BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

317 related articles for article (PubMed ID: 28405742)

  • 1. CRISPR/Cas9-mediated deletion of lncRNA Gm26878 in the distant Foxf1 enhancer region.
    Szafranski P; Karolak JA; Lanza D; Gajęcka M; Heaney J; Stankiewicz P
    Mamm Genome; 2017 Aug; 28(7-8):275-282. PubMed ID: 28405742
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Narrowing the
    Szafranski P; Herrera C; Proe LA; Coffman B; Kearney DL; Popek E; Stankiewicz P
    Clin Epigenetics; 2016; 8():112. PubMed ID: 27822317
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Two deletions overlapping a distant FOXF1 enhancer unravel the role of lncRNA LINC01081 in etiology of alveolar capillary dysplasia with misalignment of pulmonary veins.
    Szafranski P; Dharmadhikari AV; Wambach JA; Towe CT; White FV; Grady RM; Eghtesady P; Cole FS; Deutsch G; Sen P; Stankiewicz P
    Am J Med Genet A; 2014 Aug; 164A(8):2013-9. PubMed ID: 24842713
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins.
    Szafranski P; Gambin T; Dharmadhikari AV; Akdemir KC; Jhangiani SN; Schuette J; Godiwala N; Yatsenko SA; Sebastian J; Madan-Khetarpal S; Surti U; Abellar RG; Bateman DA; Wilson AL; Markham MH; Slamon J; Santos-Simarro F; Palomares M; Nevado J; Lapunzina P; Chung BH; Wong WL; Chu YWY; Mok GTK; Kerem E; Reiter J; Ambalavanan N; Anderson SA; Kelly DR; Shieh J; Rosenthal TC; Scheible K; Steiner L; Iqbal MA; McKinnon ML; Hamilton SJ; Schlade-Bartusiak K; English D; Hendson G; Roeder ER; DeNapoli TS; Littlejohn RO; Wolff DJ; Wagner CL; Yeung A; Francis D; Fiorino EK; Edelman M; Fox J; Hayes DA; Janssens S; De Baere E; Menten B; Loccufier A; Vanwalleghem L; Moerman P; Sznajer Y; Lay AS; Kussmann JL; Chawla J; Payton DJ; Phillips GE; Brosens E; Tibboel D; de Klein A; Maystadt I; Fisher R; Sebire N; Male A; Chopra M; Pinner J; Malcolm G; Peters G; Arbuckle S; Lees M; Mead Z; Quarrell O; Sayers R; Owens M; Shaw-Smith C; Lioy J; McKay E; de Leeuw N; Feenstra I; Spruijt L; Elmslie F; Thiruchelvam T; Bacino CA; Langston C; Lupski JR; Sen P; Popek E; Stankiewicz P
    Hum Genet; 2016 May; 135(5):569-586. PubMed ID: 27071622
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotype.
    Szafranski P; Liu Q; Karolak JA; Song X; de Leeuw N; Faas B; Gerychova R; Janku P; Jezova M; Valaskova I; Gibbs KA; Surrey LF; Poisson V; Bérubé D; Oligny LL; Michaud JL; Popek E; Stankiewicz P
    Hum Genet; 2019 Dec; 138(11-12):1301-1311. PubMed ID: 31686214
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Lung-specific distant enhancer cis regulates expression of FOXF1 and lncRNA FENDRR.
    Szafranski P; Gambin T; Karolak JA; Popek E; Stankiewicz P
    Hum Mutat; 2021 Jun; 42(6):694-698. PubMed ID: 33739555
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Small noncoding differentially methylated copy-number variants, including lncRNA genes, cause a lethal lung developmental disorder.
    Szafranski P; Dharmadhikari AV; Brosens E; Gurha P; Kolodziejska KE; Zhishuo O; Dittwald P; Majewski T; Mohan KN; Chen B; Person RE; Tibboel D; de Klein A; Pinner J; Chopra M; Malcolm G; Peters G; Arbuckle S; Guiang SF; Hustead VA; Jessurun J; Hirsch R; Witte DP; Maystadt I; Sebire N; Fisher R; Langston C; Sen P; Stankiewicz P
    Genome Res; 2013 Jan; 23(1):23-33. PubMed ID: 23034409
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Disruption of normal patterns of FOXF1 expression in a lethal disorder of lung development.
    Steiner LA; Getman M; Schiralli Lester GM; Iqbal MA; Katzman P; Szafranski P; Stankiewicz P; Bhattacharya S; Mariani T; Pryhuber G; Lin X; Young JL; Dean DA; Scheible K
    J Med Genet; 2020 May; 57(5):296-300. PubMed ID: 31662342
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel FOXF1 deep intronic deletion causes lethal lung developmental disorder, alveolar capillary dysplasia with misalignment of pulmonary veins.
    Szafranski P; Yang Y; Nelson MU; Bizzarro MJ; Morotti RA; Langston C; Stankiewicz P
    Hum Mutat; 2013 Nov; 34(11):1467-71. PubMed ID: 23943206
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Variable expressivity in a four-generation ACDMPV family with a non-coding hypermorphic SNV in trans to the frameshifting FOXF1 variant.
    Yıldız Bölükbaşı E; Karolak JA; Szafranski P; Gambin T; Matsika A; McManus S; Scott HS; Arts P; Ha T; Barnett CP; Rodgers J; Stankiewicz P
    Eur J Hum Genet; 2022 Oct; 30(10):1182-1186. PubMed ID: 35902696
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Inversion upstream of FOXF1 in a case of lethal alveolar capillary dysplasia with misalignment of pulmonary veins.
    Parris T; Nik AM; Kotecha S; Langston C; Helou K; Platt C; Carlsson P
    Am J Med Genet A; 2013 Apr; 161A(4):764-70. PubMed ID: 23444129
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A recurrent 8 bp frameshifting indel in FOXF1 defines a novel mutation hotspot associated with alveolar capillary dysplasia with misalignment of pulmonary veins.
    Karolak JA; Bacolla A; Liu Q; Lantz PE; Petty J; Trapane P; Panzer K; Totapally BR; Niu Z; Xiao R; Xie NG; Wu LR; Szafranski P; Zhang DY; Stankiewicz P
    Am J Med Genet A; 2019 Nov; 179(11):2272-2276. PubMed ID: 31436901
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Further refinement of the differentially methylated distant lung-specific FOXF1 enhancer in a neonate with alveolar capillary dysplasia.
    Szafranski P; Garimella RP; Mani H; Hartman R; Deutsch G; Silk A; Benheim A; Stankiewicz P
    Clin Epigenetics; 2023 Oct; 15(1):169. PubMed ID: 37865798
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of endothelial and mesenchymal FOXF1 enhancers involved in alveolar capillary dysplasia.
    Wang G; Wen B; Guo M; Li E; Zhang Y; Whitsett JA; Kalin TV; Kalinichenko VV
    Nat Commun; 2024 Jun; 15(1):5233. PubMed ID: 38898031
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The S52F FOXF1 Mutation Inhibits STAT3 Signaling and Causes Alveolar Capillary Dysplasia.
    Pradhan A; Dunn A; Ustiyan V; Bolte C; Wang G; Whitsett JA; Zhang Y; Porollo A; Hu YC; Xiao R; Szafranski P; Shi D; Stankiewicz P; Kalin TV; Kalinichenko VV
    Am J Respir Crit Care Med; 2019 Oct; 200(8):1045-1056. PubMed ID: 31199666
    [No Abstract]   [Full Text] [Related]  

