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Subject Areas on Research
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A patient with duplication (7)(p22.1pter) characterized by array-CGH.
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Amplification of the c-myc gene in human medulloblastoma cell lines and xenografts.
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Amplified C lambda and c-abl genes are on the same marker chromosome in K562 leukemia cells.
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Assignment of hexokinase types 1,2,3 (Hk1,2,3) and glucokinase (Gck) to rat chromosome band 20q11, 4q34, 17q12 and 14q21 respectively, by in situ hybridization.
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Assignment of the beta-subunit of rod photoreceptor cGMP phosphodiesterase gene PDEB (homolog of the mouse rd gene) to human chromosome 4p16.
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Assignment of the human glycogen debrancher gene to chromosome 1p21.
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Characterization of chromosome 17 abnormalities in medulloblastomas.
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Chromosomal characteristics of childhood brain tumors.
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Chromosomal composition of four permanent cultured cell lines derived from human gliomas.
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Chromosomal composition of malignant human gliomas through serial subcutaneous transplantation in athymic mice.
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Chromosomal localization of human glutamate receptor genes.
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Chromosomal organization of adrenergic receptor genes.
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Chromosomal progression of malignant human gliomas from biopsy to establishment as permanent lines in vitro.
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Cloning, mapping, and characterization of activated leukocyte-cell adhesion molecule (ALCAM), a CD6 ligand.
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De novo partial duplication of chromosome 7p in a male with autistic disorder.
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Evidence for coincident mutations in human lymphoblast clones selected for functional loss of a thymidine kinase gene.
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Genetic mapping of dinucleotide repeat polymorphisms and von Hippel-Lindau disease on chromosome 3p25-26.
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Hereditary renal cell carcinoma in the rat associated with nonrandom loss of chromosomes 5 and 6.
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In situ hybridization and translocation breakpoint mapping. I. Nonidentical 22q11 breakpoints for the t(9;22) of CML and the t(8;22) of Burkitt lymphoma.
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Intrachromosomal triplication of 2q11.2-q21 in a severely malformed infant: case report and review of triplications and their possible mechanism.
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Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients.
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Molecular and genetic characterization of a radiation-induced structural rearrangement in mouse chromosome 2 causing mutations at the limb deformity and agouti loci.
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Molecular cytogenetic analysis of the bladder carcinoma cell line BK-10 by spectral karyotyping.
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Oncogenic Kras-induced leukemogeneis: hematopoietic stem cells as the initial target and lineage-specific progenitors as the potential targets for final leukemic transformation.
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Patterns of the early, gross chromosomal changes in malignant human gliomas.
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Recombination of 4p16 DNA markers in an unusual family with Huntington disease.
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Regional localization of the human genes for S-adenosylhomocysteine hydrolase (cen----q131) and adenosine deaminase (q131----qter) on chromosome 20.
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Structural chromosomal abnormalities in human medulloblastoma.
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Subtelomeric deletions of chromosome 6p: molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher-Schinzel (3C) syndrome.
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The gene encoding the glutamate receptor subunit GluR5 is located on human chromosome 21q21.1-22.1 in the vicinity of the gene for familial amyotrophic lateral sclerosis.
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The gene that encodes the human CD20 (B1) differentiation antigen is located on chromosome 11 near the t(11;14)(q13;q32) translocation site.
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The murine Hox-2 cluster of homeo box containing genes maps distal on chromosome 11 near the tail-short (Ts) locus.
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Unbalanced translocation 46,XY,-15,+der(22)t(15;22)(q13;q11)pat: case report and review of the literature.
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cDNA cloning and chromosomal localization of the human beta-adrenergic receptor kinase.