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40 documents found
1: 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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2: 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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3: 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: In this study, the Netrin G1 (Ntng1) expression was investigated in the nucleus accumbens of mice primarily conditioned to cocaine using a place preference paradigm.
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. .
Antibodies OnlineNetrin G1 (NTNG1) .
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4: 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. .
5: 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. .
6: 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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7: 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. .
8: 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. .
9: 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. .
10: 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: This is a case-control study of the association of NTNG1 subtypes with schizophrenia among a group of individuals from a Caucasian population.
Affiliation: Department of Psychiatry, University of Arizona, Tucson, Arizona, USA. .
Antibodies OnlineNetrin G1 (NTNG1) .
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11: 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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12: 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. .
13: 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. .
14: 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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15: 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. .
16: 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. .
17: 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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18: 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: Our finding nominates the minor G allele of the NTNG1 rs628117 single nucleotide polymorphism as a risk factor for ischemic stroke at least in Armenian population.
Affiliation: Institute of Molecular Biology, National Academy of Sciences of the Republic of Armenia (NAS RA), Armenia. .
Antibodies OnlineNetrin G1 (NTNG1) .
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19: 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. .
20: Title: CDKL5 ensures excitatory synapse stability by reinforcing NGL-1-PSD95 interaction in the postsynaptic compartment and is impaired in patient iPSC-derived neurons.
Authors: Ricciardi, Sara, et.al. .
Journal: Nature cell biology (Nat Cell Biol), Vol. 14 (9): 911-23, 2012 .
Snippet: Mutations of the cyclin-dependent kinase-like 5 (CDKL5) and netrin-G1 (NTNG1) genes cause a severe neurodevelopmental disorder with clinical features that are closely related to Rett syndrome, including intellectual disability, early-onset intractable epilepsy and autism.
Affiliation: Stem Cell and Neurogenesis Unit, Division of Neuroscience, San Raffaele Scientific Institute, Via Olgettina 58, 20132 Milan, Italy. .
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