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9 documents found
1: Title: Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia Spectrum.
Authors: Karch, Celeste M, et.al. .
Journal: JAMA neurology (Jama Neurol), 2018 .
Snippet: At a conditional FDR P < .05, 22 novel ALS polymorphisms were found, including rs538622 (nearest gene, ERGIC1; P = .03 for ALS and FTD), which modifies BNIP1 expression in human brains (35 of 137 females; mean age, 59 years; P = .001).
Affiliation: Department of Psychiatry, Washington University in St Louis, St Louis, Missouri. Department of Cognitive Sciences, University of California, San Diego, La Jolla. Memory and Aging Center, Department of Neurology, University of California, San Francisco. Department of Neuroscience, Mayo Clinic College of Medicine, Jacksonville, Florida. Department of Translational Neurodegeneration, German Center for Neurodegenerative Diseases, Munich, Germany. Department of Neurology, Technical University of Munich, Munich Cluster for Systems Neurology SyNergy, Munich, Germany. Institut for Humangenetik, Justus-Liebig-Universität, Giessen, Germany. Department of Molecular Neuroscience, Institute of Neurology, University College London, London, United Kingdom. Department of Pathology and Laboratory Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia. Center for Applied Genomics, Abramson Research Center, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania. Division of Human Genetics, Abramson Research Center, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania. Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia. Laboratory of Neurogenetics, Department of Internal Medicine, Texas Tech University Health Sciences Center, Lubbock. Neuroradiology Section, Department of Radiology and Biomedical Imaging, University of California, San Francisco. Department for Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany. Institute for Clinical Epidemiology and Applied Biometry, University of Tübingen, Tübingen, Germany. Norwegian Centre for Mental Disorders Research, Institute of Clinical Medicine, University of Oslo, Oslo, Norway. Division of Mental Health and Addiction, Oslo University Hospital, Oslo, Norway. Department of Neurosciences, University of California, San Diego, La Jolla. Department of Neurosciences and Radiology, University of California, San Diego, La Jolla. .
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2: Title: Differential Expression and Significance of Endoplasmic Reticulum Golgi Intermediate Compartment 1 in Precancerous Gastric Lesions and Gastric Cancer.
Authors: Wang, Furong, et.al. .
Journal: The American journal of the medical sciences (Am J Med Sci), Vol. 355 (3): 228-234, 2018 .
Snippet: BACKGROUND: We investigated the expression of endoplasmic reticulum Golgi intermediate compartment 1 (ERGIC1) in precancerous gastric lesions and gastric cancer and the function of ERGIC in human gastric cancer cell lines.
Affiliation: Department of Pathology, the Second Hospital of Lanzhou University, Lanzhou, China; The Key Laboratory of the Digestive System Tumors of Gansu Province, the Second Hospital of Lanzhou University, Lanzhou, China; Department of General Surgery, the Second Hospital of Lanzhou University, Lanzhou, China. The Key Laboratory of the Digestive System Tumors of Gansu Province, the Second Hospital of Lanzhou University, Lanzhou, China. Department of General Surgery, the Second Hospital of Lanzhou University, Lanzhou, China; School of Life Sciences, Lanzhou University, Lanzhou, China. Department of General Surgery, the Second Hospital of Lanzhou University, Lanzhou, China. School of Life Sciences, Lanzhou University, Lanzhou, China. Department of Pathology, the Second Hospital of Lanzhou University, Lanzhou, China; School of Life Sciences, Lanzhou University, Lanzhou, China. Electronic address: liym@lzu.edu.cn. .
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3: Title: Aberrant DNA-PKcs and ERGIC1 expression may be involved in initiation of gastric cancer.
Authors: Wang, Fu-Rong, et.al. .
Journal: World journal of gastroenterology (World J Gastroenterol), Vol. 23 (33): 6119-6127, 2017 .
Snippet: The expression patterns of ERGIC1 and DNA-PKcs revealed by immunohistochemistry were consistent with the LC-MS/MS results.
Affiliation: School of Life Sciences, Lanzhou University, Lanzhou 730000, Gansu Province, China. Department of General Surgery, Second Hospital of Lanzhou University, Lanzhou 730000, Gansu Province, China. The Key Laboratory of the Digestive System Tumors of Gansu Province, Second Hospital of Lanzhou University, Lanzhou 730000, Gansu Province, China. Department of Pathology, Second Hospital of Lanzhou University, Lanzhou 730000, Gansu Province, China. .
