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Profiles of responses of immunological factors to different subtypes of Kawasaki disease.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Progressive gray matter atrophy in parkinsonian variant of multiple system atrophy assessed by using causal structural covariance network.
- Published in:
- Neuroradiology, 2024, v. 66, n. 11, p. 1931, doi. 10.1007/s00234-024-03456-2
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- Publication type:
- Article
Variation of global DNA methylation levels with age and in autistic children.
- Published in:
- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0086-y
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- Publication type:
- Article
Effect of Deep Cryogenic Treatment on Microstructure and Properties of Pure Copper Processed by Equal Channel Angular Pressing.
- Published in:
- Advanced Engineering Materials, 2019, v. 21, n. 7, p. N.PAG, doi. 10.1002/adem.201801372
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- Publication type:
- Article
Discovery of vanoxerine dihydrochloride as a CDK2/4/6 triple-inhibitor for the treatment of human hepatocellular carcinoma.
- Published in:
- Molecular Medicine, 2021, v. 27, n. 1, p. 1, doi. 10.1186/s10020-021-00269-4
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- Publication type:
- Article
Face anti-spoofing based on weighted neighborhood pixel difference pattern.
- Published in:
- Journal of Electronic Imaging, 2021, v. 30, n. 3, p. 33003, doi. 10.1117/1.JEI.30.3.033003
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- Publication type:
- Article
Identification of FLOT2 as a novel target for microRNA-34a in melanoma.
- Published in:
- Journal of Cancer Research & Clinical Oncology, 2015, v. 141, n. 6, p. 993, doi. 10.1007/s00432-014-1874-1
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- Publication type:
- Article
Risk Factors and Clinical Outcomes of Renal Thrombotic Microangiopathy in Children with Lupus Nephritis in Terms of Pathological and Clinical Features.
- Published in:
- Nephron, 2024, v. 148, n. 9, p. 609, doi. 10.1159/000538240
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- Publication type:
- Article
Feasibility of a smartphone app for prescribed exercise tutoring in patients with stable coronary heart disease.
- Published in:
- Digital Health, 2023, p. 1, doi. 10.1177/20552076231197424
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- Publication type:
- Article
Feasibility of a smartphone app for prescribed exercise tutoring in patients with stable coronary heart disease.
- Published in:
- Digital Health, 2023, v. 9, p. 1, doi. 10.1177/20552076231197424
- By:
- Publication type:
- Article
Spinocerebellar ataxia type 11 in the Chinese Han population.
- Published in:
- Neurological Sciences, 2010, v. 31, n. 1, p. 107, doi. 10.1007/s10072-009-0129-4
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- Publication type:
- Article
COMPARISON OF VIBRATION CHARACTERISTICS FOR POSTBUCKLED FGM PLATES WITH PIEZOELECTRIC FIBER REINFORCED COMPOSITE ACTUATORS.
- Published in:
- International Journal of Structural Stability & Dynamics, 2009, v. 9, n. 3, p. 533, doi. 10.1142/S021945540900317X
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- Publication type:
- Article
Interactions of genetic risks for autism and the broad autism phenotypes.
- Published in:
- Frontiers in Psychiatry, 2023, v. 14, p. 1, doi. 10.3389/fpsyt.2023.1110080
- By:
- Publication type:
- Article
Joint Analysis of Genome-Wide Association Data Reveals No Genetic Correlations Between Low Back Pain and Neurodegenerative Diseases.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.744299
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- Publication type:
- Article
Sleep Problems of Children with Autism May Independently Affect Parental Quality of Life.
- Published in:
- Child Psychiatry & Human Development, 2021, v. 52, n. 3, p. 488, doi. 10.1007/s10578-020-01035-z
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- Publication type:
- Article
Gene-Related Cerebellar Neurodegeneration in SCA3/MJD: A Case-Controlled Imaging-Genetic Study.
