Published in J Physiol on January 04, 2007
A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome. Hum Mol Genet (2008) 2.13
Preclinical research in Rett syndrome: setting the foundation for translational success. Dis Model Mech (2012) 1.66
Correction of respiratory disorders in a mouse model of Rett syndrome. Proc Natl Acad Sci U S A (2010) 1.54
Exogenous brain-derived neurotrophic factor rescues synaptic dysfunction in Mecp2-null mice. J Neurosci (2010) 1.52
Breathing disorders in Rett syndrome: progressive neurochemical dysfunction in the respiratory network after birth. Respir Physiol Neurobiol (2009) 1.46
Brainstem respiratory networks: building blocks and microcircuits. Trends Neurosci (2012) 1.37
β2-Adrenergic receptor agonist ameliorates phenotypes and corrects microRNA-mediated IGF1 deficits in a mouse model of Rett syndrome. Proc Natl Acad Sci U S A (2014) 1.23
Serotonin receptor 1A-modulated phosphorylation of glycine receptor α3 controls breathing in mice. J Clin Invest (2010) 1.21
MeCP2 is critical within HoxB1-derived tissues of mice for normal lifespan. J Neurosci (2011) 1.19
Respiratory rhythm generation in vivo. Physiology (Bethesda) (2014) 1.18
Brain activity mapping in Mecp2 mutant mice reveals functional deficits in forebrain circuits, including key nodes in the default mode network, that are reversed with ketamine treatment. J Neurosci (2012) 1.18
Pontine mechanisms of respiratory control. Compr Physiol (2012) 1.14
Synaptic microcircuit dysfunction in genetic models of neurodevelopmental disorders: focus on Mecp2 and Met. Curr Opin Neurobiol (2011) 1.12
Learning to breathe: control of the inspiratory-expiratory phase transition shifts from sensory- to central-dominated during postnatal development in rats. J Physiol (2009) 1.08
Breathing dysfunction in Rett syndrome: understanding epigenetic regulation of the respiratory network. Respir Physiol Neurobiol (2008) 1.06
Remodelling of the respiratory network in a mouse model of Rett syndrome depends on brain-derived neurotrophic factor regulated slow calcium buffering. J Physiol (2009) 1.05
The role of serotonin in respiratory function and dysfunction. Respir Physiol Neurobiol (2010) 1.05
The disruption of central CO2 chemosensitivity in a mouse model of Rett syndrome. Am J Physiol Cell Physiol (2011) 1.05
Breathing challenges in Rett syndrome: lessons learned from humans and animal models. Respir Physiol Neurobiol (2013) 1.04
Pontine respiratory activity involved in inspiratory/expiratory phase transition. Philos Trans R Soc Lond B Biol Sci (2009) 1.04
Rodent models of sleep apnea. Respir Physiol Neurobiol (2013) 0.95
A BDNF loop-domain mimetic acutely reverses spontaneous apneas and respiratory abnormalities during behavioral arousal in a mouse model of Rett syndrome. Dis Model Mech (2014) 0.94
Emergence of brain-derived neurotrophic factor-induced postsynaptic potentiation of NMDA currents during the postnatal maturation of the Kolliker-Fuse nucleus of rat. J Physiol (2008) 0.93
Pontine norepinephrine defects in Mecp2-null mice involve deficient expression of dopamine beta-hydroxylase but not a loss of catecholaminergic neurons. Biochem Biophys Res Commun (2010) 0.92
Developmental changes in brain-derived neurotrophic factor-mediated modulations of synaptic activities in the pontine Kölliker-Fuse nucleus of the rat. J Physiol (2007) 0.91
The phrenic motor nucleus in the adult mouse. Exp Neurol (2010) 0.91
GABA and glutamate pathways are spatially and developmentally affected in the brain of Mecp2-deficient mice. PLoS One (2014) 0.88
Decreased Hering-Breuer input-output entrainment in a mouse model of Rett syndrome. Front Neural Circuits (2013) 0.88
Deficiency of GABAergic synaptic inhibition in the Kölliker-Fuse area underlies respiratory dysrhythmia in a mouse model of Rett syndrome. J Physiol (2015) 0.87
