Found: 34
Select item for more details and to access through your institution.
Efficacy and Safety of SPN-812 (Extended-Release Viloxazine) in Children and Adolescents with Attention-Deficit/Hyperactivity Disorder: A Systematic Review and Meta-Analysis.
- Published in:
- Brain Sciences (2076-3425), 2023, v. 13, n. 12, p. 1627, doi. 10.3390/brainsci13121627
- By:
- Publication type:
- Article
A loss-of-function mutation p.T52S in RIPPLY3 is a potential predisposing genetic risk factor for Chinese Han conotruncal heart defect patients without the 22q11.2 deletion/duplication.
- Published in:
- 2018
- By:
- Publication type:
- journal article
A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease.
- Published in:
- BMC Genomics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12864-015-1590-5
- By:
- Publication type:
- Article
Rare copy number variation analysis identifies disease-related variants in atrioventricular septal defect patients.
- Published in:
- Frontiers in Genetics, 2023, v. 14, p. 1, doi. 10.3389/fgene.2023.1075349
- By:
- Publication type:
- Article
Prediction of Urban Taxi Travel Demand by Using Hybrid Dynamic Graph Convolutional Network Model.
- Published in:
- Sensors (14248220), 2022, v. 22, n. 16, p. 5982, doi. 10.3390/s22165982
- By:
- Publication type:
- Article
Mutation Screening of Gata4 Gene in CTD Patients Within Chinese Han Population.
- Published in:
- Pediatric Cardiology, 2017, v. 38, n. 3, p. 506, doi. 10.1007/s00246-016-1542-0
- By:
- Publication type:
- Article
Identification of diagnostic model in heart failure with myocardial fibrosis and conduction block by integrated gene co-expression network analysis.
- Published in:
- BMC Medical Genomics, 2024, v. 17, n. 1, p. 1, doi. 10.1186/s12920-024-01814-w
- By:
- Publication type:
- Article
Cost-Effectiveness and Budget Impact Analysis of Apatinib for Advanced Metastatic Gastric Cancer from the Perspective of Health Insurance System.
- Published in:
- Gastroenterology Research & Practice, 2017, p. 1, doi. 10.1155/2017/2816737
- By:
- Publication type:
- Article
Novel mutations of the SRF gene in Chinese sporadic conotruncal heart defect patients.
- Published in:
- BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01032-y
- By:
- Publication type:
- Article
Exploring the dynamical transitions on an epileptic hippocampal network model and its modulation strategy based on transcranial magneto-acoustical stimulation.
- Published in:
- Nonlinear Dynamics, 2024, v. 112, n. 11, p. 9495, doi. 10.1007/s11071-024-09476-0
- By:
- Publication type:
- Article
A Potential Relationship among Beta-Defensins Haplotype, SOX7 Duplication and Cardiac Defects.
- Published in:
- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0072515
- By:
- Publication type:
- Article
Subgroup Economic Analysis for Glioblastoma in a Health Resource-Limited Setting.
- Published in:
- PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0034588
- By:
- Publication type:
- Article
Economic Evaluation of First-Line Treatments for Metastatic Renal Cell Carcinoma: A Cost-Effectiveness Analysis in A Health Resource-Limited Setting.
- Published in:
- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0032530
- By:
- Publication type:
- Article
miR-21 Is a Promising Novel Biomarker for Lymph Node Metastasis in Patients with Gastric Cancer.
- Published in:
- Gastroenterology Research & Practice, 2012, p. 1, doi. 10.1155/2012/640168
- By:
- Publication type:
- Article
A 3 base pair deletion in TBX1 leads to reduced protein expression and transcriptional activity.
- Published in:
- Scientific Reports, 2017, p. 44165, doi. 10.1038/srep44165
- By:
- Publication type:
- Article
Identification of candidate genes for congenital heart defects on proximal chromosome 8p.
- Published in:
- Scientific Reports, 2016, p. 36133, doi. 10.1038/srep36133
- By:
- Publication type:
- Article
Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects.
- Published in:
- Genome Medicine, 2018, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13073-018-0549-y
- By:
- Publication type:
- Article
Gene-guided Gefitinib switch maintenance therapy for patients with advanced EGFR mutation-positive Non-small cell lung cancer: an economic analysis.
