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41 documents found
1: Title: Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis.
Authors: Schormair, Barbara, et.al. .
Journal: The Lancet. Neurology (Lancet Neurol), Vol. 16 (11): 898-907, 2017 .
Snippet: Gene prioritisation, enrichment, and genetic correlation analyses showed that identified pathways were related to neurodevelopment and highlighted genes linked to axon guidance (associated with SEMA6D), synapse formation (NTNG1), and neuronal specification (HOXB cluster family and MYT1).
Affiliation: Institute of Neurogenomics, Helmholtz Zentrum München, German Research Centre for Environmental Health, Neuherberg, Germany. National Institute for Health Research Blood and Transplant Unit in Donor Health and Genomics at the University of Cambridge, Strangeways Research Laboratory, University of Cambridge, Cambridge, UK; MRC/BHF Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, Strangeways Research Laboratory, University of Cambridge, Cambridge, UK; National Institute for Health Research Cambridge Biomedical Research Centre, Cambridge, UK. Max Planck Institute of Psychiatry, Munich, Germany. Sleep-Wake Disorders Centre, Department of Neurology, Hôpital Gui-de-Chauliac, INSERM U1061, CHU Montpellier, France. Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria. Department of Neurology and Centre of Clinical Neuroscience, First Faculty of Medicine and General University Hospital in Prague, Charles University, Prague, Czech Republic. Department of Neurology, Paracelsus Klinik, Osnabrueck, Germany. Department of Clinical Neurophysiology, University Medical Centre, Georg August University Göttingen, Göttingen, Germany. Clinic for Neurosurgery, University Medical Centre, Georg August University Göttingen, Göttingen, Germany; Paracelsus-Elena Hospital, Centre of Parkinsonism and Movement Disorders, Kassel, Germany. Institute of Neurogenomics, Helmholtz Zentrum München, German Research Centre for Environmental Health, Neuherberg, Germany; Department of Neurology, Philipps University Marburg, Marburg, Germany. Department of Neurology, University of Ulm, Ulm, Germany; Neuropsychiatry Centre Erding/München, Erding, Germany. Estonian Genome Centre, University of Tartu and Estonian Biocentre, Tartu, Estonia. Laboratory of Neurogenetics, Department of Neurology, Faculty of Medicine, University of Thessaly, University Hospital of Larissa, Biopolis, Larissa, Greece. Unesta Research Centre, Tampere, Finland; Department of Pulmonary Diseases, Tampere University Hospital, Tampere, Finland. Department of Cardiology and Angiology, Centre of Sleep Medicine, Charité-Universitätsmedizin Berlin, Berlin, Germany. Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA. Department of Neurology, Mayo Clinic, Jacksonville, FL, USA. National Institute for Health Research Blood and Transplant Unit in Donor Health and Genomics at the University of Cambridge, Strangeways Research Laboratory, University of Cambridge, Cambridge, UK; MRC/BHF Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, Strangeways Research Laboratory, University of Cambridge, Cambridge, UK; National Institute for Health Research Cambridge Biomedical Research Centre, Cambridge, UK; British Heart Foundation Centre of Excellence, Division of Cardiovascular Medicine, Addenbrooke's Hospital, Cambridge, UK. National Institute for Health Research Blood and Transplant Unit in Donor Health and Genomics at the University of Cambridge, Strangeways Research Laboratory, University of Cambridge, Cambridge, UK; Department of Haematology, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK; Department of Human Genetics, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, UK. National Institute for Health Research Blood and Transplant Unit in Donor Health and Genomics at the University of Cambridge, Strangeways Research Laboratory, University of Cambridge, Cambridge, UK; Department of Haematology, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK; NHS Blood and Transplant, Cambridge, UK; British Heart Foundation Centre of Excellence, Division of Cardiovascular Medicine, Addenbrooke's Hospital, Cambridge, UK; Department of Human Genetics, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, UK. NHS Blood and Transplant, Oxford, UK; Radcliffe Department of Medicine, BRC Haematology Theme and NHS Blood and Transplant, John Radcliffe Hospital, Headington, Oxford, UK; Department of Haematology and BRC Haematology Theme, Churchill Hospital, Oxford, UK. National Institute for Health