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We are analyzing https://link.springer.com/article/10.1007/bf00283614.

Title:
Human δ-aminolevulinate dehydratase: chromosomal localization to 9q34 by in situ hybridization | Human Genetics
Description:
The structural gene for human δ-aminolevulinate dehydratase (ALA-D) has been localized to chromosomal region 9q34 by in situ hybridization using a [125I]-labeled human δ-aminolevulinate dehydratase cDNA. Of the 150 silver grains analyzed, 25% were localized to chromosome 9q, while 12% and 8% were on chromosomes 1p and 13q, respectively. The single chromosomal region q34 had over 90% of the total grains observed on chromosome 9. In contrast, the grains on chromosomes 1p and 13q were dispersed, consistent with the absence of any human ALD-D pseudogenes. Southern blot analysis of somatic cell hybrids informative for ALA-D (Wang et al. 1985) also was consistent and supported the finding of only one locus for this heme biosynthetic enzyme.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Non-Profit & Charity
  • Science

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 7,643,078 visitors per month in the current month.

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How Does Link.springer.com Make Money? {💸}

We can't see how the site brings in money.

Earning money isn't the goal of every website; some are designed to offer support or promote social causes. People have different reasons for creating websites. This might be one such reason. Link.springer.com might have a hidden revenue stream, but it's not something we can detect.

Keywords {🔍}

google, scholar, human, genet, chromosome, dehydratase, gene, δaminolevulinate, article, cell, hum, hybridization, assignment, usa, situ, desnick, regional, mouse, privacy, cookies, content, genetics, chromosomal, astrin, wetmur, bishop, chromosomes, somatic, access, proc, natl, acad, sci, information, publish, search, localization, alad, cdna, acid, genetic, anderson, cytogenet, linkage, analysis, data, log, journal, research, potluri,

Topics {✒️}

month download article/chapter southern blot analysis human δ-aminolevulinate dehydratase hepatic δ-aminolevulinate dehydratase δ-aminolevulinic acid dehydratase δ-aminolveulinic acid dehydratase autosomal glucose-6-phosphate dehydrogenase delta-aminolevulinate dehydrase deficiency human α-l-iduronidase codon-optimized hema gene reveal high-frequency rflps full-length cdna clone δ-aminolevulinate dehydratase somatic cell hybridization related subjects cold spring harbor full article pdf privacy choices/manage cookies human gene map human peripheral blood human porphobilinogen deaminase hereditary hepatic porphyria situ hybridization technique european economic area nail-patella syndrome dna fragments separated ribosomal rna species arredondo-vega fx γ-globin gene mount sinai school mouse erythroleukemia cells check access homologous chromosomal segments instant access alpha-1 acid glycoprotein-1 conditions privacy policy structural gene heme biosynthetic enzyme aminolevulinate dehydratase somatic hybrids total grains observed inbred mouse strains specific enzyme immunoassay accepting optional cookies usage analysis july 1987 volume 76 chromosomal region 9q34 chromosome 11q23→11qter article log journal finder publish

Schema {🗺️}

WebPage:
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         headline:Human δ-aminolevulinate dehydratase: chromosomal localization to 9q34 by in situ hybridization
         description:The structural gene for human δ-aminolevulinate dehydratase (ALA-D) has been localized to chromosomal region 9q34 by in situ hybridization using a [125I]-labeled human δ-aminolevulinate dehydratase cDNA. Of the 150 silver grains analyzed, 25% were localized to chromosome 9q, while 12% and 8% were on chromosomes 1p and 13q, respectively. The single chromosomal region q34 had over 90% of the total grains observed on chromosome 9. In contrast, the grains on chromosomes 1p and 13q were dispersed, consistent with the absence of any human ALD-D pseudogenes. Southern blot analysis of somatic cell hybrids informative for ALA-D (Wang et al. 1985) also was consistent and supported the finding of only one locus for this heme biosynthetic enzyme.
         datePublished:
         dateModified:
         pageStart:236
         pageEnd:239
         sameAs:https://doi.org/10.1007/BF00283614
         keywords:
            Internal Medicine
            Blot Analysis
            Metabolic Disease
            Somatic Cell
            Structural Gene
            Human Genetics
            Molecular Medicine
            Gene Function
            Metabolic Diseases
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            issn:
               1432-1203
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            type:
               Periodical
               PublicationVolume
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ScholarlyArticle:
      headline:Human δ-aminolevulinate dehydratase: chromosomal localization to 9q34 by in situ hybridization
      description:The structural gene for human δ-aminolevulinate dehydratase (ALA-D) has been localized to chromosomal region 9q34 by in situ hybridization using a [125I]-labeled human δ-aminolevulinate dehydratase cDNA. Of the 150 silver grains analyzed, 25% were localized to chromosome 9q, while 12% and 8% were on chromosomes 1p and 13q, respectively. The single chromosomal region q34 had over 90% of the total grains observed on chromosome 9. In contrast, the grains on chromosomes 1p and 13q were dispersed, consistent with the absence of any human ALD-D pseudogenes. Southern blot analysis of somatic cell hybrids informative for ALA-D (Wang et al. 1985) also was consistent and supported the finding of only one locus for this heme biosynthetic enzyme.
      datePublished:
      dateModified:
      pageStart:236
      pageEnd:239
      sameAs:https://doi.org/10.1007/BF00283614
      keywords:
         Internal Medicine
         Blot Analysis
         Metabolic Disease
         Somatic Cell
         Structural Gene
         Human Genetics
         Molecular Medicine
         Gene Function
         Metabolic Diseases
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            name:Venkateswara R. Potluri
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                     name:Division of Medical Genetics, Jack and Lucy Department of Pediatrics, Mount Sinai School of Medicine, New York, USA
                     type:PostalAddress
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            type:Person
            name:Kenneth H. Astrin
            affiliation:
                  name:Mount Sinai School of Medicine
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                     name:Division of Medical Genetics, Jack and Lucy Department of Pediatrics, Mount Sinai School of Medicine, New York, USA
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            name:James G. Wetmur
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                  name:Mount Sinai School of Medicine
                  address:
                     name:Department of Microbiology, Mount Sinai School of Medicine, New York, USA
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            name:Robert J. Desnick
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                  name:Mount Sinai School of Medicine
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               name:Division of Medical Genetics, Jack and Lucy Department of Pediatrics, Mount Sinai School of Medicine, New York, USA
               type:PostalAddress
            type:Organization
      name:Kenneth H. Astrin
      affiliation:
            name:Mount Sinai School of Medicine
            address:
               name:Division of Medical Genetics, Jack and Lucy Department of Pediatrics, Mount Sinai School of Medicine, New York, USA
               type:PostalAddress
            type:Organization
      name:James G. Wetmur
      affiliation:
            name:Mount Sinai School of Medicine
            address:
               name:Department of Microbiology, Mount Sinai School of Medicine, New York, USA
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            name:Mount Sinai School of Medicine
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               name:Division of Medical Genetics, Jack and Lucy Department of Pediatrics, Mount Sinai School of Medicine, New York, USA
               type:PostalAddress
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      name:Robert J. Desnick
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      name:Department of Microbiology, Mount Sinai School of Medicine, New York, USA
      name:Division of Medical Genetics, Jack and Lucy Department of Pediatrics, Mount Sinai School of Medicine, New York, USA
      name:Division of Medical Genetics, Jack and Lucy Department of Pediatrics, Mount Sinai School of Medicine, New York, USA
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