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Список литературы на "B"

♦BA

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Bartelmez G.W., Blount M.P. (1954) The formation of neural crest from the primary optic vesicle in man. Contributions to Embryol. V.35.P.55-71

Bassel-Duby R., Hernandez M/D., Yang Q., Rochelle J.M., Seldin M.F., Williams R.S.(1994). Myocite nuclear factor, a novel winged-helix transcription factor under both developmental and neural regulation in striated myocytes Mol Cell Biol.V.14. P.4596-4605 .

Basson, C.T.,Cowley,G.S.,Solomon, S.D.,Weissman, B.,Poznanski, A.K.,Traill, T.A.,Seidman, J.G.,Seidman, C.E.(1993)The clinical and genetic spectrum of the Holt-Oram syndrome (Hand-Heart syndrome). N. Engl. J.Med.330,885-891.

Bastian J., Law S., Vogler L., Lawton A., Herrod H., Anderson S., Horowitz S., Hong R. (1989) Prediction of persistent immunodeficiency in the DiGeorge anomaly. J.Pediatr. V.115, P.391-396.

BE

Benedeczky I., Fekete E., Resch B. (1993). Ultrastructure of the developing muscle and enteric nervous system in the small intestine of human fetus. Acta Physiol.Hungarica. V.81.N 2.P.193

Behrens J, von Kries J.P, Kuhl M, Bruhn L, Wedlich D, Grosschedl R, Birchmeire W.(1996).Functional interaction of beta-catenin with the transcription factor LEF-1. Nature v.382, p 638-642.

Bergwerff M., Verberne M.E., DeRuiter M.C., Poelmann R.E., Gittenbergerger-de Groot A.C. (1998). Neural crest cell contribution to the developing circulatory system. Implication for vascular morphology? Circ.Res. V.82. P. 221-231

Berthelsen J, , Zappavigna V, Ferretti E, Mavilio F, Blasi F.1998.The novel homeoprotein Prep1 modulates Pbx-Hox protein cooperativity.EMBO J v.17:5 1434-45.

Betz U.A.K, Bloch W, van den Broek M, Yoshida K, Taga T, Kishimoto T, Addicks K, Rajewsky K, Muller W.1998.Postnatally induced inactivation of gp130 in mice results in neurologic, cardiac, hematopoietic, immunological,hepatic, and pulmonal defects.J.Exp.Med. V.188. N 10. P.1955-1965

BI

Biben C, Harvey R.P.(1997).Homeodomain factor Nkx2-5 controls left/right asymmetric expression of bHLH gene eHand during murine heart development. Genes Dev. 11:11 1357-69

Bierkamp C., McLaughin K.J., Schwarz H., Huber O., Kemler R. (1996).Embryonic heart and skin defects in mice lacking plakoglobin. Dev.Biol.180, 780-785

Bies R.D., M. Maeda, S. L. Roberds, E. Holder, T. Bohlmeyer, J. B. Young, K. P. Campbell.(1997).A 5' Dystrophin Duplication Mutation Causes Membrane Deficiency of alpha-Dystroglycan in a Family with X-linked Cardiomyopathy.J.Mol.Cell. Cardiol. v 29, n 12, p3175-3188.

Bingle CD, ., Gowan S.(1996).Oct-1 interacts with conserved motifs in the human thyroid transcription factor 1 gene minimal promoter.Biochem J. v 319 ( Pt 3): 669-74.

Bisaha J.G.,Bader D.(1991). Identification and characterization of a ventricular-specific avian myosin heavy chain, VMHC1: Expression in differentiating cardiac and skeletal muscle. Dev. Biol. V. 148. P. 355-364.

