GPR126 : A novel candidate gene implicated in autosomal recessive intellectual disability
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Title
GPR126
: A novel candidate gene implicated in autosomal recessive intellectual disability
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Volume -, Issue -, Pages -
Publisher
Wiley
Online
2018-12-14
DOI
10.1002/ajmg.a.40531
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Note: Only part of the references are listed.- Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay
- (2017) Muhammad Ansar et al. GENETICS IN MEDICINE
- Activation of Adhesion G Protein-coupled Receptors
- (2017) Lilian M. Demberg et al. JOURNAL OF BIOLOGICAL CHEMISTRY
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- (2017) Monica Ghidinelli et al. PLOS BIOLOGY
- Gpr126/Adgrg6 Has Schwann Cell Autonomous and Nonautonomous Functions in Peripheral Nerve Injury and Repair
- (2016) Amit Mogha et al. JOURNAL OF NEUROSCIENCE
- Adhesion G protein-coupled receptors in nervous system development and disease
- (2016) Tobias Langenhan et al. NATURE REVIEWS NEUROSCIENCE
- Mutations of GPR126 Are Responsible for Severe Arthrogryposis Multiplex Congenita
- (2015) Gianina Ravenscroft et al. AMERICAN JOURNAL OF HUMAN GENETICS
- LAMA2-related congenital muscular dystrophy complicated by West syndrome
- (2015) Ana Camacho et al. EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY
- LAMA2-related myopathy: Frequency among congenital and limb-girdle muscular dystrophies
- (2015) Nicoline Løkken et al. MUSCLE & NERVE
- The Adhesion GPCR GPR126 Has Distinct, Domain-Dependent Functions in Schwann Cell Development Mediated by Interaction with Laminin-211
- (2015) Sarah C. Petersen et al. NEURON
- Adhesion G protein-coupled receptors are activated by exposure of a cryptic tethered agonist
- (2015) Hannah M. Stoveken et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Integrated Sequence Analysis Pipeline Provides One-Stop Solution for Identifying Disease-Causing Mutations
- (2014) Hao Hu et al. HUMAN MUTATION
- Atypical phenotype in two patients with LAMA2 mutations
- (2014) Joana Marques et al. NEUROMUSCULAR DISORDERS
- Changes in White Matter Integrity before Conversion from Mild Cognitive Impairment to Alzheimer’s Disease
- (2014) Michaela Defrancesco et al. PLoS One
- Type IV collagen is an activating ligand for the adhesion G protein-coupled receptor GPR126
- (2014) K. J. Paavola et al. Science Signaling
- Gpr126 Functions in Schwann Cells to Control Differentiation and Myelination via G-Protein Activation
- (2013) A. Mogha et al. JOURNAL OF NEUROSCIENCE
- Degeneration and impaired regeneration of gray matter oligodendrocytes in amyotrophic lateral sclerosis
- (2013) Shin H Kang et al. NATURE NEUROSCIENCE
- Alterations of mean diffusivity in brain white matter and deep gray matter in Parkinson's disease
- (2013) Hengjun J. Kim et al. NEUROSCIENCE LETTERS
- Organ-specific function of adhesion G protein-coupled receptor GPR126 is domain-dependent
- (2013) C. Patra et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Sticky Signaling--Adhesion Class G Protein-Coupled Receptors Take the Stage
- (2013) T. Langenhan et al. Science Signaling
- Abnormal white matter microstructure in children with sensory processing disorders
- (2013) Julia P. Owen et al. NeuroImage-Clinical
- White matter tract integrity of frontostriatal circuit in attention deficit hyperactivity disorder: Association with attention performance and symptoms
- (2012) Yi-Huan Wu et al. HUMAN BRAIN MAPPING
- Deep sequencing reveals 50 novel genes for recessive cognitive disorders
- (2011) Hossein Najmabadi et al. NATURE
- Protein structure analysis of mutations causing inheritable diseases. An e-Science approach with life scientist friendly interfaces
- (2010) Hanka Venselaar et al. BMC BIOINFORMATICS
- Genotype–phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations
- (2010) Fatemeh Geranmayeh et al. NEUROMUSCULAR DISORDERS
- The Orphan Adhesion-GPCR GPR126 Is Required for Embryonic Development in the Mouse
- (2010) Helen Waller-Evans et al. PLoS One
- White Matter Impairment in Rett Syndrome: Diffusion Tensor Imaging Study with Clinical Correlations
- (2009) A. Mahmood et al. AMERICAN JOURNAL OF NEURORADIOLOGY
- A G Protein-Coupled Receptor Is Essential for Schwann Cells to Initiate Myelination
- (2009) K. R. Monk et al. SCIENCE
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