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36 documents found
1: Title: Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1.
Authors: Chen, Chih-Ping, et.al. .
Journal: Taiwanese journal of obstetrics & gynecology (Taiwan J Obstet Gynecol), Vol. 56 (6): 847-851, 2017 .
Snippet: (31,944,347-42,704,784) × 1.0 encompassing 19 Online Mendelian Inheritance of in Man (OMIM) genes including DTNA, CELF4 and SETBP1.
Affiliation: Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan; Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan; Department of Medicine, Mackay Medical College, New Taipei, Taiwan; Department of Biotechnology, Asia University, Taichung, Taiwan; School of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung, Taiwan; Institute of Clinical and Community Health Nursing, National Yang-Ming University, Taipei, Taiwan; Department of Obstetrics and Gynecology, School of Medicine, National Yang-Ming University, Taipei, Taiwan. Electronic address: cpc_mmh@yahoo.com. Department of Obstetrics and Gynecology, BIN KUN Women's & Children's Hospital, Taoyuan, Taiwan. Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan. Gene Biodesign Co. Ltd, Taipei, Taiwan. Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan. Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan; Department of Bioengineering, Tatung University, Taipei, Taiwan. .
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2: Title: Comprehensive gene and microRNA expression profiling on cardiovascular system in zebrafish co-exposured of SiNPs and MeHg.
Authors: Hu, Hejing, et.al. .
Journal: The Science of the total environment (Sci Total Environ), Vol. 607-608, 2017 .
Snippet: Major gene functions associated with cardiovascular system in the co-exposed zebrafish were discerned from the dynamic-gene-network, including stxbp1a, celf4, ahr1b and bai2.
Affiliation: Department of Toxicology and Sanitary Chemistry, School of Public Health, Capital Medical University, Beijing 100069, PR China; Beijing Key Laboratory of Environmental Toxicology, Capital Medical University, Beijing 100069, PR China. Department of Toxicology and Sanitary Chemistry, School of Public Health, Capital Medical University, Beijing 100069, PR China; Beijing Key Laboratory of Environmental Toxicology, Capital Medical University, Beijing 100069, PR China. Electronic address: jcduan@ccmu.edu.cn. Department of Toxicology and Sanitary Chemistry, School of Public Health, Capital Medical University, Beijing 100069, PR China; Beijing Key Laboratory of Environmental Toxicology, Capital Medical University, Beijing 100069, PR China. Electronic address: zwsun@ccmu.edu.cn. .
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3: Title: Microarray-based bioinformatics analysis of the combined effects of SiNPs and PbAc on cardiovascular system in zebrafish.
Authors: Hu, Hejing, et.al. .
Journal: Chemosphere, Vol. 184, 2017 .
Snippet: Key differentially expressed genes were discerned out based on the Dynamic-gene-network, including stxbp1a, ndfip2, celf4 and gsk3b.
Affiliation: Department of Toxicology and Sanitary Chemistry, School of Public Health, Capital Medical University, Beijing 100069, PR China; Beijing Key Laboratory of Environmental Toxicology, Capital Medical University, Beijing 100069, PR China. Department of Toxicology and Sanitary Chemistry, School of Public Health, Capital Medical University, Beijing 100069, PR China; Beijing Key Laboratory of Environmental Toxicology, Capital Medical University, Beijing 100069, PR China. Electronic address: jcduan@ccmu.edu.cn. .
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4: Title: Spatial and temporal expression patterns of genes around nine neuroticism-associated loci.
Authors: Ohi, Kazutaka, et.al. .
Journal: Progress in neuro-psychopharmacology & biological psychiatry (Prog Neuropsychopharmacol Biol Psychiatry), Vol. 77, 2017 .
Snippet: The temporal expression analysis revealed that the neuroticism-associated genes were divided into three expression patterns: KLHL2, CELF4 and CRHR1 were preferentially expressed during postnatal stages; PTPRD, ELAVL2 and MFHAS1 were expressed during prenatal stages; and the other three genes were not expressed during specific life stages.
Affiliation: Department of Neuropsychiatry, Kanazawa Medical University, Ishikawa, Japan. Electronic address: ohi@kanazawa-med.ac.jp. Department of Neuropsychiatry, Kanazawa Medical University, Ishikawa, Japan. .
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5: Title: Familial 18q12.2 deletion supports the role of RNA-binding protein CELF4 in autism spectrum disorders.
Authors: Barone, Rita, et.al. .
Journal: American journal of medical genetics. Part A (Am J Med Genet A), Vol. 173 (6): 1649-1655, 2017 .
Snippet: The CUGBP Elav-like family member 4 (CELF4) gene at 18q12.2 encodes a RNA-binding protein that links to RNA subsets involved in pre- and postsynaptic neurotransmission including almost 30% of potential autism-related genes.
Affiliation: Department of Clinical and Experimental Medicine, Child Neurology and Psychiatry, University of Catania, Catania, Italy. Department of Biomedical and Biotechnological Sciences, Medical Genetics, University of Catania, Catania, Italy. Laboratory of Medical Genetics, I.R.C.C.S. Associazione Oasi Maria Santissima, Troina, Italy. .
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6: Title: Integrated Epigenomics Analysis Reveals a DNA Methylation Panel for Endometrial Cancer Detection Using Cervical Scrapings.
Authors: Huang, Rui-Lan, et.al. .
Journal: Clinical cancer research : an official journal of the American Association for Cancer Research (Clin Cancer Res), Vol. 23 (1): 263-272, 2017 .
Snippet: CONCLUSIONS: This study demonstrates the potential use of methylated BHLHE22/CDO1/CELF4 panel for endometrial cancer screening of cervical scrapings.
Affiliation: Department of Obstetrics and Gynecology, Shuang Ho Hospital, Taipei Medical University, New Taipei, Taiwan. Translational epigenetic center, Shuang Ho Hospital, Taipei Medical University, New Taipei, Taiwan. Department of Obstetrics and Gynecology, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan. Department of Obstetrics and Gynecology, Wan Fang Hospital, Taipei Medical University, Taipei, Taiwan. Molecular Medicine, University of Texas, Health Science Center, San Antonio, Texas. Department of Public Health and Primary Care, Cardiovascular Epidemiology Unit, Strangeways Research Laboratory, University of Cambridge, Cambridge, United Kingdom. Department of Obstetrics and Gynecology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan. Cancer Therapy and Research Center and Departments, University of Texas, Health Science Center, San Antonio, Texas. Department of Obstetrics and Gynecology, Shuang Ho Hospital, Taipei Medical University, New Taipei, Taiwan. hclai@s.tmu.edu.tw hclai30656@gmail.com. Department and Graduate Institute of Biochemistry, National Defense Medical Center, Taipei, Taiwan. .
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7: Title: Service utilisation and costs of language impairment in children: The early language in Victoria Australian population-based study.
Authors: Le, Ha N D, et.al. .
Journal: International journal of speech-language pathology (Int J Speech Lang Pathol), Vol. 19 (4): 360-369, 2017 .
Snippet: Depending on age, the Australian adapted Clinical Evaluation of Language Fundamentals - Pre-school, 2nd Edition (CELF-P2) or the CELF, 4th Edition (CELF4) was used to assess expressive and receptive language.
Affiliation: a Population Health Strategic Research Center , Deakin Health Economics, Deakin University , Burwood , Victoria , Australia. b Center for Community Child Health , The Royal Children's Hospital , Parkville , Victoria , Australia. c Murdoch Children's Research Institute , The Royal Children's Hospital , Parkville , Victoria , Australia. d Department of Paediatrics , The University of Melbourne , Melbourne , Victoria , Australia. e Melbourne Graduate School of Education , University of Melbourne , Melbourne , Victoria , Australia. f School of Psychology and Public Health , La Trobe University , Melbourne , Victoria , Australia. g Faculty of Medicine, Melbourne School of Psychological Sciences , Dentistry, and Health Sciences, University of Melbourne , Melbourne , Victoria , Australia , and. h Menzies Health Institute Queensland , Griffith University , QLD , Australia. .
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8: Title: Genome-wide analysis of over 106 000 individuals identifies 9 neuroticism-associated loci.
Authors: Smith, D J, et.al. .
Journal: Molecular psychiatry (Mol Psychiatry), Vol. 21 (6): 749-57, 2016 .
