NOTE ON THE VARIATIONS IN AREA AND IN STAINING INTENSITY OF RED BLOOD CELLS AND ON THEIR CORRELATION

1935 ◽  
Vol 12 (6) ◽  
pp. 803-811
Author(s):  
Alfred Savage ◽  
C. H. Goulden ◽  
J. M. Isa
Keyword(s):  
Red Blood Cells ◽  
Pernicious Anemia ◽  
Human Blood ◽  
Blood Cells ◽  
Regression Line ◽  
Staining Intensity ◽  
Non Linear ◽  
Normal Human ◽  
Blood Specimens ◽  
Normal Human Blood

By means of a laborious technique, based on the use of a projection microscope and a sensitive electric photometer, it has been shown that both the areas and transparencies of stained red blood cells may be determined. From the few observations completed, it appears that, statistically, these attributes are positively correlated in normal human blood and their regression line is straight. In pernicious anemia the A/T correlation is negative. Cases of secondary anemia may show either positive or negative A/T correlations. The pathological blood specimens studied all showed non-linear A/T regression lines.

Tyrosine kinases in normal human blood cells

FEBS Letters ◽  
1986 ◽  
Vol 205 (1) ◽  
pp. 97-103 ◽  
Author(s):  
Grish C. Varshney ◽  
Jöelle'Henry ◽  
Axel Kahn ◽  
Françoise Phan-Dinh-Tuy
Keyword(s):  
Human Blood ◽  
Blood Cells ◽  
Tyrosine Kinases ◽  
Human Blood Cells ◽  
Normal Human ◽  
Normal Human Blood

scholarly journals Histochemical evidence for the differential surface labeling, uptake, and intracellular transport of a colloidal gold-labeled insulin complex by normal human blood cells.

1981 ◽  
Vol 29 (10) ◽  
pp. 1137-1149 ◽  
Author(s):  
G A Ackerman ◽  
K W Wolken
Keyword(s):  
Cell Surface ◽  
Human Blood ◽  
Binding Sites ◽  
Blood Cells ◽  
Colloidal Gold ◽  
Intracellular Transport ◽  
Insulin Binding ◽  
Human Blood Cells ◽  
Normal Human ◽  
Normal Human Blood

A colloidal gold-labeled insulin-bovine serum albumin (GIA) reagent has been developed for the ultrastructural visualization of insulin binding sites on the cell surface and for tracing the pathway of intracellular insulin translocation. When applied to normal human blood cells, it was demonstrated by both visual inspection and quantitative analysis that the extent of surface labeling, as well as the rate and degree of internalization of the insulin complex, was directly related to cell type. Further, the pathway of insulin (GIA) transport via round vesicles and by tubulo-vesicles and saccules and its subsequent fate in the hemic cells was also related to cell variety. Monocytes followed by neutrophils bound the greatest amount of labeled insulin. The majority of lymphocytes bound and internalized little GIA, however, between 5-10% of the lymphocytes were found to bind considerable quantities of GIA. Erythrocytes rarely bound the labeled insulin complex, while platelets were noted to sequester large quantities of the GIA within their extracellular canalicular system. GIA uptake by the various types of leukocytic cells appeared to occur primarily by micropinocytosis and by the direct opening of cytoplasmic tubulo-vesicles and saccules onto the cell surface in regions directly underlying surface-bound GIA. Control procedures, viz., competitive inhibition of GIA labeling using an excess of unlabeled insulin in the incubation medium, preincubation of the GIA reagent with an antibody directed toward porcine insulin, and the incorporation of 125I-insulin into the GIA reagent, indicated the specificity and selectivity of the GIA histochemical procedure for the localization of insulin binding sites.

scholarly journals Ultrastructural localization of lactoferrin in normal human blood cells: Immunoelectron microscopic observation.

1988 ◽  
Vol 28 (1) ◽  
pp. 121-126
Author(s):  
Nagahito Saito ◽  
Nobuo Takemori ◽  
Noriko Tachibana ◽  
Naoyuki Hayashishita ◽  
Keisuke Sakurada ◽  
...  
Keyword(s):  
Human Blood ◽  
Blood Cells ◽  
Microscopic Observation ◽  
Ultrastructural Localization ◽  
Human Blood Cells ◽  
Normal Human ◽  
Normal Human Blood

scholarly journals A BglII RFLP demonstrated for the II-3 gene in normal human blood cells and leukemias

1989 ◽  
Vol 17 (9) ◽  
pp. 3620-3620
Author(s):  
K. Jaquet ◽  
H. Kreipe ◽  
J. Felgner ◽  
H.J. Radzun ◽  
M.R. Parwaresch
Keyword(s):  
Human Blood ◽  
Blood Cells ◽  
Human Blood Cells ◽  
Normal Human ◽  
Normal Human Blood

scholarly journals Lysosomal acid esterase: activity and isoenzymes in separated normal human blood cells

Blood ◽  
1980 ◽  
Vol 55 (6) ◽  
pp. 891-897 ◽  
Author(s):  
HJ Radzun ◽  
MR Parwaresch ◽  
C Kulenkampff ◽  
M Staudinger ◽  
H Stein
Keyword(s):  
Human Blood ◽  
Blood Cells ◽  
Esterase Activity ◽  
Lysosomal Acid ◽  
Human Blood Cells ◽  
Normal Human ◽  
Normal Human Blood

scholarly journals On the Agglutinability of Normal Human Blood Cells

1955 ◽  
Vol 31 (6) ◽  
pp. 388-390
Author(s):  
Tanemoto FURUHATA ◽  
Takeo IIDA ◽  
Toshiyuki SEKI ◽  
Masashi HORIUCHI ◽  
Hisashi HASEBE ◽  
...  
Keyword(s):  
Human Blood ◽  
Blood Cells ◽  
Human Blood Cells ◽  
Normal Human ◽  
Normal Human Blood
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