Research Blood and Transplant Unit in Donor Health and Genomics at the University of Cambridge, Strangeways Research Laboratory, University of Cambridge, Cambridge, UK; MRC/BHF Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, Strangeways Research Laboratory, University of Cambridge, Cambridge, UK; National Institute for Health Research Cambridge Biomedical Research Centre, Cambridge, UK; British Heart Foundation Centre of Excellence, Division of Cardiovascular Medicine, Addenbrooke's Hospital, Cambridge, UK; Department of Human Genetics, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, UK. Center for Restless Legs Study, Department of Neurology, Johns Hopkins University, Baltimore, MD, USA. Department of Neurology, Methodist Neurological Institute, Houston, TX, USA. Laboratoire de Neurogénétique, Centre de Recherche, Institut Universitaire en Santé Mentale de Montréal, Montréal, QC, Canada; Département de Psychiatrie, Université de Montréal, Montréal, QC, Canada; Department of Neurology and Neurosurgery, McGill University, Montréal, QC, Canada. Département de Psychiatrie, Université de Montréal, Montréal, QC, Canada; Hôpital du Sacré-Coeur de Montréal, 67120, Center for Advanced Research in Sleep Medicine, Montréal, QC, Canada. Department of Neurology and Neurosurgery, McGill University, Montréal, QC, Canada; Montreal Neurological Institute, McGill University, Montréal, QC, Canada. Department of Health, National Institute for Health and Welfare, Helsinki, Finland; Institute of Molecular Medicine FIMM, University of Helsinki, Helsinki, Finland. Department of Molecular Biology of Cancer, Institute of Experimental Medicine, Academy of Science of Czech Republic, Prague, Czech Republic; Biomedical Centre, Faculty of Medicine in Pilsen, Charles University in Prague, Pilsen, Czech Republic. Inserm UMR1087, CNRS UMR 6291, Institut du Thorax, Nantes, France; Centre Hospitalier Universitaire (CHU) Nantes, Université de Nantes, France. Institute of Clinical Molecular Biology, Kiel University, Kiel, Germany. PopGen Biobank and Institute of Epidemiology, Christian Albrechts University Kiel, Kiel, Germany. John and Jennifer Ruddy Canadian Cardiovascular Genetics Centre, University of Ottawa Heart Institute, Ottawa, ON, Canada. Department of Medicine, Duke University School of Medicine, Durham, NC, USA; Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC, USA. Institute of Epidemiology II, Helmholtz Zentrum München, German Research Centre for Environmental Health, Neuherberg, Germany; Research Unit of Molecular Epidemiology, Helmholtz Zentrum München, German Research Centre for Environmental Health, Neuherberg, Germany; German Centre for Diabetes Research (DZD), Neuherberg, Germany. Institute of Epidemiology II, Helmholtz Zentrum München, German Research Centre for Environmental Health, Neuherberg, Germany; German Centre for Diabetes Research (DZD), Neuherberg, Germany; German Centre for Cardiovascular Disease Research (DZHK), Berlin, Germany. Department of Neurology and Neurosurgery, McGill University, Montréal, QC, Canada; Department of Human Genetics, McGill University, Montréal, QC, Canada; Montreal Neurological Institute, McGill University, Montréal, QC, Canada. Institute of Epidemiology and Social Medicine, University of Münster, Münster, Germany. National Institute for Health Research Blood and Transplant Unit in Donor Health and Genomics at the University of Cambridge, Strangeways Research Laboratory, University of Cambridge, Cambridge, UK; MRC/BHF Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, Strangeways Research Laboratory, University of Cambridge, Cambridge, UK; NHS Blood and Transplant, Cambridge, UK; National Institute for Health Research Cambridge Biomedical Research Centre, Cambridge, UK; British Heart Foundation Centre of Excellence, Division of Cardiovascular Medicine, Addenbrooke's Hospital, Cambridge, UK. 23andMe, Mountain View, CA, USA. Max Planck Institute of Psychiatry, Munich, Germany; Munich Cluster for Systems Neurology (SyNergy), Munich, Germany; Institute of Translational Medicine, University of Liverpool, Liverpool, UK. Institute of Neurogenomics, Helmholtz Zentrum München, German Research Centre for Environmental Health, Neuherberg, Germany; Munich Cluster for Systems Neurology (SyNergy), Munich, Germany; Institute of Human Genetics, Technische Universität München, Munich, Germany; Neurologische Klinik und Poliklinik, Klinikum rechts der Isar der Technischen Universität München, Munich, Germany. Electronic address: juliane.winkelmann@tum.de. .
