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Wyszukujesz frazę ""Dehydrogenase"" wg kryterium: Temat


Tytuł:
Simulations of Pathogenic E1α Variants: Allostery and Impact on Pyruvate Dehydrogenase Complex-E1 Structure and Function.
Autorzy:
Gokcan H; Department of Chemistry, Mellon College of Science, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213, United States.
Bedoyan JK; Division of Genetic and Genomic Medicine, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania 15224, United States.; Department of Pediatrics, University of Pittsburgh, Pittsburgh, Pennsylvania 15219, United States.
Isayev O; Department of Chemistry, Mellon College of Science, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213, United States.
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Źródło:
Journal of chemical information and modeling [J Chem Inf Model] 2022 Jul 25; Vol. 62 (14), pp. 3463-3475. Date of Electronic Publication: 2022 Jul 07.
Typ publikacji:
Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, N.I.H., Extramural
MeSH Terms:
Pyruvate Dehydrogenase (Lipoamide)*/chemistry
Pyruvate Dehydrogenase (Lipoamide)*/genetics
Pyruvate Dehydrogenase Complex Deficiency Disease*/genetics
Humans ; Mitochondria ; Mutation ; Pyruvate Dehydrogenase Complex/chemistry ; Pyruvate Dehydrogenase Complex/genetics
Czasopismo naukowe
Tytuł:
Randomised controlled trial of glucose-6-phosphate dehydrogenase deficient versus non-deficient red blood cell transfusion in patients with hypoproliferative anaemia.
Autorzy:
Krajibthong S; Division of Hematology, Department of Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Sahntipurna V; Transfusion Medicine Unit, King Chulalongkorn Memorial Hospital, Bangkok, Thailand.
Parnsamut C; Department of Laboratory Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Pitakpolrat P; Department of Laboratory Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Pattanapongsak W; National Blood Centre, Thai Red Cross Society, Bangkok, Thailand.
Watanaboonyongcharoen P; Transfusion Medicine Unit, King Chulalongkorn Memorial Hospital, Bangkok, Thailand.; Department of Laboratory Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Rojnuckarin P; Division of Hematology, Department of Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.; Transfusion Medicine Unit, King Chulalongkorn Memorial Hospital, Bangkok, Thailand.
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Źródło:
Transfusion medicine (Oxford, England) [Transfus Med] 2022 Aug; Vol. 32 (4), pp. 293-298. Date of Electronic Publication: 2022 May 09.
Typ publikacji:
Journal Article; Randomized Controlled Trial
MeSH Terms:
Anemia*/therapy
Glucosephosphate Dehydrogenase Deficiency*/diagnosis
Glucosephosphate Dehydrogenase Deficiency*/therapy
Bilirubin ; Erythrocyte Transfusion ; Glucosephosphate Dehydrogenase ; Haptoglobins ; Hemoglobins ; Humans
Czasopismo naukowe
Tytuł:
Lactate dehydrogenase regulates basal glucose uptake in adipocytes.
Autorzy:
Minemura T; Osaka University Graduate School of Frontier Biosciences, Japan.
Fukuhara A; Department of Metabolic Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan; Department of Adipose Management, Osaka University Graduate School of Medicine, Suita, Osaka, Japan. Electronic address: .
Otsuki M; Department of Metabolic Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Shimomura I; Department of Metabolic Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
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Źródło:
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2022 Jun 04; Vol. 607, pp. 20-27. Date of Electronic Publication: 2022 Mar 24.
Typ publikacji:
Journal Article
MeSH Terms:
Adipocytes*/metabolism
L-Lactate Dehydrogenase*/genetics
L-Lactate Dehydrogenase*/metabolism
Animals ; Glucose/metabolism ; Glucose Transporter Type 1/genetics ; Glucose Transporter Type 1/metabolism ; Glucose Transporter Type 4/metabolism ; Insulin/metabolism ; Lactate Dehydrogenase 5 ; Mice ; RNA, Small Interfering/metabolism
Czasopismo naukowe
Tytuł:
Alcohol patch test with hue-saturation-value model analysis predicts ALDH2 genetic polymorphism.
Autorzy:
Hu CY; Department of Surgery, Taipei Veterans General Hospital, Taipei City, Taiwan.
Hung CL; Cardiovascular Division, Department of Internal Medicine, MacKay Memorial Hospital, Taipei City, Taiwan; Institute of Biomedical Sciences, MacKay Medical College, New Taipei City, Taiwan; MacKay Junior College of Medicine, Nursing and Management, Taipei City, Taiwan.
Huang YC; General Internal Medicine, MacKay Memorial Hospital, Taipei City, Taiwan.
Huang PH; General Internal Medicine, MacKay Memorial Hospital, Taipei City, Taiwan.
Tseng DY; Mobile Developer, Fourdesire, Taipei City, Taiwan.
