Detalhe da pesquisa
1.
Personalized RNA neoantigen vaccines stimulate T cells in pancreatic cancer.
Nature
; 618(7963): 144-150, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-37165196
2.
Neoantigen quality predicts immunoediting in survivors of pancreatic cancer.
Nature
; 606(7913): 389-395, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35589842
3.
Novel variants in ZNF34 and other brain-expressed transcription factors are shared among early-onset MDD relatives.
Am J Med Genet B Neuropsychiatr Genet
; 171B(3): 333-41, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26823146
4.
Exploring Brain-Derived Neurotrophic Factor Val66Met Polymorphism and Extinction Learning-Based Treatment Outcome in Obsessive-Compulsive Disorder: A Pilot Study.
J Clin Psychopharmacol
; 39(1): 91-93, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30531475
5.
Pathophysiology of protein aggregation and extended phenotyping in filaminopathy.
Brain
; 135(Pt 9): 2642-60, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22961544
6.
Novel FLNC mutation in a patient with myofibrillar myopathy in combination with late-onset cerebellar ataxia.
Muscle Nerve
; 46(2): 275-82, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22806379
7.
Clinical and myopathological characteristics of desminopathy caused by a mutation in desmin tail domain.
Eur Neurol
; 68(5): 279-86, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23051780
8.
Nemaline myopathy type 6: clinical and myopathological features.
Muscle Nerve
; 42(6): 901-7, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21104864
9.
DNA sequencing errors in molecular diagnostics of filamin myopathy.
Clin Chem Lab Med
; 48(10): 1409-14, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20578970
10.
Whole genome sequencing and rare variant analysis in essential tremor families.
PLoS One
; 14(8): e0220512, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31404076
11.
A Drosophila Model of Essential Tremor.
Sci Rep
; 8(1): 7664, 2018 05 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-29769701
12.
Genetic Correlates of Spirituality/Religion and Depression: A Study in Offspring and Grandchildren at High and Low Familial Risk for Depression.
Spiritual Clin Pract (Wash D C )
; 4(1): 43-63, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29057276
13.
Associations between serotonin transporter and behavioral traits and diagnoses related to anxiety.
Psychiatry Res
; 253: 211-219, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28391138
14.
Brain derived neurotrophic factor moderates associations between maternal smoking during pregnancy and offspring behavioral disorders.
Psychiatry Res
; 245: 387-391, 2016 Nov 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-27611068
15.
Serotonin signaling modulates the effects of familial risk for depression on cortical thickness.
Psychiatry Res Neuroimaging
; 248: 83-93, 2016 Feb 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-26774425
16.
Genetic variants within the serotonin transporter associated with familial risk for major depression.
Psychiatry Res
; 228(1): 170-3, 2015 Jul 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-25920807
17.
Genetic variants in potassium channels are associated with type 2 diabetes in a Mongolian population.
J Diabetes
; 4(3): 238-42, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22151254
18.
Clinical and myopathological evaluation of early- and late-onset subtypes of myofibrillar myopathy.
Neuromuscul Disord
; 21(8): 533-42, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21676617
19.
Inheritance patterns and phenotypic features of myofibrillar myopathy associated with a BAG3 mutation.
Neuromuscul Disord
; 20(7): 438-42, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20605452
20.
In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy.
Eur J Hum Genet
; 17(5): 656-63, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19050726