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2: Title: A prognostic mutation panel for predicting cancer recurrence in stages II and III colorectal cancer.
Authors: Sho, Shonan, et.al. .
Journal: Journal of surgical oncology (J Surg Oncol), 2017 .
Snippet: RESULTS: We identified five prognostic genes (APAF1, DIAPH2, NTNG1, USP7, and VAV2), which were combined to form a prognostic mutation panel.
Affiliation: Department of Surgery, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California. Department of Surgery, VA Greater Los Angeles Healthcare System, Los Angeles, California. UCLA Center for Pancreatic Diseases, Los Angeles, California. .
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3: Title: Hyper-Methylated Loci Persisting from Sessile Serrated Polyps to Serrated Cancers.
Authors: Andrew, Angeline S, et.al. .
Journal: International journal of molecular sciences (Int J Mol Sci), Vol. 18 (3), 2017 .
Snippet: Hyper-methylated CpG loci included the known the tumor suppressor gene RET (p = 5.72 x 10-10), as well as loci in differentially methylated regions for GSG1L, MIR4493, NTNG1, MCIDAS, ZNF568, and RERG.
Affiliation: Norris Cotton Cancer Center, Geisel School of Medicine at Dartmouth, 7936 One Medical Center Drive, Lebanon, NH 03756, USA. Angeline.Andrew@dartmouth.edu. Norris Cotton Cancer Center, Geisel School of Medicine at Dartmouth, 7936 One Medical Center Drive, Lebanon, NH 03756, USA. John.A.Baron@dartmouth.edu. Department of Medicine, University of North Carolina School of Medicine, Chapel Hill, NC 27599, USA. John.A.Baron@dartmouth.edu. Norris Cotton Cancer Center, Geisel School of Medicine at Dartmouth, 7936 One Medical Center Drive, Lebanon, NH 03756, USA. Lynn.F.Butterly@dartmouth.edu. Norris Cotton Cancer Center, Geisel School of Medicine at Dartmouth, 7936 One Medical Center Drive, Lebanon, NH 03756, USA. Arief.A.Suriawinata@dartmouth.edu. Norris Cotton Cancer Center, Geisel School of Medicine at Dartmouth, 7936 One Medical Center Drive, Lebanon, NH 03756, USA. Gregory.J.Tsongalis@hitchcock.org. Norris Cotton Cancer Center, Geisel School of Medicine at Dartmouth, 7936 One Medical Center Drive, Lebanon, NH 03756, USA. Christina.M.Robinson@dartmouth.edu. Norris Cotton Cancer Center, Geisel School of Medicine at Dartmouth, 7936 One Medical Center Drive, Lebanon, NH 03756, USA. Christopher.I.Amos@dartmouth.edu. .
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4: Title: Netrin G1: its downregulation in the nucleus accumbens of cocaine-conditioned mice and genetic association in human cocaine dependence.
Authors: Kelaï, Sabah, et.al. .
Journal: Addiction biology (Addict Biol), 2017 .
Snippet: A genetic association study was then conducted on 146 multiplex families of the Collaborative study on Genetics of Alcoholism, in which seven single nucleotide polymorphisms located in the NTNG1 gene were genotyped.
Affiliation: INSERM U894, Centre de Psychiatrie & Neurosciences, University Paris Descartes, Paris, France. Centre National de la Recherche Scientifique, Unité Mixte de Recherche, France. Institut national de la santé et de la recherche médicale, Paris, France. Université Paris Descartes, Laboratoire de Neuropsychopharmacologie des Addictions, France. McGill Group for Suicide Studies, Douglas Mental Health University Institute, McGill University, Canada. Centre de Génétique Moléculaire, FRE 3144, CNRS and Gif/Orsay DNA Microarray Platform (GODMAP), France. Hôpital Sainte-Anne (CMME), University Paris Descartes, France. .
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5: Title: Targeted next generation sequencing: the diagnostic value in early-onset epileptic encephalopathy.
Authors: Gokben, Sarenur, et.al. .
Journal: Acta neurologica Belgica (Acta Neurol Belg), Vol. 117 (1): 131-138, 2017 .
Snippet: An early-onset EE gene panel including sixteen genes (ARX, CDKL5, CNTNAP2, FOLR1, FOXG1, LAMC3, MBD5, MECP2, NTNG1, PCDH19, PNKP, SCN1A, SCN1B, SCN2A, STXBP1, KCNQ2) was constituted.
