Published in Mamm Genome on September 01, 1995
PAGE-1, an X chromosome-linked GAGE-like gene that is expressed in normal and neoplastic prostate, testis, and uterus. Proc Natl Acad Sci U S A (1998) 1.24
MAGE-A1 interacts with adaptor SKIP and the deacetylase HDAC1 to repress transcription. Nucleic Acids Res (2004) 1.17
Evolution of the exon-intron structure and alternative splicing of the MAGE-A family of cancer/testis antigens. J Mol Evol (2004) 0.97
Targeted next-generation sequencing identification of mutations in patients with disorders of sex development. BMC Med Genet (2016) 0.84
Consequences of point mutations in melanoma-associated antigen 4 (MAGE-A4) protein: Insights from structural and biophysical studies. Sci Rep (2016) 0.77
MAGE-B2 autoantibody: a new biomarker for pediatric systemic lupus erythematosus. J Rheumatol (2008) 0.76
Multigeneration Inheritance through Fertile XX Carriers of an NR0B1 (DAX1) Locus Duplication in a Kindred of Females with Isolated XY Gonadal Dysgenesis. Int J Endocrinol (2012) 0.75
A Comprehensive Guide to the MAGE Family of Ubiquitin Ligases. J Mol Biol (2017) 0.75
Basic local alignment search tool. J Mol Biol (1990) 659.07
Compilation and analysis of sequences upstream from the translational start site in eukaryotic mRNAs. Nucleic Acids Res (1984) 39.52
Simple methods for estimating the numbers of synonymous and nonsynonymous nucleotide substitutions. Mol Biol Evol (1986) 36.06
CLUSTAL V: improved software for multiple sequence alignment. Comput Appl Biosci (1992) 35.52
Pattern of nucleotide substitution at major histocompatibility complex class I loci reveals overdominant selection. Nature (1988) 15.05
A gene encoding an antigen recognized by cytolytic T lymphocytes on a human melanoma. Science (1991) 14.57
Nucleotide substitution at major histocompatibility complex class II loci: evidence for overdominant selection. Proc Natl Acad Sci U S A (1989) 4.52
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules. Nature (1991) 3.59
Mammalian gene evolution: nucleotide sequence divergence between mouse and rat. J Mol Evol (1993) 2.97
Structure, chromosomal localization, and expression of 12 genes of the MAGE family. Immunogenetics (1994) 2.93
An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita. Nature (1994) 2.57
Rapid sequence evolution of the mammalian sex-determining gene SRY. Nature (1993) 2.52
Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism. Nature (1994) 2.49
Accelerated evolution in the reactive centre regions of serine protease inhibitors. Nature (1987) 2.40
Mus poschiavinus Y chromosome in the C57BL/6J murine genome causes sex reversal. Science (1982) 1.81
A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal. Nat Genet (1994) 1.78
Genetically determined sex-reversal in 46,XY humans. Science (1978) 1.76
Rapid evolution of the sex determining locus in Old World mice and rats. Nature (1993) 1.62
Heterogeneity analysis in 40 X-linked retinitis pigmentosa families. Am J Hum Genet (1994) 1.38
A strategy for the selection of transcribed sequences in the Xq28 region. Hum Mol Genet (1992) 1.28
A novel brain-specific mRNA encoding nuclear protein (necdin) expressed in neurally differentiated embryonal carcinoma cells. Biochem Biophys Res Commun (1991) 1.17
Embryonic growth and the evolution of the mammalian Y chromosome. II. Suppression of selfish Y-linked growth factors may explain escape from X-inactivation and rapid evolution of Sry. Heredity (Edinb) (1994) 0.91
A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genes. Hum Mol Genet (1992) 0.86
Identification of new markers in Xp21 between DXS28 (C7) and DMD. Genomics (1992) 0.80
Yeast artificial chromosome cloning in the glycerol kinase and adrenal hypoplasia congenita region of Xp21. Genomics (1993) 0.79
Localization of the MAGE1 gene encoding a human melanoma antigen to chromosome Xq28. Cytogenet Cell Genet (1994) 0.77
A gene encoding an antigen recognized by cytolytic T lymphocytes on a human melanoma. Science (1991) 14.57
The tripartite motif family identifies cell compartments. EMBO J (2001) 9.64
A new gene coding for a differentiation antigen recognized by autologous cytolytic T lymphocytes on HLA-A2 melanomas. J Exp Med (1994) 5.03
HSV-TK gene transfer into donor lymphocytes for control of allogeneic graft-versus-leukemia. Science (1997) 4.58
Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms. Proc Natl Acad Sci U S A (1984) 4.22
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules. Nature (1991) 3.59
The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif. EMBO J (2001) 3.42
Type 1 T regulatory cells. Immunol Rev (2001) 3.26