Lin YH; School of Medicine, College of Medicine, National Yang Ming Chiao Tung University, Taipei City, Taiwan.
Sun FJ; MacKay Junior College of Medicine, Nursing and Management, Taipei City, Taiwan; Department of Medical Research, MacKay Memorial Hospital, Taipei City, Taiwan; Institute of Biomedical Informatics, National Yang Ming Chiao Tung University, Taipei City, Taiwan.
Kao FJ; Institute of Biophotonics, National Yang Ming Chiao Tung University, Taipei City, Taiwan.
Yeh HI; Cardiovascular Division, Department of Internal Medicine, MacKay Memorial Hospital, Taipei City, Taiwan; Institute of Biomedical Sciences, MacKay Medical College, New Taipei City, Taiwan; MacKay Junior College of Medicine, Nursing and Management, Taipei City, Taiwan.
Liu YY; Cardiovascular Division, Department of Internal Medicine, MacKay Memorial Hospital, Taipei City, Taiwan; Institute of Biomedical Sciences, MacKay Medical College, New Taipei City, Taiwan; Department of Critical Care Medicine, MacKay Memorial Hospital, Taipei City, Taiwan. Electronic address: .
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Źródło:
Computers in biology and medicine [Comput Biol Med] 2022 Aug; Vol. 147, pp. 105783. Date of Electronic Publication: 2022 Jul 03.
Typ publikacji:
Journal Article
MeSH Terms:
Alcohol Dehydrogenase*/genetics
Polymorphism, Genetic*
Aldehyde Dehydrogenase, Mitochondrial/genetics ; Ethanol ; Female ; Genotype ; Humans ; Male ; Patch Tests
Czasopismo naukowe
Tytuł:
G6PD Deficiency Is Crucial for Insulin Signaling Activation in Skeletal Muscle.
Autorzy:
Jiang A; Department of Animal Genetics, Breeding and Reproduction, College of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Guo H; Department of Animal Genetics, Breeding and Reproduction, College of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Jiang X; Department of Animal Genetics, Breeding and Reproduction, College of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Tao J; Department of Animal Genetics, Breeding and Reproduction, College of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Wu W; Department of Animal Genetics, Breeding and Reproduction, College of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Liu H; Department of Animal Genetics, Breeding and Reproduction, College of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2022 Jul 04; Vol. 23 (13). Date of Electronic Publication: 2022 Jul 04.
Typ publikacji:
Journal Article
MeSH Terms:
Glucosephosphate Dehydrogenase Deficiency*/genetics
Insulin*/metabolism
Adult ; Glucose/metabolism ; Glucose 1-Dehydrogenase/metabolism ; Glucosephosphate Dehydrogenase/genetics ; Glucosephosphate Dehydrogenase/metabolism ; Humans ; Muscle, Skeletal/metabolism
Czasopismo naukowe
Tytuł:
Polymorphisms of acetaldehyde dehydrogenase 2 and alcohol dehydrogenase 1B on the malignant transformation of vocal cord leukoplakia: A Chinese cohort.
Autorzy:
Han P; Department of Otolaryngology, Head and Neck Surgery, and Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Li Y; Department of Otolaryngology, Head and Neck Surgery, and Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.; Department of Otolaryngology, Guangdong Women and Children Hospital, Guangzhou, China.
Liang F; Department of Otolaryngology, Head and Neck Surgery, and Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Ye Y; Department of Otolaryngology, Head and Neck Surgery, and Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Wang J; Department of Otolaryngology, Head and Neck Surgery, and Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Li X; Department of Pathology, Cellular and Molecular Diagnostics Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Ouyang N; Department of Pathology, Cellular and Molecular Diagnostics Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Huang X; Department of Otolaryngology, Head and Neck Surgery, and Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
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Źródło:
Molecular carcinogenesis [Mol Carcinog] 2022 May; Vol. 61 (5), pp. 472-480. Date of Electronic Publication: 2022 Jan 17.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Alcohol Dehydrogenase*/genetics
Alcohol Dehydrogenase*/metabolism
Carcinoma*
Alcohol Drinking/adverse effects ; Alcohol Drinking/genetics ; Aldehyde Dehydrogenase/metabolism ; Aldehyde Dehydrogenase, Mitochondrial/genetics ; Aldehyde Oxidoreductases ; China ; Ethanol ; Genotype ; Humans ; Leukoplakia/genetics ; Middle Aged ; Polymorphism, Genetic ; Retrospective Studies ; Vocal Cords/metabolism
Czasopismo naukowe
Tytuł:
Solvent accessibility of E1α and E1β residues with known missense mutations causing pyruvate dehydrogenase complex (PDC) deficiency: Impact on PDC-E1 structure and function.
Autorzy:
Ducich NH; Case Western Reserve University (CWRU) School of Medicine, Cleveland, Ohio, USA.
