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88 documents found
1: Title: Emerging views of mitophagy in immunity and autoimmune diseases.
Authors: Xu, Ye, et.al. .
Journal: Autophagy, 2019 .
Snippet: Abbreviations: AICD: activation induced cell death; AIM2: absent in melanoma 2; ALPL/HOPS: alkaline phosphatase, biomineralization associated; AMA: anti-mitochondrial antibodies; AMFR: autocrine motility factor receptor; ATG: autophagy-related; BCL2L13: BCL2 like 13; BNIP3: BCL2 interacting protein 3; BNIP3L/NIX: BCL2 interacting protein 3 like; CALCOCO2/NDP52: calcium binding and coiled-coil domain 2; CARD: caspase recruitment domain containing; CASP1: caspase 1; CD: Crohn disease; CGAS: cyclic GMP-AMP synthase; CXCL1: C-X-C motif chemokine ligand 1; DEN: diethylnitrosamine; DLAT/PDC-E2: dihydrolipoamide S-acetyltransferase; DNM1L/Drp1: dynamin 1 like; ESCRT: endosomal sorting complexes required for transport; FKBP8: FKBP prolyl isomerase 8; FUNDC1: Fun14 domain containing 1; GABARAP: GABA type A receptor-associated protein; HMGB1: high mobility group box 1; HPIV3: human parainfluenza virus type 3; IBD: inflammatory bowel diseases; IEC: intestinal epithelial cell; IFN: interferon; IL1B/IL-1β: interleukin 1 beta; iNK: invariant natural killer; IRGM: immunity related GTPase M; LIR: LC3-interacting region; LPS: lipopolysaccharide; LRRK2: leucine rich repeat kinase 2; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; MARCH5: membrane associated ring-CH-type finger 5; MAVS: mitochondrial antiviral signaling protein; MDV: mitochondria-derived vesicle; MFN1: mitofusin 1; MHC: major histocompatibility complex; MIF: macrophage migration inhibitory factor; mtAP: mitochondrial antigen presentation; mtDNA: mitochondrial DNA; MTOR: mechanistic target of rapamycin kinase; mtROS: mitochondrial ROS; MUL1: mitochondrial E3 ubiquitin protein ligase 1; NBR1: NBR1 autophagy cargo receptor; NFKB/NF-ĸB: nuclear factor kappa B subunit; NK: natural killer; NLR: NOD-like receptor; NLRC4: NLR family CARD domain containing 4; NLRP3: NLR family pyrin domain containing 3; OGDH: oxoglutarate dehydrogenase; OMM: outer mitochondrial membrane; OPTN: optineurin; ox: oxidized; PARK7: Parkinsonism associated deglycase; PBC: primary biliary cirrhosis; PEX13: peroxisomal biogenesis factor 13; PHB/PHB1: prohibitin; PHB2: prohibitin 2; PIK3C3/VPS34: phosphatidylinositol 3-kinase catalytic subunit type 3; PINK1: PTEN induced kinase 1; PLEKHM1: pleckstrin homology and RUN domain containing M1; PRKN/PARK2: parkin RBR E3 ubiquitin protein ligase; RAB: member RAS oncogene family; RHEB: Ras homolog: mTORC1 binding; RIPK2: receptor interacting serine/threonine kinase 2; RLR: DDX58/RIG-I like receptor; ROS: reactive oxygen species; SBD: small bile ducts; SLC2A1/GLUT1: solute carrier family 2 member 1; SLE: systemic lupus erythematosus; SMURF1: SMAD specific E3 ubiquitin protein ligase 1; SQSTM1/p62: sequestosome 1; TAX1BP1: Tax1 binding protein 1; TCR: T cell receptor; TFAM: transcription factor A: mitochondrial; Th17: T helper 17; TLR9: toll like receptor 9; TMEM173/STING: transmembrane protein 173; TNF/TNF-α: tumor necrosis factor; Ub: ubiquitin; UC: ulcerative colitis; ULK1: unc-51 like autophagy activating kinase 1; WIPI: WD repeat domain: phosphoinositide interacting; ZFYVE1/DFCP1: zinc finger FYVE-type containing 1.
