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Establishment of a PYM-resistant human tongue carcinoma cell line Tca8113/PYM and cloning of resistance-related genes
- Published in:
- 2008
- By:
- Publication type:
- Abstract
Heterozygous PGM3 Variants Are Associated With Idiopathic Focal Epilepsy With Incomplete Penetrance.
- Published in:
- Frontiers in Genetics, 2020, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.559080
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- Publication type:
- Article
Functional Investigation of a <italic>GRIN2A</italic> Variant Associated with Rolandic Epilepsy.
- Published in:
- Neuroscience Bulletin, 2018, v. 34, n. 2, p. 237, doi. 10.1007/s12264-017-0182-6
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- Publication type:
- Article
Variants in BRWD3 associated with X‐linked partial epilepsy without intellectual disability.
- Published in:
- CNS Neuroscience & Therapeutics, 2023, v. 29, n. 2, p. 727, doi. 10.1111/cns.14057
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- Publication type:
- Article
CELSR3 variants are associated with febrile seizures and epilepsy with antecedent febrile seizures.
- Published in:
- CNS Neuroscience & Therapeutics, 2022, v. 28, n. 3, p. 382, doi. 10.1111/cns.13781
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- Publication type:
- Article
CHD4 variants are associated with childhood idiopathic epilepsy with sinus arrhythmia.
- Published in:
- CNS Neuroscience & Therapeutics, 2021, v. 27, n. 10, p. 1146, doi. 10.1111/cns.13692
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- Publication type:
- Article
Heterozygous variants in USP25 cause genetic generalized epilepsy.
- Published in:
- Brain: A Journal of Neurology, 2024, v. 147, n. 10, p. 3442, doi. 10.1093/brain/awae191
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- Publication type:
- Article
UNC13B variants associated with partial epilepsy with favourable outcome.
- Published in:
- 2021
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- Publication type:
- journal article
Mitochondrial permeability transition induced by different concentrations of zinc.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Spectroscopic and microscopic studies on the mechanisms of mitochondrial toxicity induced by different concentrations of cadmium.
- Published in:
- 2011
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- Publication type:
- journal article
Efficacy and Potential MicroRNA Mechanism for Computed Tomography-Guided Percutaneous Radiofrequency Ablation of Primary Lung Cancer and Lung Metastasis from Liver Cancer.
- Published in:
- Cellular Physiology & Biochemistry (Karger AG), 2014, v. 33, n. 5, p. 1261, doi. 10.1159/000358694
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- Publication type:
- Article
CELSR1 variants are associated with partial epilepsy of childhood.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2022, v. 189, n. 7/8, p. 247, doi. 10.1002/ajmg.b.32916
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- Publication type:
- Article
Promoter Analysis of Mouse Scn3a Gene and Regulation of the Promoter Activity by GC Box and CpG Methylation.
- Published in:
- Journal of Molecular Neuroscience, 2011, v. 44, n. 2, p. 115, doi. 10.1007/s12031-011-9492-8
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- Publication type:
- Article
Non- Lactobacillus -Dominated Vaginal Microbiota Is Associated With a Tubal Pregnancy in Symptomatic Chinese Women in the Early Stage of Pregnancy: A Nested Case–Control Study.
- Published in:
- Frontiers in Cellular & Infection Microbiology, 2021, v. 11, p. 1, doi. 10.3389/fcimb.2021.659505
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- Publication type:
- Article
Retraction Note: Mir20a/106a-WTX axis regulates RhoGDIa/CDC42 signaling and colon cancer progression.
- Published in:
- 2023
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- Publication type:
- Correction Notice
Few individuals with Lennox-Gastaut syndrome have autism spectrum disorder: a comparison with Dravet syndrome.
- Published in:
- Journal of Neurodevelopmental Disorders, 2018, v. 10, n. 1, p. 1, doi. 10.1186/s11689-018-9229-x
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- Publication type:
- Article
RYR2 Mutations Are Associated With Benign Epilepsy of Childhood With Centrotemporal Spikes With or Without Arrhythmia.
- Published in:
- Frontiers in Neuroscience, 2021, v. 15, p. N.PAG, doi. 10.3389/fnins.2021.629610
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- Publication type:
- Article
DEPDC5 Variants Associated Malformations of Cortical Development and Focal Epilepsy With Febrile Seizure Plus/Febrile Seizures: The Role of Molecular Sub-Regional Effect.
- Published in:
- Frontiers in Neuroscience, 2020, v. 14, p. N.PAG, doi. 10.3389/fnins.2020.00821
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- Publication type:
- Article
Recessive LAMA5 Variants Associated With Partial Epilepsy and Spasms in Infancy.
- Published in:
- Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2022.825390
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- Publication type:
- Article
Critical Role of E1623 Residue in S3-S4 Loop of Nav1.1 Channel and Correlation Between Nature of Substitution and Functional Alteration.
