Question

1) Describe Genetics of Triplet Repeat Disorders for Fragile X-syndrome disease in terms of phenotype and...

1) Describe Genetics of Triplet Repeat Disorders for Fragile X-syndrome disease in terms of phenotype and genotype

2) Describe Ames test and its use.

3) Describe the role of P53.

4) What is Trichthiodystrophy?

Homework Answers

Answer #1

1)it is caused by abnormality in X- linked gene on x chromosome. Both male and females are equally effected because in both x chromosome is present. in this syndrome the body can't make enough protein required for brain growth and development.

2) A test used to determine the mutagenic activity of chemicals.it is used to detect that any chemical is carcinogenic or not and where the chemical cause mutation in DNA of test organism.

3) It code for a protein which regulate cell cycle. it is important in multicellular organism to suppress cancer.

4) it is a hereditary disorder characterized by short ,brittle hair with low sulphur content (sulphur deficient hair).

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
Lesch-nyhan syndrome is an x-linked, rare, recessive disease caused by a mutation in the gene encoding...
Lesch-nyhan syndrome is an x-linked, rare, recessive disease caused by a mutation in the gene encoding for hypoxanthine-guanine phosphoribosyltransferase (HPRT1). A woman’s maternal grandfather suffered from lesch-nyhan syndrome. She is concerned her male child could have lesch-nyhan syndrome. Genetically, what is the chance that this child has lesch-nyhan syndrome? a.) 0 b.) 1/8 c.) 1/4 d.) 1/16 e.) 1/2
You are studying disease X, a genetic disorder that arises from a trinucleotide repeat expansion mutation...
You are studying disease X, a genetic disorder that arises from a trinucleotide repeat expansion mutation which is a mutation where entire codons are multiplied during the replication process. The mutation is found in the CaM gene, that is a 450-base pair (bp) sequence. The trinucleotide repeat expansion results in the addition of 10 codons (30 bp) at nucleotide 150 (ie in the centre of the gene, away from the 5’ and 3’ end). The sequence of the normal gene...
You are studying disease X, a genetic disorder that arises from a trinucleotide repeat expansion mutation...
You are studying disease X, a genetic disorder that arises from a trinucleotide repeat expansion mutation which is a mutation where entire codons are multiplied during the replication process. The mutation is found in the CaM gene, that is a 450-base pair (bp) sequence. The trinucleotide repeat expansion results in the addition of 10 codons (30 bp) at nucleotide 150 (ie in the centre of the gene, away from the 5’ and 3’ end). The sequence of the normal gene...
You will be assessing the appropriateness of a new screening test for Disease X. Assume a...
You will be assessing the appropriateness of a new screening test for Disease X. Assume a population of 1000 people of whom 100 have Disease X and 900 do not have Disease X to answer questions a through i using the following 2x2 table: Disease No Disease Positive screen 80 100 Negative screen 20 800 1.      Calculate the sensitivity. 2.      Interpret your sensitivity calculation and the implications for potential use of this screening test. 3.       Calculate the specificity. 4.      Interpret your specificity calculation and...
(1) Describe how heredity and genetics influence pathophysiological alterations in the cardiovascular system. (2) What is...
(1) Describe how heredity and genetics influence pathophysiological alterations in the cardiovascular system. (2) What is the difference between pernicious anemia and iron deficiency anemia? (3) How is pulmonary edema related to congestive heart failure? Please try use reference for direct quote citation
Match the term to the description. Ex 1 = E Terms 1. Alagille                                &n
Match the term to the description. Ex 1 = E Terms 1. Alagille                                                                             Cystic Fibrosis Cri du chat Sickle Cell disease klinefelter syndrome WilliamSyndrome Jacob’s Syndrome X-linked Poly-X female Trisomy 21 Gene Linkage Down Syndrome Turner’s Syndrome Deletion Inversion Duplication 17.Fragile x syndrome 18.Hemophilia   Muscular Dystrophy Color blindness   Achondroplasia independent assortment Huntington Neurofibromatosis 25.Phenylketonuria Tay-Sachs Burkett lymphoma Mendel’s Law of Segregation Mendel’s Law of Independent Assortment Incomplete Dominance Multiple Allelic Traits 32.Polygenic Inheritance 33.Polyploidy 34.Aneuploidy Amniocentesis Chorionic Villi Sampling...
QUESTION 1 Fill in the following table Terms Similarity difference a. Enzyme and Protein b. Saturated...
QUESTION 1 Fill in the following table Terms Similarity difference a. Enzyme and Protein b. Saturated and unsaturated fat c. Phospholipid and TAG d. Molecule and atom e. Covalent and ionic bond QUESTION 4 Provide explanations for the following a.a mother and father produce a son with hemophilia even though neither have the disease themselves. If this son has children with a woman who is carrier of the disease, what is the chance of having a son who has the...
Genetics: will give a thumbs up if correct. Please show work. Thank you. 1. Red/green color...
Genetics: will give a thumbs up if correct. Please show work. Thank you. 1. Red/green color blindness is controlled by an X linked gene. A normal man and women marry. The fathers of both of these individuals are color blind but the mothers of both are homozygous normal. The probability that their first child will be color blind is: a. 1/2 b. 1/3 c. 1/4 d. 1/8 e. 0 2. If you cross a Gg (G= yellow, g=green) Ww (W=round,...
Use directional terms to describe the following: 1. The sternum is ___________ to the acromion. 2....
Use directional terms to describe the following: 1. The sternum is ___________ to the acromion. 2. The occipital bone is __________ to the nasal bone. 3. The frontal bone is ___________ to the maxilla. 4. The phalanges are __________ to the head of the humerus.
Please show WORK! In some horses, coat color is autosomal and exhibits incomplete dominance, with palamino...
Please show WORK! In some horses, coat color is autosomal and exhibits incomplete dominance, with palamino coloration intermediate to both chestnut and cremello coloration. Horses can also exhibit an immunodeficiency syndrome inherited as an X-linked recessive allele. You are a horse breeder, and cross a palamino female carrier for immunodeficiency syndrome with a normal, cremello male. 1. Use appropriate genetic notation to describe genotypes of the cross. 2. If you conducted this cross many times, what would be the expected...