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4: Title: Mutations in ERGIC1 cause Arthrogryposis Multiplex Congenita, Neuropathic type.
Authors: Reinstein, Eyal, et.al. .
Journal: Clinical genetics (Clin Genet), 2017 .
Snippet: Using whole exome sequencing, we have now identified homozygous pathogenic variant in the ERGIC1 gene within the previously defined linked region.
Affiliation: Medical Genetics Institute, Meir Medical Center, Israel. Sackler School of Medicine, Tel Aviv University, Israel. Medical Genetics Institute, Rabin Medical Center, Israel. Cancer Research Center, Chaim Sheba Medical Center, Israel. Medical Genetics institute of Maccabi HMO, Rechovot, Israel. .
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5: Title: Large-effect pleiotropic or closely linked QTL segregate within and across ten US cattle breeds.
Authors: Saatchi, Mahdi, et.al. .
Journal: BMC genomics, Vol. 15, 2014 .
Snippet: Some identified QTL regions harbor genes known to have large effects on a variety of traits in cattle such as PLAG1 and MSTN and others harbor promising candidate genes including NCAPG, ARRDC3, ERGIC1, SH3PXD2B, HMGA2, MSRB3, LEMD3, TIGAR, SEPT7, and KIRREL3.
Affiliation: Department of Animal Science, Iowa State University, Ames 50011, USA. dorian@iastate.edu. .
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6: Title: High-throughput transcriptomic and RNAi analysis identifies AIM1, ERGIC1, TMED3 and TPX2 as potential drug targets in prostate cancer.
Authors: Vainio, Paula, et.al. .
Journal: PloS one, Vol. 7 (6): e39801, 2012 .
Snippet: AIM1, ERGIC1, and TPX2 were shown to be highly expressed especially in prostate cancer tissues, and high mRNA expression of ERGIC1 and TMED3 associated with AR and ERG oncogene expression.
Affiliation: VTT Technical Research Centre of Finland, and Turku Centre for Biotechnology, University of Turku, Turku, Finland. .
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7: Title: Sec24- and ARFGAP1-dependent trafficking of GABA transporter-1 is a prerequisite for correct axonal targeting.
Authors: Reiterer, Veronika, et.al. .
Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience (J Neurosci), Vol. 28 (47): 12453-64, 2008 .
Snippet: In contrast to wild-type GAT1, GAT1-RL/AS failed to be specifically enriched at the tip of neurite extensions of CAD.a cells (a neuroblastoma cell line that can be differentiated into a neuron-like phenotype) and in the axon terminals of hippocampal neurons.
Affiliation: Institute of Pharmacology, Medical University of Vienna, 1090 Vienna, Austria. .
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8: Title: Oligomerization and interacellular localization of the glycoprotein receptor ERGIC-53 is independent of disulfide bonds.
Authors: Neve, Etienne P A, et.al. .
Journal: Journal of molecular biology (J Mol Biol), Vol. 354 (3): 556-68, 2005 .
Snippet: ERGIC-53 is a type I transmembrane lectin facilitating the efficient export of a subset of secretory glycoproteins from the endoplasmic reticulum.
Affiliation: Ludwig Institute for Cancer Research, Stockholm Branch, Karolinska Institutet, Box 240, S-17177 Stockholm, Sweden. .
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9: Title: Proteomics of endoplasmic reticulum-Golgi intermediate compartment (ERGIC) membranes from brefeldin A-treated HepG2 cells identifies ERGIC-32, a new cycling protein that interacts with human Erv46.
Authors: Breuza, Lionel, et.al. .
Journal: The Journal of biological chemistry (J Biol Chem), Vol. 279 (45): 47242-53, 2004 .
Snippet: Among the uncharacterized proteins, a 32-kDa protein termed ERGIC-32 is a novel cycling membrane protein with sequence homology to Erv41p and Erv46p, two proteins enriched in COPII vesicles of yeast.
Affiliation: Biozentrum, University of Basel, Klingelbergstrasse 70, CH-4056 Basel, Switzerland. .
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