| HC | hair cell; hairy cell; handicapped; head circumference; head compression; health care; healthy contr... |
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| HEC | hamster embryo cell; Health Education Council; human endothelial cell; hydroxyergocalciferol; hydrox... |
| HTC | hepatoma cell; hepatoma tissue culture; homozygous typing cell |
| HTLV-MA | cell membrane antigen associated with the human T-cell leukemia virus |
| ISC | immunoglobulin-secreting cells; insoluble collagen; International Society of Cardiology; Internation... |
| cell body | Used in reference to neurons, the main part of the cell around the nucleus excluding long processes such as axons and dendrites. (18 Nov 1997) |
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| cell-bound antibody | A term used for antibody on the surface of cells that may be bound either through antigen combining sites or other sites such as the Fc region. (05 Mar 2000) |
| renal cell cancer | Cancer that develops in the lining of the renal tubules, which filter the blood and produce urine. Also called renal cell carcinoma. (12 Dec 1998) |
| renal cell carcinoma | <oncology, tumour> The most common form of kidney cancer which occurs when the cells lining the renal tubule undergo cancerous changes. There are approximately 18,000 new cases of renal cell carcinoma (hypernephroma) per year in the U.S. With about 8,000 deaths annually. Smoking is considered a major risk factor. Kidney dialysis patients are at increased risk for the development of hypernephroma. Family history for renal cell carcinoma is also considered a risk factor. Symptoms include haematuria, flank pain, abdominal pain, back pain, weight loss and abdominal swelling. (27 Sep 1997) |
| cell bridges | Slender cytoplasmic strands connecting adjacent cells; in histological sections of the epidermis and other stratified squamous epithelia, the bridge's are processes attached by a desmosome and are shrinkage artifacts of fixation; true bridge's with cytoplasmic confluence exist between incompletely divided germ cells. Synonym: cell bridges, cytoplasmic bridges. (05 Mar 2000) |
| cell centre | Microtubule organising centre of the cell, the pericentriolar region. (18 Nov 1997) |
| cell cloning | The process of producing a group of cells (clones), all genetically identical, from a single ancestral cell. (12 Dec 1998) |
| cell communication | Any of several ways in which living cells of an organism communicate with one another, whether by direct contact between cells or by means of chemical signals carried by neurotransmitter substances, hormones, and cyclic AMP. (12 Dec 1998) |
| cell compartmentation | A partitioning within cells due to the selectively permeable membranes which enclose each of the separate parts, e.g., mitochondria, lysosomes, etc. (12 Dec 1998) |
| cell count | A count of the number of cells of a specific kind, usually measured per unit volume of sample. (12 Dec 1998) |
| cell culture | General term referring to the maintenance of cell strains or lines in the laboratory. (18 Nov 1997) |
| cell cycle | <cell biology, molecular biology> The sequence of events between mitotic divisions. The cycle is conventionally divided into G0, G1, (G standing for gap), S (synthesis phase during which the DNA is replicated), G2 and M (mitosis). Cells that will not divide again are considered to be in G0 and the transition from G0 to G1 is thought to commit the cell to completing the cycle and dividing. (26 Mar 1998) |
| cell cycle proteins | Proteins that control the cell division cycle. This family of proteins includes a wide variety of classes, including cyclin-dependent kinases, mitogen-activated kinases, cyclins, and phosphoprotein phosphatases (phosphoprotein phosphatase) as well as their putative substrates such as chromatin-associated proteins, cytoskeletal proteins, and transcription factors. (12 Dec 1998) |
| cell cycle restriction point | <cell biology, molecular biology> A point, late in G1, after which the cell must, normally, proceed through to division at its standard rate. (26 Mar 1998) |
| cell death | <cell biology> Cells die (nonaccidentally) either when they have completed a fixed number of division cycles (around 60, the Hayflick limit) or at some earlier stage when programmed to do so, as in digit separation in vertebrate limb morphogenesis. Whether this is due to an accumulation of errors or a programmed limit is unclear, some transformed cells have undoubtedly escaped the limit. See: apoptosis. (26 Mar 1998) |