Affiliation: Division of Child Neurology, Department of Pediatrics, Faculty of Medicine, Ege University, 35100, Izmir, Turkey. Department of Medical Genetics, Faculty of Medicine, Ege University, Izmir, Turkey. Division of Child Neurology, Department of Pediatrics, Faculty of Medicine, Ege University, 35100, Izmir, Turkey. sanem.yilmaz@ege.edu.tr. Division of Pediatric Genetics, Department of Pediatrics, Faculty of Medicine, Ege University, Izmir, Turkey. .
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6: Title: Shared Genetic Factors Involved in Celiac Disease, Type 2 Diabetes and Anorexia Nervosa Suggest Common Molecular Pathways for Chronic Diseases.
Authors: Mostowy, Joanna, et.al. .
Journal: PloS one, Vol. 11 (8): e0159593, 2016 .
Snippet: RESULTS: A total of eleven of genes were differently expressed in celiac patients compared with disease controls of which CD36, CD38, FOXP1, SELL, PPARA, PPARG, AGT previously associated with type 2 diabetes and AKAP6, NTNG1 with anorexia nervosa remained significant after correction for multiple testing.
Affiliation: Institute of Biomedicine, The Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden. Diabetes and Celiac Disease Unit, Department of Clinical Sciences, Lund University, Malmö, Sweden. Institute of Clinical Sciences, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden. Department of Pediatric Gastroenterology, Hepatology and Nutrition, Karolinska University Hospital and Division of Pediatrics, CLINTEC, Karolinska Institutet, Stockholm, Sweden. Department of Clinical Science and Education, Karolinska Institutet, Sodersjukhuset, Stockholm, Sweden. Department of Mathematical Sciences, Chalmers University of Technology, Gothenburg, Sweden. .
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7: Title: Diversification of behavior and postsynaptic properties by netrin-G presynaptic adhesion family proteins.
Authors: Zhang, Qi, et.al. .
Journal: Molecular brain (Mol Brain), Vol. 9, 2016 .
Snippet: We found that two netrin-G paralogs that recently diverged in evolution, netrin-G1 and netrin-G2 (gene symbols: Ntng1 and Ntng2, respectively), were responsible for complementary behavioral functions.
Affiliation: Laboratory for Behavioral Genetics, RIKEN Brain Science Institute, 2-1 Hirosawa, Wako, Saitama, 351-0198, Japan. zhangqi@brain.riken.jp. Laboratory for Behavioral Genetics, RIKEN Brain Science Institute, 2-1 Hirosawa, Wako, Saitama, 351-0198, Japan. gotohiromichi@brain.riken.jp. Laboratory for Behavioral Genetics, RIKEN Brain Science Institute, 2-1 Hirosawa, Wako, Saitama, 351-0198, Japan. sachiko.akiyoshi@gen.mpg.de. Laboratory for Behavioral Genetics, RIKEN Brain Science Institute, 2-1 Hirosawa, Wako, Saitama, 351-0198, Japan. prosselkov@brain.riken.jp. Laboratory for Behavioral Genetics, RIKEN Brain Science Institute, 2-1 Hirosawa, Wako, Saitama, 351-0198, Japan. sano@brain.riken.jp. Laboratory for Behavioral Genetics, RIKEN Brain Science Institute, 2-1 Hirosawa, Wako, Saitama, 351-0198, Japan. mtkwh40bg@brain.riken.jp. Laboratory for Behavioral Genetics, RIKEN Brain Science Institute, 2-1 Hirosawa, Wako, Saitama, 351-0198, Japan. yaguchi0401@gmail.com. Laboratory for Behavioral Genetics, RIKEN Brain Science Institute, 2-1 Hirosawa, Wako, Saitama, 351-0198, Japan. nakashib@brain.riken.jp. Laboratory for Behavioral Genetics, RIKEN Brain Science Institute, 2-1 Hirosawa, Wako, Saitama, 351-0198, Japan. sitohara@brain.riken.jp. .
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8: Title: Brain-specific transcriptional regulator T-brain-1 controls brain wiring and neuronal activity in autism spectrum disorders.
Authors: Huang, Tzyy-Nan, et.al. .
