Examples of 'gene are associated' in a sentence
Meaning of "gene are associated"
This phrase indicates a relationship or connection between genes and some other factors, such as traits, diseases, or specific characteristics
How to use "gene are associated" in a sentence
Basic
Advanced
gene are associated
Polymorphisms in this gene are associated with diabetes.
Defects in this gene are associated with both central and peripheral retinal degenerations.
Mutations in the PLEKHM1 gene are associated with.
Mutations in this gene are associated with agenesis of the corpus callosum with peripheral neuropathy.
Alterations in the activity ( expression ) of the FGFR2 gene are associated with certain cancers.
Mutations in this gene are associated with paroxysmal kinesigenic dyskinesia.
In mice, mutations in this gene are associated with epilepsy.
Mutations in this gene are associated with triosephosphate isomerase deficiency.
Furthermore, certain mutations in the XRCC4 gene are associated with an increased risk of cancer.
Mutations in this gene are associated with SDH-defective infantile leukoencephalopathy and mitochondrial complex II deficiency.
Bacterial strains with the cagA gene are associated with an ability to cause ulcers.
Mutation in this gene are associated with immunodeficiency, centromere instability and facial anomalies syndrome.
Various mutations in the MET gene are associated with papillary renal carcinoma.
Mutations in this gene are associated with fibrodysplasia ossificans progressive.
Rare mutations in the gene are associated with Brunner syndrome.
See also
Some mutations in this gene are associated with methylenetetrahydrofolate reductase deficiency.
For example, the alleles of Apa-I gene are associated with varying risks of depigmentation.
Defects in the leptin gene are associated with severe obesity in animals and in humans.
Mutations in the XPNPEP3 gene are associated with ciliopathy.
Mutations in this gene are associated with Rett syndrome and intellectual disability.
Mutations in the delta-globin gene are associated with Delta-thalassemia.
Mutations in this gene are associated with type II Stickler syndrome and with Marshall syndrome.
Two genetic variants in the PON1 gene are associated with reduced enzyme activity.
Mutations in this gene are associated with parietal foramina 1 and craniosynostosis type 2.
Chromosomal translocations involving the RUNX1 gene are associated with several types of leukemia including M2 AML.
Mutations in this gene are associated with slow-channel congenital myasthenic syndrome.
Mutations in this gene are associated with Scott syndrome.
Defects in this gene are associated with the development of cancers, such as gliomas.
Polymorphisms of the CRP gene are associated with the increase in its serum level.
Mutations in this gene are associated with the occurrence of adult-onset polycystic kidney disease.
Alterations of the SEPT9 gene are associated with certain cancers.
Mutation in this gene are associated with oculocerebrorenal syndrome and also with Dent's disease.
Mutations in this gene are associated with Alzheimer disease risk.
Mutations in this gene are associated with hereditary pancreatitis.
Variations in this gene are associated with a high rate of red cells in the blood.
Mutations in this gene are associated with mitochondrial complex III deficiency.
Mutations in this gene are associated with nephronophthisis type 3.
Mutations in this gene are associated with progressive myoclonic epilepsy type 5.
Mutations in the CFL2 gene are associated with nemaline myopathy.
Mutations of the VHL gene are associated with von Hippel-Lindau disease.
Mutations in this gene are associated with limb-girdle muscular dystrophies type 2A.
Mutations in this gene are associated with Sedaghatian type of spondylometaphyseal dysplasia ( SMDS ).
Polymorphisms in the CD58 gene are associated with increased risk for multiple sclerosis.
Mutations in the NLRP3 gene are associated with a number of organ specific autoimmune diseases.
Mutations in this gene are associated with Usher syndrome 2 and familial febrile seizures.
Variants of the NDUFAF1 gene are associated with hypertrophic cardiomyopathy, leukodystrophy, and cardioencephalomyopathy.
Mutations in the PRPH2 gene are associated with Vitelliform macular dystrophy.
Mutations in this gene are associated with type II vitamin D-resistant rickets.
Mutations in the PKD1 gene are associated with a poorer renal prognosis than PKD2 mutations.
Mutations in the MT-TK gene are associated with myoclonic epilepsy and ragged-red fiber disease MERRF.
You'll also be interested in:
Examples of using Associated
Show more
Taliban and associated individuals and entities
Bolivia has no chemical weapons or associated technology
Associated and secondary data centre costs
Examples of using Gene
Show more
Gene will never be able to digest them
The baldness gene was cause for dread
Gene mckinney pleaded the fifth amendment
