In the Endoplasmic Reticulum (ER). It must leave the nucleus first after transcription.
in the nucleus
Gene rearrangement actually means the rearrangement of gene in chromosomes. This can occur through 3 different ways which are inversion, translocation and transposition. These can definitely alter the chromosome and cause mutations to occur.
It can be. Basically most mutations (regardless of type; translocation, reversal, transcription, etc...) can cause hemophilia if they occur within a specific part of the genetic sequencing that codes for the production of the clotting factor proteins. This genetic sequence if found in a segment of the X chromosome.
Transcription is the process of formation of RNA. It takes place in nucleus in eukaryotes and in nucleoid in bacteria or prokaryotes .
In group translocation, chemical modification of molecule to be transport is done into the cell. Group translocation is type of active transport because metabolic energy is used during uptake of the molecule,. In bacteria the best known group translocation system is phosoenolpyruate: sugar phosphotransferase system (PTS) PEP + SUGAR --------- PYRUATE + sugar-phosphate In E.coli the PTS consists of two enzyme and a low molecular weight heat-stable protein(HPr)
in the nucleus
All Eukaryotes, that is plants and animals.
Inner mitochondrial membrane
nucleus for eukaryotes, cytoplasm for prokaryotes.
No, it takes place in both prokaryotes and eukaryotes
Leaching is another word for translocation.
translocation!
translocation
This condition is referred to as chromosomal translocation.
Gene rearrangement actually means the rearrangement of gene in chromosomes. This can occur through 3 different ways which are inversion, translocation and transposition. These can definitely alter the chromosome and cause mutations to occur.
Gene rearrangement actually means the rearrangement of gene in chromosomes. This can occur through 3 different ways which are inversion, translocation and transposition. These can definitely alter the chromosome and cause mutations to occur.
It can be. Basically most mutations (regardless of type; translocation, reversal, transcription, etc...) can cause hemophilia if they occur within a specific part of the genetic sequencing that codes for the production of the clotting factor proteins. This genetic sequence if found in a segment of the X chromosome.