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 *

221 related articles for article (PubMed ID: 9177781)

  • 1. Plectin transcript diversity: identification and tissue distribution of variants with distinct first coding exons and rodless isoforms.
    Elliott CE; Becker B; Oehler S; Castañón MJ; Hauptmann R; Wiche G
    Genomics; 1997 May; 42(1):115-25. PubMed ID: 9177781
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Unusual 5' transcript complexity of plectin isoforms: novel tissue-specific exons modulate actin binding activity.
    Fuchs P; Zörer M; Rezniczek GA; Spazierer D; Oehler S; Castañón MJ; Hauptmann R; Wiche G
    Hum Mol Genet; 1999 Dec; 8(13):2461-72. PubMed ID: 10556294
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Plectin expression patterns determine two distinct subtypes of epidermolysis bullosa simplex.
    Natsuga K; Nishie W; Akiyama M; Nakamura H; Shinkuma S; McMillan JR; Nagasaki A; Has C; Ouchi T; Ishiko A; Hirako Y; Owaribe K; Sawamura D; Bruckner-Tuderman L; Shimizu H
    Hum Mutat; 2010 Mar; 31(3):308-16. PubMed ID: 20052759
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of novel first exons in Ad4BP/SF-1 (NR5A1) gene and their tissue- and species-specific usage.
    Kimura R; Yoshii H; Nomura M; Kotomura N; Mukai T; Ishihara S; Ohba K; Yanase T; Gotoh O; Nawata H; Morohashi K
    Biochem Biophys Res Commun; 2000 Nov; 278(1):63-71. PubMed ID: 11071856
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Plectin deficiency results in muscular dystrophy with epidermolysis bullosa.
    Smith FJ; Eady RA; Leigh IM; McMillan JR; Rugg EL; Kelsell DP; Bryant SP; Spurr NK; Geddes JF; Kirtschig G; Milana G; de Bono AG; Owaribe K; Wiche G; Pulkkinen L; Uitto J; McLean WH; Lane EB
    Nat Genet; 1996 Aug; 13(4):450-7. PubMed ID: 8696340
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization.
    McLean WH; Pulkkinen L; Smith FJ; Rugg EL; Lane EB; Bullrich F; Burgeson RE; Amano S; Hudson DL; Owaribe K; McGrath JA; McMillan JR; Eady RA; Leigh IM; Christiano AM; Uitto J
    Genes Dev; 1996 Jul; 10(14):1724-35. PubMed ID: 8698233
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Human plectin: organization of the gene, sequence analysis, and chromosome localization (8q24).
    Liu CG; Maercker C; Castañon MJ; Hauptmann R; Wiche G
    Proc Natl Acad Sci U S A; 1996 Apr; 93(9):4278-83. PubMed ID: 8633055
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Comparative genomic sequence analysis and isolation of human and mouse alternative EGFR transcripts encoding truncated receptor isoforms.
    Reiter JL; Threadgill DW; Eley GD; Strunk KE; Danielsen AJ; Sinclair CS; Pearsall RS; Green PJ; Yee D; Lampland AL; Balasubramaniam S; Crossley TD; Magnuson TR; James CD; Maihle NJ
    Genomics; 2001 Jan; 71(1):1-20. PubMed ID: 11161793
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms.
    Lee PL; Gelbart T; West C; Halloran C; Beutler E
    Blood Cells Mol Dis; 1998 Jun; 24(2):199-215. PubMed ID: 9642100
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular cloning of macrophin, a human homologue of Drosophila kakapo with a close structural similarity to plectin and dystrophin.
    Okuda T; Matsuda S; Nakatsugawa S; Ichigotani Y; Iwahashi N; Takahashi M; Ishigaki T; Hamaguchi M
    Biochem Biophys Res Commun; 1999 Oct; 264(2):568-74. PubMed ID: 10529403
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel compound heterozygous mutations in the plectin gene in epidermolysis bullosa with muscular dystrophy and the use of protein truncation test for detection of premature termination codon mutations.
    Dang M; Pulkkinen L; Smith FJ; McLean WH; Uitto J
    Lab Invest; 1998 Feb; 78(2):195-204. PubMed ID: 9484717
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Conservation and expression of an alternative 3' exon of Runx2 encoding a novel proline-rich C-terminal domain.
    Terry A; Kilbey A; Vaillant F; Stewart M; Jenkins A; Cameron E; Neil JC
    Gene; 2004 Jul; 336(1):115-25. PubMed ID: 15225881
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Two isoforms of a human intersectin (ITSN) protein are produced by brain-specific alternative splicing in a stop codon.
    Guipponi M; Scott HS; Chen H; Schebesta A; Rossier C; Antonarakis SE
    Genomics; 1998 Nov; 53(3):369-76. PubMed ID: 9799604
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Plectin rodless isoform expression and its detection in mouse brain.
    Fuchs P; Spazierer D; Wiche G
    Cell Mol Neurobiol; 2005 Nov; 25(7):1141-50. PubMed ID: 16392042
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Characterization of three splice variants and genomic organization of the mouse BMAL1 gene.
    Yu W; Ikeda M; Abe H; Honma S; Ebisawa T; Yamauchi T; Honma K; Nomura M
    Biochem Biophys Res Commun; 1999 Jul; 260(3):760-7. PubMed ID: 10403839
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genomic organization and tissue-specific expression of splice variants of mouse organic anion transporting polypeptide 2.
    Ogura K; Choudhuri S; Klaassen CD
    Biochem Biophys Res Commun; 2001 Feb; 281(2):431-9. PubMed ID: 11181066
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Plectin 5'-transcript diversity: short alternative sequences determine stability of gene products, initiation of translation and subcellular localization of isoforms.
    Rezniczek GA; Abrahamsberg C; Fuchs P; Spazierer D; Wiche G
    Hum Mol Genet; 2003 Dec; 12(23):3181-94. PubMed ID: 14559777
    [TBL] [Abstract][Full Text] [Related]  

  • 18. cDNA cloning, genomic structure, and chromosome mapping of the human epithelial membrane protein CL-20 gene (EMP1), a member of the PMP22 family.
    Chen Y; Medvedev A; Ruzanov P; Marvin KW; Jetten AM
    Genomics; 1997 Apr; 41(1):40-8. PubMed ID: 9126480
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of three mouse mu-opioid receptor (MOR) gene (Oprm1) splice variants containing a newly identified alternatively spliced exon.
    Doyle GA; Rebecca Sheng X; Lin SS; Press DM; Grice DE; Buono RJ; Ferraro TN; Berrettini WH
    Gene; 2007 Feb; 388(1-2):135-47. PubMed ID: 17156941
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Revised genomic structure of the human ghrelin gene and identification of novel exons, alternative splice variants and natural antisense transcripts.
    Seim I; Collet C; Herington AC; Chopin LK
    BMC Genomics; 2007 Aug; 8():298. PubMed ID: 17727735
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.