例句與造句

1. The related diseases, which are also inherited, include spinocellebellar ataxia and spinal and bulbar muscular atrophy.
2. The related diseases, which are also inherited, include spinocerebellar ataxia and spinal and bulbar muscular atrophy.
3. Polyglutamine repeat expansion in the AR is linked to spinal and bulbar muscular atrophy ( Kennedy's disease ).
4. Spinal and bulbar muscular atrophy may share mechanistic features with other disorders caused by polyglutamine expansion, such as Huntington's disease.
5. Its role in heat shock response presents it as a target for treating related diseases like spinal and bulbar muscular atrophy ( SBMA ) and amyotrophic lateral sclerosis ( ALS ).
6. It's difficult to find spinal and bulbar muscular atrophy in a sentence. 用spinal and bulbar muscular atrophy造句挺難的
7. RAN coactivation of the AR diminishes with polyglutamine expansion within the AR, and this weak coactivation may lead to partial androgen insensitivity during the development of spinal and bulbar muscular atrophy.
8. Neurological disorders such as multiple sclerosis, post-polio syndrome, multifocal motor neuropathy, CIDP, spinal muscular atrophy, and spinal and bulbar muscular atrophy can also mimic certain aspects of the disease and should be considered.
9. Certain conditions ( e . g ., spinal muscular atrophy or spinal and bulbar muscular atrophy ) have a wide range, from infancy to adult, fatal to trivial, with different affected individuals manifesting every shade of impairment between these two extremes.
10. Other, more complex relationships have been observed as a consequence of mutated " AR "; some mutations associated with male phenotypes have been linked to male breast cancer, prostate cancer, or in the case of spinal and bulbar muscular atrophy, disease of the central nervous system.
11. These include Spinal and bulbar muscular atrophy ( trinucleotide expansion in the AR gene ), Dentatoribral-pallidoluysian atrophy ( trinucleotide expansion in the DRPLA gene ), Spinocerebellar ataxia type 1 ( trinucleotide expansion in the SCA1gene ), Machado-Joseph disease ( trinucleotide expansion in the SCA3 gene ), Myotonic dystrophy ( trinucleotide expansion in the DMPK gene ), and Friedreich's ataxia ( a trinuncleotide expansion in the X25 gene ).