Found: 23
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Discovering a change point and piecewise linear structure in a time series of organoid networks via the iso-mirror.
- Published in:
- Applied Network Science, 2023, v. 8, n. 1, p. 1, doi. 10.1007/s41109-023-00564-5
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- Publication type:
- Article
Multimodal monitoring of human cortical organoids implanted in mice reveal functional connection with visual cortex.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-35536-3
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- Publication type:
- Article
Junctional instability in neuroepithelium and network hyperexcitability in a focal cortical dysplasia human model.
- Published in:
- 2022
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- Publication type:
- journal article
Genetic Profile of Patients with Limb-Girdle Muscle Weakness in the Chilean Population.
- Published in:
- Genes, 2022, v. 13, n. 6, p. 1076, doi. 10.3390/genes13061076
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- Publication type:
- Article
Spatiotemporal activity of the pine marten Martes martes: Insights from an island population.
- Published in:
- Ecological Research, 2022, v. 37, n. 1, p. 102, doi. 10.1111/1440-1703.12269
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- Publication type:
- Article
Super-Selective Reconstruction of Causal and Direct Connectivity With Application to in vitro iPSC Neuronal Networks.
- Published in:
- Frontiers in Neuroscience, 2021, v. 15, p. 1, doi. 10.3389/fnins.2021.647877
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- Publication type:
- Article
All-Optical Electrophysiology in hiPSC-Derived Neurons With Synthetic Voltage Sensors.
- Published in:
- Frontiers in Cellular Neuroscience, 2021, v. 15, p. 1, doi. 10.3389/fncel.2021.671549
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- Publication type:
- Article
Computing Temporal Sequences Associated With Dynamic Patterns on the C. elegans Connectome.
- Published in:
- Frontiers in Systems Neuroscience, 2021, v. 14, p. N.PAG, doi. 10.3389/fnsys.2021.564124
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- Publication type:
- Article
Using iPSC Models to Understand the Role of Estrogen in Neuron–Glia Interactions in Schizophrenia and Bipolar Disorder.
- Published in:
- Cells (2073-4409), 2021, v. 10, n. 2, p. 209, doi. 10.3390/cells10020209
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- Publication type:
- Article
Splicing impact of deep exonic missense variants in CAPN3 explored systematically by minigene functional assay.
- Published in:
- Human Mutation, 2020, v. 41, n. 10, p. 1797, doi. 10.1002/humu.24083
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- Publication type:
- Article
Molecular combing reveals complex 4q35 rearrangements in Facioscapulohumeral dystrophy.
- Published in:
- Human Mutation, 2017, v. 38, n. 10, p. 1432, doi. 10.1002/humu.23304
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- Publication type:
- Article
Segregation between SMCHD1 mutation, D4Z4 hypomethylation and Facio-Scapulo- Humeral Dystrophy: a case report.
- Published in:
- BMC Medical Genetics, 2016, v. 17, p. 1, doi. 10.1186/s12881-016-0328-9
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- Publication type:
- Article
Correlation between low FAT1 expression and early affected muscle in facioscapulohumeral muscular dystrophy.
- Published in:
- Annals of Neurology, 2015, v. 78, n. 3, p. 387, doi. 10.1002/ana.24446
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- Publication type:
- Article
Identification of Variants in the 4q35 Gene FAT1 in Patients with a Facioscapulohumeral Dystrophy-Like Phenotype.
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- Human Mutation, 2015, v. 36, n. 4, p. 443, doi. 10.1002/humu.22760
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- Publication type:
- Article
Deregulation of the Protocadherin Gene <i>FAT1</i> Alters Muscle Shapes: Implications for the Pathogenesis of Facioscapulohumeral Dystrophy.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 6, p. 1, doi. 10.1371/journal.pgen.1003550
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- Publication type:
- Article
Continuous low-dose oral contraceptive in the treatment of colorectal endometriosis evaluated by rectal endoscopic ultrasonography.
- Published in:
- Acta Obstetricia et Gynecologica Scandinavica, 2012, v. 91, n. 6, p. 699, doi. 10.1111/j.1600-0412.2012.01366.x
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- Publication type:
- Article
Endoscopic rectal ultrasound and elastosonography are useful in flow chart for the diagnosis of deep pelvic endometriosis with rectal involvement.
- Published in:
- Journal of Obstetrics & Gynaecology Research, 2011, v. 37, n. 6, p. 586, doi. 10.1111/j.1447-0756.2010.01413.x
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- Publication type:
- Article
A Novel Unstable Duplication Upstream of HAS2 Predisposes to a Breed-Defining Skin Phenotype and a Periodic Fever Syndrome in Chinese Shar-Pei Dogs.
- Published in:
- PLoS Genetics, 2011, v. 7, n. 3, p. 1, doi. 10.1371/journal.pgen.1001332
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- Publication type:
- Article
Protein tyrosine kinase 7 has a conserved role in Wnt/?-catenin canonical signalling.
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- EMBO Reports, 2011, v. 12, n. 1, p. 43, doi. 10.1038/embor.2010.185
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- Publication type:
- Article
A common variant located in the 3′UTR of the RET gene is associated with protection from Hirschsprung disease.
- Published in:
- Human Mutation, 2007, v. 28, n. 2, p. 168, doi. 10.1002/humu.20397
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- Publication type:
- Article
A common haplotype at the 5′ end of the RET proto-oncogene, overrepresented in Hirschsprung patients, is associated with reduced gene expression.
- Published in:
- Human Mutation, 2005, v. 25, n. 2, p. 189, doi. 10.1002/humu.20135
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- Publication type:
- Article
Erratum to: <B>Cell-line specific chromatin acetylation at the Sox10–Pax3 enhancer site modulates the RET proto-oncogene expression</B> (FEBS 26252): [FEBS Letters 523 (2002) 123–127]
- Published in:
- 2002
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- Publication type:
- Correction notice
Cell-line specific chromatin acetylation at the Sox10–Pax3 enhancer site modulates the RET proto-oncogene expression
- Published in:
- FEBS Letters, 2002, v. 523, n. 1-3, p. 123, doi. 10.1016/S0014-5793(02)02957-5
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- Publication type:
- Article