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Journal Abstract Search

181 related items for PubMed ID: 9789042

  • 1. Complete sequencing of the Fugu WAGR region from WT1 to PAX6: dramatic compaction and conservation of synteny with human chromosome 11p13.
    Miles C, Elgar G, Coles E, Kleinjan DJ, van Heyningen V, Hastie N.
    Proc Natl Acad Sci U S A; 1998 Oct 27; 95(22):13068-72. PubMed ID: 9789042
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  • 2. Cloning and sequencing of complement component C9 and its linkage to DOC-2 in the pufferfish Fugu rubripes.
    Yeo GS, Elgar G, Sandford R, Brenner S.
    Gene; 1997 Oct 24; 200(1-2):203-11. PubMed ID: 9373156
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  • 3. Analysis of the conservation of synteny between Fugu and human chromosome 12.
    Montpetit A, Wilson MD, Chevrette M, Koop BF, Sinnett D.
    BMC Genomics; 2003 Jul 23; 4(1):30. PubMed ID: 12877756
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  • 4. Polymerase chain reaction-based risk assessment for Wilms tumor in sporadic aniridia.
    Gupta SK, De Becker I, Guernsey DL, Neumann PE.
    Am J Ophthalmol; 1998 May 23; 125(5):687-92. PubMed ID: 9625553
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  • 5. Conservation of synteny between the genome of the pufferfish (Fugu rubripes) and the region on human chromosome 14 (14q24.3) associated with familial Alzheimer disease (AD3 locus).
    Trower MK, Orton SM, Purvis IJ, Sanseau P, Riley J, Christodoulou C, Burt D, See CG, Elgar G, Sherrington R, Rogaev EI, St George-Hyslop P, Brenner S, Dykes CW.
    Proc Natl Acad Sci U S A; 1996 Feb 20; 93(4):1366-9. PubMed ID: 8643637
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  • 6. Distinct cis-essential modules direct the time-space pattern of the Pax6 gene activity.
    Kammandel B, Chowdhury K, Stoykova A, Aparicio S, Brenner S, Gruss P.
    Dev Biol; 1999 Jan 01; 205(1):79-97. PubMed ID: 9882499
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  • 7. Frequent chromosome aberrations revealed by molecular cytogenetic studies in patients with aniridia.
    Crolla JA, van Heyningen V.
    Am J Hum Genet; 2002 Nov 01; 71(5):1138-49. PubMed ID: 12386836
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  • 9. Characterization of the recombinase activating gene-1 and 2 locus in the Japanese pufferfish, Fugu rubripes.
    Peixoto BR, Mikawa Y, Brenner S.
    Gene; 2000 Apr 04; 246(1-2):275-83. PubMed ID: 10767549
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  • 10. Narrowing of the responsible region for severe developmental delay and autistic behaviors in WAGR syndrome down to 1.6 Mb including PAX6, WT1, and PRRG4.
    Yamamoto T, Togawa M, Shimada S, Sangu N, Shimojima K, Okamoto N.
    Am J Med Genet A; 2014 Mar 04; 164A(3):634-8. PubMed ID: 24357251
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  • 11. Congenital diaphragmatic hernia in WAGR syndrome.
    Scott DA, Cooper ML, Stankiewicz P, Patel A, Potocki L, Cheung SW.
    Am J Med Genet A; 2005 May 01; 134(4):430-3. PubMed ID: 15779010
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  • 17. Characterization of three genes, AKAP84, BAW and WSB1, located 3' to the neurofibromatosis type 1 locus in Fugu rubripes.
    Kehrer-Sawatzki H, Maier C, Moschgath E, Elgar G, Krone W.
    Gene; 1999 Jul 22; 235(1-2):1-11. PubMed ID: 10415327
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  • 20. Complete sex reversal in a WAGR syndrome patient.
    Le Caignec C, Delnatte C, Vermeesch JR, Boceno M, Joubert M, Lavenant F, David A, Rival JM.
    Am J Med Genet A; 2007 Nov 15; 143A(22):2692-5. PubMed ID: 17935232
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