Mears JA; Department of Pharmacology, CWRU, Cleveland, Ohio, USA.; Center for Mitochondrial Diseases, CWRU, Cleveland, Ohio, USA.
Bedoyan JK; Division of Genetic and Genomic Medicine, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.; Department of Pediatrics, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
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Źródło:
Journal of inherited metabolic disease [J Inherit Metab Dis] 2022 May; Vol. 45 (3), pp. 557-570. Date of Electronic Publication: 2022 Feb 01.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Pyruvate Dehydrogenase Complex Deficiency Disease*/genetics
Humans ; Mutation ; Mutation, Missense ; Pyruvate Dehydrogenase (Lipoamide)/chemistry ; Pyruvate Dehydrogenase (Lipoamide)/genetics ; Pyruvate Dehydrogenase (Lipoamide)/metabolism ; Pyruvate Dehydrogenase Complex/chemistry ; Pyruvate Dehydrogenase Complex/genetics ; Pyruvate Dehydrogenase Complex/metabolism ; Solvents
Czasopismo naukowe
Tytuł:
Novel imaging findings in pyruvate dehydrogenase complex (PDHc) deficiency-Results from a nationwide population-based study.
Autorzy:
Savvidou A; Department of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.; Department of Pediatrics, Region Västra Götaland, Sahlgrenska University Hospital, Gothenburg, Sweden.
Ivarsson L; Department of Radiology, Institute of Clinical Sciences, The Queen Silvia Children's Hospital, University of Gothenburg, Gothenburg, Sweden.
Naess K; Department of Medical Biochemistry and Biophysics, Karolinska Institute, Center for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden.
Eklund EA; Section for Pediatrics, Department of Clinical Sciences, Lund University, Lund, Sweden.
Lundgren J; Section for Pediatrics, Department of Clinical Sciences, Lund University, Lund, Sweden.
Dahlin M; Neuropediatric Unit, Department of Women's and Children's Health, Karolinska Institute and Astrid Lindgren Children's Hospital, Stockholm, Sweden.
Frithiof D; Department of Clinical Sciences, Umeå University, Umeå, Sweden.
Sofou K; Department of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.; Department of Pediatrics, Region Västra Götaland, Sahlgrenska University Hospital, Gothenburg, Sweden.
Darin N; Department of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.; Department of Pediatrics, Region Västra Götaland, Sahlgrenska University Hospital, Gothenburg, Sweden.
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Źródło:
Journal of inherited metabolic disease [J Inherit Metab Dis] 2022 Mar; Vol. 45 (2), pp. 248-263. Date of Electronic Publication: 2021 Dec 17.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Leukoencephalopathies*/diagnostic imaging
Leukoencephalopathies*/pathology
Pyruvate Dehydrogenase Complex Deficiency Disease*
Stroke*/pathology
Brain/pathology ; Female ; Humans ; Magnetic Resonance Imaging ; Male ; Pregnancy ; Pyruvate Dehydrogenase (Lipoamide)/genetics ; Pyruvate Dehydrogenase Complex/genetics ; Pyruvate Dehydrogenase Complex/metabolism
Czasopismo naukowe
Tytuł:
A case of G6PD Utrecht associated with β-thalassemia responding to splenectomy.
Autorzy:
Yang K; Department of Hematology, Zigong First People's Hospital, Zigong, China.
Liu X; Department of Hematology, Zigong First People's Hospital, Zigong, China.
Chen K; Department of Critical Medicine, Zigong First People's Hospital, Zigong, China.
Luo S; Department of Hematology, Zigong First People's Hospital, Zigong, China.
Kong W; Department of Pharmacy, Zigong First People's Hospital, Zigong, China.
Huang W; Department of Hematology, Zigong First People's Hospital, Zigong, China.
Xiao J; Department of Hematology, Zigong First People's Hospital, Zigong, China.
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Źródło:
Pediatric blood & cancer [Pediatr Blood Cancer] 2022 Sep; Vol. 69 (9), pp. e29837. Date of Electronic Publication: 2022 Jun 13.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Anemia, Hemolytic, Congenital Nonspherocytic*/complications
Anemia, Hemolytic, Congenital Nonspherocytic*/genetics
Glucosephosphate Dehydrogenase Deficiency*/complications
Glucosephosphate Dehydrogenase Deficiency*/genetics
beta-Thalassemia*/complications
beta-Thalassemia*/genetics
beta-Thalassemia*/surgery
Child ; Glucosephosphate Dehydrogenase/genetics ; Humans ; Male ; Splenectomy
Czasopismo naukowe
Tytuł:
Alcohol metabolism genes and risks of site-specific cancers in Chinese adults: An 11-year prospective study.
