Kirschner

Koop T, Schindler W, Kazimirov A, Scherb G, Zegenhagen J, Schulz T, Feidenhans l R and Kirschner J 1998 Electrochemical cell tor in situ x-ray diffraction under ultrapure conditions Rev. Sc/, instrum. 69 1840... 

Reif J, Zink J C, Schneider C-M and Kirschner J 1991 Effects of surface magnetism on optical second harmonic generation Phys. Rev. Lett. 67 2878-81... 

Sidney M. Cantor Frank G. Ciapetta William von Fischer Edward L. Haenisch Edwin J. Hart Stanley Kirschner John L. Lundberg Harry S. Mosher Edward E. Smissman... 

Optically active coordination compounds. S. Kirschner, Prep. Inorg. React., 1964,1,29-57 (140). 

Utilization of the Pfeiffer effect and outer-sphere complexation for the prediction of absolute configurations of optically active metal complexes. S. Kirschner and I. Bakkar, Coord. Chem. Rev., 1982,43, 325-335 (27). 

SETCHELL K D R, BROWN N M, DESAI P, ZIMMER-NECHEMIAS L, WOLFE B E, BRASHEAR W T, KIRSCHNER A s, CASSIDY A and HEUBI J E (2001) BioavailabUity of pure isoflavones in healthy humans and analysis of commercial soy isoflavone supplements. JNutr 131, 1362S-75S. 

SETCHELL K D, BROWN N M, ZIMMER-NECHEMIAS L, BRASHEAR W T, WOLFE B E, KIRSCHNER A S and HEUBI J E (2002) Evidence for lack of absorption of soy glycosides in humans, supporting the crucial role of intestinal metabolism for availability. d/n. 1 Clin Nutr. 76 (2) 447-53. 

Kirschner, M. W., Gerhart,. C. The Plausibility of Life, Yale University Press, New Haven, CT, 2005. 

Kirschner et al. [358] have observed a lower percent finish-on-yarn (FOY) for SFE as compared to solvent extraction of various fibre/textile matrices. This is rationalised as organic solvents tend to extract components from a matrix more vigorously than scCC>2 and thus remove more of the oligomer and organic components present in the fibre. SFE is a potentially softer extraction technique since it removes less of the polymer from the fibre matrix than liquid solvent extraction. 

On-line SFE-SFC-ELSD analysis of the textile and fibre finish components, butyl stearate/palmitate/myri-state, was reported [118]. Similarly, Kirschner et al. [119] used on-line SFE-pSFC for fibre finish analysis on-line SFE-SFC was also instrumental in the analysis of the total composite finish on a commercial textile thread [120]. 

Fraser PE, McLachlan DR, Surewicz WK, Mizzen CA, Snow AD, Nguyen JT, Kirschner DA. Conformation and fibrillogenesis of Alzheimer A beta peptides with selected substitution of charged residues. J Mol Biol 1994 244 64-73. 

Lomakin A, Teplow DB, Kirschner DA, Benedek GB. Kinetic theory of fibrillogenesis of amyloid beta-protein. Proc Natl Acad Sci USA 1997 94 7942-7947. 

Lomakin A, Chung DS, Benedek GB, Kirschner DA, Teplow DB. On the nucleation and growth of amyloid beta protein fibrils detection of nuclei... 

Inouye H, Fraser PE, Kirschner DA. Structure of beta-crystalline assemblies formed by Alzheimer beta-amyloid protein analogues analysis by X-ray diffraction. Biophys J 1993 64 502-519. 

Nguyen JT, Inouye H, Baldwin MA, Fletterick RJ, Cohen FE, Prusiner SB, Kirschner DA. X-ray diffraction of scrapie prion rods and PrP peptides. J Mol Biol 1995 252 412 422. 

Other phosphatases have also been identified and may be implicated in mitotic and meiotic germ cell functions. For example, INH was originally isolated from a Xenopus oocyte cell free system as an inhibitor of pre-MPF activity (Cyert and Kirschner, 1988). INH encodes a protein phosphatase 2Athat negatively regulates MPF activity by dephosphory-lating Cdc2 on thr-161 (Lee et al., 1991 Solomon et al., 1990). 

Gautier, J., Solomon, M. J., Booher, R. N., Bazan, F., and Kirschner, M. W. (1991). cdc25 is a specific tyrosine phosphatase that directly activates p34cdc2. Cell 67 197-211. 

Gerhart, J., Wu, M., and Kirschner, M. (1984). Cell cycle dynamics of an M-phase-specific cytoplasmic factor in Xenopus laevis oocytes and eggs. J. Cell Biol. 98 1247-1255. 

Karsenti, E., Bravo, R., and Kirschner, M. (1987). Phosphorylation changes associated with the early cell cycle in Xenopus eggs. Dev. Biol. 119 442-453. 

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