These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

175 related articles for article (PubMed ID: 22522965)

  • 1. Generation of conditional alleles for Foxc1 and Foxc2 in mice.
    Sasman A; Nassano-Miller C; Shim KS; Koo HY; Liu T; Schultz KM; Millay M; Nanano A; Kang M; Suzuki T; Kume T
    Genesis; 2012 Oct; 50(10):766-74. PubMed ID: 22522965
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Foxc1 and Foxc2 are necessary to maintain glomerular podocytes.
    Motojima M; Kume T; Matsusaka T
    Exp Cell Res; 2017 Mar; 352(2):265-272. PubMed ID: 28223138
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Foxc1 and Foxc2 in the Neural Crest Are Required for Ocular Anterior Segment Development.
    Seo S; Chen L; Liu W; Zhao D; Schultz KM; Sasman A; Liu T; Zhang HF; Gage PJ; Kume T
    Invest Ophthalmol Vis Sci; 2017 Mar; 58(3):1368-1377. PubMed ID: 28253399
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Murine forkhead/winged helix genes Foxc1 (Mf1) and Foxc2 (Mfh1) are required for the early organogenesis of the kidney and urinary tract.
    Kume T; Deng K; Hogan BL
    Development; 2000 Apr; 127(7):1387-95. PubMed ID: 10704385
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Characterization of Kidney and Skeleton Phenotypes of Mice Double Heterozygous for Foxc1 and Foxc2.
    Motojima M; Tanimoto S; Ohtsuka M; Matsusaka T; Kume T; Abe K
    Cells Tissues Organs; 2016; 201(5):380-9. PubMed ID: 27193493
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Conditional inactivation of Foxc1 and Foxc2 in neural crest cells leads to cardiac abnormalities.
    Sanchez J; Miyake R; Cheng A; Liu T; Iseki S; Kume T
    Genesis; 2020 Jul; 58(7):e23364. PubMed ID: 32259372
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Variants in FOXC1 and FOXC2 identified in patients with conotruncal heart defects.
    Wei W; Li B; Li F; Sun K; Jiang X; Xu R
    Genomics; 2024 May; 116(3):110840. PubMed ID: 38580085
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cell lineage- and expression-based inference of the roles of forkhead box transcription factor Foxc2 in craniofacial development.
    Takenoshita M; Takechi M; Vu Hoang T; Furutera T; Akagawa C; Namangkalakul W; Aoto K; Kume T; Miyashin M; Iwamoto T; Iseki S
    Dev Dyn; 2021 Aug; 250(8):1125-1139. PubMed ID: 33667029
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Endothelial cell specification in the somite is compromised in Pax3-positive progenitors of Foxc1/2 conditional mutants, with loss of forelimb myogenesis.
    Mayeuf-Louchart A; Montarras D; Bodin C; Kume T; Vincent SD; Buckingham M
    Development; 2016 Mar; 143(5):872-9. PubMed ID: 26839363
    [TBL] [Abstract][Full Text] [Related]  

  • 10. FOXC1 and FOXC2 Ablation Causes Abnormal Valvular Endothelial Cell Junctions and Lymphatic Vessel Formation in Myxomatous Mitral Valve Degeneration.
    Tan C; Ge ZD; Kurup S; Dyakiv Y; Liu T; Muller WA; Kume T
    Arterioscler Thromb Vasc Biol; 2024 Sep; 44(9):1944-1959. PubMed ID: 38989578
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Shear stimulation of FOXC1 and FOXC2 differentially regulates cytoskeletal activity during lymphatic valve maturation.
    Norden PR; Sabine A; Wang Y; Demir CS; Liu T; Petrova TV; Kume T
    Elife; 2020 Jun; 9():. PubMed ID: 32510325
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A complex regulatory network of transcription factors critical for ocular development and disease.
    Acharya M; Huang L; Fleisch VC; Allison WT; Walter MA
    Hum Mol Genet; 2011 Apr; 20(8):1610-24. PubMed ID: 21282189
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Disruption of foxc1 genes in zebrafish results in dosage-dependent phenotypes overlapping Axenfeld-Rieger syndrome.
    Ferre-Fernández JJ; Sorokina EA; Thompson S; Collery RF; Nordquist E; Lincoln J; Semina EV
    Hum Mol Genet; 2020 Sep; 29(16):2723-2735. PubMed ID: 32720677
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Foxc1 and Foxc2 deletion causes abnormal lymphangiogenesis and correlates with ERK hyperactivation.
    Fatima A; Wang Y; Uchida Y; Norden P; Liu T; Culver A; Dietz WH; Culver F; Millay M; Mukouyama YS; Kume T
    J Clin Invest; 2016 Jul; 126(7):2437-51. PubMed ID: 27214551
    [TBL] [Abstract][Full Text] [Related]  

  • 15.
    Almubarak A; Zhang Q; Zhang CH; Lassar AB; Kume T; Berry FB
    bioRxiv; 2023 Apr; ():. PubMed ID: 37162896
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Foxc2 in pharyngeal arch mesenchyme is important for aortic arch artery remodelling and ventricular septum formation.
    Uddin MK; Kimura W; Ishikura T; Koseki H; Yoshida N; Islam MJ; Amin MB; Nakamura K; Wu YX; Sato E; Aoto K; Miura N
    Biomed Res; 2015; 36(4):235-45. PubMed ID: 26299482
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The murine winged helix transcription factors, Foxc1 and Foxc2, are both required for cardiovascular development and somitogenesis.
    Kume T; Jiang H; Topczewska JM; Hogan BL
    Genes Dev; 2001 Sep; 15(18):2470-82. PubMed ID: 11562355
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The cooperative roles of Foxc1 and Foxc2 in cardiovascular development.
    Kume T
    Adv Exp Med Biol; 2009; 665():63-77. PubMed ID: 20429416
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Conditional knockout of Foxc2 gene in kidney: efficient generation of conditional alleles of single-exon gene by double-selection system.
    Motojima M; Ogiwara S; Matsusaka T; Kim SY; Sagawa N; Abe K; Ohtsuka M
    Mamm Genome; 2016 Feb; 27(1-2):62-9. PubMed ID: 26542959
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A critical developmental role for tgfbr2 in myogenic cell lineages is revealed in mice expressing SM22-Cre, not SMMHC-Cre.
    Frutkin AD; Shi H; Otsuka G; Levéen P; Karlsson S; Dichek DA
    J Mol Cell Cardiol; 2006 Oct; 41(4):724-31. PubMed ID: 16887142
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.