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10 documents found
1: Title: Analysis of the Human Prostate-Specific Proteome Defined by Transcriptomics and Antibody-Based Profiling Identifies TMEM79 and ACOXL as Two Putative, Diagnostic Markers in Prostate Cancer.
Authors: O'Hurley, Gillian, et.al. .
Journal: PloS one, Vol. 10 (8): e0133449, 2015 .
Snippet: In addition to previously well-known proteins we identified two poorly characterized proteins, TMEM79 and ACOXL, with potential to differentiate between benign and cancerous prostatic glands in tissue biopsies.
Affiliation: Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden; UCD School of Biomolecular and Biomedical Science, UCD Conway Institute, University College Dublin, Belfield, Dublin 4, Ireland; OncoMark Ltd, NovaUCD, Belfield Innovation Park, Belfield, Dublin 4, Ireland. Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden. Science for Life Laboratory, KTH-Royal Institute of Technology, Stockholm, Sweden. Department of Clinical Sciences Lund, Oncology and Pathology, Lund University, Skåne University Hospital, Lund, Sweden. Department of Clinical Sciences, Division of Urological Cancers, Skåne University Hospital Malmö, Lund University, Malmö, Sweden. UCD School of Biomolecular and Biomedical Science, UCD Conway Institute, University College Dublin, Belfield, Dublin 4, Ireland. .
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2: Title: Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci.
Authors: Betz, Regina C, et.al. .
Journal: Nature communications (Nat Commun), Vol. 6, 2015 .
Snippet: Outside the major histocompatibility complex, we identify two novel loci that exceed the threshold of statistical significance, containing ACOXL/BCL2L11(BIM) (2q13); GARP (LRRC32) (11q13.5),
Affiliation: Institute of Human Genetics, University of Bonn, Bonn D-53127, Germany. 1] Department of Dermatology, Columbia University, New York, New York 10032, USA [2] Department of Epidemiology, Columbia University, New York, New York 10032, USA. 1] Analytic and Translational Genetics Unit, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114, USA [2] Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02114, USA. Department of Medical Genetics, University Medical Center Utrecht, Utrecht 3584 CG, The Netherlands. 1] German Center for Neurodegenerative Diseases, Bonn D- 53175, Germany [2] Institute for Medical Biometry, Informatics and Epidemiology, University of Bonn, Bonn D-53127, Germany. 1] Institute of Human Genetics, University of Bonn, Bonn D-53127, Germany [2] Department of Genomics, Life and Brain Center, University Bonn, Bonn D-53127, Germany. Department of Dermatology, Columbia University, New York, New York 10032, USA. Department of Dermatology, MD Anderson Cancer Center, Houston, Texas 77030, USA. Department of Dermatology, University of Minnesota, Minneapolis, Minnesota 55455, USA. Department of Dermatology, University of Colorado, Denver, Colorado 80204, USA. Department of Dermatology, University of California, San Francisco, San Francisco, California 94110, USA. Department of Genetics and Development, Columbia University, New York, New York 10032, USA. Institute of Medical Informatics, Biometry, and Epidemiology, University Duisburg-Essen, Essen D-45122, Germany. Department of Dermatology, University of Münster, Münster D-48149, Germany. Department of Dermatology and Allergy, Clinical Research Center for Hair and Skin Science, Charité-Universitätsmedizin Berlin, Berlin D-10117, Germany. Department of Dermatology, University of Munich, Munich D-80337, Germany. Dermatological Practice, Hair and Nail, Wesseling D-50389, Germany. Dermatological Practice, Paderborn D-33098, Germany. Community and Family Medicine and Genetics, Dartmouth College, Hanover, New Hampshire 03755, USA. The Feinstein Institute for Medical Research, Manhasset, New York 11030, USA. Department of Medical Genetics, University of Antwerp, Antwerp BE-2650, Belgium. 1] Department of Dermatology, Columbia University, New York, New York 10032, USA [2] Department of Medicine, Columbia University, New York, New York 10032, USA. 1] Department of Medical Genetics, University Medical Center Utrecht, Utrecht 3584 CG, The Netherlands [2] Department of Epidemiology, University Medical Center Utrecht, Utrecht 3584 CG, The Netherlands. 1] Department of Dermatology, Columbia University, New York, New York 10032, USA [2] Department of Genetics and Development, Columbia University, New York, New York 10032, USA. .
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3: Title: New candidate loci identified by array-CGH in a cohort of 100 children presenting with syndromic obesity.
Authors: Vuillaume, Marie-Laure, et.al. .
Journal: American journal of medical genetics. Part A (Am J Med Genet A), Vol. 164A (8): 1965-75, 2014 .
Snippet: Proteins encoded by several of these genes are involved in lipid metabolism (ACOXL, MSMO1, MVD, and PDZK1) linked with nervous system function (BDH1 and LINGO2), neutral lipid storage (PLIN2), energy homeostasis and metabolic processes (CDH13, CNTNAP2, CPPED1, NDUFA4, PTGS2, and SOCS6).
Affiliation: CHU Bordeaux, Service de Génétique Médicale, Bordeaux, France; Univ. Bordeaux, Maladies Rares : Génétique et Métabolisme (MRGM), EA 4576, Bordeaux, France. .
