132 related articles for article (PubMed ID: 26398834)
1. Promoter methylation is not associated with FLCN irregulation in lung cyst lesions of primary spontaneous pneumothorax.
Ding Y; Zou W; Zhu C; Min H; Ma D; Chen B; Ye M; Pan Y; Cao L; Wan Y; Zhu Q; Xia H; Zhang W; Feng Y; Gao Q; Yi L
Mol Med Rep; 2015 Nov; 12(5):7770-6. PubMed ID: 26398834
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Novel in-frame deletion mutation in FLCN gene in a Korean family with recurrent primary spontaneous pneumothorax.
Kim J; Yoo JH; Kang DY; Cho NJ; Lee KA
Gene; 2012 May; 499(2):339-42. PubMed ID: 22446046
[TBL] [Abstract][Full Text] [Related]
4. A novel FLCN mutation in family members diagnosed with primary spontaneous pneumothorax.
Genc Yavuz B; Guzel Tanoglu E; Salman Yılmaz S; Colak S
Mol Genet Genomic Med; 2019 Dec; 7(12):e1003. PubMed ID: 31625278
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. FLCN intragenic deletions in Chinese familial primary spontaneous pneumothorax.
Ding Y; Zhu C; Zou W; Ma D; Min H; Chen B; Ye M; Pan Y; Cao L; Wan Y; Zhang W; Meng L; Mei Y; Yang C; Chen S; Gao Q; Yi L
Am J Med Genet A; 2015 May; 167A(5):1125-33. PubMed ID: 25807935
[TBL] [Abstract][Full Text] [Related]
7. A rapid NGS strategy for comprehensive molecular diagnosis of Birt-Hogg-Dubé syndrome in patients with primary spontaneous pneumothorax.
Zhang X; Ma D; Zou W; Ding Y; Zhu C; Min H; Zhang B; Wang W; Chen B; Ye M; Cai M; Pan Y; Cao L; Wan Y; Jin Y; Gao Q; Yi L
Respir Res; 2016 May; 17(1):64. PubMed ID: 27229674
[TBL] [Abstract][Full Text] [Related]
8. Clinical and genetic spectrum of Birt-Hogg-Dube syndrome patients in whom pneumothorax and/or multiple lung cysts are the presenting feature.
Kunogi M; Kurihara M; Ikegami TS; Kobayashi T; Shindo N; Kumasaka T; Gunji Y; Kikkawa M; Iwakami S; Hino O; Takahashi K; Seyama K
J Med Genet; 2010 Apr; 47(4):281-7. PubMed ID: 20413710
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Genotypic characteristics of Chinese patients with BHD syndrome and functional analysis of FLCN variants.
Liu K; Xu W; Tian X; Xiao M; Zhao X; Zhang Q; Qu T; Song J; Liu Y; Xu KF; Zhang X
Orphanet J Rare Dis; 2019 Oct; 14(1):223. PubMed ID: 31615547
[TBL] [Abstract][Full Text] [Related]
11. Birt-Hogg-Dube Syndrome with a Novel Mutation in the FLCN Gene.
Kayhan G; Yılmaz Demirci N; Turktas H; Ergun MA
Genet Test Mol Biomarkers; 2017 Oct; 21(10):632-634. PubMed ID: 28805452
[TBL] [Abstract][Full Text] [Related]
12. Novel folliculin (FLCN) mutation and familial spontaneous pneumothorax.
Zhu JF; Shen XQ; Zhu F; Tian L
QJM; 2017 Jan; 110(1):23-26. PubMed ID: 27486260
[TBL] [Abstract][Full Text] [Related]
13. Recurrent primary spontaneous pneumothorax in a large Chinese family: a clinical and genetic investigation.
Zheng CM; Hu XX; Gao YL; Miao JB; Li H
Chin Med J (Engl); 2019 Oct; 132(20):2402-2407. PubMed ID: 31567476
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Skin lesions of Birt-Hogg-Dubé syndrome: Clinical and histopathological findings in 31 Japanese patients who presented with pneumothorax and/or multiple lung cysts.
Iwabuchi C; Ebana H; Ishiko A; Negishi A; Mizobuchi T; Kumasaka T; Kurihara M; Seyama K
J Dermatol Sci; 2018 Jan; 89(1):77-84. PubMed ID: 29157599
[TBL] [Abstract][Full Text] [Related]
17. The Relevance of Family History Taking in the Detection and Management of Birt-Hogg-Dubé Syndrome.
Torricelli E; Occhipinti M; Cavigli E; Tancredi G; Rosi E; Rossi C; Bonaguro M; Candita L; Papi L; Novelli L; Bezzi M; Bargagli E; Voltolini L; Pistolesi M
Respiration; 2019; 98(2):125-132. PubMed ID: 31266032
[TBL] [Abstract][Full Text] [Related]
18. A de novo FLCN mutation in a patient with spontaneous pneumothorax and renal cancer; a clinical and molecular evaluation.
Menko FH; Johannesma PC; van Moorselaar RJ; Reinhard R; van Waesberghe JH; Thunnissen E; Houweling AC; Leter EM; Waisfisz Q; van Doorn MB; Starink TM; Postmus PE; Coull BJ; van Steensel MA; Gille JJ
Fam Cancer; 2013 Sep; 12(3):373-9. PubMed ID: 23264078
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Genetic analysis of familial spontaneous pneumothorax in an Indian family.
Ray A; Paul S; Chattopadhyay E; Kundu S; Roy B
Lung; 2015 Jun; 193(3):433-8. PubMed ID: 25827758
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
