Intrachromosomal gene mapping in man: Assignment of nucleoside phosphorylase to region 14cen→14q21 by interspecific hybridization of cells with a t(X;14) (p22;q21) translocation

No abstract is available for this paper.

• Publication year

  1976

• Venue

  Somatic Cell Genetics

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/BF01539240PMID 829289
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Cytological mapping of the genes assigned to the human A 1 chromosome by use of radiation-induced chromosome breakage in a human-Chinese hamster hybrid cell line

  2004cited by this paper
• Nucleoside-phosphorylase deficiency in a child with severely defective T-cell immunity and normal B-cell immunity.

  1975cited by this paper
• Reversion in expression of hypoxanthine-guanine phosphoribosyl transferase following cell hybridization.

  1975cited by this paper
• Enzyme electrophoresis on cellulose acetate gel

  1974cited by this paper
• The association of glucose phasphate isomerase expression with human chromosome 19 using somatic cell hybrids.

  1973cited by this paper
• Assignment of nucleoside phosphorylase to D-14 and localization of X-linked loci in man by somatic cell genetics.

  1973cited by this paper
• Assignment of three gene loci (PGK, HGPRT, G6PD) to the long arm of the human X chromosome by somatic cell genetics.

  1973cited by this paper
• The association of glucose phosphate isomerase expression with human chromosome 19 using somatic cell hybrids

  1973cited by this paper
• Two human X-autosome translocations identified by autoradiography and fluorescence.

  1972cited by this paper
• Linkage analysis using somatic cell hybrids.

  1972cited by this paper
• Effect of environmental pH on the efficiency of cellular hybridization.

  1972cited by this paper
• Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers).

  1972cited by this paper
• Enzyme electrophoresis on cellulose acetate gel: zymogram patterns in mgh-mouse and man--Chinese hamster somatic cell hybrids.

  1971cited by this paper
• Inherited variants of human nucleoside phosphorylase

  1971cited by this paper
• The separation of adenine and hypoxanthine-guanine phosphoribosyl transferases isoenzymes by disc gel electrophoresis

  1971cited by this paper
• Enzyme electrophoresis on cellulose acetate gel: Zymogram patterns in man-mouse and man-Chinese hamster somatic cell hybrids

  1971cited by this paper
• Mammalian cell genetics. I. Selection and characterization of mutations auxotrophic for L-glutamine or resistant to 8-azaguanine in Chinese hamster cells in vitro.

  1969cited by this paper
• A quantitative comparison of formation of spontaneous and virus-produced viable hybrids.

  1969cited by this paper
• Selection of Hybrids from Matings of Fibroblasts in vitro and Their Presumed Recombinants

  1964cited by this paper
• DNA REPLICATION PATTERNS OF HUMAN CHROMOSOMES.

  1963cited by this paper

• References

  2021cites this paper
• ASHG AWARDS AND ADDRESSES

  2014cites this paper
• ASHG AWARDS AND ADDRESSES 2012 William Allan Award: Adventures in Cytogenetics 1

  2013cites this paper
• 2012 William Allan Award: Adventures in cytogenetics.

  2013cites this paper
• DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency.

  2007cites this paper
• Partial Trisomy 14 (q23->qter) via Segregation of a 14/X Translocation

  2006cites this paper
• The Human Gene for /3 Glucuronidase is on Chromosome 7

  2006cites this paper
• Localization of DNA Sequences in Region Xp2 1 of the Human X Chromosome: Search for Molecular Markers

  2006influential citation
• X-autosome translocation with a breakpoint in Xq22 in a fertile woman and her 47,XXX infertile daughter

  2004cites this paper
• Mouse Chromosome 14

  2004cites this paper
• Balanced structural changes involving the human X: Effect on sexual phenotype

  2004cites this paper
• Comparative map for mice and humans

  2004cites this paper
• Mouse chromosome 14

  2004cites this paper
• X-Autosome translocations: Cytogenetic characteristics and their consequences

  2004cites this paper
• Regional assignment of the human gene for platelet-type phosphofructokinase (PFKP) to chromosome 10p: novel use of polyspecific rodent antisera to localize human enzyme genes

  2004cites this paper
• ICSI and the transmission of X-autosomal translocation: a three-generation evaluation of X;20 translocation: case report.