Tumor regressions observed in patients with metastatic melanoma treated with an antigenic peptide encoded by gene MAGE-3 and presented by HLA-A1. Int J Cancer (1999) 3.19
Structure, chromosomal localization, and expression of 12 genes of the MAGE family. Immunogenetics (1994) 2.93
The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency. Proc Natl Acad Sci U S A (1985) 2.88
An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita. Nature (1994) 2.57
Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism. Nature (1994) 2.49
Differentiation of T regulatory cells by immature dendritic cells. J Exp Med (2001) 2.35
Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male. Nature (1984) 2.28
Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus). Proc Natl Acad Sci U S A (1984) 2.23
A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P. Proc Natl Acad Sci U S A (2001) 2.17
Rexpression of HLA class I antigens and restoration of antigen-specific CTL response in melanoma cells following 5-aza-2'-deoxycytidine treatment. Int J Cancer (2001) 2.07
Carrier detection of Hemophilia B by using a restriction site polymorphism associated with the coagulation Factor IX gene. J Clin Invest (1984) 2.07
Canalization, genetic assimilation and preadaptation. A quantitative genetic model. Genetics (1998) 2.04
A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long arm. Nucleic Acids Res (1984) 1.93
Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome. Hum Genet (1986) 1.92
Dax1 antagonizes Sry action in mammalian sex determination. Nature (1998) 1.88
A peptide encoded by human gene MAGE-3 and presented by HLA-A2 induces cytolytic T lymphocytes that recognize tumor cells expressing MAGE-3. Eur J Immunol (1994) 1.83
A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal. Nat Genet (1994) 1.78
Genetic screening for hemophilia A (classic hemophilia) with a polymorphic DNA probe. N Engl J Med (1985) 1.67
Safety of retroviral gene marking with a truncated NGF receptor. Nat Med (2003) 1.60
Expression of human adenosine deaminase in nonhuman primates after retrovirus-mediated gene transfer. J Exp Med (1987) 1.57
Conditions for the evolution of altruism under Darwinian selection. Theor Popul Biol (1976) 1.56
Properties of the DNA-delay mutants of bacteriophage T4. Virology (1971) 1.49
Reversal of diabetes in mice by implantation of human fibroblasts genetically engineered to release mature human insulin. Hum Gene Ther (1999) 1.48
Genetic mapping of the human X chromosome: linkage analysis of the q26-q28 region that includes the fragile X locus and isolation of expressed sequences. Cold Spring Harb Symp Quant Biol (1986) 1.47
In vivo gene therapy of metachromatic leukodystrophy by lentiviral vectors: correction of neuropathology and protection against learning impairments in affected mice. Nat Med (2001) 1.46
Structural and functional features of the alpha 3 chain indicate a bridging role for chicken collagen VI in connective tissues. Biochemistry (1990) 1.45
Peripheral blood lymphocytes as target cells of retroviral vector-mediated gene transfer. Blood (1994) 1.45
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome. Proc Natl Acad Sci U S A (1989) 1.43
Risk of pocket hematoma in patients on chronic anticoagulation with warfarin undergoing electrophysiological device implantation: a comparison of different peri-operative management strategies. Eur Rev Med Pharmacol Sci (2015) 1.42
Ancient vs. recent processes as factors shaping the genetic variation of the European wild boar: are the effects of the last glaciation still detectable? Mol Ecol (2008) 1.40
Tungsten oxide nanowires grown on amorphous-like tungsten films. Nanotechnology (2015) 1.38
Herpes simplex virus thymidine kinase gene transfer for controlled graft-versus-host disease and graft-versus-leukemia: clinical follow-up and improved new vectors. Hum Gene Ther (1998) 1.34
Dendritic cells acquire the MAGE-3 human tumor antigen from apoptotic cells and induce a class I-restricted T cell response. Proc Natl Acad Sci U S A (2000) 1.33
Patients younger than 40 years with gastric carcinoma: Helicobacter pylori genotype and associated gastritis phenotype. Cancer (1999) 1.31
Mouse Dax1 expression is consistent with a role in sex determination as well as in adrenal and hypothalamus function. Nat Genet (1996) 1.31
Hierarchical TiO2 photoanode for dye-sensitized solar cells. Nano Lett (2010) 1.30
Chemotactic activity of recombinant human granulocyte colony-stimulating factor. Blood (1988) 1.30
Expression of CXCR4, the receptor for stromal cell-derived factor-1 on fetal and adult human lympho-hematopoietic progenitors. Eur J Immunol (1999) 1.29
