| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/BF00504344 |
| P953 | full work available at URL | http://link.springer.com/article/10.1007/BF00504344/fulltext.html |
| http://link.springer.com/content/pdf/10.1007/BF00504344 | ||
| http://link.springer.com/content/pdf/10.1007/BF00504344.pdf | ||
| P698 | PubMed publication ID | 120190 |
| P2093 | author name string | P. S. Gerald | |
| A. C. Leary | |||
| G. A. Bruns | |||
| V. M. Regina | |||
| B. J. Mintz | |||
| P2860 | cites work | Protein measurement with the Folin phenol reagent | Q20900776 |
| Tay-Sachs' and Sandhoff's diseases: the assignment of genes for hexosaminidase A and B to individual human chromosomes | Q24564639 | ||
| Lysosomal arylsulfatase deficiencies in humans: Chromosome assignments for arylsulfatase A and B | Q24597204 | ||
| Transfer of proteins across membranes. I. Presence of proteolytically processed and unprocessed nascent immunoglobulin light chains on membrane-bound ribosomes of murine myeloma | Q24681545 | ||
| Aconitase polymorphism in man | Q28117709 | ||
| GM1-gangliosidosis: chromosome 3 assignment of the beta-galactosidase-A gene (beta GALA) | Q28199089 | ||
| Mannosidosis: assignment of the lysosomal alpha-mannosidase B gene to chromosome 19 in man | Q35037459 | ||
| Isolation of mammalian cell mutants deficient in glucose-6-phosphate dehydrogenase activity: linkage to hypoxanthine phosphoribosyl transferase | Q35069238 | ||
| The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase | Q35108896 | ||
| Electrophoresis of arylsulfatase from normal individuals and patients with metachromatic leukodystrophy | Q35569992 | ||
| Red cell glutathione peroxidase polymorphism in Afro-Americans | Q35570310 | ||
| Resolution of granules from rabbit heterophil leukocytes into distinct populations by zonal sedimentation | Q36190289 | ||
| The development of neutrophilic polymorphonuclear leukocytes in human bone marrow | Q36270994 | ||
| Metachromatic leukodystrophy: arylsulfatase-A deficiency in skin fibroblast cultures | Q36450898 | ||
| BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes | Q36896171 | ||
| Human beta-D-N-acetylhexosaminidases A and B: expression and linkage relationships in somatic cell hybrids | Q37441049 | ||
| Microheterogeneity of arylsulfatase a from human tissues | Q39116381 | ||
| Purification, molecular weight, amino acid, and subunit composition of arylsulfatase A from human liver | Q39134983 | ||
| Human gene mapping using an X/autosome translocation | Q39443239 | ||
| Macular cherry-red spots and myoclonus with dementia: Coexistent neuraminidase and β-galactosidase deficiencies | Q39605242 | ||
| A two-year-old patient with an atypical expression of GM1-β-galactosidase deficiency: Biochemical, immunological, and cell genetic studies | Q39655192 | ||
| Assignment of structural β-galactosidase loci to human chromosomes 3 and 22 | Q39699568 | ||
| Purification and properties of a homogeneous aryl sulfatase A from rabbit liver | Q40314705 | ||
| Purification, properties and glycoprotein nature of arylsulfatase A from sheep brain | Q40340962 | ||
| Ganglioside storage disorders: recent advances | Q40807030 | ||
| Assignment of the human acid ?-glucosidase gene (?GLU) to chromosome 17 using somatic cell hybrids | Q41029888 | ||
| Biochemical and morphological characterization of azurophil and specific granules of human neutrophilic polymorphonuclear leukocytes | Q41189212 | ||
| Regional localization of aβ-galactosidase locus on human chromosome 22 | Q41360520 | ||
| Genetic linkage studies of the human glycosphingolipid ?-galactosidases | Q41364104 | ||
| Complementation studies with enucleated fibroblasts from different variants of β-galactosidase deficiency | Q41388124 | ||
| The separation and characterization of the methylumbelliferyl beta-galactosidases of human liver | Q42044547 | ||
| Linkage of genetic determinants for mouse beta-galactosidase electrophoresis and activity | Q42110954 | ||
| 8-Azaguanine resistance in mammalian cells. I. Hypoxanthine-guanine phosphoribosyltransferase | Q42274224 | ||