  2003cites this paper
• p48 Activates a UV-Damaged-DNA Binding Factor and Is Defective in Xeroderma Pigmentosum Group E Cells That Lack Binding Activity

  1998cites this paper
• THE USE OF GENE THERAPY FOR IMMUNODEFICIENCY DISEASE

  1996cites this paper
• Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features

  1995cites this paper
• Mouse chromosome 14.

  1994cites this paper
• A radiation hybrid map of human chromosome 18.

  1994cites this paper
• Generation of a human chromosome 18-specific YAC clone collection and mapping of 55 unique YACs by FISH and fingerprinting.

  1993cites this paper
• Mapping of the neural retina leucine zipper gene, Nrl, to mouse Chromosome 14

  1993cites this paper
• Genomic distribution and transcription of solitary HERV-K LTRs.

  1993cites this paper
• cDNA cloning of a liver isoform of the phosphorylase kinase alpha subunit and mapping of the gene to Xp22.2-p22.1, the region of human X-linked liver glycogenosis.

  1992cites this paper
• Comparative map for mice and humans.

  1992cites this paper
• cDNAcloning ofaliver isoform ofthephosphorylase kinase a subunit andmapping ofthegenetoXp22.2-p22.1, theregion ofhumanX-linked liver glycogenosis

  1992cites this paper
• Novel use of a chimpanzee pseudogene for chromosomal mapping of human cytochrome c oxidase subunit IV.

  1990cites this paper
• The critical region on the human Xq

  1990cites this paper
• Biologic False‐Positive Serologic Tests for Syphilis and Other Serologic Abnormalities in Autoimmune Hemolytic Anemia and Thrombocytopenic Purpura

  1989cites this paper
• Report of the committee on the genetic constitution of chromosomes 14 and 15.

  1989cites this paper
• Chromosomal Localization oftheGenefortheHuman Trifunctional Enzyme,Methylenetetrahydrofolate Dehydrogenase-Methenyltetrahydro folate Cyclohydrolase-Formyltetrahydrof olate Synthetase

  1989cites this paper
• Genetic deficiency of purine nucleoside phosphorylase in the mouse. Characterization of partially and severely enzyme deficient mutants.

  1989cites this paper
• Chromosomal localization of the gene for the human trifunctional enzyme, methylenetetrahydrofolate dehydrogenase-methenyltetrahydrofolate cyclohydrolase-formyltetrahydrofolate synthetase.

  1989cites this paper
• Human SSAV-related endogenous retroviral element: LTR-like sequence and chromosomal localization to 18q21.

  1989cites this paper
• Molecular analysis of the cDNA for human SPARC/osteonectin/BM-40: sequence, expression, and localization of the gene to chromosome 5q31-q33.

  1988cites this paper
• Comparison of nonerythroid alpha-spectrin genes reveals strict homology among diverse species

  1988cites this paper
• The gene for cystathionine beta-synthase (CBS) maps to the subtelomeric region on human chromosome 21q and to proximal mouse chromosome 17.

  1988cites this paper
• Metabolic Causes of Immune Deficiency: Mechanisms and Treatment

  1988cites this paper
• Comparison ofNonerythroid (x-Spectrin GenesReveals Strict Homology amongDiverse Species

  1988cites this paper
• Immunodeficiency and Disease

  1988cites this paper
• Cloning and expression of human nebulin cDNAs and assignment of the gene to chromosome 2q31-q32.

  1988cites this paper
• The structural gene for the M1 subunit of ribonucleotide reductase maps to chromosome 11, band p15, in human and to chromosome 7 in mouse.

