Divergent boundaries are typified in the oceanic lithosphere by the rifts of the oceanic ridge system, including the Mid-Atlantic Ridge and the East Pacific Rise, and in the continental lithosphere by rift valleys such as the famous East African Great Rift Valley. I don't know your answer choices but I hope this helps!!!!!!
Answer:
Color Blindness Fragile X Syndrome: Disorder that is the most common cause of inherited mental impairment....
Duchenne Muscular Dystrophy: Disorder caused by the lack of dystrophin...
Hemophilia Disorder: caused by the absence or minimal presence of factor Vill or factor IX...
Colour blindness (Daltonism): Disorder that affects the ability to, in most cases distinguish reds from greens
Explanation:
Fragile X syndrome is an inherited disease associated with different health problems during development including cognitive disabilities.
Duchenne is an inherited disorder caused by a mutation in the dystrophin gene that encodes a protein required for normal muscle functioning.
Hemophilia is an inherited disorder caused by mutations in the genes that encode for coagulation factors, which are required for normal blood coagulation.
Colour blindness is an inherited condition associated with the ability to distinguish red color from green color. This condition is caused by mutations in the genes that encode for red and green light-sensitive proteins.
Answer:
:ADFKL
Explanation:;kaDFS": just doing it for the points
Answer:
List three ways of reducing friction. 1.Polishing the rough surface. 2.Providing all bearings or wheels between the moving parts of a machine or vehicles reduce friction and 3.allow smooth movement as rolling friction is less than sliding friction.
Answer:
Thymidine dimers is likely to be repair as soon as it is originated but if left unrepaired then it causes frame shift mutations.
Explanation:
In case of Bacterium if UV irradiation induces covalent linkage of two thymidine present adjacently to each other or on a single strand to make thymidine dimers.
These either excised via DNA repair enzyme like Endonuclease V and the proof reading activity of DNA polymerase I enzyme help in incorporation of nucleotide by taking the unmutated original strand as a template.
These dimers if not excised before second round of replication than the sequence of newly synthesized strand will be altered. As DNA polymerase III enzyme read thymidine dimers as single thymidine nucleotide and incorporate only 1 adenine in the newly synthesizing complementary strand which results in frame shift mutations
It is the mutation in which reading frame of codons is shifted or altered due to deletion or addition of a single nucleotide.