how do the basic principles of inheritance, identified by mendel in plants, differ from those in humans?
a. they are simpler.
b. there are no mendelian traits in humans.
c. plants don’t have alleles.
d. the number of chromosomes is different; therefore, genetic principles vary.
e. there are no differences since the basic principles are the same.

e. There are no differences since the basic principles are the same.

Explanation:

The basic principles of inheritance as proposed by Mendel while working on garden pea are applied to all living beings including humans. The human also has discrete units that regulate genetic traits. These units are called genes.

Genes are present on chromosomes which in turn carry them from parent to progeny. Gametes formed in humans also follow the law of segregation and bear only one allele of each gene.

Two pairs of genes are independently segregated from each other which in turn leads to the production of parental as well as recombination gametes. Therefore, the concepts of genes, purity of gametes, the independent assortment of two pairs of genes, dominance are applicable to humans also.

sadness is not good

explanation:

transcription is a process in which information is rewritten. it is something our cells must do, in a more specialized and narrowly defined way. in biology, transcription is the process of copying out the dna sequence of a gene in the similar alphabet of rna. it needs to happen in the nucleus because that's where the dna is. dna is always inside the nucleus unless the cell is dividing.

transcription is the first step in gene expression, which involves copying a gene's dna sequence to make an rna molecule. transcription is performed by rna polymerases. it has three stages: initiation, elongation, and termination. rna molecules must be processed after transcription in eukaryotes.

explanation:

long version:

the protein synthesis consists two processes which are, transcription and translation. transcription takes place in the nucleus. it uses dna as a template to make an rna molecule. rna then leaves the nucleus and goes to a ribosome in the cytoplasm, where translation occurs. transcription is the first part of the central dogma of molecular biology: dna → rna. it is the transfer of genetic instructions in dna to messenger rna (mrna). during transcription, a strand of mrna is made that is complementary to a strand of dna.  

these three stages are:

  initiation: in which   is the beginning of transcription.occuring when the enzyme rna polymerase binds to a region of a gene called the promoter. this signals the dna to unwind so the enzyme can ‘‘read’’ the bases in one of the dna strands. the enzyme is now ready to make a strand of mrna with a complementary sequence of bases.

    elongation: in which is the addition of nucleotides to the mrna strand. rna polymerase reads the unwound dna strand and builds the mrna molecule, using complementary base pairs. there is a brief time during this process when the newly formed rna is bound to the unwound dna. during this process, an adenine (a) in the dna binds to an uracil (u) in the rna.

    termination: in which is the ending of transcription, and occurs when rna polymerase crosses a stop (termination) sequence in the gene. the mrna strand is complete, and it detaches from dna.