Journal: Frontiers in neuroscience (Front Neurosci), Vol. 9, 2015 .
Snippet: In addition to Grin2b, cell adhesion molecules-including Ntng1, Cdh8, and Cntn2-are also regulated by TBR1 to control axonal projections of amygdala.
Affiliation: Institute of Molecular Biology, Academia Sinica Taipei, Taiwan. .
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9: Title: Ethanol-related alterations in gene expression patterns in the developing murine hippocampus.
Authors: Mandal, Chanchal, et.al. .
Journal: Acta biochimica et biophysica Sinica (Acta Biochim Biophys Sin (shanghai)), Vol. 47 (8): 581-7, 2015 .
Snippet: Microarray analysis revealed that Nova1, Ntng1, Gal, Neurog2, Neurod2, and Fezf2 gene expressions are altered in the fetal hippocampus.
Affiliation: Department of Molecular and Life Science, Hanyang University, Ansan, Republic of Korea. Department of Molecular and Life Science, Hanyang University, Ansan, Republic of Korea Institute of Natural Science and Technology, Hanyang University, Ansan, Republic of Korea ygchai@hanyang.ac.kr khjung2@gmail.com. Department of Molecular and Life Science, Hanyang University, Ansan, Republic of Korea Department of Nanobiotechnology, Hanyang University, Seoul, Republic of Korea ygchai@hanyang.ac.kr khjung2@gmail.com. .
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10: Title: T-Brain-1--A Potential Master Regulator in Autism Spectrum Disorders.
Authors: Chuang, Hsiu-Chun, et.al. .
Journal: Autism research : official journal of the International Society for Autism Research (Autism Res), Vol. 8 (4): 412-26, 2015 .
Snippet: A further five of the 24 genes (Cd44, Cdh8, Cntn6, Gpc6, and Ntng1) encode membrane proteins that regulate cell adhesion and axonal outgrowth.
Affiliation: Graduate Institute of Life Sciences, National Defense Medical Center. Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan. .
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11: Title: Replication of NTNG1 association in schizophrenia.
Authors: Wilcox, James A, et.al. .
Journal: Psychiatric genetics (Psychiatr Genet), Vol. 24 (6): 266-8, 2014 .
Snippet: Netrins including NTNG1 are known to be axon guidance factors in the developing brain.
Affiliation: Department of Psychiatry, University of Arizona, Tucson, Arizona, USA. .
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12: Title: Identification of transcriptional regulatory elements for Ntng1 and Ntng2 genes in mice.
Authors: Yaguchi, Kunio, et.al. .
Journal: Molecular brain (Mol Brain), Vol. 7, 2014 .
Snippet: The Ntng1 and Ntng2 genes, encoding axonal membrane adhesion proteins netrin-G1 and netrin-G2, respectively, are paralogs that have evolved in vertebrates and are expressed in distinct neuronal subsets in a complementary manner.
Affiliation: RIKEN Brain Science Institute, 2-1 Hirosawa, Wako, Saitama, Japan. sitohara@brain.riken.jp. .
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13: Title: A genome-wide association study of calf birth weight in Holstein cattle using single nucleotide polymorphisms and phenotypes predicted from auxiliary traits.
Authors: Cole, J B, et.al. .
Journal: Journal of dairy science (J Dairy Sci), Vol. 97 (5): 3156-72, 2014 .
Snippet: Several SNP related to growth and development were found among the 25 SNP with the largest effects, including markers located within or near (≤ 100 kbp) ABCA12, FLRT2, LHX4, MAP3K5, NRAC, NTNG1, PIGN, and ZNF75A.
Affiliation: Animal Improvement Programs Laboratory, Agricultural Research Service, USDA, Beltsville, MD 20705-2350. Electronic address: john.cole@ars.usda.gov. Institute of Agricultural and Nutritional Sciences, Martin-Luther-University Halle-Wittenberg, Theodor-Lieser-Str. 11, D-06120 Halle / Saale, Germany. Animal Improvement Programs Laboratory, Agricultural Research Service, USDA, Beltsville, MD 20705-2350. .
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14: Title: Tbr1 haploinsufficiency impairs amygdalar axonal projections and results in cognitive abnormality.
Authors: Huang, Tzyy-Nan, et.al. .
Journal: Nature neuroscience (Nat Neurosci), Vol. 17 (2): 240-7, 2014 .
