Published in J Exp Zool on April 15, 2000
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A new polymorphic probe close to HLA-A. Nucleic Acids Res (1991) 1.67
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Detailed map of a region commonly amplified at 11q13-->q14 in human breast carcinoma. Cytogenet Cell Genet (1997) 1.48
A novel coding sequence belonging to a new multicopy gene family mapping within the human MHC class I region. Immunogenetics (1993) 1.47
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Differential expression assay of chromosome arm 8p genes identifies Frizzled-related (FRP1/FRZB) and Fibroblast Growth Factor Receptor 1 (FGFR1) as candidate breast cancer genes. Oncogene (1999) 1.39
Expression of the FMS/KIT-like gene FLT3 in human acute leukemias of the myeloid and lymphoid lineages. Blood (1992) 1.37
Genome-wide search for loss of heterozygosity shows extensive genetic diversity of human breast carcinomas. Cancer Res (1997) 1.33
Human FLT3/FLK2 gene: cDNA cloning and expression in hematopoietic cells. Blood (1993) 1.32
MOZ is fused to p300 in an acute monocytic leukemia with t(8;22). Genes Chromosomes Cancer (2000) 1.30
The mapping of the human 52-kD Ro/SSA autoantigen gene to human chromosome 11, and its polymorphisms. Am J Hum Genet (1993) 1.24
Murine FGF-12 and FGF-13: expression in embryonic nervous system, connective tissue and heart. Mech Dev (1997) 1.22
The t(6;8)(q27;p11) translocation in a stem cell myeloproliferative disorder fuses a novel gene, FOP, to fibroblast growth factor receptor 1. Blood (1999) 1.21
Structure and expression of human fibroblast growth factor-10. J Biol Chem (1997) 1.20
FGFR1 is fused to the centrosome-associated protein CEP110 in the 8p12 stem cell myeloproliferative disorder with t(8;9)(p12;q33). Blood (2000) 1.20
Frequent generation of oncogenes by in vitro recombination of TRK protooncogene sequences. Proc Natl Acad Sci U S A (1988) 1.15
Fibroblast growth factor receptor-4 shows novel features in genomic structure, ligand binding and signal transduction. EMBO J (1992) 1.14
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Homeobox gene clusters and the human paralogy map. FEBS Lett (2001) 1.13
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B30.2-like domain proteins: a growing family. Biochem Biophys Res Commun (1997) 1.09
let-756, a C. elegans fgf essential for worm development. Oncogene (1999) 1.02
Cloning, structural analysis, and mapping of the B30 and B7 multigenic families to the major histocompatibility complex (MHC) and other chromosomal regions. Immunogenetics (1997) 1.01
The family of Caenorhabditis elegans tyrosine kinase receptors: similarities and differences with mammalian receptors. Genome Res (1999) 1.00
Characterization of FIM-FGFR1, the fusion product of the myeloproliferative disorder-associated t(8;13) translocation. J Biol Chem (1999) 1.00
Coparalogy: physical and functional clusterings in the human genome. Biochem Biophys Res Commun (2001) 0.98
Evolutionary study of multigenic families mapping close to the human MHC class I region. J Mol Evol (1993) 0.96
Structure and evolution of a member of a new subfamily of GTP-binding proteins mapping to the human MHC class I region. Mamm Genome (1994) 0.95
A susceptibility region for myasthenia gravis extending into the HLA-class I sector telomeric to HLA-C. Hum Immunol (1999) 0.94
New highly polymorphic microsatellite marker in linkage disequilibrium with HLA-B. Hum Immunol (1996) 0.94
The human interleukin-1 alpha gene is located on the long arm of chromosome 2 at band q13. Blood (1989) 0.94
The MHC big bang. Immunol Rev (1999) 0.93
Chromosome region 8p11-p21: refined mapping and molecular alterations in breast cancer. Genes Chromosomes Cancer (1998) 0.92
gamma-heregulin is the product of a chromosomal translocation fusing the DOC4 and HGL/NRG1 genes in the MDA-MB-175 breast cancer cell line. Oncogene (1999) 0.91
Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13). Proc Natl Acad Sci U S A (1998) 0.91
DOK4 and DOK5: new Dok-related genes expressed in human T cells. Genes Immun (2003) 0.89
Cloning, localization, and structure of new members of the butyrophilin gene family in the juxta-telomeric region of the major histocompatibility complex. Immunogenetics (1997) 0.89
The chromosome region containing the highly polymorphic HLA class I genes displays limited large scale variability in the human population. EMBO J (1988) 0.88
Chromosomal mapping of two novel human FGF genes, FGF11 and FGF12. Genomics (1997) 0.87
A continuous restriction map from HLA-E to HLA-F. Structural comparison between different HLA-A haplotypes. Immunogenetics (1992) 0.87
Creation of an HLA-A2/HLA-Aw69 alloantigenic determinant on an HLA-A3 molecule by site-directed mutagenesis. J Immunol (1987) 0.86
Assignment of FGF13 to human chromosome band Xq21 by in situ hybridization. Cytogenet Cell Genet (1997) 0.84
FGF6 modulates the expression of fibroblast growth factor receptors and myogenic genes in muscle cells. Exp Cell Res (1996) 0.84
