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Increased Wnt and Notch signaling: a clue to the renal disease in Schimke immuno-osseous dysplasia?
Morimoto, Marie; Myung, Clara; Beirnes, Kimberly; Choi, Kunho; Asakura, Yumi; Bokenkamp, Arend; Bonneau, Dominique; Brugnara, Milena; Charrow, Joel; Colin, Estelle; Davis, Amira; Deschenes, Georges; Gentile, Mattia; Giordano, Mario; Gormley, Andrew K; Govender, Rajeshree; Joseph, Mark; Keller, Kory; Lerut, Evelyne; Levtchenko, Elena; Massella, Laura; Mayfield, Christy; Najafian, Behzad; Parham, David; Spranger, Jurgen; Stenzel, Peter; Yis, Uluc; Yu, Zhongxin; Zonana, Jonathan; Hendson, Glenda; Boerkoel, Cornelius F.
Afiliación
  • Morimoto M; Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.
  • Myung C; Child & Family Research Institute, Vancouver, BC, Canada.
  • Beirnes K; Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.
  • Choi K; Child & Family Research Institute, Vancouver, BC, Canada.
  • Asakura Y; Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.
  • Bokenkamp A; Child & Family Research Institute, Vancouver, BC, Canada.
  • Bonneau D; Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.
  • Brugnara M; Child & Family Research Institute, Vancouver, BC, Canada.
  • Charrow J; Department of Endocrinology & Metabolism, Kanagawa Children's Medical Center, Yokohama, Japan.
  • Colin E; Department of Pediatric Nephrology, VU University Medical Center, Amsterdam, The Netherlands.
  • Davis A; Département de Biochimie et Génétique, Centre Hospitalier Universitaire d'Angers, Angers, France.
  • Deschenes G; Department of Pediatrics, University of Verona, Verona, Italy.
  • Gentile M; Division of Genetics, Birth Defects and Metabolism, Ann and Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Giordano M; Département de Biochimie et Génétique, Centre Hospitalier Universitaire d'Angers, Angers, France.
  • Gormley AK; Seattle Children's Hospital, Seattle, WA, USA.
  • Govender R; Département de Pédiatrie, Hôpital Robert Debré, Paris, France.
  • Joseph M; Department of Medical Genetics, Hospital Di Venere - ASL Bari, Bari, Italy.
  • Keller K; Pediatric Nephrology and Dialysis Unit, Ospedale Pediatrico Giovanni XXIII, Bari, Italy.
  • Lerut E; Department of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.
  • Levtchenko E; Department of Pediatrics and Child Health, Nelson R. Mandela School of Medicine, University of KwaZulu-Natal, Durban, South Africa.
  • Massella L; Department of Pediatric Nephrology, Phoenix Children's Hospital, Phoenix, AZ, USA.
  • Mayfield C; Child Development and Rehabiliation Center, Oregon Institute on Disability & Development, Oregon Health & Science University, Portland, OR, USA.
  • Najafian B; Department of Pathology, University Hospitals Leuven, Leuven, Belgium.
  • Parham D; Department of Pediatric Nephrology, University Hospitals Leuven, Leuven, Belgium.
  • Spranger J; Division of Nephrology, Bambino Gesù Children's Hospital and Research Institute, Rome, Italy.
  • Stenzel P; Warren Clinic Family Medicine, Tulsa, OK, USA.
  • Yis U; Department of Pathology, University of Washington, Seattle, WA, USA.
  • Yu Z; Department of Pathology, Children's Hospital Los Angeles and Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
  • Zonana J; Children's Hospital, University of Mainz, Mainz, Germany.
  • Hendson G; Department of Pathology, Oregon Health and Science University, Portland, OR, USA.
  • Boerkoel CF; Department of Pediatrics, Division of Child Neurology, Dokuz Eylül University, School of Medicine, Izmir, Turkey.
Orphanet J Rare Dis ; 11(1): 149, 2016 11 05.
Article en En | MEDLINE | ID: mdl-27816064
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Texto completo: 1 Colección: 01-internacional Asunto principal: Osteocondrodisplasias / Arteriosclerosis / Embolia Pulmonar / Glomeruloesclerosis Focal y Segmentaria / Proteínas Wnt / Receptores Notch / Síndromes de Inmunodeficiencia / Enfermedades Renales / Síndrome Nefrótico Límite: Animals / Child / Child, preschool / Humans / Male Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2016 Tipo del documento: Article País de afiliación: Canadá
Texto completo
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Texto completo: 1 Colección: 01-internacional Asunto principal: Osteocondrodisplasias / Arteriosclerosis / Embolia Pulmonar / Glomeruloesclerosis Focal y Segmentaria / Proteínas Wnt / Receptores Notch / Síndromes de Inmunodeficiencia / Enfermedades Renales / Síndrome Nefrótico Límite: Animals / Child / Child, preschool / Humans / Male Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2016 Tipo del documento: Article País de afiliación: Canadá