Snippet: Loss of a copy of the Tbr1 gene altered the expression of Ntng1, Cntn2 and Cdh8 and reduced both inter- and intra-amygdalar connections.
Affiliation: 1] Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan. [2]. 1] Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan. [2] Graduate Institute of Life Sciences, National Defense Medical Center, Taipei, Taiwan. [3]. Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan. Institute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan. 1] Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan. [2] Graduate Institute of Life Sciences, National Defense Medical Center, Taipei, Taiwan. .
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15: Title: Stress susceptibility-specific phenotype associated with different hippocampal transcriptomic responses to chronic tricyclic antidepressant treatment in mice.
Authors: Lisowski, Pawel, et.al. .
Journal: BMC neuroscience (Bmc Neurosci), Vol. 14, 2013 .
Snippet: We observed the upregulation of Igf2 and the genes involved in neurogenesis (HA: Sema3f, Ntng1, Gbx2, Efna5, and Rora; LA: Otx2, Rarb, and Drd1a) in both mouse lines.
Affiliation: Department of Molecular Biology, Institute of Genetics and Animal Breeding, Polish Academy of Sciences, Postepu 36A, 05-552, Magdalenka, Jastrzebiec n/Warsaw, Poland. p.lisowski@ighz.pl. .
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16: Title: Transcriptome profile at different physiological stages reveals potential mode for curly fleece in Chinese tan sheep.
Authors: Kang, Xiaolong, et.al. .
Journal: PloS one, Vol. 8 (8): e71763, 2013 .
Snippet: The hair-related important differentially expressed genes (SPINK4, FGF21, ESRα, EphA3, NTNG1 and GPR110) were confirmed by qPCR analysis.
Affiliation: Department of Animal Genetics and Breeding, National Engineering Laboratory for Animal Breeding, MOA Laboratory of Animal Genetics and Breeding, College of Animal Science and Technology, China Agricultural University, Beijing, China ; College of Agriculture, Ningxia University, Yinchuan, People's Republic of China. .
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17: Title: FUS-mediated alternative splicing in the nervous system: consequences for ALS and FTLD.
Authors: Orozco, Denise, et.al. .
Journal: Journal of molecular medicine (Berlin, Germany) (J Mol Med), Vol. 91 (12): 1343-54, 2013 .
Snippet: Several groups have shown that FUS binds broadly to many transcripts in the brain and have also identified a plethora of putative splice targets; however, only ABLIM1, BRAF, Ewing sarcoma protein R1 (EWSR1), microtubule-associated protein tau (MAPT), NgCAM cell adhesion molecule (NRCAM), and netrin G1 (NTNG1) have been identified in at least three of four studies.
Affiliation: German Center for Neurodegenerative Diseases (DZNE), Munich, Germany. .
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18: Title: Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review.
Authors: Chen, Chih-Ping, et.al. .
Journal: Gene, Vol. 529 (1): 169-75, 2013 .
Snippet: We discuss the genotype-phenotype correlation of the involved genes of ALX3, RBM15, NTNG1, SLC25A24, GPSM2, TBX15 and NOTCH2 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 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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19: Title: The netrin G1 gene rs628117 polymorphism is associated with ischemic stroke.
Authors: Stepanyan, Ani, et.al. .
Journal: Neuroscience letters (Neurosci Lett), Vol. 549, 2013 .
Snippet: Genomic DNA samples of ischemic stroke patients and controls were genotyped for netrin G1 gene (NTNG1) rs628117 single nucleotide polymorphism using polymerase chain reaction with sequence-specific primers.
Affiliation: Institute of Molecular Biology, National Academy of Sciences of the Republic of Armenia (NAS RA), Armenia. .
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20: Title: DNA methylation profile dynamics of tissue-dependent and differentially methylated regions during mouse brain development.
Authors: Hirabayashi, Keiji, et.al. .
Journal: BMC genomics, Vol. 14, 2013 .
Snippet: We identified T-DMRs with different DNA methylation statuses between E11.5NSph and E14.5NSph at genes involved in neural development and/or associated with neurological disorders in humans, such as Dclk1, Nrcam, Nfia, and Ntng1.
Affiliation: Laboratory of Cellular Biochemistry, Department of Animal Resource Sciences/Veterinary Medical Sciences, The University of Tokyo, Yayoi 1-1-1, Bunkyo-ku, Tokyo 113-8657, Japan. .
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