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Список литературы на "D"

♦DA


Dabiri GA. , Turnacioglu KK, Sanger JM, Sanger JW (1997). Myofibrillogenesis visualized in living embryonic cardiomyocytes. Proc Natl Acad Sci U S A. V.94:17 9493-8
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de la Chapelle A., Herva R.,Koivista M.,Aula P. (1981). A deletion in chromosome 22 can cause DiGeorge syndrome. Hum. Genet.57,253-256
De Haan R.L.(1964). Cell intractions and oriented movements during developmen. J.Exp. Z00l. V. 157. P. 127-238
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Demczuk S., Desmaze C., Aikem M., Prieur M., Ledeist F., Sanson M., Rouleau G., Thomas G., Aurias A. (1994) Molecular cytogenetic analysis of a series of 23 DiGeorge syndrome patients by fluorescence in situ hybridization. Ann Genet. V.37, P.60-65
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DeRuiter M.C.,Poelman R.E., Mentink M.M.T., VanIpern L., Gittenberg-de Groot A.C.(1992). Тhe early formation of the vascular system in quail Embryo. Development of Vascular System in the embryo: A Concept of the Origin of Systematic-Pulmonary Collateral Arteries P. 99-128
DeRuiter M.C., Poelmann R.E, Mentink M.M, Vaniperen L, Gittenberger-De-Groot A.C. (1993). Early formation of the vascular system in quail embryos. Anat.Rec. V.235 No 2. P. 261-274
DeRuiter M.C., Poelmann RE; VanMunsteren JC; Mironov V; Markwald RR; Gittenberger-de Groot AC.(1997). Embryonic endothelial cells transdifferentiate into mesenchymal cells expressing smooth muscle actins in vivo and in vitro Circ Res. V.80(4):444-51
Desmaze C., Scambler P., Prieur M., Halford S., Sidi D., Ledeist F., Aurias A. (1993) Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization. Hum.Genet. V.90, P.663-665
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Dickson M.C., Slager H.G., Duffie E., Mummery C.L., Akhurst R.J.(1993). RNA and protein localisations of TGF beta 2 in the early mouse embryo suggest an involvenebt in cardiac development Develop. V.117. N 3. P. 626-639

DR


Dono R., Scalera L., Pacifico F., Acampora D., Persico M.G., Simeone A..(1993). The murine cripto gene: expression during mesoderm induction and early heart morphogenesis. Develop. V.118. No.4. P. 1157-1168

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Driscoll D.A., Budarf M.L., Emanuel B.S. (1992) A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11. Am.J.Hum.Genet. V.50, P.924-933
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Drysdale T.A., Patterson K.D, Saha M, Krieg P.A. (1997) Retinoic acid can block differentiation of the myocardium after heart specification. Dev Biol . V.188:2 205-15

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Duncan S.A..(2000) Transcriptional regulation of liver development. Devel.Dyn.V.219. N 2. P. 131-142
Durandy A., Ledeist F., Fischer A.,Driscelli P. (1986) Impaired T8 lymphocyte-mediated suppressive activity in patients with partial DiGeorge syndrome. J.Clin.Immunol. V.6 P.265-270
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