Published in Gene on February 07, 2001
Quantitative proteomic identification of MAZ as a transcriptional regulator of muscle-specific genes in skeletal and cardiac myocytes. Mol Cell Biol (2008) 1.01
Glutamate receptor activation evokes calpain-mediated degradation of Sp3 and Sp4, the prominent Sp-family transcription factors in neurons. J Neurochem (2007) 0.96
The transcription factor SP4 is reduced in postmortem cerebellum of bipolar disorder subjects: control by depolarization and lithium. Bipolar Disord (2011) 0.94
Specificity protein (Sp) transcription factors Sp1, Sp3 and Sp4 are non-oncogene addiction genes in cancer cells. Oncotarget (2016) 0.89
Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE). Birth Defects Res A Clin Mol Teratol (2012) 0.80
Genetic polymorphisms in the thioredoxin 2 (TXN2) gene and risk for spina bifida. Am J Med Genet A (2009) 0.78
Overexpression and clinical significance of MYC-associated zinc finger protein in pancreatic carcinoma. Onco Targets Ther (2016) 0.75
MYC associated zinc finger protein promotes the invasion and metastasis of hepatocellular carcinoma by inducing epithelial mesenchymal transition. Oncotarget (2016) 0.75
The Nuclear Orphan Receptor NR4A1 Regulates β1-Integrin Expression in Pancreatic and Colon Cancer Cells and Can Be Targeted by NR4A1 Antagonists. Mol Carcinog (2017) 0.75
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy. Nature (1998) 3.86
A tale of three fingers: the family of mammalian Sp/XKLF transcription factors. Nucleic Acids Res (1999) 3.68
Serum anti-GQ1b IgG antibody is associated with ophthalmoplegia in Miller Fisher syndrome and Guillain-Barré syndrome: clinical and immunohistochemical studies. Neurology (1993) 3.31
Sp1-mediated transcriptional activation is repressed by Sp3. EMBO J (1994) 3.27
Serum IgG antibody to ganglioside GQ1b is a possible marker of Miller Fisher syndrome. Ann Neurol (1992) 3.04
Cloning by recognition site screening of two novel GT box binding proteins: a family of Sp1 related genes. Nucleic Acids Res (1992) 2.89
Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve alpha-dystroglycan. The role of a novel O-mannosyl-type oligosaccharide in the binding of alpha-dystroglycan with laminin. J Biol Chem (1997) 2.38
Benefit of IVIG for long-standing ataxic sensory neuronopathy with Sjögren's syndrome. IV immunoglobulin. Neurology (2003) 2.37
SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein. Hum Mol Genet (2001) 2.30
Distinct roles of the co-activators p300 and CBP in retinoic-acid-induced F9-cell differentiation. Nature (1998) 2.25
Double-blind and placebo-controlled study of lithium for adolescent bipolar disorders with secondary substance dependency. J Am Acad Child Adolesc Psychiatry (1998) 2.16
HIP1, a human homologue of S. cerevisiae Sla2p, interacts with membrane-associated huntingtin in the brain. Nat Genet (1997) 2.09
Preferential activation of different I waves by transcranial magnetic stimulation with a figure-of-eight-shaped coil. Exp Brain Res (1997) 2.03
Paired-pulse magnetic stimulation of the human motor cortex: differences among I waves. J Physiol (1998) 1.96
Expanded polyglutamine stretches interact with TAFII130, interfering with CREB-dependent transcription. Nat Genet (2000) 1.92
ATF-2 has intrinsic histone acetyltransferase activity which is modulated by phosphorylation. Nature (2000) 1.89
Post mortem changes and regional distribution of substance P in the rat and mouse nervous system. Brain Res (1976) 1.82
Transcription factor Sp3 is essential for post-natal survival and late tooth development. EMBO J (2000) 1.77
Ganglioside composition of the human cranial nerves, with special reference to pathophysiology of Miller Fisher syndrome. Brain Res (1997) 1.76
An inhibitor domain in Sp3 regulates its glutamine-rich activation domains. EMBO J (1996) 1.68
Reduction of GluR2 RNA editing, a molecular change that increases calcium influx through AMPA receptors, selective in the spinal ventral gray of patients with amyotrophic lateral sclerosis. Ann Neurol (1999) 1.67
Different members of the Sp1 multigene family exert opposite transcriptional regulation of the long terminal repeat of HIV-1. Nucleic Acids Res (1994) 1.65
The distribution of substance P immunoreactive fibers in the rat central nervous system. J Comp Neurol (1978) 1.63
Magnetic stimulation over the cerebellum in humans. Ann Neurol (1995) 1.61
Specificity of signaling by STAT1 depends on SH2 and C-terminal domains that regulate Ser727 phosphorylation, differentially affecting specific target gene expression. EMBO J (2001) 1.59
Further analysis of interleukin-2 receptor subunit expression on the different human peripheral blood mononuclear cell subsets. Blood (1998) 1.56
