Forensics Quiz 4 Flashcards

1
Q

Drug Interaction: Synergism

A

increases effects of drugs through combination of drugsT

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2
Q

Drug Interaction:Tolerance

A

Effect of drug decreases due t prior exposure

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3
Q

Elimination from Body

A

1.Excrete in urine-majority of time
2.Sweat it out
3.Vomit
4.Exhaling

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4
Q

Alcohol

A

ethanol creates to a CNS depressant

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5
Q

BAC

A

blood alcohol concentration

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6
Q

g/dL

A

numbers of grams present in liters of blood

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7
Q

Factors that determine BAC

A

1.Bodyweight/height
2.presence/absence of food in stomach
3.Gender
4.Metabolism
5.Tolerance(experienced new drinker)
6.Genetics
7.Type of drink
8.size of drink
9.Rate of consumption
10.medication

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8
Q

Alcohol level indicator:.02 g/dl

A

most people begin feel some effect from alcohol

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9
Q

Alcohol level indicator:.04 g/dl

A

definite feeling of relaation

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10
Q

Alcohol level indicator:.06 g/dl

A

most people less able to make rational descisions

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11
Q

Alcohol level indicator:.08 g/dl

A

definite impairment in motor coordination skills, ability to drive is compromised

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12
Q

Alcohol level indicator:12 g/dl

A

vomiting may occur inexperienced drinkers

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13
Q

Alcohol level indicator:.15g/dl

A

balance is seriously compromised

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14
Q

Alcohol level indicator:.4g/dl

A

most people lose consciousness may die

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15
Q

Field Sobriety Test

A

1.Waling and turning
2.Stand on one foot
3.horizontal gaze nystagmus(must use formal names on test)
Follow the moving object(pen) with your eyes when your uni you have a hard time steadily following(jerking manner)
4.breathalyzer(all is a a volatile vapor

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16
Q

DNA

A

deoxyribonucleic acid
-information that serves as a blueprint for our existence
-2 types-mitochondrial and nuclear)
-shaped like a ladder
-rungs are nucleotides(base),H has the DNA

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17
Q

Dna has

A

4bases,adenine,thymine,guanine,cystocine

18
Q

Nuclear Dna

A

-Adenline always pairs w/ Tymine A-T
-Guanine always pairs w/Cytostine G-C
-they also never pair w/themselves

19
Q

Central Dogma

A

genetic information flows:in one direction from DNA to RNA(transcription)
-RNA turns to protein(translation)

20
Q

RNA-ribonucleic acid

A

uses adenine, Uracil, Guanine, Cytosine
-A-U and G-C connect

21
Q

Replication

A

created identical DNA strands

22
Q

Transcription

A

conversion of DNA to RNA
-there are 20 types of amino acids
for every 3 bases it is called a codon(triplet of nucleotides)

23
Q

Mutations Types(from OG DNA strand) step 1

A
  1. alter base
    GAUCC AGAG(DNA)
    CUGG UCU(RNA)
    leu. val (amino)
24
Q

Mutations Types(from OG DNA strand) step 2

A

2.skip base
-dfferent codon than the original strand both are different methods

25
Q

DNA to RNA

A

DNA(ATCG) to RNA (AUCG)
-20 amino acids

26
Q

Nuclear DNA

A

arranged in structures called chromosomes

27
Q

humans have how many chromosomes and how much from each parent

A

-humans have 46 chromosomes
-23 from dad
-23 from mom
-23 pairs

28
Q

chromosomes

A

-through chromosomes that each person in hearts the physical emotion characteristics from both parents

29
Q

gene

A

genetic code contained in portions of the chromosome

30
Q

alleles

A

different forms of a gene

31
Q

dominant

A

expressed allele
-a allele and B allele

32
Q

recessive

A

silent allele
-O allele

33
Q

Blood Type Groups and their Genotypes

A

Blood Type A- AA,AO
Blood Type B-BB,BO
Blood Type AB-AB
Blood Type O-OO

34
Q

genotypes

A

genetic makeup

35
Q

phenotypes

A

characteristics that are visible

36
Q

Polymerse Chain Reaction(PCR)

A

developed by Dr. Kery Mullins in 1983

37
Q

Gregor Mendel

A

-1860s
-mendelinan heriditary.genetics

38
Q

Punnet Square

A

indicated all potential progeny genotypes

39
Q
A

Ross Syndrome
Retinitis Pigmentosa
Sex linked means x linked
-affected males can not pass the trait to their off spring
-pass the gene to all their daughters
-unless the daughter also receivesth genes from her mother, she is a phenotypically normal carrier of the trait

40
Q

Sex linked(x linked)

A

Sex-linked (X-linked) Inheritance: When a condition is X-linked, it means the gene causing the condition is located on the X chromosome