Affiliation: a Division of Gastroenterology and Hepatology, Key Laboratory of Gastroenterology and Hepatology, Ministry of Health , Inflammatory Bowel Disease Research Center , Shanghai , China. b Renji Hospital, School of Medicine , Shanghai Jiao Tong University , Shanghai , China. c Shanghai Institute of Digestive Disease , Shanghai , China. .
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2: Title: The HGF-MET axis coordinates liver cancer metabolism and autophagy for chemotherapeutic resistance.
Authors: Huang, Xing, et.al. .
Journal: Autophagy, 2019 .
Snippet: Abbreviations: ALDO: aldolase, fructose-bisphosphate; CQ: chloroquine; DLAT/PDCE2: dihydrolipoamide S-acetyltransferase; EMT: epithelial-mesenchymal transition; ENO: enolase; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; GLS/GLS1: glutaminase; GLUL/GS: glutamine-ammonia ligase; GPI/PGI: glucose-6-phosphate isomerase; HCC: hepatocellular carcinoma; HGF: hepatocyte growth factor; HK: hexokinase; LDH: lactate dehydrogenase; LIHC: liver hepatocellular carcinoma; LIR: LC3-interacting region; PDH: pyruvate dehydrogenase; PDHA1: pyruvate dehydrogenase E1 alpha 1 subunit; PDHX: pyruvate dehydrogenase complex component X; PFK: phosphofructokinase; PK: pyruvate kinase; RTK: receptor tyrosine kinase; TCGA: The Cancer Genome Atlas.
Affiliation: a The Key Laboratory of Precision Diagnosis and Treatment for Hepatobiliary and Pancreatic Tumor of Zhejiang Province , First Affiliated Hospital, School of Medicine, Zhejiang University , Hangzhou , Zhejiang , China. b The Key Laboratory of Developmental Genes and Human Disease , Institute of Life Sciences, Southeast University , Nanjing , Jiangsu , China. c The Therapeutic Antibody Research Center of SEU-Alphamab , Southeast University , Nanjing , China. .
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3: Title: Alternol eliminates excessive ATP production by disturbing Krebs cycle in prostate cancer.
Authors: Li, Changlin, et.al. .
Journal: The Prostate (Prostate), 2019 .
Snippet: RESULTS: Among 14 verified protein targets, four were Krebs cycle enzymes, fumarate hydratase (FH), malate dehydrogenase-2 (MDH2), dihydrolipoamide acetyltransferase (DLAT) in pyruvate dehydrogenase complex (PDHC) and dihydrolipoamide S-succinyltransferase (DLST) in a-ketoglutarate dehydrogenase complex (KGDHC).
Affiliation: Institute of Precision Medicine, Jining Medical University, Jining, China. Department of Urology, The University of Kansas Medical Center, Kansas City, Kansas. Department of Radiation Oncology, The First Affiliated Hospital, Xi'An Jiaotong University School of Medicine, Xi'An, China. Department of Pharmacology, Toxicology & Therapeutics, The University of Kansas Medical Center, Kansas City, Kansas. Department of Pharmaceutical Chemistry, The University of Kansas, Lawrence, Kansas. Department of Biochemistry & Molecular Biology, The University of Kansas Medical Center, Kansas City, Kansas. .
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4: Title: Altered Proteins in the Hippocampus of Patients with Mesial Temporal Lobe Epilepsy.
Authors: Persike, Daniele Suzete, et.al. .
Journal: Pharmaceuticals (Basel, Switzerland) (Pharmaceuticals (basel)), Vol. 11 (4), 2018 .
Snippet: The following proteins were found to be up-regulated in patients: isoform 1 of serum albumin (ALB), proton ATPase catalytic subunit A (ATP6V1A), heat shock protein 70 (HSP70), dihydropyrimidinase-related protein 2 (DPYSL2), isoform 1 of myelin basic protein (MBP), and dihydrolipoamide S-acethyltransferase (DLAT).