Autorzy:
Im PK; Clinical Trial Service Unit and Epidemiological Studies Unit (CTSU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Yang L; Clinical Trial Service Unit and Epidemiological Studies Unit (CTSU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.; Medical Research Council Population Health Research Unit (MRC PHRU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Kartsonaki C; Clinical Trial Service Unit and Epidemiological Studies Unit (CTSU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.; Medical Research Council Population Health Research Unit (MRC PHRU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Chen Y; Clinical Trial Service Unit and Epidemiological Studies Unit (CTSU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.; Medical Research Council Population Health Research Unit (MRC PHRU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Guo Y; Chinese Academy of Medical Sciences, Beijing, China.
Du H; Clinical Trial Service Unit and Epidemiological Studies Unit (CTSU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.; Medical Research Council Population Health Research Unit (MRC PHRU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Lin K; Clinical Trial Service Unit and Epidemiological Studies Unit (CTSU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Kerosi R; Clinical Trial Service Unit and Epidemiological Studies Unit (CTSU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Hacker A; Clinical Trial Service Unit and Epidemiological Studies Unit (CTSU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Liu J; NCDs Prevention and Control Department, Wuzhong CDC, Suzhou, China.
Yu C; Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, China.
Lv J; Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, China.
Walters RG; Clinical Trial Service Unit and Epidemiological Studies Unit (CTSU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.; Medical Research Council Population Health Research Unit (MRC PHRU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Li L; Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, China.
Chen Z; Clinical Trial Service Unit and Epidemiological Studies Unit (CTSU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.; Medical Research Council Population Health Research Unit (MRC PHRU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Millwood IY; Clinical Trial Service Unit and Epidemiological Studies Unit (CTSU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.; Medical Research Council Population Health Research Unit (MRC PHRU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.
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Corporate Authors:
China Kadoorie Biobank (CKB) Collaborative Group
Źródło:
International journal of cancer [Int J Cancer] 2022 May 15; Vol. 150 (10), pp. 1627-1639. Date of Electronic Publication: 2022 Jan 20.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Alcohol Dehydrogenase*/genetics
Esophageal Neoplasms*/epidemiology
Esophageal Neoplasms*/genetics
Adult ; Alcohol Drinking/adverse effects ; Alcohol Drinking/genetics ; Aldehyde Dehydrogenase/genetics ; Aldehyde Dehydrogenase, Mitochondrial/genetics ; Asians/genetics ; Female ; Genotype ; Humans ; Male ; Polymorphism, Single Nucleotide ; Prospective Studies ; Risk Factors
Czasopismo naukowe
Tytuł:
Impact and potential mechanism of effects of chronic moderate alcohol consumption on cardiac function in aldehyde dehydrogenase 2 gene heterozygous mice.
Autorzy:
Hu Q; Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Chen H; Heart Center of Fujian Province, Union Hospital, Fujian Medical University, Fuzhou, China.; Department of Cardiology, Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University, Shanghai, China.
Shen C; Department of Cardiology, Affiliated Hospital of Jining Medical University, Jining, China.
Zhang B; Department of Cardiology, Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University, Shanghai, China.; NHC Key Laboratory of Viral Heart Diseases, Shanghai, China.; Key Laboratory of Viral Heart Diseases, Chinese Academy of Medical Sciences, Shanghai, China.
Weng X; Department of Cardiology, Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University, Shanghai, China.; NHC Key Laboratory of Viral Heart Diseases, Shanghai, China.; Key Laboratory of Viral Heart Diseases, Chinese Academy of Medical Sciences, Shanghai, China.
Sun X; Department of Cardiology, Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University, Shanghai, China.; NHC Key Laboratory of Viral Heart Diseases, Shanghai, China.; Key Laboratory of Viral Heart Diseases, Chinese Academy of Medical Sciences, Shanghai, China.
Liu J; Department of Cardiology, Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University, Shanghai, China.; NHC Key Laboratory of Viral Heart Diseases, Shanghai, China.; Key Laboratory of Viral Heart Diseases, Chinese Academy of Medical Sciences, Shanghai, China.
Dong Z; Department of Cardiology, Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University, Shanghai, China.; NHC Key Laboratory of Viral Heart Diseases, Shanghai, China.; Key Laboratory of Viral Heart Diseases, Chinese Academy of Medical Sciences, Shanghai, China.
Hu K; Institutes of Biomedical Sciences, Fudan University, Shanghai, China.; Department of Cardiology, Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University, Shanghai, China.
Ge J; Institutes of Biomedical Sciences, Fudan University, Shanghai, China.; Department of Cardiology, Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University, Shanghai, China.; NHC Key Laboratory of Viral Heart Diseases, Shanghai, China.; Key Laboratory of Viral Heart Diseases, Chinese Academy of Medical Sciences, Shanghai, China.
