820-4. PubMed ID: 14627671
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Birt-Hogg-Dubé syndrome with clear-cell and oncocytic renal tumour and trichoblastoma associated with a novel FLCN mutation.
    Imada K; Dainichi T; Yokomizo A; Tsunoda T; Song YH; Nagasaki A; Sawamura D; Nishie W; Shimizu H; Fukagawa S; Urabe K; Furue M; Hashimoto T; Naito S
    Br J Dermatol; 2009 Jun; 160(6):1350-3. PubMed ID: 19416240
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. Birt-Hogg-Dubé (BHD) syndrome: report of two novel germline mutations in the folliculin (FLCN) gene.
    Palmirotta R; Donati P; Savonarola A; Cota C; Ferroni P; Guadagni F
    Eur J Dermatol; 2008; 18(4):382-6. PubMed ID: 18573707
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations of the Birt Hogg Dube gene in patients with multiple lung cysts and recurrent pneumothorax.
    Gunji Y; Akiyoshi T; Sato T; Kurihara M; Tominaga S; Takahashi K; Seyama K
    J Med Genet; 2007 Sep; 44(9):588-93. PubMed ID: 17496196
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification and characterization of Birt-Hogg-Dubé associated renal carcinoma.
    Murakami T; Sano F; Huang Y; Komiya A; Baba M; Osada Y; Nagashima Y; Kondo K; Nakaigawa N; Miura T; Kubota Y; Yao M; Kishida T
    J Pathol; 2007 Apr; 211(5):524-531. PubMed ID: 17323425
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Birt-Hogg-Dubé gene mutations in human endometrial carcinomas with microsatellite instability.
    Fujii H; Jiang W; Matsumoto T; Miyai K; Sashara K; Ohtsuji N; Hino O
    J Pathol; 2006 Jul; 209(3):328-35. PubMed ID: 16691634
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detection of 1733insC mutations in an Asian family with Birt-Hogg-Dubé syndrome.
    Kawasaki H; Sawamura D; Nakazawa H; Hattori N; Goto M; Sato-Matsumura KC; Akiyama M; Shimizu H
    Br J Dermatol; 2005 Jan; 152(1):142-5. PubMed ID: 15656814
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dubé syndrome.
    Schmidt LS; Nickerson ML; Warren MB; Glenn GM; Toro JR; Merino MJ; Turner ML; Choyke PL; Sharma N; Peterson J; Morrison P; Maher ER; Walther MM; Zbar B; Linehan WM
    Am J Hum Genet; 2005 Jun; 76(6):1023-33. PubMed ID: 15852235
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Kidney-targeted Birt-Hogg-Dube gene inactivation in a mouse model: Erk1/2 and Akt-mTOR activation, cell hyperproliferation, and polycystic kidneys.
    Baba M; Furihata M; Hong SB; Tessarollo L; Haines DC; Southon E; Patel V; Igarashi P; Alvord WG; Leighty R; Yao M; Bernardo M; Ileva L; Choyke P; Warren MB; Zbar B; Linehan WM; Schmidt LS
    J Natl Cancer Inst; 2008 Jan; 100(2):140-54. PubMed ID: 18182616
    [TBL] [Abstract][Full Text] [Related]  

  • 13. High frequency of somatic frameshift BHD gene mutations in Birt-Hogg-Dubé-associated renal tumors.
    Vocke CD; Yang Y; Pavlovich CP; Schmidt LS; Nickerson ML; Torres-Cabala CA; Merino MJ; Walther MM; Zbar B; Linehan WM
    J Natl Cancer Inst; 2005 Jun; 97(12):931-5. PubMed ID: 15956655
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [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]  

  • 16. Investigation of the Birt-Hogg-Dube tumour suppressor gene (FLCN) in familial and sporadic colorectal cancer.
    Nahorski MS; Lim DH; Martin L; Gille JJ; McKay K; Rehal PK; Ploeger HM; van Steensel M; Tomlinson IP; Latif F; Menko FH; Maher ER
    J Med Genet; 2010 Jun; 47(6):385-90. PubMed ID: 20522427
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Spontaneous pneumothorax as the first manifestation of a hereditary condition with an increased renal cancer risk].
    Johannesma PC; Lammers JW; van Moorselaar RJ; Starink TM; Postmus PE; Menko FH
    Ned Tijdschr Geneeskd; 2009; 153():A581. PubMed ID: 19857281
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Birt-Hogg-Dubé syndrome: clinical and genetic studies of 20 families.
    Leter EM; Koopmans AK; Gille JJ; van Os TA; Vittoz GG; David EF; Jaspars EH; Postmus PE; van Moorselaar RJ; Craanen ME; Starink TM; Menko FH
    J Invest Dermatol; 2008 Jan; 128(1):45-9. PubMed ID: 17611575
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.