Affiliation: Departamento de Neurologia/Neurocirurgia, Escola Paulista de Medicina, Universidade Federal de São Paulo⁻UNIFESP, Rua Pedro de Toledo, 669, CEP, São Paulo 04039-032, Brazil. daniele_persike@protonmail.com. Department of Medicinal Chemistry, College of Pharmacy, University of Dohuk-UoD, Kurdistan Region 1006AJ, Iraq. daniele_persike@protonmail.com. Departamento de Neurologia/Neurocirurgia, Escola Paulista de Medicina, Universidade Federal de São Paulo⁻UNIFESP, Rua Pedro de Toledo, 669, CEP, São Paulo 04039-032, Brazil. edumarques83@gmail.com. INSERM U1114, Neuropsychologie Cognitive et Physiopathologie de la Schizophrenie, 1 pl de l'Hopital, 67091 Strasbourg, France. edumarques83@gmail.com. Departamento de Micro-Imuno-Parasito, Disciplina de Biologia Celular, Escola Paulista de Medicina, UNIFESP, São Paulo 04039-032, Brasil. mikota_bio@yahoo.com.br. Departamento de Neurologia/Neurocirurgia, Escola Paulista de Medicina, Universidade Federal de São Paulo⁻UNIFESP, Rua Pedro de Toledo, 669, CEP, São Paulo 04039-032, Brazil. yacubian@terra.com.br. Departamento de Neurologia/Neurocirurgia, Escola Paulista de Medicina, Universidade Federal de São Paulo⁻UNIFESP, Rua Pedro de Toledo, 669, CEP, São Paulo 04039-032, Brazil. ricardoscenteno@gmail.com. Instituto do Coração (INCOR), Departamento de Anatomia Patológica, Faculdade de Medicina da Universidade de São Paulo (FMUSP), São Paulo 04039-032, Brasil. mauroczn@hotmail.com. Departamento de Neurologia/Neurocirurgia, Escola Paulista de Medicina, Universidade Federal de São Paulo⁻UNIFESP, Rua Pedro de Toledo, 669, CEP, São Paulo 04039-032, Brazil. fernandesepm@gmail.com. .
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5: Title: Proteomics and metabolomics identify molecular mechanisms of aging potentially predisposing for chronic lymphocytic leukemia.
Authors: Mayer, Rupert Laurenz, et.al. .
Journal: Molecular & cellular proteomics : MCP (Mol Cell Proteomics), 2017 .
Snippet: Mass spectrometric proteomics data have been made fully accessible via ProteomeXchange with identifier PXD006570-PXD006572, PXD006576, PXD006578 and PXD006589-PXD006591. Remarkably, B cells from aged controls displayed significant regulation of proteins related to stress management in mitochondria and ROS stress such as DLAT, FIS1 and NDUFAB1, and DNA repair including RAD9A, MGMT and XPA.
Affiliation: University of Vienna, Austria. Karl Landsteiner Society, Austria. Medical University of Vienna, Department of Laboratory Medicine, Austria. University of Vienna, Faculty of Chemistry, Department of Analytical Chemistry. University of Vienna, Department of Analytical Chemistry, Austria. University Hospital of Regensburg, Department of Internal Medicine III, Haematology & Oncology. Department of Analytical Chemistry, University of Vienna, Austria. Department of Analytical Chemistry, University of Vienna, Austria christopher.gerner@univie.ac.at. .
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6: Title: Immunometabolic profiling of T cells from patients with relapsing-remitting multiple sclerosis reveals an impairment in glycolysis and mitochondrial respiration.
Authors: La Rocca, Claudia, et.al. .
Journal: Metabolism: clinical and experimental (Metabolism), Vol. 77, 2017 .
Snippet: These results were also corroborated at biochemical level by a reduced expression of the glycolitic enzymes aldolase, enolase 1, hexokinase I, and by reduction of Krebs cycle enzymes dihydrolipoamide-S-acetyl transferase (DLAT) and dihydrolipoamide-S-succinyl transferase (DLST).
