Detalhe da pesquisa
1.
Psychiatric Disorders and lncRNAs: A Synaptic Match.
Int J Mol Sci
; 21(9)2020 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-32344798
2.
Emerging Role of Genetic Alterations Affecting Exosome Biology in Neurodegenerative Diseases.
Int J Mol Sci
; 20(17)2019 Aug 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-31450727
3.
Multiple Layers of CDK5R1 Regulation in Alzheimer's Disease Implicate Long Non-Coding RNAs.
Int J Mol Sci
; 19(7)2018 Jul 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29997370
4.
Functional characterization of CDK5 and CDK5R1 mutations identified in patients with non-syndromic intellectual disability.
J Hum Genet
; 61(4): 283-93, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26657932
5.
hnRNPA2/B1 and nELAV proteins bind to a specific U-rich element in CDK5R1 3'-UTR and oppositely regulate its expression.
Biochim Biophys Acta
; 1839(6): 506-16, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24792867
6.
ADAP2 in heart development: a candidate gene for the occurrence of cardiovascular malformations in NF1 microdeletion syndrome.
J Med Genet
; 51(7): 436-43, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24711647
7.
PURPL and NEAT1 Long Non-Coding RNAs Are Modulated in Vascular Smooth Muscle Cell Replicative Senescence.
Biomedicines
; 11(12)2023 Dec 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38137449
8.
Lost in HELLS: Disentangling the mystery of SALNR existence in senescence cellular models.
PLoS One
; 18(5): e0286104, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37252915
9.
Noonan syndrome associated with both a new Jnk-activating familial SOS1 and a de novo RAF1 mutations.
Am J Med Genet A
; 152A(9): 2176-84, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20683980
10.
Candidate Genes and MiRNAs Linked to the Inverse Relationship Between Cancer and Alzheimer's Disease: Insights From Data Mining and Enrichment Analysis.
Front Genet
; 10: 846, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31608105
11.
Breakpoint characterization of a novel NF1 multiexonic deletion: a case showing expression of the mutated allele.
Neurogenetics
; 9(2): 95-100, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18196300
12.
The 3' untranslated region of human Cyclin-Dependent Kinase 5 Regulatory subunit 1 contains regulatory elements affecting transcript stability.
BMC Mol Biol
; 8: 111, 2007 Dec 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-18053171
13.
The miR-15/107 Family of microRNA Genes Regulates CDK5R1/p35 with Implications for Alzheimer's Disease Pathogenesis.
Mol Neurobiol
; 54(6): 4329-4342, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27343180
14.
The Long Non-Coding RNAs in Neurodegenerative Diseases: Novel Mechanisms of Pathogenesis.
Curr Alzheimer Res
; 13(11): 1219-1231, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27338628
15.
A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome.
Am J Med Genet A
; 152A(4): 1043-5, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20358625
16.
Centaurin-α2 interacts with ß-tubulin and stabilizes microtubules.
PLoS One
; 7(12): e52867, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23285209
17.
The role of miR-103 and miR-107 in regulation of CDK5R1 expression and in cellular migration.
PLoS One
; 6(5): e20038, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21625387
18.
MicroRNA-23b mediates urokinase and c-met downmodulation and a decreased migration of human hepatocellular carcinoma cells.
FEBS J
; 276(11): 2966-82, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19490101
19.
Characterisation of a non-recurrent familial translocation t(7;9)(q11.23;p24.3) points to a recurrent involvement of the Williams-Beuren syndrome region in chromosomal rearrangements.
J Hum Genet
; 51(1): 68-75, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-16328081
20.
Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with non-syndromic mental retardation.
Neurogenetics
; 7(1): 59-66, 2006 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-16425041