Transcription mapping in a 700-kb region around the DXS52 locus in Xq28: isolation of six novel transcripts and a novel ATPase isoform (hPMCA5).

Basic Local Alignment Search Tool

1990 • 12,947 citations

Genomic sequencing.

1984 • 8,343 citations

A Gene Encoding an Antigen Recognized by Cytolytic T Lymphocytes on a Human Melanoma

1991 • 3,493 citations

A nonapeptide encoded by human gene MAGE-1 is recognized on HLA-A1 by cytolytic T lymphocytes directed against tumor antigen MZ2-E.

1992 • 694 citations

Structure, chromosomal localization, and expression of 12 genes of the MAGE family

1994 • 595 citations

Exon amplification: a strategy to isolate mammalian genes based on RNA splicing.

1991 • 425 citations

THE ISOCHORE ORGANIZATION OF THE HUMAN GENOME

1989 • 369 citations

Direct selection: a method for the isolation of cDNAs encoded by large genomic regions.

1991 • 271 citations

cDNA selection: efficient PCR approach for the selection of cDNAs encoded in large chromosomal DNA fragments.

1991 • 211 citations

The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency.

1985 • 204 citations

Cloning of Human Genes Encoding Novel G Protein-Coupled Receptors

1994 • 151 citations

Sequence and expression pattern of the human MAGE2 gene

1994 • 144 citations

Human biglycan gene. Putative promoter, intron-exon junctions, and chromosomal localization

1991 • 136 citations

Molecular cloning and centrosomal localization of human caltractin.

1993 • 128 citations

Assignment of the gene for dyskeratosis congenita to Xq28

1986 • 122 citations

The Melanoma Antigen Gene (MAGE) Family Is Clustered in the Chromosomal Band Xq28

1995 • 121 citations

A strategy for the selection of transcribed sequences in the Xq28 region

1992 • 121 citations

Plasma membrane Ca2+-ATPase isoforms: distribution of mRNAs in rat brain by in situ hybridization

1992 • 117 citations

Barth syndrome: Clinical features and confirmation of gene localisation to distal Xq28

1993 • 117 citations

KpnI families of long, interspersed repetitive DNAs in human and other primate genomes

1982 • 101 citations

Physical map of human Xq27-qter: localizing the region of the fragile X mutation.

1991 • 76 citations

Transcriptional organization of a 450-kb region of the human X chromosome in Xq28.

1993 • 72 citations

Multilocus analysis of the fragile X syndrome

1988 • 59 citations

Mapping of DNA markers close to the fraglle site on the human X chromosome at Xq25–3

1987 • 57 citations

Structure of the rat plasma membrane Ca(2+)-ATPase isoform 3 gene and characterization of alternative splicing and transcription products. Skeletal muscle-specific splicing results in a plasma membrane Ca(2+)-ATPase with a novel calmodulin-binding domain.

1992 • 56 citations

Isochores and CpG Islands in YAC Contigs in Human Xq26.1-qter

1993 • 54 citations

construction of a transcription map of a 300 kb region around the human G6PD locus by direst cDNA selection

1993 • 53 citations

Localisation of the MRX3 gene for non-specific X linked mental retardation.

1991 • 53 citations

Fine mapping of the human biglycan (BGN) gene within the Xq28 region employing a hybrid cell panel

1992 • 46 citations

YAC Contig Organization and CpG Island Analysis in Xq28

1994 • 45 citations

Exclusion mapping of the X-linked dominant chondrodysplasia punctata/ichthyosis/cataract/short stature (Happle) syndrome: possible involvement of an unstable pre-mutation

1992 • 43 citations

Localization of two genes encoding plasma membrane Ca<sup>2</sup><sup>+</sup> ATPases isoforms 2 (ATP2B2) and 3 (ATP2B3) to human chromosomes 3p26→p25 and Xq28, respectively

1994 • 42 citations

Oto-palato-digital syndrome type I: further evidence for assignment of the locus to Xq28

1991 • 37 citations

A trace display and editing program for data from fluorescence based sequencing machines

1991 • 36 citations

Linkage to Xq28 in a family with nonspecific X-linked mental retardation

1992 • 34 citations

Gene mapping and serendipity. The locus for torticollis, keloids, cryptorchidism and renal dysplasia (31430, McKusick) is at Xq28, distal to the G6PD locus

1982 • 33 citations

Waisman syndrome, a human X-linked recessive basal ganglia disorder with mental retardation: Localization to Xq27.3-qter

1991 • 31 citations

THE ASSOCIATION OF DYSKERATOSIS CONGENITA AND FANCONI'S ANÆMIA

1965 • 30 citations

Physical and genetic mapping of polymorphic loci in Xq28 (DXS15, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosome.

1990 • 28 citations

Close linkage of the murine locus bare patches to the X-linked visual pigment gene: Implications for mapping human X-linked dominant chondrodysplasia punctata

1990 • 28 citations

Identification of human chromosome 9 specific genes using exon amplification

1993 • 28 citations

A YAC clone map spanning 7.5 megabases of human chromosome band Xq28

1994 • 27 citations

An archipelago of CpG islands in Xq28: identification and fine mapping of 20 new CpG islands of the human X chromosome

1992 • 22 citations

ACTIVE IMMUNIZATION AGAINST TETANUS

1953 • 16 citations

Completion of the physical map of Xq28: the location of the gene for L1CAM on the human X Chromosome

1992 • 14 citations

A 2.3-Mb Yeast Artificial Chromosome Contig Spanning from Gabra3 to G6pd on the Mouse X Chromosome

1994 • 14 citations

Efficiency and specificity of gene isolation by exon amplification

1993 • 14 citations

Physical mapping of DXS134 close to the DXS52 locus

1989 • 14 citations

Refined mapping of caltractin in human Xq28 and in the homologous region of the mouse X Chromosome places the gene within the bare patches (Bpa) and striated (Str) critical regions

1995 • 12 citations

COMMENTARY: So many needles, so much hay

1995 • 10 citations