Kölliker–Fuse neurons send collateral projections to multiple hypoxia-activated and nonactivated structures in rat brainstem and spinal cord. Brain Struct Funct (2012) 0.87
Control of breathing by interacting pontine and pulmonary feedback loops. Front Neural Circuits (2013) 0.86
Ponto-medullary nuclei involved in the generation of sequential pharyngeal swallowing and concomitant protective laryngeal adduction in situ. J Physiol (2014) 0.86
Progressive Changes in a Distributed Neural Circuit Underlie Breathing Abnormalities in Mice Lacking MeCP2. J Neurosci (2016) 0.84
Characterization of the MeCP2R168X knockin mouse model for Rett syndrome. PLoS One (2014) 0.83
Inflammatory lung disease in Rett syndrome. Mediators Inflamm (2014) 0.82
Use-dependent learning and memory of the Hering-Breuer inflation reflex in rats. Exp Physiol (2008) 0.82
Effect of Sarizotan, a 5-HT1a and D2-like receptor agonist, on respiration in three mouse models of Rett syndrome. Am J Respir Cell Mol Biol (2014) 0.82
Pinpointing brainstem mechanisms responsible for autonomic dysfunction in Rett syndrome: therapeutic perspectives for 5-HT1A agonists. Front Physiol (2014) 0.81
A selective 5-HT1a receptor agonist improves respiration in a mouse model of Rett syndrome. J Appl Physiol (1985) (2013) 0.81
Habituation without NMDA Receptor-Dependent Desensitization of Hering-Breuer Apnea Reflex in a Mecp2 Mutant Mouse Model of Rett Syndrome. Front Integr Neurosci (2011) 0.81
Effects of glycinergic inhibition failure on respiratory rhythm and pattern generation. Prog Brain Res (2014) 0.78
Multiscale fingerprinting of neuronal functional connectivity. Brain Struct Funct (2014) 0.78
Learning to breathe: habituation of Hering-Breuer inflation reflex emerges with postnatal brainstem maturation. Respir Physiol Neurobiol (2014) 0.77
Network models predict that reduced excitatory fluctuations can give rise to hippocampal network hyper-excitability in MeCP2-null mice. PLoS One (2014) 0.77
Habituation, desensitization and sensitization of the Hering Breuer reflex in normal and Mecp2 /y knockout mice. J Physiol (2007) 0.77
Autonomic breathing abnormalities in Rett syndrome: caregiver perspectives in an international database study. J Neurodev Disord (2017) 0.75
Blockade of dorsolateral pontine 5HT1A receptors destabilizes the respiratory rhythm in C57BL6/J wild-type mice. Respir Physiol Neurobiol (2016) 0.75
Post-inspiratory discharges are the centrepiece of respiratory disrhythmia in a gene knockout model of Rett syndrome. J Physiol (2007) 0.75
GlyT2-Dependent Preservation of MECP2-Expression in Inhibitory Neurons Improves Early Respiratory Symptoms but Does Not Rescue Survival in a Mouse Model of Rett Syndrome. Front Physiol (2016) 0.75
Chronic serotonin-norepinephrine reuptake transporter inhibition modifies basal respiratory output in adult mouse in vitro and in vivo. Respir Physiol Neurobiol (2012) 0.75
D-cycloserine improves synaptic transmission in an animal mode of Rett syndrome. PLoS One (2017) 0.75
Pathogenesis of Lethal Aspiration Pneumonia in Mecp2-null Mouse Model for Rett Syndrome. Sci Rep (2017) 0.75
Breathing abnormalities in animal models of Rett syndrome a female neurogenetic disorder. Respir Physiol Neurobiol (2016) 0.75
The Kölliker-Fuse nucleus: a review of animal studies and the implications for cranial nerve function in humans. Eur Arch Otorhinolaryngol (2015) 0.75
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet (1999) 22.84
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome. Nat Genet (2001) 9.82
Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice. Nat Genet (2001) 8.64
A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases. Ann Neurol (1983) 6.80
Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3. Neuron (2002) 5.71
Looking for inspiration: new perspectives on respiratory rhythm. Nat Rev Neurosci (2006) 4.70
Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett syndrome. Proc Natl Acad Sci U S A (2005) 4.52
