How a common variant in the growth factor receptor gene, NTRK1, affects white matter

BioArchitecture

Volumn 2, Issue 5, 2012, Pages 181-184

  Braskie, Meredith N ^a   Jahanshad, Neda ^a   Toga, Arthur W ^a   McMahon, Katie L ^b   de Zubicaray, Greig I ^b   Martin, Nicholas G ^c   Wright, Margaret J ^c   Thompson, Paul M ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF QUEENSLAND   (Australia)

^c QIMR BERGHOFER MEDICAL RESEARCH INSTITUTE   (Australia)

Author keywords

Development; Diffusion tensor imaging; Fractional anisotropy; Growth factor; Myelin; Neurotrophic tyrosine kinase receptor 1; Neurotrophin; Radial diffusivity; Schizophrenia; Tropomyosin related kinase receptor A

Indexed keywords

GROWTH FACTOR RECEPTOR; PROTEIN TYROSINE KINASE A;

ARTICLE; BRAIN REGION; CORTICAL THICKNESS (BRAIN); DIFFUSION TENSOR IMAGING; GENE EXPRESSION REGULATION; GENE LOCUS; GENETIC ASSOCIATION; GENETIC CODE; GENETIC RISK; GENETIC VARIABILITY; HETEROZYGOTE; HUMAN; MISSENSE MUTATION; MYELIN SHEATH; NEUROANATOMY; NEUROIMAGING; NEUROTROPHIC TYROSINE KINASE RECEPTOR 1 GENE; RECEPTOR GENE; RISK ASSESSMENT; SIGNAL TRANSDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM; WHITE MATTER; GENETICS; LEUKOENCEPHALOPATHY; METABOLISM; PATHOLOGY;

GENETIC VARIATION; HUMANS; LEUKOENCEPHALOPATHIES; RECEPTOR, TRKA; WHITE MATTER;

EID: 84898344072     PISSN: 19490992     EISSN: 1949100X     Source Type: Journal    
DOI: 10.4161/bioa.22190     Document Type: Article

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