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Wyświetlanie 1-12 z 12
Tytuł :
Genome-Wide Association for HbA1c in Malay Identified Deletion on SLC4A1 that Influences HbA1c Independent of Glycemia.
Autorzy :
Chai JF; Saw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore, Singapore.
Kao SL; Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore and National University Health System, Singapore, Singapore.
Wang C; Department of Epidemiology and Biostatistics, Key Laboratory for Environment and Health, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.; Genome Institute of Singapore, Agency for Science, Technology and Research, Singapore.
Lim VJ; Saw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore, Singapore.
Khor IW; Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore and National University Health System, Singapore, Singapore.
Dou J; Department of Epidemiology and Biostatistics, Key Laboratory for Environment and Health, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.; Genome Institute of Singapore, Agency for Science, Technology and Research, Singapore.
Podgornaia AI; Merck Research Laboratories, Kenilworth, New Jersey.
Chothani S; Genome Institute of Singapore, Agency for Science, Technology and Research, Singapore.
Cheng CY; Singapore Eye Research Institute, Singapore National Eye Centre, Singapore, Singapore.; Ophthalmology & Visual Sciences Academic Clinical Program (Eye ACP), Duke-NUS Medical School, Singapore, Singapore.; Department of Ophthalmology, Yong Loo Lin School of Medicine, National University of Singapore and National University Health System, Singapore, Singapore.
Sabanayagam C; Singapore Eye Research Institute, Singapore National Eye Centre, Singapore, Singapore.; Ophthalmology & Visual Sciences Academic Clinical Program (Eye ACP), Duke-NUS Medical School, Singapore, Singapore.
Wong TY; Singapore Eye Research Institute, Singapore National Eye Centre, Singapore, Singapore.; Ophthalmology & Visual Sciences Academic Clinical Program (Eye ACP), Duke-NUS Medical School, Singapore, Singapore.; Department of Ophthalmology, Yong Loo Lin School of Medicine, National University of Singapore and National University Health System, Singapore, Singapore.
van Dam RM; Saw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore, Singapore.; Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore and National University Health System, Singapore, Singapore.; Department of Nutrition, Harvard T.H Chan School of Public Health, Boston, Massachusetts.
Liu J; Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore and National University Health System, Singapore, Singapore.; Genome Institute of Singapore, Agency for Science, Technology and Research, Singapore.
Reilly DF; Merck Research Laboratories, Kenilworth, New Jersey.; Janssen Pharmaceuticals Inc, Titusville, New Jersey.
Paterson AD; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Canada.; Divisions of Epidemiology and Biostatistics, Dalla Lana School of Public Health, University of Toronto, Canada.
Sim X; Saw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore, Singapore.
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Źródło :
The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 2020 Dec 01; Vol. 105 (12).
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
TaxoNN: ensemble of neural networks on stratified microbiome data for disease prediction.
Autorzy :
Sharma D; Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada M5T 3M7.
Paterson AD; Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada M5T 3M7.; Genetics and Genome Biology Program, The Hospital for Sick Children, Toronto, ON, Canada, M5G 1X8.
Xu W; Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada M5T 3M7.; Department of Biostatistics, Princess Margaret Cancer Center, University Health Network, Toronto, ON, Canada, M5G 2C1.
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Źródło :
Bioinformatics (Oxford, England) [Bioinformatics] 2020 Nov 01; Vol. 36 (17), pp. 4544-4550.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Association of systemic lupus erythematosus (SLE) genetic susceptibility loci with lupus nephritis in childhood-onset and adult-onset SLE.
Autorzy :
Webber D; Division of Rheumatology, Department of Pediatrics, University of Toronto, Toronto, Canada.
Cao J; Genetics & Genome Biology, Research Institute, SickKids Hospital, Toronto, Canada.
Dominguez D; Division of Rheumatology, Department of Pediatrics, University of Toronto, Toronto, Canada.
Gladman DD; Krembil Research Institute, Toronto Western Hospital, Toronto, Canada.
Levy DM; Division of Rheumatology, Department of Pediatrics, University of Toronto, Toronto, Canada.
Ng L; Division of Rheumatology, Department of Pediatrics, University of Toronto, Toronto, Canada.
Paterson AD; Genetics & Genome Biology, Research Institute, SickKids Hospital, Toronto, Canada.