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The uteroglobin gene region: hormonal regulation, repetitive elements and complete nucleotide sequence of the gene. Nucleic Acids Res (1983) 1.52
Endothelin: a novel peptide in the posterior pituitary system. Science (1990) 1.51
Anti-GQ1b antibody as a factor predictive of mechanical ventilation in Guillain-Barré syndrome. Neurology (2004) 1.50
p300 and ATF-2 are components of the DRF complex, which regulates retinoic acid- and E1A-mediated transcription of the c-jun gene in F9 cells. Genes Dev (1998) 1.50
Elevated serum fibroblast growth factor 21 is associated with hypertension in community-dwelling adults. J Hum Hypertens (2012) 1.49
Transcription factor Sp3 is regulated by acetylation. Nucleic Acids Res (2001) 1.47
Local modulation by 11beta-hydroxysteroid dehydrogenase of glucocorticoid effects on the activity of 15-hydroxyprostaglandin dehydrogenase in human chorion and placental trophoblast cells. J Clin Endocrinol Metab (1999) 1.44
Screening for imprinted genes by allelic message display: identification of a paternally expressed gene impact on mouse chromosome 18. Proc Natl Acad Sci U S A (1997) 1.43
Relationship of 25-hydroxyvitamin D with all-cause and cardiovascular disease mortality in older community-dwelling adults. Eur J Clin Nutr (2009) 1.42
N-acetylgalactosaminyl GD1a is a target molecule for serum antibody in Guillain-Barré syndrome. Ann Neurol (1994) 1.41
Intracortical inhibition of the motor cortex is normal in chorea. J Neurol Neurosurg Psychiatry (1999) 1.41
Simultaneous detection of RNA and protein by in situ hybridization and immunological staining. J Histochem Cytochem (2001) 1.38
Ataxin-3, the MJD1 gene product, interacts with the two human homologs of yeast DNA repair protein RAD23, HHR23A and HHR23B. Hum Mol Genet (2000) 1.38
Cognitive performance in a high-functioning community-dwelling elderly population. J Gerontol (1993) 1.35
Functional analyses of the transcription factor Sp4 reveal properties distinct from Sp1 and Sp3. J Biol Chem (1995) 1.34
Phosphorylation of the adenovirus E1A-associated 300 kDa protein in response to retinoic acid and E1A during the differentiation of F9 cells. EMBO J (1995) 1.33
Percutaneous closure of perimembranous ventricular septal defects with the eccentric Amplatzer device: multicenter follow-up study. Pediatr Cardiol (2005) 1.33
Hypothetical versus real willingness to pay in the health care sector: results from a field experiment. J Health Econ (2001) 1.30
Impaired ossification in mice lacking the transcription factor Sp3. Mech Dev (2001) 1.29
Substance P: depletion in the dorsal horn of rat spinal cord after section of the peripheral processes of primary sensory neurons. Brain Res (1979) 1.28
TOK-1, a novel p21Cip1-binding protein that cooperatively enhances p21-dependent inhibitory activity toward CDK2 kinase. J Biol Chem (2000) 1.28
High Sp1/Sp3 ratios in epithelial cells during epithelial differentiation and cellular transformation correlate with the activation of the HPV-16 promoter. Virology (1996) 1.27
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Interhemispheric facilitation of the hand motor area in humans. J Physiol (2001) 1.26
Differential transcriptional regulation of c-myc promoter through the same DNA binding sites targeted by Sp1-like proteins. Oncogene (1995) 1.26
Low dietary diversity is a predictor of child stunting in rural Bangladesh. Eur J Clin Nutr (2010) 1.25
Neurobehavioral and neurophysiological observations in six year old children with low lead levels in East and West Germany. Neurotoxicology (1994) 1.24
Release and metabolism of substance P in rat hypothalamus. Nature (1976) 1.24
Abnormal gene product identified in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) brain. Nat Genet (1995) 1.23
Ipsilateral cortico-cortical inhibition of the motor cortex in various neurological disorders. J Neurol Sci (1996) 1.22
Requirement of expression of P-glycoprotein on human natural killer leukemia cells for cell-mediated cytotoxicity. Biochem Pharmacol (1998) 1.22
PQBP-1, a novel polyglutamine tract-binding protein, inhibits transcription activation by Brn-2 and affects cell survival. Hum Mol Genet (1999) 1.21
Sp1 trans-activation of cell cycle regulated promoters is selectively repressed by Sp3. Biochemistry (1995) 1.21
c-myc activation renders proliferation of Epstein-Barr virus (EBV)-transformed cells independent of EBV nuclear antigen 2 and latent membrane protein 1. Proc Natl Acad Sci U S A (1996) 1.20
Formic acid dissolves aggregates of an N-terminal huntingtin fragment containing an expanded polyglutamine tract: applying to quantification of protein components of the aggregates. Biochem Biophys Res Commun (2000) 1.20
Members of the Sp transcription factor family control transcription from the uteroglobin promoter. J Biol Chem (1995) 1.18
