Published in J Neurosci Res on September 01, 2000
The NF1 tumor suppressor critically regulates TSC2 and mTOR. Proc Natl Acad Sci U S A (2005) 3.49
Soluble AXL: a possible circulating biomarker for neurofibromatosis type 1 related tumor burden. PLoS One (2014) 1.39
Molecular dissection of isolated disease features in mosaic neurofibromatosis type 1. Am J Hum Genet (2007) 1.33
Class III beta-tubulin is a component of the mitotic spindle in multiple cell types. J Histochem Cytochem (2008) 1.09
The development of cutaneous neurofibromas. Am J Pathol (2011) 1.04
EGFR-STAT3 signaling promotes formation of malignant peripheral nerve sheath tumors. Oncogene (2013) 0.94
Exploring the somatic NF1 mutational spectrum associated with NF1 cutaneous neurofibromas. Eur J Hum Genet (2011) 0.86
CK2 blockade causes MPNST cell apoptosis and promotes degradation of β-catenin. Oncotarget (2016) 0.79
Pathogenesis of vestibular schwannoma in ring chromosome 22. BMC Med Genet (2009) 0.79
Immortalization of human normal and NF1 neurofibroma Schwann cells. Lab Invest (2016) 0.76
Partial Blindness to Submicron Topography in NF1 Haploinsufficient Cultured Fibroblasts Indicates a New Function of Neurofibromin in Regulation of Mechanosensoric. Mol Syndromol (2012) 0.75
The role of nerve microenvironment for neurofibroma development. Oncotarget (2016) 0.75
Prognostic effect of weight loss prior to chemotherapy in cancer patients. Eastern Cooperative Oncology Group. Am J Med (1980) 6.12
End-of-life decisions in neonatal intensive care: physicians' self-reported practices in seven European countries. EURONIC Study Group. Lancet (2000) 4.01
The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication. Nat Genet (1992) 2.18
Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS. Neurology (2004) 2.14
Schwann cells harbor the somatic NF1 mutation in neurofibromas: evidence of two different Schwann cell subpopulations. Hum Mol Genet (2000) 1.84
Lithium in patients with amyotrophic lateral sclerosis (LiCALS): a phase 3 multicentre, randomised, double-blind, placebo-controlled trial. Lancet Neurol (2013) 1.65
Nerve injury, axonal degeneration and neural regeneration: basic insights. Brain Pathol (1999) 1.63
The clinical features of homozygous alpha 2(I) collagen deficient osteogenesis imperfecta. J Med Genet (1984) 1.56
Single-void urine samples can be used to estimate quantitative microalbuminuria. Diabetes Care (1987) 1.54
Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A. Nat Genet (1992) 1.43
Randomized comparison of three adriamycin regimens for metastatic soft tissue sarcomas. J Clin Oncol (1987) 1.42
Hearing loss in facioscapulohumeral dystrophy. Eur J Pediatr (1986) 1.28
Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophy. Hum Mol Genet (2000) 1.26
FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients. J Med Genet (2004) 1.24
Cloning and characterization of SDF-1gamma, a novel SDF-1 chemokine transcript with developmentally regulated expression in the nervous system. Eur J Neurosci (2000) 1.23
A specific 37,000-dalton protein that accumulates in regenerating but not in nonregenerating mammalian nerves. Science (1985) 1.18
Magnetic stimulation of motor cortex and nerve roots in children. Maturation of cortico-motoneuronal projections. Electroencephalogr Clin Neurophysiol (1991) 1.15
Retroviral-mediated gene transfer of the peripheral myelin protein PMP22 in Schwann cells: modulation of cell growth. EMBO J (1995) 1.14
Intracranial germ cell tumors: a comprehensive update of the European data. Neuropediatrics (1994) 1.14
Isolation and characterization of Schwann cells from neurofibromatosis type 2 patients. Neurobiol Dis (1998) 1.12
The syndrome of autosomal recessive pontocerebellar hypoplasia, microcephaly, and extrapyramidal dyskinesia (pontocerebellar hypoplasia type 2): compiled data from 10 pedigrees. Neurology (1995) 1.12
Adhesive properties of proteolipid protein are responsible for the compaction of CNS myelin sheaths. J Neurosci (1995) 1.10
Axon-regulated expression of a Schwann cell transcript that is homologous to a 'growth arrest-specific' gene. EMBO J (1991) 1.10
The CNS lesion scar: new vistas on an old regeneration barrier. Cell Tissue Res (1998) 1.09
