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The molecular mechanisms of Axenfeld-Rieger syndrome

Brad A Amendt

Georgetown, Tex. : Landes Bioscience/Eurekah.com ; New York, N.Y. : Springer Science+Business Media ©2005

Online access

  • Title:
    The molecular mechanisms of Axenfeld-Rieger syndrome
  • Author: Brad A Amendt
  • Subjects: Axenfeld-Rieger syndrome -- Molecular aspects; Abnormalities, Multiple -- genetics; Gene Expression Regulation, Developmental -- physiology; Transcription Factors -- metabolism; Abnormalities, Multiple -- genetics; Gene Expression Regulation, Developmental -- physiology; Transcription Factors -- metabolism; Axenfeld-Rieger syndrome -- Molecular aspects
  • Contents: Identification of the gene involved in 4q25-linked Axenfeld-Rieger syndrome, PITX2 / Elena V. Semina -- Winged helix/forkhead transcription factors and Rieger syndrome / Darryl Y. Nishimura and Ruth E. Swiderski -- Rieger syndrome and PAX6 deletion / Ruth Riise -- The molecular and biochemical basis of Axenfeld-Rieger syndrome / Brad A. Amendt -- Role of PITX2 in the pituitary gland / Hoonkyo Suh [and others] -- Expression and function of PITX2 in chick heart looping / Xueyan Yu, Shusheng Wang, and YiPing Chen -- The multiple roles of PITX2 in heart development / James F. Martin -- The role of PITX2 in tooth development / Brad A. Amendt -- PITX genes and ocular development / Elena V. Semina -- An overview of Axenfeld-Rieger syndrome and the anterior segment developmental disorders / Brad A. Amendt.
    Annotation The Molecular Mechanisms of Axenfeld-Rieger Syndrome describes the current research and clinical findings of the heterogeneous disorder termed Axenfeld-Rieger Syndrome (ARS). The book provides an in-depth analysis of this phenotypic diverse disorder and is designed to detail the current molecular and biochemical research involved in studying genetic defects. This book brings together the complete analysis of a human genetic defect using humans, mouse and chick epigenetic and genetic studies, combined with cell culture and in vitro analyses. It is a comprehensive study of a unique set of genes and their mutant activities. A molecular basis for the genetic and phenotypic anomalies observed in ARS patients is provided, with especially detailed descriptions of eye, tooth, and heart development.
  • Publisher: Georgetown, Tex. : Landes Bioscience/Eurekah.com ; New York, N.Y. : Springer Science+Business Media
  • Creation Date: ©2005
  • Physical Description: 1 online resource (106 pages) : illustrations..
  • Language: English
  • Identifier: ISBN1423735072;ISBN9781423735076;ISBN9781587066207;ISBN1587066203
  • Source: 01GALI USG ALMA
  • OCLC Number: 209910200
  • NZ MMS ID: 9910004247302931
  • IZ MMS ID: 996008454102948$$IAUGUSTA
    995078324102938$$ICCGA
    997059833902954$$IKSU
    994579823902954$$IKSU
    991718424102956$$ISSU
    9937771273902959$$IUGA

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