Related references
Note: Only part of the references are listed.Purinergic signaling in human pluripotent stem cells is regulated by the housekeeping gene encoding hypoxanthine guanine phosphoribosyltransferase
Lina Mastrangelo et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Purinergic signalling: From normal behaviour to pathological brain function
Geoffrey Burnstock et al.
PROGRESS IN NEUROBIOLOGY (2011)
Purinergic signaling in neural development
Herbert Zimmermann
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY (2011)
Human neural stem cells: a model system for the study of Lesch-Nyhan disease neurological aspects
Silvia Cristini et al.
HUMAN MOLECULAR GENETICS (2010)
Deficiency of the Housekeeping Gene Hypoxanthine-Guanine Phosphoribosyltransferase (HPRT) Dysregulates Neurogenesis
Ghiabe-Henri Guibinga et al.
MOLECULAR THERAPY (2010)
Pediatric neurological syndromes and inborn errors of purine metabolism
Marcella Camici et al.
NEUROCHEMISTRY INTERNATIONAL (2010)
Rho and Ras GTPases in Axon Growth, Guidance, and Branching
Alan Hall et al.
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2010)
Lesch-Nyhan disease: from mechanism to model and back again
H. A. Jinnah
DISEASE MODELS & MECHANISMS (2009)
Hypoxanthine-guanine phosphoribosyl transferase regulates early developmental programming of dopamine neurons: implications for Lesch-Nyhan disease pathogenesis
Irene Ceballos-Picot et al.
HUMAN MOLECULAR GENETICS (2009)
Inborn errors of purine and pyrimidine metabolism
A. Jurecka
JOURNAL OF INHERITED METABOLIC DISEASE (2009)
Trophic functions of nucleotides in the central nervous system
Joseph T. Neary et al.
TRENDS IN NEUROSCIENCES (2009)
Consequences of impaired purine recycling in dopaminergic neurons
J. C. Lewers et al.
NEUROSCIENCE (2008)
Functions of rac GTPases during neuronal development
Ivan De Curtis
DEVELOPMENTAL NEUROSCIENCE (2008)
A human neuronal tissue culture model for Lesch-Nyhan disease
Thomas L. Shirley et al.
JOURNAL OF NEUROCHEMISTRY (2007)
Basal ganglia dopamine loss due to defect in purine recycling
Kiyoshi Egami et al.
NEUROBIOLOGY OF DISEASE (2007)
Gene duplication and inactivation in the HPRT gene family
Alaine C. Keebaugh et al.
GENOMICS (2007)
Delineation of the motor disorder of Lesch-Nyhan disease
HA Jinnah et al.
BRAIN (2006)
A Golgi study of neuronal architecture in a genetic mouse model for Lesch-Nyhan disease
I Mikolaenko et al.
NEUROBIOLOGY OF DISEASE (2005)
Behavioral aspects of Lesch-Nyhan disease and its variants
DJ Schretlen et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2005)
Disorders of purine and pyrimidine metabolism
WL Nyhan
MOLECULAR GENETICS AND METABOLISM (2005)
Abnormal Purine and Pyrimidine Nucleotide Content in Primary Astroglia Cultures from Hypoxanthine-Guanine Phosphoribosyltransferase-Deficient Transgenic Mice
Dori Pelled et al.
JOURNAL OF NEUROCHEMISTRY (2003)
Oxidative stress and dopamine deficiency in a genetic mouse model of Lesch-Nyhan disease
JE Visser et al.
DEVELOPMENTAL BRAIN RESEARCH (2002)
Neurocognitive functioning in Lesch-Nyhan disease and partial hypoxanthine-guanine phosphoribosyltransferase deficiency
DJ Schretlen et al.
JOURNAL OF THE INTERNATIONAL NEUROPSYCHOLOGICAL SOCIETY (2001)
Rho GTPases in neuronal morphogenesis
LQ Luo
NATURE REVIEWS NEUROSCIENCE (2000)
The spectrum of inherited mutations causing HPRT deficiency: 75 new cases and a review of 196 previously reported cases
HA Jinnah et al.
MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH (2000)
Lesch-Nyhan disease and the basal ganglia
JE Visser et al.
BRAIN RESEARCH REVIEWS (2000)
Characterization of the dopamine defect in primary cultures of dopaminergic neurons from hypoxanthine phosphoribosyltransferase knockout mice
DW Smith et al.
MOLECULAR THERAPY (2000)
Elevated UTP and CTP content in cultured neurons from HPRT-deficient transgenic mice
S Brosh et al.
JOURNAL OF MOLECULAR NEUROSCIENCE (2000)
Share Paper
