BRAF somatic mutation contributes to intrinsic epileptogenicity in pediatric brain tumors
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Dong Seok Kim | Jae Seok Lim | Se-Bum Paik | Hoon-Chul Kang | W. Heo | Jinju Han | M. Shong | Junjeong Choi | Jaeson Jang | Geurim Son | Sungwook Han | Jeong Ho Lee | Byung Ouk Park | Hyunjoo Lee | H. Koh | Hyungguk Kim | Daeyoup Lee | S. H. Kim
[1] Dong Seok Kim,et al. Somatic Mutations in TSC1 and TSC2 Cause Focal Cortical Dysplasia. , 2017, American journal of human genetics.
[2] M. Honavar,et al. Low-grade epilepsy-associated neuroepithelial tumours — the 2016 WHO classification , 2016, Nature Reviews Neurology.
[3] A. Odawara,et al. Physiological maturation and drug responses of human induced pluripotent stem cell-derived cortical neuronal networks in long-term culture , 2016, Scientific Reports.
[4] G. Reifenberger,et al. The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary , 2016, Acta Neuropathologica.
[5] Guoping Feng,et al. Adult Restoration of Shank3 Expression Rescues Selective Autistic-Like Phenotypes , 2016, Nature.
[6] [World Health Organization classification of tumours of the central nervous system: a summary]. , 2016, Zhonghua bing li xue za zhi = Chinese journal of pathology.
[7] I. Scheffer,et al. Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures , 2015, Nature Communications.
[8] L. Mortier,et al. Cerebrospinal fluid concentrations of vemurafenib in patients treated for brain metastatic BRAF-V600 mutated melanoma , 2015, Melanoma research.
[9] Seok-Gu Kang,et al. Brain somatic mutations in MTOR cause focal cortical dysplasia type II leading to intractable epilepsy , 2015, Nature Medicine.
[10] T. Aune,et al. Expression and functions of long noncoding RNAs during human T helper cell differentiation , 2015, Nature Communications.
[11] A. Fatemi,et al. A novel variant in GABRB2 associated with intellectual disability and epilepsy , 2014, American journal of medical genetics. Part A.
[12] C. Bernard,et al. The transcription factor NRSF contributes to epileptogenesis by selective repression of a subset of target genes , 2014, eLife.
[13] Oriane Trouillard,et al. De novo mutations in HCN1 cause early infantile epileptic encephalopathy , 2014, Nature Genetics.
[14] Markus Wolff,et al. GRIN2B Mutations in West Syndrome and Intellectual Disability with Focal Epilepsy , 2014, Annals of neurology.
[15] C. Vecht,et al. Seizure characteristics and prognostic factors of gliomas , 2013, Epilepsia.
[16] Dongfang Li,et al. Genome sequencing of 161 Mycobacterium tuberculosis isolates from China identifies genes and intergenic regions associated with drug resistance , 2013, Nature Genetics.
[17] K. Blomgren,et al. Brain development in rodents and humans: Identifying benchmarks of maturation and vulnerability to injury across species , 2013, Progress in Neurobiology.
[18] Ethan M. Goldberg,et al. Mechanisms of epileptogenesis: a convergence on neural circuit dysfunction , 2013, Nature Reviews Neuroscience.
[19] Heather L. Mulder,et al. Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas , 2013, Nature Genetics.
[20] Dongsup Kim,et al. Human histone H3K79 methyltransferase DOT1L protein binds actively transcribing RNA polymerase II to regulate gene expression. , 2013, The Journal of Biological Chemistry.
[21] Dongsup Kim,et al. Human Histone H3K79 Methyltransferase DOT1L Methyltransferase Binds Actively Transcribing RNA Polymerase II to Regulate Gene Expression* , 2012, The Journal of Biological Chemistry.
[22] Jyothi Arikkath,et al. Culturing pyramidal neurons from the early postnatal mouse hippocampus and cortex , 2012, Nature Protocols.
[23] E. Eichler,et al. Epi4K: Gene discovery in 4,000 genomes , 2012 .
[24] S. Vaidhyanathan,et al. Impact of P-Glycoprotein (ABCB1) and Breast Cancer Resistance Protein (ABCG2) on the Brain Distribution of a Novel BRAF Inhibitor: Vemurafenib (PLX4032) , 2012, Journal of Pharmacology and Experimental Therapeutics.
[25] Darcy Mcmullin. Epi4K: Gene discovery in 4,000 genomes , 2012, Epilepsia.
[26] E. Aronica,et al. Long‐Term Epilepsy‐Associated Tumors , 2012, Brain pathology.
