BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

312 related articles for article (PubMed ID: 10783262)

  • 1. Characterization of human retinal fascin gene (FSCN2) at 17q25: close physical linkage of fascin and cytoplasmic actin genes.
    Tubb BE; Bardien-Kruger S; Kashork CD; Shaffer LG; Ramagli LS; Xu J; Siciliano MJ; Bryan J
    Genomics; 2000 Apr; 65(2):146-56. PubMed ID: 10783262
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Retinal fascin: functional nature, subcellular distribution, and chromosomal localization.
    Saishin Y; Ishikawa R; Ugawa S; Guo W; Ueda T; Morimura H; Kohama K; Shimizu H; Tano Y; Shimada S
    Invest Ophthalmol Vis Sci; 2000 Jul; 41(8):2087-95. PubMed ID: 10892848
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Testis fascin (FSCN3): a novel paralog of the actin-bundling protein fascin expressed specifically in the elongate spermatid head.
    Tubb B; Mulholland DJ; Vogl W; Lan ZJ; Niederberger C; Cooney A; Bryan J
    Exp Cell Res; 2002 Apr; 275(1):92-109. PubMed ID: 11925108
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sequence variations in the retinal fascin FSCN2 gene in a Spanish population with autosomal dominant retinitis pigmentosa or macular degeneration.
    Gamundi MJ; Hernan I; Maseras M; Baiget M; Ayuso C; Borrego S; Antiñolo G; Millán JM; Valverde D; Carballo M
    Mol Vis; 2005 Nov; 11():922-8. PubMed ID: 16280978
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cloning and characterization of the canine photoreceptor specific cone-rod homeobox (CRX) gene and evaluation as a candidate for early onset photoreceptor diseases in the dog.
    Akhmedov NB; Baldwin VJ; Zangerl B; Kijas JW; Hunter L; Minoofar KD; Mellersh C; Ostrander EA; Acland GM; Farber DB; Aguirre GD
    Mol Vis; 2002 Mar; 8():79-84. PubMed ID: 11951083
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Human bZIP transcription factor gene NRL: structure, genomic sequence, and fine linkage mapping at 14q11.2 and negative mutation analysis in patients with retinal degeneration.
    Farjo Q; Jackson A; Pieke-Dahl S; Scott K; Kimberling WJ; Sieving PA; Richards JE; Swaroop A
    Genomics; 1997 Oct; 45(2):395-401. PubMed ID: 9344665
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Refinement of the RP17 locus for autosomal dominant retinitis pigmentosa, construction of a YAC contig and investigation of the candidate gene retinal fascin.
    Bardien-Kruger S; Greenberg J; Tubb B; Bryan J; Queimado L; Lovett M; Ramesar RS
    Eur J Hum Genet; 1999 Apr; 7(3):332-8. PubMed ID: 10234509
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Targeted disruption of FSCN2 gene induces retinopathy in mice.
    Yokokura S; Wada Y; Nakai S; Sato H; Yao R; Yamanaka H; Ito S; Sagara Y; Takahashi M; Nakamura Y; Tamai M; Noda T
    Invest Ophthalmol Vis Sci; 2005 Aug; 46(8):2905-15. PubMed ID: 16043865
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genomic organization and mutation analysis of the gene encoding lecithin retinol acyltransferase in human retinal pigment epithelium.
    Ruiz A; Kuehn MH; Andorf JL; Stone E; Hageman GS; Bok D
    Invest Ophthalmol Vis Sci; 2001 Jan; 42(1):31-7. PubMed ID: 11133845
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutation of human retinal fascin gene (FSCN2) causes autosomal dominant retinitis pigmentosa.
    Wada Y; Abe T; Takeshita T; Sato H; Yanashima K; Tamai M
    Invest Ophthalmol Vis Sci; 2001 Sep; 42(10):2395-400. PubMed ID: 11527955
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genomic organization of the JEM-1 (BLZF1) gene on human chromosome 1q24: molecular cloning and analysis of its promoter region.
    Tong JH; Fant X; Benoit G; Chen SJ; Chen Z; Lanotte M
    Genomics; 2000 Nov; 69(3):380-90. PubMed ID: 11056056
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The actin-bundling protein fascin is involved in the formation of dendritic processes in maturing epidermal Langerhans cells.
    Ross R; Ross XL; Schwing J; Längin T; Reske-Kunz AB
    J Immunol; 1998 Apr; 160(8):3776-82. PubMed ID: 9558080
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Isolation, characterization and evolution of nine pufferfish (Fugu rubripes) actin genes.
    Venkatesh B; Tay BH; Elgar G; Brenner S
    J Mol Biol; 1996 Jun; 259(4):655-65. PubMed ID: 8683572
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mammalian orthologs of C. elegans unc-119 highly expressed in photoreceptors.
    Swanson DA; Chang JT; Campochiaro PA; Zack DJ; Valle D
    Invest Ophthalmol Vis Sci; 1998 Oct; 39(11):2085-94. PubMed ID: 9761287
    [TBL] [Abstract][Full Text] [Related]  

  • 15. RINX(VSX1), a novel homeobox gene expressed in the inner nuclear layer of the adult retina.
    Hayashi T; Huang J; Deeb SS
    Genomics; 2000 Jul; 67(2):128-39. PubMed ID: 10903837
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Isolation of a cDNA encoding a photoreceptor cell-specific actin-bundling protein: retinal fascin.
    Saishin Y; Shimada S; Morimura H; Sato K; Ishimoto I; Tano Y; Tohyama M
    FEBS Lett; 1997 Sep; 414(2):381-6. PubMed ID: 9315724
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cloning, mapping, and expression of two novel actin genes, actin-like-7A (ACTL7A) and actin-like-7B (ACTL7B), from the familial dysautonomia candidate region on 9q31.
    Chadwick BP; Mull J; Helbling LA; Gill S; Leyne M; Robbins CM; Pinkett HW; Makalowska I; Maayan C; Blumenfeld A; Axelrod FB; Brownstein M; Gusella JF; Slaugenhaupt SA
    Genomics; 1999 Jun; 58(3):302-9. PubMed ID: 10373328
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic and physical mapping of human recoverin: a gene expressed in retinal photoreceptors.
    Wiechmann AF; Akots G; Hammarback JA; Pettenati MJ; Rao PN; Bowden DW
    Invest Ophthalmol Vis Sci; 1994 Feb; 35(2):325-31. PubMed ID: 7906682
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Isolation and characterization of a zebrafish homologue of the cone rod homeobox gene.
    Liu Y; Shen Y; Rest JS; Raymond PA; Zack DJ
    Invest Ophthalmol Vis Sci; 2001 Feb; 42(2):481-7. PubMed ID: 11157887
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cloning of a portion of the chromosomal gene and cDNA for human beta-fodrin, the nonerythroid form of beta-spectrin.
    Chang JG; Scarpa A; Eddy RL; Byers MG; Harris AS; Morrow JS; Watkins P; Shows TB; Forget BG
    Genomics; 1993 Aug; 17(2):287-93. PubMed ID: 8406479
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.