- Published in:
- Frontiers in Neurology, 2019, p. 1, doi. 10.3389/fneur.2019.01025
- By:
- Publication type:
- Article
Prevalence of Autism Spectrum Disorder in China: A Nationwide Multi-center Population-based Study Among Children Aged 6 to 12 Years.
- Published in:
- Neuroscience Bulletin, 2020, v. 36, n. 9, p. 961, doi. 10.1007/s12264-020-00530-6
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- Publication type:
- Article
Modifying the Autism Spectrum Rating Scale (6-18 years) to a Chinese Context: An Exploratory Factor Analysis.
- Published in:
- Neuroscience Bulletin, 2017, v. 33, n. 2, p. 175, doi. 10.1007/s12264-017-0104-7
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- Publication type:
- Article
Chinese Norms for the Autism Spectrum Rating Scale.
- Published in:
- Neuroscience Bulletin, 2017, v. 33, n. 2, p. 161, doi. 10.1007/s12264-017-0105-6
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- Publication type:
- Article
Novel West syndrome candidate genes in a Chinese cohort.
- Published in:
- CNS Neuroscience & Therapeutics, 2018, v. 24, n. 12, p. 1196, doi. 10.1111/cns.12860
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- Publication type:
- Article
Updated frequency analysis of spinocerebellar ataxia in China.
- Published in:
- 2018
- By:
- Publication type:
- Letter
Rare GCH1 heterozygous variants contributing to Parkinson's disease.
- Published in:
- 2017
- By:
- Publication type:
- Letter
Ubiquitin-related network underlain by (CAG)n loci modulate age at onset in Machado-Joseph disease.
- Published in:
- 2017
- By:
- Publication type:
- Letter
ATXN2 polymorphism modulates age at onset in Machado-Joseph disease.
- Published in:
- 2016
- By:
- Publication type:
- journal article
MORC2 mutations in a cohort of Chinese patients with Charcot-Marie-Tooth disease type 2.
- Published in:
- Brain: A Journal of Neurology, 2016, v. 139, n. 10, p. e56, doi. 10.1093/brain/aww156
- By:
- Publication type:
- Article
(CAG)n loci as genetic modifiers of age-at-onset in patients with Machado-Joseph disease from mainland China.
- Published in:
- 2016
- By:
- Publication type:
- Letter
Predictive Nomogram of RAGE Genetic Polymorphisms and Metabolic Risk Factors for Myocardial Infarction Risk in a Han Chinese Population.
- Published in:
- Angiology, 2017, v. 68, n. 10, p. 877, doi. 10.1177/0003319717696622
- By:
- Publication type:
- Article
Screening for distress in patients with primary brain tumor using distress thermometer: a systematic review and meta-analysis.
- Published in:
- 2018
- By:
- Publication type:
- journal article
18β-Glycyrrhetinic acid preferentially blocks late Na current generated by ΔKPQ Nav1.5 channels.
- Published in:
- Acta Pharmacologica Sinica, 2012, v. 33, n. 6, p. 752, doi. 10.1038/aps.2012.22
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- Publication type:
- Article
Parkin, PINK1, and DJ-1 form a ubiquitin E3 ligase complex promoting unfolded protein degradation.
- Published in:
- Journal of Clinical Investigation, 2009, v. 119, n. 3, p. 650, doi. 10.1172/JCI37617
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- Publication type:
- Article
The dominant role of the atmospheric component of coupled models in ENSO amplitude simulations.
- Published in:
- Climate Dynamics, 2019, v. 52, n. 7/8, p. 4833, doi. 10.1007/s00382-018-4416-8
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- Publication type:
- Article
Identification of the Largest SCA36 Pedigree in Asia: with Multimodel Neuroimaging Evaluation for the First Time.
- Published in:
- Cerebellum, 2022, v. 21, n. 3, p. 358, doi. 10.1007/s12311-021-01304-0
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- Publication type:
- Article
Lithium Chloride Alleviates Neurodegeneration Partly by Inhibiting Activity of GSK3β in a SCA3 Drosophila Model.
