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Nature1971; 232(5309); 312-315; doi: 10.1038/232312a0

Non-random X chromosome expression in female mules and hinnies.

Abstract: No abstract available
Publication Date: 1971-07-30 PubMed ID: 5094834DOI: 10.1038/232312a0Google Scholar: Lookup
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  • Journal Article

Cite This Article

APA
Hamerton JL, Richardson BJ, Gee PA, Allen WR, Short RV. (1971). Non-random X chromosome expression in female mules and hinnies. Nature, 232(5309), 312-315. https://doi.org/10.1038/232312a0

Publication

ISSN: 0028-0836
NlmUniqueID: 0410462
Country: England
Language: English
Volume: 232
Issue: 5309
Pages: 312-315

Researcher Affiliations

Hamerton, J L
    Richardson, B J
      Gee, P A
        Allen, W R
          Short, R V

            MeSH Terms

            • Animals
            • Clone Cells
            • Culture Techniques
            • DNA Replication
            • Electrophoresis
            • Female
            • Fibroblasts / cytology
            • Genes
            • Glucosephosphate Dehydrogenase / analysis
            • Horses
            • Hybridization, Genetic
            • Pedigree
            • Perissodactyla
            • Sex Chromosomes

            Citations

            This article has been cited 9 times.
            1. Wang X, Miller DC, Clark AG, Antczak DF. Random X inactivation in the mule and horse placenta. Genome Res 2012 Oct;22(10):1855-63.
              doi: 10.1101/gr.138487.112pubmed: 22645258google scholar: lookup
            2. Hitzeroth HW, Bender K. Age-dependency of somatic selection in South African Negro G-6-PD heterozygotes. Hum Genet 1981;58(3):338-43.
              doi: 10.1007/BF00294934pubmed: 7327555google scholar: lookup
            3. Disteche CM, Swisshelm K, Forbes S, Pagon RA. X-inactivation patterns in lymphocytes and skin fibroblasts of three cases of X-autosome translocations with abnormal phenotypes. Hum Genet 1984;66(1):71-6.
              doi: 10.1007/BF00275190pubmed: 6698557google scholar: lookup
            4. Cohen MM, Lin CC, Sybert V, Orecchio EJ. Two human X-autosome translocations identified by autoradiography and fluorescence. Am J Hum Genet 1972 Sep;24(5):583-97.
              pubmed: 5054227
            5. Beutler E, Kuhl W. Biochemical and electrophoretic studies of -galactosidase in normal man, in patients with Fabry's disease, and in Equidae. Am J Hum Genet 1972 May;24(3):237-49.
              pubmed: 5028964
            6. Johnston PG, VandeBerg JL, Sharman GB. Inheritance of erythrocyte glucose 6-phosphate dehydrogenase in the red-necked wallaby, Macropus rufogriseus (Desmarest), consistent with paternal X inactivation. Biochem Genet 1975 Apr;13(3-4):235-42.
              doi: 10.1007/BF00486017pubmed: 1147889google scholar: lookup
            7. Serov OL, Zakijan SM, Kulichkov VA. Analysis of mechanisms regulating the expression of parental alleles at the GPD locus in mule erythrocytes. Biochem Genet 1978 Jun;16(5-6):379-86.
              doi: 10.1007/BF00484205pubmed: 736879google scholar: lookup
            8. Ropers HH, Wolff G, Hitzeroth HW. Preferential X inactivation in human placenta membranes: is the paternal X inactive in early embryonic development of female mammals?. Hum Genet 1978 Sep 19;43(3):265-73.
              doi: 10.1007/BF00278833pubmed: 700701google scholar: lookup
            9. Disteche CM, Eicher EM, Latt SA. Late replication in an X-autosome translocation in the mouse: correlation with genetic inactivation and evidence for selective effects during embryogenesis. Proc Natl Acad Sci U S A 1979 Oct;76(10):5234-8.
              doi: 10.1073/pnas.76.10.5234pubmed: 291940google scholar: lookup