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4: Title: Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services.
Authors: Roberts, Jennifer L, et.al. .
Journal: Gene, Vol. 535 (1): 70-8, 2014 .
Snippet: We report our experience with the use of the 105 K and 180K oligonucleotide microarrays in 215 consecutive patients referred with either autism or autism spectrum disorders (ASD) or developmental delay/learning disability for genetic services at the University of Kansas Medical Center during the past 4 years (2009-2012).
Affiliation: Departments of Psychiatry, Behavioral Sciences and Pediatrics, The University of Kansas, Medical Center, Kansas City, KS, USA. CombiMatrix Diagnostics, Irvine, CA, USA. Department of Neurology, The University of Kansas Medical Center, Kansas City, KS, USA; King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia. Departments of Psychiatry, Behavioral Sciences and Pediatrics, The University of Kansas, Medical Center, Kansas City, KS, USA. Electronic address: mbutler4@kumc.edu. .
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5: Title: Whole Genome Association Studies of Residual Feed Intake and Related Traits in the Pig.
Authors: Onteru, Suneel K, et.al. .
Journal: PloS one, Vol. 8 (6): e61756, 2013 .
Snippet: The Bayesian approach identified associations of genomic regions containing insulin release genes (e.g., GLP1R, CDKAL, SGMS1) with RFI and ADFI, of regions with energy homeostasis (e.g., MC4R, PGM1, GPR81) and muscle growth related genes (e.g., TGFB1) with ADG, and of fat metabolism genes (e.g., ACOXL, AEBP1) with BF.
Affiliation: Department of Animal Science and Center for Integrated Animal Genomics, Iowa State University, Ames, Iowa, United States of America. .
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6: Title: Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
Authors: Berndt, Sonja I, et.al. .
Journal: Nature genetics (Nat Genet), Vol. 45 (8): 868-76, 2013 .
Snippet: In the meta-analysis, we identified ten independent associated SNPs in nine new loci at 10q23.31 (ACTA2 or FAS (ACTA2/FAS), P=1.22×10(-14)), 18q21.33 (BCL2, P=7.76×10(-11)), 11p15.5 (C11orf21, P=2.15×10(-10)), 4q25 (LEF1, P=4.24×10(-10)), 2q33.1 (CASP10 or CASP8 (CASP10/CASP8), P=2.50×10(-9)), 9p21.3 (CDKN2B-AS1, P=1.27×10(-8)), 18q21.32 (PMAIP1, P=2.51×10(-8)), 15q15.1 (BMF, P=2.71×10(-10)) and 2p22.2 (QPCT, P=1.68×10(-8)), as well as an independent signal at an established locus (2q13, ACOXL, P=2.08×10(-18)).
Affiliation: Division of Cancer Epidemiology and Genetics, National Cancer Institute (NCI), Bethesda, Maryland, USA. .
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7: Title: Five linkage regions each harbor multiple type 2 diabetes genes in the African American subset of the GENNID Study.
Authors: Hasstedt, Sandra J, et.al. .
Journal: Journal of human genetics (J Hum Genet), Vol. 58 (6): 378-83, 2013 .
Snippet: The associated genes included 3 previously reported to associate with T2D or related traits (GRB10, NEDD4L, LIPG) and 24 novel candidate genes, including genes in lipid metabolism (ACOXL) and cell-cell and cell-matrix adhesion (MAGI2, CLDN4, CTNNA2).
Affiliation: Department of Human Genetics, University of Utah, Salt Lake City, UT 84112 5330, USA. sandy@genetics.utah.edu .
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8: Title: A genome-wide assessment of variability in human serum metabolism.
Authors: Hong, Mun-Gwan, et.al. .
Journal: Human mutation (Hum Mutat), Vol. 34 (3): 515-24, 2013 .
Snippet: Biological pathway analysis implicated ACADM, ACADS, ACAD8, ACAD10, ACAD11, and ACOXL, reflecting significant enrichment of genes with acyl-CoA dehydrogenase activity.
Affiliation: Department of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, Sweden. .
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9: Title: Genetic analysis of 16 NMR-lipoprotein fractions in humans, the GOLDN study.
Authors: Kraja, Aldi T, et.al. .
Journal: Lipids, Vol. 48 (2): 155-65, 2013 .
Snippet: Five proxy genes, (ACOXL, FAM84B, NXPH1, STK40 and VAPA) showed pleiotropic effects.
Affiliation: Division of Statistical Genomics, Washington University School of Medicine, 4444 Forest Park Ave, Campus Box 8506, St. Louis, MO 63108, USA. aldi@wustl.edu .
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10: Title: Genetic susceptibility for chronic lymphocytic leukemia among Chinese in Hong Kong.
Authors: Lan, Qing, et.al. .
Journal: European journal of haematology (Eur J Haematol), Vol. 85 (6): 492-5, 2010 .
Snippet: Polymorphisms in SP140 and ACOXL were also associated with risk of CLL.
Affiliation: Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD 20892-7240, USA. qingl@mail.nih.gov .
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