Snippet: Other associated loci included interesting candidate genes on chromosome 1 (GRIK3 (glutamate receptor ionotropic kainate 3)), chromosome 4 (KLHL2 (Kelch-like protein 2)), chromosome 17 (CRHR1 (corticotropin-releasing hormone receptor 1) and MAPT (microtubule-associated protein Tau)) and on chromosome 18 (CELF4 (CUGBP elav-like family member 4)).
Affiliation: Institute of Health and Wellbeing, University of Glasgow, Glasgow, UK. MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK. Centre for Cognitive Ageing and Cognitive Epidemiology, Department of Psychology, University of Edinburgh, Edinburgh, UK. School of Life Sciences, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK. QIMR Berghofer Medical Research Institute, Herston, QLD, Australia. Medical Research Council Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK. MRC Lifecourse Epidemiology Unit, University of Southampton, Southampton General Hospital, Southampton, UK. Generation Scotland, Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK. Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA. Analytical and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA. Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA. Division of Psychiatry, University of Edinburgh, Edinburgh, UK. Division of Population Health Sciences, University of Dundee, Dundee, UK. Medical Genetics Section, Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK. .
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9: Title: Impacts of Salmonella enterica Serovar Typhimurium and Its speG Gene on the Transcriptomes of In Vitro M Cells and Caco-2 Cells.
Authors: Wang, Ke-Chuan, et.al. .
Journal: PloS one, Vol. 11 (4): e0153444, 2016 .
Snippet: The immune responses of in vitro M cells and Caco-2 cells can differ and reply on speG or not, with speG-dependent regulation of KYL4, SCTR, IL6, TNF, and CELF4 in Caco-2 cells, JUN, KLF6, and KCTD11 in M cells, or speG-independent modulation of ZFP36 in both cells.
Affiliation: Division of Pediatric Gastroenterology and Hepatology, Department of Pediatrics, Shuang Ho Hospital, Taipei Medical University, Taipei, Taiwan. Department of Pediatrics, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan. Graduate Institute of Biochemical and Biomedical Engineering, National Taipei University of Technology, Taipei, Taiwan. .
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10: Title: Clinical and Genetic Determinants of Cardiomyopathy Risk among Hematopoietic Cell Transplantation Survivors.
Authors: Leger, Kasey J, et.al. .
Journal: Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation (Biol Blood Marrow Transplant), Vol. 22 (6): 1094-101, 2016 .
Snippet: We replicated several previously reported genetic associations among early-onset cardiomyopathy cases, including rs1786814 in CELF4, rs2232228 in HAS3, and rs17863783 in UGT1A6.
Affiliation: Department of Pediatrics, University of Washington, Seattle Children's Hospital, Seattle, Washington. Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington. Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington; Department of Medicine, University of Washington, Seattle, Washington. Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington. Department of Pediatrics, University of Washington, Seattle Children's Hospital, Seattle, Washington; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington. Electronic address: ericchow@u.washington.edu. .
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11: Title: CELF4 Variant and Anthracycline-Related Cardiomyopathy: A Children's Oncology Group Genome-Wide Association Study.
Authors: Wang, Xuexia, et.al. .
Journal: Journal of clinical oncology : official journal of the American Society of Clinical Oncology (J Clin Oncol), Vol. 34 (8): 863-70, 2016 .
Snippet: CONCLUSION: We report a modifying effect of a polymorphism of CELF4 (rs1786814) on the dose-dependent association between anthracyclines and cardiomyopathy, which possibly occurs through a pathway that involves the expression of abnormally spliced TNNT2 variants.
