Medical Glossary

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19186
medical terms

Mitochondrial heteroplasmy




Mitochondrial heteroplasmy

An atypical condition characterized by the presence of more than one type of mitochondrial DNA in a single individual. Normally, each individual has only one type of mitochondrial DNA, inherited from his or her mother through the egg at fertilization. (Mitochondria from the sperm are systematically eliminated by the egg at fertilization.)Cloned organisms may exhibit mitochondrial heteroplasmy (having a mixture of mitochondria from both the donor cell and the recipient egg) because this elimination system may be bypassed during the cloning process.

RELATED TERMS
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Atypical
Not typical, not usual, not normal, abnormal. Atypical is often used to refer to the appearance of precancerous or cancerous cells.

Condition
The term "condition" has a number of biomedical meanings including the following: 1.An unhealthy state, such as in "this is a progressive condition." 2.A state of fitness, such as "getting into condition." 3.Something that is essential to the occurrence of something else; essentially a "precondition." 4.As a verb: to cause a change in something so that a response that was previously associated with a certain stimulus becomes associated with another stimulus; to condition a person, as in behavioral conditioning.

DNA
Deoxyribo-Nucleic acid. DNA molecules carry the genetic information necessary for the organization and functioning of most living cells and control the inheritance of characteristics.

Fertilization
The combining of the genetic material carried by sperm and egg to create an embryo. Normally occurs inside the fallopian tube (in vivo) but may also occur in a petri dish (in vitro).

Sperm
A sperm cell, or spermatozoon (pl. spermatozoa) (in Greek: sperm = semen and zoon = alive), is the haploid cell that is the male gamete. It is carried in fluid called semen, and is capable of fertilising an egg cell to form a zygote. A zygote can grow into a new organism, such as a human. Sperm cells contain half of the genetic information needed to create life. Generally, the sex of the offspring is determined by the sperm, through the chromosomal pair "XX" (for a female) or "XY" (for a male).

Heteroplasmy
An atypical condition characterized by the presence of more than one type of mitochondrial DNA in a single individual. Normally, each individual has only one type of mitochondrial DNA, inherited from his or her mother through the egg at fertilization. (Mitochondria from the sperm are systematically eliminated by the egg at fertilization.)

Mitochondria
Self-replicating membrane-bound cytoplasmic organelles in most eukaryotic cells that complete the breakdown of glucose. Singular: mitochondrium.

Donor
A person who gives an organ, tissue or blood to another person. A compatible donor is a person who has the same tissue and blood types as the person who receives the organ, tissue or blood.

Cell
Fundamental structural unit of all life. The cell consists primarily of an outer plasma membrane, which separates it from the environment; the genetic material (DNA), which encodes heritable information for the maintainance of life; and the cytoplasm, a heterogeneous assemblage of ions, molecules, and fluid.

Recipient
A patient who receives an organ, tissue or blood from another person.

Cloning
The production of a clone. (For the purpose of this report, generating an individual animal or person that derives its nuclear genes from a diploid cell taken from an embryo, fetus, or born individual of the same species.)



SIMILAR TERMS
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Mitochondria
Self-replicating membrane-bound cytoplasmic organelles in most eukaryotic cells that complete the breakdown of glucose. Singular: mitochondrium.

Mitochondrion
Plural: mitochondria. A cellular structure in the cytoplasm that provides energy to the cell. Each cell contains many mitochondria. In humans, a single mitochondrion contains 37 genes on a circular mitochondrial DNA, compared with about 35,000 genes contained in the nuclear DNA.

Mitochondrium
Self-replicating membrane-bound cytoplasmic organelles in most eukaryotic cells that complete the breakdown of glucose. Plural: mitochondria.

Mitogen
A substance that stimulates the proliferation of many different clones of lymphocytes.

Mitomycin
Mitomycin is a prescription or over-the-counter drug which is (or once was) approved in the United States and possibly in other countries. Active ingredient(s): mitomycin.

Mitosis
The division of the cell's nucleus and nuclear material of a cell; consists of four stages: prophase, metaphase, anaphase, and telophase. Mitosis occurs only in eukaryotes. The DNA of the cell is replicated during interphase of the cell cycle and then segregated during the four phases of mitosis.

Mitoxantrone
Mitoxantrone is a prescription or over-the-counter drug which is (or once was) approved in the United States and possibly in other countries. Active ingredient(s): mitoxantrone.



PREVIOUS AND NEXT TERMS
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Mycoplasma
Very common sexually transmitted disease or urinary tract infection caused by a bacteria-like organism in the urethra and reproductive system.

Myelogram
A specific X-ray study that uses an injection of a dye or contrast material into the spinal canal to allow careful evaluation of the spinal canal and nerve roots.

Male factor infertility
Condition in which a male patient is infertile for such reasons as very low sperm count, sperm that cannot swim properly, sperm that are unable to penetrate the egg, or blocked sperm ducts.

Methylation
A biochemical process involving the addition of chemical tags called methyl groups (-CH3) to DNA. Methylation can be a signal for a gene or a section of a chromosome to turn off gene expression and become inactive or "silent".

Minor H antigens
Or minor histocompatibility antigens. A group of proteins (in addition to those encoded by the major histocompatibility complex (MHC) that can cause transplant tissue rejection. Minor H antigens can cause tissue rejection even when donor and recipient are matched for MHC. Immune response to minor H antigens is far less potent than response to MHC-encoded proteins, so the rejection is a slower process.

Mitochondrial heteroplasmy

Mitochondrion
Plural: mitochondria. A cellular structure in the cytoplasm that provides energy to the cell. Each cell contains many mitochondria. In humans, a single mitochondrion contains 37 genes on a circular mitochondrial DNA, compared with about 35,000 genes contained in the nuclear DNA.

Monozygotic twins
Twins derived from one egg and one sperm (often called identical twins).

Morula
The preimplantation embryo 3-4 days after fertilization, when it is a solid mass composed of 12-32 cells (blastomeres). After the eight-cell stage, the cells of the preimplantation embryo begin to adhere to each other more tightly, becoming "compacted". The resulting embryo resembles a mulberry and is called a morula (Latin: morus = mulberry).

Multipotent stem cells
Stem cells from the embryo, fetus, or adult, whose progeny are of multiple differentiated cell types and usually, but not necessarily, all of a particular tissue, organ, or physiological system.

Mutation
A change in DNA that alters a gene and thus the gene's product, leading in some cases to deformity or disease. Mutations can occur spontaneously during cell division or can be triggered by environmental stresses, such as sunlight, radiation, and chemicals.

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This dictionary contains 19186 terms.







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