Recombinant mouse phosphatidylinostol transfer protein β has a major and a minor site of phosphorylation

2000 ◽  
Vol 28 (5) ◽  
pp. A360-A360
Author(s):  
C. M. van Tiel ◽  
M. A. Paasman ◽  
J. Westerman ◽  
G. T. Snoek ◽  
K. W. A. Wirtz
Keyword(s):  
Transfer Protein ◽  
Recombinant Mouse ◽  
Minor Site ◽  
A Minor

scholarly journals Selective hepatic uptake of synthetic glycoproteins: mannosaminated ribonuclease A dimer and serum albumin.

1979 ◽  
Vol 74 (4) ◽  
pp. 495-509 ◽  
Author(s):  
G Wilson
Keyword(s):  
Serum Albumin ◽  
Reductive Amination ◽  
Hepatic Uptake ◽  
Ribonuclease A ◽  
Liver Uptake ◽  
Lysine Residues ◽  
Minor Site ◽  
Pancreatic Ribonuclease A ◽  
A Minor ◽  
Derivatives Of

The influence of mannose-containing oligosaccharides on the tissue uptake of glycoproteins has been examined with synthetic glycoconjugates. Oligosaccharides obtained from the acetolysis of bakers' yeast mannan have been coupled to the lysine residues of the cross-linked dimer of bovine pancreatic ribonuclease A and of human serum albumin by reductive amination with cyanoborohydride. 14C-labeled derivatives of the two proteins containing two to four mannopyranose residues per 10,000 mol wt were administered intravenously to rats. There was selective (70-80%) uptake of these derivatives by the liver within 10-15 min after injection. A minor site of uptake was the spleen. The extent of hepatic uptake was a function of the number and size of the mannooligosaccharide residues coupled. With the nonglycosaminated derivatives the liver uptake was less than 5%. Related studies have shown that mannose-containing glycoproteins are taken up by both the endothelial and Kupffer cells of the liver; thus, reductive mannosamination may provide a means of directing to these cells proteins of potential therapeutic interest.

Dormancy in Pinusmonticola seed related to stratification time, seed coat, and genetics

1987 ◽  
Vol 17 (4) ◽  
pp. 294-298 ◽  
Author(s):  
R. J. Hoff
Keyword(s):  
Seed Coat ◽  
White Pine ◽  
Hard Seed ◽  
Physiological Conditions ◽  
Western White Pine ◽  
Minor Site ◽  
Coat Layer ◽  
A Minor ◽  
Hard Seed Coat

The inner layer of the seed coat, a papery membrane, and physiological conditions of the gametophyte–embryo were shown to be major sites of dormancy in seed of western white pine. The hard seed coat layer was a minor site. With no stratification, 7% of the seeds were not dormant, 9% were dormant because of the hard seed coat, 34% were dormant because of the inner seed coat, and 50% were dormant because of physiological conditions of the gametophyte–embryo. These values varied with stratification times and seed lots (families).

Quantitative digestion of fresh herbage by sheep: III. The movement of Mg, Ca, P, K and Na in the digestive tract

1974 ◽  
Vol 82 (2) ◽  
pp. 321-330 ◽  
Author(s):  
N. D. Grace ◽  
M. J. Ulyatt ◽  
J. C. Macrae
Keyword(s):  
Small Intestine ◽  
Large Intestine ◽  
Dry Matter ◽  
Mineral Elements ◽  
High Intake ◽  
Faecal Excretion ◽  
Once Daily ◽  
Short Rotation ◽  
Minor Site ◽  
A Minor

SummarySheep prepared either with a rumen cannula, or with a rumen cannula plus re-entrant cannulae in the duodenum and ileum were fed fresh ‘Ruanui’ perennial ryegrass (R), ‘Manawa’ short-rotation ryegrass (M) and white clover (C) at dry-matter intakes ranging from 450 to 1000 g/24 h. Paper impregnated with chromic oxide was given once daily via the rumen fistula as a marker.Amounts of Mg, Ca, P, K and Na entering and leaving the small intestine and excreted in the faeces were regressed against the intake of each element for each sheep and these equations (all, other than the faecal excretion of Na, significant (P < 0·05)) were used to calculate the extent of apparent absorption or secretion in the stomach, the small intestine and the large intestine at two levels of OM intake (500 and 800 g daily).Quantities of Mg (at high intake), Ca and K (except sheep fed M) leaving the stomach were significantly lower (P < 0·05), while the amounts of P and Na were significantly higher (P < 0·01) than the amounts consumed. Quantities of Mg (at high intakes) and Ca leaving the small intestine were significantly higher (P < 0·05) while amounts of P, K and Na (at high intakes) were significantly lower (P < 0·05) than the corresponding quantities entering the small intestine. At both intakes in the case of Na and at the higher intakes in the case of the other mineral elements, quantities of Mg, Ca (except sheep fed C), P, K and Na excreted in the faeces were significantly less (P < 0·05) than the amounts entering the large intestine.Thus at the higher intakes there were net absorptions of Mg, Ca and K (except sheep fed M) from, and net secretions of P and Na into, the stomach. The small intestine was the major site of net absorption for P and K and a minor site for Na, while a net secretion of Mg and Ca occurred into this region. Net absorption of Mg, Ca, P, K and Na occurred from the large intestine at the higher intakes.The retention of Mg, Ca and P is discussed in relation to the animals' minimal daily requirements of these elements.

Rating Post-Operative Backs (Part I)

1997 ◽  
Vol 2 (4) ◽  
pp. 1-3
Author(s):  
James B. Talmage
Keyword(s):  
Spinal Stenosis ◽  
Foot Drop ◽  
Neurogenic Claudication ◽  
Root Damage ◽  
Fourth Edition ◽  
Minor Strain ◽  
Injury Model ◽  
Strain Type ◽  
A Minor ◽  
Anterior Tibialis

Abstract The AMA Guides to the Evaluation of Permanent Impairment, Fourth Edition, uses the Injury Model to rate impairment in people who have experienced back injuries. Injured individuals who have not required surgery can be rated using differentiators. Challenges arise when assessing patients whose injuries have been treated surgically before the patient is rated for impairment. This article discusses five of the most common situations: 1) What is the impairment rating for an individual who has had an injury resulting in sciatica and who has been treated surgically, either with chemonucleolysis or with discectomy? 2) What is the impairment rating for an individual who has a back strain and is operated on without reasonable indications? 3) What is the impairment rating of an individual with sciatica and a foot drop (major anterior tibialis weakness) from L5 root damage? 4) What is the rating for an individual who is injured, has true radiculopathy, undergoes a discectomy, and is rated as Category III but later has another injury and, ultimately, a second disc operation? 5) What is the impairment rating for an older individual who was asymptomatic until a minor strain-type injury but subsequently has neurogenic claudication with severe surgical spinal stenosis on MRI/myelography? [Continued in the September/October 1997 The Guides Newsletter]

Pelvic Impairments

2018 ◽  
Vol 23 (4) ◽  
pp. 9-10
Author(s):  
James Talmage ◽  
Jay Blaisdell
Keyword(s):  
Pelvic Ring ◽  
Reproductive Organs ◽  
High Impact ◽  
Pelvic Fractures ◽  
Motor Dysfunction ◽  
Impact Event ◽  
Concomitant Injuries ◽  
Rating Process ◽  
Pass Through ◽  
A Minor

Abstract Pelvic fractures are relatively uncommon, and in workers’ compensation most pelvic fractures are the result of an acute, high-impact event such as a fall from a roof or an automobile collision. A person with osteoporosis may sustain a pelvic fracture from a lower-impact injury such as a minor fall. Further, major parts of the bladder, bowel, reproductive organs, nerves, and blood vessels pass through the pelvic ring, and traumatic pelvic fractures that result from a high-impact event often coincide with damaged organs, significant bleeding, and sensory and motor dysfunction. Following are the steps in the rating process: 1) assign the diagnosis and impairment class for the pelvis; 2) assign the functional history, physical examination, and clinical studies grade modifiers; and 3) apply the net adjustment formula. Because pelvic fractures are so uncommon, raters may be less familiar with the rating process for these types of injuries. The diagnosis-based methodology for rating pelvic fractures is consistent with the process used to rate other musculoskeletal impairments. Evaluators must base the rating on reliable data when the patient is at maximum medical impairment and must assess possible impairment from concomitant injuries.

Conjugated Linoleic Acid Causes a Marked Increase in Liver α-Tocopherol and Liver α-Tocopherol Transfer Protein in C57BL/6 J Mice

2010 ◽  
Vol 80 (1) ◽  
pp. 65-73 ◽  
Author(s):  
Pei-Min Chao ◽  
Wan-Hsuan Chen ◽  
Chun-Huei Liao ◽  
Huey-Mei Shaw
Keyword(s):  
Antioxidant Enzymes ◽  
Linoleic Acid ◽  
Conjugated Linoleic Acid ◽  
Thiobarbituric Acid ◽  
Control Group ◽  
Thiobarbituric Acid Reactive Substances ◽  
Control Groups ◽  
Protein Levels ◽  
Transfer Protein ◽  
And Control

Conjugated linoleic acid (CLA) is a collective term for the positional and geometric isomers of a conjugated diene of linoleic acid (C18:2, n-6). The aims of the present study were to evaluate whether levels of hepatic α-tocopherol, α-tocopherol transfer protein (α-TTP), and antioxidant enzymes in mice were affected by a CLA-supplemented diet. C57BL/6 J mice were divided into the CLA and control groups, which were fed, respectively, a 5 % fat diet with or without 1 g/100 g of CLA (1:1 mixture of cis-9, trans-11 and trans-10, cis-12) for four weeks. α-Tocopherol levels in plasma and liver were significantly higher in the CLA group than in the control group. Liver α-TTP levels were also significantly increased in the CLA group, the α-TTP/β-actin ratio being 2.5-fold higher than that in control mice (p<0.01). Thiobarbituric acid-reactive substances were significantly decreased in the CLA group (p<0.01). There were no significant differences between the two groups in levels of three antioxidant enzymes (superoxide dismutase, glutathione peroxidase, and catalase). The accumulation of liver α-tocopherol seen with the CLA diet can be attributed to the antioxidant potential of CLA and the ability of α-TTP induction. The lack of changes in antioxidant enzyme protein levels and the reduced lipid peroxidation in the liver of CLA mice are due to α-tocopherol accumulation.

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