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 *

137 related articles for article (PubMed ID: 12748961)

  • 41. BOP, a regulator of right ventricular heart development, is a direct transcriptional target of MEF2C in the developing heart.
    Phan D; Rasmussen TL; Nakagawa O; McAnally J; Gottlieb PD; Tucker PW; Richardson JA; Bassel-Duby R; Olson EN
    Development; 2005 Jun; 132(11):2669-78. PubMed ID: 15890826
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Cooperative activation of atrial naturetic peptide promoter by dHAND and MEF2C.
    Zang MX; Li Y; Xue LX; Jia HT; Jing H
    J Cell Biochem; 2004 Dec; 93(6):1255-66. PubMed ID: 15486975
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Expression of Sox transcription factors in the developing mouse pancreas.
    Lioubinski O; Müller M; Wegner M; Sander M
    Dev Dyn; 2003 Jul; 227(3):402-8. PubMed ID: 12815626
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Dominant-negative
    Villani R; Hodgson S; Legrand J; Greaney J; Wong HY; Pichol-Thievend C; Adolphe C; Wainwight B; Francois M; Khosrotehrani K
    Development; 2017 May; 144(10):1887-1895. PubMed ID: 28512199
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Slow and fast fiber isoform gene expression is systematically altered in skeletal muscle of the Sox6 mutant, p100H.
    Hagiwara N; Ma B; Ly A
    Dev Dyn; 2005 Oct; 234(2):301-11. PubMed ID: 16124007
    [TBL] [Abstract][Full Text] [Related]  

  • 46. SoxF genes: Key players in the development of the cardio-vascular system.
    Francois M; Koopman P; Beltrame M
    Int J Biochem Cell Biol; 2010 Mar; 42(3):445-8. PubMed ID: 19733255
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Severe growth retardation and short life span of double-mutant mice lacking Xpa and exon 15 of Xpg.
    Shiomi N; Mori M; Kito S; Harada YN; Tanaka K; Shiomi T
    DNA Repair (Amst); 2005 Mar; 4(3):351-7. PubMed ID: 15661658
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Transcription profiling of inner ears from Pou4f3(ddl/ddl) identifies Gfi1 as a target of the Pou4f3 deafness gene.
    Hertzano R; Montcouquiol M; Rashi-Elkeles S; Elkon R; Yücel R; Frankel WN; Rechavi G; Möröy T; Friedman TB; Kelley MW; Avraham KB
    Hum Mol Genet; 2004 Sep; 13(18):2143-53. PubMed ID: 15254021
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Structure, mapping, and expression of human SOX18.
    Pennisi DJ; James KM; Hosking B; Muscat GE; Koopman P
    Mamm Genome; 2000 Dec; 11(12):1147-9. PubMed ID: 11130989
    [No Abstract]   [Full Text] [Related]  

  • 50. A dominant-negative SOX18 mutant disrupts multiple regulatory layers essential to transcription factor activity.
    McCann AJ; Lou J; Moustaqil M; Graus MS; Blum A; Fontaine F; Liu H; Luu W; Rudolffi-Soto P; Koopman P; Sierecki E; Gambin Y; Meunier FA; Liu Z; Hinde E; Francois M
    Nucleic Acids Res; 2021 Nov; 49(19):10931-10955. PubMed ID: 34570228
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Sox18 expression in blood vessels and feather buds during chicken embryogenesis.
    Olsson JE; Kamachi Y; Penning S; Muscat GE; Kondoh H; Koopman P
    Gene; 2001 Jun; 271(2):151-8. PubMed ID: 11418236
    [TBL] [Abstract][Full Text] [Related]  

  • 52. The human SOX18 gene: cDNA cloning and high resolution mapping.
    Stanojcić S; Stevanović M
    Biochim Biophys Acta; 2000 Jun; 1492(1):237-41. PubMed ID: 10858556
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Cytoplasmic plaque formation in hemidesmosome development is dependent on SoxF transcription factor function.
    Oommen S; Francois M; Kawasaki M; Murrell M; Kawasaki K; Porntaveetus T; Ghafoor S; Young NJ; Okamatsu Y; McGrath J; Koopman P; Sharpe PT; Ohazama A
    PLoS One; 2012; 7(9):e43857. PubMed ID: 22962592
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Genotype-phenotype correlation of mouse pde6b mutations.
    Hart AW; McKie L; Morgan JE; Gautier P; West K; Jackson IJ; Cross SH
    Invest Ophthalmol Vis Sci; 2005 Sep; 46(9):3443-50. PubMed ID: 16123450
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Evaluation of Lama5 as a candidate for the mouse ragged (Ra) mutation.
    Durkin ME; Albrechtsen R; Chambers DM; Abbott CM; Wewer UM
    Biochem Biophys Res Commun; 1998 Sep; 250(1):125-30. PubMed ID: 9735344
    [TBL] [Abstract][Full Text] [Related]  

  • 56. A novel missense mutation in the mouse hairless gene causes irreversible hair loss: genetic and molecular analyses of Hr m1Enu.
    Nam Y; Kim JK; Cha DS; Cho JW; Cho KH; Yoon S; Yoon JB; Oh YS; Suh JG; Han SS; Song CW; Yoon SK
    Genomics; 2006 Apr; 87(4):520-6. PubMed ID: 16455232
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Mef2c is a direct transcriptional target of ISL1 and GATA factors in the anterior heart field during mouse embryonic development.
    Dodou E; Verzi MP; Anderson JP; Xu SM; Black BL
    Development; 2004 Aug; 131(16):3931-42. PubMed ID: 15253934
    [TBL] [Abstract][Full Text] [Related]  

  • 58. A conserved transcriptional enhancer that specifies Tyrp1 expression to melanocytes.
    Murisier F; Guichard S; Beermann F
    Dev Biol; 2006 Oct; 298(2):644-55. PubMed ID: 16934245
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Transcription factors Sox8 and Sox10 perform non-equivalent roles during oligodendrocyte development despite functional redundancy.
    Stolt CC; Lommes P; Friedrich RP; Wegner M
    Development; 2004 May; 131(10):2349-58. PubMed ID: 15102707
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A novel SOX18 mutation uncovered in Jordanian patient with hypotrichosis-lymphedema-telangiectasia syndrome by Whole Exome Sequencing.
    Bastaki F; Mohamed M; Nair P; Saif F; Tawfiq N; Al-Ali MT; Brandau O; Hamzeh AR
    Mol Cell Probes; 2016 Feb; 30(1):18-21. PubMed ID: 26631803
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.