Touma Z; Krembil Research Institute, Toronto Western Hospital, Toronto, Canada.
Urowitz MB; Krembil Research Institute, Toronto Western Hospital, Toronto, Canada.
Wither JE; Krembil Research Institute, Toronto Western Hospital, Toronto, Canada.
Silverman ED; Division of Rheumatology, Department of Pediatrics, University of Toronto, Toronto, Canada.; Division of Translational Medicine Research Institute, Toronto, Canada.
Hiraki LT; Division of Rheumatology, Department of Pediatrics, University of Toronto, Toronto, Canada.; Child Health Evaluative Sciences, Research Institute, SickKids Hospital, Toronto, Canada.
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Źródło :
Rheumatology (Oxford, England) [Rheumatology (Oxford)] 2020 Jan 01; Vol. 59 (1), pp. 90-98.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Age of Onset*
Genetic Loci/*genetics
Genetic Predisposition to Disease/*genetics
Lupus Erythematosus, Systemic/*genetics
Lupus Nephritis/*genetics
Adolescent ; Adult ; Child ; European Continental Ancestry Group/genetics ; Female ; Genetic Predisposition to Disease/ethnology ; Genotype ; Humans ; Logistic Models ; Lupus Erythematosus, Systemic/ethnology ; Lupus Nephritis/ethnology ; Male ; Odds Ratio ; Polymorphism, Single Nucleotide/genetics ; Risk Factors ; Young Adult
Czasopismo naukowe
Tytuł :
gpart: human genome partitioning and visualization of high-density SNP data by identifying haplotype blocks.
Autorzy :
Kim SA; The Research Institute of Basic Sciences, Seoul National University, Seoul, South Korea.
Brossard M; Prosserman Centre for Health Research, The Lunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, ON, Canada.
Roshandel D; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
Paterson AD; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.; Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada.
Bull SB; Prosserman Centre for Health Research, The Lunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, ON, Canada.; Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada.
Yoo YJ; Department of Mathematics Education, Seoul National University, Seoul, South Korea.; Interdisciplinary Program in Bioinformatics, Seoul National University, Seoul, South Korea.
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Źródło :
Bioinformatics (Oxford, England) [Bioinformatics] 2019 Nov 01; Vol. 35 (21), pp. 4419-4421.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Genome, Human*
Polymorphism, Single Nucleotide*
Haplotypes ; Humans ; Linkage Disequilibrium ; Software
Czasopismo naukowe
Tytuł :
Analysis of Genetic Association of Intestinal Permeability in Healthy First-degree Relatives of Patients with Crohn's Disease.
Autorzy :
Turpin W; Zane Cohen Centre for Digestive Diseases, Mount Sinai Hospital, Toronto, Ontario, Canada.; Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Espin-Garcia O; Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
Bedrani L; Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Madsen K; University of Alberta, Edmonton, Alberta, Canada.
Meddings JB; Department of Medicine, Cumming School of Medicine, Calgary, Alberta, Canada.
Raygoza Garay JA; Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Silverberg MS; Zane Cohen Centre for Digestive Diseases, Mount Sinai Hospital, Toronto, Ontario, Canada.
Smith MI; Zane Cohen Centre for Digestive Diseases, Mount Sinai Hospital, Toronto, Ontario, Canada.; Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Griffiths AM; Division of Gastroenterology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Moayyedi P; Department of Medicine, McMaster University, Farncombe Family Digestive Health Research Institute, Hamilton, Ontario, Canada.
Marshall JK; Department of Medicine, McMaster University, Farncombe Family Digestive Health Research Institute, Hamilton, Ontario, Canada.
Mack D; Division of Gastroenterology, Hepatology & Nutrition, Children's Hospital of Eastern Ontario and University of Ottawa, Ottawa, Ontario, Canada.
Seidman EG; Inflammatory Bowel Disease Centre, Division of Gastroenterology, McGill University Health Centre (MUHC), Montreal, Quebec, Canada.
Ropeleski M; Gastrointestinal Diseases Research Unit, Department of Medicine, Queen's University, Kingston, Ontario, Canada.
Feagan BG; Departments of Medicine, Epidemiology, and Biostatistics University of Western Ontario, London, Ontario, Canada.