- Published in:
- Cerebellum, 2013, v. 12, n. 6, p. 892, doi. 10.1007/s12311-013-0498-3
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- Publication type:
- Article
Development of Chinese genetic reference panel for Fragile X Syndrome and its application to the screen of 10,000 Chinese pregnant women and women planning pregnancy.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 6, p. 1, doi. 10.1002/mgg3.1236
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- Publication type:
- Article
Elevated serum ghrelin, tumor necrosis factor-α and interleukin-6 in congenital heart disease.
- Published in:
- Pediatrics International, 2016, v. 58, n. 4, p. 259, doi. 10.1111/ped.12773
- By:
- Publication type:
- Article
Cross-Disorder Analysis of De Novo Variants Increases the Power of Prioritising Candidate Genes.
- Published in:
- Life (2075-1729), 2021, v. 11, n. 3, p. 233, doi. 10.3390/life11030233
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- Publication type:
- Article
Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family.
- Published in:
- Journal of Human Genetics, 2015, v. 60, n. 3, p. 119, doi. 10.1038/jhg.2014.114
- By:
- Publication type:
- Article
Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: a unique SLC26A4 mutation spectrum.
- Published in:
- Journal of Human Genetics, 2007, v. 52, n. 6, p. 492, doi. 10.1007/s10038-007-0139-0
- By:
- Publication type:
- Article
A syndactyly type IV locus maps to 7q36.
- Published in:
- Journal of Human Genetics, 2007, v. 52, n. 6, p. 561, doi. 10.1007/s10038-007-0150-5
- By:
- Publication type:
- Article
A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigree.
- Published in:
- Journal of Human Genetics, 2002, v. 47, n. 12, p. 635, doi. 10.1007/s100380200098
- By:
- Publication type:
- Article
Primary familial brain calcification presenting with parkinsonism and motor complications caused by a novel SLC20A2 variant: a case report.
- Published in:
- Frontiers in Neurology, 2024, p. 1, doi. 10.3389/fneur.2024.1382534
- By:
- Publication type:
- Article
The Collective Contribution of Atmospheric and Oceanic Components to ENSO Asymmetry.
- Published in:
- Atmosphere, 2019, v. 10, n. 8, p. 469, doi. 10.3390/atmos10080469
- By:
- Publication type:
- Article
Wavelet packet and support vector machine analysis of series DC ARC fault detection in photovoltaic system.
- Published in:
- IEEJ Transactions on Electrical & Electronic Engineering, 2019, v. 14, n. 2, p. 192, doi. 10.1002/tee.22797
- By:
- Publication type:
- Article
Essential sequence of the N-terminal cytoplasmic localization-related domain of huntingtin and its effect on huntingtin aggregates.
- Published in:
- SCIENCE CHINA Life Sciences, 2011, v. 54, n. 4, p. 342, doi. 10.1007/s11427-011-4151-4
- By:
- Publication type:
- Article
Vitamin D-related genes are subjected to significant de novo mutation burdens in autism spectrum disorder.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 5, p. 568, doi. 10.1002/ajmg.b.32543
- By:
- Publication type:
- Article
Hutchinson-Gilford progeria syndrome accompanied by severe skeletal abnormalities in two Chinese siblings: two case reports.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Genotype and phenotype correlations for SHANK3 de novo mutations in neurodevelopmental disorders.
- Published in:
- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 12, p. 2668, doi. 10.1002/ajmg.a.40666
- By:
- Publication type:
- Article
P3-346: TMP21 degradation is mediated by the ubiquitin-proteasome pathway
- Published in:
- 2008
- By:
- Publication type:
- Abstract
P1-298: Differential transcriptional regulation of PEN-2 and APH-1A, two key components of the gamma-secretase complex
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P1-298: Differential transcriptional regulation of PEN-2 and APH-1A, two key components of the gamma-secretase complex
- Published in:
- 2006
- By:
- Publication type:
- Abstract