Steroidogenic factor 1 and Dax-1 colocalize in multiple cell lineages: potential links in endocrine development. Mol Endocrinol (1996) 1.28
Human CD34(+) cells express CXCR4 and its ligand stromal cell-derived factor-1. Implications for infection by T-cell tropic human immunodeficiency virus. Blood (1999) 1.27
Genetic diversity within and between European pig breeds using microsatellite markers. Anim Genet (2006) 1.26
Cytotoxic T-lymphocyte clones from different patients display limited T-cell-receptor variable-region gene usage in HLA-A2-restricted recognition of the melanoma antigen Melan-A/MART-1. Proc Natl Acad Sci U S A (1995) 1.24
A Fas-based suicide switch in human T cells for the treatment of graft-versus-host disease. Blood (2001) 1.23
Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesis. Hum Mol Genet (1998) 1.22
Transfer of the HSV-tk gene into donor peripheral blood lymphocytes for in vivo modulation of donor anti-tumor immunity after allogeneic bone marrow transplantation. Hum Gene Ther (1995) 1.20
An in vivo model of somatic cell gene therapy for human severe combined immunodeficiency. Science (1991) 1.19
Characterization of natural peptide ligands for HLA-B*4402 and -B*4403: implications for peptide involvement in allorecognition of a single amino acid change in the HLA-B44 heavy chain. Tissue Antigens (1994) 1.19
Effect of topical ketanserin administration on intraocular pressure. Br J Ophthalmol (1993) 1.15
Quantitative trait loci affecting milk yield and protein percentage in a three-country Brown Swiss population. J Dairy Sci (2008) 1.14
The expression pattern of a mouse doublesex-related gene is consistent with a role in gonadal differentiation. Mech Dev (2000) 1.14
Barriers to gene flow estimated by surname distribution in Italy. Ann Hum Genet (1993) 1.14
A deletion map of the human Yq11 region: implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis. Genomics (1991) 1.12
Clinical indications for cardiac computed tomography. From the Working Group of the Cardiac Radiology Section of the Italian Society of Medical Radiology (SIRM). Radiol Med (2012) 1.12
A new submicroscopic deletion that refines the 9p region for sex reversal. Genomics (2000) 1.12
Identification of five MAGE-A1 epitopes recognized by cytolytic T lymphocytes obtained by in vitro stimulation with dendritic cells transduced with MAGE-A1. J Immunol (1999) 1.11
Comparison of prenatal muscle tissue expression profiles of two pig breeds differing in muscle characteristics. J Anim Sci (2006) 1.09
The N-terminus of the fragile X mental retardation protein contains a novel domain involved in dimerization and RNA binding. Biochemistry (2003) 1.07
A first comparative map of copy number variations in the sheep genome. Genomics (2010) 1.06
Natural cytotoxicity on tumour cells of human macrophages obtained from diverse anatomical sites. Clin Exp Immunol (1980) 1.06
Inhibition of natural killer activity by human bronchoalveolar macrophages. J Immunol (1982) 1.05
Copy number variation and missense mutations of the agouti signaling protein (ASIP) gene in goat breeds with different coat colors. Cytogenet Genome Res (2009) 1.05
Phase Ib study of NGR-hTNF, a selective vascular targeting agent, administered at low doses in combination with doxorubicin to patients with advanced solid tumours. Br J Cancer (2009) 1.03
Hierarchically organized nanostructured TiO2 for photocatalysis applications. Nanotechnology (2008) 1.02
A transcriptional silencing domain in DAX-1 whose mutation causes adrenal hypoplasia congenita. Mol Endocrinol (1997) 1.02
Alteration of expression of muscle specific isoforms of the fragile X related protein 1 (FXR1P) in facioscapulohumeral muscular dystrophy patients. J Med Genet (2008) 1.01
Modulation of GvHD by suicide-gene transduced donor T lymphocytes: clinical applications in mismatched transplantation. Cytotherapy (2005) 1.00
Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26-q27. Hum Genet (1987) 1.00
MAGE BAGE and GAGE genes expression in fresh epithelial ovarian carcinomas. Int J Cancer (1996) 1.00
The porcine fat mass and obesity associated (FTO) gene is associated with fat deposition in Italian Duroc pigs. Anim Genet (2008) 0.99
Hematopoietic histoincompatibility reactions by NK cells in vitro: model for genetic resistance to marrow grafts. Science (1985) 0.99
Optimal management of traumatic aortic injury. Eur J Vasc Endovasc Surg (2008) 0.99
Identification of tumour rejection antigens recognized by T lymphocytes. Cancer Surv (1992) 0.98
Comparison between cationic polymers and lipids in mediating systemic gene delivery to the lungs. Gene Ther (1999) 0.97
Acquisition of intact allogeneic human leukocyte antigen molecules by human dendritic cells. Blood (2000) 0.97