Tetracycline-inducible transgene expression mediated by a single AAV vector. Gene Ther (2003) 1.08
Ataxia-deafness-retardation syndrome in three sisters. Neuropediatrics (1987) 1.07
Phase II trial of ifosfamide with mesna in previously treated metastatic sarcoma. Cancer Treat Rep (1985) 1.07
Goldenhar, Möbius and hypoglossia-hypodactyly anomalies in a patient: syndrome or association? Eur J Pediatr (1996) 1.06
Overloaded endoplasmic reticulum-Golgi compartments, a possible pathomechanism of peripheral neuropathies caused by mutations of the peripheral myelin protein PMP22. J Neurosci (1998) 1.06
Papillon-Lefèvre syndrome--successful treatment with a combination of retinoid and concurrent systematic periodontal therapy: case reports. Quintessence Int (1995) 1.06
Rho-dependent regulation of cell spreading by the tetraspan membrane protein Gas3/PMP22. Mol Biol Cell (1999) 1.05
Peripheral myelin protein-22 is expressed in rat and mouse brain and spinal cord motoneurons. Eur J Neurosci (1995) 1.05
Glycosaminoglycan-binding properties and secondary structure of the C-terminus of netrin-1. Biochem Biophys Res Commun (2000) 1.04
Transduction of wild-type merlin into human schwannoma cells decreases schwannoma cell growth and induces apoptosis. Hum Mol Genet (2002) 1.04
Mallory body-like inclusions in a hereditary congenital neuromuscular disease. Muscle Nerve (1983) 1.04
Multiple intracranial juvenile xanthogranulomas. Case report. J Neurosurg (2000) 1.03
On the ultrastructural diversity and essence of residual bodies in neuronal ceroid-lipofuscinosis. Mech Ageing Dev (1979) 1.02
Amplification of the MET gene in glioma. Genes Chromosomes Cancer (1995) 1.01
CT and MRI of congenital sinonasal ossifying fibroma. Neuroradiology (1999) 1.01
Mitotic recombination effects homozygosity for NF1 germline mutations in neurofibromas. Nat Genet (2001) 1.00
A comparison of adriamycin versus vincristine and adriamycin, and cyclophosphamide versus vincristine, actinomycin-D, and cyclophosphamide for advanced sarcoma. Cancer (1982) 1.00
Gianotti-Crosti syndrome associated with Epstein-Barr virus infection. Pediatr Dermatol (1997) 0.98
[Ring chromosome 8 (46,XY, 8 r) in a boy with debility (author's transl)]. Klin Padiatr (1973) 0.98
A study of eye movements in sleeping newborn infants. Brain Res (1967) 0.97
Experimental strategies to promote axonal regeneration after traumatic central nervous system injury. Prog Neurobiol (1998) 0.97
Expression of specific sheath cell proteins during peripheral nerve growth and regeneration in mammals. J Cell Biol (1986) 0.97
Emery-Dreifuss muscular dystrophy: disease spectrum and differential diagnosis. Neuropediatrics (1988) 0.96
Differential expression of the small chondroitin/dermatan sulfate proteoglycans decorin and biglycan after injury of the adult rat brain. Brain Res (1995) 0.96
Megalencephaly, mega corpus callosum, and complete lack of motor development: a previously undescribed syndrome. Am J Med Genet (1998) 0.95
Fibre type disproportion in the rigid spine syndrome. Neuropadiatrie (1977) 0.95
Exteroceptive and tendon reflexes in various behavioural states in the newborn infant. Biol Neonat (1967) 0.95
Peripheral myelin protein 22 and protein zero: a novel association in peripheral nervous system myelin. J Neurosci (1999) 0.95
Mutation-dependent alteration in cellular distribution of peripheral myelin protein 22 in nerve biopsies from Charcot-Marie-Tooth type 1A. Brain (2000) 0.94
Fetal CNS damage after exposure to maternal trauma during pregnancy. Acta Paediatr (1996) 0.94
A reliable method to reduce collagen scar formation in the lesioned rat spinal cord. J Neurosci Methods (2001) 0.94
Influence of elevated expression of rat wild-type PMP22 and its mutant PMP22Trembler on cell growth of NIH3T3 fibroblasts. Cell Tissue Res (1997) 0.94
Increased dopaminergic neurotransmission in therapy-naïve asymptomatic HIV patients is not associated with adaptive changes at the dopaminergic synapses. J Neural Transm (Vienna) (2010) 0.94
Regeneration-associated high level expression of apolipoprotein D mRNA in endoneurial fibroblasts of peripheral nerve. EMBO J (1990) 0.93
