Answer:
tRNA
Transfer ribonucleic acid (tRNA) is a type of RNA molecule that helps decode a messenger RNA (mRNA) sequence into a protein. tRNAs function at specific sites in the ribosome during translation, which is a process that synthesizes a protein from an mRNA molecule.
Answer:
A. Will only phosphorylate glycogen synthase (GS) after GS has been phosphorylated by casein kinase.
Explanation:
Glycogen synthase kinase (GSK) is a type of enzyme capable of phosphorylating serine and threonine residues on the glycogen synthase (GS). The insulin hormone activates the synthesis of glycogen by dephosphorylating GS, but it is a mechanism that depends on the previous phosphorylation of GS by Casein Kinase (CK). GSK is also known to phosphorylate the insulin receptor (IRS), and thus controlling glucose metabolism.
Answer:
Uhh-
Explanation:
Bruh there's no pic so ... I dunno lol. Just in case this helps you, hypothesis means an educated guess. There's different meanings, for science it's an idea. But mostly it means guessing.
I didn't help Ik XD
And
Sorry
I
Couldn't
Helppp
.............
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Answer:
The option 'All cells contain a nucleus' is not a part of the cell theory.
Explanation:
The cell theory proposed by scientists illustrates that every organism whether prokaryotic or eukaryotic is made up of a cell or different kinds of cells. It also that explains that cells are made from living things. According to the cell theory, cells are termed as the basic unit of life, without which life is not possible.
The cell theory does not claim that every cell must have a nucleus because many cells like cells of prokaryotes lack nucleus. Their genetic material is dispersed in the cytoplasm.
Answer:
Gene therapy
Explanation:
Gene therapy can be defined as the methodologies used to modify/restore the expression of target genes and thus cure and treat genetic disorders. Gene therapy approaches consist of delivering specific nucleic acids (either RNA or DNA) in the cells of the individual to be treated. Some of the most important gene therapy approaches include the use of small interfering RNAs (siRNAs) in order to block target gene expression, adenovirus vectors to insert genes into host cells, the use of the CRISPR-Cas9 genome editing system to insert specific sequences by the mechanism of homologous recombination, etc.
