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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

125 related items for PubMed ID: 8980123

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Cross-species homology of the CLN3 gene.
    Taschner PE, de Vos N, Breuning MH.
    Neuropediatrics; 1997 Feb; 28(1):18-20. PubMed ID: 9151313
    [Abstract] [Full Text] [Related]

  • 6. Strategy for mutation detection in CLN3: characterisation of two Finnish mutations.
    Munroe PB, O'Rawe AM, Mitchison HM, Järvelä IE, Santavuori P, Lerner TJ, Taschner PE, Gardiner RM, Mole SE.
    Neuropediatrics; 1997 Feb; 28(1):15-7. PubMed ID: 9151312
    [Abstract] [Full Text] [Related]

  • 7. A yeast model for the study of Batten disease.
    Pearce DA, Sherman F.
    Proc Natl Acad Sci U S A; 1998 Jun 09; 95(12):6915-8. PubMed ID: 9618513
    [Abstract] [Full Text] [Related]

  • 8. Farnesylation of Batten disease CLN3 protein.
    Pullarkat RK, Morris GN.
    Neuropediatrics; 1997 Feb 09; 28(1):42-4. PubMed ID: 9151320
    [Abstract] [Full Text] [Related]

  • 9. Structure of the CLN3 gene and predicted structure, location and function of CLN3 protein.
    Mitchison HM, Taschner PE, Kremmidiotis G, Callen DF, Doggett NA, Lerner TJ, Janes RB, Wallace BA, Munroe PB, O'Rawe AM, Gardiner RM, Mole SE.
    Neuropediatrics; 1997 Feb 09; 28(1):12-4. PubMed ID: 9151311
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Gene symbol: CLN3. Disease: Juvenile neuronal ceroid lipofuscinosis (Batten disease).
    Leman AR, Pearce DA, Rothberg PG.
    Hum Genet; 2005 May 09; 116(6):544. PubMed ID: 15991331
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Defective lysosomal arginine transport in juvenile Batten disease.
    Ramirez-Montealegre D, Pearce DA.
    Hum Mol Genet; 2005 Dec 01; 14(23):3759-73. PubMed ID: 16251196
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Action of BTN1, the yeast orthologue of the gene mutated in Batten disease.
    Pearce DA, Ferea T, Nosel SA, Das B, Sherman F.
    Nat Genet; 1999 May 01; 22(1):55-8. PubMed ID: 10319861
    [Abstract] [Full Text] [Related]

  • 20. Experimental models of NCL: the yeast model.
    Pearce DA.
    Adv Genet; 2001 May 01; 45():205-16. PubMed ID: 11332774
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.