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pro vyhledávání: '"Reilly ML"'
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Autor:
Kim C, Tang G, Pogue-Geile KL, Costantino JP, Baehner FL, Baker J, Cronin MT, Watson D, Shak S, Bohn OL, Fumagalli D, Taniyama Y, Lee A, Reilly ML, Vogel VG, McCaskill-Stevens W, Ford LG, Geyer CE Jr, Wickerham DL, Wolmark N
Publikováno v:
Journal of Clinical Oncology; 11/1/2011, Vol. 29 Issue 31, p4160-4167, 8p
Autor:
Kemper NS; Department of Psychology, University at Albany, State University of New York., Reilly ML; New York State Office of Mental Health., Freeman NJ; New York State Office of Mental Health., Sandler JC; New York State Office of Mental Health.
Publikováno v:
Law and human behavior [Law Hum Behav] 2024 Feb; Vol. 48 (1), pp. 67-82. Date of Electronic Publication: 2024 Jan 22.
Autor:
Reilly ML; Imagine Institute, Laboratory of Inherited Kidney Diseases, Institut National de la Santé et de la Recherche Médicale (INSERM) Unités Mixtes de Recherche (UMR) 1163, Université Paris Cité, Paris, France., Ain NU; School of Biological Sciences, University of the Punjab, Lahore, Pakistan.; Department of Molecular Medicine and Surgery and Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden., Muurinen M; Folkhälsan Research Center, Helsinki, Finland.; Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Research Program for Clinical and Molecular Metabolism, University of Helsinki, Helsinki, Finland., Tata A; Imagine Institute, Laboratory of Inherited Kidney Diseases, Institut National de la Santé et de la Recherche Médicale (INSERM) Unités Mixtes de Recherche (UMR) 1163, Université Paris Cité, Paris, France., Huber C; Imagine Institute, Laboratory of Molecular and Physiopathological bases of Osteochondrodysplasia, Institut National de la Santé et de la Recherche Médicale (INSERM) Unités Mixtes de Recherche (UMR) 1163, Université Paris Cité, Paris, France.; Department of Genetics, Reference Centre for Skeletal Dysplasia, Assistance Publique-Hôpitaux de Paris, Necker-Enfants Malades Hospital, Paris, France., Simon M; Department of Medical Genetics, University Medical Centre Utrecht, Utrecht, The Netherlands., Ishaq T; School of Biological Sciences, University of the Punjab, Lahore, Pakistan., Shaw N; Department of Endocrinology & Diabetes, Birmingham Children's Hospital, Birmingham, UK.; Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, UK., Rusanen S; Folkhälsan Research Center, Helsinki, Finland., Pekkinen M; Folkhälsan Research Center, Helsinki, Finland.; Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Research Program for Clinical and Molecular Metabolism, University of Helsinki, Helsinki, Finland., Högler W; Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, UK.; Department of Paediatrics and Adolescent Medicine, Johannes Kepler University Linz, Linz, Austria., Knapen MFCM; Department of Obstetrics and Fetal Medicine, Erasmus Medical Center, Rotterdam, The Netherlands., van den Born M; Department of Clinical Genetics, Erasmus MC, University Medical Center, Rotterdam, The Netherlands., Saunier S; Imagine Institute, Laboratory of Inherited Kidney Diseases, Institut National de la Santé et de la Recherche Médicale (INSERM) Unités Mixtes de Recherche (UMR) 1163, Université Paris Cité, Paris, France., Naz S; School of Biological Sciences, University of the Punjab, Lahore, Pakistan., Cormier-Daire V; Imagine Institute, Laboratory of Molecular and Physiopathological bases of Osteochondrodysplasia, Institut National de la Santé et de la Recherche Médicale (INSERM) Unités Mixtes de Recherche (UMR) 1163, Université Paris Cité, Paris, France.; Department of Genetics, Reference Centre for Skeletal Dysplasia, Assistance Publique-Hôpitaux de Paris, Necker-Enfants Malades Hospital, Paris, France., Benmerah A; Imagine Institute, Laboratory of Inherited Kidney Diseases, Institut National de la Santé et de la Recherche Médicale (INSERM) Unités Mixtes de Recherche (UMR) 1163, Université Paris Cité, Paris, France., Makitie O; Department of Molecular Medicine and Surgery and Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.; Folkhälsan Research Center, Helsinki, Finland.; Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Research Program for Clinical and Molecular Metabolism, University of Helsinki, Helsinki, Finland.
Publikováno v:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research [J Bone Miner Res] 2022 Sep; Vol. 37 (9), pp. 1642-1652. Date of Electronic Publication: 2022 Jul 19.