| Human ?-glucuronidase: Assignment of the structural gene to chromosome 7 using somatic cell hybrids | Q43414366 | ||
| Assignment of a structural gene for beta-glucuronidase to human chromosome C7. | Q44436387 | ||
| Purification and properties of arylsulfatase. A from human urine | Q44812061 | ||
| Expression of alpha-D-mannosidase in man-hamster somatic cell hybrids | Q45172083 | ||
| Lactosylceramide beta-galactosidase in human sphingolipidoses. Evidence for two genetically distinct enzymes | Q45303454 | ||
| Size and charge isomer separation and estimation of molecular weights of proteins by disc gel electrophoresis | Q47401199 | ||
| Human acid phosphatase in somatic cell hybrids. | Q47830945 | ||
| Biochemical and immunological studies of purified mouse beta-galactosidase | Q48435842 | ||
| Heterogeneity of human hepatic H-acetyl-beta-D-hexosaminidose. A activity toward natural glycosphingolipid substrates | Q48475421 | ||
| GM1 ganglioside beta-galactosidase. A. Purification and studies of the enzyme from human liver | Q48497743 | ||
| Ganglioside GM1 beta-galactosidase: studies in human liver and brain | Q48620347 | ||
| Arylsulphatases in human brain: separation, purification, and certain properties of the two soluble arylsulphatases | Q48848174 | ||
| The status of the gene map of the human chromosomes | Q51051769 | ||
| X-Linkage of Human α-Galactosidase | Q54593626 | ||
| GM1-gangliosidosis: Chromosome 3 assignment of the?-galactosidase-A gene (? GAL A ) | Q56866497 | ||
| Assignment of the gene locus for human ?-l-fucosidase to chromosome 1 by analysis of somatic cell hybrids | Q67281499 | ||
| Aconitase (E.C. 4.2.1.3) mitochondrial locus mapped to human chromosome 22: studies with Chinese hamster--human somatic cell hybrids | Q67427064 | ||
| Nongenetic heterogeneity of mouse beta-galactosidase | Q67586615 | ||
| Differential staining of interspecific chromosomes in somatic cell hybrids by alkaline Giemsa stain | Q68273532 | ||
| Maroteaux-Lamy disease (mucopolysaccharidosis VI), subtype A: deficiency of a N-acetylgalactosamine-4-sulfatase | Q68354874 | ||
| Identification of human chromosomes by DNA-binding fluorescent agents | Q70137712 | ||
| Differential effect of chloride ions on β-galactosidase isoenzymes: A method for separate assay | Q70540483 | ||
| A correlation of intracellular cerebroside sulfatase activity in fibroblasts with latency in metachromatic leukodystrophy | Q70609536 | ||
| Loss of human genetic markers in man--Chinese hamster somatic cell hybrids | Q71068742 | ||
| Glutathion peroxidase. I. Isolation and determinations of molecular weight | Q71771388 | ||
| Cerebroside 3-sulfate as a physiological substrate of arylsulfatase A | Q72037242 | ||
| DISC ELECTROPHORESIS IN POLYACRYLAMIDE GELS: EXTENSION TO NEW CONDITIONS OF PH AND BUFFER | Q77121484 | ||
| The assay of arylsulphatases A and B in human urine | Q78694080 | ||
| A sex-linked type of gargoylism | Q83241206 | ||
| A monospecific antibody to human sulfatase A. Preparation, characterization and significance | Q93824907 | ||
| P433 | issue | 11-12 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | biochemistry | Q7094 |
| genetics | Q7162 | ||
| P304 | page(s) | 1031-1059 | |
| P577 | publication date | 1979-12-01 | |
| P1433 | published in | Biochemical Genetics | Q15765855 |
| P1476 | title | Human lysosomal genes: Arylsulfatase A and ?-Galactosidase | |
| Human lysosomal genes: arylsulfatase A and beta-galactosidase | |||
| P478 | volume | 17 |
| Q35248105 | A deletion map of the WAGR region on chromosome 11. |
| Q35200781 | A highly polymorphic locus in human DNA revealed by probes from cosmid 1-5 maps to chromosome 2q35----37 |
| Q35197517 | Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP |
| Q37686616 | Assignment of the gene coding for the T3-delta subunit of the T3-T-cell receptor complex to the long arm of human chromosome 11 and to mouse chromosome 9. |
| Q35201575 | Assignment of the gene for acid beta-glucosidase to human chromosome 1 |
| Q28287336 | Assignment of the human gamma-crystallin gene cluster (CRYG) to the long arm of chromosome 2, region q33-36 |
