493 related articles for article (PubMed ID: 19733897)
1. Novel intronic germline FLCN gene mutation in a patient with multiple ipsilateral renal neoplasms.
Gatalica Z; Lilleberg SL; Vranic S; Eyzaguirre E; Orihuela E; Velagaleti G
Hum Pathol; 2009 Dec; 40(12):1813-9. PubMed ID: 19733897
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. A new locus-specific database (LSDB) for mutations in the folliculin (FLCN) gene.
Lim DH; Rehal PK; Nahorski MS; Macdonald F; Claessens T; Van Geel M; Gijezen L; Gille JJ; Giraud S; Richard S; van Steensel M; Menko FH; Maher ER
Hum Mutat; 2010 Jan; 31(1):E1043-51. PubMed ID: 19802896
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Birt-Hogg-Dubé syndrome: Clinical and molecular aspects of recently identified kidney cancer syndrome.
Hasumi H; Baba M; Hasumi Y; Furuya M; Yao M
Int J Urol; 2016 Mar; 23(3):204-10. PubMed ID: 26608100
[TBL] [Abstract][Full Text] [Related]
8. FLCN gene-mutated renal cell neoplasms: mother and daughter cases with a novel germline mutation.
Nagashima Y; Furuya M; Gotohda H; Takagi S; Hes O; Michal M; Grossmann P; Tanaka R; Nakatani Y; Kuroda N
Int J Urol; 2012 May; 19(5):468-70. PubMed ID: 22211584
[TBL] [Abstract][Full Text] [Related]
9. Early onset of renal cancer in a family with Birt-Hogg-Dubé syndrome.
Kluijt I; de Jong D; Teertstra HJ; Axwijk PH; Gille JJ; Bell K; van Rens A; van der Velden AW; Middelton L; Horenblas S
Clin Genet; 2009 Jun; 75(6):537-43. PubMed ID: 19320655
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Birt Hogg-Dubé syndrome-associated FLCN mutations disrupt protein stability.
Nahorski MS; Reiman A; Lim DH; Nookala RK; Seabra L; Lu X; Fenton J; Boora U; Nordenskjöld M; Latif F; Hurst LD; Maher ER
Hum Mutat; 2011 Aug; 32(8):921-9. PubMed ID: 21538689
[TBL] [Abstract][Full Text] [Related]
12. Interaction of folliculin (Birt-Hogg-Dubé gene product) with a novel Fnip1-like (FnipL/Fnip2) protein.
Takagi Y; Kobayashi T; Shiono M; Wang L; Piao X; Sun G; Zhang D; Abe M; Hagiwara Y; Takahashi K; Hino O
Oncogene; 2008 Sep; 27(40):5339-47. PubMed ID: 18663353
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Birt-Hogg-Dubé syndrome in a patient with localized fibrofolliculomas and a novel mutation in the FLCN gene.
Alonso-González J; Rodríguez-Pazos L; Fernández-Redondo V; Vega-Gliemmo A; Toribio J
Int J Dermatol; 2011 Aug; 50(8):968-71. PubMed ID: 21781069
[TBL] [Abstract][Full Text] [Related]
15. Association between Birt Hogg Dube syndrome and cancer predisposition.
Palmirotta R; Savonarola A; Ludovici G; Donati P; Cavaliere F; DE Marchis ML; Ferroni P; Guadagni F
Anticancer Res; 2010 Mar; 30(3):751-7. PubMed ID: 20392993
[TBL] [Abstract][Full Text] [Related]
16. Birt-Hogg-Dubé syndrome: clinical and genetic studies of 10 French families.
Kluger N; Giraud S; Coupier I; Avril MF; Dereure O; Guillot B; Richard S; Bessis D
Br J Dermatol; 2010 Mar; 162(3):527-37. PubMed ID: 19785621
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. [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]
19. Mutation analysis of the FLCN gene in Chinese patients with sporadic and familial isolated primary spontaneous pneumothorax.
Ren HZ; Zhu CC; Yang C; Chen SL; Xie J; Hou YY; Xu ZF; Wang DJ; Mu DK; Ma DH; Wang Y; Ye MH; Ye ZR; Chen BF; Wang CG; Lin J; Qiao D; Yi L
Clin Genet; 2008 Aug; 74(2):178-83. PubMed ID: 18505456
[TBL] [Abstract][Full Text] [Related]
20. Characterization of a splice-site mutation in the tumor suppressor gene FLCN associated with renal cancer.
Bartram MP; Mishra T; Reintjes N; Fabretti F; Gharbi H; Adam AC; Göbel H; Franke M; Schermer B; Haneder S; Benzing T; Beck BB; Müller RU
BMC Med Genet; 2017 May; 18(1):53. PubMed ID: 28499369
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]