Autor:
Carretero-Rodriguez L; School of Life Sciences, University of Sussex, Brighton BN7 9QG, United Kingdom., Guðjónsdóttir R; School of Life Sciences, University of Sussex, Brighton BN7 9QG, United Kingdom., Poparic I; Department of Developmental Neurobiology, King's College London, London SE1 1UL, United Kingdom., Reilly ML; School of Life Sciences, University of Sussex, Brighton BN7 9QG, United Kingdom., Chol M; Department of Developmental Neurobiology, King's College London, London SE1 1UL, United Kingdom., Bianco IH; Department of Neuroscience, Physiology and Pharmacology, University College London, London WC1E 6BT, United Kingdom., Chiapello M; Cambridge Centre for Proteomics, Cambridge Systems Biology Centre, Department of Biochemistry, University of Cambridge, Cambridge CB2 1QR, United Kingdom., Feret R; Institute for Sustainable Plant Protection, National Research Council, 10135 Torino, Italy., Deery MJ; Institute for Sustainable Plant Protection, National Research Council, 10135 Torino, Italy., Guthrie S; School of Life Sciences, University of Sussex, Brighton BN7 9QG, United Kingdom s.guthrie@sussex.ac.uk.
Publikováno v:
The Journal of neuroscience : the official journal of the Society for Neuroscience [J Neurosci] 2021 Aug 04; Vol. 41 (31), pp. 6652-6672. Date of Electronic Publication: 2021 Jun 24.
Autor:
Pejskova P; Department of Histology and Embryology, Masaryk University, Faculty of Medicine, Brno, Czech Republic., Reilly ML; Laboratory of Hereditary Kidney Diseases, Institut National de la Santé et de la Recherche Médicale UMR 1163, Paris University, Imagine Institute, Paris, France.; Paris Diderot University, Paris, France., Bino L; Department of Histology and Embryology, Masaryk University, Faculty of Medicine, Brno, Czech Republic., Bernatik O; Department of Histology and Embryology, Masaryk University, Faculty of Medicine, Brno, Czech Republic., Dolanska L; Department of Histology and Embryology, Masaryk University, Faculty of Medicine, Brno, Czech Republic., Ganji RS; Central European Institute of Technology, Brno, Czech Republic., Zdrahal Z; Central European Institute of Technology, Brno, Czech Republic., Benmerah A; Laboratory of Hereditary Kidney Diseases, Institut National de la Santé et de la Recherche Médicale UMR 1163, Paris University, Imagine Institute, Paris, France., Cajanek L; Department of Histology and Embryology, Masaryk University, Faculty of Medicine, Brno, Czech Republic.
Publikováno v:
The Journal of cell biology [J Cell Biol] 2020 Jun 01; Vol. 219 (6).
Autor:
Thomas S; Laboratory of Embryology and Genetics of Human Malformation, INSERM UMR 1163, Paris Descartes University, Imagine Institute, 75015, Paris, France., Boutaud L; Laboratory of Embryology and Genetics of Human Malformation, INSERM UMR 1163, Paris Descartes University, Imagine Institute, 75015, Paris, France., Reilly ML; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Paris Descartes University, Imagine Institute, 75015, Paris, France.; Paris Diderot University, 75013, Paris, France., Benmerah A; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Paris Descartes University, Imagine Institute, 75015, Paris, France.
Publikováno v:
Biology of the cell [Biol Cell] 2019 Sep; Vol. 111 (9), pp. 217-231. Date of Electronic Publication: 2019 Jun 17.
Autor:
Reilly ML; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Paris Descartes University, Imagine Institute, Paris, 75015, France.; Paris Diderot University, Paris, 75013, France., Benmerah A; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Paris Descartes University, Imagine Institute, Paris, 75015, France.
Publikováno v:
Biology of the cell [Biol Cell] 2019 Apr; Vol. 111 (4), pp. 79-94. Date of Electronic Publication: 2019 Feb 15.