Learning and memory and synaptic plasticity are impaired in a mouse model of Rett syndrome. J Neurosci (2006) 3.69
An update on clinically applicable diagnostic criteria in Rett syndrome. Comments to Rett Syndrome Clinical Criteria Consensus Panel Satellite to European Paediatric Neurology Society Meeting, Baden Baden, Germany, 11 September 2001. Eur J Paediatr Neurol (2002) 3.26
Neural pathways underlying vocal control. Neurosci Biobehav Rev (2002) 3.01
Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2. Proc Natl Acad Sci U S A (2005) 2.90
Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3. Hum Mol Genet (2004) 2.89
A novel functional neuron group for respiratory rhythm generation in the ventral medulla. J Neurosci (2003) 2.82
Distribution of N-methyl-D-aspartate-sensitive L-[3H]glutamate-binding sites in rat brain. J Neurosci (1985) 2.66
Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome. Neurobiol Dis (2005) 2.44
Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized. Nat Rev Genet (2006) 2.42
Synaptic connections between medullary respiratory neurons and considerations on the genesis of respiratory rhythm. Prog Neurobiol (1990) 2.26
Mecp2 deficiency disrupts norepinephrine and respiratory systems in mice. J Neurosci (2005) 2.20
Characterisation of breathing and associated central autonomic dysfunction in the Rett disorder. Arch Dis Child (2001) 1.80
Mechanisms of respiratory rhythm generation. Curr Opin Neurobiol (1992) 1.66
The Kölliker-Fuse nucleus gates the postinspiratory phase of the respiratory cycle to control inspiratory off-switch and upper airway resistance in rat. Eur J Neurosci (2006) 1.62
Hyperventilation in the awake state: potentially treatable component of Rett syndrome. Arch Dis Child (1988) 1.61
Modeling the ponto-medullary respiratory network. Respir Physiol Neurobiol (2004) 1.49
EEG and respiration in Rett syndrome. Acta Neurol Scand (1991) 1.48
Rett syndrome: a suggested staging system for describing impairment profile with increasing age towards adolescence. Am J Med Genet Suppl (1986) 1.48
Rett syndrome: analysis of deaths in the British survey. Eur Child Adolesc Psychiatry (1997) 1.43
Rett syndrome: epidemiology and geographical variability. Eur Child Adolesc Psychiatry (1997) 1.25
Respiratory neurons mediating the Breuer-Hering reflex prolongation of expiration in rat. J Neurosci (1996) 1.23
Functional and structural models of pontine modulation of mechanoreceptor and chemoreceptor reflexes. Respir Physiol Neurobiol (2004) 1.20
Neurochemical development of brain stem nuclei involved in the control of respiration. Respir Physiol Neurobiol (2005) 1.17
Defect in normal developmental increase of the brain biogenic amine concentrations in the mecp2-null mouse. Neurosci Lett (2005) 1.13
The ventral medullary respiratory network of the mature mouse studied in a working heart-brainstem preparation. J Physiol (1996) 1.09
Glycinergic inhibition is essential for co-ordinating cranial and spinal respiratory motor outputs in the neonatal rat. J Physiol (2002) 1.08
Polysomnographic characteristics of patients with Rett syndrome. J Pediatr (1994) 1.02
Respiratory activity in neonatal rats. Auton Neurosci (2000) 1.01
Cerebrospinal fluid biogenic amines and biopterin in Rett syndrome. Ann Neurol (1989) 1.01
Respiration-related afferents to parabrachial pontine regions. Respir Physiol Neurobiol (2004) 1.00
Assessment of the maturity-related brainstem functions reveals the heterogeneous phenotypes and facilitates clinical management of Rett syndrome. Brain Dev (2005) 0.99
Functional organization of respiratory neurones: a brief review of current questions and speculations. Exp Physiol (2004) 0.99
Role of pontile mechanisms in the neurogenesis of eupnea. Respir Physiol Neurobiol (2004) 0.98
Development of adaptive behaviour of the respiratory network: implications for the pontine Kolliker-Fuse nucleus. Respir Physiol Neurobiol (2004) 0.98