- Published in:
- BMC Cancer, 2013, v. 13, n. 1, p. 1, doi. 10.1186/1471-2407-13-39
- By:
- Publication type:
- Article
Gene-guided gefitinib switch maintenance therapy for patients with advanced EGFR mutation-positive non-small cell lung cancer: an economic analysis.
- Published in:
- 2013
- By:
- Publication type:
- journal article
MiRNA-26a Contributes to the Acquisition of Malignant Behaviors of Doctaxel- Resistant Lung Adenocarcinoma Cells through Targeting EZH2.
- Published in:
- Cellular Physiology & Biochemistry (Karger AG), 2017, v. 41, n. 2, p. 583, doi. 10.1159/000457879
- By:
- Publication type:
- Article
Patients Carrying 9q31.1-q32 Deletion Share Common Features with Cornelia de Lange Syndrome.
- Published in:
- Cellular Physiology & Biochemistry (Karger AG), 2015, v. 35, n. 1, p. 270, doi. 10.1159/000369694
- By:
- Publication type:
- Article
CITED2 Mutations in Conserved Regions Contribute to Conotruncal Heart Defects in Chinese Children.
- Published in:
- DNA & Cell Biology, 2017, v. 36, n. 7, p. 589, doi. 10.1089/dna.2017.3701
- By:
- Publication type:
- Article
Duplication and Deletion of CFC1 Associated with Heterotaxy Syndrome.
- Published in:
- DNA & Cell Biology, 2015, v. 34, n. 2, p. 101, doi. 10.1089/dna.2014.2616
- By:
- Publication type:
- Article
Exome Sequencing Identifies a Novel MYH7 p.G407C Mutation Responsible for Familial Hypertrophic Cardiomyopathy.
- Published in:
- DNA & Cell Biology, 2014, v. 33, n. 10, p. 699, doi. 10.1089/dna.2014.2483
- By:
- Publication type:
- Article
Cost-effectiveness analysis of adjuvant chemotherapies in patients presenting with gastric cancer after D2 gastrectomy.
- Published in:
- BMC Cancer, 2014, v. 14, n. 1, p. 1, doi. 10.1186/1471-2407-14-984
- By:
- Publication type:
- Article
Economic evaluation of radiotherapy for early breast cancer after breast-conserving surgery in a health resource-limited setting.
- Published in:
- Breast Cancer Research & Treatment, 2012, v. 136, n. 2, p. 547, doi. 10.1007/s10549-012-2268-1
- By:
- Publication type:
- Article
CTL Attenuation Regulated by PS1 in Cancer-Associated Fibroblast.
- Published in:
- Frontiers in Immunology, 2020, v. 11, p. 1, doi. 10.3389/fimmu.2020.00999
- By:
- Publication type:
- Article
Rare Copy Number Variants Identify Novel Genes in Sporadic Total Anomalous Pulmonary Vein Connection.
- Published in:
- Frontiers in Genetics, 2018, p. N.PAG, doi. 10.3389/fgene.2018.00559
- By:
- Publication type:
- Article
Copy Number Variants and Exome Sequencing Analysis in Six Pairs of Chinese Monozygotic Twins Discordant for Congenital Heart Disease.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Predisposition to atrioventricular septal defects may be caused by SOX7 variants that impair interaction with GATA4.
- Published in:
- Molecular Genetics & Genomics, 2022, v. 297, n. 3, p. 671, doi. 10.1007/s00438-022-01859-5
- By:
- Publication type:
- Article
Research on Experimental and Simulated Temperature Control Performance of Power Batteries Based on Composite Phase Change Materials.
- Published in:
- World Electric Vehicle Journal, 2024, v. 15, n. 7, p. 302, doi. 10.3390/wevj15070302
- By:
- Publication type:
- Article
JAG1 loss‑of‑function mutations contributed to Alagille syndrome in two Chinese families.
- Published in:
- Molecular Medicine Reports, 2018, v. 18, n. 2, p. 2356, doi. 10.3892/mmr.2018.9217
- By:
- Publication type:
- Article
Variants in a cis-regulatory element of TBX1 in conotruncal heart defect patients impair GATA6-mediated transactivation.
- Published in:
- 2021
- By:
- Publication type:
- journal article
A Novel Short-Time Passenger Flow Prediction Method for Urban Rail Transit: CEEMDAN-CSSA-LSTM Model Based on Station Classification.
- Published in:
- Engineering Letters, 2023, v. 31, n. 4, p. 1894
- By:
- Publication type:
- Article