Affiliation: Laboratorio di Immunologia, Istituto per l'Endocrinologia e l'Oncologia Sperimentale, Consiglio Nazionale delle Ricerche (IEOS-CNR), Napoli, Italy. Dipartimento di Medicina Clinica e Chirurgia, Università degli Studi di Napoli "Federico II", Napoli, Italy. Dipartimento di Neuroscienze, Scienze Riproduttive ed Odontostomatologiche, Università degli Studi di Napoli "Federico II", Napoli, Italy. Dipartimento di Neurologia, Centro regionale di Sclerosi Multipla, Azienda Ospedaliera "A. Cardarelli", Napoli, Italy. Centro Neurologico Terapie Sperimentali, Dipartimento di Neuroscienze, Salute Mentale e Organi di Senso, Università degli Studi di Roma "La Sapienza", Roma, Italy; IRCCS Istituto Neurologico Mediterraneo (INM) Neuromed, Pozzilli (IS), Italy. IRCCS Istituto Neurologico Mediterraneo (INM) Neuromed, Pozzilli (IS), Italy; Unità di Neurologia, Dipartimento di Medicina dei Sistemi, Università degli Studi di Roma "Tor Vergata", Roma, Italy. Dipartimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze Materno-infantili, Facoltà di Medicina e Chirurgia, Università degli Studi di Genova, Genova, Italy; Ospedale Policlinico San Martino IRCCS, Genova, Italy. Global Medical Affairs Fertility, Merck KGaA, Darmstadt, Germany. Medical Affairs, Merck Serono S.p.A., Italy. Laboratorio di Immunologia, Istituto per l'Endocrinologia e l'Oncologia Sperimentale, Consiglio Nazionale delle Ricerche (IEOS-CNR), Napoli, Italy; Dipartimento di Medicina Molecolare e Biotecnologie Mediche, Università degli Studi di Napoli "Federico II", Napoli, Italy. Electronic address: giuseppe.matarese@unina.it. .
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7: Title: Commensal Propionibacterium strain UF1 mitigates intestinal inflammation via Th17 cell regulation.
Authors: Colliou, Natacha, et.al. .
Journal: The Journal of clinical investigation (J Clin Invest), 2017 .
Snippet: The induction of Th17 cells was dependent on bacterial dihydrolipoamide acetyltransferase (DlaT), a major protein expressed on the P. UF1 surface layer (S-layer).
Affiliation: Department of Infectious Diseases and Immunology. Division of Gastroenterology, Hepatology & Nutrition, Department of Medicine. Department of Physiological Sciences. Division of Neonatology, Department of Pediatrics, and. Interdisciplinary Center for Biotechnology Research, University of Florida, Gainesville, Florida, USA. Department of Microbiology and Immunology, Loyola University Chicago, Maywood, Illinois, USA. Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia, USA. .
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8: Title: Widening of the safe trajectory range during subaxial cervical pedicle screw placement: advantages of a curved pedicle probe and laterally located starting point without creating a funnel-shaped hole.
Authors: Lee, Subum, et.al. .
Journal: Journal of neurosurgery. Spine (J Neurosurg Spine), Vol. 27 (2): 150-157, 2017 .
Snippet: The mean df/Df values were 0.64, 0.62, 0.63, 0.63, and 1.24 on the C3-7 levels, respectively.
Affiliation: Department of Neurological Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul; and. Departments of 2 Neurology and. Neurological Surgery, Gangneung Asan Hospital, University of Ulsan College of Medicine, Gangneung, Korea. .
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9: Title: Evaluation of impact of an external breast shield (FlexiShield) in electronic brachytherapy for breast IORT: A phantom study.
Authors: Kim, Yongbok, et.al. .
Journal: Brachytherapy, Vol. 16 (3): 597-607, 2017 May - Jun .
Snippet: For 45 pairs of MVCT scans, balloon deformation was measured in superior-inferior (dSI) dimension on coronal and sagittal planes and anterior-posterior (dAP) and lateral (dLAT) dimensions on the equatorial plane of balloon.