- Published in:
- Frontiers in Molecular Neuroscience, 2022, v. 14, p. 1, doi. 10.3389/fnmol.2021.797628
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- Publication type:
- Article
Isorhamnetin Downregulates MMP2 and MMP9 to Inhibit Development of Rheumatoid Arthritis through SRC/ERK/CREB Pathway.
- Published in:
- Chinese Journal of Integrative Medicine, 2024, v. 30, n. 4, p. 299, doi. 10.1007/s11655-023-3753-6
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- Publication type:
- Article
Optimization of in silico tools for predicting genetic variants: individualizing for genes with molecular sub-regional stratification.
- Published in:
- Briefings in Bioinformatics, 2020, v. 21, n. 5, p. 1776, doi. 10.1093/bib/bbz115
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- Publication type:
- Article
CCDC88C variants are associated with focal epilepsy and genotype–phenotype correlation.
- Published in:
- Clinical Genetics, 2024, v. 105, n. 4, p. 397, doi. 10.1111/cge.14476
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- Publication type:
- Article
Association between HLA and Stevens-Johnson Syndrome Induced by Carbamazepine in Southern Han Chinese: Genetic Markers besides B*1502?
- Published in:
- Basic & Clinical Pharmacology & Toxicology, 2012, v. 111, n. 1, p. 58, doi. 10.1111/j.1742-7843.2012.00868.x
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- Publication type:
- Article
Immunological features and functional analysis of anti-CFH autoantibodies in patients with atypical hemolytic uremic syndrome.
- Published in:
- Pediatric Nephrology, 2019, v. 34, n. 2, p. 269, doi. 10.1007/s00467-018-4074-4
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- Publication type:
- Article
The clinical and laboratory features of Chinese Han anti-factor H autoantibody-associated hemolytic uremic syndrome.
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 5, p. 811, doi. 10.1007/s00467-016-3562-7
- By:
- Publication type:
- Article
GRIN2A Variants Associated With Idiopathic Generalized Epilepsies.
- Published in:
- Frontiers in Molecular Neuroscience, 2021, v. 14, p. 1, doi. 10.3389/fnmol.2021.720984
- By:
- Publication type:
- Article
TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large‐Sample Study.
- Published in:
- Movement Disorders, 2022, v. 37, n. 3, p. 545, doi. 10.1002/mds.28865
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- Publication type:
- Article
The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in China.
- Published in:
- 2020
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- Publication type:
- journal article
Tailoring microstructures of CoCrFeNiNb<sub>0.25</sub> hypoeutectic high-entropy alloy by hot deformation.
- Published in:
- Rare Metals, 2022, v. 41, n. 6, p. 2028, doi. 10.1007/s12598-021-01932-9
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- Publication type:
- Article
Risk factors for renal outcomes in children with antineutrophil cytoplasmic antibody-associated vasculitis: a nationwide retrospective study in China.
- Published in:
- World Journal of Pediatrics, 2024, v. 20, n. 5, p. 506, doi. 10.1007/s12519-023-00753-3
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- Publication type:
- Article
Clinical characteristics of hemolytic uremic syndrome secondary to cobalamin C disorder in Chinese children.
- Published in:
- World Journal of Pediatrics, 2015, v. 11, n. 3, p. 276, doi. 10.1007/s12519-015-0032-4
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- Publication type:
- Article
The SCN1A Mutation Database: Updating Information and Analysis of the Relationships among Genotype, Functional Alteration, and Phenotype.
- Published in:
- Human Mutation, 2015, v. 36, n. 6, p. 573, doi. 10.1002/humu.22782
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- Publication type:
- Article
Research progress of salt-tolerance genes in soybean.
- Published in:
- Chinese Journal of Oil Crop Sciences, 2020, v. 42, n. 4, p. 512, doi. 10.19802/j.issn.1007-9084.2020167
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- Publication type:
- Article
CS2164, a novel multi-target inhibitor against tumor angiogenesis, mitosis and chronic inflammation with anti-tumor potency.
- Published in:
- Cancer Science, 2017, v. 108, n. 3, p. 469, doi. 10.1111/cas.13141
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- Publication type:
- Article
<italic>ARHGEF9</italic> mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variation.
- Published in:
- Neurogenetics, 2018, v. 19, n. 1, p. 9, doi. 10.1007/s10048-017-0528-2
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- Publication type:
- Article
Floral Transcriptome Analyses of Four Paphiopedilum Orchids with Distinct Flowering Behaviors and Development of Simple Sequence Repeat Markers.
- Published in:
- Plant Molecular Biology Reporter, 2015, v. 33, n. 6, p. 1928, doi. 10.1007/s11105-015-0886-6
- By:
- Publication type:
- Article
Proline-rich transmembrane protein 2-negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients.
- Published in:
- 2018
- By:
- Publication type:
- journal article