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PMID: 4546820 Published · ppublish English Journal Article

Histidinaemia in mouse and man.

Archives of disease in childhood ·Vol. 49 ·No. 7 ·1974-07-00 ·Pages 545-52

Bulfield G, Kacser H

Abstract

暂无摘要

MeSH Terms
Amino Acid Metabolism, Inborn Errors/genetics Animals Brain Chemistry Chromosome Aberrations Chromosome Disorders Congenital Abnormalities/etiology Disease Models, Animal Female Genes, Recessive Histidine/analysis,blood Histidine Ammonia-Lyase/metabolism Homozygote Humans Intellectual Disability/etiology Liver/analysis Male Mice Movement Disorders/etiology Mutation Postural Balance Vestibule, Labyrinth/abnormalities
Chemicals
Histidine Histidine Ammonia-Lyase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Bulfield G
Kacser H
References (16)
16 references, click to expand
  1. Comparative studies of the Chediak-Higashi syndrome.
    Am J Pathol. 1967 Oct;51(4):553-71 PMID: 6057596
  2. Histidinaemia.
    Biochem J. 1969 Feb;111(3):4P-6P PMID: 5767058
  3. Acatalasemia in the mouse and other species.
    Biochem Genet. 1970 Feb;4(1):135-55 PMID: 4986298
  4. Phosphorylase kinase deficiency.
    Biochem Genet. 1970 Feb;4(1):187-94 PMID: 5444101
  5. Intelligent, small for dates baby born to oligophrenic phenylketonuric mother after low phenylalanine diet during pregnancy.
    Pediatrics. 1970 Aug;46(2):235-9 PMID: 5432154
  6. Speech and histidinemia: methodology and evaluation of four cases.
    Dev Med Child Neurol. 1970 Oct;12(5):596-603 PMID: 5477943
  7. Maternal histidinaemia.
    Arch Dis Child. 1971 Feb;46(245):119-21 PMID: 5555485
  8. An intravenous histidine load test for the detection of heterozygotes for histidinaemia.
    Clin Chim Acta. 1971 Jul;33(2):462-4 PMID: 5119323
  9. Management of inherited metabolic disease.
    Br Med J. 1972 May 6;2(5809):329-36 PMID: 4553819
  10. Histidinaemia. Study of relation between clinical and biological findings in 7 subjects.
    Arch Dis Child. 1972 Apr;47(252):190-200 PMID: 5023465
  11. Screening for inherited metabolic disease by plasma chromatography (Scriver) in a large city.
    Br Med J. 1972 Jul 1;3(5817):7-13 PMID: 5039582
  12. Histidinaemic mutant in the mouse.
    Nature. 1973 Jul 13;244(5411):77-9 PMID: 4583487
  13. A familial disturbance of histidine metabolism.
    N Engl J Med. 1961 Aug 3;265:221-4 PMID: 13704885
  14. Effect of genic substitution on the incorporation of tyrosine into the melanin of mouse skin.
    Arch Biochem Biophys. 1962 Mar;96:562-8 PMID: 13880466
  15. CHILDREN OF MOTHERS WITH PHENYLKETONURIA.
    J Pediatr. 1963 Sep;63:461-2 PMID: 14061035
  16. Anterior pituitary cytology of the dwarf mouse.
    Anat Rec. 1959 Sep;135:43-9 PMID: 13819893
Article Info
Journal
Archives of disease in childhood
Abbr.
Arch Dis Child
ISSN
1468-2044
DOI
10.1136/adc.49.7.545
Published
1974-07-00
Pages
545-52
Language
English
Region
England
NLM ID
0372434
PMCID
PMC1648897
Subset
IM
External Links
PubMed source DOI: 10.1136/adc.49.7.545 PMC Full Text View journal details
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