4.4 Article

Expression and distribution of creatine transporter and creatine kinase (brain isoform) in developing and mature rat cochlear tissues

Related references

Note: Only part of the references are listed.
Article Genetics & Heredity

Clinical features and X-inactivation in females heterozygous for creatine transporter defect

J. M. van de Kamp et al.

CLINICAL GENETICS (2011)

Article Endocrinology & Metabolism

Language disorder with mild intellectual disability in a child affected by a novel mutation of SLC6A8 gene

R. Battini et al.

MOLECULAR GENETICS AND METABOLISM (2011)

Article Multidisciplinary Sciences

Creatine Transporter (CrT; Slc6a8) Knockout Mice as a Model of Human CrT Deficiency

Matthew R. Skelton et al.

PLOS ONE (2011)

Review Biochemistry & Molecular Biology

Synthesis and transport of creatine in the CNS: importance for cerebral functions

Elidie Beard et al.

JOURNAL OF NEUROCHEMISTRY (2010)

Article Biochemistry & Molecular Biology

Differential expression of P2Y receptors in the rat cochlea during development

Lin-Chien Huang et al.

PURINERGIC SIGNALLING (2010)

Review Neurosciences

Purinergic signaling in special senses

Gary D. Housley et al.

TRENDS IN NEUROSCIENCES (2009)

Review Neurosciences

Functions and effects of creatine in the central nervous system

Robert H. Andres et al.

BRAIN RESEARCH BULLETIN (2008)

Article Multidisciplinary Sciences

The origin of spontaneous activity in the developing auditory system

Nicolas X. Tritsch et al.

NATURE (2007)

Article Clinical Neurology

Severe epilepsy in X-linked creatine transporter defect (CRTR-D)

Maria Margherita Mancardi et al.

EPILEPSIA (2007)

Article Neurosciences

Hair bundles are specialized for ATP delivery via creatine kinase

Jung-Bum Shin et al.

NEURON (2007)

Review Neurosciences

Supporting sensory transduction: cochlear fluid homeostasis and the endocochlear potential

Philine Wangemann

JOURNAL OF PHYSIOLOGY-LONDON (2006)

Review Biochemistry & Molecular Biology

Mitochondrial creatine kinase in human health and disease

U Schlattner et al.

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2006)

Article Endocrinology & Metabolism

X-linked creatine transporter defect: A report on two unrelated boys with a severe clinical phenotype

IM Anselm et al.

JOURNAL OF INHERITED METABOLIC DISEASE (2006)

Article Cell Biology

Creatine transporter localization in developing and adult retina: importance of creatine to retinal function

ML Acosta et al.

AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2005)

Article Neurosciences

Developmental regulation of neuron-specific P2X3 receptor expression in the rat cochlea

LC Huang et al.

JOURNAL OF COMPARATIVE NEUROLOGY (2005)

Article Neurosciences

Purinergic modulation of cochlear partition resistance and its effect on the endocochlear potential in the guinea pig

PR Thorne et al.

JARO-JOURNAL OF THE ASSOCIATION FOR RESEARCH IN OTOLARYNGOLOGY (2004)

Article Genetics & Heredity

High prevalence of SLC6A8 deficiency in X-linked mental retardation

EH Rosenberg et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2004)

Article Biochemistry & Molecular Biology

Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice

A Dedeoglu et al.

JOURNAL OF NEUROCHEMISTRY (2003)

Article Endocrinology & Metabolism

X-linked creatine transporter defect: An overview

GS Salomons et al.

JOURNAL OF INHERITED METABOLIC DISEASE (2003)

Review Audiology & Speech-Language Pathology

K+ cycling and the endocochlear potential

P Wangemann

HEARING RESEARCH (2002)

Article Genetics & Heredity

X-linked creatine-transporter gene (SLC6A8) defect:: A new creatine-deficiency syndrome

GS Salomons et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2001)