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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 3
2001 2
2002 3
2003 5
2004 5
2005 4
2006 6
2007 4
2008 11
2009 3
2010 7
2011 10
2012 10
2013 10
2014 7
2015 10
2016 13
2017 11
2018 7
2019 6
2020 2
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Article attribute
Article type
Publication date

gene_pubmed for PMID: 201163

120 results
Results by year
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Page 1
A novel FLCN mutation in family members diagnosed with primary spontaneous pneumothorax.
Genc Yavuz B, Guzel Tanoglu E, Salman Yılmaz S, Colak S. Genc Yavuz B, et al. Mol Genet Genomic Med. 2019 Dec;7(12):e1003. doi: 10.1002/mgg3.1003. Epub 2019 Oct 18. Mol Genet Genomic Med. 2019. PMID: 31625278 Free PMC article.
Loss of FLCN inhibits canonical WNT signaling via TFE3.
Kennedy JC, Khabibullin D, Hougard T, Nijmeh J, Shi W, Henske EP. Kennedy JC, et al. Hum Mol Genet. 2019 Oct 1;28(19):3270-3281. doi: 10.1093/hmg/ddz158. Hum Mol Genet. 2019. PMID: 31272105
BHD-associated kidney cancer exhibits unique molecular characteristics and a wide variety of variants in chromatin remodeling genes.
Hasumi H, Furuya M, Tatsuno K, Yamamoto S, Baba M, Hasumi Y, Isono Y, Suzuki K, Jikuya R, Otake S, Muraoka K, Osaka K, Hayashi N, Makiyama K, Miyoshi Y, Kondo K, Nakaigawa N, Kawahara T, Izumi K, Teranishi J, Yumura Y, Uemura H, Nagashima Y, Metwalli AR, Schmidt LS, Aburatani H, Linehan WM, Yao M. Hasumi H, et al. Hum Mol Genet. 2018 Aug 1;27(15):2712-2724. doi: 10.1093/hmg/ddy181. Hum Mol Genet. 2018. PMID: 29767721 Free PMC article.
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. Hou X, et al. BMC Med Genet. 2018 Jan 22;19(1):14. doi: 10.1186/s12881-017-0519-z. BMC Med Genet. 2018. PMID: 29357828 Free PMC article.
Detection of Folliculin Gene Mutations in Two Chinese Families with Birt-Hogg-Dube Syndrome.
Liu L, Yang K, Wang X, Shi Z, Yang Y, Yuan Y, Guo T, Xiao X, Luo H. Liu L, et al. Biomed Res Int. 2017;2017:8751384. doi: 10.1155/2017/8751384. Epub 2017 Jul 12. Biomed Res Int. 2017. PMID: 28785590 Free PMC article.
Birt-Hogg-Dubé syndrome: a rare cause of familial spontaneous pneumothorax.
Luk HM, Tong TM, Lo IF. Luk HM, et al. Hong Kong Med J. 2017 Aug;23(4):416.e4-5. doi: 10.12809/hkmj165022. Hong Kong Med J. 2017. PMID: 28775225 Free article. No abstract available.
Clinical and genetic characteristics of chinese patients with Birt-Hogg-Dubé syndrome.
Liu Y, Xu Z, Feng R, Zhan Y, Wang J, Li G, Li X, Zhang W, Hu X, Tian X, Xu KF, Zhang X. Liu Y, et al. Orphanet J Rare Dis. 2017 May 30;12(1):104. doi: 10.1186/s13023-017-0656-7. Orphanet J Rare Dis. 2017. PMID: 28558743 Free PMC article.
A Case of Birt-Hogg-Dubé (BHD) Syndrome Harboring a Novel Folliculin (FLCN) Gene Mutation.
Yukawa T, Fukazawa T, Yoshida M, Morita I, Kato K, Monobe Y, Furuya M, Naomoto Y. Yukawa T, et al. Am J Case Rep. 2016 Oct 26;17:788-792. doi: 10.12659/ajcr.899407. Am J Case Rep. 2016. PMID: 27780965 Free PMC article.
Genetic screening of the FLCN gene identify six novel variants and a Danish founder mutation.
Rossing M, Albrechtsen A, Skytte AB, Jensen UB, Ousager LB, Gerdes AM, Nielsen FC, Hansen TV. Rossing M, et al. J Hum Genet. 2017 Feb;62(2):151-157. doi: 10.1038/jhg.2016.118. Epub 2016 Oct 13. J Hum Genet. 2017. PMID: 27734835
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