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1.
The Continuous Adaptive Challenge Played by Arboviruses: An In Silico Approach to Identify a Possible Interplay between Conserved Viral RNA Sequences and Host RNA Binding Proteins (RBPs).
Int J Mol Sci
; 24(13)2023 Jul 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-37446229
2.
Novel Germline PHD2 Variant in a Metastatic Pheochromocytoma and Chronic Myeloid Leukemia, but in the Absence of Polycythemia.
Medicina (Kaunas)
; 58(8)2022 Aug 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-36013579
3.
An emerging role for BAG3 in gynaecological malignancies.
Br J Cancer
; 125(6): 789-797, 2021 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-34099896
4.
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins.
Clin Genet
; 95(3): 368-374, 2019 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-30471091
5.
BAG3 Protein Is Over-Expressed in Endometrioid Endometrial Adenocarcinomas.
J Cell Physiol
; 232(2): 309-311, 2017 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-27414463
6.
Characterization of two de novoKCNT1 mutations in children with malignant migrating partial seizures in infancy.
Mol Cell Neurosci
; 72: 54-63, 2016 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-26784557
7.
Pancreatic Cancer-Secreted Proteins: Targeting Their Functions in Tumor Microenvironment.
Cancers (Basel)
; 15(19)2023 Oct 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-37835519
8.
Spike-mediated viral membrane fusion is inhibited by a specific anti-IFITM2 monoclonal antibody.
Antiviral Res
; 211: 105546, 2023 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-36669656
9.
What Have We Learned from Patients Who Have Arboleda-Tham Syndrome Due to a De Novo KAT6A Pathogenic Variant with Impaired Histone Acetyltransferase Function? A Precise Clinical Description May Be Critical for Genetic Testing Approach and Final Diagnosis.
Genes (Basel)
; 14(1)2023 01 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-36672906
10.
FACILITATE: A real-world, multicenter, prospective study investigating the utility of a rapid, fully automated real-time PCR assay versus local reference methods for detecting epidermal growth factor receptor variants in NSCLC.
Pathol Oncol Res
; 29: 1610707, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-36798672
11.
Neutrophil-to-Lymphocyte Ratio Is a Major Prognostic Factor in Non-small Cell Lung Carcinoma Patients Undergoing First Line Immunotherapy With Pembrolizumab.
Cancer Diagn Progn
; 3(1): 44-52, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-36632583
12.
An in silico pipeline approach uncovers a potentially intricate network involving spike SARS-CoV-2 RNA, RNA vaccines, host RNA-binding proteins (RBPs), and host miRNAs at the cellular level.
J Genet Eng Biotechnol
; 20(1): 129, 2022 Sep 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-36066672
13.
McKusick-Kaufman or Bardet-Biedl syndrome? A new borderline case in an Italian nonconsanguineous healthy family.
Indian J Hum Genet
; 17(2): 94-6, 2011 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-22090721
14.
In Silico Analysis of Possible Interaction between Host Genomic Transcription Factors (TFs) and Zika Virus (ZikaSPH2015) Strain with Combinatorial Gene Regulation; Virus Versus Host-The Game Reloaded.
Pathogens
; 10(1)2021 Jan 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-33466592
15.
Pathogenic DNM1L Variant (1085G>A) Linked to Infantile Progressive Neurological Disorder: Evidence of Maternal Transmission by Germline Mosaicism and Influence of a Contemporary in cis Variant (1535T>C).
Genes (Basel)
; 12(9)2021 08 24.
Artículo
en Inglés
| MEDLINE | ID: mdl-34573276
16.
A SARS-CoV-2 host infection model network based on genomic human Transcription Factors (TFs) depletion.
Heliyon
; 6(10): e05010, 2020 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-32984567
17.
Rising Roles of Small Noncoding RNAs in Cotranscriptional Regulation: In Silico Study of miRNA and piRNA Regulatory Network in Humans.
Genes (Basel)
; 11(5)2020 04 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-32365489
18.
Germline Mutation in KIF1Bß Gene Associated with Loss of Heterozygosity: Usefulness of Next-Generation Sequencing in the Genetic Screening of Patients with Pheochromocytoma.
Int J Endocrinol
; 2020: 3671396, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32565791
19.
The recurrent SETBP1 c.2608G > A, p.(Gly870Ser) variant in a patient with Schinzel-Giedion syndrome: an illustrative case of the utility of whole exome sequencing in a critically ill neonate.
Ital J Pediatr
; 46(1): 74, 2020 May 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-32460883
20.
Novel association of MEN1 gene mutations with parathyroid carcinoma.
Oncol Lett
; 14(1): 23-30, 2017 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-28693130