Jacobson K; British Columbia Children's Hospital, British Columbia Children's Hospital Research Institute, University of British Columbia, Vancouver, British Columbia, Canada.
Turner D; The Juliet Keidan Institute of Pediatric Gastroenterology and Nutrition, Shaare Zedek Medical Center, The Hebrew University of Jerusalem, Jerusalem, Israel.
Walters T; Division of Gastroenterology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Paterson AD; Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.; Genetics and Genome Biology, The Hospital for Sick Children Research Institute, The Hospital for Sick Children, Toronto, Ontario, Canada.
Xu W; Division of Biostatistics, Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
Croitoru K; Zane Cohen Centre for Digestive Diseases, Mount Sinai Hospital, Toronto, Ontario, Canada.; Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
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Corporate Authors :
CCC GEM Project Research Consortium
Źródło :
Inflammatory bowel diseases [Inflamm Bowel Dis] 2019 Oct 18; Vol. 25 (11), pp. 1796-1804.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Family*
Gene-Environment Interaction*
Crohn Disease/*physiopathology
Intestinal Mucosa/*physiology
Adolescent ; Adult ; Child ; Crohn Disease/genetics ; Female ; Genome-Wide Association Study ; Humans ; Lactulose/analysis ; Logistic Models ; Male ; Mannitol/analysis ; Permeability ; Polymorphism, Single Nucleotide ; Young Adult
Czasopismo naukowe
Tytuł :
IBD Genetic Risk Profile in Healthy First-Degree Relatives of Crohn's Disease Patients.
Autorzy :
Kevans D; Zane Cohen Centre for Digestive Diseases, Mount Sinai Hospital, Toronto, ON, Canada Division of Gastroenterology, Department of Medicine, University of Toronto, Toronto, ON, Canada.
Silverberg MS; Zane Cohen Centre for Digestive Diseases, Mount Sinai Hospital, Toronto, ON, Canada Division of Gastroenterology, Department of Medicine, University of Toronto, Toronto, ON, Canada.
Borowski K; Zane Cohen Centre for Digestive Diseases, Mount Sinai Hospital, Toronto, ON, Canada.
Griffiths A; Division of Gastroenterology, Hepatology and Nutrition, Department of Paediatrics, The Hospital for Sick Children, Toronto, ON, Canada.
Xu W; Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada.
Onay V; Zane Cohen Centre for Digestive Diseases, Mount Sinai Hospital, Toronto, ON, Canada.
Paterson AD; The Hospital for Sick Children Research Institute, The Hospital for Sick Children, Toronto, ON, Canada.
Knight J; Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON, Canada Institute of Medical Science, University of Toronto, Toronto, ON, Canada Department of Psychiatry, University of Toronto, Toronto, ON, Canada.
Croitoru K; Zane Cohen Centre for Digestive Diseases, Mount Sinai Hospital, Toronto, ON, Canada Division of Gastroenterology, Department of Medicine, University of Toronto, Toronto, ON, Canada .
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Corporate Authors :
GEM Project
Źródło :
Journal of Crohn's & colitis [J Crohns Colitis] 2016 Feb; Vol. 10 (2), pp. 209-15. Date of Electronic Publication: 2015 Oct 28.
Typ publikacji :
Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Family*
Genetic Predisposition to Disease*
Polymorphism, Single Nucleotide*
Crohn Disease/*genetics
Nod2 Signaling Adaptor Protein/*genetics
Adolescent ; Adult ; Alleles ; Child ; Female ; Gene Frequency ; Genotype ; Humans ; Male ; Pedigree ; Prospective Studies ; Risk Factors ; Young Adult
Czasopismo naukowe
Tytuł :
PMPCA mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxia.
Autorzy :
Jobling RK; 1 Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
Assoum M; 2 Inserm, UMR_S 910, 13385, Marseille, France 3 Aix Marseille Université, GMGF, 13385, Marseille, France.
Gakh O; 4 Department of Paediatric and Adolescent Medicine and Mayo Clinic Children's Centre, Mayo Clinic, Rochester, MN, USA.
Blaser S; 5 Division of Neuroradiology, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Raiman JA; 1 Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
Mignot C; 6 Département de Génétique, Unité de Génétique Clinique, APHP, Groupe Hospitalier Pitié-Salpêtrière; Centre de Référence Maladies Rares 'Déficiences Intellectuelles de Causes Rares'; Groupe de Recherche Clinique UPMC Univ Paris 06; Paris, France.