Sun A; Institutes of Biomedical Sciences, Fudan University, Shanghai, China.; Department of Cardiology, Shanghai Institute of Cardiovascular Diseases, Zhongshan Hospital, Fudan University, Shanghai, China.; NHC Key Laboratory of Viral Heart Diseases, Shanghai, China.; Key Laboratory of Viral Heart Diseases, Chinese Academy of Medical Sciences, Shanghai, China.
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Źródło:
Alcoholism, clinical and experimental research [Alcohol Clin Exp Res] 2022 May; Vol. 46 (5), pp. 707-723. Date of Electronic Publication: 2022 Apr 20.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Alcohol Drinking*/genetics
Alcohol Drinking*/metabolism
Aldehyde Dehydrogenase, Mitochondrial*/genetics
Aldehyde Dehydrogenase, Mitochondrial*/metabolism
Aldehyde Dehydrogenase/metabolism ; Animals ; Calcium-Calmodulin-Dependent Protein Kinase Type 2/genetics ; Calcium-Calmodulin-Dependent Protein Kinase Type 2/metabolism ; Calcium-Calmodulin-Dependent Protein Kinase Type 2/pharmacology ; Ethanol/pharmacology ; Mice ; Myocytes, Cardiac/metabolism ; Ryanodine Receptor Calcium Release Channel/metabolism ; Ryanodine Receptor Calcium Release Channel/pharmacology
Czasopismo naukowe
Tytuł:
Aldehyde Dehydrogenase Enzyme Functions in Acute Leukemia Stem Cells.
Autorzy:
Dancik GM; Department of Computer Science, Eastern Connecticut State University, Willimantic, CT 06226, USA.
Voutsas IF; Cancer Immunology & Immunotherapy Center, Saint Savas Cancer Hospital, 11522 Athens, Greece.
Vlahopoulos S; First Department of Pediatrics, National and Kapodistrian University of Athens, 11527 Goudi-Athens, Greece.
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Źródło:
Frontiers in bioscience (Scholar edition) [Front Biosci (Schol Ed)] 2022 Mar 08; Vol. 14 (1), pp. 8.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms:
Aldehyde Dehydrogenase*/genetics
Aldehyde Dehydrogenase*/metabolism
Leukemia, Myeloid, Acute*/drug therapy
Acetaldehyde/metabolism ; Aldehyde Dehydrogenase, Mitochondrial ; Animals ; Humans ; Mice ; Stem Cells
Czasopismo naukowe
Tytuł:
Glucose-6-phosphate dehydrogenase deficiency is more prevalent in Duffy-null red blood cell transfusion in sickle cell disease.
Autorzy:
Yee ME; Center for Transfusion and Cellular Therapies, Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.; Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, Georgia, USA.; Department of Pediatrics, Division of Hematology/Oncology, Emory University School of Medicine, Atlanta, Georgia, USA.
Francis RO; Department of Pathology and Cell Biology, Columbia University Medical Center, New York Presbyterian Hospital, New York, New York, USA.
Luban NLC; Center for Cancer and Blood Disorders, Children's National Medical Center, Departments of Hematology and Laboratory Medicine, George Washington University School of Medicine and Health Sciences, Washington, DC, USA.
Easley KA; Department of Biostatistics and Bioinformatics, Rollins School of Public Health, Atlanta, Georgia, USA.
Lough CM; Lifesouth Community Blood Centers, Gainesville, Florida, USA.
Roback JD; Center for Transfusion and Cellular Therapies, Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.
Josephson CD; Center for Transfusion and Cellular Therapies, Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.; Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, Georgia, USA.; Department of Pediatrics, Division of Hematology/Oncology, Emory University School of Medicine, Atlanta, Georgia, USA.
Fasano RM; Center for Transfusion and Cellular Therapies, Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.; Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Atlanta, Georgia, USA.
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Źródło:
Transfusion [Transfusion] 2022 Mar; Vol. 62 (3), pp. 551-555. Date of Electronic Publication: 2022 Jan 19.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Anemia, Sickle Cell*/genetics
Anemia, Sickle Cell*/therapy
Glucosephosphate Dehydrogenase Deficiency*/epidemiology
Glucosephosphate Dehydrogenase Deficiency*/genetics
Blood Transfusion ; Child ; Erythrocyte Transfusion/adverse effects ; Erythrocytes ; Glucosephosphate Dehydrogenase ; Humans
Czasopismo naukowe
Tytuł:
Aldehydes, Aldehyde Metabolism, and the ALDH2 Consortium.
Autorzy:
Rwere F; Department of Anesthesiology, Perioperative and Pain Medicine, School of Medicine, Stanford University, Stanford, CA 94305, USA.
Yu X; Department of Anesthesiology, Perioperative and Pain Medicine, School of Medicine, Stanford University, Stanford, CA 94305, USA.
