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

181 related items for PubMed ID: 9789042

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Structures, sequence characteristics, and synteny relationships of the transcription factor E4TF1, the splicing factor U2AF35 and the cystathionine beta synthetase genes from Fugu rubripes.
    Tassone F, Villard L, Clancy K, Gardiner K.
    Gene; 1999 Jan 21; 226(2):211-23. PubMed ID: 9931491
    [Abstract] [Full Text] [Related]

  • 23. [Aniridia-Wilms tumor association].
    Imaizumi K.
    Ryoikibetsu Shokogun Shirizu; 2000 Jan 21; (30 Pt 5):327-8. PubMed ID: 11057248
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26. Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene.
    Glaser T, Walton DS, Maas RL.
    Nat Genet; 1992 Nov 21; 2(3):232-9. PubMed ID: 1345175
    [Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. A LINE element is present at the site of a 300-kb deletion starting in intron 10 of the PAX6 gene in a case of familial aniridia.
    Drechsler M, Royer-Pokora B.
    Hum Genet; 1996 Sep 21; 98(3):297-303. PubMed ID: 8707297
    [Abstract] [Full Text] [Related]

  • 29. Characterization of the Fugu rubripes NLK and FN5 genes flanking the NF1 (Neurofibromatosis type 1) gene in the 5' direction and mapping of the human counterparts.
    Kehrer-Sawatzki H, Moschgath E, Maier C, Legius E, Elgar G, Krone W.
    Gene; 2000 Jun 13; 251(1):63-71. PubMed ID: 10863097
    [Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31. Mutation in the PAX6 gene in twenty patients with aniridia.
    Chao LY, Huff V, Strong LC, Saunders GF.
    Hum Mutat; 2000 Jun 13; 15(4):332-9. PubMed ID: 10737978
    [Abstract] [Full Text] [Related]

  • 32. Comparative analysis of a 229-kb medaka genomic region, containing the zic1 and zic4 genes, with Fugu, human, and mouse.
    Ohtsuka M, Kikuchi N, Ozato K, Inoko H, Kimura M.
    Genomics; 2004 Jun 13; 83(6):1063-71. PubMed ID: 15177559
    [Abstract] [Full Text] [Related]

  • 33. Genomic structure and comparative analysis of nine Fugu genes: conservation of synteny with human chromosome Xp22.2-p22.1.
    Brunner B, Todt T, Lenzner S, Stout K, Schulz U, Ropers HH, Kalscheuer VM.
    Genome Res; 1999 May 13; 9(5):437-48. PubMed ID: 10330123
    [Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36. Genomic structure and expression of parathyroid hormone-related protein gene (PTHrP) in a teleost, Fugu rubripes.
    Power DM, Ingleton PM, Flanagan J, Canario AV, Danks J, Elgar G, Clark MS.
    Gene; 2000 May 30; 250(1-2):67-76. PubMed ID: 10854780
    [Abstract] [Full Text] [Related]

  • 37. The evolution of WT1 sequence and expression pattern in the vertebrates.
    Kent J, Coriat AM, Sharpe PT, Hastie ND, van Heyningen V.
    Oncogene; 1995 Nov 02; 11(9):1781-92. PubMed ID: 7478606
    [Abstract] [Full Text] [Related]

  • 38. Conserved synteny between the Fugu and human PTEN locus and the evolutionary conservation of vertebrate PTEN function.
    Yu WP, Pallen CJ, Tay A, Jirik FR, Brenner S, Tan YH, Venkatesh B.
    Oncogene; 2001 Sep 06; 20(39):5554-61. PubMed ID: 11571655
    [Abstract] [Full Text] [Related]

  • 39. Mosaic deletion 11p13 in a child with dopamine beta-hydroxylase deficiency--case report and review of the literature.
    Erez A, Li J, Geraghty MT, Ben-Shachar S, Cooper ML, Mensing DE, Vonalt KD, Ou Z, Pursley AN, Chinault AC, Patel A, Cheung SW, Sahoo T.
    Am J Med Genet A; 2010 Mar 06; 152A(3):732-6. PubMed ID: 20186791
    [Abstract] [Full Text] [Related]

  • 40. Three patients with hallucal polydactyly and WAGR syndrome, including discordant expression of Wilms tumor in MZ twins.
    Brémond-Gignac D, Gérard-Blanluet M, Copin H, Bitoun P, Baumann C, Crolla JA, Benzacken B, Verloes A.
    Am J Med Genet A; 2005 May 01; 134(4):422-5. PubMed ID: 15779023
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 10.