Affiliation: Xuexia Wang, University of Wisconsin-Milwaukee, Milwaukee, WI; Can-Lan Sun, Molly Mather, Saro H. Armenian, City of Hope, Duarte; Jerome I. Rotter, Kent D. Taylor, Yii-Der Ida Chen, Los Angeles Biomedical Research Institute at Harbor-University of California, Los Angeles, Torrance, CA; Adolfo Quiñones-Lombraña, Javier G. Blanco, State University of New York at Buffalo, Buffalo; Kevin C. Oeffinger, Memorial Sloan Kettering Cancer Center, New York, NY; Purnima Singh, Wendy Landier, Lindsey Hageman, Smita Bhatia, University of Alabama at Birmingham, Birmingham, AL; Naomi Winick, University of Texas Southwestern Medical Center, Dallas; Zoann E. Dreyer, Texas Children's Cancer Center, Houston, TX; Jill P. Ginsberg, Childrens Hospital of Philadelphia, Philadelphia, PA; Joseph P. Neglia, University of Minnesota, Minneapolis, MN; Sharon M. Castellino, Emory University and Children's Healthcare of Atlanta, Atlanta, GA; and Melissa M. Hudson, Leslie L. Robison, St Jude Children's Research Hospital, Memphis, TN. Xuexia Wang, University of Wisconsin-Milwaukee, Milwaukee, WI; Can-Lan Sun, Molly Mather, Saro H. Armenian, City of Hope, Duarte; Jerome I. Rotter, Kent D. Taylor, Yii-Der Ida Chen, Los Angeles Biomedical Research Institute at Harbor-University of California, Los Angeles, Torrance, CA; Adolfo Quiñones-Lombraña, Javier G. Blanco, State University of New York at Buffalo, Buffalo; Kevin C. Oeffinger, Memorial Sloan Kettering Cancer Center, New York, NY; Purnima Singh, Wendy Landier, Lindsey Hageman, Smita Bhatia, University of Alabama at Birmingham, Birmingham, AL; Naomi Winick, University of Texas Southwestern Medical Center, Dallas; Zoann E. Dreyer, Texas Children's Cancer Center, Houston, TX; Jill P. Ginsberg, Childrens Hospital of Philadelphia, Philadelphia, PA; Joseph P. Neglia, University of Minnesota, Minneapolis, MN; Sharon M. Castellino, Emory University and Children's Healthcare of Atlanta, Atlanta, GA; and Melissa M. Hudson, Leslie L. Robison, St Jude Children's Research Hospital, Memphis, TN. sbhatia@peds.uab.edu. .
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12: Title: Improving comprehension in adolescents with severe receptive language impairments: a randomized control trial of intervention for coordinating conjunctions.
Authors: Ebbels, Susan H, et.al. .
Journal: International journal of language & communication disorders / Royal College of Speech & Language Therapists (J Commun Disord), Vol. 49 (1): 30-48, 2014 Jan-Feb .
Snippet: METHODS & PROCEDURES: Fourteen participants (aged 11;3-16;1) with severe RELI (mean standard scores: CELF4 ELS = 48, CELF4 RLS = 53 and TROG-2 = 57), but higher non-verbal (Matrices = 83) and visual perceptual skills (Test of Visual Perceptual Skills (TVPS) = 86) were randomly assigned to two groups: therapy versus waiting controls.
Affiliation: Moor House School, Oxted, UK; Division of Psychology and Language Sciences, University College London, London, UK. .
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13: Title: Prenatal diagnosis of de novo interstitial deletions involving 5q23.1-q23.3 and 18q12.1-q12.3 by array CGH using uncultured amniocytes in a pregnancy with fetal interrupted aortic arch and atrial septal defect.
Authors: Chen, Chih-Ping, et.al. .
Journal: Gene, Vol. 531 (2): 496-501, 2013 .
Snippet: We discuss the genotype-phenotype correlation and the consequence of haploinsufficiency of FBN2, DTNA and CELF4 in this case.
Affiliation: Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan; Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan; Department of Medicine, Mackay Medical College, New Taipei City, Taiwan; Department of Biotechnology, Asia University, Taichung, Taiwan; School of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung, Taiwan; Institute of Clinical and Community Health Nursing, National Yang-Ming University, Taipei, Taiwan; Department of Obstetrics and Gynecology, School of Medicine, National Yang-Ming University, Taipei, Taiwan. Electronic address: cpc_mmh@yahoo.com. .
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14: Title: The expression analysis of Sfrs10 and Celf4 during mouse retinal development.
Journal: Gene expression patterns : GEP (Gene Expr Patterns), Vol. 13 (8): 425-36, 2013 .
Snippet: Here we report the expression of an ASF, serine-arginine rich splicing factor 10 (Sfrs10) and a mRNA translation regulation factor, CUGBP, elav like family member 4 (Celf4) in the developing mouse retina.