[27] Pablo Cingolani,et al. © 2012 Landes Bioscience. Do not distribute. , 2022 .
[28] Frances S. Chance,et al. Erratum: Orthogonal micro-organization of orientation and spatial frequency in primate primary visual cortex , 2013, Nature Neuroscience.
[29] David R. Kelley,et al. Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks , 2012, Nature Protocols.
[30] M. Bennett,et al. Repressor element-1 silencing transcription factor (REST)-dependent epigenetic remodeling is critical to ischemia-induced neuronal death , 2012, Proceedings of the National Academy of Sciences.
[31] C. Bernard,et al. Neuron‐restrictive silencer factor‐mediated hyperpolarization‐activated cyclic nucleotide gated channelopathy in experimental temporal lobe epilepsy , 2011, Annals of neurology.
[32] P. V. van Rijen,et al. Activation of Toll-like receptor, RAGE and HMGB1 signalling in malformations of cortical development. , 2011, Brain : a journal of neurology.
[33] F. Tamanoi,et al. Activating mutations of TOR (target of rapamycin) , 2011, Genes to cells : devoted to molecular & cellular mechanisms.
[34] H. Ropers,et al. Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes , 2010, Nature Genetics.
[35] Cole Trapnell,et al. Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation. , 2010, Nature biotechnology.
[36] J. C. Baayen,et al. Expression and localization of voltage dependent potassium channel Kv4.2 in epilepsy associated focal lesions , 2009, Neurobiology of Disease.
[37] J. Reis-Filho,et al. Oncogenic Braf induces melanocyte senescence and melanoma in mice. , 2009, Cancer cell.
[38] L. Cantley,et al. PI3K pathway alterations in cancer: variations on a theme , 2008, Oncogene.
[39] Young Seok Park,et al. Factors contributing to resectability and seizure outcomes in 44 patients with ganglioglioma , 2008, Clinical Neurology and Neurosurgery.
[40] Arjen van Ooyen,et al. Low-frequency stimulation induces stable transitions in stereotypical activity in cortical networks. , 2008, Biophysical journal.
[41] B. Scheithauer,et al. The 2007 WHO classification of tumours of the central nervous system , 2007, Acta Neuropathologica.
[42] C. Vecht,et al. Epilepsy in patients with brain tumours: epidemiology, mechanisms, and management , 2007, The Lancet Neurology.
[43] E. Aronica,et al. Inhibitory networks in epilepsy-associated gangliogliomas and in the perilesional epileptic cortex , 2007, Epilepsy Research.
[44] E. Aronica,et al. Differential Cellular Gene Expression in Ganglioglioma , 2007, Epilepsia.
[45] E. Aronica,et al. Differential expression patterns of chloride transporters, Na+-K+-2Cl−-cotransporter and K+-Cl−-cotransporter, in epilepsy-associated malformations of cortical development , 2007, Neuroscience.
[46] C. Cianchetti,et al. Increased sensitivity of the neuronal nicotinic receptor alpha 2 subunit causes familial epilepsy with nocturnal wandering and ictal fear. , 2006, American journal of human genetics.
[47] C. Pritchard,et al. Expression of endogenous oncogenic V600EB-raf induces proliferation and developmental defects in mice and transformation of primary fibroblasts. , 2005, Cancer research.
[48] Steven Petrou,et al. GABRD encoding a protein for extra- or peri-synaptic GABAA receptors is a susceptibility locus for generalized epilepsies. , 2004, Human molecular genetics.
[49] H. Lester,et al. NRSF causes cAMP-sensitive suppression of sodium current in cultured hippocampal neurons. , 2002, Journal of neurophysiology.
[50] I. Blümcke,et al. Gangliogliomas: An Intriguing Tumor Entity Associated With Focal Epilepsies , 2002, Journal of neuropathology and experimental neurology.
[51] C. Stiles,et al. Molecular mechanisms controlling cortical gliogenesis , 2002, Current Opinion in Neurobiology.
[52] Wei-Yang Lu,et al. Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy , 2002, Nature Genetics.
[53] P. Brehm,et al. Regulation of Neuronal Traits by a Novel Transcriptional Complex , 2001, Neuron.
[54] E. Perucca. The Management of Refractory Idiopathic Epilepsies , 2001, Epilepsia.
[55] David A. Williams,et al. Mutant GABAA receptor γ2-subunit in childhood absence epilepsy and febrile seizures , 2001, Nature Genetics.
[56] P. Chiaravelli. Variations on a theme. , 1990, Journal of the American Dental Association.
[57] J. Sneep,et al. With a summary , 1945 .