Affiliation: Department of Radiation Oncology, The University of Arizona, Tucson, AZ. Electronic address: yongbokkim@email.arizona.edu. Department of Radiation Oncology, The University of Arizona, Tucson, AZ. .
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10: Title: Identification and Verification of Potential Therapeutic Target Genes in Berberine-Treated Zucker Diabetic Fatty Rats through Bioinformatics Analysis.
Authors: Wu, Yang Sheng, et.al. .
Journal: PloS one, Vol. 11 (11): e0166378, 2016 .
Snippet: These results suggested that the RHOA, MAPK4, SGK494, DOT1L, SETD2, ME3 and DLAT genes are potential therapeutic target genes for the treatment of diabetes.
Affiliation: College of Pharmacy, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, People's Republic of China. College of Life Science, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, People's Republic of China. .
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11: Title: E4F1 controls a transcriptional program essential for pyruvate dehydrogenase activity.
Authors: Lacroix, Matthieu, et.al. .
Journal: Proceedings of the National Academy of Sciences of the United States of America (Proc Natl Acad Sci U S A), Vol. 113 (39): 10998-1003, 2016 .
Snippet: E4F1 controls a set of four genes [dihydrolipoamide acetlytransferase (Dlat), dihydrolipoyl dehydrogenase (Dld), mitochondrial pyruvate carrier 1 (Mpc1), and solute carrier family 25 member 19 (Slc25a19)] involved in pyruvate oxidation and reported to be individually mutated in human metabolic syndromes.
Affiliation: Institut de Recherche en Cancérologie de Montpellier, Montpellier F-34298, France; INSERM, U1194, Montpellier F-34298, France; Université Montpellier, Montpellier F-34090, France; Institut du Cancer Montpellier, Montpellier F-34298, France; Equipe labellisée Ligue Contre le Cancer, 75013 Paris, France; Institut de Recherche en Cancérologie de Montpellier, Montpellier F-34298, France; INSERM, U1194, Montpellier F-34298, France; Université Montpellier, Montpellier F-34090, France; Institut du Cancer Montpellier, Montpellier F-34298, France; Equipe labellisée Ligue Contre le Cancer, 75013 Paris, France; Institut de Génétique Moléculaire de Montpellier, UMR5535, CNRS, Montpellier F-34293, France; Institut de Génétique Moléculaire de Montpellier, UMR5535, CNRS, Montpellier F-34293, France; CNRS, UMR7216, Epigenetics and Cell Fate, University Paris Diderot, Sorbonne Paris Cite, 75013 Paris, France; Université Montpellier, Montpellier F-34090, France; Dynamique Musculaire et Métabolisme, Institut National de la Recherche Agronomique, UMR866, F-34060 Montpellier, France; Université de Toulouse, Institut National des Sciences Appliquées, Université Paul Sabatié, Institut National Polytechnique, F-31077 Toulouse, France; UMR792 Ingénierie des Systèmes Biologiques et des Procédés, Institut National de la Recherche Agronomique, F-31400 Toulouse, France; CNRS, UMR5504, F-31400 Toulouse, France; Institut de Recherche en Cancérologie de Montpellier, Montpellier F-34298, France; INSERM, U1194, Montpellier F-34298, France; Université Montpellier, Montpellier F-34090, France; Institut du Cancer Montpellier, Montpellier F-34298, France; Montpellier Network of Experimental Histology, BioCampus, CNRS, UMS3426, F-34094 Montpellier, France; Department of Biochemistry, Bicêtre Hospital, 94270 Le Kremlin Bicetre, France. Institut de Recherche en Cancérologie de Montpellier, Montpellier F-34298, France; INSERM, U1194, Montpellier F-34298, France; Université Montpellier, Montpellier F-34090, France; Institut du Cancer Montpellier, Montpellier F-34298, France; Equipe labellisée Ligue Contre le Cancer, 75013 Paris, France; laurent.lecam@inserm.fr claude.sardet@inserm.fr. Institut de Recherche en Cancérologie de Montpellier, Montpellier F-34298, France; INSERM, U1194, Montpellier F-34298, France; Université Montpellier, Montpellier F-34090, France; Institut du Cancer Montpellier, Montpellier F-34298, France; Equipe labellisée Ligue Contre le Cancer, 75013 Paris, France; Institut de Génétique Moléculaire de Montpellier, UMR5535, CNRS, Montpellier F-34293, France; laurent.lecam@inserm.fr claude.sardet@inserm.fr. .