Multifunctional laryngeal motoneurons: an intracellular study in the cat. J Neurosci (1999) 0.97
Excitatory and inhibitory synaptic inputs shape the discharge pattern of pump neurons of the nucleus tractus solitarii in the rat. Exp Brain Res (1999) 0.94
Rett syndrome: biogenic amines and metabolites in postmortem brain. Pediatr Neurol (1990) 0.92
Serotonin transporter abnormality in the dorsal motor nucleus of the vagus in Rett syndrome: potential implications for clinical autonomic dysfunction. J Neuropathol Exp Neurol (2005) 0.91
Expression of N-methyl-D-aspartate receptor subunits in the rat parabrachial and Kölliker-Fuse nuclei and in selected pontomedullary brainstem nuclei. J Comp Neurol (1999) 0.90
Communication and oral-motor function in Rett syndrome. Dev Med Child Neurol (1990) 0.88
Eating difficulties in girls with Rett syndrome compared with other developmental disabilities. J Am Diet Assoc (2003) 0.88
Respiration patterns during feeding in Rett syndrome. Dev Med Child Neurol (1997) 0.84
Reduced expression of neuropeptides can be related to respiratory disturbances in Rett syndrome. Brain Dev (2001) 0.81
Factors influencing neural activity in parabrachial regions during cat vocalizations. Exp Brain Res (1992) 0.81
Commentary on eupneic breathing patterns and gasping. Respir Physiol Neurobiol (2003) 0.79
Rett syndrome: revised diagnostic criteria and nomenclature. Ann Neurol (2010) 4.03
Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study. Lancet Neurol (2012) 3.29
5-HT4(a) receptors avert opioid-induced breathing depression without loss of analgesia. Science (2003) 2.28
Folate receptor alpha defect causes cerebral folate transport deficiency: a treatable neurodegenerative disorder associated with disturbed myelin metabolism. Am J Hum Genet (2009) 2.07
Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease. Am J Hum Genet (2004) 2.03
Deletion of the mouse glycine transporter 2 results in a hyperekplexia phenotype and postnatal lethality. Neuron (2003) 1.97
Low BCR-ABL expression levels in hematopoietic precursor cells enable persistence of chronic myeloid leukemia under imatinib. Blood (2011) 1.81
Treatment of early onset multiple sclerosis with subcutaneous interferon beta-1a. Neurology (2005) 1.65
Pediatric multiple sclerosis: detection of clinically silent lesions by multimodal evoked potentials. J Pediatr (2006) 1.61
Lack of the Kir4.1 channel subunit abolishes K+ buffering properties of astrocytes in the ventral respiratory group: impact on extracellular K+ regulation. J Neurophysiol (2005) 1.57
Correction of respiratory disorders in a mouse model of Rett syndrome. Proc Natl Acad Sci U S A (2010) 1.54
X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects. Biochim Biophys Acta (2006) 1.51
T-cell homeostasis in pediatric multiple sclerosis: old cells in young patients. Neurology (2013) 1.51
Genotype-phenotype analysis in patients with giant axonal neuropathy (GAN). Neuromuscul Disord (2007) 1.49
Breathing disorders in Rett syndrome: progressive neurochemical dysfunction in the respiratory network after birth. Respir Physiol Neurobiol (2009) 1.46
Common infectious agents in multiple sclerosis: a case-control study in children. Mult Scler (2007) 1.44
Anti-myelin oligodendrocyte glycoprotein antibodies in pediatric patients with optic neuritis. Arch Neurol (2012) 1.43
Combined inhibition of cellular pathways as a future therapeutic option in fatal anaplastic thyroid cancer. Endocrine (2012) 1.42
Comparison of ATP-binding cassette transporter interactions with the tyrosine kinase inhibitors imatinib, nilotinib, and dasatinib. Drug Metab Dispos (2010) 1.41
Clinical and biochemical spectrum of D-bifunctional protein deficiency. Ann Neurol (2006) 1.41
Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model. J Mol Med (Berl) (2010) 1.40
Genotype and protein expression after bone marrow transplantation for adrenoleukodystrophy. Arch Neurol (2007) 1.38
