Výsledky vyhledávání - "Aizencang, G I"

Periodical

Uroporphyrinogen III synthase. An alternative promoter controls erythroid-specific expression in the murine gene.

Autor: Aizencang, G I, Bishop, D F, Forrest, D, Astrin, K H, Desnick, R J

Publikováno v: Journal of Biological Chemistry; January 2000, Vol. 275 Issue: 4 p2295-304, 10p

Periodical

Identification and characterization of hydroxymethylbilane synthase mutations causing acute intermittent porphyria: Evidence for an ancestral founder of the common G111R mutation

Autor: Siervi, A. De, Rossetti, M. V., Parera, V. E., Astrin, K. H., Aizencang, G. I., Glass, I. A., Batlle, A. M. del C., Desnick, R. J.

Publikováno v: American Journal of Medical Genetics. Part A; 8 October 1999, Vol. 86 Issue: 4 p366-375, 10p

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Akademický článek

Uroporphyrinogen III synthase erythroid promoter mutations in adjacent GATA1 and CP2 elements cause congenital erythropoietic porphyria.

Autor: Solis C; Department of Human Genetics, Mount Sinai School of Medicine, Fifth Avenue at 100th Street, New York, NY 10029, USA., Aizencang GI, Astrin KH, Bishop DF, Desnick RJ

Publikováno v: The Journal of clinical investigation [J Clin Invest] 2001 Mar; Vol. 107 (6), pp. 753-62.

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Akademický článek

Identification and characterization of hydroxymethylbilane synthase mutations causing acute intermittent porphyria: evidence for an ancestral founder of the common G111R mutation.

Autor: De Siervi A; Department of Human Genetics, Mount Sinai School of Medicine, New York, New York 10029, USA., Rossetti MV, Parera VE, Astrin KH, Aizencang GI, Glass IA, Batlle AM, Desnick RJ

Publikováno v: American journal of medical genetics [Am J Med Genet] 1999 Oct 08; Vol. 86 (4), pp. 366-75.

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