Chen CH; Department of Chemical and Systems Biology, School of Medicine, Stanford University, Stanford, CA 94305, USA.
Gross ER; Department of Anesthesiology, Perioperative and Pain Medicine, School of Medicine, Stanford University, Stanford, CA 94305, USA.
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Źródło:
Biomolecules [Biomolecules] 2022 May 30; Vol. 12 (6). Date of Electronic Publication: 2022 May 30.
Typ publikacji:
Editorial; Research Support, N.I.H., Extramural
MeSH Terms:
Aldehyde Dehydrogenase*/genetics
Aldehyde Dehydrogenase*/metabolism
Aldehydes*/metabolism
Acetaldehyde ; Aldehyde Dehydrogenase, Mitochondrial/genetics
Raport
Tytuł:
Acquired glucose 6-phosphate dehydrogenase (G6PD) deficiency in a patient with Chronic Myelomonocytic Leukemia.
Autorzy:
Naville AS; Laboratory of Haematology, University Hospital of Bordeaux, Bordeaux, France.
Lazaro E; Internal medicine department, University Hospital of Bordeaux, Bordeaux, France.
Boutin J; Laboratory of Biochemistry, University Hospital of Bordeaux, Bordeaux, France.; INSERM, BMGIC, University of Bordeaux, Bordeaux, France.; Laboratory of Excellence Gr-Ex, Paris, France.
Prot-Leurent C; Internal medicine department, University Hospital of Bordeaux, Bordeaux, France.
Mansier O; Laboratory of Haematology, University Hospital of Bordeaux, Bordeaux, France.
Richard E; Laboratory of Biochemistry, University Hospital of Bordeaux, Bordeaux, France.; INSERM, BMGIC, University of Bordeaux, Bordeaux, France.; Laboratory of Excellence Gr-Ex, Paris, France.
Augis V; Laboratory of Haematology, University Hospital of Bordeaux, Bordeaux, France.
Weinmann L; Laboratory of Haematology, University Hospital of Bordeaux, Bordeaux, France.
Fuster V; Laboratory of Haematology, University Hospital of Bordeaux, Bordeaux, France.
Vial JP; Laboratory of Haematology, University Hospital of Bordeaux, Bordeaux, France.
Ged C; Laboratory of Biochemistry, University Hospital of Bordeaux, Bordeaux, France.; INSERM, BMGIC, University of Bordeaux, Bordeaux, France.; Laboratory of Excellence Gr-Ex, Paris, France.
Dulucq S; Laboratory of Haematology, University Hospital of Bordeaux, Bordeaux, France.
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Źródło:
British journal of haematology [Br J Haematol] 2022 May; Vol. 197 (4), pp. e45-e48. Date of Electronic Publication: 2022 Jan 06.
Typ publikacji:
Letter
MeSH Terms:
Glucosephosphate Dehydrogenase Deficiency*/complications
Glucosephosphate Dehydrogenase Deficiency*/genetics
Leukemia, Myelomonocytic, Chronic*/complications
Leukemia, Myelomonocytic, Juvenile*
Erythrocytes ; Glucose ; Glucosephosphate Dehydrogenase ; Humans ; Oxidoreductases ; Phosphates
Opinia redakcyjna
Tytuł:
Variation in Glucose-6-Phosphate Dehydrogenase activity following acute malaria.
Autorzy:
Ley B; Global and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, Australia.
Alam MS; Infectious Diseases Division, International Centre for Diarrheal Diseases Research, Bangladesh, Mohakhali, Dhaka, Bangladesh.
Satyagraha AW; Eijkman Institute for Molecular Biology, Jakarta, Indonesia.
Phru CS; Infectious Diseases Division, International Centre for Diarrheal Diseases Research, Bangladesh, Mohakhali, Dhaka, Bangladesh.
Thriemer K; Global and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, Australia.
Tadesse D; Arba Minch University, College of Medicine & Health Sciences, Arba Minch, Ethiopia.
Shibiru T; Arba Minch University, College of Medicine & Health Sciences, Arba Minch, Ethiopia.
Hailu A; Arba Minch University, College of Medicine & Health Sciences, Arba Minch, Ethiopia.
Kibria MG; Infectious Diseases Division, International Centre for Diarrheal Diseases Research, Bangladesh, Mohakhali, Dhaka, Bangladesh.
Hossain MS; Infectious Diseases Division, International Centre for Diarrheal Diseases Research, Bangladesh, Mohakhali, Dhaka, Bangladesh.
Rahmat H; Eijkman Institute for Molecular Biology, Jakarta, Indonesia.
Poespoprodjo JR; Timika Malaria Research Program, Papuan Health and Community Development Foundation, Timika, Papua.; Centre for Child Health-PRO, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia.
