Detalhe da pesquisa
1.
Variants in EXOSC9 Disrupt the RNA Exosome and Result in Cerebellar Atrophy with Spinal Motor Neuronopathy.
Am J Hum Genet
; 102(5): 858-873, 2018 05 03.
Artigo
Inglês
| MEDLINE | ID: mdl-29727687
2.
Second-generation compound for the modulation of utrophin in the therapy of DMD.
Hum Mol Genet
; 24(15): 4212-24, 2015 Aug 01.
Artigo
Inglês
| MEDLINE | ID: mdl-25935002
3.
Advances in genetic therapeutic strategies for Duchenne muscular dystrophy.
Exp Physiol
; 100(12): 1458-67, 2015 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-26140505
4.
RNA exosome mutations in pontocerebellar hypoplasia alter ribosome biogenesis and p53 levels.
Life Sci Alliance
; 3(8)2020 08.
Artigo
Inglês
| MEDLINE | ID: mdl-32527837
5.
Consistency in reference radiotherapy dosimetry: resolution of an apparent conundrum when (60)Co is the reference quality for charged-particle and photon beams.
Phys Med Biol
; 58(19): 6593-621, 2013 Oct 07.
Artigo
Inglês
| MEDLINE | ID: mdl-24018471
6.
On the uncertainties of photon mass energy-absorption coefficients and their ratios for radiation dosimetry.
Phys Med Biol
; 57(8): 2117-36, 2012 Apr 21.
Artigo
Inglês
| MEDLINE | ID: mdl-22451262