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12: Title: E4F1-mediated control of pyruvate dehydrogenase activity is essential for skin homeostasis.
Authors: Goguet-Rubio, Perrine, et.al. .
Journal: Proceedings of the National Academy of Sciences of the United States of America (Proc Natl Acad Sci U S A), Vol. 113 (39): 11004-9, 2016 .
Snippet: E4F1 deficiency in basal keratinocytes resulted in deregulated expression of dihydrolipoamide acetyltransferase (Dlat), a gene encoding the E2 subunit of the mitochondrial pyruvate dehydrogenase (PDH) complex.
Affiliation: Institut de Recherche en Cancérologie de Montpellier, Montpellier F-34298, France; INSERM U1194, Montpellier F-34298, France; University of Montpellier, Montpellier F-34090, France; Institut Régional du Cancer de Montpellier, Montpellier F-34298, France; Equipe labellisée Ligue Contre le Cancer, 75013 Paris, France; Institut de Recherche en Cancérologie de Montpellier, Montpellier F-34298, France; University of Montpellier, Montpellier F-34090, France; Réseau d'Histologie Expérimentale de Montpellier, BioCampus, CNRS-UMS3426, F-34094 Montpellier, France; Institut de Recherche en Cancérologie de Montpellier, Montpellier F-34298, France; INSERM U1194, Montpellier F-34298, France; University of Montpellier, Montpellier F-34090, France; Institut Régional du Cancer de Montpellier, Montpellier F-34298, France; Equipe labellisée Ligue Contre le Cancer, 75013 Paris, France; Institut de Génétique Moléculaire de Montpellier, CNRS-UMR5535, Montpellier 34293, France; Department of Physiology, University of Lausanne, 1005 Lausanne, Switzerland; Institut de Génétique Moléculaire de Montpellier, CNRS-UMR5535, Montpellier 34293, France; Epigenetics and Cell Fate, University Paris Diderot, Sorbonne Paris Cite, UMR7216 CNRS, Paris 75013, France; University of Montpellier, Montpellier F-34090, France; Institut de Génétique Moléculaire de Montpellier, CNRS-UMR5535, Montpellier 34293, France; Institut de Recherche en Cancérologie de Montpellier, Montpellier F-34298, France; INSERM U1194, Montpellier F-34298, France; University of Montpellier, Montpellier F-34090, France; Institut Régional du Cancer de Montpellier, Montpellier F-34298, France; Réseau d'Histologie Expérimentale de Montpellier, BioCampus, CNRS-UMS3426, F-34094 Montpellier, France; Institut de Recherche en Cancérologie de Montpellier, Montpellier F-34298, France; INSERM U1194, Montpellier F-34298, France; University of Montpellier, Montpellier F-34090, France; Institut Régional du Cancer de Montpellier, Montpellier F-34298, France; Institut de la Clinique de la Souris-Mouse Clinical Institute, PHENOMIN, CNRS-UMR7104, INSERM U964, Université de Strasbourg, Illkirch, France. Institut de Recherche en Cancérologie de Montpellier, Montpellier F-34298, France; INSERM U1194, Montpellier F-34298, France; University of Montpellier, Montpellier F-34090, France; Institut Régional du Cancer de Montpellier, Montpellier F-34298, France; Equipe labellisée Ligue Contre le Cancer, 75013 Paris, France; matthieu.lacroix@inserm.fr laurent.lecam@inserm.fr. .
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13: Title: Difficulties in recognition of pyruvate dehydrogenase complex deficiency on the basis of clinical and biochemical features. The role of next-generation sequencing.
Authors: Ciara, E, et.al. .
