Negative Autoregulation ofGTF2IRD1in Williams-Beuren Syndrome via a Novel DNA Binding Mechanism

Journal of Biological Chemistry - United States
doi 10.1074/jbc.m109.086660
Full Text
Abstract

Available in full text

Date
Authors
Publisher

American Society for Biochemistry & Molecular Biology (ASBMB)

Related search

Metabolic Abnormalities in Williams–Beuren Syndrome

Journal of Medical Genetics
Genetics
2015English

An Atypical 7q11.23 Deletion in a Normal IQ Williams–Beuren Syndrome Patient

European Journal of Human Genetics
Genetics
2009English

Detection of Deletions at 7q11.23 in Williams-Beuren Syndrome by Polymorphic Markers

Clinics
Medicine
2011English

Human Induced Pluripotent Stem Cell Derived Neurons as a Model for Williams-Beuren Syndrome

Molecular Brain
Molecular NeuroscienceMolecular BiologyCellular
2015English

Clinical and Molecular Cytogenetic Study of 38 Williams-Beuren Syndrome Tunisian Patients

Open Journal of Genetics
2014English

Determination and Functional Analysis of the Consensus Binding Site for TFII-I Family Member BEN, Implicated in Williams-Beuren Syndrome

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
2008English

Observation of a Parental Inversion Variant in a Rare Williams–Beuren Syndrome Family With Two Affected Children

Human Genetics
Genetics
2005English

"The Impact of Psychiatric Disorders in the Evolution of Patients With Williams-Beuren Syndrome"

BULLETIN OF INTEGRATIVE PSYCHIATRY
2020English

Williams-Beuren Syndrome: Cardiovascular Abnormalities in 20 Patients Diagnosed With Fluorescence in Situ Hybridization

Arquivos Brasileiros de Cardiologia
Cardiovascular MedicineCardiology
2003English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy