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Wyszukujesz frazę ""Cudré-Cung, Hong-Phuc"" wg kryterium: Autor


Wyświetlanie 1-14 z 14
Tytuł :
New in vitro model derived from brain-specific Mut-/- mice confirms cerebral ammonium accumulation in methylmalonic aciduria
Autorzy :
Remacle, Noémie
Forny, Patrick
Cudré-Cung, Hong-Phuc
Gonzalez-Melo, Mary
do Vale-Pereira, Sónia
Henry, Hugues
Teav, Tony
Gallart-Ayala, Hector
Braissant, Olivier
Baumgartner, Matthias
Ballhausen, Diana
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Temat :
Medical Clinic
610 Medicine & health
Źródło :
Remacle, Noémie; Forny, Patrick; Cudré-Cung, Hong-Phuc; Gonzalez-Melo, Mary; do Vale-Pereira, Sónia; Henry, Hugues; Teav, Tony; Gallart-Ayala, Hector; Braissant, Olivier; Baumgartner, Matthias; Ballhausen, Diana (2018). New in vitro model derived from brain-specific Mut-/- mice confirms cerebral ammonium accumulation in methylmalonic aciduria. Molecular Genetics and Metabolism, 124(4):266-277.
Tytuł :
Immunolocalization of glutaryl-CoA dehydrogenase (GCDH) in adult and embryonic rat brain and peripheral tissues
Autorzy :
Braissant, Olivier
Jafari, Paris
Remacle, Noémie
Cudré-Cung, Hong-Phuc
Do Vale Pereira, Sonia
Ballhausen, Diana
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Temat :
Medical Clinic
610 Medicine & health
General Neuroscience
Źródło :
Braissant, Olivier; Jafari, Paris; Remacle, Noémie; Cudré-Cung, Hong-Phuc; Do Vale Pereira, Sonia; Ballhausen, Diana (2017). Immunolocalization of glutaryl-CoA dehydrogenase (GCDH) in adult and embryonic rat brain and peripheral tissues. Neuroscience, 343:355-363.
Tytuł :
Ammonium accumulation and chemokine decrease in culture media of Gcdh−/− 3D reaggregated brain cell cultures.
Autorzy :
Cudré-Cung, Hong-Phuc (AUTHOR) thanh-hong-phuc.cung@chuv.ch
Remacle, Noémie (AUTHOR)
do Vale-Pereira, Sonia (AUTHOR)
Gonzalez, Mary (AUTHOR)
Henry, Hugues (AUTHOR)
Ivanisevic, Julijana (AUTHOR)
Schmiesing, Jessica (AUTHOR)
Mühlhausen, Chris (AUTHOR)
Braissant, Olivier (AUTHOR)
Ballhausen, Diana (AUTHOR)
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Źródło :
Molecular Genetics & Metabolism. Apr2019, Vol. 126 Issue 4, p416-428. 13p.
Czasopismo naukowe
Tytuł :
The first knock-in rat model for glutaric aciduria type I allows further insights into pathophysiology in brain and periphery.
Autorzy :
Gonzalez Melo, Mary (AUTHOR)
Remacle, Noémie (AUTHOR)
Cudré-Cung, Hong-Phuc (AUTHOR)
Roux, Clothilde (AUTHOR)
Poms, Martin (AUTHOR)
Cudalbu, Cristina (AUTHOR)
Barroso, Madalena (AUTHOR)
Gersting, Søren Waldemar (AUTHOR)
Feichtinger, René Günther (AUTHOR)
Mayr, Johannes Adalbert (AUTHOR)
Costanzo, Michele (AUTHOR)
Caterino, Marianna (AUTHOR)
Ruoppolo, Margherita (AUTHOR)
Rüfenacht, Véronique (AUTHOR)
Häberle, Johannes (AUTHOR)
Braissant, Olivier (AUTHOR)
Ballhausen, Diana (AUTHOR)
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Źródło :
Molecular Genetics & Metabolism. Jun2021, Vol. 133 Issue 2, p157-181. 25p.
Czasopismo naukowe
Tytuł :
The first knock-in rat model for glutaric aciduria type I allows further insights into pathophysiology in brain and periphery.
Autorzy :
Gonzalez Melo M; Pediatric Metabolic Unit, Pediatrics, Woman-Mother-Child Department, University of Lausanne and University Hospital of Lausanne, Switzerland. Electronic address: .
Remacle N; Pediatric Metabolic Unit, Pediatrics, Woman-Mother-Child Department, University of Lausanne and University Hospital of Lausanne, Switzerland.