Affiliation: Department of Physiology and Neurobiology, University of Connecticut, Storrs, CT 06269, United States. .
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15: Title: Development of GMDR-GPU for gene-gene interaction analysis and its application to WTCCC GWAS data for type 2 diabetes.
Authors: Zhu, Zhixiang, et.al. .
Journal: PloS one, Vol. 8 (4): e61943, 2013 .
Snippet: Through an exhaustive search of pair-wise interactions and a selected search of three- to five-way interactions conditioned on significant pair-wise results, we identified 24 core SNPs in six genes (FTO: rs9939973, rs9940128, rs9922047, rs1121980, rs9939609, rs9930506; TSPAN8: rs1495377; TCF7L2: rs4074720, rs7901695, rs4506565, rs4132670, rs10787472, rs11196205, rs10885409, rs11196208; L3MBTL3: rs10485400, rs4897366; CELF4: rs2852373, rs608489; RUNX1: rs445984, rs1040328, rs990074, rs2223046, rs2834970) that appear to be important for T2D.
Affiliation: Institute of Bioinformatics, Zhejiang University, Hangzhou, China. .
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16: Title: CELF4 regulates translation and local abundance of a vast set of mRNAs, including genes associated with regulation of synaptic function.
Authors: Wagnon, Jacy L, et.al. .
Journal: PLoS genetics (Plos Genet), Vol. 8 (11): e1003067, 2012 .
Snippet: Among biological processes associated with CELF4 targets that accumulate in neuropil of mutants, regulation of synaptic plasticity and transmission are the most prominent.
Affiliation: The Jackson Laboratory, Bar Harbor, Maine, United States of America. .
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17: Title: Aberrant sodium channel activity in the complex seizure disorder of Celf4 mutant mice.
Authors: Sun, Wenzhi, et.al. .
Journal: The Journal of physiology (J Physiol), Vol. 591 (1): 241-55, 2013 .
Snippet: Mice deficient for CELF4, a neuronal RNA-binding protein, have a complex seizure disorder that includes both convulsive and non-convulsive seizures, and is dependent upon Celf4 gene dosage and mouse strain background.
Affiliation: The Jackson Laboratory, 600 Main Street, Bar Harbor, ME 04609-1500, USA. .
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18: Title: Haploinsufficiency of CELF4 at 18q12.2 is associated with developmental and behavioral disorders, seizures, eye manifestations, and obesity.
Authors: Halgren, Christina, et.al. .
Journal: European journal of human genetics : EJHG (Eur J Hum Genet), Vol. 20 (12): 1315-9, 2012 .
Snippet: Our study illustrates the utility of high-resolution genome-wide techniques in identifying neurodevelopmental and neurobehavioral genes, and it adds to the growing evidence, including a transgenic mouse model, that CELF4 is important for human brain development.
Affiliation: Department of Cellular and Molecular Medicine, Wilhelm Johannsen Centre for Functional Genome Research, University of Copenhagen, Faculty of Health Sciences, Copenhagen, Denmark. halgren@sund.ku.dk .
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19: Title: Development of a method for the purification and culture of rodent astrocytes.
Authors: Foo, Lynette C, et.al. .
Journal: Neuron, Vol. 71 (5): 799-811, 2011 .
Snippet: Whereas astrocyte progenitor cells can be cultured from neonatal brain, culture of mature astrocytes from postnatal brain has not been possible.
Affiliation: Stanford University School of Medicine, Department of Neurobiology, Stanford, CA 94305, USA. lfoo@stanford.edu .
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20: Title: Etiology of a genetically complex seizure disorder in Celf4 mutant mice.
Authors: Wagnon, J L, et.al. .
Journal: Genes, brain, and behavior (Genes Brain Behav), Vol. 10 (7): 765-77, 2011 .
Snippet: Mice deficient for the gene encoding the RNA-binding protein CELF4 (CUGBP, ELAV-like family member 4) have a complex seizure phenotype that includes both convulsive and non-convulsive seizures, depending upon gene dosage and strain background, modeling genetically complex epilepsy.
Affiliation: The Jackson Laboratory, Bar Harbor, ME 04609-1500, USA. .
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