Transcription factor IRF4 determines germinal center formation through follicular T-helper cell differentiation. Proc Natl Acad Sci U S A (2012) 1.32
5-HT7 receptor is coupled to G alpha subunits of heterotrimeric G12-protein to regulate gene transcription and neuronal morphology. J Neurosci (2005) 1.31
Large deletions of the MECP2 gene detected by gene dosage analysis in patients with Rett syndrome. Hum Mutat (2004) 1.28
RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infection. Nat Genet (2009) 1.22
Serotonin receptor 1A-modulated phosphorylation of glycine receptor α3 controls breathing in mice. J Clin Invest (2010) 1.21
Acute disseminated encephalomyelitis followed by recurrent or monophasic optic neuritis in pediatric patients. Mult Scler (2012) 1.19
The expanding clinical and genetic spectrum of ATP1A3-related disorders. Neurology (2014) 1.18
Mitochondrial organization and motility probed by two-photon microscopy in cultured mouse brainstem neurons. Exp Cell Res (2005) 1.16
Activation of XII motoneurons and premotor neurons during various oropharyngeal behaviors. Respir Physiol Neurobiol (2005) 1.16
Early breathing defects after moderate hypoxia or hypercapnia in a mouse model of Rett syndrome. Respir Physiol Neurobiol (2009) 1.11
Oral treatment with desipramine improves breathing and life span in Rett syndrome mouse model. Respir Physiol Neurobiol (2007) 1.11
Diversity of functional astroglial properties in the respiratory network. J Neurosci (2004) 1.09
Serotonin targets inhibitory synapses to induce modulation of network functions. Philos Trans R Soc Lond B Biol Sci (2009) 1.07
Differential modulation of I(h) by 5-HT receptors in mouse CA1 hippocampal neurons. Eur J Neurosci (2002) 1.07
Choroid plexus transcytosis and exosome shuttling deliver folate into brain parenchyma. Nat Commun (2013) 1.06
Molecular analysis of SUMF1 mutations: stability and residual activity of mutant formylglycine-generating enzyme determine disease severity in multiple sulfatase deficiency. Hum Mutat (2008) 1.06
Spontaneous central apneas occur in the C57BL/6J mouse strain. Respir Physiol Neurobiol (2007) 1.05
The role of serotonin in respiratory function and dysfunction. Respir Physiol Neurobiol (2010) 1.05
SUMF1 mutations affecting stability and activity of formylglycine generating enzyme predict clinical outcome in multiple sulfatase deficiency. Eur J Hum Genet (2011) 1.04
Pontine respiratory activity involved in inspiratory/expiratory phase transition. Philos Trans R Soc Lond B Biol Sci (2009) 1.04
rnaset2 mutant zebrafish model familial cystic leukoencephalopathy and reveal a role for RNase T2 in degrading ribosomal RNA. Proc Natl Acad Sci U S A (2011) 1.02
Cerebral involvement in axonal Charcot-Marie-Tooth neuropathy caused by mitofusin2 mutations. J Neurol (2008) 1.01
Heterodimerization of serotonin receptors 5-HT1A and 5-HT7 differentially regulates receptor signalling and trafficking. J Cell Sci (2012) 1.00
Rational diagnostic strategy for Zellweger syndrome spectrum patients. Eur J Hum Genet (2009) 1.00
Identification of twelve novel mutations in patients with classic and variant forms of maple syrup urine disease. Hum Mutat (2003) 1.00
5-HT7R/G12 signaling regulates neuronal morphology and function in an age-dependent manner. J Neurosci (2012) 0.99
Stimulation- and palmitoylation-dependent changes in oligomeric conformation of serotonin 5-HT1A receptors. Biochim Biophys Acta (2008) 0.99
Identification of ten novel mutations in patients with eIF2B-related disorders. Hum Mutat (2005) 0.99
Monitoring of donor chimerism in sorted CD34+ peripheral blood cells allows the sensitive detection of imminent relapse after allogeneic stem cell transplantation. Haematologica (2009) 0.98
Organelle interplay in peroxisomal disorders. Trends Mol Med (2009) 0.98
Clinical diagnosis, biochemical findings and MRI spectrum of peroxisomal disorders. Biochim Biophys Acta (2012) 0.98
