Combined defects

Maguire MP, Paredes AM, Riess RW 1991 The desynaptic mutant of maize as a combined defect of synaptonemal complex and chiasma maintenance. Genome 34 879-887 May GS, McGoldrick CA, Holt CL, Denison SH 1992 The bimB3 mutation of Aspergillus nidulans uncouples DNA replication from the completion of mitosis. J Biol Chem 267 15737-15743... 

Results obtained in this way were helpful, but of limited value. The analyses told us whether or not the bile was supersaturated with cholesterol, but did not tell us whether the abnormality was due to too much cholesterol, too few bile acids, too few phospholipids or to some combined defect. The next step, therefore, was to measure the hour-by-hour bile lipid-secretion rates using marker-corrected perfusion techniques. These assume that, in response to the perfusion stimulus (such as an intra-duodenal amino acid mixture), the gallbladder remains tonically contracted throughout and steady-state conditions ensue. 

Compare the photoabsorption and PL properties of NBO in Si02 with those of the NBO-OV combination defects. Flow the presence of OVs affects the PL bands ... 

Since the Xbar/R Charts for the oven cure data show that the curing process is now in control, there should be a corresponding shift downward in the defect rate. This improvement in the defect rate can be illustrated by combining defect data from before and after the process change onto the same C-chart. 

Clinically, cochlear ototoxicity is more frequent and easier to detect than vestibular toxicity combined defects are relatively rare. Symptoms of cochlear damage include tinnitus, hearing loss, pressure, and sometimes pain in the ear. The manifestations of vestibular toxicity are dizziness, vertigo, ataxia, and nystagmus. These are often overlooked in severely ill, bed-ridden patients. 

It would seem that there is much room for the application of CAEM to the study of the oxidation of carbons. It would be interesting to try to combine defect decoration techniques with CAEM, or to follow oxidation at higher conversions using the technique. 

Olchovsky, D., Bruno, J.E, Wood, T.L., Gelato, M.C., Leidy, J.W., Jr, Gilbert, J.M., Jr Berelowitz, M. (1990) Altered pituitary growth hormone (GH) regulation in streptozotocin-diabetic rats a combined defect of hypothalamic somatostatin and GH-releasing factor. Endocrinology 126, 53-61. 

To identify the antiferroelectric phase, texture observation of the homeotropic cells of racemic compounds is very effective. In the SmC phase, only the schlieren texture with four brushes is observable and that with two brushes is prohibited, because of the head-and-tail inequivalence of the C-director. In the SmCA phase, however, the schlieren texture with two brushes is sometimes seen, as shown in Figure 9.8 [18], [19]. The existence can be explained by taking into account a screw dislocation, as illustrated in Figure 9.9. The discontinuous change (7r-wall) of the C-director is compensated by the screw dislocation. This defect is a combined defect of a disclination and a dislocation, i.e., adispiration [18], [19]. 

Figure 9.9. Model structure of the two-brush defect i.e., dispiration, a combined defect of a wedge disclination and a screw dislocation.

In addition to these two types of sialidosis, there are patients with a combined defect of neuraminidase and p-galactosidase (Wenger etal. 1978, Andria etal. 1978, OK.ADAetal. 1979), possibly caused by a common defect in the biosynthetic processing of the two enzymes (Hoogeveen etal. 1980). A neuraminidase deficiency has also been observed in patients with mucolipidosis II (I-cell disease) and mucolipidosis III (Strecker etal. 1976, Thomas etal. 1976). In these disorders, however, the neuraminidase deficiency is but one of many lysosomal hydrolase deficiencies, presumably due to a defect in the proper compart-mentalization of these enzymes (Neufeld 1974). 

The ice crystalline stmcture can contain many kinds of point defects, dislocations, and planar defects in common with other crystalline materials [3]. For point defects, there are several categories in ice molecular defects, impurity defects, electronic defects, protonic defects, and combined defects. Dislocations in the ice stmcture... 

Bartlett, K., Ng, H. and Leonard, J.V. (1980), A combined defect of three mitochondrial carboxylases presenting as biotin-responsive 3-methylcrotonyl-glycinuria and 3-hydroxyisovalerate aciduria. Clin. Chim. Acta, 100,183. 

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