Roze E; 7 Sorbonne Université, UPMC Univ Paris 06, UM 75, ICM, F-75013 Paris, France 8 Inserm, U 1127, ICM, F-75013 Paris, France 9 Cnrs, UMR 7225, ICM, F-75013 Paris, France 10 ICM, Paris, F-75013 Paris, France 11 AP-HP, Hôpital de la Salpêtrière, Département de Neurologie, F-75013, Paris, France.
Dürr A; 7 Sorbonne Université, UPMC Univ Paris 06, UM 75, ICM, F-75013 Paris, France 8 Inserm, U 1127, ICM, F-75013 Paris, France 9 Cnrs, UMR 7225, ICM, F-75013 Paris, France 10 ICM, Paris, F-75013 Paris, France 12 AP-HP, Hôpital de la Salpêtrière, Département de Génétique et Cytogénétique, F-75013, Paris, France.
Brice A; 7 Sorbonne Université, UPMC Univ Paris 06, UM 75, ICM, F-75013 Paris, France 8 Inserm, U 1127, ICM, F-75013 Paris, France 9 Cnrs, UMR 7225, ICM, F-75013 Paris, France 10 ICM, Paris, F-75013 Paris, France 12 AP-HP, Hôpital de la Salpêtrière, Département de Génétique et Cytogénétique, F-75013, Paris, France.
Lévy N; 2 Inserm, UMR_S 910, 13385, Marseille, France 3 Aix Marseille Université, GMGF, 13385, Marseille, France 13 Département de Génétique Médicale, Hôpital d'Enfants de la Timone, AP-HM, Marseille, France.
Prasad C; 14 Medical Genetics Program, Department of Pediatrics, London Health Sciences Centre, London, Ontario, Canada.
Paton T; 15 The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
Paterson AD; 15 The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
Roslin NM; 15 The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
Marshall CR; 15 The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada.
Desvignes JP; 2 Inserm, UMR_S 910, 13385, Marseille, France 3 Aix Marseille Université, GMGF, 13385, Marseille, France.
Roëckel-Trevisiol N; 2 Inserm, UMR_S 910, 13385, Marseille, France 3 Aix Marseille Université, GMGF, 13385, Marseille, France.
Scherer SW; 15 The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada 16 McLaughlin Centre and Department of Molecular Genetics, University of Toronto.
Rouleau GA; 17 Montreal Neurological Institute and Hospital and Department of Neurology and Neurosurgery, McGill University, Montreal, QC, Canada.
Mégarbané A; 18 Unité de Génétique Médicale and Laboratoire Associé Inserm UMR S_910, Faculté de Médecine, Université Saint Joseph, Beirut, Lebanon 19 Institut Jérôme Lejeune, Paris, France.
Isaya G; 4 Department of Paediatric and Adolescent Medicine and Mayo Clinic Children's Centre, Mayo Clinic, Rochester, MN, USA.
Delague V; 2 Inserm, UMR_S 910, 13385, Marseille, France 3 Aix Marseille Université, GMGF, 13385, Marseille, France .
Yoon G; 1 Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada 20 Division of Neurology, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada .
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Źródło :
Brain : a journal of neurology [Brain] 2015 Jun; Vol. 138 (Pt 6), pp. 1505-17. Date of Electronic Publication: 2015 Mar 25.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Metalloendopeptidases/*genetics
Mitochondrial Proteins/*metabolism
Mutation/*genetics
Protein Subunits/*genetics
Spinocerebellar Degenerations/*genetics
Spinocerebellar Degenerations/*metabolism
Adult ; Child ; Humans ; Lebanon ; Lymphocytes/metabolism ; Male ; Metalloendopeptidases/metabolism ; Pedigree ; Protein Subunits/metabolism ; Young Adult
SCR Disease Name :
Spinocerebellar Ataxia, Autosomal Recessive 2
Czasopismo naukowe
Tytuł :
Genome-wide scan for loci of adolescent obesity and their relationship with blood pressure.
Autorzy :
Melka MG; The Hospital for Sick Children, Toronto, Canada.
