Pregnancy and Inheritance Flashcards

(47 cards)

1
Q

a fluid-filled sphere of cells that enters the uterine cavity

A

blastocyst

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2
Q

cells produced by cleavage

A

blastomeres

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3
Q

the developing individual from week nine of pregnancy until birth

A

fetus

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4
Q

the outer covering of cells of the blastocyst

A

trophoblast

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5
Q

membrane derived from trophoblast

A

chorion

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6
Q

early divisions of the zygote

A

cleavage

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7
Q

a solid sphere of cells still surrounded by the zona pellicuda

A

morula

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8
Q

event in which differentiation into the three primary germ layers occurs

A

gastrulation

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9
Q

embryonic development of structures that will become the nervous system

A

neurulation

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10
Q

the formation of blood vessels to support the developing embryo

A

angiogenesis

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11
Q

result of the fusion of female and male pronuclei

A

zygote

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12
Q

stimulates the corpus luteum to continue production of progesterone and estrogens

A

human chorionic gonadotropin

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13
Q

increases the flexibility of the pubic symphysis and helps dilate the uterine cervix during labor

A

relaxin

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14
Q

secreted by the placenta; helps establish the timing of birth and increases the secretion of cortisol for fetal lung maturation

A

corticotropin-releasing hormone

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15
Q

helps prepare mammary glands for lactation; regulates certain aspects of maternal and fetal metabolism

A

human chorionic somatomammotropin

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16
Q

stimulates uterine contractions; responsible for the milk ejection reflex

A

oxytocin

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17
Q

promotes milk synthesis and secretion; inhibited by progesterone during pregnancy

A

prolactin

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18
Q

the penetration of a secondary oocyte by a single sperm cell

A

syngamy

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19
Q

fertilization of a secondary oocyte by more than one sperm

20
Q

the attachment of a blastocyst to the endometrium

21
Q

the fusion of the genetic material from a haploid sperm and a haploid secondary oocyte into a single diploid nucleus

A

fertilization

22
Q

the induction by the female reproductive tract of functional changes in sperm that allow them to fertilize a secondary oocyte

23
Q

the examination of embryonic or fetal cells sloughed off into the amniotic fluid

A

amniocentesis

24
Q

an abnormal condition of pregnancy characterized by sudden hypertension, large amounts of protein in urine, and generalized edema

25
noninvasive test that can detect fetal neural tube defects
maternal AFP test
26
the process of giving birth
parturition
27
the period of time (about 6 weeks) during which the maternal reproductive organs and physiology return to the prepregnancystate
puerperium
28
plays an important role in induction whereby an inducing tissue stimulates the development of an unspecialized responding tissue into a specialized tissue
notochord
29
finger-like projections of the chorion that bring maternal and fetal blood vessels into close proximity
chorionic villi
30
serves as an early site of blood vessel formation
allantois
31
the fetal portion is formed by the chorionic villi and the maternal portion is formed by the decidua basalis of the endometrium; allows oxygen and nutrients to diffuse from maternal blood into fetal blood
placenta
32
contains the vascular connections between mother and fetus
umbilical cord
33
interchange of portions of nonhomologous chromosomes
translocation
34
heterozygous individuals who possess a recessive gene (but do not express it) and can pass the gene on to their offspring
carriers
35
inactivated X chromosome in females
Barr body
36
refers to a person with the same alleles on homologous chromosomes
homozygous
37
a homozygous dominant, homozygous recessive, or heterozygous genetic makeup; the actual gene arrangement
genotype
38
refers to how the genetic makeup is expressed in the body; the physical or outward expression of a gene
phenotype
39
neither member of the allelic pair is dominant over the other, and the heterozygote has a phenotype intermediate between the homozygous dominant and the homozygous recessive
incomplete dominance
40
permanent inheritable change in an allele that produces a different variant of the same trait
mutation
41
traits linked to the X chromosome
sex-linked inheritance
42
refers to an individual with different alleles on homologous chromosomes
heterozygous
43
a cell in which one or more chromosomes of a set is added or deleted
aneuploid
44
inheritance based on genes that have more than two alternative forms; an example is the inheritance of blood type
multiple-allele inheritance
45
abnormal number of chromosomes due to failure of homologous chromosomes or chromatids to separate
nondisjunction
46
the two alternative forms of a gene that code for the same trait and are at the same location on homologous chromosomes
alleles
47
the control of inherited traits by the combined effects of many genes
polygenic inheritance