Cudré-Cung HP; Pediatric Metabolic Unit, Pediatrics, Woman-Mother-Child Department, University of Lausanne and University Hospital of Lausanne, Switzerland.
Roux C; Service of Clinical Chemistry, University of Lausanne and University Hospital of Lausanne, Switzerland. Electronic address: .
Poms M; Klinische Chemie und Biochemie Universitäts-Kinderspital Zürich, Switzerland. Electronic address: .
Cudalbu C; CIBM Center for Biomedical Imaging, Switzerland; Animal Imaging and Technology, Ecole Polytechnique Fédérale de Lausanne, Lausanne, Switzerland. Electronic address: .
Barroso M; University Children's Research, , University Medical Center Hamburg-Eppendorf, Hamburg, Germany. Electronic address: .
Gersting SW; University Children's Research, , University Medical Center Hamburg-Eppendorf, Hamburg, Germany. Electronic address: .
Feichtinger RG; Department of Pediatrics, University Hospital Salzburg, Paracelsus Medical University, Salzburg, Austria. Electronic address: .
Mayr JA; Department of Pediatrics, University Hospital Salzburg, Paracelsus Medical University, Salzburg, Austria. Electronic address: .
Costanzo M; Department of Molecular Medicine and Medical Biotechnology, School of Medicine, University of Naples Federico II, 80131 Naples, Italy; CEINGE - Biotecnologie Avanzate s.c.ar.l., 80145 Naples, Italy. Electronic address: .
Caterino M; Department of Molecular Medicine and Medical Biotechnology, School of Medicine, University of Naples Federico II, 80131 Naples, Italy; CEINGE - Biotecnologie Avanzate s.c.ar.l., 80145 Naples, Italy. Electronic address: .
Ruoppolo M; Department of Molecular Medicine and Medical Biotechnology, School of Medicine, University of Naples Federico II, 80131 Naples, Italy; CEINGE - Biotecnologie Avanzate s.c.ar.l., 80145 Naples, Italy. Electronic address: .
Rüfenacht V; Division of Metabolism and Children's Research Center, University Children's Hospital Zurich, Zurich, Switzerland. Electronic address: .
Häberle J; Division of Metabolism and Children's Research Center, University Children's Hospital Zurich, Zurich, Switzerland. Electronic address: .
Braissant O; Service of Clinical Chemistry, University of Lausanne and University Hospital of Lausanne, Switzerland. Electronic address: .
Ballhausen D; Pediatric Metabolic Unit, Pediatrics, Woman-Mother-Child Department, University of Lausanne and University Hospital of Lausanne, Switzerland. Electronic address: .
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Źródło :
Molecular genetics and metabolism [Mol Genet Metab] 2021 Jun; Vol. 133 (2), pp. 157-181. Date of Electronic Publication: 2021 Apr 18.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Amino Acid Metabolism, Inborn Errors/*genetics
Brain/*metabolism
Brain Diseases, Metabolic/*genetics
Gliosis/*genetics
Glutaryl-CoA Dehydrogenase/*deficiency
Glutaryl-CoA Dehydrogenase/*genetics
Amino Acid Metabolism, Inborn Errors/metabolism ; Amino Acid Metabolism, Inborn Errors/pathology ; Animals ; Arginine/metabolism ; Brain/pathology ; Brain Diseases, Metabolic/metabolism ; Brain Diseases, Metabolic/pathology ; Creatine/blood ; Disease Models, Animal ; Gene Knock-In Techniques ; Gliosis/metabolism ; Gliosis/pathology ; Glutaryl-CoA Dehydrogenase/metabolism ; Humans ; Lysine/metabolism ; Metabolism, Inborn Errors/genetics ; Metabolism, Inborn Errors/metabolism ; Rats
SCR Disease Name :
Glutaric Acidemia I
Czasopismo naukowe
Tytuł :
Ammonium accumulation and chemokine decrease in culture media of Gcdh 3D reaggregated brain cell cultures.
Autorzy :
Cudré-Cung HP; Pediatric Metabolic Disease Unit, Department of Pediatrics, Lausanne University Hospital, Chemin de Mont-Paisible 18, 1011 Lausanne, Switzerland. Electronic address: thanh-hong-phuc.cung@chuv.ch.
Remacle N; Pediatric Metabolic Disease Unit, Department of Pediatrics, Lausanne University Hospital, Chemin de Mont-Paisible 18, 1011 Lausanne, Switzerland. Electronic address: .
do Vale-Pereira S; Pediatric Metabolic Disease Unit, Department of Pediatrics, Lausanne University Hospital, Chemin de Mont-Paisible 18, 1011 Lausanne, Switzerland.