Khan WA; Infectious Diseases Division, International Centre for Diarrheal Diseases Research, Bangladesh, Mohakhali, Dhaka, Bangladesh.
Simpson JA; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Australia.
Price RN; Global and Tropical Health Division, Menzies School of Health Research and Charles Darwin University, Darwin, Australia.; Centre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom.; Mahidol-Oxford Tropical Medicine Research Unit (MORU), Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
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Źródło:
PLoS neglected tropical diseases [PLoS Negl Trop Dis] 2022 May 11; Vol. 16 (5), pp. e0010406. Date of Electronic Publication: 2022 May 11 (Print Publication: 2022).
Typ publikacji:
Journal Article
MeSH Terms:
Antimalarials*/adverse effects
Glucosephosphate Dehydrogenase Deficiency*/complications
Malaria*/epidemiology
Malaria, Falciparum*/complications
Malaria, Vivax*/complications
Malaria, Vivax*/drug therapy
Cross-Sectional Studies ; Glucosephosphate Dehydrogenase/genetics ; Hemolysis ; Humans ; Primaquine/therapeutic use
SCR Disease Name:
Acute malaria
Czasopismo naukowe
Tytuł:
Aldehyde dehydrogenase 2 and PARP1 interaction modulates hepatic HDL biogenesis by LXRα-mediated ABCA1 expression.
Autorzy:
Li L; CAS Key Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institute of Nutrition and Health (SINH), University of the Chinese Academy of Sciences (UCAS), Chinese Academy of Sciences (CAS), Shanghai, China.
Zhong S; CAS Key Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institute of Nutrition and Health (SINH), University of the Chinese Academy of Sciences (UCAS), Chinese Academy of Sciences (CAS), Shanghai, China.
Li R; School of Life Science and Technology, ShanghaiTech University, Shanghai, China.
Liang N; CAS Key Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institute of Nutrition and Health (SINH), University of the Chinese Academy of Sciences (UCAS), Chinese Academy of Sciences (CAS), Shanghai, China.
Zhang L; CAS Key Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institute of Nutrition and Health (SINH), University of the Chinese Academy of Sciences (UCAS), Chinese Academy of Sciences (CAS), Shanghai, China.
Xia S; School of Life Science and Technology, ShanghaiTech University, Shanghai, China.
Xu X; CAS Key Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institute of Nutrition and Health (SINH), University of the Chinese Academy of Sciences (UCAS), Chinese Academy of Sciences (CAS), Shanghai, China.
Chen X; CAS Key Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institute of Nutrition and Health (SINH), University of the Chinese Academy of Sciences (UCAS), Chinese Academy of Sciences (CAS), Shanghai, China.
Chen S; CAS Key Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institute of Nutrition and Health (SINH), University of the Chinese Academy of Sciences (UCAS), Chinese Academy of Sciences (CAS), Shanghai, China.
Tao Y; CAS Key Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institute of Nutrition and Health (SINH), University of the Chinese Academy of Sciences (UCAS), Chinese Academy of Sciences (CAS), Shanghai, China.
Yin H; CAS Key Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institute of Nutrition and Health (SINH), University of the Chinese Academy of Sciences (UCAS), Chinese Academy of Sciences (CAS), Shanghai, China.; School of Life Science and Technology, ShanghaiTech University, Shanghai, China.; Key Laboratory of Food Safety Risk Assessment, Ministry of Health, Beijing, China.
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Źródło:
JCI insight [JCI Insight] 2022 Apr 08; Vol. 7 (7). Date of Electronic Publication: 2022 Apr 08.
Typ publikacji:
Journal Article
MeSH Terms:
ATP Binding Cassette Transporter 1*/genetics
ATP Binding Cassette Transporter 1*/metabolism
Aldehyde Dehydrogenase*/metabolism
Lipoproteins, HDL*/biosynthesis
Liver*/metabolism
Liver X Receptors*/genetics
Liver X Receptors*/metabolism
Aldehyde Dehydrogenase, Mitochondrial ; Animals ; Cardiovascular Diseases/metabolism ; Humans ; Mice ; Poly (ADP-Ribose) Polymerase-1 ; Transcriptional Activation
Czasopismo naukowe
Tytuł:
Aldehyde Dehydrogenase 1B1 Is Implicated in DNA Damage Response in Human Colorectal Adenocarcinoma.
Autorzy:
Tsochantaridis I; Department of Molecular Biology & Genetics, Faculty of Health Sciences, Democritus University of Thrace, 68100 Alexandroupolis, Greece.
Kontopoulos A; Department of Molecular Biology & Genetics, Faculty of Health Sciences, Democritus University of Thrace, 68100 Alexandroupolis, Greece.
Voulgaridou GP; Department of Molecular Biology & Genetics, Faculty of Health Sciences, Democritus University of Thrace, 68100 Alexandroupolis, Greece.
