TLS Online TPP Program

#Question id: 31145


A set of small GTP-binding proteins, associate with transport vesicles and act as key regulators of vesicle trafficking to and fusion with the appropriate target membrane, known as: 

#Unit 2. Cellular Organization
  1. Sar1 proteins
  2. Rab proteins
  3. ARF proteins
  4. Dynamin proteins
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TLS Online TPP Program

#Question id: 15369

#Unit 4. Cell Communication and Cell Signaling

Changes in DNA methylation, as well as changes in the activity of histone-modifying enzymes or chromatin-remodeling complexes, are major drivers of tumorigenesis,
a. Hypermethylation of CpG dinucleotides of TSG gene causes cancer.
b. Hypomethylation of CpG dinucleotides of proto-oncogenes causes cancer.
c. SWI/SNF plays a role in repressing the expression of E2F genes.
d. Gain of SWI/SNF function, just like loss of Rb function.
Which of the statements are INCORRECT;

TLS Online TPP Program

#Question id: 15376

#Unit 13. Methods in Biology

If a protein made up of three subunit α2βγ (Mr. of α = 25000, β = 50000, γ = 75000) which of the following correctly representing SDS and Native (buffer) gel

TLS Online TPP Program

#Question id: 15378

#Unit 8. Inheritance Biology

You find a pink geranium in your flowerbed of red geraniums. Seeds from self fertilization of this plant produce ¼ red plants, ½ pink plants, and ¼ white plants. When considering the visible phenotype, which explanation is most likely?

TLS Online TPP Program

#Question id: 15379

#Unit 8. Inheritance Biology

What are the possible offspring from a type A mother and a type AB father?

TLS Online TPP Program

#Question id: 15380

#Unit 8. Inheritance Biology

In soybeans, resistance to sudden death syndrome (SDS) is inherited as a dominant condition. In some cases, individuals that are not resistant to SDS (but whose parents were) can pass the trait on to their progeny. This is an example of which of the following?

TLS Online TPP Program

#Question id: 15381

#Unit 8. Inheritance Biology

Neurofibromatosis is a condition in humans which is generally inherited in a dominant fashion. Assuming this disorder is 90% penetrant, what is the chance that a single child born to a father with neurofibromatosis and a mother known not to carry the mutation will have the disorder?