  1988cites this paper
• Restriction of human adenovirus replication in Chinese hamster cell lines and their hybrids with human cells.

  1987cites this paper
• Report of the committee on the genetic constitution of chromosomes 13, 14, 15 amd 16.

  1987cites this paper
• The human tyrosine aminotransferase gene mapped to the long arm of chromosome 16 (region 16q22→q24) by somatic cell hybrid analysis and in situ hybridization

  1986cites this paper
• Human Luteinizing hormone-releasing hormone gene (LHRH) is located on short arm of chromosome 8 (region 8p11.2 → p21)

  1986cites this paper
• Genes for synapsin I, a neuronal phosphoprotein, map to conserved regions of human and murine X chromosomes.

  1986cites this paper
• Transforming growth factor β gene maps to human chromosome 19 long arm and to mouse chromosome 7

  1986cites this paper
• Multiple, distinct forms of bovine and human protein kinase C suggest diversity in cellular signaling pathways.

  1986cites this paper
• The human C-reactive protein gene (CRP) and serum amyloid P component gene (APCS) are located on the proximal long arm of chromosome 1

  1986cites this paper
• Regional assignments of three polymorphic DNA segments on human chromosome 15

  1986cites this paper
• Human tissue-type plasminogen activator gene located near chromosomal breakpoint in myeloproliferative disorder.

  1986cites this paper
• Genetic and cytogenetic localisation of the homeo box containing genes on mouse chromosome 6 and human chromosome 7.

  1986cites this paper
• The terminal deoxynucleotidyltransferase gene is located on human chromosome 10 (10q23----q24) and on mouse chromosome 19.

  1986cites this paper
• An expressed beta-tubulin gene, TUBB, is located on the short arm of human chromosome 6 and two related sequences are dispersed on chromosomes 8 and 13.

  1986cites this paper
• The neu gene: an erbB-homologous gene distinct from and unlinked to the gene encoding the EGF receptor.

  1985cites this paper
• Assignment of the structural gene for subunit M1 of human ribonucleotide reductase to the short arm of chromosome 11.

  1985cites this paper
• Balanced reciprocal translocations: risk factors for aneuploid segregant viability

  1985cites this paper
• ADA and PNP Deficiencies: How It All Began

  1985cites this paper
• Mapping of transforming growth factor alpha gene on human chromosome 2 close to the breakpoint of the Burkitt's lymphoma t(2;8) variant translocation.

  1985cites this paper
• The pronatriodilatin gene is located on the distal short arm of human chromosome 1 and on mouse chromosome 4.

  1985cites this paper
• Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.

  1985cites this paper
• Report of the Committee on the Genetic Constitution of Chromosomes 13, 14, 15 and 16.

  1985cites this paper
• The primary immunodeficiencies. (2).

  1984cites this paper
• Random X inactivation resulting in mosaic nullisomy of region Xp21.1----p21.3 associated with heterozygosity for ornithine transcarbamylase deficiency and for chronic granulomatous disease.

  1984cites this paper
• Human chromosomal mapping of genes for insulin-like growth factors I and II and epidermal growth factor

  1984cites this paper
• Assignment of the human gene for the low density lipoprotein receptor to chromosome 19: synteny of a receptor, a ligand, and a genetic disease.

  1984cites this paper
• Partial trisomy 14 (q23 leads to qter) via segregation of a 14/X translocation.

  1983cites this paper
• The human gene for the beta subunit of nerve growth factor is located on the proximal short arm of chromosome 1.

  1983cites this paper
• Oncogene from human EJ bladder carcinoma is located on the short arm of chromosome 11.

  1983cites this paper
• Familial Systemic Lupus Erythematosus: Immunogenetic Studies in Eight Families

  1983cites this paper
• Activation of humanα1-antitrypsin gene in rat hepatoma × human fetal liver cell hybrids depends on presence of human chromosome 14

  1983cites this paper
• The N-ras oncogene assigned to the short arm of human chromosome 1.

