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  • Human small intestine showing villi and glands. The cytokeratinin the cells is stained blue, the cell nuclei are stained red and the endothelial cells lining the blood vessels are stained green.
  • Human small intestine showing villi and glands. The cytokeratin in the cells is stained blue, the cell nuclei are stained red and the endothelial cells lining the blood vessels are stained green.
  • Blood cells (of a goose or guillemot?): four figures. Ink and crayon, possibly by D. Gascoigne Lillie, ca 1906.
  • Blood vessels in the retina showing the endothelial cells in red and the vascular contents in green. Surrounding cell nuclei are stained blue.
  • Blood cells in myeloid leukaemia stained with Ehrlich's triple stain, as seen under a microscope. Watercolour after A. Goodall, 1912.
  • Cellular architecture of normal human skin imaged by whole mount tissue microscopy. Human skin has a rich network of white blood cells (specifically dendritic cells, T cells and macrophages) which form sheaths around blood vessels. In this image, T cells (stained for CD3; red) dendritic cells (stained for MHC class II; green) and macrophages (stained for LYVE-1; blue with some cells showing a tinge of green) can be seen. Cell nuclei have been stained with DAPI (grey). This normal cellular architecture is grossly disrupted in diseased skin (see related images). X10 magnification. Scale bar (white) represents 200 micrometres.
  • Cellular architecture of normal human skin imaged by whole mount tissue microscopy. Human skin has a rich network of white blood cells (specifically dendritic cells, T cells and macrophages) which form sheaths around blood vessels. In this image, T cells (stained for CD3; red) dendritic cells (stained for MHC class II; green) and macrophages (stained for LYVE-1; blue with some cells showing a tinge of green) can be seen. Cell nuclei have been stained with DAPI (grey). This normal cellular architecture is grossly disrupted in diseased skin (see related images). X20 magnification. Scale bar (white) represents 100 micrometres.
  • Cellular architecture of human skin lymphoma imaged by whole mount tissue microscopy. Normal human skin has a rich network of white blood cells (specifically dendritic cells, T cells and macrophages) which form sheaths around blood vessels. In diseased skin, such as in skin lymphoma as seen here, this normal architecture becomes distorted. In this image, lots of T cells (stained for CD3; red), dendritic cells (stained for CD11c; green) and macrophages (stained for LYVE-1; blue) have infiltrated the skin. X20 magnification. Scale bar (white) represents 100 micrometres.
  • Cellular architecture of normal human skin imaged by whole mount tissue microscopy. Human skin has a rich network of white blood cells (specifically dendritic cells, T cells and macrophages) which form sheaths around blood vessels. In this image, blood vessels (string-like structures stained for CD31; red), lymphatic vessels (ribbon-like structures stained for LYVE-1; blue) and dendritic cells (stained for CD11c; green) can be seen. Macrophages (stained for LYVE-1; blue) are also present. This normal cellular architecture is grossly disrupted in diseased skin (see related images). X10 magnification. Scale bar (white) represents 200 micrometres.
  • Cellular architecture of normal human skin imaged by whole mount tissue microscopy. Human skin has a rich network of white blood cells (specifically dendritic cells, T cells and macrophages) which form sheaths around blood vessels. This image was taken greater than 150 micrometres beneath the junction that joins the dermal and epidermal layers of the skin (dermo-epidermal junction). At this level, dendritic cells (stained for CD11c; green) and macrophages (stained for LYVE-1; blue) form clusters around blood vessels (stained for CD31; red). This normal cellular architecture is grossly disrupted in diseased skin (see related images). Scale bar (white) represents 100 micrometres.
  • Cellular architecture of normal human skin imaged by whole mount tissue microscopy. Human skin has a rich network of white blood cells (specifically dendritic cells, T cells and macrophages) which form sheaths around blood vessels. This image was taken less than 20 micrometres beneath the junction that joins the dermal and epidermal layers of the skin (dermo-epidermal junction). At this level, dendritic cells (stained for CD11c; green) form clusters around and between blood capillary loops (stained for CD31; red). The blind-ended tips of initial lymphatic vessels are just visible (stained for LYVE-1; blue) at this level. This normal cellular architecture is grossly disrupted in diseased skin (see related images). Scale bar (white) represents 200 micrometres.
  • Cellular architecture of normal human skin imaged by whole mount tissue microscopy. Human skin has a rich network of white blood cells (specifically dendritic cells, T cells and macrophages) which form sheaths around blood vessels. This image was taken directly beneath the junction that joins the dermal and epidermal layers of the skin (dermo-epidermal junction). At this level, the capillary network (stained for CD31; red) is visualised against a lawn of autofluorescent dermal papillae (finger-like projections of the dermis; green) scattered with dendritic cells (stained for CD11c; green) and macrophages (stained for LYVE-1; blue). This normal cellular architecture is grossly disrupted in diseased skin (see related images). Scale bar (white) represents 200 micrometres.
  • Diagnostic test for Fragile X, using presence (normal) or absence (Fragile X syndrome) of FMR-1 protein. FMR-1 protein expression in blood cells has been made visible with antibodies against the FMR-1 protein. The presence of FMR-1 protein is made visible as red staining. a: red staining in cells of normal individual. b/c: absence of staining in male patient. d: female patient; one cell is showing staining and in the other cell there is an absence of staining - this individual is a carrier.
  • Human white blood cell
  • Human white blood cell
  • Cell death around scleral blood vessels
  • TEM of leukocytes (white blood cell)
  • White blood cell - polymorphonuclear leucocyte
  • White blood cell - polymorphonuclear leucocyte
  • Cancer cell migrating through blood vessel
  • White blood cell - polymorphonuclear leucocyte - neutrophil
  • The Coulter automatic blood cell counter and cell size analyzer : another giant step forward in the field of hematology / Coulter Electronics.
  • The Coulter automatic blood cell counter and cell size analyzer : another giant step forward in the field of hematology / Coulter Electronics.
  • The Coulter automatic blood cell counter and cell size analyzer : another giant step forward in the field of hematology / Coulter Electronics.
  • A dripping blood droplet against a yellow background representing an advertisement for blood banks as part of the AIDS prevention scheme by the AIIMS Blood Transfusion Service and NGO AIDS Cell, New Delhi. Colour lithograph by N.R. Nanda, ca. 1994.
  • A dripping blood droplet against a yellow background representing an advertisement for blood banks as part of the AIDS prevention scheme by the AIIMS Blood Transfusion Service and NGO AIDS Cell, New Delhi. Colour lithograph by N.R. Nanda, ca. 1994.
  • A sunflower, a symbol of bringing life back by giving blood; an AIDS prevention advertisement by the AIIMS Blood Transfusion Service and NGO AIDS Cell, New Delhi. Colour lithograph by N.R. Nanda, ca. January 1994.
  • A sunflower, a symbol of bringing life back by giving blood; an AIDS prevention advertisement by the AIIMS Blood Transfusion Service and NGO AIDS Cell, New Delhi. Colour lithograph by N.R. Nanda, ca. January 1994.
  • A human white blood cell (CD4) being attacked by the HIV virus; an AIDS prevention advertisement by The Ministry of Education Training, Vietnam. Colour lithograph, ca. 1995.
  • A blood transfusion bag representing an advertisement for sterilisation of needles and syringes to prevent AIDS; by the NGO AIDS Cell Centre for Community Medicine in New Delhi. Colour lithograph by Ayuha (?), ca. December 1992.