Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1977 Dec;14(6):389–398. doi: 10.1136/jmg.14.6.389

Mendelian inheritance or transmissible agent? The lesson Kuru and the Australia antigen.

P S Harper
PMCID: PMC1013633  PMID: 146739

Full text

PDF
389

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Arnott E. J., Crawfurd M. D., Toghill P. J. Anterior lenticonus and Alport's syndrome. Br J Ophthalmol. 1966 Jul;50(7):390–403. doi: 10.1136/bjo.50.7.390. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. BENNETT J. H., RHODES F. A., ROBSON H. N. A possible genetic basis for kuru. Am J Hum Genet. 1959 Jun;11(2 Pt 1):169–187. [PMC free article] [PubMed] [Google Scholar]
  3. BLUMBERG B. S., ALTER H. J., VISNICH S. A "NEW" ANTIGEN IN LEUKEMIA SERA. JAMA. 1965 Feb 15;191:541–546. doi: 10.1001/jama.1965.03080070025007. [DOI] [PubMed] [Google Scholar]
  4. BLUMBERG B. S., DRAY S., ROBINSON J. C. Antigen polymorphism of a low-density beta-lipoprotein. Allotypy in human serum. Nature. 1962 May 19;194:656–658. doi: 10.1038/194656a0. [DOI] [PubMed] [Google Scholar]
  5. BLUMBERG B. S. POLYMORPHISMS OF THE SERUM PROTEINS AND THE DEVELOPMENT OF ISO-PRECIPITINS IN TRANSFUSED PATIENTS. Bull N Y Acad Med. 1964 May;40:377–386. [PMC free article] [PubMed] [Google Scholar]
  6. Bevan E. A., Herring A. J., Mitchell D. J. Preliminary characterization of two species of dsRNA in yeast and their relationship to the "killer" character. Nature. 1973 Sep 14;245(5420):81–86. doi: 10.1038/245081b0. [DOI] [PubMed] [Google Scholar]
  7. Bird E. D., Caro A. J., Pilling J. B. A sex related factor in the inheritance of Huntington's chorea. Ann Hum Genet. 1974 Jan;37(3):255–260. doi: 10.1111/j.1469-1809.1974.tb01833.x. [DOI] [PubMed] [Google Scholar]
  8. Blumberg B. S., Larouzé B., London W. T., Werner B., Hesser J. E., Millman I., Saimot G., Payet M. The relation of infection with the hepatitis B agent to primary hepatic carcinoma. Am J Pathol. 1975 Dec;81(3):669–682. [PMC free article] [PubMed] [Google Scholar]
  9. Brackenbridge C. J. The relation of sex of affected parent to the age at onset of Huntington's disease. J Med Genet. 1973 Dec;10(4):333–336. [PMC free article] [PubMed] [Google Scholar]
  10. Brackenridge C. J. A genetic and statistical study of some sex-related factors in Huntington's disease. Clin Genet. 1971;2(5):267–286. doi: 10.1111/j.1399-0004.1971.tb00288.x. [DOI] [PubMed] [Google Scholar]
  11. Bruckman C., Berry H. K., Dasenbrock R. J. Histidinemia in two successive generations. Am J Dis Child. 1970 Mar;119(3):221–227. doi: 10.1001/archpedi.1970.02100050223007. [DOI] [PubMed] [Google Scholar]
  12. Bulfield G., Kacser H. Histidinaemia in mouse and man. Arch Dis Child. 1974 Jul;49(7):545–552. doi: 10.1136/adc.49.7.545. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. CONSTANTINIDIS J., GARRONE G., de AJURIAGUERRA [The inheritance of senile psychoses]. Encephale. 1962 Jul-Aug;51:301–344. [PubMed] [Google Scholar]
  14. Clarke C. A. Prevention of rhesus iso-immunisation. Semin Hematol. 1969 Apr;6(2):201–224. [PubMed] [Google Scholar]
  15. Dickinson A. G., Meikle V. M. Host-genotype and agent effects in scrapie incubation: change in allelic interaction with different strains of agent. Mol Gen Genet. 1971;112(1):73–79. doi: 10.1007/BF00266934. [DOI] [PubMed] [Google Scholar]
