Restoration of the cholesterol metabolism in 3T3 cell lines derived from the sphingomyelinosis mouse (spm/spm) by transfer of a human chromosome 18

[1]  E. Nanba,et al.  A cell line derived from sphingomyelinosis mouse shows alterations in intracellular cholesterol metabolism similar to those in type C Niemann-Pick disease. , 1992, Cell structure and function.

[2]  M. Oshimura,et al.  Structure of the human pituitary adenylate cyclase activating polypeptide (PACAP) gene. , 1992, Biochimica et biophysica acta.

[3]  R. Rousson,et al.  Niemann-Pick disease type C: An update , 1991, Journal of Inherited Metabolic Disease.

[4]  Tomomasa Watanabe,et al.  A molecular genetic linkage map of mouse chromosome 18, includingspm, Grl-1, Fim-2/c-fms, andMbp , 1991, Biochemical Genetics.

[5]  D. Adler,et al.  Regional assignment of the human acid sphingomyelinase gene (SMPD1) by PCR analysis of somatic cell hybrids and in situ hybridization to 11p15.1----p15.4. , 1991, Genomics.

[6]  Y. Nakamura,et al.  Human chromosome 9 can complement UV sensitivity of xeroderma pigmentosum group A cells. , 1990, Mutation research.

[7]  S. Kodama,et al.  Restoration of radiation resistance in ataxia telangiectasia cells by the introduction of normal human chromosome 11. , 1990, Mutation research.

[8]  M. Oshimura,et al.  Introduction of normal chromosome 3p modulates the tumorigenicity of a human renal cell carcinoma cell line YCR. , 1990, Oncogene.

[9]  Kathleen R. Cho,et al.  Identification of a chromosome 18q gene that is altered in colorectal cancers. , 1990, Science.

[10]  D. Cogan,et al.  Clinical spectrum of Niemann‐Pick disease type C , 1989, Neurology.

[11]  M. Oshimura,et al.  Construction of Mouse A9 Clones Containing a Single Human Chromosome Tagged with Neomycin‐resistance Gene via Microcell Fusion , 1989, Japanese journal of cancer research : Gann.

[12]  M. Oshimura,et al.  Construction of Mouse A9 Clones Containing a Single Human Chromosome (X/Autosome Translocation) via Micro‐cell Fusion , 1989, Japanese journal of cancer research : Gann.

[13]  Y. Nakamura,et al.  Twelve loci form a continuous linkage map for human chromosome 18. , 1988, Genomics.

[14]  R. Brady,et al.  Type-C Niemann-Pick disease: low density lipoprotein uptake is associated with premature cholesterol accumulation in the Golgi complex and excessive cholesterol storage in lysosomes. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[15]  R. Brady,et al.  Niemann‐Pick disease group C: clinical variability and diagnosis based on defective cholesterol esterification: A collaborative study on 70 patients , 1988, Clinical genetics.

[16]  R. Brady,et al.  Type C Niemann-Pick disease. Lysosomal accumulation and defective intracellular mobilization of low density lipoprotein cholesterol. , 1988, The Journal of biological chemistry.

[17]  L. Hood,et al.  DNA length polymorphism located 5' to the human myelin basic protein gene. , 1987, American journal of human genetics.

[18]  T. Mohandas,et al.  Assignment of the prealbumin (PALB) gene (familial amyloidotic polyneuropathy) to human chromosome region 18q11.2–q12.1 , 1987, Human Genetics.

[19]  R. Brady,et al.  A defect in cholesterol esterification in Niemann-Pick disease (type C) patients. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[20]  K. C. Reed,et al.  Rapid transfer of DNA from agarose gels to nylon membranes. , 1985, Nucleic acids research.

[21]  M. Oshimura,et al.  Nonrandom loss of chromosome 15 in Syrian hamster tumours induced by v-Ha-ras plus v-myc oncogenes , 1985, Nature.

[22]  T. Kitagawa,et al.  A lysosomal storage disorder in mice: A model of Niemann-Pick disease , 1982, Journal of Inherited Metabolic Disease.

[23]  T. Kitagawa,et al.  Sphingomyelinosis, a new mutation in the mouse: a model of Niemann-Pick disease in humans. , 1982, The Journal of heredity.

[24]  Carl W. Schmid,et al.  Partial nucleotide sequence of the 300-nucleotide interspersed repeated human DNA sequences , 1980, Nature.

[25]  E. Southern Detection of specific sequences among DNA fragments separated by gel electrophoresis. , 1975, Journal of molecular biology.

[26]  S. Goss,et al.  New method for mapping genes in human chromosomes , 1975, Nature.

[27]  M. Oshimura,et al.  Multiple chromosomes carrying tumor suppressor activity, via microcell-mediated chromosome transfer, for various tumor cell lines. , 1989, Princess Takamatsu symposia.

[28]  R. Rousson,et al.  Sphingomyelinase and Niemann-Pick Disease , 1986 .

[29]  H. Kruth,et al.  Quantification of low density lipoprotein binding and cholesterol accumulation by single human fibroblasts using fluorescence microscopy. , 1980, Journal of lipid research.

[30]  J. Shay,et al.  Nuclear control of tumorigenicity in cells reconstructed by PEG-induced fusion of cell fragments. , 1979, Journal of supramolecular structure.

[31]  M. Yoshida,et al.  Differential Staining of Parental Chromosomes in Interspecific Cell Hybrids with a Combined Quinacrine and 33258 Hoechst Technique , 1975 .