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Свободная субъединица хорионического гонадотропина человека как маркер синдрома Дауна (стр. 3 из 3)

Lapthorn A. J., Hariris D. C., Littlejohn A. et al. Crystal structure of human chorionic gonadotropin. // Nature. 1994. 369.9: 455-61.

McDonald N. Q., Lapatto R., Murray-Rust J. et al. New protein fold revealed by 2.3 A resolution crystal structure of nerve growth factor // Nature. 1991. 354: 411-14.

Schlunegger M. P., Grutter M. G. An unusual feature reveal to end by the crystal structure at 2.2 A resolution of human transforming growth factor-β2. // Nature. 1992. 358: 430-34.

Oefner C., Darey A., Winkler F. K. et al. Crystal structure of human platelet-derived growth factor B. // EMBO J. 1992. 11: 3921-26.

Elliot M., Kardana A., Lustbader J. W., Cole L. A. Carbohydrate and peptide structure of the α- and β-subunits of human chorionic gonadotropin from normal and aberrant pregnancy and choriocarcinoma.// Endocrine. 1988. 5: 2221-33.

Boorstein W. R., Vamvakopoulos N. C., Fiddes J. C. Human chorionic gonadotropin β-subunit is encoded by at least eight genes arranged in tandem, inverted pairs. // Nature. 1982. 300: 419-22.

Policastro P., Ovitt C. E., Hoshina M. et al. The β-subunit of human chorionic gonadotropin is encoded by multiple genes. // JBC. 1983. 258: 11492-99.

Boothby M., Kukowska J., Boime I. Imbalanced of human choriogonadotropin alpha, beta subunits reflects the steady state levels of the corresponding mRNAs. // JBC. 1983. 258: 9250-53.

Blithe D. L., Iles R. K. The role of glycosylation in regulating the glycoprotein hormone free alpha-subunit and free beta-subunit combination in the extraembryonic coelomic fluid of early pregnancy. // Endocrinology. 1995. 136: 903-910.

Cole L. A., Kardana A., Park S-Y., Braustein G. D. The deactivation of hCG by nicking and dissociation.// J. of clin. End. and Metab. 1993; 76(3): 704-10.

Spencer K., Macri J. N., Carpenter P. et al. Stability of intact chorionic gonaotropin in serum. Liquid whole blood and dried whole-blood filter-paper. // Clin. Chem. 1993. 39/6: 1064-68.

Cole L. A, Kardana A., Andrade-Gordon P. et al. The heterogeneity of hCG: III. The occurence, biological and immunological activities of nicked hCG. // Endocrinology. 1991. 129: 1559-67.

Cole L. A. Immunoassay of human chorionic gonadotropin, its free subunits, and metabolites. // Clin Chem. 1997; 43(12): 2233-43.

Pittaway D. E , Reiosh R. L. , Wentz A. C. Doubling times of human chorionic ginadotropin increase in early viable intrauterine pregnancies. // Am. J. Obstet. Gynecol. 1985. 152: 299-302.

Aspillaga M. O., Whittaker P. G., Taylor A., Lind T. Some new aspects of the endocrinological response to pregnancy. // Br. J. Obstet. Gynecol. 1983. 90: 596-603.

Cole L. A., Seifer D. B., Kardana A., Braunstein G. D. Selecting human chorionic gonadotropin immunoassays: consideration of cross-reacting molecules in first-trimester pregnancy serum and urine. //Am. J. Obstet. Gynecol. 1993; 168: 1580-6.

Rao C. V., Griffin L. P., Carman F. R. Gonadotorpin receptors in human corpora lutea of the menstrual cycle and pregnancy. // Am. J. Obstet. Gynecol. 128: 146-153.

Macri N., Kasturi R. V. , Krantz D. A. et al. Maternal serum Down syndrome screening: free beta-protein is a more effective marker than human chorionic gonadotropin. // Am. J. Obstet. Gynecol. 1990; 163: 1248-53.

Cuckle H. S., Iles R. K., Chard T. Urinary β-core human chorionic gonadotropin: a new approach to Downs syndrome screening. Prenat. Diagn. 1994; 14: 953-8.

Cole L. A. New perspectives in measuring human chorionic gonadotropin levels for measuring and monitoring trophoblast disease. // J. Reprod. Med. 1994; 74: 212-6.

Berkowitz R., Ozturk M., Goldstein D. et al. Human chorionic gonadotropin and free subunits serum levels in patients with partial and complete hydatidiform moles. // Obstet. Gynecol. 1989; 74: 212-6.

Leshin L. Prenatal testing for Down syndrome. At http://www.ds-health.com/prenatal.html

Кащеева Т. К., Полынцев Д. Г., Шаповалов В. В. и др. Опыт использования автоматизированной системы расчета риска патологии плода // Terra Medica. 2002; 1: 20-22.

Macri J. N., Spencer K., Aitken D. et al. First trimester free beta (hCG) screening for Down syndrome. Prenat. Diagn. 1993; 13: 557-62.

Macintosh M. C, Iles R., Teisner B. et al. Maternal serum human chorionic gonadotropin and pregnancy-associated plasma protein A, markers for fetal Down syndrome. Prenat. Diagn. 1994; 14: 203-8.

Haddow J. E., Palomaki G. E , Knight G. J. et al. Screening of maternal serum for fetal Downs syndrome in the first trimester. // The New Engl. J. of Med. 1998; 338 (14): 955-61.

Khasaeli M. B., England B. G, Dieterle R. C. et al. Development and characterisation of a monoclonal antibody which distinuishes the β-subunit of human chorionic gonadotropin in the presence of hCG. // Endocrin. 1981; 109: 1290.

Ong C. Y., Liao A. W., Spencer K. et al. First trimester maternal serum free β human chorionic gonaditropin and pregnancy associated plasma protein A as predictors of pregnancy complications. BJOG 2000; 107: 1265-70.

Dirnhofer S., Klieber R., DeLeeuw R. et al. Functional and immunological relevance of the COOH-terminal extension of human horionic gonadotropin β: implications for the WHO birth vaccine. // Faseb. J. 1993. 7, 1381-85.

Berger P., Klieber R., Panmoung W. et al. Monoclonal antibodies against the free subunits of human chorionic gonadotropin. // J. Endocrinol. 1990; 125: 301-9.

Qin Q., Christiansen M., Lovgren T. et al. Dual-label time-resolved immunofluorometric assay for simultaneous determination of pregnancy-associated plasma protein A and free β-subunit of human chorionic gonadotropin. // J. Immunol. Meth. 1997; 205: 169-175.