  16. Dickinson A. G., Stamp J. T., Renwick C. C. Maternal and lateral transmission of scrapie in sheep. J Comp Pathol. 1974 Jan;84(1):19–25. doi: 10.1016/0021-9975(74)90023-1. [DOI] [PubMed] [Google Scholar]
  17. Duffy P., Wolf J., Collins G., DeVoe A. G., Streeten B., Cowen D. Letter: Possible person-to-person transmission of Creutzfeldt-Jakob disease. N Engl J Med. 1974 Mar 21;290(12):692–693. [PubMed] [Google Scholar]
  18. Emery J. L. Pathology with reference to the bile retention syndrome. Postgrad Med J. 1974 Jun;50(584):344–347. doi: 10.1136/pgmj.50.584.344. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. GAJDUSEK D. C. Kuru: an appraisal of five years of investigation. Eugen Q. 1962 Mar;9:69–74. doi: 10.1080/19485565.1962.9987505. [DOI] [PubMed] [Google Scholar]
  20. GAJDUSEK D. C., ZIGAS V. Degenerative disease of the central nervous system in New Guinea; the endemic occurrence of kuru in the native population. N Engl J Med. 1957 Nov 14;257(20):974–978. doi: 10.1056/NEJM195711142572005. [DOI] [PubMed] [Google Scholar]
  21. GAJDUSEK D. C., ZIGAS V. Kuru; clinical, pathological and epidemiological study of an acute progressive degenerative disease of the central nervous system among natives of the Eastern Highlands of New Guinea. Am J Med. 1959 Mar;26(3):442–469. doi: 10.1016/0002-9343(59)90251-7. [DOI] [PubMed] [Google Scholar]
  22. Gajdusek D. C., Alpers M. Genetic studies in relation of kuru. I. Cultural, historical, and demographic background. Am J Hum Genet. 1972 Nov;24(Suppl):1–38. [PMC free article] [PubMed] [Google Scholar]
  23. Gajdusek D. C., Gibbs C. J., Alpers M. Experimental transmission of a Kuru-like syndrome to chimpanzees. Nature. 1966 Feb 19;209(5025):794–796. doi: 10.1038/209794a0. [DOI] [PubMed] [Google Scholar]
  24. Gajdusek D. C., Gibbs C. J., Jr Familial and sporadic chronic neurological degenerative disorders transmitted from man to primates. Adv Neurol. 1975;10:291–317. [PubMed] [Google Scholar]
  25. Gajdusek D. C. Kuru and Creutzfeldt-Jakob disease. Experimental models of noninflammatory degenerative slow virus disease of the central nervous system. Ann Clin Res. 1973 Oct;5(5):254–261. [PubMed] [Google Scholar]
  26. Gibbs C. J., Jr, Gajdusek D. C., Asher D. M., Alpers M. P., Beck E., Daniel P. M., Matthews W. B. Creutzfeldt-Jakob disease (spongiform encephalopathy): transmission to the chimpanzee. Science. 1968 Jul 26;161(3839):388–389. doi: 10.1126/science.161.3839.388. [DOI] [PubMed] [Google Scholar]
  27. Harper P. S., Dyken P. R. Early-onset dystrophia myotonica. Evidence supporting a maternal environmental factor. Lancet. 1972 Jul 8;2(7767):53–55. doi: 10.1016/s0140-6736(72)91548-6. [DOI] [PubMed] [Google Scholar]
  28. Helske T., Nevanlinna H. R. Familial accumulation of carriers of Au antigen. J Med Genet. 1973 Sep;10(3):270–272. doi: 10.1136/jmg.10.3.270. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Hesser J. E., Economidou J., Blumberg B. S. Hepatitis B surface antigen (Australia antigen) in parents and sex ratio of offspring in a Greek population. Hum Biol. 1975 Dec;47(4):415–425. [PubMed] [Google Scholar]
