Detalhe da pesquisa
1.
Multiple early factors anticipate post-acute COVID-19 sequelae.
Cell
; 185(5): 881-895.e20, 2022 03 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35216672
2.
Multi-Omics Resolves a Sharp Disease-State Shift between Mild and Moderate COVID-19.
Cell
; 183(6): 1479-1495.e20, 2020 12 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33171100
3.
Genetic modifiers of Huntington disease differentially influence motor and cognitive domains.
Am J Hum Genet
; 109(5): 885-899, 2022 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35325614
4.
Expanding student nurse placement activity in Welsh care homes: An evaluation study.
Int J Nurs Pract
; : e13242, 2024 Feb 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38332422
5.
Genetic and Functional Analyses Point to FAN1 as the Source of Multiple Huntington Disease Modifier Effects.
Am J Hum Genet
; 107(1): 96-110, 2020 07 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32589923
6.
'It's tough. It is hard': A qualitative interview study of staff and volunteers caring for hospice in-patients with delirium.
Palliat Med
; 37(7): 993-1005, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37129262
7.
Translating qualitative data into intervention content using the Theoretical Domains Framework and stakeholder co-design: a worked example from a study of cervical screening attendance in older women.
BMC Health Serv Res
; 22(1): 610, 2022 May 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35524217
8.
FAN1 modifies Huntington's disease progression by stabilizing the expanded HTT CAG repeat.
Hum Mol Genet
; 28(4): 650-661, 2019 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30358836
9.
The unique information and communication needs of men affected by prostate cancer: A qualitative study of men's experience.
Eur J Cancer Care (Engl)
; 30(6): e13503, 2021 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-34549483
10.
Population-specific genetic modification of Huntington's disease in Venezuela.
PLoS Genet
; 14(5): e1007274, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29750799
11.
MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1.
Brain
; 2019 Jun 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-31216018
12.
Genetic modifiers of Mendelian disease: Huntington's disease and the trinucleotide repeat disorders.
Hum Mol Genet
; 26(R2): R83-R90, 2017 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28977442
13.
A modifier of Huntington's disease onset at the MLH1 locus.
Hum Mol Genet
; 26(19): 3859-3867, 2017 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28934397
14.
The HTT CAG-Expansion Mutation Determines Age at Death but Not Disease Duration in Huntington Disease.
Am J Hum Genet
; 98(2): 287-98, 2016 Feb 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-26849111
15.
RNA-Seq of Huntington's disease patient myeloid cells reveals innate transcriptional dysregulation associated with proinflammatory pathway activation.
Hum Mol Genet
; 25(14): 2893-2904, 2016 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27170315
16.
DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases.
Ann Neurol
; 79(6): 983-90, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-27044000
17.
Reconstitution of Formylglycine-generating Enzyme with Copper(II) for Aldehyde Tag Conversion.
J Biol Chem
; 290(25): 15730-15745, 2015 Jun 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-25931126
18.
Generating aldehyde-tagged antibodies with high titers and high formylglycine yields by supplementing culture media with copper(II).
BMC Biotechnol
; 16: 23, 2016 Feb 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-26911368
19.
Decreasing the expression of PICALM reduces endocytosis and the activity of ß-secretase: implications for Alzheimer's disease.
BMC Neurosci
; 17(1): 50, 2016 07 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-27430330
20.
Reply: The repeat variant in MSH3 is not a genetic modifier for spinocerebellar ataxia type 3 and Friedreich's ataxia.
Brain
; 143(4): e26, 2020 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32154840