Differentially expressed genes after peripheral nerve injury. J Neurosci Res (1995) 0.93
A neurotrophic factor (NTF) released from primary glial cultures supports survival and fiber outgrowth of cultured hippocampal neurons. J Neurosci Res (1982) 0.93
Molecular mechanisms of cellular interactions in peripheral nerve regeneration. Curr Opin Neurol (2001) 0.93
Macrophages in the peripheral nervous system and astroglia in the central nervous system of rat commonly express apolipoprotein E during development but differ in their response to injury. Neurosci Lett (1986) 0.92
Impaired intercellular adhesion and immature adherens junctions in merlin-deficient human primary schwannoma cells. Glia (2008) 0.92
Congenital myopathy with cytoplasmic bodies. Neuropediatrics (1981) 0.92
Occurrence and characterization of peripheral nerve involvement in neurofibromatosis type 2. Brain (2002) 0.91
High-resolution multipinhole single-photon-emission computed tomography in experimental and human arthritis. Arthritis Rheum (2006) 0.91
Inhibition of collagen IV deposition promotes regeneration of injured CNS axons. Eur J Neurosci (1999) 0.90
A second alternative transcript of the gap junction gene connexin32 is expressed in murine Schwann cells and modulated in injured sciatic nerve. Eur J Cell Biol (1996) 0.90
A functional association between merlin and HEI10, a cell cycle regulator. Oncogene (2006) 0.90
Differential expression of two mRNA species indicates a dual function of peripheral myelin protein PMP22 in cell growth and myelination. J Neurosci Res (1994) 0.90
Reflexes and their relationship to behavioural state in the newborn. Acta Paediatr Scand (1968) 0.89
Amplified met gene linked to double minutes in human glioblastoma. Eur J Cancer (1993) 0.88
Paraneoplastic limbic encephalitis in two teenage girls. Neuropediatrics (1998) 0.88
The collagenous lesion scar--an obstacle for axonal regeneration in brain and spinal cord injury. Restor Neurol Neurosci (2001) 0.88
Sonographic tissue characterisation in thyroid gland diagnosis. A correlation between sonography and histology. Klin Wochenschr (1985) 0.88
Studies on the effects of altered PMP22 expression during myelination in vitro. J Neurosci Res (1997) 0.87
Proteins of peripheral myelin are associated with glycosphingolipid/cholesterol-enriched membranes. J Neurosci Res (2002) 0.87
Magnetoelectrical stimulation of motor cortex in children with motor disturbances. Electroencephalogr Clin Neurophysiol (1992) 0.87
GABA and glutamate receptor development of cultured neurons from rat hippocampus, septal region, and neocortex. Synapse (1990) 0.86
Peripheral myelin protein-22 expression in Charcot-Marie-Tooth disease type 1a sural nerve biopsies. J Neurosci Res (1994) 0.86
Aplasia cutis congenita and enlarged parietal foramina (Catlin marks) in a family. Acta Paediatr (1995) 0.86
Spontaneous activity and recurrent inhibition in cultured hippocampal networks. Synapse (1993) 0.85
Polygraphic sleep study in craniopagus twins (where is the sleep transmitter?). J Neurol Neurosurg Psychiatry (1972) 0.85
Coexpression of PMP22 gene with MBP and P0 during de novo myelination and nerve repair. Glia (1993) 0.85
A morphological study of non-Japanese congenital muscular dystrophy associated with cerebral lesions. Brain Dev (1983) 0.85
A form of congenital muscular dystrophy. Brain Dev (1980) 0.85
MRI abnormalities in neurofibromatosis type 1 (NF1): a study of men and mice. Brain Dev (1999) 0.84
Basal membrane-depleted scar in lesioned CNS: characteristics and relationships with regenerating axons. Neuroscience (1999) 0.84
Morphologic and chemical biopsy findings in mucolipidosis IV. Clin Neuropathol (1982) 0.84
Pathogenesis of Charcot-Marie-Tooth 1A (CMT1A) neuropathy. Trends Neurosci (1998) 0.84
Changes in iron-regulatory gene expression occur in human cell culture models of Parkinson's disease. Neurochem Int (2011) 0.84
Insulin-like growth factor-binding protein-1 (IGFBP-1) regulates human schwannoma proliferation, adhesion and survival. Oncogene (2011) 0.84
The ontogeny of sensory perception in preterm infants. Eur J Pediatr (1977) 0.84
Somato-sensory evoked responses in newborn infants. Electroencephalogr Clin Neurophysiol (1968) 0.84