| Q41646652 | Characterization of N-myc amplification in a human neuroblastoma cell line by clones isolated following the phenol emulsion reassociation technique and by hexagonal field gel electrophoresis |
| Q70184689 | Chromosome 13 restriction fragment length polymorphisms |
| Q24676714 | Cloning and chromosomal localization of the human cytoskeletal alpha-actinin gene reveals linkage to the beta-spectrin gene |
| Q28278760 | Cloning of human alpha 1(X) collagen DNA and localization of the COL10A1 gene to the q21-q22 region of human chromosome 6 |
| Q35199889 | Complementation of multiple sulfatase deficiency in somatic cell hybrids |
| Q36415470 | Construction of a chromosome 16-enriched phage library and characterization of several DNA segments from 16p. |
| Q37690152 | Differential amplification, assembly, and relocation of multiple DNA sequences in human neuroblastomas and neuroblastoma cell lines |
| Q35200843 | Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to chromosome 19. |
| Q36424470 | Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to human chromosome 12q. |
| Q34547155 | Genetic analysis of patients with retinitis pigmentosa using a cloned cDNA probe for the human gamma subunit of cyclic GMP phosphodiesterase |
| Q24297786 | Human GAP-43: its deduced amino acid sequence and chromosomal localization in mouse and human |
| Q70338524 | Human beta-galactosidase and alpha-neuraminidase deficient mucolipidosis: genetic complementation analysis of the neuraminidase deficiency |
| Q35604219 | Human inhibitor of the first component of complement, C1: characterization of cDNA clones and localization of the gene to chromosome 11 |
| Q24307950 | Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease |
| Q24309376 | Human smooth muscle myosin heavy chain gene mapped to chromosomal region 16q12 |
| Q24599567 | Isolation of amplified DNA sequences from IMR-32 human neuroblastoma cells: facilitation by fluorescence-activated flow sorting of metaphase chromosomes |
| Q35611528 | Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome |
| Q35245858 | Localization of gelsolin proximal to ABL on chromosome 9 |
| Q44265975 | Localization of the gene for the vitamin B12 binding protein, transcobalamin II, near the centromere on mouse chromosome 11, linked with the hemoglobin alpha-chain locus |
| Q35198537 | Localization of the human angiogenin gene to chromosome band 14q11, proximal to the T cell receptor alpha/delta locus |
| Q35588259 | Mapping of the human APOB gene to chromosome 2p and demonstration of a two-allele restriction fragment length polymorphism |
| Q24617856 | Molecular characterization of sialophorin (CD43), the lymphocyte surface sialoglycoprotein defective in Wiskott-Aldrich syndrome |
| Q68304589 | Molecular cloning and chromosomal localization of a gene coding for human cardiac myosin heavy-chain |
| Q67916359 | On the structure and chromosome location of the 72- and 92-kDa human type IV collagenase genes |
| Q48421777 | Park Spearin Gerald: a tribute |
| Q72498550 | Regional assignment of arylsulfatase A, mitochondrial aconitase and NADH-cytochrome b5 reductase by somatic cell hybridization |
| Q36249664 | Regional assignment of the structural gene for human alpha-L-iduronidase |
| Q24602000 | Structure, chromosome location, and expression of the human smooth muscle (enteric type) gamma-actin gene: evolution of six human actin genes |
| Q70174991 | The 35 kd pulmonary surfactant-associated protein is encoded on chromosome 10 |
| Q34606178 | The gene encoding the epsilon subunit of the T3/T-cell receptor complex maps to chromosome 11 in humans and to chromosome 9 in mice |
| Q44264378 | The human T cell antigen Leu-2 (T8) is encoded on chromosome 2. |
| Q24681840 | The human mannose-binding protein gene. Exon structure reveals its evolutionary relationship to a human pulmonary surfactant gene and localization to chromosome 10 |
| Q45041223 | Transposition and amplification of oncogene-related sequences in human neuroblastomas |
Search more.