Bernard M
Mahboubi A
Abrahamowicz M
Paterson AD
Syme C
Lourdusamy A
Schumann G
Leonard GT
Perron M
Richer L
Veillette S
Gaudet D
Paus T
Pausova Z
Pokaż więcej
Źródło :
The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 2012 Jan; Vol. 97 (1), pp. E145-50. Date of Electronic Publication: 2011 Oct 19.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Genetic Loci*/genetics
Genetic Loci*/physiology
Genome-Wide Association Study*
Blood Pressure/*genetics
Obesity/*genetics
Adolescent ; Age of Onset ; Blood Pressure/physiology ; Body Mass Index ; Canada/epidemiology ; Child ; Chromosome Mapping ; Female ; Genetic Predisposition to Disease ; Humans ; Hypertension/complications ; Hypertension/genetics ; Male ; Obesity/complications ; Obesity/epidemiology ; Obesity/physiopathology ; Quebec/epidemiology ; Validation Studies as Topic
Czasopismo naukowe
Tytuł :
Identification of LTBP2 on chromosome 14q as a novel candidate gene for bone mineral density variation and fracture risk association.
Autorzy :
Cheung CL; Department of Medicine, The University of Hong Kong, Pokfulam, Hong Kong, China.
Sham PC
Chan V
Paterson AD
Luk KD
Kung AW
Pokaż więcej
Źródło :
The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 2008 Nov; Vol. 93 (11), pp. 4448-55. Date of Electronic Publication: 2008 Aug 12.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 14*
Polymorphism, Single Nucleotide*
Bone Density/*genetics
Fractures, Bone/*epidemiology
Fractures, Bone/*genetics
Latent TGF-beta Binding Proteins/*genetics
3T3 Cells ; Animals ; Asian Continental Ancestry Group/genetics ; Cells, Cultured ; China ; Chromosome Mapping ; Genetic Linkage ; Genetic Variation ; Genome, Human ; Genotype ; Humans ; Mice ; Microsatellite Repeats ; Osteoblasts/cytology ; Osteoblasts/physiology ; Prevalence ; Quantitative Trait Loci ; Risk Factors
Czasopismo naukowe
Tytuł :
Monozygotic twins exhibit numerous epigenetic differences: clues to twin discordance?
Autorzy :
Petronis A; The Krembil Family Epigenetics Laboratory, Centre for Addiction and Mental Health, 250 College Street, Toronto, Ontario, M5T 1R8 Canada. />Gottesman II
Kan P
Kennedy JL
Basile VS
Paterson AD
Popendikyte V
Pokaż więcej
Źródło :
Schizophrenia bulletin [Schizophr Bull] 2003; Vol. 29 (1), pp. 169-78.
Typ publikacji :
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Twin Study
MeSH Terms :
Epigenesis, Genetic/*genetics
Twins/*genetics
Twins/*psychology
Twins, Monozygotic/*genetics
Twins, Monozygotic/*psychology
Adolescent ; Adult ; DNA Methylation ; Humans ; Male ; Promoter Regions, Genetic ; Receptors, Dopamine D2/genetics
Czasopismo naukowe
Tytuł :
PKD3-to be or not to be?
Autorzy :
Paterson AD
Pei Y
Pokaż więcej
Źródło :
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association [Nephrol Dial Transplant] 1999 Dec; Vol. 14 (12), pp. 2965-6.
Typ publikacji :
Comment; Letter
MeSH Terms :
Polycystic Kidney, Autosomal Dominant/*genetics
Genetic Linkage ; Humans ; Membrane Proteins/genetics ; Proteins/genetics ; TRPP Cation Channels
Opinia redakcyjna
Tytuł :
Schizophrenia: an epigenetic puzzle?
Autorzy :
Petronis A; Department of Psychiatry, University of Toronto, Centre of Addiction and Mental Health, Ontario, Canada. />Paterson AD
Kennedy JL
Pokaż więcej
Źródło :
Schizophrenia bulletin [Schizophr Bull] 1999; Vol. 25 (4), pp. 639-55.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms :
Schizophrenia*/genetics
Schizophrenia*/metabolism
Schizophrenia*/virology
Dopamine/metabolism ; Humans
Czasopismo naukowe
    Wyświetlanie 1-12 z 12

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