Journal: Molecular genetics and metabolism reports (Unknown Journal), Vol. 7, 2016 .
Snippet: Pyruvate dehydrogenase complex (PDHc) defect is a well-known cause of mitochondrial disorders (MD) with at least six responsible genes (PDHA1, PDHB, DLAT, DLD, PDHX, PDP1).
Affiliation: Department of Medical Genetics, The Children's Memorial Health Institute, Warsaw, Poland. Department of Pediatrics, Nutrition and Metabolic Diseases, The Children's Memorial Health Institute, Warsaw, Poland. Department of Pathology, The Children's Memorial Health Institute, Warsaw, Poland. Department of Pediatrics, Paracelsus Medical University, Salzburg, Austria. Department of Biochemistry and Experimental Medicine, The Children's Memorial Health Institute, Warsaw, Poland. Department of Child Neurology, Chorzowskie Centrum Pediatrii i Onkologii, Chorzów, Poland. Department of Pediatrics, Endocrinology, Diabetology, Metabolic Diseases and Cardiology, Pomeranian Medical University, Szczecin, Poland. Department of Medical Genetics, Warsaw Medical University, Warsaw, Poland. Department of Medical Genetics, The Children's Memorial Health Institute, Warsaw, Poland; Department of Pediatrics, Nutrition and Metabolic Diseases, The Children's Memorial Health Institute, Warsaw, Poland. .
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14: Title: How accurate is size-specific dose estimate in pediatric body CT examinations?
Authors: Karmazyn, Boaz, et.al. .
Journal: Pediatric radiology (Pediatr Radiol), Vol. 46 (9): 1234-40, 2016 .
Snippet: We calculated the following in each child: (1) SSDEs based on DAP, DLAT, DAP+LAT, DED, and body weight, and (2) SSDE based on software calculation of mean water-equivalent diameter ([Formula: see text] adopted standard within our study).
Affiliation: Department of Radiology, Riley Hospital for Children, 705 Riley Drive, Room 1053, Indianapolis, IN, 46202, USA. bkarmazy@iupui.edu. Department of Radiology and Imaging Sciences, Indiana University School of Medicine, Indianapolis, IN, USA. bkarmazy@iupui.edu. Department of Radiation Oncology, Indiana University School of Medicine, Indianapolis, IN, USA. CT Clinical Science, Philips Healthcare, Highland Heights, OH, USA. Department of Biostatistics, Indiana University School of Medicine, Indianapolis, IN, USA. Department of Radiology and Imaging Sciences, Indiana University School of Medicine, Indianapolis, IN, USA. .
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15: Title: Deletion of Galectin-3 Enhances Xenobiotic Induced Murine Primary Biliary Cholangitis by Facilitating Apoptosis of BECs and Release of Autoantigens.
Journal: Scientific reports (Sci Rep), Vol. 6, 2016 .
Snippet: Galectin-3 (Gal-3) is a carbohydrate binding lectin, with multiple roles in inflammatory diseases and autoimmunity including its antiapoptotic effect on epithelial cells.
Affiliation: Center for Molecular Medicine and Stem Cell Research, Faculty of Medical Sciences, University of Kragujevac, Serbia. Department of Internal Medicine, Faculty of Medical Sciences, University of Kragujevac, Serbia. Division of Rheumatology, Allergy and Clinical Immunology, University of California at Davis School of Medicine, Davis, CA, USA. .
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16: Title: Xenobiotics and loss of tolerance in primary biliary cholangitis.
Authors: Wang, Jinjun, et.al. .
Journal: World journal of gastroenterology (World J Gastroenterol), Vol. 22 (1): 338-48, 2016 .
Snippet: The serologic hallmark of PBC are the presence of high titer anti-mitochondrial autoantibodies (AMA) that recognize the lipoyl domain of the mitochondrial pyruvate dehydrogenase E2 (PDC-E2) subunit.
Affiliation: Jinjun Wang, Guoxiang Yang, Alana Mari Dubrovsky, Jinjung Choi, Patrick SC Leung, Division of Rheumatology, Allergy and Clinical Immunology, University of California at Davis, School of Medicine, Davis, CA 95616, United States. .