Bisgrove D.A,R.Godbout (1999). Differential expression AP-2,alpha; and AP-2,beta; in the developing chick retina: repression of R-FABP promotor activity by AP-2 Devel.Dyn. V.214. N 3. P. 195-206

BL

C.S.Blagden,S.M.Hughes(1999).Extrinsic influences on limb muscle organization Cell Tissue Res. V.296. No 1. P. 141-150

Blankenship T.N., Petterson P.E., Hendrickx A.G. (1996). Emigration of neural crest cells from macaque optic vesicles is correlated with discontinuities in its basement membrane J.Anat V.188. P. 473-483

Blanchard E.M, Iizuka K, Christe M,Conner D.A, Geisterfer A, Schoen F.J, Maughan D.W, Seidman C.E,Seidman J.G (1997). Targeted ablation of the murine α-tropomyosin gene. Circ.Res. V.81(6):1005-1010.

Blaschke RJ;., Monaghan AP; Schiller S; Schechinger B; Rao E; Padilla-Nash H; Ried T; Rappold G.A. (1998). SHOT, a SHOX-related homeobox gene, is implicated in craniofacial, brain, heart, and limb development Proc Natl Acad Sci U S A V.95(5):2406-11.

BO

Bockman D.E. (1997). Development of the thymus Microsc.Res. & Technique V.38 N 3. P.209-215

Bogdanov Y., Rubino A, Burnstock G(1998). Characterisation of subtypes of the P2X and P2Y families of ATP receptors in the foetal human heart.Life Sci V.62:8 697-703

Bordi C., D'Adda T, Azzoni C, Ferraro G.(2000). Classification of gastric endocrine cells at the light and electron microscopical levelsMicr. Res. & Technol. V.48. No2. P.258-271

BR

Brannan C I., Perkins A. S., Vogel K. S, Ratner N, Nordlund M. L, Reid S.W, Buchberg A. M, Jenkins N. A, Parada L. F, Copeland N. G. (1994). Targeted disruption ofthe neurofibromatosis type 1 gene leads to developmental abnormalities in heart and various neural crest derived tissues Genes& Dev V.8, P.1019-1029.

Bresnick A.R.(1999). Molecular mechanisms of nonmuscle myosin-II regulation Cur.Opin.in Cell Biol. V.11. No 1. P. 26-33

Britz-Cunningham S.H., Shah M. M, Zuppan C. W, Fletcher W. H. (1995).Mutations of the connexin43 gap junction gene in patients with heart malformations and defects of laterality New Eng J.Med. V.332, 1323- 1329 .

Brooks P.C., Stromblad S., Sanders L.C., von Schalscha T.L., Aimes R.T, Stetler-Stevenson W.G., Quigley J.P. Cheresh D. A. (1996) Localization of matrix metalloproteinase MMP-2 to the surface of invasive cells by interaction with integrin alfa v beta 3. Cell V.85, P.683-693.

BU

Budarf, M.L., Collins, J.,Gong, W.,Roe, B.,Wang, Z.,Bailey, L.C.,Sellinger, B.,Michaud, D.,Driscoll, D.A.,Emanuel, B.S. (1995) Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene. Nat. Genet.10,269-277 .

Burch G.H., Bedolli M.A., McDonough S., Rosenthal S.M.,Bristow J.(1995). Embryonic expression of tenascin-X suggest a role in limb, muscle, and heart development. Dev.Dyn. V.203.No.4. P.491-504.

Burke B.A., Johnson D., Gilbert E.F., Drut R.M., Ludwig J., Wick M.R. (1987) Thyrocalcitonin-containing cells in the DiGeorge anomaly. Human.Pathol. V.18, P.355-360.

Burke D., Wilkes D., Blundell T. L. and Malcolm S. (1998) Fibroblast growth factor receptors: lessons from the genes Trends in Biochemical Sciences .V 23. N 1. P.59-62

Burn, J., Takao, A.,Wilson, D.,Cross, I.,Momma, K.,Wadey, R.,Scambler, P.,Goodship, J.(1993) Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11. J. Med. Genet.30,807-812(822-824).

BY

Byeon M.K., Sugi Y, Markwald R.R, Hoffman S. (1995). NCAM polypeptides in heart development: assotiation with Z discs of form that contain the muscle-specific domain. J.Cell Biol.V.128,N 1-2,P. 209-221.

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