Identification of mouse Jun dimerization protein 2 as a novel repressor of ATF-2. FEBS Lett (2001) 1.18
APP717 missense mutation affects the ratio of amyloid beta protein species (A beta 1-42/43 and a beta 1-40) in familial Alzheimer's disease brain. J Biol Chem (1994) 1.18
Binding of the ubiquitous cellular transcription factors Sp1 and Sp3 to the ZI domains in the Epstein-Barr virus lytic switch BZLF1 gene promoter. Virology (1997) 1.18
Pulmonary hypertension after operations for congenital heart disease: analysis of risk factors and management. J Thorac Cardiovasc Surg (1996) 1.17
Human huntingtin derived from YAC transgenes compensates for loss of murine huntingtin by rescue of the embryonic lethal phenotype. Hum Mol Genet (1996) 1.17
Topographical localization of the Onuf's nuclear neurons innervating the rectal and vesical striated sphincter muscles: a retrograde fluorescent double labeling in cat and dog. Neurosci Lett (1980) 1.17
Transcriptional regulation of the CLC-K1 promoter by myc-associated zinc finger protein and kidney-enriched Krüppel-like factor, a novel zinc finger repressor. Mol Cell Biol (2000) 1.17
Shortening of simple reaction time by peripheral electrical and submotor-threshold magnetic cortical stimulation. Exp Brain Res (1997) 1.17
Serum antibody against a peripheral nerve myelin ganglioside, LM1, in Guillain-Barré syndrome. J Neurol Sci (1999) 1.15
Characterization of dp6troglycan-laminin interaction in peripheral nerve. J Neurochem (1996) 1.15
Surgical management of complete atrioventricular septal defects. A twenty-year experience. J Thorac Cardiovasc Surg (1995) 1.15
1.55 µm InAs/GaAs quantum dots and high repetition rate quantum dot SESAM mode-locked laser. Sci Rep (2012) 1.15
Deregulation of the proto-oncogene c-myc through t(8;22) translocation in Burkitt's lymphoma. Oncogene (1999) 1.15
Mechanism of gene regulation by steroid hormones. J Steroid Biochem (1986) 1.14
Identification of the gene for a novel liver-related putative tumor suppressor at a high-frequency loss of heterozygosity region of chromosome 8p23 in human hepatocellular carcinoma. Hepatology (2000) 1.14
Optimization of the medium composition for production of mycelial biomass and exo-polymer by Grifola frondosa GF9801 using response surface methodology. Bioresour Technol (2005) 1.14
Ancestral differences in the distribution of the delta 2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington disease. Hum Mol Genet (1995) 1.13
Abundant expression and cytoplasmic aggregations of [alpha]1A voltage-dependent calcium channel protein associated with neurodegeneration in spinocerebellar ataxia type 6. Hum Mol Genet (1999) 1.12
Expression of transforming growth factor-beta 1 and its relation to endomysial fibrosis in progressive muscular dystrophy. Am J Pathol (1994) 1.12
Autophagy prevents irradiation injury and maintains stemness through decreasing ROS generation in mesenchymal stem cells. Cell Death Dis (2013) 1.12
Decrease of a peptide in the cat spinal cord after upper cervical transection. Neurosci Lett (1981) 1.12
Evidence for a new variant CYP2D6 allele CYP2D6J in a Japanese population associated with lower in vivo rates of sparteine metabolism. Pharmacogenetics (1993) 1.12
The Stat3/5 locus encodes novel endoplasmic reticulum and helicase-like proteins that are preferentially expressed in normal and neoplastic mammary tissue. Genomics (2001) 1.12
Distal myopathy with rimmed vacuoles: novel mutations in the GNE gene. Neurology (2002) 1.11
JNK activation is associated with intracellular beta-amyloid accumulation. Brain Res Mol Brain Res (2000) 1.11
Magnetic stimulation of corticospinal pathways at the foramen magnum level in humans. Ann Neurol (1994) 1.11
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Organization of apatite crystals in human woven bone. Bone (2003) 1.10
Anti-GQ1b IgG antibody is associated with ataxia as well as ophthalmoplegia. Muscle Nerve (1999) 1.10
Polymorphisms of ACE2 gene are associated with essential hypertension and antihypertensive effects of Captopril in women. Clin Pharmacol Ther (2007) 1.10
Facilitatory effect of tonic voluntary contraction on responses to motor cortex stimulation. Electroencephalogr Clin Neurophysiol (1995) 1.08
Caveolin-3 upregulation activates beta-secretase-mediated cleavage of the amyloid precursor protein in Alzheimer's disease. J Neurosci (1999) 1.08
alpha-Synuclein affects the MAPK pathway and accelerates cell death. J Biol Chem (2001) 1.08
Complex phenotype of mice homozygous for a null mutation in the Sp4 transcription factor gene. Genes Cells (2001) 1.08
Endothelin localizes in the dorsal horn and acts on the spinal neurones: possible involvement of dihydropyridine-sensitive calcium channels and substance P release. Neurosci Lett (1989) 1.07