Gonzalez M; Pediatric Metabolic Disease Unit, Department of Pediatrics, Lausanne University Hospital, Chemin de Mont-Paisible 18, 1011 Lausanne, Switzerland. Electronic address: .
Henry H; Service of Clinical Chemistry, Lausanne University Hospital, Rue du Bugnon 46, 1011 Lausanne, Switzerland.
Ivanisevic J; Metabolomics Platform, Faculty of Biology and Medicine, University of Lausanne, Rue du Bugnon 19, 1005 Lausanne, Switzerland. Electronic address: .
Schmiesing J; Department of Biochemistry, University Medical Center Hamburg-Eppendorf, University Children's Hospital, Martinistrasse 52, 20246 Hamburg, Germany. Electronic address: .
Mühlhausen C; Department of Biochemistry, University Medical Center Hamburg-Eppendorf, University Children's Hospital, Martinistrasse 52, 20246 Hamburg, Germany. Electronic address: .
Braissant O; Service of Clinical Chemistry, Lausanne University Hospital, Rue du Bugnon 46, 1011 Lausanne, Switzerland. Electronic address: .
Ballhausen D; Pediatric Metabolic Disease Unit, Department of Pediatrics, Lausanne University Hospital, Chemin de Mont-Paisible 18, 1011 Lausanne, Switzerland. Electronic address: .
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Źródło :
Molecular genetics and metabolism [Mol Genet Metab] 2019 Apr; Vol. 126 (4), pp. 416-428. Date of Electronic Publication: 2019 Jan 18.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Ammonium Compounds/*analysis
Brain/*cytology
Chemokines/*analysis
Culture Media/*analysis
Glutaryl-CoA Dehydrogenase/*genetics
Amino Acid Metabolism, Inborn Errors/genetics ; Ammonium Compounds/metabolism ; Animals ; Brain/drug effects ; Brain/pathology ; Brain Diseases, Metabolic/genetics ; Cell Culture Techniques ; Chemokines/metabolism ; Culture Media/metabolism ; Glutaryl-CoA Dehydrogenase/deficiency ; Lysine/pharmacology ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Tissue Scaffolds
SCR Disease Name :
Glutaric Acidemia I
Czasopismo naukowe
Tytuł :
Ammonium accumulation is a primary effect of 2-methylcitrate exposure in an in vitro model for brain damage in methylmalonic aciduria.
Autorzy :
Cudré-Cung HP; Center of Molecular Diseases, Lausanne University Hospital, Switzerland.
Zavadakova P; Center of Molecular Diseases, Lausanne University Hospital, Switzerland.
do Vale-Pereira S; Center of Molecular Diseases, Lausanne University Hospital, Switzerland.
Remacle N; Center of Molecular Diseases, Lausanne University Hospital, Switzerland.
Henry H; Biomedicine, Innovation & Development, Lausanne University Hospital, Switzerland.
Ivanisevic J; Metabolomics Research Platform, Faculty of Biology and Medicine, University of Lausanne, Switzerland.
Tavel D; Department of Physiology, Lausanne University, Switzerland.
Braissant O; Biomedicine, Lausanne University Hospital, Switzerland.
Ballhausen D; Center of Molecular Diseases, Lausanne University Hospital, Switzerland. Electronic address: .
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Źródło :
Molecular genetics and metabolism [Mol Genet Metab] 2016 Sep; Vol. 119 (1-2), pp. 57-67. Date of Electronic Publication: 2016 Jul 30.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Amino Acid Metabolism, Inborn Errors/*metabolism
Ammonium Compounds/*metabolism
Brain Injuries/*metabolism
Citrates/*toxicity
Amino Acid Chloromethyl Ketones/pharmacology ; Amino Acid Metabolism, Inborn Errors/chemically induced ; Amino Acid Metabolism, Inborn Errors/physiopathology ; Ammonium Compounds/toxicity ; Animals ; Apoptosis/drug effects ; Brain Injuries/chemically induced ; Brain Injuries/pathology ; Caspase 3/metabolism ; Cell Culture Techniques ; Culture Media/chemistry ; Glutamine/metabolism ; Humans ; Neurons/drug effects ; Neurons/metabolism ; Neurons/pathology ; Quinolines/pharmacology ; Rats
SCR Disease Name :
Methylmalonic acidemia
Czasopismo naukowe
    Wyświetlanie 1-14 z 14

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