Answer:
By transfecting small activating RNAs
Explanation:
Small activating RNAs (saRNAs) are an emerging class of non-coding RNAs (ncRNAs) that are capable of activating gene expression at transcriptional level. The saRNAs are small double-stranded RNAs (dsRNAs) that bind to promoter sequences in order to activate the expression of target genes. These molecules are structurally similar to small interfering RNAs (siRNAs), i.e., they also have a size of 21 nucleotides and two overhang nucleotides at the 3' end of both strands.
Answer:
Smooth Muscle
Explanation:
In the digestive tract it's called the muscularis mucosa.
Answer:
Anton Von Leeuwenhoek is the name
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.
You need to know if the parents trait are dominant or recessive
