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32 Cards in this Set

  • Front
  • Back

carrier

an individual who is heterozygous for a recessive disorder

pedigree

a diagram that traces the inhiertance of a popular trait through several generations

incomplete dominanace

the heterozygous phenotype is an intermediate phenotype between the two homozygous phenotypes

codominance

both alleles are expressed in the heterozygous condition

multiple alleles

forms of inheritance are determined by more than two alleles

epistasis

the interaction of one allele hiding the effects of another allele

sex chromosome

determine an individual's gender

autosome

the 22 pairs of chromosomes, excluding the sex chromosomes

sex-linked trait

traits controlled by genes located on the x-chromosome

polygenic trait

traits such as skin color, height, eye color, and fingerprint pattern

karyotype

the pairs of homologous chromosomes arranged in decreasing size to produce a micrograph

telomere

a protective cap the chromosome ends in

nondisjunction

cell division where sister chromatids fail to seperate

double helix

twisted ladder shape, formed by two strands of DNA

nucleosome

a phosphate group in DNA that creates a negative charge, which attracts the DNA to the positivley charged histone protiens

semiconservative replication

parental strands of DNA seperate, serve as templates, and produce DNA molecules that have one strand of parental DNA and one strand of new DNA

DNA polymerase

catalyzes the addition of appropriate nucleotides to the new DNA strand

okazaki fragment

synthesized discontinuosly small segmets

RNA

a nucleic acid similar to DNA

messenger DNA

long strands of RNA nucleotides that are formed complentary to one strand of DNA

ribosomal RNA

type of RNA that associates with proteins to form ribosomes to direct the synthesis of a specific person

transfer RNA

smaller segments of RNA nucleotides that transport amino acids to the ribosome

transcription

the DNA code is transferred to mRNA in the nucleus

RNA polymerase

an enzyme that regulates RNA synthesis

intron

intervening segments

exon

the coding sequences that remain in the final mRNA

codon

the three-base code in the DNA or mRNA

translation

process in which mRNA attaches to the ribosome and a protein is assembled

gene regulation

the ability of an organism to control which genes are transcribed in response to the enviorment

operon

a section of DNA that contain the genes for the proteins needed for a specific metabolic pathway

mutation

a permanent change that occurs in a cell's DNA

mutagen

substances that cause mutations