  • 16. Prenatal Detection of a
    Bzdęga K; Kutkowska-Kaźmierczak A; Deutsch GH; Plaskota I; Smyk M; Niemiec M; Barczyk A; Obersztyn E; Modzelewski J; Lipska I; Stankiewicz P; Gajecka M; Rydzanicz M; Płoski R; Szczapa T; Karolak JA
    Genes (Basel); 2023 Feb; 14(3):. PubMed ID: 36980834
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Perturbation of semaphorin and VEGF signaling in ACDMPV lungs due to FOXF1 deficiency.
    Karolak JA; Gambin T; Szafranski P; Maywald RL; Popek E; Heaney JD; Stankiewicz P
    Respir Res; 2021 Jul; 22(1):212. PubMed ID: 34315444
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Alveolar capillary dysplasia with misalignment of the pulmonary veins and hypoplastic left heart sequence caused by an in frame deletion within FOXF1.
    Bourque DK; Fonseca IC; Staines A; Teitelbaum R; Axford MM; Jobling R; Chiasson D; Chitayat D
    Am J Med Genet A; 2019 Jul; 179(7):1325-1329. PubMed ID: 31074124
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Comparative analyses of lung transcriptomes in patients with alveolar capillary dysplasia with misalignment of pulmonary veins and in foxf1 heterozygous knockout mice.
    Sen P; Dharmadhikari AV; Majewski T; Mohammad MA; Kalin TV; Zabielska J; Ren X; Bray M; Brown HM; Welty S; Thevananther S; Langston C; Szafranski P; Justice MJ; Kalinichenko VV; Gambin A; Belmont J; Stankiewicz P
    PLoS One; 2014; 9(4):e94390. PubMed ID: 24722050
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genome wide DNA methylation analysis of alveolar capillary dysplasia lung tissue reveals aberrant methylation of genes involved in development including the FOXF1 locus.
    Slot E; Boers R; Boers J; van IJcken WFJ; Tibboel D; Gribnau J; Rottier R; de Klein A
    Clin Epigenetics; 2021 Jul; 13(1):148. PubMed ID: 34325731
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.