Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Uhlendorf BW"'
Publikováno v:
American Journal of Clinical Pathology. 36:555-558
Publikováno v:
New England Journal of Medicine. 280:686-688
Prenatal diagnosis was accomplished for two women who had previously borne children affected with genetic disorders of mucopolysaccharide metabolism — the Hurler syndrome (autosomal recessive) in one case and the Hunter syndrome (X-linked recessive
Publikováno v:
Scopus-Elsevier
Myosins and myosin light chain kinases have been isolated from a cloned line of myoblasts (L5/A10) as this cell line undergoes differentiation toward adult muscle. At least three myosin isozymes were obtained during this developmental process. Initia
Publikováno v:
Pediatric research. 7(7)
Extract: Cystathionine synthase activities are reported for extracts of fibroblasts grown from 39 control subjects, 47 homocystinuric individuals, and 10 parents of cystathionine synthase-deficient patients. Among the group with homocystinuria, fibro
Publikováno v:
Cell differentiation [Cell Differ] 1985 Aug; Vol. 17 (2), pp. 105-14.
Publikováno v:
Pediatric research [Pediatr Res] 1976 Mar; Vol. 10 (3), pp. 179-83.
Autor:
Dillon MJ, England JM, Gompertz D, Goodey PA, Grant DB, Hussein HA, Linnell JC, Matthews DM, Mudd SH, Newns GH, Seakins JW, Uhlendorf BW, Wise IJ
Publikováno v:
Clinical science and molecular medicine [Clin Sci Mol Med] 1974 Jul; Vol. 47 (1), pp. 43-61.
Publikováno v:
Biochemistry [Biochemistry] 1981 Jun 09; Vol. 20 (12), pp. 3511-6.
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry [Clin Chim Acta] 1975 Jan 06; Vol. 58 (1), pp. 51-9.
Publikováno v:
Pediatric research [Pediatr Res] 1969 Nov; Vol. 3 (6), pp. 532-7.