The Two Different Means of Achieving Dosage Compensation for X-linked Genes Employed by Drosophila and Mammals
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[1] B. Childs,et al. X-Linked 6-Phosphogluconate Dehydrogenase in Drosophila: Subunit Associations , 1965, Science.
[2] A. Robinson. THE ASSAY OF GALACTOKINASE AND GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE ACTIVITY IN HUMAN ERYTHROCYTES , 1963, The Journal of Experimental Medicine.
[3] B. Childs,et al. DEMONSTRATION OF TWO POPULATIONS OF CELLS IN THE HUMAN FEMALE HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATE DEHYDROGENASE VARIANTS. , 1963, Proceedings of the National Academy of Sciences of the United States of America.
[4] W. Valentine,et al. Pyruvate kinase (PK) deficiency hereditary nonspherocytic hemolytic anemia. , 1962, Blood.
[5] Virgil F. Fairbanks,et al. THE NORMAL HUMAN FEMALE AS A MOSAIC OF X-CHROMOSOME ACTIVITY: STUDIES USING THE GENE FOR G-6-PD-DEFICIENCY AS A MARKER , 1962 .
[6] M. Lyon. Gene Action in the X-chromosome of the Mouse (Mus musculus L.) , 1961, Nature.
[7] S. C. Madden,et al. Immunologic evidence of catalase deficiency in human hereditary acatalasemia. , 1961, Laboratory investigation; a journal of technical methods and pathology.
[8] R. Blattner. Antihemophilic globulin levels in carriers of hemophilia A , 1961 .
[9] S. Rapaport,et al. Anti-hemophilic globulin levels in carriers of hemophilia A. , 1960, The Journal of clinical investigation.
[10] Graham Jb,et al. A study of the carrier state for plasma thromboplastin component (PTC, Christmas factor) deficiency, utilizing a new assay procedure. , 1960 .
[11] Y. Ogura,et al. Hypocatalasemia: a new genetic carrier state. , 1960, The Journal of clinical investigation.
[12] E. P. Anderson,et al. Congenital galactosemia, a single enzymatic block in galactose metabolism. , 1956, Science.