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17: Title: Identification of a novel mitochondrial interacting protein of C1QBP using subcellular fractionation coupled with CoIP-MS.
Authors: Chen, Ruibing, et.al. .
Journal: Analytical and bioanalytical chemistry (Anal Bioanal Chem), Vol. 408 (6): 1557-64, 2016 .
Snippet: Using this method, a novel C1QBP interacting protein, dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial (DLAT) was identified and validated.
Affiliation: Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy; Research Center of Basic Medical Sciences; School of Medical Laboratory, Tianjin Medical University, Tianjin, 300070, China. chenruibing@tijmu.edu.cn. Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy; Research Center of Basic Medical Sciences; School of Medical Laboratory, Tianjin Medical University, Tianjin, 300070, China. Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy; Research Center of Basic Medical Sciences; School of Medical Laboratory, Tianjin Medical University, Tianjin, 300070, China. zhangning@tijmu.edu.cn. .
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18: Title: Specific protein changes contribute to the differential muscle mass loss during ageing.
Authors: Capitanio, Daniele, et.al. .
Journal: Proteomics, Vol. 16 (4): 645-56, 2016 .
Snippet: High levels of dihydrolipoyllysine-residue acetyltransferase (Dlat) and ATP synthase subunit alpha (Atp5a1) are detected in triceps and gastrocnemius, respectively.
Affiliation: Department of Biomedical Sciences for Health, University of Milan, Milan, Italy. IRCCS Policlinico San Donato, San Donato Milanese (MI), Italy. Institute of Bioimaging and Molecular Physiology, National Research Council, Segrate (MI) - Cefalù (PA), Italy. Department of Pharmacological and Biomolecular Sciences, University of Milan, Milan, Italy. .
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19: Title: Making Sense of Autoantibodies in Cholestatic Liver Diseases.
Authors: Marzorati, Simona, et.al. .
Journal: Clinics in liver disease (Clin Liver Dis), Vol. 20 (1): 33-46, 2016 .
Snippet: Primary biliary cirrhosis (PBC) and primary sclerosing cholangitis (PSC) are the most common chronic cholestatic liver diseases (CLD) in adults and are associated with immune mechanisms.
Affiliation: Liver Unit and Center for Autoimmune Liver Diseases, Humanitas Clinical and Research Center, Via A. Manzoni 113, Rozzano, Milan 20089, Italy; Department of Electronics, Information and Bioengineering, Politecnico di Milano, via Ponzio 34/5, Milan 20133, Italy. Liver Unit and Center for Autoimmune Liver Diseases, Humanitas Clinical and Research Center, Via A. Manzoni 113, Rozzano, Milan 20089, Italy; Division of Rheumatology, Allergy, and Clinical Immunology, University of California Davis, GBSF, 451 Health Science Drive, Davis, CA 95616, USA. Liver Unit and Center for Autoimmune Liver Diseases, Humanitas Clinical and Research Center, Via A. Manzoni 113, Rozzano, Milan 20089, Italy. Electronic address: ana.lleo@humanitas.it. .
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20: Title: E1 of α-ketoglutarate dehydrogenase defends Mycobacterium tuberculosis against glutamate anaplerosis and nitroxidative stress.
Authors: Maksymiuk, Christina, et.al. .
Journal: Proceedings of the National Academy of Sciences of the United States of America (Proc Natl Acad Sci U S A), Vol. 112 (43): E5834-43, 2015 .
Snippet: We also show that pyruvate decarboxylase (AceE), the E1 component of pyruvate dehydrogenase (PDHC), can participate in AceE/DlaT/AhpD/AhpC, using pyruvate as a source of electrons for reductase action.
Affiliation: Department of Microbiology and Immunology, Weill Cornell Medical College, New York, NY 10065; Department of Medicine, Weill Cornell Medical College, New York, NY 10065. Department of Microbiology and Immunology, Weill Cornell Medical College, New York, NY 10065; cnathan@med.cornell.edu. .
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