C. Are vascular is the answer
The question is incomplete as it misses the options which are:
Cancer cells do not exhibit density dependent inhibition
Cancer cells do not require growth factors
Cancer cells do not exhibit anchorage dependence
Cancer cells ignore typical cell cycle checkpoints
Answer:
The correct answer will be option- Cancer cells do not exhibit anchorage dependence
Explanation:
A cell becomes tumour forming cell or cancerous cell when the cell undergoes some mutation in the DNA which causes uncontrolled cell division without differentiation.
As a result of the mutation, these cancerous cells show various properties which are present in the normal cells nut absent in cancerous cells like the cancerous cells lack the anchorage dependence.
Anchorage dependence is the property of the cells or the group of cells in which the cells maintain their adherence to the other layer of cells to communicate with each other.
Thus, the cancerous cells lack the anchorage dependence
Answer: DF508 mutation. A Genetic, Hereditary, Autosomal and Recessive Mutation.
Explanation:
Cystic fibrosis (CF) is a recessive autosomal lethal disease, it is most common on Caucasoid populations. Its diagnosis is suggested by the clinical features of chronic obstructive pulmonary disease, persistent pulmonary colonization (particularly with mucoid Pseudomonas strains), meconium ileus, pancreatic insufficiency with or familiarity history of the disease. The FC gene is large, with about 250 Kb of genomic DNA, 27 exons representing about 5% of genomic DNA; encodes a 6.5 kb transcribed mRNA. This mRNA is transcribed into a protein of 1480 amino acid called CFTR (Regulator Transmembrane Conductance Cystic Fibrosis). When a three-base pair deletion, adenosine-thymine-thymine (ATT) identified in the CFTR gene, exon 10, it results in the loss of a single amino acid phenylalanine at position 508 of the protein. This mutation is called DF508; “D” stands for deletion and “F” for phenylalanine amino acid.
If I’m not incorrect, DNA is made from amino acids
Answer:
C. More than 5 fingers/toes on each hand/foot
Explanation:
According to the given information, polydactyly is an autosomal dominant trait which means that the phenotype would be expressed in both homozygous dominant and heterozygous dominant genotype.
The given genotype is heterozygous dominant. The individuals with heterozygous dominant genotype would exhibit the polydactyly and would have more than 5 fingers and toes on each hand and foot.