Autor:
Reilly ML; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Imagine Institute, Paris, France.; Paris Diderot University, Department of Life Sciences, Paris, France., Stokman MF; Department of Genetics, University Medical Center Utrecht, Utrecht University, JE Utrecht, Netherlands., Magry V; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Imagine Institute, Paris, France., Jeanpierre C; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Imagine Institute, Paris, France., Alves M; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Imagine Institute, Paris, France., Paydar M; Institute for Research in Immunology and Cancer, Département de médecine, Université de Montréal, PO Box 6128, Station Centre-Ville, Montréal, QC, Canada., Hellinga J; Department of Biomedical and Molecular Sciences, Queen's University, Kingston, ON K7L 3N6, Canada., Delous M; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Imagine Institute, Paris, France., Pouly D; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Imagine Institute, Paris, France., Failler M; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Imagine Institute, Paris, France., Martinovic J; Unit of Fetal Pathology, Antoine Béclère Hospital, AP-HP, Clamart, France.; INSERM U-788, Génétique/Neurogénétique, 94270 Le Kremlin-Bicêtre, France., Loeuillet L; Service d'Histologie-Embryologie-Cytogénétique, Hôpital Necker-Enfants Malades, AP-HP, Paris, France., Leroy B; Service d'Anatomie et de Cytologie Pathologiques, Centre hospitalier intercommunal de Poissy, Saint Germain en Laye, France., Tantau J; Service d'Anatomie et de Cytologie Pathologiques, Centre hospitalier intercommunal de Poissy, Saint Germain en Laye, France., Roume J; Service de Génétique, Centre hospitalier intercommunal de Poissy, 78100 Saint Germain en Laye, France., Gregory-Evans CY; Department of Ophthalmology, University of British Columbia, Vancouver, BC V6T 1Z4, Canada., Shan X; Department of Ophthalmology, University of British Columbia, Vancouver, BC V6T 1Z4, Canada., Filges I; Medical Genetics, Institute of Medical Genetics and Pathology, University Hospital of Basel, University of Basel, Basel, Switzerland.; Department of Clinical Research, University Hospital of Basel, University of Basel, Basel, Switzerland.; Department of Genetics, University of British Columbia, Vancouver, BC V6T 1Z4, Canada., Allingham JS; Department of Biomedical and Molecular Sciences, Queen's University, Kingston, ON K7L 3N6, Canada., Kwok BH; Institute for Research in Immunology and Cancer, Département de médecine, Université de Montréal, PO Box 6128, Station Centre-Ville, Montréal, QC, Canada., Saunier S; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Imagine Institute, Paris, France., Giles RH; Department of Nephrology and Hypertension, University Medical Center Utrecht, Utrecht University, 3512 JE Utrecht, Netherlands., Benmerah A; Laboratory of Hereditary Kidney Diseases, INSERM UMR 1163, Imagine Institute, Paris, France.
Publikováno v:
Human molecular genetics [Hum Mol Genet] 2019 Mar 01; Vol. 28 (5), pp. 778-795.
Autor:
Cavallin M; Laboratory of Embryology and Genetics of Congenital Malformations, INSERM UMR1163, Imagine Institute, Paris, France; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France; Pediatric Neurology APHP- Necker Enfants Malades University Hospital, Paris, France. Electronic address: mara.cavallin@institutimagine.org., Maillard C; Laboratory of Embryology and Genetics of Congenital Malformations, INSERM UMR1163, Imagine Institute, Paris, France; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France; Pediatric Neurology APHP- Necker Enfants Malades University Hospital, Paris, France., Hully M; Pediatric Neurology APHP- Necker Enfants Malades University Hospital, Paris, France; Centre de Référence 'Déficiences intellectuelles de causes rares', APHP- Necker Enfants Malades University Hospital, Paris, France., Philbert M; Laboratory of Embryology and Genetics of Congenital Malformations, INSERM UMR1163, Imagine Institute, Paris, France; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France; Pediatric Neurology APHP- Necker Enfants Malades University Hospital, Paris, France., Boddaert N; Pediatric Radiology APHP- Necker Enfants Malades University Hospital, Paris, France; Image- Institut Imagine, INSERM UMR1163, Paris Descartes University, Hôpital Necker Enfants Malades, Paris, France., Reilly ML; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France; Laboratory of inherited kidney diseases, INSERM UMR1163, Imagine Institute, Paris, France; Paris Diderot University, 75013, Paris, France., Nitschké P; Bioinformatic Core Facility, INSERM UMR1163, Imagine Institute, Paris, France., Bery A; Laboratory of Embryology and Genetics of Congenital Malformations, INSERM UMR1163, Imagine Institute, Paris, France; Genetics and development of the cerebral cortex, Institut Imagine, Paris, France. Electronic address: amandine.bery@inserm.fr., Bahi-Buisson N; Laboratory of Embryology and Genetics of Congenital Malformations, INSERM UMR1163, Imagine Institute, Paris, France; Paris Descartes-Sorbonne Paris Cité University, Imagine Institute, Paris, France; Pediatric Neurology APHP- Necker Enfants Malades University Hospital, Paris, France; Centre de Référence 'Déficiences intellectuelles de causes rares', APHP- Necker Enfants Malades University Hospital, Paris, France; Genetics and development of the cerebral cortex, Institut Imagine, Paris, France. Electronic address: nadia.bahi-buisson@nck.aphp.fr.
Publikováno v:
European journal of medical genetics [Eur J Med Genet] 2018 Dec; Vol. 61 (12), pp. 729-732. Date of Electronic Publication: 2018 May 25.