Detalhe da pesquisa
1.
Exosomal microRNAs in Parkinson's disease: insights into biomarker potential and disease pathology.
Neurol Sci
; 2024 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38532190
2.
Functional assessment of DNA extraction methods from frozen human blood samples for Sanger sequencing analysis.
Cell Mol Biol (Noisy-le-grand)
; 69(8): 25-33, 2023 Aug 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-37715434
3.
Local regulation of the Srs2 helicase by the SUMO-like domain protein Esc2 promotes recombination at sites of stalled replication.
Genes Dev
; 29(19): 2067-80, 2015 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26443850
4.
Esc2 promotes Mus81 complex-activity via its SUMO-like and DNA binding domains.
Nucleic Acids Res
; 45(1): 215-230, 2017 Jan 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27694623
5.
DNA bending facilitates the error-free DNA damage tolerance pathway and upholds genome integrity.
EMBO J
; 33(4): 327-40, 2014 Feb 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-24473148
6.
Role of Copeptin in Predicting Postoperative Hyponatremia and Hypernatremia in Patients Undergoing Endoscopic Pituitary Adenoma Surgery.
Neurosurgery
; 2024 Mar 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38551356
7.
Identification of novel endogenous control miRNAs in heart failure for normalization of qPCR data.
Int J Biol Macromol
; 261(Pt 2): 129714, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38286377
8.
Resequencing the complete SNCA locus in Indian patients with Parkinson's disease.
NPJ Parkinsons Dis
; 10(1): 85, 2024 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38622158
9.
C12orf57 pathogenic variants: a unique cause of developmental encephalopathy in a south Indian child.
J Genet
; 1012022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35791610
10.
MutT Homolog1 has multifaceted role in glioma and is under the apparent orchestration by Hypoxia Inducible factor1 alpha.
Life Sci
; 264: 118673, 2021 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33130078
11.
DNA damage response and repair pathway modulation by non-histone protein methylation: implications in neurodegeneration.
J Cell Commun Signal
; 14(1): 31-45, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31749026
12.
Mus81-Mms4 endonuclease is an Esc2-STUbL-Cullin8 mitotic substrate impacting on genome integrity.
Nat Commun
; 11(1): 5746, 2020 11 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33184279
13.
Movement Disorders in GRIA2-Related Disorder - Expanding the Genetic Spectrum of Developmental Dyskinetic Encephalopathy.
Mov Disord Clin Pract
; 10(8): 1222-1224, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37635778
14.
Generalized Stiffness in Hereditary Hyperekplexia Responsive to Trihexyphenidyl: A Novel Finding.
Clin Pediatr (Phila)
; : 99228231203300, 2023 Oct 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-37899614
15.
Correction to: DNA damage response and repair pathway modulation by non-histone protein methylation: implications in neurodegeneration.
J Cell Commun Signal
; 15(1): 151, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-32990932
16.
Asymmetric DNA methylation by dimeric EcoP15I DNA methyltransferase.
Biochimie
; 128-129: 70-82, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27422119
17.
Corrigendum to "MutT Homolog1 has multifaceted role in glioma and is under the apparent orchestration by Hypoxia Inducible factor1 alpha" [Life Sci. Available online 29 October 2020, 118673].
Life Sci
; 265: 118810, 2021 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33303203
18.
SUMO-mediated global and local control of recombination.
Cell Cycle
; 15(2): 160-1, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26587752