Two polymorphisms at the locus D698 defined by a YAC. Nucleic Acids Res (1990) 0.84
HLA-E is the only class I gene that escapes CpG methylation and is transcriptionally active in the trophoblast-derived human cell line JAR. Immunogenetics (1993) 0.84
Chromosomal localizations of mouse Fgf2 and Fgf5 genes. Mamm Genome (1992) 0.83
Neuropeptides in the sympathetic innervations of the cochlea. Adv Otorhinolaryngol (1990) 0.83
t(6;8), t(8;9) and t(8;13) translocations associated with stem cell myeloproliferative disorders have close or identical breakpoints in chromosome region 8p11-12. Oncogene (1998) 0.82
Characterization of the region of the short arm of chromosome 8 amplified in breast carcinoma. Oncogene (1995) 0.82
Identification and characterization of a beta proteasome subunit cluster in the Japanese pufferfish (Fugu rubripes). J Immunol (2000) 0.82
Cell cycle-dependent expression of early viral genes in one group of simian virus 40-transformed rat cells. EMBO J (1984) 0.82
In situ hybridization localizes the human OTF3 to chromosome 6p21.3-->p22 and OTF3L to 12p13. Cytogenet Cell Genet (1993) 0.82
The human FGF9 gene maps to chromosomal region 13q11-q12. Genomics (1995) 0.82
Integrated map of the chromosome 8p12-p21 region, a region involved in human cancers and Werner syndrome. Genomics (1996) 0.81
The 8p12 myeloproliferative disorder. t(8;19)(p12;q13.3): a novel translocation involving the FGFR1 gene. Br J Haematol (2000) 0.81
Electron microscopic studies of silver-strained proteins in nucleolar organizer regions: location in nucleoli of rat sympathetic neurons during light and dark periods. J Cell Sci (1981) 0.80
Assignment of Fgf12 to mouse chromosome bands 16B1-->B3 by in situ hybridization. Cytogenet Cell Genet (1997) 0.80
Mouse fgf9 (fibroblast growth factor 9) is localized on chromosome 14. Mamm Genome (1997) 0.80
Molecular analysis of the human MHC class I region using yeast artificial chromosome clones. Immunogenetics (1990) 0.80
YAC-assisted cloning of a putative G-protein mapping to the MHC class I region. Genomics (1992) 0.80
Physical mapping between the S and HLA-E genes in the human MHC class I region: construction of a BAC, PAC, and cosmid contig. Immunogenetics (1998) 0.80
Combined and sequential effects of human IL-3 and GM-CSF on the proliferation of CD34+ hematopoietic cells from cord blood. Blood (1989) 0.80
Coexistence of putative neuroactive substances in lateral olivocochlear neurons of rat and guinea pig. Hear Res (1987) 0.80
Differences between human sperm and somatic cell DNA in CpG methylation within the HLA class I chromosomal region. Am J Reprod Immunol (1993) 0.80
Molecular linkage of the human CTLA4 and CD28 Ig-superfamily genes in yeast artificial chromosomes. Genomics (1992) 0.80
A rigorous method for multigenic families' functional annotation: the peptidyl arginine deiminase (PADs) proteins family example. BMC Genomics (2005) 0.79
The 11q13 amplicon of a mammary carcinoma cell line. Genes Chromosomes Cancer (1990) 0.79
The human myelin oligodendrocyte glycoprotein (MOG) gene: complete nucleotide sequence and structural characterization. Genomics (1995) 0.79
Sequence analysis of full length cDNA for enhancing factor/phospholipase A2. Indian J Exp Biol (1998) 0.79
Characterization of a yeast artificial chromosome from human chromosome band 13q12 containing the FLT1 and FLT3 receptor-type tyrosine kinase genes. Cytogenet Cell Genet (1994) 0.79
Familial screening for genetic haemochromatosis by means of DNA markers. J Med Genet (1992) 0.78
Cytotoxic activity of a diptheria toxin/FGF6 mitotoxin on human tumour cell lines. Oncogene (1997) 0.77
A case of inv(8)(p11q24) associated with acute myeloid leukemia involves the MOZ and CBP genes in a masked t(8;16). Genes Chromosomes Cancer (1999) 0.77
Chronobiological studies on the nucleolus. Chronobiol Int (1985) 0.77
Analysis of HLA-A/B recombinant families with new polymorphic markers. Hum Immunol (1993) 0.77
Nucleotide sequence of the BALB/c H-2T region gene, T3d. Immunogenetics (1992) 0.77
A 3.1-Mb YAC contig within the Werner syndrome region, on the short arm of human chromosome 8. Cytogenet Cell Genet (1996) 0.77
A first map of the porcine major histocompatibility complex class I region. Tissue Antigens (1998) 0.77
Production and functional characterization of human recombinant FGF-6 protein. Cell Growth Differ (1991) 0.76
Expressed sequence tags identify human isologs of the ARF-dependent phospholipase D. Biochem Biophys Res Commun (1996) 0.76
Mapping of the Olf89 and Rfp genes to the rat genome: comparison with the mouse and human and new insights into the evolution of the rodent genome. Cytogenet Cell Genet (1997) 0.76
A precise meiotic map in the class I region of the human major histocompatibility complex. Genomics (1995) 0.76
Identification of a YAC spanning the translocation breakpoint t(8;22) associated with acute monocytic leukemia. Genes Chromosomes Cancer (1996) 0.76
Myelin oligodendrocyte glycoprotein (MOG) gene polymorphisms and multiple sclerosis: no evidence of disease association with MOG. J Neuroimmunol (1995) 0.75