  1983cites this paper
• Assignment of the human gene for muscle-type phosphofructokinase (PFKM) to chromosome 1 (region cen→q32) using somatic cell hybrids and monoclonal anti-M antibody

  1982cites this paper
• Structural anomalies of the X chromosome: personal observation and review of non‐mosaic cases

  1982cites this paper
• Genetic factors predisposing to autoimmune diseases. Autoimmune hemolytic anemia, chronic thrombocytopenic purpura, and systemic lupus erythematosus.

  1982cites this paper
• Requirement of the human chromosome 11 long arm for replication of herpes simplex virus type 1 in nonpermissive Chinese hamster x human diploid fibroblast hybrids

  1982cites this paper
• Assignment of first random restriction fragment length polymorphism (RFLP) locus ((D14S1) to a region of human chromosome 14.

  1982influential citation
• 3:1 meiotic disjunction in a mother with a balanced translocation, 46,XX,t(5,14)(p15;q13) resulting in tertiary trisomy and tertiary monosomy offspring.

  1982cites this paper
• Report of the committee on the genetic constitution of chromosomes 13 to 22. Oslo Conference (1981): Sixth International Workshop on Human Gene Mapping.

  1982cites this paper
• tigated in 10 families having more than one affected member.

  1982cites this paper
• Genetic defects in human purine and pyrimidine metabolism.

  1982cites this paper
• An Mr = 52,000 peptide can mediate effects on cholera toxin on adenylate cyclase in intact cells.

  1981cites this paper
• Conserved autosomal syntenic group on mouse (MMU) chromosome 15 and human (HSA) chromosome 22: assignment of a gene for arylsulfatase A to MMU 15 and regional mapping of DIA1, ARSA, and ACO2 on HSA 22.

  1981cites this paper
• Assignment of the human gene for liver-type 6-phosphofructokinase isozyme (PFKL) to chromosome 21 by using somatic cell hybrids and monoclonal anti-L antibody.

  1981cites this paper
• Immunodeficiency syndromes associated with inherited metabolic disorders.

  1981cites this paper
• Assignment of genes to the human X chromosome by the two-dimensional electrophoretic analysis of total cell proteins from rodent-human somatic cell hybrids.

  1981cites this paper
• Immunologic precursors of autoimmune hematologic disorders. Autoimmune hematologic disorders. Autoimmune hemolytic anemia and thrombocytopenic purpura.

  1981cites this paper
• The beta-globin gene is on the short arm of human chromosome 11.

  1980cites this paper
• The β-globin gene is on the short arm of human chromosome 11

  1980cites this paper
• Genes coding for sensitivity to interferon (IfRec) and soluble superoxide dismutase (SOD-1) are linked in mouse and man and map to mouse chromosome 16.

  1980cites this paper
• Gonadal dysgenesis in a patient with an X;3 translocation: case report and review.

  1980cites this paper
• Genetics of the cell surface: Assignment of genes coding for external membrane proteins to human chromosomes 10 and 14

  1979cites this paper
• Spontaneous expression of murine endogenous viruses in hamster X mouse hybrid cells

  1979cites this paper
• Report of the committee on the genetic constitution of chromosomes 13, 14, 15, 16, 17, 18, 19, 20, 21, and 22.

  1979cites this paper
• Association of human chromosome 14 with a ts defect in G1 of Chinese hamster K12 cells.

  1979cites this paper
• Confirmation of regional assignment of nucleoside phosphorylase to band 14q13 by gene-dosage studies

  1979cites this paper
• Requirement of human chromosomes 19, 6 and possibly 3 for infection of hamster x human hybrid cells with baboon M7 type C virus.

  1979cites this paper
• Assignment of a gene required for infection with endogenous baboon virus to human chromosome 19.

  1978cites this paper