Two different targeting signals direct human peroxisomal membrane protein 22 to peroxisomes. J Biol Chem (2001) 0.98
Microduplication of 3p26.3 in nonsyndromic intellectual disability indicates an important role of CHL1 for normal cognitive function. Neuropediatrics (2013) 0.98
Leukoencephalopathy with accumulated succinate is indicative of SDHAF1 related complex II deficiency. Orphanet J Rare Dis (2012) 0.96
8-OH-DPAT suppresses spontaneous central apneas in the C57BL/6J mouse strain. Respir Physiol Neurobiol (2007) 0.96
Localization of the mouse 5-hydroxytryptamine(1A) receptor in lipid microdomains depends on its palmitoylation and is involved in receptor-mediated signaling. Mol Pharmacol (2007) 0.95
Live cell FRET microscopy: homo- and heterodimerization of two human peroxisomal ABC transporters, the adrenoleukodystrophy protein (ALDP, ABCD1) and PMP70 (ABCD3). J Biol Chem (2007) 0.95
The 5-hydroxytryptamine(1A) receptor is stably palmitoylated, and acylation is critical for communication of receptor with Gi protein. J Biol Chem (2003) 0.95
Quantitative measurement of cAMP concentration using an exchange protein directly activated by a cAMP-based FRET-sensor. Biophys J (2008) 0.94
Natalizumab use in pediatric multiple sclerosis. Arch Neurol (2008) 0.94
Extensive acute axonal damage in pediatric multiple sclerosis lesions. Ann Neurol (2015) 0.94
Emergence of brain-derived neurotrophic factor-induced postsynaptic potentiation of NMDA currents during the postnatal maturation of the Kolliker-Fuse nucleus of rat. J Physiol (2008) 0.93
Suppression of nonsense mutations in Rett syndrome by aminoglycoside antibiotics. Pediatr Res (2009) 0.93
Peroxisome formation requires the endoplasmic reticulum channel protein Sec61. Traffic (2012) 0.93
Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patients. Hum Mutat (2006) 0.93
Palmitoylation of the 5-hydroxytryptamine4a receptor regulates receptor phosphorylation, desensitization, and beta-arrestin-mediated endocytosis. Mol Pharmacol (2005) 0.92
Developmental changes in the BDNF-induced modulation of inhibitory synaptic transmission in the Kölliker-Fuse nucleus of rat. Eur J Neurosci (2007) 0.92
Peroxisomes are juxtaposed to strategic sites on mitochondria. Mol Biosyst (2014) 0.92
Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin. Am J Hum Genet (2012) 0.91
Developmental changes in brain-derived neurotrophic factor-mediated modulations of synaptic activities in the pontine Kölliker-Fuse nucleus of the rat. J Physiol (2007) 0.91
Imaging of respiratory-related population activity with single-cell resolution. Am J Physiol Cell Physiol (2006) 0.91
Maintenance of eupnea of in situ and in vivo rats following riluzole: a blocker of persistent sodium channels. Respir Physiol Neurobiol (2006) 0.91
The dual role of the orexin/hypocretin system in modulating wakefulness and respiratory drive. Curr Opin Pulm Med (2008) 0.91
Structure of tripeptidyl-peptidase I provides insight into the molecular basis of late infantile neuronal ceroid lipofuscinosis. J Biol Chem (2008) 0.90
The 5-hydroxytryptamine(4a) receptor is palmitoylated at two different sites, and acylation is critically involved in regulation of receptor constitutive activity. J Biol Chem (2001) 0.90
Mesenchymal stem cells obtained after bone marrow transplantation or peripheral blood stem cell transplantation originate from host tissue. Ann Hematol (2005) 0.90
Pelizaeus-Merzbacher-like disease is caused not only by a loss of connexin47 function but also by a hemichannel dysfunction. Eur J Hum Genet (2010) 0.90
Disturbances of breathing in Rett syndrome: results from patients and animal models. Adv Exp Med Biol (2008) 0.90
Serial proton MR spectroscopy and diffusion tensor imaging in infantile Balo's concentric sclerosis. Neuroradiology (2008) 0.89
Multimodal therapy for vertebral involvement of systemic mastocytosis. Spine (Phila Pa 1976) (2009) 0.89