Examples of 'mutations cause' in a sentence

Meaning of "mutations cause"

mutations cause: This phrase indicates that changes in genetic material lead to certain outcomes or effects, often in the context of biological or evolutionary discussions

How to use "mutations cause" in a sentence

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mutations cause
These mutations cause the cells to grow uncontrollably.
Biologists long thought they understood how genetic mutations cause disease.
Mutations cause high levels of mortality.
Only some mutations cause disease.
Mutations cause increase in information.
Nonsense and missense mutations cause the most severe phenotypes.
Mutations cause many different variances in genes, and the majority are harmless.
Three of the four missense mutations cause nonconservative changes in amino acids.
For some time now, the science community has known that genetic mutations cause disease.
These mutations cause different degrees of androgen insensitivity.
Researchers stil do not know what gene mutations cause most types of leukaemia.
Some mutations cause the production of an abnormally short protein.
The molecular mechanisms by which these two mutations cause muscular dystrophy remain unknown.
The mutations cause a decrease in secretion of trimeric procollagen molecules.
There are several mechanisms by which these mutations cause problems with the CFTR protein.

See also

Tau mutations cause autosomal dominant frontal temporal dementia.
Inhibition of FCA activity to cause late flowering fca mutations cause late flowering of Arabidopsis.
Not all mutations cause problems.
In summary, impaired CFTR function by several mutations cause cystic fibrosis.
Other mutations cause the protein to be longer than normal.
Lab method sheds light on how genetic mutations cause inherited Parkinson 's disease.
Gene mutations cause this protein to accumulate in the vessel wall.
Like the inherited changes, all somatic TIE2 mutations cause hyperphosphorylation in vitro.
Missense mutations cause a single amino acid change within the protein.
The exact molecular mechanism ( or mechanisms ) by which SOD1 mutations cause disease are unknown.
These mutations cause normal cells in your prostate to start growing abnormally.
In addition, it has been shown that DNM2 mutations cause autosomal dominant centronuclear myopathy ( CNM ).
These mutations cause the cell to make prion proteins with an abnormal structure.
They are now investigating how PINK1 mutations cause Parkinson 's disease.
Most of the mutations cause amino acid changes in the extracellular domain.
In recent years, 23 gene loci have been found, in which mutations cause hereditary Parkinson's disease.
Most mutations cause microcephaly while some specific changes appear to result in macrocephaly.
POLR1C and POLR1D gene mutations cause an additional 2 % of cases.
These mutations cause increased channel activity and associated increased neuronal excitability.
In human, HNF1B heterozygous mutations cause the MODY5 pathology.
The mutations cause cells to divide relentlessly or lose their normal ability to die.
On the contrary, two RTK mutations cause drastic inhibition of the corresponding kinase activity.
The mutations cause the cells to grow out of control and become cancerous cells.
The majority of these mutations cause dramatic defects in p53 function.
Those mutations cause retinoblasts to grow out of control and form a tumour called retinoblastoma.
Some inherited DNA mutations cause syndromes that are linked with an increased risk of osteosarcoma.
These mutations cause myofibril and myocyte structural abnormalities and possible deficiencies in force generation.
First, the reported mutations cause severe alterations of the predicted protein structure.
Both mutations cause decreased enzyme activity of ADPG PPase in the endosperm.
Why do BRCA1 mutations cause predominantly breast and ovarian cancer?
SPOP mutations cause elevation of BET proteins in prostate cancer patient specimens.
Furthermore, duplication mutations cause a familial PD phenotype that more closely resembles late-onset, idiopathic PD.
Why mutations cause disease in some people but not in others?
For example, NEFL mutations cause type 2E Charcot-Marie-Tooth motor neuropathy.
NPHP gene mutations cause defects in signaling resulting in flaws of planar cell polarity.

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Examples of using Mutations
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