Tsifintaris M; Department of Molecular Biology & Genetics, Faculty of Health Sciences, Democritus University of Thrace, 68100 Alexandroupolis, Greece.
Triantafyllou C; Department of Molecular Biology & Genetics, Faculty of Health Sciences, Democritus University of Thrace, 68100 Alexandroupolis, Greece.
Pappa A; Department of Molecular Biology & Genetics, Faculty of Health Sciences, Democritus University of Thrace, 68100 Alexandroupolis, Greece.
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Źródło:
Cells [Cells] 2022 Jun 24; Vol. 11 (13). Date of Electronic Publication: 2022 Jun 24.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Adenocarcinoma*/genetics
Colorectal Neoplasms*/genetics
Colorectal Neoplasms*/pathology
Aldehyde Dehydrogenase 1 Family/*metabolism
Aldehyde Dehydrogenase, Mitochondrial/*metabolism
Aldehyde Dehydrogenase/metabolism ; Aldehyde Dehydrogenase, Mitochondrial/genetics ; DNA Damage ; DNA-Binding Proteins/metabolism ; Humans ; Ubiquitin-Protein Ligases/metabolism ; X-ray Repair Cross Complementing Protein 1/genetics
Czasopismo naukowe
Tytuł:
Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong.
Autorzy:
Xu JX; Central Laboratory, Chaozhou Central Hospital Affiliated to Southern Medical University, Chaozhou, 521021, Guangdong Province, People's Republic of China.
Lin F; Central Laboratory, Chaozhou Central Hospital Affiliated to Southern Medical University, Chaozhou, 521021, Guangdong Province, People's Republic of China.
Chen ZK; School of Food Engineering and Biotechnology, Hanshan Normal University, Chaozhou, 521021, Guangdong Province, People's Republic of China.
Luo ZY; Central Laboratory, Chaozhou Central Hospital Affiliated to Southern Medical University, Chaozhou, 521021, Guangdong Province, People's Republic of China.
Zhan XF; Central Laboratory, Chaozhou Central Hospital Affiliated to Southern Medical University, Chaozhou, 521021, Guangdong Province, People's Republic of China.
Wu JR; Central Laboratory, Chaozhou Central Hospital Affiliated to Southern Medical University, Chaozhou, 521021, Guangdong Province, People's Republic of China.
Ma YB; Department of Pediatrics, Chaozhou Central Hospital Affiliated to Southern Medical University, Chaozhou, 521021, Guangdong Province, People's Republic of China.
Li JD; Department of Pediatrics, Chaozhou Central Hospital Affiliated to Southern Medical University, Chaozhou, 521021, Guangdong Province, People's Republic of China.
Yang LY; Precision Medical Center, People's Hospital of Yangjiang Affiliated to Guangdong Medical University, No. 42 Dongshan Road, Yangjiang, 529500, Guangdong Province, People's Republic of China. .
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Źródło:
BMC pediatrics [BMC Pediatr] 2021 Dec 11; Vol. 21 (1), pp. 564. Date of Electronic Publication: 2021 Dec 11.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Glucosephosphate Dehydrogenase Deficiency*/complications
Glucosephosphate Dehydrogenase Deficiency*/genetics
Glucuronosyltransferase*/genetics
Hyperbilirubinemia, Neonatal*/genetics
Genotype ; Glucosephosphate Dehydrogenase/genetics ; Heterozygote ; Humans ; Infant, Newborn ; Mutation ; Retrospective Studies
Czasopismo naukowe
Tytuł:
Management of children with glucose-6-phosphate dehydrogenase deficiency presenting with acute haemolytic crisis during the SARs-COV-2 pandemic.
Autorzy:
Elalfy M; Paediatrics Department, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Adly A; Paediatrics Department, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Eltonbary K; Paediatrics Department, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Elghamry I; Paediatrics Department, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Elalfy O; Complementary Medicine Department, National Research Center, Giza, Egypt.
Maebid M; Paediatrics Department, Faculty of Medicine, Beni-Suef University, Beni Suef, Egypt.
Elsayh K; Paediatrics Department, Faculty of Medicine, Assuit University, Assiut, Egypt.
Elsayed HN; Ain Shams University Hospitals Blood Bank, Cairo, Egypt.
El Ekiaby M; Shabrawishy Blood Bank, Giza, Egypt.
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Źródło:
Vox sanguinis [Vox Sang] 2022 Jan; Vol. 117 (1), pp. 80-86. Date of Electronic Publication: 2021 Jun 08.
Typ publikacji:
Journal Article
MeSH Terms:
COVID-19*
Glucosephosphate Dehydrogenase Deficiency*/epidemiology
Blood Transfusion ; Child ; Glucosephosphate Dehydrogenase ; Humans ; Pandemics ; SARS-CoV-2
Czasopismo naukowe

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