  30. JACOB H., PYRKOSCH W., STRUBE H. Die erbliche Form der Creutzfeldt-Jakobschen Krankheit (Familie Backer). Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr. 1950;184(7):653–674. doi: 10.1007/BF00344941. [DOI] [PubMed] [Google Scholar]
  31. JOHNSON D. R. Hairpin-tail: a case of post-reductional gene action in the mouse egg. Genetics. 1974 Apr;76(4):795–805. doi: 10.1093/genetics/76.4.795. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Kacser H., Bulfield G., Wallace M. E. Histidinaemic mutant in the mouse. Nature. 1973 Jul 13;244(5411):77–79. doi: 10.1038/244077a0. [DOI] [PubMed] [Google Scholar]
  33. London W. T., Sutnick A. I., Blumberg B. S. Australia antigen and acute viral hepatitis. Ann Intern Med. 1969 Jan;70(1):55–59. doi: 10.7326/0003-4819-70-1-55. [DOI] [PubMed] [Google Scholar]
  34. MABRY C. C., DENNISTON J. C., NELSON T. L., SON C. D. MATERNAL PHENYLKETONURIA. A CAUSE OF MENTAL RETARDATION IN CHILDREN WITHOUT THE METABOLIC DEFECT. N Engl J Med. 1963 Dec 26;269:1404–1408. doi: 10.1056/NEJM196312262692604. [DOI] [PubMed] [Google Scholar]
  35. Neville B. G., Harris R. F., Stern D. J., Stern J. Maternal histidinaemia. Arch Dis Child. 1971 Feb;46(245):119–121. doi: 10.1136/adc.46.245.119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Obayashi A., Okochi K., Mayumi M. Familial clustering of asymptomatic carriers of Australia antigen and patients with chronic liver disease or primary liver cancer. Gastroenterology. 1972 Apr;62(4):618–625. [PubMed] [Google Scholar]
  37. PERKOFF G. T., STEPHENS F. E., DOLOWITZ D. A., TYLER F. H. A clinical study of hereditary interstitial pyelonephritis. AMA Arch Intern Med. 1951 Aug;88(2):191–200. doi: 10.1001/archinte.1951.03810080059006. [DOI] [PubMed] [Google Scholar]
  38. POULSON D. F., SAKAGUCHI B. Nature of "sex-ratio" agent in Drosophila. Science. 1961 May 12;133(3463):1489–1490. doi: 10.1126/science.133.3463.1489. [DOI] [PubMed] [Google Scholar]
  39. Preus M., Fraser F. C. Genetics of hereditary nephropathy with deafness (Alport's disease). Clin Genet. 1971;2(6):331–337. doi: 10.1111/j.1399-0004.1971.tb00293.x. [DOI] [PubMed] [Google Scholar]
  40. SJOGREN T., SJOGREN H., LINDGREN A. G. Morbus Alzheimer and morbus Pick; a genetic, clinical and patho-anatomical study. Acta Psychiatr Neurol Scand Suppl. 1952;82:1–152. [PubMed] [Google Scholar]
  41. Shaw R. F., Glover R. A. Abnormal Segregation in Hereditary Renal Disease with Deafness. Am J Hum Genet. 1961 Mar;13(1 Pt 1):89–97. [PMC free article] [PubMed] [Google Scholar]
  42. Sutnick A. I., London W. T., Blumberg B. S. Australia antigen: a genetic basis for chronic liver disease and hepatoma? Ann Intern Med. 1971 Mar;74(3):443–444. [PubMed] [Google Scholar]
  43. Tishler P. V., Rosner B. The genetics of the Alport syndrome. Birth Defects Orig Artic Ser. 1974;10(4):93–99. [PubMed] [Google Scholar]
  44. Trouche A. M., Gigonnet J. M., Dorche C., Nivelon-Chevallier A., Nivelon J. L., Alison M. Les enfants nés de mère phénylcétonurique. A propos d'une nouvelle fratrie. Pediatrie. 1974 Jan-Feb;29(1):33–50. [PubMed] [Google Scholar]
  45. Wallace D. C. A new manifestation of Leber's disease and a new explanation for the agency responsible for its unusual pattern of inheritance. Brain. 1970;93(1):121–132. doi: 10.1093/brain/93.1.121. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES