Results 161 to 170 of about 40,012 (197)
RENAL‐CHIP converts 1 mL of peripheral blood into a biopsy‐equivalent readout of renal‐allograft fate. By magnetic capture and release of donor‐derived circulating podocytes through a herringbone microfluidic chip, 84% capture, 96% release and single‐cell RNA evidence of rejection‐specific immunity are achieved.
Juan Song +11 more
wiley +1 more source
To address multidrug‐resistant urinary tract infections (MDR‐UTIs), we developed Cu‐ZIF8‐Ru nanozyme featuring an asymmetric Cu─N─Ru catalytic site. This unique structure enhances multienzyme‐mimetic activity, eradicating resistant bacteria by inducing a cuproptosis‐like death pathway through intracellular Cu2+ accumulation and energy depletion.
Guanlin Li +9 more
wiley +1 more source
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Critical Care Medicine, 2003
To review current knowledge about cell-free hemoglobin solutions.A computerized MEDLINE search was used to retrieve all studies concerning cell-free hemoglobin solutions from 1990 to 2003. The reference lists of all available review articles and primary studies were also reviewed to identify references not identified in the computerized search.All ...
Creteur, Jacques, Vincent, Jean Louis
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To review current knowledge about cell-free hemoglobin solutions.A computerized MEDLINE search was used to retrieve all studies concerning cell-free hemoglobin solutions from 1990 to 2003. The reference lists of all available review articles and primary studies were also reviewed to identify references not identified in the computerized search.All ...
Creteur, Jacques, Vincent, Jean Louis
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Hemoglobin, 1990
About 70 variants of Hb A with associated hemolytic disorders have been reported during the past 30 years. I have classified them according to four grades of severity of chronic hemolysis. Acute episodes of severe hemolysis may be seen in all classes.
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About 70 variants of Hb A with associated hemolytic disorders have been reported during the past 30 years. I have classified them according to four grades of severity of chronic hemolysis. Acute episodes of severe hemolysis may be seen in all classes.
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Unstable Hemoglobins, Hemoglobins with Altered Oxygen Affinity, and M-Hemoglobins
Pediatric Clinics of North America, 1980Most patients with chronic Heinz body anemia do not require treatment. Dietary folic acid supplementation is recommended when hemolysis is chronic and severe. During infection, patients should be observed carefully because of the possibility of aplastic or hemolytic crises.
E P, Vichinsky, B H, Lubin
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2005
Hemoglobin degradation by Plasmodium is a massive catabolic process within the parasite food vacuole that is important for the organism's survival in its host erythrocyte. A proteolytic pathway is responsible for generating amino acids from hemoglobin.
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Hemoglobin degradation by Plasmodium is a massive catabolic process within the parasite food vacuole that is important for the organism's survival in its host erythrocyte. A proteolytic pathway is responsible for generating amino acids from hemoglobin.
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Spectrophotometry of Hemoglobin and Hemoglobin Derivatives
1983Publisher Summary This chapter presents a discussion of spectrophotometry of hemoglobin and hemoglobin derivatives. Many special photometers (hemoglobinometers, oximeters, etc.) presently available for the determination of hemoglobin and hemoglobin derivatives are mentioned only incidentally.
E J, van Kampen, W G, Zijlstra
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Ontogeny of hemoglobins: Evidence for hemoglobin M
Developmental Biology, 1974Abstract A new autosomal codominant hemoglobin mutation alters hemoglobin M of the primitive red cell line and hemoglobin D found in definitive cells. That Hb M and Hb D are altered by the same gene mutation supports the idea that Hb M shares a polypeptide chain with Hb D.
R W, Keane +3 more
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Hemoglobin Variants in Koreans: Hemoglobin G Taegu
Science, 1967Hemoglobin G Taegu, an electrophoretically slow hemoglobin with a structural anomaly believed to be in the β-T-3 section of the beta chain, was the only variant found among 6700 normal Koreans. Four subjects, 0.06 percent, had the G-hemoglobin variant in addition to normal hemoglobin A. Hemoglobin E, known in numerous groups from Southeast Asia and the
R Q, Blackwell, J T, Huang, I H, Ro
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