Albin

Albin, S. L. and Crefield, P. J. 1994 Getting Started - Concurrent Engineering for a Medium Sized Manufacturer. Journal of Manufacturing Systems, 13(1), 48-58. 

In the body, proteins are built up by a series of reactions that in general produce a specific sequence of amino adds. Even tiny errors in this sequence may have serious effects. Among the genetic diseases known to be caused by improper sequencing are hemophilia, sickle cell anemia, and albinism. Sickle cell anemia is caused by the substitution of one valine unit for a glutamic add unit in a chain containing 146 monomers. 

Chaudhari AM, Woudenberg TM, Albin M, Goodson KE (1998) Transient liquid crystal thermometry of microfabricated PCR vessel arrays. J Microelectromech Sys 7 345-355 Cheng P, Wu WY (2006) Mesoscale and microscale phase heat transfer. In Greene G, Cho Y, Hartnett J, Bar-Cohen A (eds) Advances in heat transfer, vol 39. Elsevier, Amsterdam Choi SB, Barron RF, Warrington RQ (1991) Fluid flow and heat transfer in micro- tubes. ASME DSC 40 89-93... 

Nineteen women underwent amniocentesis for the determination of fetal sex. Several different X-llnked abnormalities constituted the Indications for this procedure, and these Included hemophilia A, hemophilia B, Duchenne muscular dystrophy, optic albinism, X-llnked mental retardation, the Lesch-Nyhan syndrome (due to dlflclency of hypoxanthlne-guanlne phosphorlbosyltransferase, and Fabry s disease (due to deficiency of an a-galact-osldase). Fourteen of the fetuses were male. Including one which turned out to be a set of twins, and most of the male pregnancies were terminated. The sex determination being carried out for Fabry s disease Is of particular Interest, since In this case It was desired to find out whether the fetus was a female. 

COWARD L, KIRK M, ALBIN N and BARNES s (1996) Analysis of plasma isoflavones by reversed-phase HPLC-multiple reaction ion monitoring-mass spectrometry. Clin Chim Acta. 247 (1-2) 121-42. 

Albin, D. M., Wubben, J. E., and Gabert, V. M., Effect of hydrolysis time on the determination of amino acids in samples of soybean products with ion-exchange chromatography or precolumn derivatization with phenyl isothiocyanate,. Agr. Food Chem., 48, 1684, 2000. 

Giebel, L. B., and Spritz, R.A. (1992). The molecular basis of type I (tyrosinase-deficient) human oculocutaneous albinism. Pigment Cell Res. Suppl. 2 101-106. 

King, R. A., Mentink, M. M., and Oetting, W. S. (1991). Non-random distribution of missense mutations within the human tyrosinase gene in type I (tyrosinase-related) oculocutaneous albinism. Mol. Biol. Med. 8 19-29. 

Schmidt, A., and Beermann, F. (1994). Molecular basis of dark-eyed albinism in the mouse. Proc. Natl. Acad. Sci. USA 91 4756-4760. 

G Albin, TA Horbett, BD Ratner. Glucose-sensitive membranes for controlled release of insulin. In J Kost, ed. Pulsed and Self-Regulated Drug Delivery. Boca Raton, FL CRC Press, 1990, pp 159-185. 

Albin R., Koeppe R., Chervin R. et al. (2000). Decreased striatal dopaminergic innervation in REM sleep behavior disorder. Neurology. 55, 1410-12. 

Albin R., Young A., Penney J. (1989). The functional anatomy of basal ganglia disorders. Trends Neurosci. 12, 366-75. 

LN Amankwa, M Albin, WG Kuhr. Trends Anal Chem 11 114-120, 1992. 

GTA Kovac, K Petersen, M Albin. Anal Chem 68 407A-412A, 1996. 

Albin, D. Noufi, R. Tuttle, J. Goral, J. Risbud, S. H. 1988. Composition-structure relationships for multisource evaporated copper gallium selenide (CuGaSe2) thin films. J. Appl. Phys. 64 4903 1908. 

Reiner, A., Albin, R. L., Anderson, K. D. et al. Differential loss of striatal projection neurons in Huntington disease. Proc. Natl Acad. Sci. USA 85 5733-5737,1988. 

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