science Flashcards
(22 cards)
allele
any of several forms of a gene, usually arising through mutation, that are responsible for hereditary variation.
genotype
the sum total of genes transmitted from parent to offspring.
phenotype
the appearance of an organism resulting from the interaction of the genotype and the environment.
homozygous
having identical pairs of genes for any given pair of hereditary characteristics.
heterozygous
Immunology. pertaining to an antigen that elicits a reaction in a nonspecific antibody.
dominate trait
In genetics, a trait that will appear in the offspring if one of the parents contributes it. ( Compare recessive trait.)
reccessive trait
3.
the condition of being definite, distinct, or clearly o
mitosis
the usual method of cell division
meiosis
consisting of chromosome conjugation and two cell divisions
identical twins
one of a pair of twins who develop from a single fertilized ovum and therefore have the same genotype, are of the same sex, and usually resemble each other closely.
fraternal twins
one of a pair of twins, not necessarily resembling each other, or of the same sex, that develop from two separately fertilized ova.
sex-linked disorder
disorder from your gender
chromosomes
the human species has 23 pairs, designated 1 to 22 in order of decreasing size and X and Y for the female and male sex chromosomes respectively.
gene
a linear sequence of nucleotides along a segment of DNA that provides the coded instructions for synthesis of RNA
DNA
deoxyribonucleic acid: an extremely long macromolecule that is the main component of chromosomes and is the material that transfers genetic characteristics in all life forms
DNA replication
is the process of producing two identical replicas from one original DNA molecule. This biological process occurs in all living organisms
doble helix
the spiral arrangement of the two complementary strands of DNA.
chargaff’s rule
Structures cell membranes Preventive and therapeutic effects
mutation
a sudden departure from the parent type in one or more heritable characteristics, caused by a change in a gene or a chromosome.
deletion
type of chromosomal aberration in which a segment of the chromosome is removed or lost.
insertion
the manner or place of attachment, as of an organ.
attachment of a part or organ, with special reference to the site or manner of such attachment.
substitution
a person or thing acting or serving in place of another.