Examples of 'mutations in the gene' in a sentence
Meaning of "mutations in the gene"
Mutations in the gene denote changes or alterations that occur in the genetic material of an organism. It refers to variations or modifications in the DNA sequence, which can result in different traits or characteristics. Mutations in the gene can have various effects, including genetic disorders, diseases, or evolutionary changes
How to use "mutations in the gene" in a sentence
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mutations in the gene
Different mutations in the gene require different oligonucleotide drugs.
Do not they realise societies can only evolve through mutations in the gene pool.
How mutations in the gene cause disease is not yet clear.
Strains with protease impairment include derivatives with mutations in the gene lon and htpR.
Some mutations in the gene cause people to feel more pain.
The disease is associated with mutations in the gene MeCP2.
Mutations in the gene cause a group of syndromes known as ectodermal dysplasias.
Sclerosteosis is caused by mutations in the gene that encode for the sclerostin protein.
Mutations in the gene may bring on weakened connective tissue throughout the body.
We show here that heterozygous mutations in the gene MYCN are present in Feingold syndrome.
Mutations in the gene encoding the LDL receptor are known to cause familial hypercholesterolaemia.
Some people naturally have mutations in the gene that help protect them from HIV infection.
Mutations in the gene CRTAP causes this type.
People with AID have mutations in the gene that makes ALDP.
Such mutations in the gene coding sequence are typically sufficient to inactivate the gene.
See also
It can be caused by mutations in the gene PLOD1.
Some mutations in the gene for adenosine deaminase cause it not to be expressed.
It is caused by is caused by mutations in the gene MECP2.
Compensating mutations in the gene encoding the second species in the complex can be selected.
Alström syndrome is a rare genetic disorder caused by mutations in the gene ALMS1.
Rare mutations in the gene are associated with Brunner syndrome.
You should know . Evolution is all about mutations in the gene pool.
It is caused by mutations in the gene that codes for fibroblast growth factor receptor 2.
Many cases of Wilson 's Disease occur due to spontaneous mutations in the gene.
Maternal lethal mutations in the gene encoding C.
Mutations in the gene BRG1 give resistance to hormones in lung cancer.
Previous studies have identified mutations in the gene mylk4 to be important in breast cancer.
Mutations in the gene are responsible for a common form of syndromic deafness, Pendred syndrome.
They can also be made by introducing mutations in the gene encoding the B-toxin.
Mutations in the gene for PINK1 are known to cause inherited Parkinson disease.
Abstract, Cystic fibrosis is an autosomic recessive disease due to mutations in the gene CFTR.
NF1 is caused by mutations in the gene that makes a protein called neurofibromin.
One of them may be Huntington \ 's disease caused by mutations in the gene IT15.
AOA2 is associated with mutations in the gene SETX, which encodes the protein senataxin.
A related neurocutaneous syndrome may be caused by mutations in the gene ALDH18A1 P5CS.
More than 20 mutations in the gene are known to date.
Mutations in the gene causing ichthyosis vulgaris [ 12 ] are extremely common in some populations.
It has been associated with mutations in the gene that codes for KERATIN-9.
Mutations in the gene responsible for MTHFR creation lead to decreased L-methylfolate production [ R ].
Both diseases are caused by mutations in the gene CLCN1 encoding the ClC-1 ion channel.
Mutations in the gene ITGA6 accounts for about 5 % of all cases of EB-PA.
CAPS are caused by a range of mutations in the gene CIAS1 ( also known as NALP3 ).
Al . Mutations in the gene for.
The disease is caused by mutations in the gene coding for pantothenate kinase 2 ( PANK2 ).
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The baldness gene was cause for dread
Gene mckinney pleaded the fifth amendment
Examples of using Mutations
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Ecstasy causes serious mutations in animal brains
These mutations most likely are compensatory mutations
Most loss of function mutations are selected against
